Variant report

Variant	nsv525378
Chromosome Location	chr7:25605725-25615221
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	chr7:25605520-25605894	K562	blood:	n/a	n/a
2	ARID3A	chr7:25605491-25605914	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:25608534-25608799	K562	blood:	n/a	n/a
4	ARID3A	chr7:25608009-25608865	HepG2	liver:	n/a	n/a
5	ATF1	chr7:25608157-25608836	K562	blood:	n/a	n/a
6	ATF3	chr7:25605486-25605782	GM12878	blood:	n/a	n/a
7	ATF3	chr7:25605508-25605772	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr7:25605551-25605757	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:25608673-25608795	K562	blood:	n/a	n/a
10	BCLAF1	chr7:25605559-25605843	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:25608040-25608849	HepG2	liver:	n/a	n/a
12	BHLHE40	chr7:25608184-25608761	A549	lung:	n/a	n/a
13	BHLHE40	chr7:25608114-25608813	K562	blood:	n/a	n/a
14	BHLHE40	chr7:25608156-25608401	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:25608186-25608493	HepG2	liver:	n/a	n/a
16	BRCA1	chr7:25611641-25611759	GM12878	blood:	n/a	n/a
17	BRCA1	chr7:25605500-25605835	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr7:25608095-25608803	K562	blood:	n/a	n/a
19	CBX3	chr7:25608127-25608926	HCT-116	colon:	n/a	n/a
20	CEBPB	chr7:25605503-25605884	A549	lung:	n/a	chr7:25605716-25605729
21	CEBPB	chr7:25605426-25605977	A549	lung:	n/a	chr7:25605716-25605729
22	CEBPB	chr7:25608502-25608749	K562	blood:	n/a	n/a
23	CEBPB	chr7:25605529-25605881	Hela-S3	cervix:	n/a	chr7:25605716-25605729
24	CEBPB	chr7:25605525-25605849	H1-hESC	embryonic stem cell:	n/a	chr7:25605716-25605729
25	CHD1	chr7:25608644-25608665	GM12878	blood:	n/a	n/a
26	CREB1	chr7:25607934-25608880	HepG2	liver:	n/a	n/a
27	CREB1	chr7:25608148-25608387	A549	lung:	n/a	n/a
28	CREB1	chr7:25608078-25608416	A549	lung:	n/a	n/a
29	CREB1	chr7:25608444-25608890	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr7:25608469-25608898	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr7:25608600-25608750	HUVEC	blood vessel:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
32	CTCF	chr7:25608605-25608757	Kidney_OC	kidney:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
33	CTCF	chr7:25605566-25605807	Fibrobl	skin:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
34	CTCF	chr7:25605640-25605790	K562	blood:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
35	CTCF	chr7:25608459-25608918	K562	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
36	CTCF	chr7:25608620-25608770	GM12868	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
37	CTCF	chr7:25608640-25608790	HAc	cerebellar:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
38	CTCF	chr7:25606781-25606819	GM10266	blood:	n/a	n/a
39	CTCF	chr7:25608513-25608864	K562	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
40	CTCF	chr7:25605544-25605845	GM10266	blood:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
41	CTCF	chr7:25605437-25605829	H1-hESC	embryonic stem cell:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
42	CTCF	chr7:25608577-25608829	GM12878	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
43	CTCF	chr7:25605620-25605770	GM12867	blood:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
44	CTCF	chr7:25608240-25608390	GM12869	blood:	n/a	n/a
45	CTCF	chr7:25605254-25606051	K562	blood:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
46	CTCF	chr7:25605620-25605770	GM12868	blood:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
47	CTCF	chr7:25605600-25605750	GM12875	blood:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
48	CTCF	chr7:25608620-25608770	GM12875	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
49	CTCF	chr7:25608640-25608790	GM12870	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
50	CTCF	chr7:25608660-25608810	SK-N-SH_RA	brain:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:25608634-25608684	AG09309	skin:	n/a
2	chr7:25608305-25608355	AG09309	skin:	n/a
3	chr7:25608323-25608373	HCPEpiC	choroid plexus:	n/a
4	chr7:25608634-25608684	HRE	kidney:	n/a
5	chr7:25608323-25608373	H1-hESC	embryonic stem cell:	embryo
6	chr7:25608305-25608355	AG10803	skin:	n/a
7	chr7:25608634-25608684	HEEpiC	esophagus:	n/a
8	chr7:25608323-25608373	BJ	skin:	n/a
9	chr7:25608323-25608373	SAEC	small airway:	n/a
10	chr7:25608323-25608373	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:25608305-25608355	GM12892	blood:	n/a
12	chr7:25608323-25608373	HRCEpiC	kidney:	n/a
13	chr7:25608323-25608373	HCF	heart:	n/a
14	chr7:25608305-25608355	Jurkat	blood:	n/a
15	chr7:25608305-25608355	ProgFib	skin:	n/a
16	chr7:25608323-25608373	HCT-116	colon:	n/a
17	chr7:25608673-25608723	AG04450	lung:	fetal
18	chr7:25608673-25608723	LNCaP	prostate:	n/a
19	chr7:25608305-25608355	AoSMC	blood vessel:	n/a
20	chr7:25608323-25608373	HIPEpiC	eye:	n/a
21	chr7:25608305-25608355	Hepatocyte	liver:	n/a
22	chr7:25608323-25608373	PFSK-1	brain:	n/a
23	chr7:25608305-25608355	HRPEpiC	eye:	n/a
24	chr7:25608323-25608373	ECC-1	luminal epithelium:	n/a
25	chr7:25608673-25608723	Jurkat	blood:	n/a
26	chr7:25608673-25608723	HEK293	kidney:	embryo
27	chr7:25608323-25608373	NT2-D1	testis:	n/a
28	chr7:25608305-25608355	HIPEpiC	eye:	n/a
29	chr7:25608634-25608684	BJ	skin:	n/a
30	chr7:25608673-25608723	T-47D	breast:	n/a
31	chr7:25608305-25608355	MCF-7	breast:	n/a
