Variant report

Variant	nsv981607
Chromosome Location	chr7:149483488-149506591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:991)
CpG islands
(count:672)
Chromatin interactive
region (count:63)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:991 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:149497005-149497192	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:149487148-149487379	K562	blood:	n/a	n/a
3	ATF3	chr7:149487245-149487558	K562	blood:	n/a	n/a
4	BACH1	chr7:149484599-149484951	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:149487050-149487759	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:149487231-149487628	K562	blood:	n/a	n/a
7	BHLHE40	chr7:149486849-149486853	K562	blood:	n/a	n/a
8	BHLHE40	chr7:149484475-149485102	K562	blood:	n/a	n/a
9	BHLHE40	chr7:149496880-149497163	K562	blood:	n/a	n/a
10	BHLHE40	chr7:149489080-149489398	K562	blood:	n/a	n/a
11	BHLHE40	chr7:149485581-149486169	HepG2	liver:	n/a	n/a
12	BHLHE40	chr7:149493429-149493435	K562	blood:	n/a	n/a
13	BHLHE40	chr7:149504258-149504411	K562	blood:	n/a	n/a
14	BHLHE40	chr7:149485665-149486197	K562	blood:	n/a	n/a
15	BRCA1	chr7:149487336-149487411	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr7:149487111-149487573	K562	blood:	n/a	n/a
17	CBX3	chr7:149484431-149485045	K562	blood:	n/a	n/a
18	CCNT2	chr7:149487187-149487786	K562	blood:	n/a	n/a
19	CCNT2	chr7:149491898-149491995	K562	blood:	n/a	n/a
20	CCNT2	chr7:149484506-149485004	K562	blood:	n/a	chr7:149484696-149484705
21	CCNT2	chr7:149497332-149497377	K562	blood:	n/a	n/a
22	CHD1	chr7:149487296-149487304	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr7:149496953-149497118	K562	blood:	n/a	n/a
24	CHD2	chr7:149487166-149487489	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr7:149484645-149484858	K562	blood:	n/a	n/a
26	CHD2	chr7:149500859-149501041	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr7:149487976-149487977	K562	blood:	n/a	n/a
28	CHD2	chr7:149490130-149490136	K562	blood:	n/a	n/a
29	CHD2	chr7:149485848-149485866	HepG2	liver:	n/a	n/a
30	CHD2	chr7:149493537-149493564	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr7:149487284-149487439	K562	blood:	n/a	n/a
32	CREB1	chr7:149487206-149487708	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr7:149504360-149504510	HUVEC	blood vessel:	n/a	chr7:149504449-149504470 chr7:149504450-149504463 chr7:149504447-149504465 chr7:149504448-149504464
34	CTCF	chr7:149504265-149504623	GM12878	blood:	n/a	chr7:149504449-149504470 chr7:149504450-149504463 chr7:149504447-149504465 chr7:149504448-149504464
35	CTCF	chr7:149484677-149484858	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr7:149497060-149497210	HL-60	blood:	n/a	n/a
37	CTCF	chr7:149504360-149504510	GM12867	blood:	n/a	chr7:149504449-149504470 chr7:149504450-149504463 chr7:149504447-149504465 chr7:149504448-149504464
38	CTCF	chr7:149493514-149493641	GM12891	blood:	n/a	n/a
39	CTCF	chr7:149504360-149504510	Caco-2	colon:	n/a	chr7:149504449-149504470 chr7:149504450-149504463 chr7:149504447-149504465 chr7:149504448-149504464
40	CTCF	chr7:149504340-149504490	GM12878	blood:	n/a	chr7:149504449-149504470 chr7:149504450-149504463 chr7:149504447-149504465 chr7:149504448-149504464
41	CTCF	chr7:149487280-149487430	HCFaa	heart:	n/a	n/a
42	CTCF	chr7:149484640-149484790	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr7:149484700-149484850	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr7:149503705-149503710	GM12891	blood:	n/a	n/a
45	CTCF	chr7:149504360-149504510	GM12869	blood:	n/a	chr7:149504449-149504470 chr7:149504450-149504463 chr7:149504447-149504465 chr7:149504448-149504464
46	CTCF	chr7:149484647-149484869	A549	lung:	n/a	n/a
47	CTCF	chr7:149504320-149504470	GM12874	blood:	n/a	chr7:149504449-149504470 chr7:149504450-149504463 chr7:149504447-149504465 chr7:149504448-149504464
48	CTCF	chr7:149484640-149484790	GM12868	blood:	n/a	n/a
49	CTCF	chr7:149504384-149504469	GM12891	blood:	n/a	chr7:149504450-149504463 chr7:149504447-149504465 chr7:149504448-149504464
50	CTCF	chr7:149484473-149485100	K562	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149484880-149484930	AG04450	lung:	fetal
2	chr7:149484880-149484930	AG04450	lung:	fetal
3	chr7:149484985-149485035	HMEC	breast:	n/a
4	chr7:149485981-149486031	PFSK-1	brain:	n/a
5	chr7:149488213-149488263	HRCEpiC	kidney:	n/a
6	chr7:149484880-149484930	NHBE	bronchial:	n/a
7	chr7:149485740-149485790	IMR90	lung:	fetal
8	chr7:149484880-149484930	ECC-1	luminal epithelium:	n/a
9	chr7:149487677-149487727	Caco-2	colon:	n/a
10	chr7:149487749-149487799	A549	lung:	n/a
11	chr7:149485981-149486031	HepG2	liver:	n/a
12	chr7:149489783-149489833	NT2-D1	testis:	n/a
