Variant report

Variant	esv2763622
Chromosome Location	chr7:12375528-12424583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:272)
CpG islands
(count:183)
Chromatin interactive
region (count:49)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:12391517-12391830	K562	blood:	n/a	n/a
2	ATF2	chr7:12397170-12397485	GM12878	blood:	n/a	n/a
3	BACH1	chr7:12409290-12409383	K562	blood:	n/a	n/a
4	BCL3	chr7:12397240-12397520	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:12391626-12391783	K562	blood:	n/a	n/a
6	BHLHE40	chr7:12412689-12412834	GM12878	blood:	n/a	n/a
7	CCNT2	chr7:12383002-12383143	K562	blood:	n/a	n/a
8	CCNT2	chr7:12422140-12422303	K562	blood:	n/a	n/a
9	CCNT2	chr7:12405891-12406052	K562	blood:	n/a	n/a
10	CCNT2	chr7:12391547-12391847	K562	blood:	n/a	n/a
11	CCNT2	chr7:12418952-12419019	K562	blood:	n/a	n/a
12	CCNT2	chr7:12403056-12403099	K562	blood:	n/a	n/a
13	CEBPB	chr7:12413219-12413802	K562	blood:	n/a	chr7:12413407-12413418
14	CEBPB	chr7:12413265-12413569	H1-hESC	embryonic stem cell:	n/a	chr7:12413407-12413418
15	CEBPB	chr7:12413221-12413469	K562	blood:	n/a	chr7:12413407-12413418
16	CEBPB	chr7:12413202-12413543	A549	lung:	n/a	chr7:12413407-12413418
17	CEBPB	chr7:12413224-12413590	HepG2	liver:	n/a	chr7:12413407-12413418
18	CEBPB	chr7:12413230-12413569	A549	lung:	n/a	chr7:12413407-12413418
19	CEBPB	chr7:12418167-12418474	K562	blood:	n/a	chr7:12418334-12418345 chr7:12418333-12418346 chr7:12418333-12418344
20	CEBPB	chr7:12413251-12413595	IMR90	lung:	n/a	chr7:12413407-12413418
21	CEBPB	chr7:12418196-12418500	HepG2	liver:	n/a	chr7:12418334-12418345 chr7:12418333-12418346 chr7:12418333-12418344
22	CEBPB	chr7:12376804-12377018	IMR90	lung:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
23	CEBPB	chr7:12413170-12413593	A549	lung:	n/a	chr7:12413407-12413418
24	CEBPB	chr7:12376796-12377033	K562	blood:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
25	CEBPB	chr7:12376790-12377114	A549	lung:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
26	CEBPB	chr7:12413201-12413548	ECC-1	luminal epithelium:	n/a	chr7:12413407-12413418
27	CEBPB	chr7:12413235-12413751	Hela-S3	cervix:	n/a	chr7:12413407-12413418
28	CEBPB	chr7:12413192-12413834	K562	blood:	n/a	chr7:12413407-12413418
29	CEBPB	chr7:12422917-12423570	Hela-S3	cervix:	n/a	chr7:12422959-12422970
30	CEBPB	chr7:12376799-12377121	HepG2	liver:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
31	CEBPB	chr7:12397108-12397677	GM12878	blood:	n/a	n/a
32	CHD2	chr7:12409741-12410041	K562	blood:	n/a	n/a
33	CHD2	chr7:12418162-12418528	K562	blood:	n/a	n/a
34	CHD2	chr7:12403775-12403837	K562	blood:	n/a	n/a
35	CHD2	chr7:12409281-12409385	K562	blood:	n/a	n/a
36	CHD2	chr7:12408202-12408583	K562	blood:	n/a	n/a
37	CHD2	chr7:12404357-12404706	K562	blood:	n/a	n/a
38	CHD2	chr7:12405468-12405540	K562	blood:	n/a	n/a
39	CHD2	chr7:12391646-12391710	K562	blood:	n/a	n/a
40	CTCF	chr7:12423157-12423247	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr7:12409440-12409590	SK-N-SH_RA	brain:	n/a	n/a
42	CUX1	chr7:12413704-12413756	K562	blood:	n/a	n/a
43	CUX1	chr7:12424107-12424438	K562	blood:	n/a	n/a
44	CUX1	chr7:12420650-12420776	GM12878	blood:	n/a	n/a
45	E2F4	chr7:12420638-12420788	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr7:12380533-12380704	MCF10A-Er-Src	breast:	n/a	n/a
47	ELF1	chr7:12391547-12391792	K562	blood:	n/a	chr7:12391648-12391661
48	EP300	chr7:12413426-12413824	K562	blood:	n/a	n/a
49	EP300	chr7:12391588-12391816	K562	blood:	n/a	n/a
50	EP300	chr7:12382017-12382153	K562	blood:	n/a	chr7:12382116-12382125

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12411370-12411420	H1-hESC	embryonic stem cell:	embryo
2	chr7:12376625-12376675	A549	lung:	n/a
3	chr7:12411370-12411420	GM12891	blood:	n/a
4	chr7:12376625-12376675	AoSMC	blood vessel:	n/a
5	chr7:12411370-12411420	PANC-1	pancreas:	n/a
6	chr7:12376625-12376675	T-47D	breast:	n/a
7	chr7:12410026-12410076	ovcar-3	ovarian:	n/a
8	chr7:12376625-12376675	ProgFib	skin:	n/a
9	chr7:12376625-12376675	AG04450	lung:	fetal
10	chr7:12411370-12411420	Hepatocyte	liver:	n/a
11	chr7:12410026-12410076	HEEpiC	esophagus:	n/a
12	chr7:12410026-12410076	SK-N-SH	brain:	n/a
13	chr7:12410026-12410076	GM12892	blood:	n/a
14	chr7:12410026-12410076	Hela-S3	cervix:	n/a
15	chr7:12376625-12376675	HCF	heart:	n/a
16	chr7:12410026-12410076	SKMC	muscle:	n/a
17	chr7:12411370-12411420	HNPCEpiC	eye:	n/a
18	chr7:12376625-12376675	AG10803	skin:	n/a
19	chr7:12410026-12410076	HUVEC	blood vessel:	n/a
20	chr7:12411370-12411420	HRE	kidney:	n/a
21	chr7:12410026-12410076	MCF-7	breast:	n/a
22	chr7:12376625-12376675	SK-N-SH	brain:	n/a
23	chr7:12410026-12410076	HRCEpiC	kidney:	n/a
24	chr7:12410026-12410076	Caco-2	colon:	n/a
25	chr7:12410026-12410076	A549	lung:	n/a
26	chr7:12411370-12411420	AG09309	skin:	n/a
27	chr7:12410026-12410076	GM19239	blood:	n/a
28	chr7:12410026-12410076	CMK	blood:	n/a
29	chr7:12411370-12411420	HCF	heart:	n/a
30	chr7:12411370-12411420	AG10803	skin:	n/a
31	chr7:12410026-12410076	BE2_C	brain:	n/a
32	chr7:12411370-12411420	SAEC	small airway:	n/a
33	chr7:12411370-12411420	SK-N-MC	brain:	n/a
34	chr7:12411370-12411420	AG04449	skin:	fetal
35	chr7:12411370-12411420	ProgFib	skin:	n/a
36	chr7:12411370-12411420	PFSK-1	brain:	n/a
37	chr7:12376625-12376675	BJ	skin:	n/a
38	chr7:12376625-12376675	HUVEC	blood vessel:	n/a
39	chr7:12411370-12411420	K562	blood:	n/a
40	chr7:12410026-12410076	ECC-1	luminal epithelium:	n/a
41	chr7:12376625-12376675	HNPCEpiC	eye:	n/a
42	chr7:12411370-12411420	SK-N-SH	brain:	n/a
43	chr7:12410026-12410076	Hepatocyte	liver:	n/a
44	chr7:12411370-12411420	AG09319	gingival:	n/a
45	chr7:12411370-12411420	HMEC	breast:	n/a
46	chr7:12376625-12376675	GM12891	blood:	n/a
47	chr7:12411370-12411420	Caco-2	colon:	n/a
