Variant report

Variant	nsv1018430
Chromosome Location	chr7:39455497-39643569
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2349)
CpG islands
(count:1343)
Chromatin interactive
region (count:84)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2349 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:39504617-39504923	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:39619920-39620322	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:39559568-39560308	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:39605696-39606077	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:39528586-39528662	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:39559554-39559774	K562	blood:	n/a	n/a
7	ARID3A	chr7:39629196-39629849	K562	blood:	n/a	n/a
8	ATF1	chr7:39629296-39629800	K562	blood:	n/a	n/a
9	ATF1	chr7:39620042-39620358	K562	blood:	n/a	n/a
10	ATF1	chr7:39544575-39544759	K562	blood:	n/a	n/a
11	ATF2	chr7:39629257-39629794	GM12878	blood:	n/a	n/a
12	ATF2	chr7:39629214-39629775	GM12878	blood:	n/a	n/a
13	ATF2	chr7:39605695-39606255	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:39620059-39620415	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:39629324-39629589	K562	blood:	n/a	n/a
16	ATF3	chr7:39629296-39629758	K562	blood:	n/a	n/a
17	BACH1	chr7:39504641-39505056	K562	blood:	n/a	n/a
18	BACH1	chr7:39504575-39505029	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:39623626-39623709	K562	blood:	n/a	n/a
20	BACH1	chr7:39460082-39460104	K562	blood:	n/a	n/a
21	BACH1	chr7:39605642-39605702	K562	blood:	n/a	n/a
22	BACH1	chr7:39605695-39606256	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr7:39629280-39629727	GM12878	blood:	n/a	chr7:39629520-39629531
24	BATF	chr7:39504633-39504960	GM12878	blood:	n/a	n/a
25	BATF	chr7:39629347-39629718	GM12878	blood:	n/a	chr7:39629520-39629531
26	BATF	chr7:39504666-39504886	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:39629238-39629667	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:39629312-39629663	GM12878	blood:	n/a	n/a
29	BCL3	chr7:39556282-39556573	GM12878	blood:	n/a	n/a
30	BCL3	chr7:39629295-39629695	GM12878	blood:	n/a	n/a
31	BCL3	chr7:39605532-39606336	A549	lung:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
32	BCLAF1	chr7:39605565-39606356	GM12878	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
33	BCLAF1	chr7:39605736-39606198	K562	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
34	BCLAF1	chr7:39605624-39606257	GM12878	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
35	BHLHE40	chr7:39556351-39556520	K562	blood:	n/a	n/a
36	BHLHE40	chr7:39629275-39629703	K562	blood:	n/a	n/a
37	BHLHE40	chr7:39559598-39559764	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:39629250-39629748	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:39605270-39606262	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:39559617-39559759	K562	blood:	n/a	n/a
41	BHLHE40	chr7:39619986-39620611	K562	blood:	n/a	n/a
42	BHLHE40	chr7:39605211-39606254	K562	blood:	n/a	n/a
43	BHLHE40	chr7:39555294-39555818	K562	blood:	n/a	n/a
44	BHLHE40	chr7:39620025-39620654	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:39620025-39620413	HepG2	liver:	n/a	n/a
46	BRCA1	chr7:39590462-39590468	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr7:39522396-39522445	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr7:39629193-39629730	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr7:39605671-39606201	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr7:39629167-39629814	HCT-116	colon:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39605683-39605733	HCPEpiC	choroid plexus:	n/a
2	chr7:39605683-39605733	HCPEpiC	choroid plexus:	n/a
3	chr7:39606013-39606063	PrEC	prostate:	n/a
4	chr7:39500288-39500338	GM12892	blood:	n/a
5	chr7:39605536-39605586	GM12892	blood:	n/a
6	chr7:39606071-39606121	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:39500223-39500273	HRPEpiC	eye:	n/a
8	chr7:39503619-39503669	ProgFib	skin:	n/a
9	chr7:39612363-39612413	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:39606071-39606121	Caco-2	colon:	n/a
11	chr7:39472716-39472766	HAEpiC	amniotic membrane:	n/a
12	chr7:39605790-39605840	HMEC	breast:	n/a
13	chr7:39606071-39606121	MCF10A-Er-Src	breast:	n/a
14	chr7:39605683-39605733	AG10803	skin:	n/a
15	chr7:39472716-39472766	HepG2	liver:	n/a
16	chr7:39612363-39612413	CMK	blood:	n/a
17	chr7:39605790-39605840	U87	brain:	n/a
18	chr7:39605790-39605840	HL-60	blood:	n/a
19	chr7:39606071-39606121	PFSK-1	brain:	n/a
20	chr7:39503619-39503669	NB4	blood:	n/a
21	chr7:39605805-39605855	LNCaP	prostate:	n/a
22	chr7:39605883-39605933	NHDF-neo	bronchial:	n/a
