Variant report

Variant	nsv888636
Chromosome Location	chr7:84117594-84334498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1763)
CpG islands
(count:366)
Chromatin interactive
region (count:64)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1763 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

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	chr7:84302368-84302402	K562	blood:	n/a	n/a
4	ARID3A	chr7:84332343-84332393	K562	blood:	n/a	n/a
5	ARID3A	chr7:84287580-84287954	K562	blood:	n/a	n/a
6	ATF1	chr7:84331188-84331414	K562	blood:	n/a	n/a
7	ATF1	chr7:84323619-84323645	K562	blood:	n/a	n/a
8	ATF1	chr7:84298510-84298929	K562	blood:	n/a	n/a
9	ATF1	chr7:84120076-84120312	K562	blood:	n/a	n/a
10	ATF1	chr7:84292651-84292819	K562	blood:	n/a	n/a
11	ATF1	chr7:84259630-84259842	K562	blood:	n/a	n/a
12	ATF1	chr7:84305022-84305312	K562	blood:	n/a	n/a
13	ATF3	chr7:84165356-84165961	A549	lung:	n/a	n/a
14	ATF3	chr7:84165333-84165902	A549	lung:	n/a	n/a
15	ATF3	chr7:84154321-84154946	A549	lung:	n/a	n/a
16	ATF3	chr7:84154180-84154816	A549	lung:	n/a	n/a
17	ATF3	chr7:84331078-84331730	A549	lung:	n/a	n/a
18	ATF3	chr7:84158579-84159198	A549	lung:	n/a	n/a
19	BACH1	chr7:84127424-84127445	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:84314329-84314388	K562	blood:	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	chr7:84153993-84154944	A549	lung:	n/a	chr7:84154006-84154015
25	BCL3	chr7:84165334-84165953	A549	lung:	n/a	n/a
26	BCL3	chr7:84165165-84166072	A549	lung:	n/a	n/a
27	BCL3	chr7:84158630-84159471	A549	lung:	n/a	n/a
28	BCL3	chr7:84330997-84331738	A549	lung:	n/a	n/a
29	BCL3	chr7:84158463-84159465	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	chr7:84330839-84331723	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr7:84302255-84302599	GM12878	blood:	n/a	n/a
35	BRCA1	chr7:84154330-84154744	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr7:84304850-84305429	Hela-S3	cervix:	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	chr7:84232979-84233116	K562	blood:	n/a	n/a
40	CBX3	chr7:84261530-84261866	K562	blood:	n/a	n/a
41	CCNT2	chr7:84255504-84255628	K562	blood:	n/a	n/a
42	CCNT2	chr7:84305040-84305328	K562	blood:	n/a	n/a
43	CCNT2	chr7:84298566-84298780	K562	blood:	n/a	n/a
44	CEBPB	chr7:84178758-84179104	HepG2	liver:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
45	CEBPB	chr7:84159800-84160116	A549	lung:	n/a	chr7:84159971-84159984
46	CEBPB	chr7:84178114-84178352	K562	blood:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
47	CEBPB	chr7:84161478-84161912	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr7:84158697-84159164	A549	lung:	n/a	n/a
49	CEBPB	chr7:84153993-84154751	A549	lung:	n/a	chr7:84154228-84154241 chr7:84154618-84154629
50	CEBPB	chr7:84178742-84179124	IMR90	lung:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84330779-84330829	SK-N-MC	brain:	n/a
2	chr7:84177905-84177955	IMR90	lung:	fetal
3	chr7:84330779-84330829	AG09309	skin:	n/a
4	chr7:84161222-84161272	BJ	skin:	n/a
5	chr7:84267140-84267190	PANC-1	pancreas:	n/a
6	chr7:84161222-84161272	HMEC	breast:	n/a
7	chr7:84277775-84277825	HRE	kidney:	n/a
8	chr7:84161420-84161470	Caco-2	colon:	n/a
9	chr7:84161222-84161272	MCF-7	breast:	n/a
10	chr7:84267140-84267190	PFSK-1	brain:	n/a
11	chr7:84161420-84161470	AoSMC	blood vessel:	n/a
12	chr7:84277775-84277825	HCT-116	colon:	n/a
13	chr7:84267140-84267190	K562	blood:	n/a
