Variant report

Variant	nsv887631
Chromosome Location	chr7:12360805-12434771
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:930)
CpG islands
(count:305)
Chromatin interactive
region (count:66)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:930 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12361928-12362236	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:12424775-12425636	K562	blood:	n/a	n/a
3	ARID3A	chr7:12428736-12429092	K562	blood:	n/a	n/a
4	ARID3A	chr7:12425885-12425929	K562	blood:	n/a	n/a
5	ARID3A	chr7:12361970-12362233	K562	blood:	n/a	n/a
6	ATF1	chr7:12424857-12425489	K562	blood:	n/a	n/a
7	ATF1	chr7:12391517-12391830	K562	blood:	n/a	n/a
8	ATF1	chr7:12360907-12361152	K562	blood:	n/a	n/a
9	ATF2	chr7:12397170-12397485	GM12878	blood:	n/a	n/a
10	BACH1	chr7:12409290-12409383	K562	blood:	n/a	n/a
11	BATF	chr7:12362561-12362908	GM12878	blood:	n/a	chr7:12362724-12362735
12	BATF	chr7:12362529-12362819	GM12878	blood:	n/a	chr7:12362724-12362735
13	BCL11A	chr7:12362543-12362825	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:12362562-12362789	GM12878	blood:	n/a	n/a
15	BCL3	chr7:12397240-12397520	GM12878	blood:	n/a	n/a
16	BCL3	chr7:12370808-12371350	K562	blood:	n/a	n/a
17	BCLAF1	chr7:12424838-12425482	K562	blood:	n/a	n/a
18	BHLHE40	chr7:12371392-12371475	A549	lung:	n/a	n/a
19	BHLHE40	chr7:12361210-12361233	K562	blood:	n/a	n/a
20	BHLHE40	chr7:12362651-12362754	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:12412689-12412834	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:12431674-12431880	K562	blood:	n/a	n/a
23	BHLHE40	chr7:12391626-12391783	K562	blood:	n/a	n/a
24	BRCA1	chr7:12363238-12363314	GM12878	blood:	n/a	n/a
25	CBX3	chr7:12424861-12425408	K562	blood:	n/a	n/a
26	CCNT2	chr7:12422140-12422303	K562	blood:	n/a	n/a
27	CCNT2	chr7:12424779-12425447	K562	blood:	n/a	n/a
28	CCNT2	chr7:12383002-12383143	K562	blood:	n/a	n/a
29	CCNT2	chr7:12405891-12406052	K562	blood:	n/a	n/a
30	CCNT2	chr7:12430237-12430378	K562	blood:	n/a	n/a
31	CCNT2	chr7:12403056-12403099	K562	blood:	n/a	n/a
32	CCNT2	chr7:12360909-12361396	K562	blood:	n/a	n/a
33	CCNT2	chr7:12391547-12391847	K562	blood:	n/a	n/a
34	CCNT2	chr7:12418952-12419019	K562	blood:	n/a	n/a
35	CCNT2	chr7:12432707-12432774	K562	blood:	n/a	n/a
36	CEBPB	chr7:12376799-12377121	HepG2	liver:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
37	CEBPB	chr7:12413170-12413593	A549	lung:	n/a	chr7:12413407-12413418
38	CEBPB	chr7:12413201-12413548	ECC-1	luminal epithelium:	n/a	chr7:12413407-12413418
39	CEBPB	chr7:12413202-12413543	A549	lung:	n/a	chr7:12413407-12413418
40	CEBPB	chr7:12365869-12365957	K562	blood:	n/a	chr7:12365903-12365914 chr7:12365903-12365916 chr7:12365903-12365916 chr7:12365903-12365916
41	CEBPB	chr7:12360899-12361157	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:12428774-12429020	K562	blood:	n/a	n/a
43	CEBPB	chr7:12418167-12418474	K562	blood:	n/a	chr7:12418334-12418345 chr7:12418333-12418346 chr7:12418333-12418344
44	CEBPB	chr7:12428720-12429075	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr7:12428710-12429085	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:12427225-12427566	K562	blood:	n/a	chr7:12427390-12427401
47	CEBPB	chr7:12376796-12377033	K562	blood:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
48	CEBPB	chr7:12413224-12413590	HepG2	liver:	n/a	chr7:12413407-12413418
49	CEBPB	chr7:12413230-12413569	A549	lung:	n/a	chr7:12413407-12413418
50	CEBPB	chr7:12365884-12365914	H1-hESC	embryonic stem cell:	n/a	chr7:12365903-12365914

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12411370-12411420	AG04449	skin:	fetal
2	chr7:12370351-12370401	AG04449	skin:	fetal
3	chr7:12370351-12370401	HAEpiC	amniotic membrane:	n/a
4	chr7:12363490-12363540	SK-N-MC	brain:	n/a
5	chr7:12411370-12411420	HCM	heart:	n/a
6	chr7:12370351-12370401	AG04450	lung:	fetal
7	chr7:12363490-12363540	MCF10A-Er-Src	breast:	n/a
8	chr7:12363490-12363540	U87	brain:	n/a
9	chr7:12411370-12411420	HCT-116	colon:	n/a
10	chr7:12411370-12411420	HNPCEpiC	eye:	n/a
11	chr7:12376625-12376675	GM12892	blood:	n/a
12	chr7:12410026-12410076	HCPEpiC	choroid plexus:	n/a
13	chr7:12370351-12370401	MCF-7	breast:	n/a
14	chr7:12411370-12411420	HEK293	kidney:	embryo
15	chr7:12370351-12370401	Hepatocyte	liver:	n/a
16	chr7:12411370-12411420	GM12892	blood:	n/a
17	chr7:12410026-12410076	NHBE	bronchial:	n/a
18	chr7:12370351-12370401	AG09309	skin:	n/a
19	chr7:12376625-12376675	HCF	heart:	n/a