32	chr7:25608634-25608684	GM06990	blood:	n/a
33	chr7:25608323-25608373	NH-A	brain:	n/a
34	chr7:25608673-25608723	GM06990	blood:	n/a
35	chr7:25608323-25608373	GM12891	blood:	n/a
36	chr7:25608323-25608373	AG09319	gingival:	n/a
37	chr7:25608305-25608355	HUVEC	blood vessel:	n/a
38	chr7:25608673-25608723	NHBE	bronchial:	n/a
39	chr7:25608634-25608684	NHDF-neo	bronchial:	n/a
40	chr7:25608673-25608723	K562	blood:	n/a
41	chr7:25608323-25608373	K562	blood:	n/a
42	chr7:25608305-25608355	RPTEC	kidney:	n/a
43	chr7:25608323-25608373	HL-60	blood:	n/a
44	chr7:25608305-25608355	AG04450	lung:	fetal
45	chr7:25608634-25608684	PrEC	prostate:	n/a
46	chr7:25608323-25608373	Hepatocyte	liver:	n/a
47	chr7:25608673-25608723	SK-N-SH_RA	brain:	n/a
48	chr7:25608673-25608723	AoSMC	blood vessel:	n/a
49	chr7:25608323-25608373	HCM	heart:	n/a
50	chr7:25608323-25608373	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:25256547..25257067-chr7:25608230..25609163,2	K562	blood:
2	chr7:25430622..25431559-chr7:25605393..25606130,7	MCF-7	breast:
3	chr7:25429098..25432014-chr7:25608292..25610212,2	K562	blood:
4	chr7:25433157..25433791-chr7:25605378..25606157,2	MCF-7	breast:
5	chr7:25608970..25611945-chr7:25612045..25614894,3	MCF-7	breast:
6	chr7:25433474..25434141-chr7:25605268..25606353,4	K562	blood:
7	chr7:25298470..25299852-chr7:25605228..25606576,11	MCF-7	breast:
8	chr7:25430704..25431525-chr7:25608219..25609114,4	K562	blood:
9	chr7:25428848..25430407-chr7:25605173..25606452,6	MCF-7	breast:
10	chr7:25430463..25431643-chr7:25605112..25606187,14	K562	blood:
11	chr7:25614579..25616228-chr7:25892925..25895334,2	K562	blood:
12	chr7:25605147..25606187-chr7:25890189..25892015,14	MCF-7	breast:
13	chr7:25605629..25606130-chr7:26404535..26405453,2	K562	blood:
14	chr7:25298951..25300126-chr7:25605192..25606795,18	K562	blood:
15	chr7:25428818..25429573-chr7:25605415..25606098,2	K562	blood:
16	chr7:25605406..25606179-chr7:25890948..25891905,5	K562	blood:
17	chr7:25429055..25432240-chr7:25604579..25606349,45	MCF-7	breast:
18	chr7:25298973..25299854-chr7:25605283..25606167,4	MCF-7	breast:
19	chr7:25608198..25609026-chr7:25891099..25891911,6	MCF-7	breast:
20	chr7:25596711..25599628-chr7:25603188..25605911,2	K562	blood:
21	chr7:25432296..25432868-chr7:25605222..25605812,2	MCF-7	breast:
22	chr7:25299061..25300348-chr7:25608226..25609143,4	K562	blood:
23	chr7:25605314..25606102-chr7:25891008..25891805,3	MCF-7	breast:
24	chr7:25430634..25431513-chr7:25608350..25609015,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPVF-4	chr7:25607521-25607592	XLOC_006381

Variant related genes	Relation type
ENSG00000222101	TF binding region
ENSG00000222101	CpG island
ENSG00000222101	chromatin interactions

Extended variants
information (count: 424 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10240053	chr7:25605725-25605726	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563299360	chr7:25605760-25605761	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs374960046	chr7:25605764-25605765	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs188126370	chr7:25605808-25605809	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs544632277	chr7:25605812-25605813	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs564527042	chr7:25605826-25605827	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs73084000	chr7:25605868-25605869	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149726771	chr7:25605883-25605884	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs553935817	chr7:25605942-25605943	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs529106889	chr7:25606001-25606002	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs191860324	chr7:25606009-25606010	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs115678801	chr7:25606032-25606033	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs144561073	chr7:25606034-25606035	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs550963519	chr7:25606045-25606046	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs2952523	chr7:25606113-25606114	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs183890977	chr7:25606117-25606118	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2952524	chr7:25606120-25606121	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs75965819	chr7:25606152-25606153	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs116207386	chr7:25606208-25606209	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs556059670	chr7:25606211-25606212	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs576027897	chr7:25606223-25606224	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2999577	chr7:25606273-25606274	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs80151297	chr7:25606337-25606338	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs577995890	chr7:25606387-25606388	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs540703273	chr7:25606443-25606444	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs560419644	chr7:25606463-25606464	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2938115	chr7:25606484-25606485	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs139631490	chr7:25606485-25606486	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs562394694	chr7:25606503-25606504	