Variant report

Variant	nsv932955
Chromosome Location	chr1:76189923-76190791
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:536)
CpG islands
(count:549)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76190282-76190610	K562	blood:	n/a	n/a
2	ARID3A	chr1:76189663-76190663	HepG2	liver:	n/a	n/a
3	ATF2	chr1:76190039-76190752	GM12878	blood:	n/a	n/a
4	ATF2	chr1:76190068-76190614	GM12878	blood:	n/a	n/a
5	ATF2	chr1:76190083-76190371	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:76190205-76190643	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr1:76189929-76190427	A549	lung:	n/a	chr1:76190084-76190097
8	BCLAF1	chr1:76190073-76190790	K562	blood:	n/a	chr1:76190687-76190696 chr1:76190084-76190097
9	BCLAF1	chr1:76190094-76190732	GM12878	blood:	n/a	chr1:76190687-76190696
10	BCLAF1	chr1:76190090-76190760	K562	blood:	n/a	chr1:76190687-76190696
11	BCLAF1	chr1:76190088-76190821	GM12878	blood:	n/a	chr1:76190687-76190696
12	BHLHE40	chr1:76189760-76190902	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:76189589-76190874	K562	blood:	n/a	n/a
14	BRCA1	chr1:76190213-76190351	HepG2	liver:	n/a	n/a
15	BRCA1	chr1:76189124-76190021	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr1:76190236-76190749	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr1:76189673-76190677	K562	blood:	n/a	chr1:76189836-76189847
18	CCNT2	chr1:76189838-76190765	K562	blood:	n/a	chr1:76190097-76190106
19	CEBPB	chr1:76189564-76190590	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:76189622-76190465	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:76190305-76190606	K562	blood:	n/a	n/a
22	CEBPD	chr1:76190000-76190696	HepG2	liver:	n/a	n/a
23	CEBPD	chr1:76189679-76190655	K562	blood:	n/a	n/a
24	CEBPD	chr1:76189856-76190047	HepG2	liver:	n/a	n/a
25	CEBPD	chr1:76190183-76190426	HepG2	liver:	n/a	n/a
26	CHD1	chr1:76190567-76191049	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr1:76190098-76192501	GM12878	blood:	n/a	n/a
28	CHD2	chr1:76189686-76190782	K562	blood:	n/a	n/a
29	CHD2	chr1:76189623-76190791	GM12878	blood:	n/a	n/a
30	CHD2	chr1:76189638-76190788	HepG2	liver:	n/a	n/a
31	CHD2	chr1:76189594-76190760	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr1:76189822-76190834	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr1:76189883-76190650	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr1:76189573-76190868	HepG2	liver:	n/a	n/a
35	CREB1	chr1:76189887-76190731	A549	lung:	n/a	n/a
36	CTBP2	chr1:76189947-76190697	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr1:76190160-76190310	AG04449	skin:	n/a	n/a
38	CTCF	chr1:76190266-76190324	NHEK	skin:	n/a	n/a
39	CTCF	chr1:76189960-76190110	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr1:76190087-76190552	GM12878	blood:	n/a	n/a
41	CTCF	chr1:76189994-76189996	GM12891	blood:	n/a	n/a
42	CTCF	chr1:76189979-76189991	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr1:76190320-76190470	GM12869	blood:	n/a	n/a
44	CTCF	chr1:76189960-76190110	GM12865	blood:	n/a	n/a
45	CTCF	chr1:76190420-76190570	HepG2	liver:	n/a	n/a
46	CTCF	chr1:76190280-76190430	HMEC	breast:	n/a	n/a
47	CTCF	chr1:76189920-76190070	AG04449	skin:	n/a	n/a
48	CTCF	chr1:76190060-76190350	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr1:76190243-76190345	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:76190230-76190352	Fibrobl	skin:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76190140-76190190	NT2-D1	testis:	n/a
2	chr1:76190172-76190222	HEEpiC	esophagus:	n/a
3	chr1:76190040-76190090	Caco-2	colon:	n/a
4	chr1:76189954-76190004	CMK	blood:	n/a
5	chr1:76190008-76190058	AG09319	gingival:	n/a
6	chr1:76189945-76189995	MCF-7	breast:	n/a
7	chr1:76189954-76190004	GM19239	blood:	n/a
8	chr1:76189954-76190004	AG09319	gingival:	n/a
9	chr1:76190172-76190222	H1-hESC	embryonic stem cell:	embryo
10	chr1:76189945-76189995	A549	lung:	n/a
11	chr1:76190428-76190478	HMEC	breast:	n/a
12	chr1:76190428-76190478	AG09319	gingival:	n/a
13	chr1:76189945-76189995	U87	brain:	n/a
14	chr1:76190140-76190190	BE2_C	brain:	n/a
15	chr1:76190428-76190478	HL-60	blood:	n/a
16	chr1:76190140-76190190	HEEpiC	esophagus:	n/a
17	chr1:76190428-76190478	HRCEpiC	kidney:	n/a
18	chr1:76190140-76190190	AG10803	skin:	n/a
19	chr1:76190666-76190716	AG04450	lung:	fetal
20	chr1:76189945-76189995	HUVEC	blood vessel:	n/a
21	chr1:76189954-76190004	HepG2	liver:	n/a
22	chr1:76190040-76190090	HEEpiC	esophagus:	n/a
23	chr1:76190428-76190478	T-47D	breast:	n/a
24	chr1:76189954-76190004	SK-N-SH_RA	brain:	n/a
25	chr1:76190666-76190716	A549	lung:	n/a
26	chr1:76190435-76190485	HRCEpiC	kidney:	n/a
27	chr1:76190435-76190485	BE2_C	brain:	n/a
28	chr1:76190172-76190222	GM12892	blood:	n/a
29	chr1:76190040-76190090	CMK	blood:	n/a
30	chr1:76189945-76189995	AG10803	skin:	n/a
31	chr1:76190666-76190716	HMEC	breast:	n/a
32	chr1:76190666-76190716	RPTEC	kidney:	n/a
33	chr1:76190428-76190478	GM12878	blood:	n/a
34	chr1:76189945-76189995	SAEC	small airway:	n/a
35	chr1:76189954-76190004	ProgFib	skin:	n/a
36	chr1:76190172-76190222	Caco-2	colon:	n/a
37	chr1:76190666-76190716	Caco-2	colon:	n/a
38	chr1:76190172-76190222	AG09319	gingival:	n/a
39	chr1:76190666-76190716	HRCEpiC	kidney:	n/a
40	chr1:76190435-76190485	HCF	heart:	n/a