20	chr7:12376625-12376675	SK-N-MC	brain:	n/a
21	chr7:12376625-12376675	PANC-1	pancreas:	n/a
22	chr7:12376625-12376675	MCF-7	breast:	n/a
23	chr7:12410026-12410076	RPTEC	kidney:	n/a
24	chr7:12410026-12410076	A549	lung:	n/a
25	chr7:12410026-12410076	HL-60	blood:	n/a
26	chr7:12376625-12376675	GM06990	blood:	n/a
27	chr7:12410026-12410076	HRPEpiC	eye:	n/a
28	chr7:12363490-12363540	HIPEpiC	eye:	n/a
29	chr7:12376625-12376675	HepG2	liver:	n/a
30	chr7:12411370-12411420	CMK	blood:	n/a
31	chr7:12363490-12363540	NHDF-neo	bronchial:	n/a
32	chr7:12411370-12411420	T-47D	breast:	n/a
33	chr7:12410026-12410076	SK-N-SH	brain:	n/a
34	chr7:12363490-12363540	PANC-1	pancreas:	n/a
35	chr7:12370351-12370401	SK-N-MC	brain:	n/a
36	chr7:12411370-12411420	SAEC	small airway:	n/a
37	chr7:12376625-12376675	AG09319	gingival:	n/a
38	chr7:12411370-12411420	HCF	heart:	n/a
39	chr7:12370351-12370401	HIPEpiC	eye:	n/a
40	chr7:12376625-12376675	HCT-116	colon:	n/a
41	chr7:12410026-12410076	GM12891	blood:	n/a
42	chr7:12370351-12370401	AG10803	skin:	n/a
43	chr7:12370351-12370401	HCM	heart:	n/a
44	chr7:12410026-12410076	SAEC	small airway:	n/a
45	chr7:12376625-12376675	NB4	blood:	n/a
46	chr7:12370351-12370401	BJ	skin:	n/a
47	chr7:12410026-12410076	CMK	blood:	n/a
48	chr7:12411370-12411420	NT2-D1	testis:	n/a
49	chr7:12370351-12370401	HEK293	kidney:	embryo
50	chr7:12370351-12370401	HUVEC	blood vessel:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:12408712..12411098-chr7:12427407..12429029,2	K562	blood:
2	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
3	chr7:12408674..12410212-chr7:12426957..12428907,2	K562	blood:
4	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
5	chr7:12391134..12392692-chr7:12402911..12404517,2	K562	blood:
6	chr7:12428351..12429175-chr7:12529458..12530800,4	MCF-7	breast:
7	chr7:12422294..12424938-chr7:12449157..12451879,2	K562	blood:
8	chr7:12408712..12411098-chr7:12427407..12429029,2	K562	blood:
9	chr7:12354059..12356452-chr7:12416852..12418898,2	K562	blood:
10	chr7:12401550..12404872-chr7:12410854..12415444,4	K562	blood:
11	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
12	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
13	chr7:12398772..12400728-chr7:12416119..12417972,2	K562	blood:
14	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
15	chr7:12251087..12251775-chr7:12361635..12362202,4	MCF-7	breast:
16	chr7:12362049..12364322-chr7:12365857..12368217,3	K562	blood:
17	chr7:12359587..12361942-chr7:12364993..12366787,2	K562	blood:
18	chr7:12402068..12405586-chr7:12406959..12410606,5	K562	blood:
19	chr7:12382799..12385098-chr7:12438700..12441052,2	K562	blood:
20	chr7:12414352..12417133-chr7:12443944..12445537,2	K562	blood:
21	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
22	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
23	chr7:12359785..12361369-chr7:12363361..12365480,2	K562	blood:
24	chr7:12408799..12410708-chr7:12417249..12418833,2	K562	blood:
25	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
26	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
27	chr7:12398772..12400728-chr7:12416119..12417972,2	K562	blood:
28	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
29	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
30	chr7:12359587..12361942-chr7:12364993..12366787,2	K562	blood:
31	chr7:12380686..12382573-chr7:12386582..12389339,2	K562	blood:
32	chr7:12421246..12422799-chr7:12438154..12440817,2	K562	blood:
33	chr7:12252737..12254776-chr7:12374517..12377204,2	K562	blood:
34	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
35	chr7:12423183..12428504-chr7:12441656..12445145,7	K562	blood:
36	chr7:12408799..12410708-chr7:12417249..12418833,2	K562	blood:
37	chr7:12250726..12252615-chr7:12403379..12404987,2	MCF-7	breast:
38	chr7:12426277..12428963-chr7:12530535..12533181,2	K562	blood:
39	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
40	chr7:12428677..12429434-chr7:12476625..12477415,2	K562	blood:
41	chr7:12391914..12394742-chr7:12414391..12416688,2	K562	blood:
42	chr7:12376678..12378667-chr7:12443118..12444758,2	K562	blood:
43	chr7:12106923..12107696-chr7:12361667..12362587,3	MCF-7	breast:
44	chr7:12382924..12384916-chr7:12389053..12391966,2	K562	blood:
45	chr7:12399201..12400947-chr7:12402626..12404166,2	K562	blood:
46	chr7:12399201..12400947-chr7:12402626..12404166,2	K562	blood:
47	chr4:173623488..173624406-chr7:12420850..12421512,2	MCF-7	breast:
48	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
49	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
50	chr7:12356830..12359604-chr7:12404989..12406571,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THSD7A-5	chr7:12376785-12377015	expReg_chr7_1125_-
2	lnc-THSD7A-7	chr7:12380807-12381047	expReg_chr7_1129_-
3	lnc-THSD7A-6	chr7:12378965-12379591	expReg_chr7_1128_-
4	lnc-THSD7A-4	chr7:12370513-12370823	NONHSAT119227
5	lnc-THSD7A-4	chr7:12373091-12373352	NONHSAT119227
6	lnc-THSD7A-8	chr7:12381149-12381601	expReg_chr7_1130_-

No data

Variant related genes	Relation type
VWDE	TF binding region
VWDE	CpG island
ENSG00000203523	chromatin interactions
ENSG00000106460	chromatin interactions
ENSG00000146530	chromatin interactions

Extended variants
information (count: 3413 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3413 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2356167	chr7:12360805-12360806	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186925100	chr7:12360849-12360850	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73290451	chr7:12360858-12360859	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs13437654	chr7:12360883-12360884	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552151089	chr7:12360901-12360902	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571248869	chr7:12360910-12360911	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536907207	chr7:12360934-12360935	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550366225	chr7:12360954-12360955	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7782613	chr7:12360956-12360957	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs191773874	chr7:12360974-12360975	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138000948	chr7:12360988-12360989	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572833258	chr7:12361098-12361099	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73290452	chr7:12361162-12361163	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs73679941	chr7:12361172-12361173	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs576015920	chr7:12361216-12361217	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544871077	chr7:12361287-12361288	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149478473	chr7:12361291-12361292	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574941684	chr7:12361323-12361324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73679942	chr7:12361329-12361330	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs182893890	chr7:12361334-12361335	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12699362	chr7:12361337-12361338	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs186863971	chr7:12361344-12361345	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74865431	chr7:12361350-12361351	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34234902	chr7:12361411-12361412	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114554536	chr7:12361416-12361417	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150539511	chr7:12361444-12361445	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576214709	chr7:12361508-12361509	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114958862	chr7:12361528-12361529	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191749177	chr7:12361572-12361573	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143052033	chr7:12361607-12361608	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73679943	chr7:12361608-12361609	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs80317059	chr7:12361611-12361612	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370735104	chr7:12361627-12361628	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182113901	chr7:12361647-12361648	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558587868	chr7:12361654-12361655	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6971849	chr7:12361678-12361679	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs73679945	chr7:12361700-12361701	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs555277086	chr7:12361719-12361720	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566345731	chr7:12361744-12361745	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540863563	chr7:12361745-12361746	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554033629	chr7:12361765-12361766	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs77046567	