Variant report

Variant	nsv1016072
Chromosome Location	chr7:70297559-70358327
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	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
3	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:70321901-70322317	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
8	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
9	CEBPB	chr7:70299440-70299798	HepG2	liver:	n/a	chr7:70299603-70299614
10	CEBPB	chr7:70314283-70314959	H1-hESC	embryonic stem cell:	n/a	chr7:70314674-70314686
11	CEBPB	chr7:70349310-70349766	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr7:70299455-70299763	K562	blood:	n/a	chr7:70299603-70299614
13	CEBPB	chr7:70299422-70299775	IMR90	lung:	n/a	chr7:70299603-70299614
14	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:70299521-70299730	H1-hESC	embryonic stem cell:	n/a	chr7:70299603-70299614
16	CEBPB	chr7:70299453-70299778	A549	lung:	n/a	chr7:70299603-70299614
17	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
18	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
19	CHD2	chr7:70323263-70323459	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr7:70314201-70315062	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr7:70349262-70350113	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:70321862-70322262	H1-hESC	embryonic stem cell:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
23	CTCF	chr7:70320557-70320642	HepG2	liver:	n/a	n/a
24	CTCF	chr7:70322000-70322150	HFF	foreskin:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
25	CTCF	chr7:70321923-70322300	K562	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
26	CTCF	chr7:70321980-70322130	Caco-2	colon:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
27	CTCF	chr7:70322020-70322170	RPTEC	kidney:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
28	CTCF	chr7:70322400-70322550	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr7:70322008-70322189	A549	lung:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
30	CTCF	chr7:70322020-70322170	AG04450	lung:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
31	CTCF	chr7:70321960-70322217	A549	lung:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
32	CTCF	chr7:70321992-70322160	A549	lung:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
33	CTCF	chr7:70321960-70322110	A549	lung:	n/a	chr7:70322093-70322106 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
34	CTCF	chr7:70322060-70322210	HAc	cerebellar:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
35	CTCF	chr7:70321895-70322287	T-47D	breast:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
36	CTCF	chr7:70322020-70322170	AG10803	skin:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
37	CTCF	chr7:70321660-70321810	SAEC	small airway:	n/a	n/a
38	CTCF	chr7:70322040-70322190	BJ	skin:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
39	CTCF	chr7:70322020-70322170	HPF	lung:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
40	CTCF	chr7:70322000-70322150	GM12872	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
41	CTCF	chr7:70321865-70322315	H1-hESC	embryonic stem cell:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
42	CTCF	chr7:70322020-70322170	HepG2	liver:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
43	CTCF	chr7:70321982-70322243	ECC-1	luminal epithelium:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
44	CTCF	chr7:70321742-70321780	GM12878	blood:	n/a	n/a
45	CTCF	chr7:70321398-70321473	GM10266	blood:	n/a	n/a
46	CTCF	chr7:70322040-70322190	HAc	cerebellar:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
47	CTCF	chr7:70321930-70322265	K562	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
48	CTCF	chr7:70322000-70322150	GM12801	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
49	CTCF	chr7:70322420-70322570	AG09309	skin:	n/a	n/a
50	CTCF	chr7:70321851-70322315	T-47D	breast:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70311532-70311582	LNCaP	prostate:	n/a
2	chr7:70311532-70311582	LNCaP	prostate:	n/a
3	chr7:70311532-70311582	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:70311321-70311371	HIPEpiC	eye:	n/a
5	chr7:70311321-70311371	HUVEC	blood vessel:	n/a
6	chr7:70322401-70322451	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:70311435-70311485	AG10803	skin:	n/a
8	chr7:70322401-70322451	GM19239	blood:	n/a
9	chr7:70311321-70311371	GM19239	blood:	n/a
10	chr7:70311321-70311371	HCT-116	colon:	n/a
11	chr7:70311321-70311371	HL-60	blood:	n/a
12	chr7:70311321-70311371	NHDF-neo	bronchial:	n/a
13	chr7:70322401-70322451	AG09319	gingival:	n/a
14	chr7:70311321-70311371	NHBE	bronchial:	n/a
15	chr7:70311435-70311485	ovcar-3	ovarian:	n/a
16	chr7:70311321-70311371	HNPCEpiC	eye:	n/a
17	chr7:70322401-70322451	NHDF-neo	bronchial:	n/a
18	chr7:70311532-70311582	AG10803	skin:	n/a
19	chr7:70311435-70311485	Jurkat	blood:	n/a
20	chr7:70311321-70311371	BE2_C	brain:	n/a
21	chr7:70311321-70311371	K562	blood:	n/a
22	chr7:70311532-70311582	MCF10A-Er-Src	breast:	n/a
23	chr7:70311532-70311582	PFSK-1	brain:	n/a
24	chr7:70311532-70311582	HCT-116	colon:	n/a
25	chr7:70322401-70322451	HRPEpiC	eye:	n/a
26	chr7:70311435-70311485	AG09309	skin:	n/a
27	chr7:70311321-70311371	T-47D	breast:	n/a
28	chr7:70322401-70322451	A549	lung:	n/a
29	chr7:70311532-70311582	IMR90	lung:	fetal
30	chr7:70311321-70311371	GM06990	blood:	n/a
31	chr7:70311532-70311582	GM12892	blood:	n/a
32	chr7:70311532-70311582	HEEpiC	esophagus:	n/a
33	chr7:70322401-70322451	ProgFib	skin:	n/a
34	chr7:70311532-70311582	GM06990	blood:	n/a
35	chr7:70311532-70311582	HCPEpiC	choroid plexus:	n/a
36	chr7:70311321-70311371	Jurkat	blood:	n/a
37	chr7:70322401-70322451	HCM	heart:	n/a
38	chr7:70322401-70322451	CMK	blood:	n/a
39	chr7:70311532-70311582	HCF	heart:	n/a
40	chr7:70311435-70311485	ProgFib	skin:	n/a
41	chr7:70311321-70311371	AG09319	gingival:	n/a
42	chr7:70311435-70311485	A549	lung:	n/a
43	chr7:70311321-70311371	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:70311435-70311485	NHBE	bronchial:	n/a
45	chr7:70311321-70311371	GM12878	blood:	n/a
46	chr7:70322401-70322451	SKMC	muscle:	n/a
47	chr7:70322401-70322451	HRE	kidney:	n/a
48	chr7:70322401-70322451	HAEpiC	amniotic membrane:	n/a
49	chr7:70311532-70311582	NH-A	brain:	n/a
50	chr7:70322401-70322451	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
2	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
3	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
4	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
5	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
6	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
7	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
8	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
9	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
10	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
11	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
12	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
13	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
14	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AUTS2-3	chr7:70302724-70302999	NONHSAT121342