23	chr7:39606002-39606052	PrEC	prostate:	n/a
24	chr7:39609343-39609393	BE2_C	brain:	n/a
25	chr7:39605536-39605586	MCF10A-Er-Src	breast:	n/a
26	chr7:39472716-39472766	GM19239	blood:	n/a
27	chr7:39606002-39606052	HNPCEpiC	eye:	n/a
28	chr7:39605861-39605911	AoSMC	blood vessel:	n/a
29	chr7:39569916-39569966	HCPEpiC	choroid plexus:	n/a
30	chr7:39606280-39606330	AG04450	lung:	fetal
31	chr7:39605683-39605733	GM12878	blood:	n/a
32	chr7:39609343-39609393	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:39605883-39605933	NT2-D1	testis:	n/a
34	chr7:39605861-39605911	HRCEpiC	kidney:	n/a
35	chr7:39500288-39500338	ECC-1	luminal epithelium:	n/a
36	chr7:39606002-39606052	HMEC	breast:	n/a
37	chr7:39606071-39606121	HEK293	kidney:	embryo
38	chr7:39605861-39605911	HMEC	breast:	n/a
39	chr7:39605996-39606046	HRE	kidney:	n/a
40	chr7:39606013-39606063	NT2-D1	testis:	n/a
41	chr7:39503619-39503669	BE2_C	brain:	n/a
42	chr7:39612363-39612413	HUVEC	blood vessel:	n/a
43	chr7:39605536-39605586	AG04450	lung:	fetal
44	chr7:39500288-39500338	AG10803	skin:	n/a
45	chr7:39606280-39606330	HepG2	liver:	n/a
46	chr7:39503619-39503669	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:39605996-39606046	GM12878	blood:	n/a
48	chr7:39500288-39500338	HCM	heart:	n/a
49	chr7:39606002-39606052	Hela-S3	cervix:	n/a
50	chr7:39605790-39605840	HUVEC	blood vessel:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:39616830..39619300-chr7:39660316..39662885,2	K562	blood:
2	chr7:39605618..39607861-chr7:39772706..39774759,2	K562	blood:
3	chr7:39538609..39540979-chr7:39546036..39547767,2	K562	blood:
4	chr7:39619675..39620675-chr7:39785462..39786424,9	MCF-7	breast:
5	chr7:39538705..39540633-chr7:39541459..39543564,2	K562	blood:
6	chr7:39493293..39495900-chr7:39499088..39502872,3	K562	blood:
7	chr10:3888800..3889300-chr7:39632378..39632982,2	MCF-7	breast:
8	chr7:39610504..39612853-chr7:39613535..39615540,2	K562	blood:
9	chr7:39559251..39560178-chr7:39581010..39581845,2	K562	blood:
10	chr7:39620191..39622665-chr7:39628141..39629776,2	K562	blood:
11	chr7:39493099..39494043-chr7:39559206..39560190,4	MCF-7	breast:
12	chr7:39619773..39620623-chr7:39785550..39786165,2	MCF-7	breast:
13	chr7:39613001..39614812-chr7:39768164..39770870,2	K562	blood:
14	chr7:39620191..39622665-chr7:39628141..39629776,2	K562	blood:
15	chr7:39621618..39625232-chr7:39625771..39627613,3	K562	blood:
16	chr7:39567068..39569157-chr7:39570895..39573557,2	K562	blood:
17	chr7:39573042..39574543-chr7:39580412..39582259,2	K562	blood:
18	chr7:39493116..39494045-chr7:39504502..39505143,2	K562	blood:
19	chr7:39619733..39620697-chr7:39781534..39782496,5	K562	blood:
20	chr7:39643128..39644638-chr7:39660434..39662671,2	MCF-7	breast:
21	chr7:39498982..39501819-chr7:39501974..39504808,2	K562	blood:
22	chr7:39638996..39641307-chr7:39643111..39644755,2	K562	blood:
23	chr7:39620146..39620721-chr7:39781543..39782233,2	MCF-7	breast:
24	chr7:39559251..39560178-chr7:39581010..39581845,2	K562	blood:
25	chr7:39640592..39642673-chr7:39644409..39647009,2	K562	blood:
26	chr7:39492607..39495001-chr7:39495505..39498185,2	K562	blood:
27	chr7:39619730..39620271-chr7:39781971..39782566,2	MCF-7	breast:
28	chr7:39492607..39495001-chr7:39495505..39498185,2	K562	blood:
29	chr7:39629985..39632213-chr7:39633896..39637546,5	K562	blood:
30	chr7:39575609..39577326-chr7:39580919..39582737,2	MCF-7	breast:
31	chr7:39493293..39495900-chr7:39499088..39502872,3	K562	blood:
32	chr7:39538609..39540979-chr7:39546036..39547767,2	K562	blood:
33	chr7:39619917..39620450-chr7:39831240..39831746,2	K562	blood:
34	chr7:39609139..39613691-chr7:39613860..39617111,6	K562	blood:
35	chr7:39515006..39518001-chr7:39520059..39523009,2	K562	blood:
36	chr7:39573042..39574543-chr7:39580412..39582259,2	K562	blood:
37	chr7:39597542..39600192-chr7:39605435..39607184,2	MCF-7	breast:
38	chr7:39608617..39610852-chr7:39611782..39613419,2	K562	blood:
39	chr7:39581559..39584136-chr7:39585096..39587437,2	K562	blood:
40	chr7:39597430..39600567-chr7:39603197..39606224,3	MCF-7	breast:
41	chr7:39630501..39633434-chr7:39759020..39762831,5	K562	blood:
42	chr7:39453463..39455969-chr7:39846035..39848815,2	K562	blood:
43	chr7:38836232..38836866-chr7:39504695..39505205,2	MCF-7	breast:
44	chr7:39515006..39518001-chr7:39520059..39523009,2	K562	blood:
45	chr7:38836537..38837171-chr7:39559252..39560166,3	MCF-7	breast:
46	chr7:39623431..39626186-chr7:39627006..39629338,2	MCF-7	breast:
47	chr7:39538705..39540633-chr7:39541459..39543564,2	K562	blood:
48	chr7:39567068..39569157-chr7:39570895..39573557,2	K562	blood:
49	chr7:39612446..39614989-chr7:39616627..39618783,2	MCF-7	breast:
50	chr7:39603623..39606050-chr7:39662280..39665105,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POU6F2-1	chr7:39510687-39510841	NONHSAT120203
2	lnc-C7orf11-7	chr7:39605742-39605838	ENSG00000227172.2
3	lnc-C7orf11-7	chr7:39605742-39605943	XLOC_006414
4	lnc-C7orf11-7	chr7:39585249-39585492	XLOC_006414
5	lnc-C7orf11-7	chr7:39605742-39605838	XLOC_006414
6	lnc-C7orf11-7	chr7:39593475-39593543	XLOC_006414
7	lnc-RALA-3	chr7:39622404-39622930	NONHSAT120209
8	lnc-POU6F2-1	chr7:39529969-39530208	NONHSAT120203
9	lnc-C7orf11-7	chr7:39585245-39585492	ENSG00000227172.2
10	lnc-C7orf11-14	chr7:39608975-39609797	NONHSAT120207
11	lnc-C7orf11-7	chr7:39593494-39593543	XLOC_006414
12	lnc-C7orf11-7	chr7:39593475-39593543	ENSG00000227172.2
13	lnc-POU6F2-1	chr7:39532643-39532694	NONHSAT120203
14	lnc-POU6F2-1	chr7:39504691-39504775	NONHSAT120203

No data

Variant related genes	Relation type
ENSG00000236015	TF binding region
YAE1D1	TF binding region
POU6F2	TF binding region
ENSG00000227172	TF binding region
ENSG00000236015	CpG island
YAE1D1	CpG island
POU6F2	CpG island
ENSG00000227172	CpG island
ENSG00000236015	chromatin interactions
ENSG00000006451	chromatin interactions
ENSG00000006715	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000227172	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000241127	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000106536	chromatin interactions
ENSG00000188185	chromatin interactions

Extended variants
information (count: 6038 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6038 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543812304	chr7:39455516-39455517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142587585	chr7:39455526-39455527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561852486	chr7:39455558-39455559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574488169	chr7:39455559-39455560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs71728454	chr7:39455693-39455694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs57579748	chr7:39455733-39455734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113863961	chr7:39455772-39455773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6948411	chr7:39455788-39455789	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs573084784	chr7:39455792-39455793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76698012	chr7:39455837-39455838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35763272	chr7:39455924-39455925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565412669	chr7:39455953-39455954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182824901	chr7:39455961-39455962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550659840	chr7:39455991-39455992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576303488	chr7:39455999-39456000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs117544650	chr7:39456006-39456007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185255410	chr7:39456057-39456058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189961048	chr7:39456063-39456064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538806959	chr7:39456096-39456097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371399096	chr7:39456118-39456119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182662800	chr7:39456208-39456209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564581220	chr7:39456212-39456213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538132276	chr7:39456219-39456220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188923007	chr7:39456303-39456304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34171316	chr7:39456327-39456328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs118080333	chr7:39456362-39456363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573637835	chr7:39456364-39456365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558012109	chr7:39456413-39456414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531942673	chr7:39456414-39456415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540557414	chr7:39456424-39456425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs193099813	chr7:39456435-39456436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150928608	chr7:39456458-39456459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140752733	chr7:39456459-39456460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575889739	chr7:39456579-39456580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143191045	chr7:39456602-39456603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113027047	chr7:39456638-39456639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2024100	