Variant report

Variant	nsv888635
Chromosome Location	chr7:84086502-84344258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1892)
CpG islands
(count:427)
Chromatin interactive
region (count:68)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:84305107-84305335	K562	blood:	n/a	n/a
2	ARID3A	chr7:84120218-84120406	K562	blood:	n/a	chr7:84120371-84120387 chr7:84120370-84120386
3	ARID3A	chr7:84332343-84332393	K562	blood:	n/a	n/a
4	ARID3A	chr7:84302368-84302402	K562	blood:	n/a	n/a
5	ARID3A	chr7:84287580-84287954	K562	blood:	n/a	n/a
6	ATF1	chr7:84259630-84259842	K562	blood:	n/a	n/a
7	ATF1	chr7:84292651-84292819	K562	blood:	n/a	n/a
8	ATF1	chr7:84323619-84323645	K562	blood:	n/a	n/a
9	ATF1	chr7:84331188-84331414	K562	blood:	n/a	n/a
10	ATF1	chr7:84120076-84120312	K562	blood:	n/a	n/a
11	ATF1	chr7:84305022-84305312	K562	blood:	n/a	n/a
12	ATF1	chr7:84298510-84298929	K562	blood:	n/a	n/a
13	ATF3	chr7:84154321-84154946	A549	lung:	n/a	n/a
14	ATF3	chr7:84165333-84165902	A549	lung:	n/a	n/a
15	ATF3	chr7:84165356-84165961	A549	lung:	n/a	n/a
16	ATF3	chr7:84154180-84154816	A549	lung:	n/a	n/a
17	ATF3	chr7:84158579-84159198	A549	lung:	n/a	n/a
18	ATF3	chr7:84331078-84331730	A549	lung:	n/a	n/a
19	BACH1	chr7:84314329-84314388	K562	blood:	n/a	n/a
20	BACH1	chr7:84127424-84127445	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr7:84305070-84305360	GM12878	blood:	n/a	n/a
22	BATF	chr7:84305143-84305369	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:84177692-84177958	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr7:84158630-84159471	A549	lung:	n/a	n/a
25	BCL3	chr7:84165334-84165953	A549	lung:	n/a	n/a
26	BCL3	chr7:84330997-84331738	A549	lung:	n/a	n/a
27	BCL3	chr7:84153993-84154944	A549	lung:	n/a	chr7:84154006-84154015
28	BCL3	chr7:84158463-84159465	A549	lung:	n/a	n/a
29	BCL3	chr7:84165165-84166072	A549	lung:	n/a	n/a
30	BHLHE40	chr7:84244524-84244740	K562	blood:	n/a	n/a
31	BHLHE40	chr7:84305313-84305318	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:84158325-84159418	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr7:84304850-84305429	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr7:84330839-84331723	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr7:84154330-84154744	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr7:84302255-84302599	GM12878	blood:	n/a	n/a
37	CBX3	chr7:84331137-84331706	HCT-116	colon:	n/a	n/a
38	CBX3	chr7:84330750-84331792	HCT-116	colon:	n/a	n/a
39	CBX3	chr7:84261530-84261866	K562	blood:	n/a	n/a
40	CBX3	chr7:84232979-84233116	K562	blood:	n/a	n/a
41	CCNT2	chr7:84298566-84298780	K562	blood:	n/a	n/a
42	CCNT2	chr7:84255504-84255628	K562	blood:	n/a	n/a
43	CCNT2	chr7:84305040-84305328	K562	blood:	n/a	n/a
44	CEBPB	chr7:84304860-84305527	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:84178130-84178390	HepG2	liver:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
46	CEBPB	chr7:84153993-84154751	A549	lung:	n/a	chr7:84154228-84154241 chr7:84154618-84154629
47	CEBPB	chr7:84329881-84330244	A549	lung:	n/a	n/a
48	CEBPB	chr7:84329805-84330202	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr7:84152060-84152260	HepG2	liver:	n/a	chr7:84152181-84152194 chr7:84152182-84152193
50	CEBPB	chr7:84121967-84122330	ECC-1	luminal epithelium:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84107482-84107532	AG09319	gingival:	n/a
2	chr7:84177905-84177955	HUVEC	blood vessel:	n/a
3	chr7:84161420-84161470	PANC-1	pancreas:	n/a
4	chr7:84177905-84177955	SKMC	muscle:	n/a
5	chr7:84330779-84330829	HCT-116	colon:	n/a
6	chr7:84277775-84277825	HL-60	blood:	n/a
7	chr7:84161420-84161470	SK-N-SH_RA	brain:	n/a
8	chr7:84177905-84177955	Caco-2	colon:	n/a
9	chr7:84267140-84267190	Jurkat	blood:	n/a
10	chr7:84107482-84107532	NB4	blood:	n/a
11	chr7:84161222-84161272	NT2-D1	testis:	n/a
12	chr7:84277775-84277825	RPTEC	kidney:	n/a
13	chr7:84161222-84161272	AG04449	skin:	fetal
14	chr7:84161420-84161470	ProgFib	skin:	n/a
15	chr7:84177905-84177955	HCF	heart:	n/a
16	chr7:84330779-84330829	AG04449	skin:	fetal
17	chr7:84161222-84161272	Caco-2	colon:	n/a
18	chr7:84107482-84107532	SAEC	small airway:	n/a
19	chr7:84161222-84161272	SK-N-SH_RA	brain:	n/a
20	chr7:84177905-84177955	GM19239	blood:	n/a
21	chr7:84267140-84267190	Hela-S3	cervix:	n/a
22	chr7:84161222-84161272	PrEC	prostate:	n/a
23	chr7:84161420-84161470	PFSK-1	brain:	n/a
24	chr7:84267140-84267190	NT2-D1	testis:	n/a
25	chr7:84277775-84277825	HRCEpiC	kidney:	n/a
26	chr7:84161420-84161470	NH-A	brain:	n/a
27	chr7:84177905-84177955	Hepatocyte	liver:	n/a