41	chr1:76190428-76190478	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:76189945-76189995	BJ	skin:	n/a
43	chr1:76190428-76190478	BE2_C	brain:	n/a
44	chr1:76190666-76190716	HUVEC	blood vessel:	n/a
45	chr1:76189945-76189995	HMEC	breast:	n/a
46	chr1:76190435-76190485	GM06990	blood:	n/a
47	chr1:76190008-76190058	AG04450	lung:	fetal
48	chr1:76190666-76190716	GM19239	blood:	n/a
49	chr1:76190666-76190716	GM12878	blood:	n/a
50	chr1:76189945-76189995	NH-A	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76188764..76194417-chr1:76259356..76264333,14	K562	blood:
2	chr1:76187424..76195796-chr1:76248839..76258922,52	K562	blood:
3	chr1:76189917..76190733-chr20:34329839..34330374,2	Hela-S3	cervix:
4	chr1:76189902..76190712-chr1:144533703..144534665,2	Hela-S3	cervix:
5	chr1:76189545..76190479-chr8:125486401..125487035,2	Hela-S3	cervix:
6	chr1:76189700..76190212-chr9:130565796..130566746,2	Hela-S3	cervix:
7	chr1:76190052..76193339-chr1:76196508..76198872,3	K562	blood:
8	chr1:76189532..76190105-chr1:76251441..76252104,2	MCF-7	breast:
9	chr1:76189501..76190437-chr1:76251743..76252335,2	NB4	blood:
10	chr1:76189767..76190677-chr19:2475779..2476409,2	Hela-S3	cervix:
11	chr1:76186306..76195796-chr1:76248732..76266552,73	K562	blood:
12	chr1:76189028..76194220-chr1:76209012..76215464,6	K562	blood:
13	chr1:76188769..76191418-chr1:76197121..76200007,3	MCF-7	breast:
14	chr1:76188658..76192178-chr1:76249968..76253902,5	MCF-7	breast:
15	chr1:19971033..19971998-chr1:76190390..76190915,2	Hela-S3	cervix:
16	chr1:76188740..76191486-chr1:76199573..76201902,4	K562	blood:
17	chr1:76190185..76192141-chr1:76251658..76253401,2	MCF-7	breast:

No data

Variant related genes	Relation type
ACADM	TF binding region
ENSG00000178193	TF binding region
ACADM	CpG island
ENSG00000178193	CpG island
ENSG00000131051	chromatin interactions
ENSG00000201487	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000137955	chromatin interactions
ENSG00000117054	chromatin interactions
ENSG00000057468	chromatin interactions
ENSG00000181227	chromatin interactions
ENSG00000206620	chromatin interactions
ENSG00000245149	chromatin interactions
ENSG00000158747	chromatin interactions
ENSG00000170881	chromatin interactions
ENSG00000207241	chromatin interactions
ENSG00000136877	chromatin interactions
ENSG00000099860	chromatin interactions

Extended variants
information (count: 61 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:61 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576513198	chr1:76189924-76189925	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
2	rs537794866	chr1:76189937-76189938	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
3	rs558494664	chr1:76189939-76189940	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
4	rs61797339	chr1:76189946-76189947	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs574117609	chr1:76189957-76189958	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
6	rs541416173	chr1:76189962-76189963	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
7	rs553376990	chr1:76190012-76190013	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
8	rs578156664	chr1:76190023-76190024	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
9	rs545133313	chr1:76190036-76190037	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
10	rs114802787	chr1:76190037-76190038	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
11	rs531405752	chr1:76190055-76190056	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs114005461	chr1:76190072-76190073	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
13	rs574519305	chr1:76190106-76190107	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
14	rs1251076	chr1:76190111-76190112	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs113112056	chr1:76190153-76190154	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
16	rs150066561	chr1:76190157-76190158	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
17	rs374976396	chr1:76190162-76190163	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
18	rs547003002	chr1:76190195-76190196	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
19	rs565294797	chr1:76190207-76190208	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
20	rs17848068	chr1:76190216-76190217	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551184035	chr1:76190305-76190306	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs563406308	chr1:76190321-76190322	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs61124994	chr1:76190331-76190332	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs537233466	chr1:76190345-76190346	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs554660770	chr1:76190349-76190350	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs556054701	chr1:76190376-76190377	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs567983446	chr1:76190381-76190382	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs535303084	chr1:76190393-76190394	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs371418479	chr1:76190404-76190405	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs553414128	chr1:76190407-76190408	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs373731510	