Variant report

Variant	nsv831044
Chromosome Location	chr7:80721773-80918591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1673)
CpG islands
(count:183)
Chromatin interactive
region (count:159)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1673 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:80764746-80764765	K562	blood:	n/a	n/a
2	ARID3A	chr7:80788684-80788908	K562	blood:	n/a	n/a
3	ARID3A	chr7:80835779-80836220	K562	blood:	n/a	n/a
4	ARID3A	chr7:80846463-80846580	K562	blood:	n/a	n/a
5	ARID3A	chr7:80784778-80785691	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:80790861-80791516	K562	blood:	n/a	n/a
7	ARID3A	chr7:80838216-80838678	K562	blood:	n/a	n/a
8	ARID3A	chr7:80886356-80886529	K562	blood:	n/a	n/a
9	ARID3A	chr7:80874461-80874519	K562	blood:	n/a	n/a
10	ATF1	chr7:80788785-80789022	K562	blood:	n/a	n/a
11	ATF1	chr7:80838347-80838672	K562	blood:	n/a	n/a
12	ATF2	chr7:80874627-80875086	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr7:80788680-80789097	K562	blood:	n/a	n/a
14	ATF3	chr7:80803048-80803628	A549	lung:	n/a	n/a
15	ATF3	chr7:80838360-80838725	K562	blood:	n/a	n/a
16	ATF3	chr7:80790660-80791118	A549	lung:	n/a	n/a
17	ATF3	chr7:80790695-80791322	K562	blood:	n/a	n/a
18	BACH1	chr7:80893571-80893822	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:80764741-80764956	K562	blood:	n/a	n/a
20	BACH1	chr7:80886355-80886632	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:80893499-80893817	K562	blood:	n/a	n/a
22	BCL11A	chr7:80874764-80874978	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL3	chr7:80802786-80803832	A549	lung:	n/a	n/a
24	BCL3	chr7:80784785-80785737	A549	lung:	n/a	n/a
25	BCL3	chr7:80803015-80803706	A549	lung:	n/a	n/a
26	BCL3	chr7:80790622-80791131	A549	lung:	n/a	n/a
27	BHLHE40	chr7:80838287-80838633	K562	blood:	n/a	n/a
28	BHLHE40	chr7:80790639-80791371	K562	blood:	n/a	n/a
29	BHLHE40	chr7:80788780-80788968	K562	blood:	n/a	n/a
30	BHLHE40	chr7:80814503-80814642	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:80780304-80780460	HepG2	liver:	n/a	n/a
32	BHLHE40	chr7:80790692-80790965	A549	lung:	n/a	n/a
33	BRCA1	chr7:80802930-80803818	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr7:80822827-80823135	K562	blood:	n/a	n/a
35	CBX3	chr7:80889513-80889730	K562	blood:	n/a	n/a
36	CBX3	chr7:80838275-80838711	K562	blood:	n/a	n/a
37	CBX3	chr7:80889413-80889815	K562	blood:	n/a	n/a
38	CBX3	chr7:80896810-80897106	K562	blood:	n/a	n/a
39	CBX3	chr7:80790612-80791138	HCT-116	colon:	n/a	n/a
40	CBX3	chr7:80889474-80889879	HCT-116	colon:	n/a	n/a
41	CBX3	chr7:80913796-80914251	HCT-116	colon:	n/a	n/a
42	CBX3	chr7:80791024-80791413	K562	blood:	n/a	n/a
43	CBX3	chr7:80873489-80873978	HCT-116	colon:	n/a	n/a
44	CCNT2	chr7:80737702-80737827	K562	blood:	n/a	n/a
45	CCNT2	chr7:80838362-80838771	K562	blood:	n/a	n/a
46	CCNT2	chr7:80791073-80791398	K562	blood:	n/a	n/a
47	CCNT2	chr7:80818957-80819157	K562	blood:	n/a	n/a
48	CCNT2	chr7:80834045-80834218	K562	blood:	n/a	n/a
49	CEBPB	chr7:80864200-80864399	K562	blood:	n/a	n/a
50	CEBPB	chr7:80784837-80785516	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80732349-80732399	HCT-116	colon:	n/a
2	chr7:80750194-80750244	AG09319	gingival:	n/a
3	chr7:80750194-80750244	Caco-2	colon:	n/a
4	chr7:80732349-80732399	HCM	heart:	n/a
5	chr7:80750194-80750244	NHDF-neo	bronchial:	n/a
6	chr7:80732349-80732399	HCPEpiC	choroid plexus:	n/a
7	chr7:80750194-80750244	HL-60	blood:	n/a
8	chr7:80750194-80750244	SK-N-SH_RA	brain:	n/a
9	chr7:80732349-80732399	T-47D	breast:	n/a
10	chr7:80771132-80771182	ECC-1	luminal epithelium:	n/a
11	chr7:80771132-80771182	BJ	skin:	n/a
12	chr7:80771132-80771182	HIPEpiC	eye:	n/a
13	chr7:80732349-80732399	HMEC	breast:	n/a
14	chr7:80750194-80750244	HCT-116	colon:	n/a
15	chr7:80771132-80771182	RPTEC	kidney:	n/a
16	chr7:80732349-80732399	HRE	kidney:	n/a
17	chr7:80771132-80771182	HEK293	kidney:	embryo
18	chr7:80771132-80771182	ProgFib	skin:	n/a
19	chr7:80750194-80750244	K562	blood:	n/a
20	chr7:80732349-80732399	GM19239	blood:	n/a
21	chr7:80771132-80771182	HepG2	liver:	n/a
22	chr7:80750194-80750244	HepG2	liver:	n/a
23	chr7:80771132-80771182	MCF-7	breast:	n/a
24	chr7:80750194-80750244	HEEpiC	esophagus:	n/a
25	chr7:80771132-80771182	HAEpiC	amniotic membrane:	n/a