48	chr7:12410026-12410076	GM12878	blood:	n/a
49	chr7:12410026-12410076	PFSK-1	brain:	n/a
50	chr7:12376625-12376675	NHBE	bronchial:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12391914..12394742-chr7:12414391..12416688,2	K562	blood:
2	chr7:12408674..12410212-chr7:12426957..12428907,2	K562	blood:
3	chr7:12391134..12392692-chr7:12402911..12404517,2	K562	blood:
4	chr7:12398772..12400728-chr7:12416119..12417972,2	K562	blood:
5	chr7:12399201..12400947-chr7:12402626..12404166,2	K562	blood:
6	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
7	chr7:12252737..12254776-chr7:12374517..12377204,2	K562	blood:
8	chr7:12401893..12405448-chr7:12416442..12419735,3	K562	blood:
9	chr7:12382924..12384916-chr7:12389053..12391966,2	K562	blood:
10	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
11	chr7:12408712..12411098-chr7:12427407..12429029,2	K562	blood:
12	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
13	chr7:12402068..12405586-chr7:12406959..12410606,5	K562	blood:
14	chr7:12401550..12404872-chr7:12410854..12415444,4	K562	blood:
15	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
16	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
17	chr4:173623488..173624406-chr7:12420850..12421512,2	MCF-7	breast:
18	chr7:12391914..12394742-chr7:12414391..12416688,2	K562	blood:
19	chr7:12408799..12410708-chr7:12417249..12418833,2	K562	blood:
20	chr7:12391134..12392692-chr7:12402911..12404517,2	K562	blood:
21	chr7:12380686..12382573-chr7:12386582..12389339,2	K562	blood:
22	chr7:12423183..12428504-chr7:12441656..12445145,7	K562	blood:
23	chr7:12399201..12400947-chr7:12402626..12404166,2	K562	blood:
24	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
25	chr7:12356830..12359604-chr7:12404989..12406571,2	K562	blood:
26	chr7:12401893..12405448-chr7:12416442..12419735,3	K562	blood:
27	chr7:12408799..12410708-chr7:12417249..12418833,2	K562	blood:
28	chr7:12401550..12404872-chr7:12410854..12415444,4	K562	blood:
29	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
30	chr7:12382924..12384916-chr7:12389053..12391966,2	K562	blood:
31	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
32	chr7:12422294..12424938-chr7:12449157..12451879,2	K562	blood:
33	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
34	chr7:12376678..12378667-chr7:12443118..12444758,2	K562	blood:
35	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
36	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
37	chr7:12421246..12422799-chr7:12438154..12440817,2	K562	blood:
38	chr7:12380686..12382573-chr7:12386582..12389339,2	K562	blood:
39	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
40	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
41	chr7:12402068..12405586-chr7:12406959..12410606,5	K562	blood:
42	chr7:12382799..12385098-chr7:12438700..12441052,2	K562	blood:
43	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
44	chr7:12250726..12252615-chr7:12403379..12404987,2	MCF-7	breast:
45	chr7:12414352..12417133-chr7:12443944..12445537,2	K562	blood:
46	chr7:12354059..12356452-chr7:12416852..12418898,2	K562	blood:
47	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
48	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
49	chr7:12398772..12400728-chr7:12416119..12417972,2	K562	blood:

(count:4 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2224 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2224 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185514837	chr7:12375563-12375564	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs74626405	chr7:12375667-12375668	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs78493184	chr7:12375668-12375669	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs367551600	chr7:12375673-12375674	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs78646430	chr7:12375674-12375675	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs537915649	chr7:12375683-12375684	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs554629821	chr7:12375686-12375687	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs138386323	chr7:12375706-12375707	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs574523410	chr7:12375754-12375755	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs79222040	chr7:12375766-12375767	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs201785224	chr7:12375767-12375768	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs565483238	chr7:12375774-12375775	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs374822025	chr7:12375776-12375777	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs544020247	chr7:12375778-12375779	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs370171246	chr7:12375779-12375780	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs373415584	chr7:12375809-12375810	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs544895591	chr7:12375832-12375833	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs576179035	chr7:12375842-12375843	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs565035253	chr7:12375871-12375872	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs200181513	chr7:12375872-12375873	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs376084422	chr7:12375947-12375948	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs530707040	chr7:12375949-12375950	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs188711103	chr7:12375954-12375955	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs560962762	chr7:12375960-12375961	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs137918880	chr7:12375983-12375984	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs80045192	chr7:12375995-12375996	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs377386471	chr7:12376035-12376036	