chr1:76190426-76190427	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs371787277	chr1:76190435-76190436	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs59932454	chr1:76190439-76190440	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376904926	chr1:76190449-76190450	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs367734665	chr1:76190456-76190457	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs545522153	chr1:76190458-76190459	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs201646499	chr1:76190483-76190484	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs372088389	chr1:76190489-76190490	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs375492495	chr1:76190513-76190514	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs369431746	chr1:76190550-76190551	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs369417973	chr1:76190564-76190565	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs116034618	chr1:76190568-76190569	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs1251075	chr1:76190569-76190570	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs561520228	chr1:76190605-76190606	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs529155733	chr1:76190611-76190612	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs540887454	chr1:76190629-76190630	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs377704457	chr1:76190643-76190644	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs558964981	chr1:76190664-76190665	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs371104977	chr1:76190677-76190678	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs1251074	chr1:76190690-76190691	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Melanoma	17363583	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
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
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76189000-76191200	Active TSS	Brain Hippocampus Middle	brain
2	chr1:76189000-76191400	Active TSS	A549	lung
3	chr1:76189000-76191600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:76189000-76191600	Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr1:76189200-76190000	Flanking Active TSS	HUVEC	blood vessel
6	chr1:76189200-76191000	Active TSS	Fetal Brain Male	brain
7	chr1:76189200-76191400	Active TSS	Duodenum Smooth Muscle	Duodenum
8	chr1:76189200-76191600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:76189200-76191600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:76189200-76191600	Active TSS	Brain Anterior Caudate	brain
11	chr1:76189200-76191800	Active TSS	Esophagus	oesophagus
12	chr1:76189200-76191800	Active TSS	HSMM	muscle
13	chr1:76189200-76192000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr1:76189200-76192400	Active TSS	HMEC	breast
15	chr1:76189200-76192400	Active TSS	NHDF-Ad	bronchial
16	chr1:76189400-76190000	Flanking Active TSS	Primary hematopoietic stem cells	blood
17	chr1:76189400-76190000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:76189400-76190000	Active TSS	Brain Germinal Matrix	brain
19	chr1:76189400-76190000	Active TSS	Right Atrium	heart
20	chr1:76189400-76190000	Flanking Active TSS	NH-A	brain
21	chr1:76189400-76190800	Active TSS	Monocytes-CD14+_RO01746	blood
22	chr1:76189400-76191200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:76189400-76191200	Active TSS	Fetal Heart	heart
24	chr1:76189400-76191200	Active TSS	Fetal Kidney	kidney
25	chr1:76189400-76191400	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr1:76189400-76191400	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr1:76189400-76191400	Active TSS	Muscle Satellite Cultured Cells	--
28	chr1:76189400-76191400	Active TSS	Aorta	Aorta
29	chr1:76189400-76191400	Active TSS	Fetal Muscle Trunk	muscle
30	chr1:76189400-76191400	Active TSS	Rectal Smooth Muscle	rectum
31	chr1:76189400-76191600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:76189400-76191600	Active TSS	Fetal Muscle Leg	muscle
33	chr1:76189400-76191600	Active TSS	Fetal Thymus	thymus
34	chr1:76189400-76191600	Active TSS	HSMMtube	muscle
35	chr1:76189400-76191600	Active TSS	Osteobl	bone
36	chr1:76189400-76191800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr1:76189400-76191800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:76189400-76191800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr1:76189400-76191800	Active TSS	Fetal Stomach	stomach
40	chr1:76189400-76191800	Active TSS	Psoas Muscle	Psoas
41	chr1:76189400-76191800	Active TSS	Right Ventricle	heart
42	chr1:76189400-76192000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr1:76189400-76192000	Active TSS	HepG2	liver
44	chr1:76189400-76192000	Active TSS	NHLF	lung
45	chr1:76189400-76192200	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr1:76189400-76192200	Active TSS	Ovary	ovary
47	chr1:76189400-76192400	Active TSS	Colonic Mucosa	Colon
48	chr1:76189600-76190000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr1:76189600-76190000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
50	chr1:76189600-76190000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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