13	chr7:149484798-149484848	ECC-1	luminal epithelium:	n/a
14	chr7:149484798-149484848	MCF-7	breast:	n/a
15	chr7:149489783-149489833	HRPEpiC	eye:	n/a
16	chr7:149488213-149488263	GM12878	blood:	n/a
17	chr7:149488213-149488263	HEEpiC	esophagus:	n/a
18	chr7:149485981-149486031	AoSMC	blood vessel:	n/a
19	chr7:149484798-149484848	NH-A	brain:	n/a
20	chr7:149484798-149484848	AoSMC	blood vessel:	n/a
21	chr7:149485981-149486031	HRE	kidney:	n/a
22	chr7:149489783-149489833	GM12891	blood:	n/a
23	chr7:149485981-149486031	AG09309	skin:	n/a
24	chr7:149487338-149487388	Hepatocyte	liver:	n/a
25	chr7:149485981-149486031	GM12878	blood:	n/a
26	chr7:149485712-149485762	NHBE	bronchial:	n/a
27	chr7:149485740-149485790	CMK	blood:	n/a
28	chr7:149484985-149485035	GM19239	blood:	n/a
29	chr7:149485981-149486031	ProgFib	skin:	n/a
30	chr7:149487677-149487727	K562	blood:	n/a
31	chr7:149487749-149487799	HRCEpiC	kidney:	n/a
32	chr7:149487338-149487388	SKMC	muscle:	n/a
33	chr7:149485712-149485762	HMEC	breast:	n/a
34	chr7:149485740-149485790	LNCaP	prostate:	n/a
35	chr7:149487677-149487727	NH-A	brain:	n/a
36	chr7:149485712-149485762	NHDF-neo	bronchial:	n/a
37	chr7:149485740-149485790	SK-N-MC	brain:	n/a
38	chr7:149485712-149485762	GM12892	blood:	n/a
39	chr7:149485712-149485762	NH-A	brain:	n/a
40	chr7:149489783-149489833	AG09309	skin:	n/a
41	chr7:149485981-149486031	AG09319	gingival:	n/a
42	chr7:149487338-149487388	ovcar-3	ovarian:	n/a
43	chr7:149487749-149487799	PrEC	prostate:	n/a
44	chr7:149485712-149485762	AG09319	gingival:	n/a
45	chr7:149487749-149487799	ECC-1	luminal epithelium:	n/a
46	chr7:149485740-149485790	NHDF-neo	bronchial:	n/a
47	chr7:149487677-149487727	HL-60	blood:	n/a
48	chr7:149484985-149485035	NHDF-neo	bronchial:	n/a
49	chr7:149487677-149487727	MCF-7	breast:	n/a
50	chr7:149484798-149484848	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:149486923..149488789-chr7:149516308..149518311,2	MCF-7	breast:
2	chr7:149439409..149439997-chr7:149486897..149487877,2	K562	blood:
3	chr7:149476551..149479010-chr7:149504345..149507000,2	K562	blood:
4	chr7:149495710..149497643-chr7:149503377..149505393,2	K562	blood:
5	chr7:149497731..149501879-chr7:149502628..149506798,7	K562	blood:
6	chr7:149475777..149478196-chr7:149495163..149497885,2	K562	blood:
7	chr7:149484679..149488642-chr7:149489546..149492770,6	MCF-7	breast:
8	chr7:149484023..149486893-chr7:149499166..149501510,2	K562	blood:
9	chr7:149503784..149507213-chr7:149507288..149510780,3	MCF-7	breast:
10	chr7:149473801..149475401-chr7:149492673..149494757,2	MCF-7	breast:
11	chr7:149482558..149484845-chr7:149519799..149522299,2	K562	blood:
12	chr7:149484191..149484692-chr7:149580431..149580931,2	K562	blood:
13	chr7:149489220..149491723-chr7:149504339..149506284,2	K562	blood:
14	chr7:149484023..149486893-chr7:149499166..149501510,2	K562	blood:
15	chr7:149501055..149503338-chr7:149561332..149564151,2	MCF-7	breast:
16	chr7:149499623..149502288-chr7:149502769..149505265,4	K562	blood:
17	chr7:149478286..149483291-chr7:149484543..149488292,6	K562	blood:
18	chr7:149467684..149471867-chr7:149482733..149487472,6	K562	blood:
19	chr7:149332468..149334868-chr7:149493693..149495718,2	K562	blood:
20	chr7:149503783..149504300-chr7:149546267..149547084,2	MCF-7	breast:
21	chr7:149504416..149504923-chr7:149545982..149546934,2	K562	blood:
22	chr7:149470464..149473149-chr7:149495554..149497306,2	MCF-7	breast:
23	chr7:149433441..149435598-chr7:149486933..149488751,2	K562	blood:
24	chr7:149504930..149508041-chr7:149510970..149514779,4	MCF-7	breast:
25	chr7:149359887..149360749-chr7:149496598..149497119,2	MCF-7	breast:
26	chr7:149409957..149411791-chr7:149503300..149505720,2	K562	blood:
27	chr7:149359338..149360344-chr7:149496249..149497433,4	K562	blood:
28	chr7:149492594..149494537-chr7:149501792..149504524,2	MCF-7	breast:
29	chr7:149484679..149488642-chr7:149489546..149492770,6	MCF-7	breast:
30	chr7:149450620..149451175-chr7:149496361..149497222,2	MCF-7	breast:
31	chr7:149450477..149451367-chr7:149496593..149497103,2	MCF-7	breast:
32	chr7:149320947..149323521-chr7:149506280..149508125,2	K562	blood:
33	chr7:149487842..149489605-chr7:149493457..149495726,2	MCF-7	breast:
34	chr7:149478680..149481554-chr7:149493903..149496392,2	MCF-7	breast:
35	chr7:149471379..149473903-chr7:149490121..149491823,3	MCF-7	breast:
36	chr7:149499623..149502288-chr7:149502769..149505265,4	K562	blood:
37	chr7:149486170..149487742-chr7:149495791..149498541,2	K562	blood:
38	chr7:149359416..149360312-chr7:149486909..149487857,5	K562	blood:
39	chr7:149469665..149471242-chr7:149492952..149494694,2	K562	blood:
40	chr7:149495710..149497643-chr7:149503377..149505393,2	K562	blood:
41	chr7:149416557..149419178-chr7:149484233..149488617,3	K562	blood:
42	chr7:149419111..149421649-chr7:149493906..149495599,2	K562	blood:
43	chr7:149503718..149504886-chr7:149546056..149546960,4	MCF-7	breast:
44	chr7:149503805..149505965-chr7:149519208..149521069,2	MCF-7	breast:
45	chr7:149486170..149487742-chr7:149495791..149498541,2	K562	blood:
46	chr7:149377419..149380079-chr7:149485808..149488196,2	K562	blood:
47	chr7:149468811..149471165-chr7:149492241..149495834,3	K562	blood:
48	chr7:149471231..149473426-chr7:149502540..149505740,3	MCF-7	breast:
49	chr7:149471644..149473259-chr7:149495701..149497872,2	MCF-7	breast:
50	chr7:149140254..149143048-chr7:149504984..149507887,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF862-1	chr7:149496922-149497125	NONHSAT124049
2	lnc-ZNF862-1	chr7:149493695-149493834	NONHSAT124049
3	lnc-ZNF862-1	chr7:149494360-149494432	NONHSAT124049

No data

Variant related genes	Relation type
SSPO	TF binding region
SSPO	CpG island
ENSG00000133619	chromatin interactions
ENSG00000197558	chromatin interactions
ENSG00000106479	chromatin interactions
ENSG00000181444	chromatin interactions
ENSG00000133624	chromatin interactions

Extended variants
information (count: 1466 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374239239	chr7:149483539-149483540	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs554025550	chr7:149483574-149483575	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs141968084	chr7:149483596-149483597	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs572610838	chr7:149483606-149483607	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566619198	chr7:149483627-149483628	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538468683	chr7:149483647-149483648	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs76505709	chr7:149483649-149483650	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs3779111	chr7:149483671-149483672	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185640939	chr7:149483721-149483722	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs34960784	chr7:149483731-149483732	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs537425513	chr7:149483764-149483765	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs557430524	chr7:149483831-149483832	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs78421504	chr7:149483896-149483897	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs543062968	chr7:149483897-149483898	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559603504	chr7:149483912-149483913	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs3779112	chr7:149483917-149483918	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531719330	chr7:149483930-149483931	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs180750556	chr7:149483952-149483953	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs565219503	chr7:149483982-149483983	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531145638	chr7:149483999-149484000	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550153718	chr7:149484005-149484006	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560987843	chr7:149484010-149484011	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs529664743	chr7:149484024-149484025	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs546638930	chr7:149484036-149484037	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs3823697	chr7:149484048-149484049	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs562764684	chr7:149484060-149484061	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs552436323	chr7:149484072-149484073	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs185197217	chr7:149484077-149484078	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs538189104	chr7:149484124-149484125	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs533124998	chr7:149484149-149484150	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs113218964	chr7:149484165-149484166	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs573939683	chr7:149484187-149484188	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs7796804	chr7:149484204-149484205	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553404725	chr7:149484266-149484267	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs573284400	chr7:149484277-149484278	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs370218469	chr7:149484321-149484322	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs145161782	chr7:149484326-149484327	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs565181001	chr7:149484329-149484330	