26	chr7:80732349-80732399	MCF10A-Er-Src	breast:	n/a
27	chr7:80771132-80771182	SK-N-MC	brain:	n/a
28	chr7:80771132-80771182	PFSK-1	brain:	n/a
29	chr7:80750194-80750244	NB4	blood:	n/a
30	chr7:80750194-80750244	MCF-7	breast:	n/a
31	chr7:80771132-80771182	AG09319	gingival:	n/a
32	chr7:80732349-80732399	SK-N-SH	brain:	n/a
33	chr7:80732349-80732399	MCF-7	breast:	n/a
34	chr7:80750194-80750244	BJ	skin:	n/a
35	chr7:80750194-80750244	HAEpiC	amniotic membrane:	n/a
36	chr7:80750194-80750244	IMR90	lung:	fetal
37	chr7:80771132-80771182	HL-60	blood:	n/a
38	chr7:80750194-80750244	ovcar-3	ovarian:	n/a
39	chr7:80771132-80771182	Hepatocyte	liver:	n/a
40	chr7:80732349-80732399	NH-A	brain:	n/a
41	chr7:80771132-80771182	K562	blood:	n/a
42	chr7:80771132-80771182	IMR90	lung:	fetal
43	chr7:80771132-80771182	HCF	heart:	n/a
44	chr7:80750194-80750244	PFSK-1	brain:	n/a
45	chr7:80732349-80732399	NT2-D1	testis:	n/a
46	chr7:80732349-80732399	AoSMC	blood vessel:	n/a
47	chr7:80771132-80771182	LNCaP	prostate:	n/a
48	chr7:80771132-80771182	Hela-S3	cervix:	n/a
49	chr7:80750194-80750244	HCF	heart:	n/a
50	chr7:80771132-80771182	AG04450	lung:	fetal

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:80507279..80509626-chr7:80810573..80812155,2	MCF-7	breast:
2	chr7:80562846..80565574-chr7:80788453..80790857,2	MCF-7	breast:
3	chr7:80570519..80573316-chr7:80792715..80798037,5	MCF-7	breast:
4	chr3:64009122..64009628-chr7:80743049..80743848,2	MCF-7	breast:
5	chr7:80886551..80889533-chr7:80889914..80891522,2	MCF-7	breast:
6	chr7:80573388..80575762-chr7:80724562..80727160,2	MCF-7	breast:
7	chr7:80762464..80764169-chr7:80767281..80770291,3	K562	blood:
8	chr7:80550385..80552330-chr7:80878720..80881431,3	MCF-7	breast:
9	chr7:80811160..80813261-chr7:80817973..80820541,2	K562	blood:
10	chr7:80821792..80824304-chr7:80825021..80828118,3	MCF-7	breast:
11	chr7:80788382..80789329-chr7:80797240..80797887,3	MCF-7	breast:
12	chr7:80794786..80796336-chr7:80796368..80797899,2	MCF-7	breast:
13	chr7:80735961..80738195-chr7:80820318..80822112,2	MCF-7	breast:
14	chr7:80543196..80546765-chr7:80879476..80881407,3	MCF-7	breast:
15	chr7:80545653..80550046-chr7:80890283..80894244,7	MCF-7	breast:
16	chr7:80786547..80788746-chr7:80790222..80791891,2	MCF-7	breast:
17	chr7:80788038..80791953-chr7:80793633..80797401,3	MCF-7	breast:
18	chr7:80545954..80551359-chr7:80730647..80734192,4	MCF-7	breast:
19	chr7:80788533..80789298-chr7:80797276..80797921,3	MCF-7	breast:
20	chr7:80762464..80764120-chr7:80767823..80770291,2	K562	blood:
21	chr7:80873781..80875540-chr7:80877890..80879810,2	MCF-7	breast:
22	chr7:80548614..80550203-chr7:80841572..80844375,2	MCF-7	breast:
23	chr7:80840881..80842505-chr7:80847101..80849411,2	K562	blood:
24	chr7:80786119..80788066-chr7:80797479..80799282,2	MCF-7	breast:
25	chr7:80779464..80781511-chr7:80784882..80787080,2	MCF-7	breast:
26	chr7:80792450..80794527-chr7:80797989..80800904,2	MCF-7	breast:
27	chr7:80781139..80783357-chr7:80784311..80786613,2	MCF-7	breast:
28	chr7:80783252..80785229-chr7:80787279..80788864,2	MCF-7	breast:
29	chr7:80840881..80842505-chr7:80847101..80849411,2	K562	blood:
30	chr7:80788038..80791953-chr7:80793633..80797401,3	MCF-7	breast:
31	chr7:80547175..80549639-chr7:80793412..80796966,3	MCF-7	breast:
32	chr7:80811160..80813261-chr7:80817973..80820541,2	K562	blood:
33	chr7:80788533..80789298-chr7:80797276..80797921,3	MCF-7	breast:
34	chr7:80550453..80552011-chr7:80727282..80729460,2	MCF-7	breast:
35	chr7:80571738..80573248-chr7:80725803..80727635,2	MCF-7	breast:
36	chr7:80539272..80542140-chr7:80885838..80888215,3	MCF-7	breast:
37	chr7:80783452..80785528-chr7:80926720..80928385,2	MCF-7	breast:
38	chr7:80820849..80823481-chr7:80826763..80829018,2	K562	blood:
39	chr7:80565444..80567748-chr7:80788627..80790911,2	MCF-7	breast:
40	chr7:80883750..80886703-chr7:80894705..80896223,2	MCF-7	breast:
41	chr7:80548728..80550741-chr7:80899992..80902009,2	MCF-7	breast:
42	chr7:80762464..80764169-chr7:80767281..80770291,3	K562	blood:
43	chr7:80820849..80823481-chr7:80826038..80829018,5	K562	blood:
44	chr7:80570676..80574921-chr7:80787209..80790875,5	MCF-7	breast:
45	chr7:80852495..80856208-chr7:80856677..80858955,3	K562	blood:
46	chr7:80768507..80770416-chr7:80771855..80773597,2	K562	blood:
47	chr7:80749693..80751206-chr7:80754360..80756638,2	MCF-7	breast:
48	chr7:80887573..80889363-chr7:80895949..80898235,2	MCF-7	breast:
49	chr7:80788690..80790506-chr7:80884567..80886518,2	MCF-7	breast:
50	chr7:80878793..80880678-chr7:80882418..80884824,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD36-4	chr7:80820714-80821325	NONHSAT121757

No data

Variant related genes	Relation type
ENSG00000237896	TF binding region
ENSG00000226671	TF binding region
ENSG00000237896	CpG island
ENSG00000226671	CpG island
ENSG00000124171	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000226671	chromatin interactions
ENSG00000237896	chromatin interactions
ENSG00000075223	chromatin interactions

Extended variants
information (count: 7639 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:7639 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573125530	chr7:80721791-80721792	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs542043200	chr7:80721803-80721804	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540871675	chr7:80721861-80721862	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371885322	chr7:80721876-80721877	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs180815200	chr7:80721898-80721899	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs561914132	chr7:80721924-80721925	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376723714	chr7:80722000-80722001	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575543970	chr7:80722001-80722002	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544533397	chr7:80722004-80722005	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564156681	chr7:80722012-80722013	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374527625	chr7:80722034-80722035	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185873516	chr7:80722036-80722037	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148989777	chr7:80722089-80722090	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188490601	chr7:80722095-80722096	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs377197484	chr7:80722102-80722103	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528962166	chr7:80722153-80722154	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143745567	chr7:80722159-80722160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569024617	chr7:80722273-80722274	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181627847	chr7:80722275-80722276	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150963375	chr7:80722280-80722281	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570856386	chr7:80722361-80722362	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs78410583	chr7:80722372-80722373	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs137980182	chr7:80722402-80722403	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553306608	chr7:80722413-80722414	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140752169	chr7:80722423-80722424	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371638210	chr7:80722457-80722458	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555545495	chr7:80722495-80722496	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575431113	chr7:80722498-80722499	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544930526	chr7:80722534-80722535	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144610095	chr7:80722552-80722553	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185955406	chr7:80722564-80722565	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs539863341	chr7:80722595-80722596	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2697227	chr7:80722649-80722650	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs386715123	chr7:80722650-80722651	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs6968574	chr7:80722663-80722664	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs549095060	chr7:80722722-80722723	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs199910733	chr7:80722822-80722823	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs138548827	chr7:80722872-80722873	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs192032686	