28	chr7:84177905-84177955	SK-N-SH	brain:	n/a
29	chr7:84161222-84161272	K562	blood:	n/a
30	chr7:84177905-84177955	AoSMC	blood vessel:	n/a
31	chr7:84277775-84277825	H1-hESC	embryonic stem cell:	embryo
32	chr7:84330779-84330829	T-47D	breast:	n/a
33	chr7:84161222-84161272	GM12891	blood:	n/a
34	chr7:84330779-84330829	PFSK-1	brain:	n/a
35	chr7:84330779-84330829	SK-N-SH	brain:	n/a
36	chr7:84267140-84267190	HRCEpiC	kidney:	n/a
37	chr7:84330779-84330829	PANC-1	pancreas:	n/a
38	chr7:84161420-84161470	AoSMC	blood vessel:	n/a
39	chr7:84267140-84267190	K562	blood:	n/a
40	chr7:84267140-84267190	SK-N-MC	brain:	n/a
41	chr7:84107482-84107532	HRCEpiC	kidney:	n/a
42	chr7:84107482-84107532	HCPEpiC	choroid plexus:	n/a
43	chr7:84267140-84267190	HAEpiC	amniotic membrane:	n/a
44	chr7:84267140-84267190	HEK293	kidney:	embryo
45	chr7:84161420-84161470	GM06990	blood:	n/a
46	chr7:84161420-84161470	SK-N-MC	brain:	n/a
47	chr7:84161420-84161470	HEK293	kidney:	embryo
48	chr7:84267140-84267190	Hepatocyte	liver:	n/a
49	chr7:84277775-84277825	HEK293	kidney:	embryo
50	chr7:84330779-84330829	GM12892	blood:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:84165149..84165684-chr7:84582450..84583007,2	MCF-7	breast:
2	chr7:84312169..84314896-chr7:84317846..84320190,3	K562	blood:
3	chr7:84315326..84318065-chr7:84325058..84327523,3	K562	blood:
4	chr7:84231197..84234055-chr7:84234117..84236974,2	K562	blood:
5	chr7:84243619..84244378-chr7:84650207..84650987,2	MCF-7	breast:
6	chr7:84250435..84252517-chr7:84252923..84255018,2	K562	blood:
7	chr7:84293189..84295299-chr7:84297078..84299323,2	K562	blood:
8	chr7:84302626..84304689-chr7:84308409..84311060,2	MCF-7	breast:
9	chr7:84158432..84159047-chr7:84499527..84500086,2	MCF-7	breast:
10	chr7:84158595..84159433-chr7:84240484..84241224,2	MCF-7	breast:
11	chr7:84297350..84299613-chr7:84307072..84309162,2	K562	blood:
12	chr7:84275439..84277976-chr7:84279778..84282553,2	K562	blood:
13	chr7:84165588..84166207-chr7:84499370..84499987,2	MCF-7	breast:
14	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
15	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
16	chr7:84112762..84114363-chr7:84117900..84119846,2	K562	blood:
17	chr7:84319553..84321871-chr7:84324252..84327875,3	K562	blood:
18	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
19	chr7:84297350..84299961-chr7:84307072..84309162,3	K562	blood:
20	chr7:84312169..84314896-chr7:84317846..84320190,3	K562	blood:
21	chr3:161089345..161090957-chr7:84248345..84250491,2	MCF-7	breast:
22	chr7:84158367..84158951-chr7:84240610..84241382,2	MCF-7	breast:
23	chr7:84138849..84140536-chr7:84143161..84145231,2	K562	blood:
24	chr7:84172414..84174090-chr7:84421942..84424878,2	K562	blood:
25	chr7:84305279..84307187-chr7:84308599..84311252,2	K562	blood:
26	chr7:84158595..84159433-chr7:84240484..84241224,2	MCF-7	breast:
27	chr7:84119833..84120591-chr7:84650307..84651093,2	K562	blood:
28	chr7:84107857..84110395-chr7:84114744..84117396,2	K562	blood:
29	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
30	chr7:84158432..84159358-chr7:84499153..84500086,4	MCF-7	breast:
31	chr1:149857245..149858849-chr7:84173495..84175226,2	MCF-7	breast:
32	chr7:84119744..84120746-chr7:84652245..84653462,3	MCF-7	breast:
33	chr7:84297350..84299613-chr7:84307072..84309162,2	K562	blood:
34	chr7:84319553..84321871-chr7:84324252..84327875,3	K562	blood:
35	chr7:84316486..84318065-chr7:84325058..84327513,2	K562	blood:
36	chr7:84231197..84234055-chr7:84234117..84236974,2	K562	blood:
37	chr7:84311385..84314153-chr7:84316076..84317631,2	K562	blood:
38	chr7:84119826..84120501-chr7:84652111..84652970,2	K562	blood:
39	chr7:84244149..84244717-chr7:84651890..84652789,2	MCF-7	breast:
40	chr7:83568691..83570764-chr7:84108131..84110174,2	K562	blood:
41	chr7:84120092..84120731-chr7:84650207..84651023,2	MCF-7	breast:
42	chr7:84117622..84122447-chr7:84123148..84126860,4	K562	blood:
43	chr7:84273543..84275443-chr7:84283712..84286350,2	K562	blood:
44	chr7:84311385..84314153-chr7:84316076..84317631,2	K562	blood:
45	chr7:84112762..84114363-chr7:84117900..84119846,2	K562	blood:
46	chr7:84158367..84158951-chr7:84240610..84241382,2	MCF-7	breast:
47	chr7:84138849..84140536-chr7:84143161..84145231,2	K562	blood:
48	chr7:84305279..84307187-chr7:84308599..84311252,2	K562	blood:
49	chr7:83904428..83905120-chr7:84165177..84165677,2	MCF-7	breast:
50	chr7:84165204..84166004-chr7:84499385..84500020,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-2	chr7:84213467-84213634	NR_110080
2	lnc-GRM3-2	chr7:84200295-84204159	XLOC_006159