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs374721737	chr7:149484434-149484435	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs369038014	chr7:149484482-149484483	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs575531691	chr7:149484490-149484491	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs372766610	chr7:149484492-149484493	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375318586	chr7:149484493-149484494	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs369655758	chr7:149484500-149484501	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs373174623	chr7:149484501-149484502	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs111741862	chr7:149484527-149484528	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs188422566	chr7:149484550-149484551	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs181493696	chr7:149484563-149484564	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs374636900	chr7:149484577-149484578	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs10262505	chr7:149484590-149484591	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149473800-149534800	Weak transcription	Right Atrium	heart
2	chr7:149475000-149484400	Weak transcription	Pancreas	Pancrea
3	chr7:149480000-149484800	Weak transcription	Left Ventricle	heart
4	chr7:149480800-149484200	Weak transcription	K562	blood
5	chr7:149480800-149484600	Weak transcription	Gastric	stomach
6	chr7:149480800-149484800	Weak transcription	Esophagus	oesophagus
7	chr7:149480800-149486800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr7:149481000-149484400	Weak transcription	Lung	lung
9	chr7:149481000-149485200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:149481200-149484200	Weak transcription	Fetal Lung	lung
11	chr7:149481200-149484400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:149481200-149484400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:149481200-149484400	Weak transcription	Right Ventricle	heart
14	chr7:149481400-149484400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:149483000-149484200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:149484200-149484400	Enhancers	K562	blood
17	chr7:149484200-149485000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:149484400-149484600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:149484400-149484600	Bivalent Enhancer	Fetal Intestine Large	intestine
20	chr7:149484400-149484600	Enhancers	A549	lung
21	chr7:149484400-149484800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr7:149484400-149484800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:149484400-149484800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
24	chr7:149484400-149485000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr7:149484400-149485000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
26	chr7:149484400-149485000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:149484400-149485000	Enhancers	Pancreas	Pancrea
28	chr7:149484400-149485200	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr7:149484400-149485200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:149484400-149485200	Enhancers	Right Ventricle	heart
31	chr7:149484400-149485200	Flanking Active TSS	K562	blood
32	chr7:149484400-149485400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
33	chr7:149484400-149485400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
34	chr7:149484400-149485600	Enhancers	Lung	lung
35	chr7:149484600-149484800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
36	chr7:149484600-149484800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
37	chr7:149484600-149484800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:149484600-149484800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr7:149484600-149484800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:149484600-149484800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:149484600-149484800	Bivalent Enhancer	Fetal Lung	lung
42	chr7:149484600-149484800	Bivalent Enhancer	Fetal Thymus	thymus
43	chr7:149484600-149485000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
44	chr7:149484600-149485000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:149484600-149485000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr7:149484600-149485000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
47	chr7:149484600-149485200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:149484600-149485200	Enhancers	Gastric	stomach
49	chr7:149484600-149485200	Active TSS	A549	lung
50	chr7:149484600-149485400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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