chr7:39456652-39456653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs530103460	chr7:39456653-39456654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568994783	chr7:39456689-39456690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183654681	chr7:39456784-39456785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373975552	chr7:39457031-39457032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112812766	chr7:39457041-39457042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10262012	chr7:39457096-39457097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs530332181	chr7:39457138-39457139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs578057821	chr7:39457240-39457241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551035088	chr7:39457341-39457342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548533530	chr7:39457378-39457379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187511805	chr7:39457410-39457411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570926882	chr7:39457439-39457440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537779268	chr7:39457474-39457475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	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
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39454600-39460600	Weak transcription	Brain Germinal Matrix	brain
2	chr7:39455000-39462000	Weak transcription	Fetal Muscle Leg	muscle
3	chr7:39455200-39456200	Enhancers	Fetal Intestine Small	intestine
4	chr7:39455400-39455600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:39456800-39457000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:39460600-39460800	Enhancers	Brain Germinal Matrix	brain
7	chr7:39460600-39461200	Enhancers	Fetal Brain Male	brain
8	chr7:39460600-39461600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:39460600-39462400	Enhancers	HSMMtube	muscle
10	chr7:39460800-39461200	Weak transcription	Brain Germinal Matrix	brain
11	chr7:39460800-39461400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr7:39460800-39461600	Enhancers	Fetal Brain Female	brain
13	chr7:39461000-39461400	Enhancers	HSMM	muscle
14	chr7:39461200-39462400	Enhancers	Brain Germinal Matrix	brain
15	chr7:39462000-39462600	Enhancers	Fetal Muscle Leg	muscle
16	chr7:39462400-39463200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:39462600-39463000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:39462600-39463000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr7:39462600-39463400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:39462600-39463400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:39462600-39470800	Weak transcription	Fetal Muscle Leg	muscle
22	chr7:39462800-39463600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:39466600-39467600	Weak transcription	HSMM	muscle
24	chr7:39467200-39468400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr7:39467400-39468400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:39467400-39468400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:39467400-39468400	Enhancers	Muscle Satellite Cultured Cells	--
28	chr7:39467400-39468400	Enhancers	HMEC	breast
29	chr7:39467400-39468600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:39467400-39469400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:39467600-39468200	Enhancers	Colon Smooth Muscle	Colon
32	chr7:39467600-39468400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr7:39467600-39468400	Enhancers	Aorta	Aorta
34	chr7:39467600-39468400	Enhancers	Rectal Smooth Muscle	rectum
35	chr7:39467600-39468400	Enhancers	NH-A	brain
36	chr7:39467600-39469000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr7:39467600-39469200	Enhancers	NHDF-Ad	bronchial
38	chr7:39467600-39469400	Enhancers	A549	lung
39	chr7:39467600-39469400	Enhancers	HSMM	muscle
40	chr7:39467600-39469400	Enhancers	HSMMtube	muscle
41	chr7:39467800-39468200	Enhancers	NHEK	skin
42	chr7:39467800-39469000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:39468000-39468400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:39468000-39468400	Enhancers	Stomach Smooth Muscle	stomach
45	chr7:39468400-39469000	Weak transcription	Rectal Smooth Muscle	rectum
46	chr7:39468400-39469200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:39468400-39471000	Weak transcription	Aorta	Aorta
48	chr7:39468400-39473800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr7:39468600-39469000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:39469000-39469200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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