Variant related genes	Relation type
ENSG00000236978	TF binding region
ENSG00000236978	CpG island

Extended variants
information (count: 2294 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2294 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549209330	chr7:70297573-70297574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577910477	chr7:70297590-70297591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545416168	chr7:70297623-70297624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569039034	chr7:70297707-70297708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143320935	chr7:70297723-70297724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531457800	chr7:70297730-70297731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549570911	chr7:70297753-70297754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150894290	chr7:70297790-70297791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139369721	chr7:70297846-70297847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75818003	chr7:70297851-70297852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376443905	chr7:70297876-70297877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530422948	chr7:70297878-70297879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183713178	chr7:70297883-70297884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539428482	chr7:70297886-70297887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150042903	chr7:70297888-70297889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185832889	chr7:70297893-70297894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533712821	chr7:70297919-70297920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370884952	chr7:70297964-70297965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs58050373	chr7:70298095-70298096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10252997	chr7:70298109-70298110	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs28559780	chr7:70298170-70298171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs200567809	chr7:70298200-70298201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200048629	chr7:70298201-70298202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567623186	chr7:70298221-70298222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28545657	chr7:70298241-70298242	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556352539	chr7:70298246-70298247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556125961	chr7:70298247-70298248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191077827	chr7:70298253-70298254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374462191	chr7:70298254-70298255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545409245	chr7:70298267-70298268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560592763	chr7:70298292-70298293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374284964	chr7:70298298-70298299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28638367	chr7:70298299-70298300	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs542832889	chr7:70298307-70298308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561513809	chr7:70298328-70298329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528989739	chr7:70298331-70298332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28878291	chr7:70298350-70298351	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs375239413	chr7:70298354-70298355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562573197	chr7:70298355-70298356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532763460	chr7:70298360-70298361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368032710	chr7:70298363-70298364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372266860	chr7:70298366-70298367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58500578	chr7:70298367-70298368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs58349919	chr7:70298395-70298396	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs561298628	chr7:70298426-70298427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9691227	chr7:70298427-70298428	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs9691230	chr7:70298441-70298442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs578062648	chr7:70298445-70298446	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs201173637	chr7:70298452-70298453	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs544064738	chr7:70298456-70298457	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70294800-70298600	Weak transcription	NHEK	skin
2	chr7:70294800-70298600	Weak transcription	Osteobl	bone
3	chr7:70295000-70298400	Weak transcription	NH-A	brain
4	chr7:70295000-70298600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:70295200-70298600	Weak transcription	HSMM	muscle
6	chr7:70295400-70300200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:70295400-70301800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:70298400-70298800	Enhancers	NH-A	brain
9	chr7:70298600-70298800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:70298600-70299000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:70298600-70299000	Enhancers	HSMM	muscle
12	chr7:70298600-70299000	Enhancers	NHEK	skin
13	chr7:70298600-70299000	Enhancers	Osteobl	bone
14	chr7:70298800-70299000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:70299000-70300000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:70299000-70300200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:70299200-70299600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr7:70299400-70299600	Weak transcription	Liver	Liver
19	chr7:70299800-70300400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
20	chr7:70300200-70300800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:70300200-70301200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr7:70300800-70301000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:70300800-70301200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:70301200-70312200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:70301200-70314200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr7:70301400-70302000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr7:70301800-70302000	Enhancers	H9 Cell Line	embryonic stem cell
28	chr7:70303000-70303600	Enhancers	Esophagus	oesophagus
29	chr7:70303200-70303800	Enhancers	HepG2	liver
30	chr7:70310400-70310600	Active TSS	HSMM	muscle
31	chr7:70310600-70310800	Flanking Active TSS	HSMM	muscle
32	chr7:70314200-70315000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr7:70314200-70315000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:70315000-70321600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr7:70316000-70316800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr7:70316800-70321600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr7:70319400-70320000	Enhancers	Fetal Stomach	stomach
38	chr7:70319800-70320400	Enhancers	H9 Cell Line	embryonic stem cell
39	chr7:70320200-70320400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr7:70320400-70320600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:70320400-70321200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr7:70320600-70321600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr7:70320600-70321800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:70321200-70323600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr7:70321400-70322000	Enhancers	Fetal Muscle Trunk	muscle
46	chr7:70321400-70322200	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr7:70321400-70322800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr7:70321400-70325000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:70321600-70322000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr7:70321600-70322000	Enhancers	Placenta	Placenta

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