Variant report

Variant	nsv900442
Chromosome Location	chr13:69223307-69387266
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:61)
Chromatin interactive
region (count:50)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:69282536-69282692	K562	blood:	n/a	n/a
2	ARID3A	chr13:69384973-69385035	HepG2	liver:	n/a	n/a
3	ATF2	chr13:69287464-69287949	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:69266329-69266484	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:69265322-69265590	K562	blood:	n/a	n/a
6	BACH1	chr13:69271864-69271997	K562	blood:	n/a	n/a
7	BACH1	chr13:69318094-69318108	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr13:69240994-69241236	GM12878	blood:	n/a	n/a
9	BCL11A	chr13:69287549-69287790	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr13:69287512-69287888	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr13:69288465-69288682	H1-hESC	embryonic stem cell:	n/a	chr13:69288578-69288587
12	BHLHE40	chr13:69282521-69282769	K562	blood:	n/a	n/a
13	BRCA1	chr13:69358761-69358834	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr13:69282455-69282835	K562	blood:	n/a	n/a
15	CBX3	chr13:69271695-69271977	K562	blood:	n/a	n/a
16	CCNT2	chr13:69271798-69271998	K562	blood:	n/a	n/a
17	CCNT2	chr13:69282518-69282742	K562	blood:	n/a	n/a
18	CEBPB	chr13:69282521-69282816	K562	blood:	n/a	n/a
19	CEBPB	chr13:69295467-69295806	K562	blood:	n/a	n/a
20	CEBPB	chr13:69295475-69295749	HepG2	liver:	n/a	n/a
21	CEBPB	chr13:69295505-69295707	A549	lung:	n/a	n/a
22	CEBPB	chr13:69334695-69335004	HepG2	liver:	n/a	chr13:69334825-69334834 chr13:69334823-69334834
23	CEBPB	chr13:69384656-69384934	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr13:69228532-69228846	IMR90	lung:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
25	CEBPB	chr13:69228553-69228762	A549	lung:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
26	CEBPB	chr13:69287513-69287988	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr13:69334704-69334988	A549	lung:	n/a	chr13:69334825-69334834 chr13:69334823-69334834
28	CEBPB	chr13:69268765-69268935	A549	lung:	n/a	n/a
29	CEBPB	chr13:69268809-69269015	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr13:69268752-69269047	HepG2	liver:	n/a	n/a
31	CEBPB	chr13:69384657-69384933	K562	blood:	n/a	n/a
32	CEBPB	chr13:69268802-69269108	K562	blood:	n/a	n/a
33	CEBPB	chr13:69334660-69334974	IMR90	lung:	n/a	chr13:69334825-69334834 chr13:69334823-69334834
34	CEBPB	chr13:69291799-69292137	HepG2	liver:	n/a	n/a
35	CEBPB	chr13:69228540-69228837	K562	blood:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
36	CEBPB	chr13:69334712-69334967	K562	blood:	n/a	chr13:69334825-69334834 chr13:69334823-69334834
37	CEBPB	chr13:69335928-69336158	HepG2	liver:	n/a	chr13:69336008-69336021 chr13:69336010-69336019 chr13:69336010-69336019 chr13:69336010-69336019 chr13:69336008-69336021 chr13:69336009-69336020 chr13:69336008-69336019 chr13:69336010-69336019
38	CEBPB	chr13:69228505-69228846	HepG2	liver:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
39	CEBPB	chr13:69310378-69310560	HepG2	liver:	n/a	chr13:69310425-69310436
40	CEBPB	chr13:69282532-69282841	K562	blood:	n/a	n/a
41	CEBPB	chr13:69228574-69228763	H1-hESC	embryonic stem cell:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
42	CEBPB	chr13:69223398-69223677	Hela-S3	cervix:	n/a	chr13:69223512-69223524
43	CEBPB	chr13:69323960-69324263	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr13:69334713-69334884	H1-hESC	embryonic stem cell:	n/a	chr13:69334825-69334834 chr13:69334823-69334834
45	CEBPB	chr13:69295493-69295769	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr13:69299808-69299984	K562	blood:	n/a	n/a
47	CEBPB	chr13:69268761-69269087	IMR90	lung:	n/a	n/a
48	CHD1	chr13:69287835-69288438	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr13:69282486-69282641	K562	blood:	n/a	n/a
50	CTCF	chr13:69384900-69385050	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:69261665-69261715	AoSMC	blood vessel:	n/a
2	chr13:69261665-69261715	HEEpiC	esophagus:	n/a
3	chr13:69261665-69261715	NHDF-neo	bronchial:	n/a
4	chr13:69261665-69261715	PFSK-1	brain:	n/a
5	chr13:69261665-69261715	AG09309	skin:	n/a
6	chr13:69261665-69261715	T-47D	breast:	n/a
7	chr13:69261665-69261715	A549	lung:	n/a
8	chr13:69261665-69261715	AG04449	skin:	fetal
9	chr13:69261665-69261715	GM12891	blood:	n/a
10	chr13:69261665-69261715	SAEC	small airway:	n/a
11	chr13:69261665-69261715	HL-60	blood:	n/a
12	chr13:69261665-69261715	HCF	heart:	n/a
13	chr13:69261665-69261715	HIPEpiC	eye:	n/a
14	chr13:69261665-69261715	HAEpiC	amniotic membrane:	n/a
