Variant report

Variant	nsv606277
Chromosome Location	chr7:13907827-13967377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:13915440-13915557	K562	blood:	n/a	n/a
2	ARID3A	chr7:13959750-13960140	K562	blood:	n/a	n/a
3	ATF1	chr7:13959834-13960225	K562	blood:	n/a	n/a
4	ATF1	chr7:13934044-13934292	K562	blood:	n/a	n/a
5	BHLHE40	chr7:13915327-13915479	K562	blood:	n/a	n/a
6	BHLHE40	chr7:13959838-13960065	K562	blood:	n/a	n/a
7	BRCA1	chr7:13959665-13960170	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr7:13919496-13920313	HCT-116	colon:	n/a	n/a
9	CBX3	chr7:13919485-13920390	HCT-116	colon:	n/a	n/a
10	CBX3	chr7:13959551-13960396	HCT-116	colon:	n/a	n/a
11	CBX3	chr7:13948217-13948986	HCT-116	colon:	n/a	n/a
12	CBX3	chr7:13959648-13960390	HCT-116	colon:	n/a	n/a
13	CCNT2	chr7:13945243-13945446	K562	blood:	n/a	n/a
14	CEBPB	chr7:13959668-13960221	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:13928817-13928939	K562	blood:	n/a	chr7:13928854-13928865
16	CEBPB	chr7:13937479-13937812	IMR90	lung:	n/a	chr7:13937627-13937640 chr7:13937628-13937639 chr7:13937627-13937640 chr7:13937586-13937597 chr7:13937627-13937638 chr7:13937585-13937596
17	CEBPB	chr7:13943701-13944070	K562	blood:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
18	CEBPB	chr7:13948068-13949024	HCT-116	colon:	n/a	chr7:13948234-13948247
19	CEBPB	chr7:13959726-13960325	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr7:13948318-13948725	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:13948360-13948639	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:13928771-13928971	HepG2	liver:	n/a	chr7:13928854-13928865
23	CEBPB	chr7:13943706-13944047	HepG2	liver:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
24	CEBPB	chr7:13935047-13935258	HepG2	liver:	n/a	chr7:13935149-13935160
25	CEBPB	chr7:13948119-13948927	HCT-116	colon:	n/a	chr7:13948234-13948247
26	CEBPB	chr7:13937516-13937723	HepG2	liver:	n/a	chr7:13937627-13937640 chr7:13937628-13937639 chr7:13937627-13937640 chr7:13937586-13937597 chr7:13937627-13937638 chr7:13937585-13937596
27	CEBPB	chr7:13943733-13944059	ECC-1	luminal epithelium:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
28	CEBPB	chr7:13943727-13943994	K562	blood:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
29	CEBPB	chr7:13943812-13943971	H1-hESC	embryonic stem cell:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
30	CEBPB	chr7:13943752-13944082	ECC-1	luminal epithelium:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
31	CEBPB	chr7:13943774-13943999	K562	blood:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
32	CEBPB	chr7:13928758-13928975	IMR90	lung:	n/a	chr7:13928854-13928865
33	CEBPB	chr7:13943707-13944054	A549	lung:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
34	CEBPB	chr7:13943678-13944033	Hela-S3	cervix:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
35	CEBPB	chr7:13959724-13960187	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:13943530-13944071	IMR90	lung:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
37	CEBPB	chr7:13923797-13923997	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:13932728-13932820	A549	lung:	n/a	n/a
39	CEBPB	chr7:13943702-13944046	A549	lung:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
40	CHD2	chr7:13919878-13919971	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr7:13959631-13960239	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr7:13962900-13963050	HCFaa	heart:	n/a	n/a
43	CTCF	chr7:13934684-13934862	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr7:13962782-13963055	IMR90	lung:	n/a	n/a
45	CTCF	chr7:13919820-13919970	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr7:13928534-13928592	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr7:13962900-13963050	HCT-116	colon:	n/a	n/a
48	CTCF	chr7:13934710-13934828	K562	blood:	n/a	n/a
49	CTCF	chr7:13919660-13919810	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr7:13962840-13962990	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13960140-13960190	HL-60	blood:	n/a
2	chr7:13960140-13960190	HL-60	blood:	n/a
3	chr7:13935467-13935517	NH-A	brain:	n/a
4	chr7:13960140-13960190	HEK293	kidney:	embryo
5	chr7:13960140-13960190	HRPEpiC	eye:	n/a
6	chr7:13960140-13960190	HCPEpiC	choroid plexus:	n/a
7	chr7:13960140-13960190	Hepatocyte	liver:	n/a
8	chr7:13960140-13960190	LNCaP	prostate:	n/a
9	chr7:13960140-13960190	ECC-1	luminal epithelium:	n/a
10	chr7:13935467-13935517	HNPCEpiC	eye:	n/a
11	chr7:13960140-13960190	ovcar-3	ovarian:	n/a
12	chr7:13960140-13960190	HUVEC	blood vessel:	n/a
13	chr7:13960140-13960190	HRE	kidney:	n/a
14	chr7:13960140-13960190	Hela-S3	cervix:	n/a
15	chr7:13960140-13960190	T-47D	breast:	n/a
16	chr7:13935467-13935517	PFSK-1	brain:	n/a
17	chr7:13935467-13935517	HUVEC	blood vessel:	n/a
18	chr7:13935467-13935517	HEEpiC	esophagus:	n/a
19	chr7:13960140-13960190	HMEC	breast:	n/a
20	chr7:13960140-13960190	NH-A	brain:	n/a
21	chr7:13960140-13960190	GM12878	blood:	n/a
22	chr7:13935467-13935517	BJ	skin:	n/a
23	chr7:13935467-13935517	AG09309	skin:	n/a
24	chr7:13935467-13935517	RPTEC	kidney:	n/a
25	chr7:13960140-13960190	NB4	blood:	n/a
26	chr7:13935467-13935517	AG04450	lung:	fetal
27	chr7:13960140-13960190	ProgFib	skin:	n/a
28	chr7:13935467-13935517	HAEpiC	amniotic membrane:	n/a
29	chr7:13935467-13935517	SK-N-SH_RA	brain:	n/a