3	lnc-SEMA3A-1	chr7:84157438-84158146	NONHSAT121788
4	lnc-GRM3-2	chr7:84200294-84200423	NONHSAT121790
5	lnc-GRM3-2	chr7:84213466-84213638	NONHSAT121790
6	lnc-GRM3-2	chr7:84178521-84178569	NONHSAT121790
7	lnc-GRM3-2	chr7:84200295-84200423	XLOC_006159
8	lnc-GRM3-2	chr7:84178463-84178569	NR_110080
9	lnc-GRM3-2	chr7:84161792-84161923	NR_110080
10	lnc-GRM3-2	chr7:84161792-84161923	XLOC_006159
11	lnc-GRM3-2	chr7:84213467-84213638	XLOC_006159
12	lnc-GRM3-2	chr7:84200295-84200423	NR_110080
13	lnc-GRM3-2	chr7:84178463-84178569	XLOC_006159
14	lnc-GRM3-2	chr7:84178522-84178569	XLOC_006159

No data

Variant related genes	Relation type
ENSG00000235139	TF binding region
RPL7P30	TF binding region
ENSG00000265050	TF binding region
SEMA3A	TF binding region
ENSG00000235139	CpG island
RPL7P30	CpG island
ENSG00000265050	CpG island
SEMA3A	CpG island
ENSG00000184260	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000075213	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000196542	chromatin interactions
ARFIP1	miRNA target sites
ARHGAP1	miRNA target sites
ARFGEF1	miRNA target sites

Extended variants
information (count: 7395 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:7395 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1228966	chr7:84086502-84086503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555550759	chr7:84086530-84086531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576267464	chr7:84086549-84086550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190282009	chr7:84086630-84086631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs180681911	chr7:84086693-84086694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538801696	chr7:84086757-84086758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559477572	chr7:84086856-84086857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1228967	chr7:84086868-84086869	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs16887713	chr7:84086924-84086925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs563202750	chr7:84086934-84086935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565064443	chr7:84086972-84086973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530859289	chr7:84086975-84086976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375334029	chr7:84086982-84086983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185395522	chr7:84087089-84087090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567453947	chr7:84087179-84087180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528564023	chr7:84087187-84087188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7810450	chr7:84087254-84087255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571823914	chr7:84087274-84087275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192143622	chr7:84087283-84087284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184012894	chr7:84087345-84087346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188652050	chr7:84087349-84087350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537086124	chr7:84087377-84087378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555389825	chr7:84087395-84087396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573812369	chr7:84087399-84087400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374534012	chr7:84087447-84087448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541143596	chr7:84087547-84087548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552759806	chr7:84087571-84087572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116814933	chr7:84087586-84087587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544830797	chr7:84087606-84087607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560953443	chr7:84087611-84087612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373622427	chr7:84087619-84087620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148530998	chr7:84087698-84087699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575176816	chr7:84087714-84087715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368769813	chr7:84087721-84087722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542639689	chr7:84087756-84087757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35989680	chr7:84087766-84087767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397791133	chr7:84087772-84087773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549728225	chr7:84087797-84087798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78568673	