15	chr13:69261665-69261715	GM19239	blood:	n/a
16	chr13:69261665-69261715	NB4	blood:	n/a
17	chr13:69261665-69261715	GM06990	blood:	n/a
18	chr13:69261665-69261715	ProgFib	skin:	n/a
19	chr13:69261665-69261715	AG09319	gingival:	n/a
20	chr13:69261665-69261715	H1-hESC	embryonic stem cell:	embryo
21	chr13:69261665-69261715	AG10803	skin:	n/a
22	chr13:69261665-69261715	HEK293	kidney:	embryo
23	chr13:69261665-69261715	SK-N-SH_RA	brain:	n/a
24	chr13:69261665-69261715	HNPCEpiC	eye:	n/a
25	chr13:69261665-69261715	HRPEpiC	eye:	n/a
26	chr13:69261665-69261715	GM12878	blood:	n/a
27	chr13:69261665-69261715	MCF-7	breast:	n/a
28	chr13:69261665-69261715	MCF10A-Er-Src	breast:	n/a
29	chr13:69261665-69261715	LNCaP	prostate:	n/a
30	chr13:69261665-69261715	RPTEC	kidney:	n/a
31	chr13:69261665-69261715	HCM	heart:	n/a
32	chr13:69261665-69261715	HUVEC	blood vessel:	n/a
33	chr13:69261665-69261715	HCT-116	colon:	n/a
34	chr13:69261665-69261715	GM12892	blood:	n/a
35	chr13:69261665-69261715	SK-N-SH	brain:	n/a
36	chr13:69261665-69261715	SK-N-MC	brain:	n/a
37	chr13:69261665-69261715	HRE	kidney:	n/a
38	chr13:69261665-69261715	NH-A	brain:	n/a
39	chr13:69261665-69261715	NHBE	bronchial:	n/a
40	chr13:69261665-69261715	CMK	blood:	n/a
41	chr13:69261665-69261715	BJ	skin:	n/a
42	chr13:69261665-69261715	BE2_C	brain:	n/a
43	chr13:69261665-69261715	K562	blood:	n/a
44	chr13:69261665-69261715	SKMC	muscle:	n/a
45	chr13:69261665-69261715	Hela-S3	cervix:	n/a
46	chr13:69261665-69261715	HCPEpiC	choroid plexus:	n/a
47	chr13:69261665-69261715	Caco-2	colon:	n/a
48	chr13:69261665-69261715	HRCEpiC	kidney:	n/a
49	chr13:69261665-69261715	HepG2	liver:	n/a
50	chr13:69261665-69261715	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:69287232..69288836-chr13:69289519..69291070,2	MCF-7	breast:
2	chr13:69281888..69284510-chr13:69284969..69287100,2	K562	blood:
3	chr13:69259900..69260965-chr13:69319275..69320290,3	MCF-7	breast:
4	chr13:69255286..69258231-chr13:69263633..69265493,2	K562	blood:
5	chr13:69258057..69262640-chr13:69318281..69322115,7	MCF-7	breast:
6	chr13:69261144..69263388-chr13:69284618..69286596,2	MCF-7	breast:
7	chr13:69285714..69286598-chr13:69319387..69320170,3	MCF-7	breast:
8	chr13:69260112..69260846-chr13:69285482..69286306,2	MCF-7	breast:
9	chr13:69287232..69288836-chr13:69289519..69291070,2	MCF-7	breast:
10	chr13:69259973..69261382-chr13:69319364..69320393,8	MCF-7	breast:
11	chr13:69259880..69261273-chr13:69319408..69320273,7	MCF-7	breast:
12	chr13:69259986..69260836-chr13:69285583..69286413,2	MCF-7	breast:
13	chr13:69315131..69317872-chr13:69317923..69322288,4	K562	blood:
14	chr13:69302476..69304966-chr13:69305880..69307759,2	K562	blood:
15	chr13:69259897..69261382-chr13:69319281..69320393,15	MCF-7	breast:
16	chr13:69305922..69307461-chr13:69310294..69313098,2	MCF-7	breast:
17	chr13:69254844..69257160-chr13:69257337..69259897,2	K562	blood:
18	chr13:69285777..69286462-chr13:69319713..69320490,3	MCF-7	breast:
19	chr13:69259973..69261382-chr13:69319364..69320393,8	MCF-7	breast:
20	chr13:69310540..69313201-chr13:69349262..69351035,2	K562	blood:
21	chr13:69259880..69261273-chr13:69319408..69320273,7	MCF-7	breast:
22	chr13:69260117..69261169-chr13:69319440..69320437,6	MCF-7	breast:
23	chr13:69302476..69304966-chr13:69305880..69307759,2	K562	blood:
24	chr13:69259986..69260836-chr13:69285583..69286413,2	MCF-7	breast:
25	chr13:69232704..69235680-chr13:69237810..69239831,2	K562	blood:
26	chr13:69254844..69257160-chr13:69257337..69259897,2	K562	blood:
27	chr13:69266497..69268743-chr13:69269469..69272027,2	MCF-7	breast:
28	chr13:69385279..69388108-chr13:69393931..69396561,2	K562	blood:
29	chr13:69259900..69260965-chr13:69319275..69320290,3	MCF-7	breast:
30	chr13:69305922..69307461-chr13:69310294..69313098,2	MCF-7	breast:
31	chr13:69285777..69286462-chr13:69319713..69320490,3	MCF-7	breast:
32	chr13:69260112..69260846-chr13:69285482..69286306,2	MCF-7	breast:
33	chr13:69213639..69216422-chr13:69230531..69232946,2	K562	blood:
34	chr13:69290266..69293012-chr13:69294530..69297103,2	K562	blood:
35	chr13:69259897..69261382-chr13:69319281..69320393,15	MCF-7	breast:
36	chr13:69261144..69263388-chr13:69284618..69286596,2	MCF-7	breast:
37	chr13:69258923..69261156-chr13:69263100..69265480,2	K562	blood:
38	chr13:69258057..69262640-chr13:69318281..69322115,7	MCF-7	breast:
39	chr13:69290266..69293012-chr13:69294530..69297103,2	K562	blood:
40	chr13:69310540..69313201-chr13:69349262..69351035,2	K562	blood:
41	chr13:69258923..69261156-chr13:69263100..69265480,2	K562	blood:
42	chr13:69342465..69344656-chr13:69450218..69452422,2	K562	blood:
43	chr13:69281888..69284510-chr13:69284969..69287100,2	K562	blood:
44	chr13:69269070..69271450-chr13:69274161..69276898,2	K562	blood:
45	chr13:69232704..69235680-chr13:69237810..69239831,2	K562	blood:
46	chr13:69315131..69317872-chr13:69317923..69322288,4	K562	blood:
47	chr13:69269070..69271450-chr13:69274161..69276898,2	K562	blood:
48	chr13:69285714..69286598-chr13:69319387..69320170,3	MCF-7	breast:
49	chr13:69260117..69261169-chr13:69319440..69320437,6	MCF-7	breast:
50	chr13:69255286..69258231-chr13:69263633..69265493,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BORA-26	chr13:69228704-69229182	NONHSAT034236
2	lnc-KLHL1-8	chr13:69267938-69268213	NONHSAT034237

No data

Variant related genes	Relation type
RPL12P34	TF binding region
RN7SL761P	TF binding region
RPL12P34	CpG island
RN7SL761P	CpG island
ENSG00000243671	chromatin interactions

Extended variants
information (count: 2537 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2537 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551300143	chr13:69224030-69224031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555387179	chr13:69224036-69224037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561526295	chr13:69224102-69224103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79946055	chr13:69224112-69224113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546549426	chr13:69224114-69224115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566325096	chr13:69224142-69224143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538757114	chr13:69224260-69224261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193183984	chr13:69224312-69224313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568755857	chr13:69224356-69224357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9541483	chr13:69224399-69224400	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs556084996	chr13:69225965-69225966	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs7991638	chr13:69225991-69225992	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs575629640	chr13:69225992-69225993	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs368731016	chr13:69226047-69226048	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs372965707	chr13:69226055-69226056	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs287378	chr13:69226057-69226058	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs114108345	chr13:69226061-69226062	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs527495153	chr13:69226083-69226084	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs538986123	chr13:69226097-69226098	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs547246092	chr13:69226098-69226099	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs190291359	chr13:69226108-69226109	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs551556875	chr13:69226115-69226116	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs144505783	chr13:69226136-69226137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs35269619	chr13:69226142-69226143	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs34351387	chr13:69226148-69226149	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs181645373	chr13:69226205-69226206	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs287379	chr13:69226209-69226210	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs568428890	chr13:69226239-69226240	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534427801	chr13:69226242-69226243	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs287380	chr13:69226299-69226300	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs34669350	chr13:69226314-69226315	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs147368616	chr13:69226407-69226408	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs376992395	chr13:69226408-69226409	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs539784877	chr13:69226444-69226445	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs66972690	chr13:69226454-69226455	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs398117487	chr13:69226455-69226456	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs35738967	chr13:69226463-69226464	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs542153395	chr13:69226465-69226466	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs375895179	chr13:69226569-69226570	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs12428605	chr13:69226586-69226587	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs287381	