30	chr7:13935467-13935517	NHDF-neo	bronchial:	n/a
31	chr7:13935467-13935517	Caco-2	colon:	n/a
32	chr7:13935467-13935517	HepG2	liver:	n/a
33	chr7:13935467-13935517	HCT-116	colon:	n/a
34	chr7:13960140-13960190	NHDF-neo	bronchial:	n/a
35	chr7:13935467-13935517	ProgFib	skin:	n/a
36	chr7:13935467-13935517	NHBE	bronchial:	n/a
37	chr7:13935467-13935517	HL-60	blood:	n/a
38	chr7:13960140-13960190	AG04449	skin:	fetal
39	chr7:13935467-13935517	Jurkat	blood:	n/a
40	chr7:13960140-13960190	BE2_C	brain:	n/a
41	chr7:13935467-13935517	SK-N-SH	brain:	n/a
42	chr7:13935467-13935517	GM12878	blood:	n/a
43	chr7:13935467-13935517	SAEC	small airway:	n/a
44	chr7:13960140-13960190	PANC-1	pancreas:	n/a
45	chr7:13960140-13960190	RPTEC	kidney:	n/a
46	chr7:13935467-13935517	ovcar-3	ovarian:	n/a
47	chr7:13960140-13960190	HCF	heart:	n/a
48	chr7:13935467-13935517	MCF-7	breast:	n/a
49	chr7:13960140-13960190	PFSK-1	brain:	n/a
50	chr7:13960140-13960190	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:13929540..13931526-chr7:13932770..13934783,2	K562	blood:
2	chr7:13937992..13940139-chr7:13941426..13943158,2	K562	blood:
3	chr7:13931063..13934018-chr7:13935773..13937430,2	K562	blood:
4	chr7:13940952..13942572-chr7:13946206..13948609,2	K562	blood:
5	chr7:13921967..13924964-chr7:13941231..13943091,2	K562	blood:
6	chr7:13941782..13943979-chr7:13946074..13948883,2	K562	blood:
7	chr7:13946657..13948257-chr7:13950013..13952270,2	K562	blood:
8	chr7:13940952..13942572-chr7:13946206..13948609,2	K562	blood:
9	chr7:13929540..13931526-chr7:13932770..13934783,2	K562	blood:
10	chr7:13946657..13948257-chr7:13950013..13952270,2	K562	blood:
11	chr7:13929008..13930898-chr7:13949066..13950636,2	K562	blood:
12	chr7:13898559..13901034-chr7:13906643..13908176,2	K562	blood:
13	chr7:13934057..13934906-chr7:14497131..14498025,4	MCF-7	breast:
14	chr7:13934709..13935267-chr7:14497324..14498029,2	MCF-7	breast:
15	chr7:13953124..13955887-chr7:14024617..14027108,2	K562	blood:
16	chr7:13937992..13940139-chr7:13941426..13943158,2	K562	blood:
17	chr7:13964325..13967217-chr7:14020611..14022495,2	K562	blood:
18	chr7:13921967..13924964-chr7:13941231..13943091,2	K562	blood:
19	chr7:13961833..13964592-chr7:14031302..14033936,2	K562	blood:
20	chr7:13894294..13896373-chr7:13930641..13933578,2	K562	blood:
21	chr7:13929008..13930898-chr7:13949066..13950636,2	K562	blood:
22	chr7:13931063..13934018-chr7:13935773..13937430,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL4A-8	chr7:13934333-13934794	NONHSAT119259

Variant related genes	Relation type
ETV1	TF binding region
ENSG00000213875	TF binding region
ETV1	CpG island
ENSG00000213875	CpG island
ENSG00000006468	chromatin interactions
ENSG00000224330	chromatin interactions

Extended variants
information (count: 2467 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2467 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs251994	chr7:13907827-13907828	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74496589	chr7:13907838-13907839	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs151128433	chr7:13907839-13907840	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs140041993	chr7:13907840-13907841	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150299251	chr7:13907866-13907867	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564662230	chr7:13907881-13907882	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530505223	chr7:13907887-13907888	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs372911907	chr7:13907923-13907924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs116398790	chr7:13907931-13907932	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529645229	chr7:13907935-13907936	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs546587469	chr7:13907938-13907939	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs377336644	chr7:13907946-13907947	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs137964478	chr7:13907955-13907956	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538858023	chr7:13907956-13907957	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552380521	chr7:13907964-13907965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571806147	chr7:13907971-13907972	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537534014	chr7:13907995-13907996	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557373982	chr7:13908057-13908058	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567558378	chr7:13908111-13908112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536610475	chr7:13908159-13908160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568627247	chr7:13910609-13910610	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs559098428	chr7:13910614-13910615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs563010358	chr7:13910639-13910640	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs547989873	chr7:13910662-13910663	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs570597629	chr7:13910669-13910670	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs539532750	chr7:13910690-13910691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs555937101	chr7:13910707-13910708	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs79375394	chr7:13910708-13910709	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs535070580	