chr7:80722946-80722947	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551680051	chr7:80723007-80723008	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs565083404	chr7:80723052-80723053	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1528389	chr7:80723062-80723063	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546600974	chr7:80723074-80723075	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs34696699	chr7:80723118-80723119	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs184188982	chr7:80723133-80723134	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547196066	chr7:80723144-80723145	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs113377499	chr7:80723167-80723168	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs145387415	chr7:80723229-80723230	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs58754250	chr7:80723232-80723233	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs10677742	chr7:80723252-80723253	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80723800-80724200	Enhancers	A549	lung
2	chr7:80724200-80724800	Flanking Active TSS	A549	lung
3	chr7:80724200-80725000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:80724200-80725200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:80724400-80724800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:80724400-80724800	Enhancers	Adipose Nuclei	Adipose
7	chr7:80724400-80724800	Enhancers	Stomach Mucosa	stomach
8	chr7:80724800-80725000	Enhancers	A549	lung
9	chr7:80725000-80725200	Flanking Active TSS	A549	lung
10	chr7:80725200-80725800	Enhancers	A549	lung
11	chr7:80725200-80729000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:80725800-80727000	Weak transcription	A549	lung
13	chr7:80727000-80727200	Enhancers	A549	lung
14	chr7:80727200-80727800	Flanking Active TSS	A549	lung
15	chr7:80727800-80729600	Enhancers	A549	lung
16	chr7:80729000-80729600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:80738400-80743400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr7:80739400-80740800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:80739600-80740800	Enhancers	A549	lung
20	chr7:80739800-80740600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:80739800-80741400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:80739800-80741400	Enhancers	HMEC	breast
23	chr7:80739800-80741400	Enhancers	HSMM	muscle
24	chr7:80739800-80741600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:80739800-80742400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:80739800-80742400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:80739800-80743200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:80740000-80740400	Enhancers	HSMMtube	muscle
29	chr7:80740200-80741400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:80740200-80741400	Enhancers	Primary hematopoietic stem cells	blood
31	chr7:80740200-80741400	Enhancers	Fetal Lung	lung
32	chr7:80740200-80741400	Enhancers	NHDF-Ad	bronchial
33	chr7:80740200-80741600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr7:80740200-80741600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:80740200-80741800	Enhancers	NH-A	brain
36	chr7:80740200-80741800	Enhancers	Osteobl	bone
37	chr7:80740200-80742400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr7:80740200-80743600	Enhancers	Colon Smooth Muscle	Colon
39	chr7:80740400-80740800	Weak transcription	HSMMtube	muscle
40	chr7:80740400-80741200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr7:80740400-80741400	Enhancers	Rectal Smooth Muscle	rectum
42	chr7:80740800-80741200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:80740800-80741200	Enhancers	Stomach Smooth Muscle	stomach
44	chr7:80740800-80741400	Enhancers	HSMMtube	muscle
45	chr7:80740800-80741800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:80740800-80741800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:80740800-80742000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr7:80740800-80742600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:80741000-80741200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:80741000-80741200	Enhancers	HUES64 Cell Line	embryonic stem cell

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