chr13:69226605-69226606	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs541389975	chr13:69226611-69226612	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs113386258	chr13:69226644-69226645	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs8181870	chr13:69226649-69226650	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs77659666	chr13:69226678-69226679	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185826601	chr13:69226710-69226711	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs533145089	chr13:69226752-69226753	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs550105689	chr13:69226779-69226780	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs571249669	chr13:69228483-69228484	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs287382	chr13:69228533-69228534	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22737080	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69224000-69224400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr13:69238800-69239000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:69247400-69247800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:69250600-69252000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr13:69250800-69251000	Enhancers	HSMM	muscle
6	chr13:69251000-69251400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:69251000-69252000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr13:69251200-69252200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr13:69252000-69253000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr13:69252000-69253000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr13:69252800-69253200	Enhancers	Placenta Amnion	Placenta Amnion
12	chr13:69253000-69253200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr13:69253000-69253200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr13:69253000-69253400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr13:69253200-69256400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr13:69253200-69260200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr13:69258400-69260200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr13:69260200-69260600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr13:69260200-69260800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr13:69260200-69260800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr13:69260200-69264600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr13:69260400-69260800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr13:69260600-69261400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr13:69260600-69262800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr13:69260800-69262200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:69260800-69262200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr13:69260800-69262200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr13:69262000-69262800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr13:69262200-69262400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr13:69262200-69262600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr13:69262200-69262600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr13:69262200-69262600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:69262200-69262800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr13:69262200-69262800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr13:69262400-69262800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr13:69262600-69282600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr13:69264600-69265000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:69264600-69265000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr13:69264600-69265000	Enhancers	Brain Germinal Matrix	brain
40	chr13:69266000-69266800	Enhancers	K562	blood
41	chr13:69266800-69272400	Weak transcription	K562	blood
42	chr13:69271200-69272600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr13:69271600-69271800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr13:69271800-69272000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:69271800-69272200	Enhancers	Placenta Amnion	Placenta Amnion
46	chr13:69271800-69272400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr13:69272000-69275000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr13:69272400-69272800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr13:69272400-69273000	Enhancers	K562	blood
50	chr13:69275000-69275400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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