chr7:13910712-13910713	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs78514586	chr7:13910714-13910715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs6962343	chr7:13910748-13910749	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs548603398	chr7:13910764-13910765	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs535199205	chr7:13910798-13910799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs115179741	chr7:13910825-13910826	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs146828009	chr7:13910850-13910851	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs138077580	chr7:13913608-13913609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149543312	chr7:13913616-13913617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144162676	chr7:13913625-13913626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140005025	chr7:13913626-13913627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549050064	chr7:13913627-13913628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539713752	chr7:13913635-13913636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530004729	chr7:13913657-13913658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568992037	chr7:13913660-13913661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546862380	chr7:13913692-13913693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs118087466	chr7:13913717-13913718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532304708	chr7:13913758-13913759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551921216	chr7:13913803-13913804	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs571687261	chr7:13913829-13913830	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs141962629	chr7:13913846-13913847	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs576338304	chr7:13913859-13913860	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	21298110	CNVD
Glioblastoma multiforme	22122801	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Prostate cancer	17079440	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13913600-13913800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:13913800-13914000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:13913800-13914000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:13913800-13914000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:13913800-13914000	Enhancers	NHLF	lung
6	chr7:13913800-13914000	Enhancers	Osteobl	bone
7	chr7:13913800-13914200	Enhancers	Dnd41	blood
8	chr7:13913800-13914800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:13914000-13914200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:13914000-13914400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr7:13914000-13914400	Flanking Active TSS	NHLF	lung
12	chr7:13914000-13914400	Flanking Active TSS	Osteobl	bone
13	chr7:13914000-13914600	Enhancers	HSMM	muscle
14	chr7:13914000-13914800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:13914000-13914800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:13914000-13915000	Enhancers	Fetal Lung	lung
17	chr7:13914000-13915200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr7:13914000-13915400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:13914000-13915400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:13914000-13915600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:13914200-13914600	Flanking Active TSS	Dnd41	blood
22	chr7:13914200-13914600	Active TSS	NHDF-Ad	bronchial
23	chr7:13914200-13914800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:13914200-13914800	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr7:13914400-13914800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
26	chr7:13914400-13914800	Active TSS	Osteobl	bone
27	chr7:13914400-13915000	Enhancers	NHLF	lung
28	chr7:13914400-13915200	Enhancers	NH-A	brain
29	chr7:13914600-13915000	Enhancers	NHDF-Ad	bronchial
30	chr7:13914600-13915400	Enhancers	Dnd41	blood
31	chr7:13914600-13919000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:13914600-13919400	Weak transcription	HSMM	muscle
33	chr7:13914800-13915000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:13914800-13915000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:13914800-13915000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:13914800-13915200	Enhancers	Osteobl	bone
37	chr7:13914800-13915400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:13914800-13915800	Enhancers	K562	blood
39	chr7:13915000-13915200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:13915000-13919400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:13915000-13919400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:13915000-13919400	Weak transcription	NHDF-Ad	bronchial
43	chr7:13915000-13919600	Weak transcription	NHLF	lung
44	chr7:13915200-13918400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr7:13915200-13919000	Weak transcription	Osteobl	bone
46	chr7:13915200-13919400	Weak transcription	NH-A	brain
47	chr7:13915200-13919800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:13915400-13918800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr7:13917000-13917800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr7:13917800-13919800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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