chr7:12361773-12361774	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73679947	chr7:12361794-12361795	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs527551277	chr7:12361796-12361797	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2024441	chr7:12361834-12361835	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs370442130	chr7:12361841-12361842	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs111292037	chr7:12361843-12361844	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112287921	chr7:12361852-12361853	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73679948	chr7:12361853-12361854	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138523946	chr7:12361875-12361876	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Multiple myeloma	17550852	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12351000-12367600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:12354400-12405000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:12354800-12364800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:12358000-12361800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:12360000-12362400	Enhancers	A549	lung
6	chr7:12360200-12361000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:12360400-12362400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr7:12360400-12367600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:12360400-12367800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr7:12360600-12361000	Genic enhancers	K562	blood
11	chr7:12361000-12361200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr7:12361000-12361600	Strong transcription	K562	blood
13	chr7:12361000-12363000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:12361200-12367800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr7:12361600-12363600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr7:12361600-12367000	Weak transcription	K562	blood
17	chr7:12362200-12362400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:12362200-12363800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr7:12362200-12364000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr7:12362400-12362800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:12362800-12363400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr7:12363000-12363200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:12363200-12363600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:12363200-12364000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:12363400-12367600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr7:12363400-12367800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:12363600-12367400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr7:12363600-12367600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr7:12363800-12367600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr7:12363800-12392800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr7:12364000-12367200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr7:12364000-12367600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr7:12366000-12369800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:12367000-12372000	Strong transcription	K562	blood
35	chr7:12367200-12368200	Enhancers	Fetal Intestine Large	intestine
36	chr7:12367200-12371800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:12367400-12372000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr7:12367600-12367800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:12367600-12367800	Enhancers	Pancreas	Pancrea
40	chr7:12367600-12368200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:12367600-12368200	Enhancers	Fetal Intestine Small	intestine
42	chr7:12367600-12368400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr7:12367600-12368400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr7:12367600-12368800	Enhancers	H9 Cell Line	embryonic stem cell
45	chr7:12367600-12368800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr7:12367600-12369000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr7:12367600-12369000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr7:12367600-12372000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr7:12367800-12368200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:12367800-12368600	Genic enhancers	iPS-20b Cell Line	embryonic stem cell

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