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs575892536	chr7:12376044-12376045	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs567057009	chr7:12376069-12376070	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs532814042	chr7:12376080-12376081	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552369942	chr7:12376082-12376083	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs569143066	chr7:12376109-12376110	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs73290495	chr7:12376110-12376111	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs55664102	chr7:12376156-12376157	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs60783223	chr7:12376175-12376176	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs77595649	chr7:12376209-12376210	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs117683026	chr7:12376241-12376242	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs73292356	chr7:12376288-12376289	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs552889215	chr7:12376306-12376307	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs58252466	chr7:12376307-12376308	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs111377470	chr7:12376400-12376401	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs565347272	chr7:12376417-12376418	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs575556989	chr7:12376425-12376426	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544408836	chr7:12376426-12376427	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs143796241	chr7:12376432-12376433	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs569834545	chr7:12376459-12376460	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs560973348	chr7:12376461-12376462	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs528857413	chr7:12376498-12376499	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs146254600	chr7:12376516-12376517	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs539871342	chr7:12376526-12376527	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12354400-12405000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:12363800-12392800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:12368200-12433200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:12368800-12376600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:12370400-12376200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:12370400-12384800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:12370600-12379000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:12371800-12376200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:12372000-12375800	Weak transcription	K562	blood
10	chr7:12372000-12376200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:12372000-12376400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:12372000-12376600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr7:12372000-12376600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr7:12372000-12376600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr7:12372000-12379800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:12373400-12375800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:12375800-12377000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:12375800-12387200	Strong transcription	K562	blood
19	chr7:12376200-12376800	Genic enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:12376200-12377000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:12376200-12377200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr7:12376400-12385800	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr7:12376600-12377000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr7:12376600-12377000	Genic enhancers	H9 Cell Line	embryonic stem cell
25	chr7:12376600-12377000	Genic enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:12376600-12377200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr7:12376800-12385800	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr7:12377000-12378400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr7:12377000-12379000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr7:12377000-12379400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:12377000-12385000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr7:12377000-12408000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr7:12377200-12378400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr7:12377200-12380400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr7:12378400-12380600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
36	chr7:12378400-12385600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr7:12379000-12382800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:12379000-12386000	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr7:12379400-12382800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr7:12379800-12381800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:12380200-12380600	Enhancers	Brain Germinal Matrix	brain
42	chr7:12380400-12381800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
43	chr7:12380600-12393400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr7:12381800-12390400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:12381800-12429000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr7:12382800-12385000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:12382800-12390800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:12383400-12401800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr7:12384800-12385400	Strong transcription	H1 Cell Line	embryonic stem cell
50	chr7:12385000-12385600	Strong transcription	ES-I3 Cell Line	embryonic stem cell

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