chr7:84087857-84087858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191753182	chr7:84087860-84087861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547078499	chr7:84087925-84087926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183713250	chr7:84087932-84087933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532786744	chr7:84087950-84087951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569482118	chr7:84087959-84087960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2527537	chr7:84087962-84087963	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs551603158	chr7:84087991-84087992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79957367	chr7:84088024-84088025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186846283	chr7:84088055-84088056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2706902	chr7:84088111-84088112	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs200634127	chr7:84088243-84088244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84085400-84093600	Weak transcription	NHDF-Ad	bronchial
2	chr7:84090000-84091200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:84090400-84090600	Enhancers	Fetal Brain Female	brain
4	chr7:84090600-84091200	Weak transcription	Fetal Brain Female	brain
5	chr7:84091000-84092000	Enhancers	Fetal Brain Male	brain
6	chr7:84091200-84092000	Enhancers	Fetal Brain Female	brain
7	chr7:84091600-84092200	Enhancers	Fetal Stomach	stomach
8	chr7:84093600-84096400	Strong transcription	NHDF-Ad	bronchial
9	chr7:84094400-84101600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr7:84095600-84100000	Weak transcription	Adipose Nuclei	Adipose
11	chr7:84096000-84097600	Weak transcription	Fetal Muscle Leg	muscle
12	chr7:84096400-84098400	Weak transcription	NHDF-Ad	bronchial
13	chr7:84098400-84098800	Enhancers	HUVEC	blood vessel
14	chr7:84098400-84098800	Strong transcription	NHDF-Ad	bronchial
15	chr7:84098400-84099000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:84098600-84099000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:84098800-84107000	Weak transcription	NHDF-Ad	bronchial
18	chr7:84100000-84100400	Enhancers	Adipose Nuclei	Adipose
19	chr7:84103400-84104200	Enhancers	Colon Smooth Muscle	Colon
20	chr7:84106800-84107600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr7:84107000-84107400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr7:84107000-84107600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:84107000-84107600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:84107000-84107600	Genic enhancers	NHDF-Ad	bronchial
25	chr7:84107000-84107800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:84107000-84107800	Enhancers	HMEC	breast
27	chr7:84107000-84108000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr7:84107000-84108000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr7:84107000-84109600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr7:84107000-84109600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:84107200-84107600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:84107200-84109800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr7:84107400-84107600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:84107600-84108600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr7:84107600-84108600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:84107600-84108600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr7:84107600-84114800	Weak transcription	NHDF-Ad	bronchial
38	chr7:84107600-84116600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr7:84107800-84108200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr7:84108000-84108400	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr7:84108000-84108400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr7:84108200-84109600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr7:84108400-84109400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:84108400-84109800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr7:84108600-84108800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr7:84108600-84108800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:84108600-84109600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr7:84109200-84120000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr7:84110400-84110600	Enhancers	Rectal Smooth Muscle	rectum
50	chr7:84110600-84111800	Weak transcription	Rectal Smooth Muscle	rectum

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