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs111241694	chr7:25606511-25606512	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs532339187	chr7:25606569-25606570	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs551299655	chr7:25606590-25606591	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs552134585	chr7:25606595-25606596	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs17727166	chr7:25606612-25606613	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547452875	chr7:25606654-25606655	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572199824	chr7:25606656-25606657	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567264510	chr7:25606659-25606660	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs145303000	chr7:25606696-25606697	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs73693126	chr7:25606731-25606732	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs77850212	chr7:25606735-25606736	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs538535385	chr7:25606748-25606749	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs558517712	chr7:25606792-25606793	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs12531920	chr7:25606871-25606872	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114258296	chr7:25606881-25606882	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs560608365	chr7:25606914-25606915	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs147629622	chr7:25606916-25606917	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs372376699	chr7:25606917-25606918	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs2960821	chr7:25606956-25606957	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190116789	chr7:25606960-25606961	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs531446468	chr7:25607021-25607022	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
Melanoma	18172304	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
Endometrioid adenocarcinoma	16974079	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25604000-25606000	Enhancers	Colon Smooth Muscle	Colon
2	chr7:25604000-25606200	Enhancers	Fetal Lung	lung
3	chr7:25604600-25608200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:25604800-25608200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr7:25605200-25606400	Weak transcription	Fetal Stomach	stomach
6	chr7:25605200-25606800	Enhancers	Fetal Kidney	kidney
7	chr7:25605400-25606000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:25605400-25606000	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr7:25605400-25607000	Enhancers	Stomach Mucosa	stomach
10	chr7:25605600-25606800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr7:25606000-25606400	Weak transcription	Colon Smooth Muscle	Colon
12	chr7:25606000-25607400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr7:25606200-25608000	Weak transcription	Fetal Lung	lung
14	chr7:25606400-25606600	Enhancers	Fetal Stomach	stomach
15	chr7:25606600-25607000	Enhancers	Gastric	stomach
16	chr7:25606800-25607000	Enhancers	Rectal Smooth Muscle	rectum
17	chr7:25607000-25607800	Weak transcription	Stomach Mucosa	stomach
18	chr7:25607400-25608000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr7:25607800-25608800	Enhancers	Stomach Mucosa	stomach
20	chr7:25608000-25608200	Enhancers	Liver	Liver
21	chr7:25608000-25608200	Enhancers	Colon Smooth Muscle	Colon
22	chr7:25608000-25608200	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr7:25608000-25608200	Enhancers	HepG2	liver
24	chr7:25608000-25608200	Enhancers	K562	blood
25	chr7:25608000-25608400	Enhancers	Fetal Heart	heart
26	chr7:25608000-25608400	Enhancers	Fetal Lung	lung
27	chr7:25608000-25608600	Flanking Active TSS	A549	lung
28	chr7:25608000-25608800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr7:25608200-25608400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:25608200-25608400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
31	chr7:25608200-25608600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:25608200-25608600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:25608200-25608600	Enhancers	H9 Cell Line	embryonic stem cell
34	chr7:25608200-25608600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:25608200-25608600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:25608200-25608600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:25608200-25608600	Flanking Active TSS	Liver	Liver
38	chr7:25608200-25608600	Enhancers	Placenta	Placenta
39	chr7:25608200-25608600	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr7:25608200-25608600	Flanking Active TSS	HepG2	liver
41	chr7:25608200-25608600	Flanking Active TSS	K562	blood
42	chr7:25608200-25608800	Enhancers	Pancreas	Pancrea
43	chr7:25608200-25609000	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr7:25608400-25608600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:25608400-25608600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr7:25608400-25609200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:25608400-25613400	Weak transcription	Fetal Lung	lung
48	chr7:25608600-25608800	Enhancers	Liver	Liver
49	chr7:25608600-25608800	Active TSS	A549	lung
50	chr7:25608600-25608800	Active TSS	HepG2	liver

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