14	chr7:84277775-84277825	HUVEC	blood vessel:	n/a
15	chr7:84330779-84330829	HepG2	liver:	n/a
16	chr7:84277775-84277825	Hepatocyte	liver:	n/a
17	chr7:84267140-84267190	GM12892	blood:	n/a
18	chr7:84277775-84277825	HIPEpiC	eye:	n/a
19	chr7:84267140-84267190	SK-N-SH_RA	brain:	n/a
20	chr7:84267140-84267190	HRPEpiC	eye:	n/a
21	chr7:84161222-84161272	AG10803	skin:	n/a
22	chr7:84177905-84177955	GM06990	blood:	n/a
23	chr7:84177905-84177955	GM19239	blood:	n/a
24	chr7:84161222-84161272	H1-hESC	embryonic stem cell:	embryo
25	chr7:84330779-84330829	HNPCEpiC	eye:	n/a
26	chr7:84177905-84177955	HepG2	liver:	n/a
27	chr7:84161222-84161272	SKMC	muscle:	n/a
28	chr7:84161222-84161272	HRPEpiC	eye:	n/a
29	chr7:84177905-84177955	SK-N-SH	brain:	n/a
30	chr7:84330779-84330829	BJ	skin:	n/a
31	chr7:84161222-84161272	HepG2	liver:	n/a
32	chr7:84161222-84161272	NB4	blood:	n/a
33	chr7:84177905-84177955	AG09309	skin:	n/a
34	chr7:84161222-84161272	PrEC	prostate:	n/a
35	chr7:84330779-84330829	HAEpiC	amniotic membrane:	n/a
36	chr7:84161222-84161272	NHBE	bronchial:	n/a
37	chr7:84161222-84161272	HIPEpiC	eye:	n/a
38	chr7:84161420-84161470	HNPCEpiC	eye:	n/a
39	chr7:84267140-84267190	HCPEpiC	choroid plexus:	n/a
40	chr7:84277775-84277825	IMR90	lung:	fetal
41	chr7:84177905-84177955	A549	lung:	n/a
42	chr7:84177905-84177955	BE2_C	brain:	n/a
43	chr7:84267140-84267190	HRE	kidney:	n/a
44	chr7:84161222-84161272	AG09309	skin:	n/a
45	chr7:84177905-84177955	NB4	blood:	n/a
46	chr7:84161420-84161470	AG04449	skin:	fetal
47	chr7:84161420-84161470	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:84330779-84330829	HUVEC	blood vessel:	n/a
49	chr7:84277775-84277825	GM19239	blood:	n/a
50	chr7:84277775-84277825	AoSMC	blood vessel:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
2	chr7:84119826..84120501-chr7:84652111..84652970,2	K562	blood:
3	chr7:84275439..84277976-chr7:84279778..84282553,2	K562	blood:
4	chr7:84119833..84120591-chr7:84650307..84651093,2	K562	blood:
5	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
6	chr7:84158367..84158951-chr7:84240610..84241382,2	MCF-7	breast:
7	chr7:84165149..84166023-chr7:84582151..84583096,5	MCF-7	breast:
8	chr7:84165149..84165684-chr7:84582450..84583007,2	MCF-7	breast:
9	chr7:84165144..84166088-chr7:84499191..84500054,5	MCF-7	breast:
10	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
11	chr7:84120092..84120731-chr7:84650207..84651023,2	MCF-7	breast:
12	chr7:84158367..84158951-chr7:84240610..84241382,2	MCF-7	breast:
13	chr7:84297350..84299961-chr7:84307072..84309162,3	K562	blood:
14	chr7:84215550..84219199-chr7:84222001..84225003,3	K562	blood:
15	chr7:84315326..84318065-chr7:84325058..84327523,3	K562	blood:
16	chr7:84312169..84314896-chr7:84317846..84320190,3	K562	blood:
17	chr7:84298376..84301290-chr7:84302394..84304217,2	MCF-7	breast:
18	chr7:84293189..84295299-chr7:84297078..84299323,2	K562	blood:
19	chr7:84316486..84318065-chr7:84325058..84327513,2	K562	blood:
20	chr7:84311385..84314153-chr7:84316076..84317631,2	K562	blood:
21	chr7:84275439..84277976-chr7:84279778..84282553,2	K562	blood:
22	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
23	chr7:84315326..84318065-chr7:84325058..84327523,3	K562	blood:
24	chr7:84319553..84321871-chr7:84324252..84327875,3	K562	blood:
25	chr7:84302626..84304689-chr7:84308409..84311060,2	MCF-7	breast:
26	chr7:84273543..84275443-chr7:84283712..84286350,2	K562	blood:
27	chr7:84312169..84314896-chr7:84317846..84320190,3	K562	blood:
28	chr7:84112762..84114363-chr7:84117900..84119846,2	K562	blood:
29	chr7:84172414..84174090-chr7:84421942..84424878,2	K562	blood:
30	chr7:84165204..84166004-chr7:84499385..84500020,2	MCF-7	breast:
31	chr7:84250435..84252517-chr7:84252923..84255018,2	K562	blood:
32	chr7:84319553..84321871-chr7:84324252..84327875,3	K562	blood:
33	chr7:84293189..84295299-chr7:84297078..84299323,2	K562	blood:
34	chr7:84215550..84219199-chr7:84222001..84225003,3	K562	blood:
35	chr7:84158595..84159433-chr7:84240484..84241224,2	MCF-7	breast:
36	chr7:83904428..83905120-chr7:84165177..84165677,2	MCF-7	breast:
37	chr7:84231197..84234055-chr7:84234117..84236974,2	K562	blood:
38	chr7:84297350..84299613-chr7:84307072..84309162,2	K562	blood:
39	chr7:84138849..84140536-chr7:84143161..84145231,2	K562	blood:
40	chr7:84158432..84159047-chr7:84499527..84500086,2	MCF-7	breast:
41	chr7:84305279..84307187-chr7:84308599..84311252,2	K562	blood:
42	chr7:84325930..84329136-chr7:84329688..84332999,3	K562	blood:
43	chr7:84325930..84329136-chr7:84329688..84332999,3	K562	blood:
44	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
45	chr7:84158595..84159433-chr7:84240484..84241224,2	MCF-7	breast:
46	chr7:84244149..84244717-chr7:84651890..84652789,2	MCF-7	breast:
47	chr7:84158432..84159358-chr7:84499153..84500086,4	MCF-7	breast:
48	chr7:84305279..84307187-chr7:84308599..84311252,2	K562	blood:
49	chr7:84302626..84304689-chr7:84308409..84311060,2	MCF-7	breast:
50	chr7:84243619..84244378-chr7:84650207..84650987,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-2	chr7:84161792-84161923	XLOC_006159
2	lnc-GRM3-2	chr7:84200295-84204159	XLOC_006159
3	lnc-GRM3-2	chr7:84200294-84200423	NONHSAT121790
4	lnc-SEMA3A-1	chr7:84157438-84158146	NONHSAT121788
5	lnc-GRM3-2	chr7:84200295-84200423	XLOC_006159
6	lnc-GRM3-2	chr7:84213466-84213638	NONHSAT121790
7	lnc-GRM3-2	chr7:84200295-84200423	NR_110080
8	lnc-GRM3-2	chr7:84178463-84178569	NR_110080
9	lnc-GRM3-2	chr7:84213467-84213638	XLOC_006159
10	lnc-GRM3-2	chr7:84178522-84178569	XLOC_006159
11	lnc-GRM3-2	chr7:84213467-84213634	NR_110080
12	lnc-GRM3-2	chr7:84161792-84161923	NR_110080
13	lnc-GRM3-2	chr7:84178521-84178569	NONHSAT121790
14	lnc-GRM3-2	chr7:84178463-84178569	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
ENSG00000202077	chromatin interactions
ENSG00000184260	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: 6194 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6194 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16887725	chr7:84117594-84117595	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189282183	chr7:84117608-84117609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs202016976	chr7:84117627-84117628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78558304	chr7:84117628-84117629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79006179	chr7:84117631-84117632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111966108	chr7:84117632-84117633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371812440	chr7:84117633-84117634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72268602	chr7:84117634-84117635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71558792	chr7:84117635-84117636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555207913	chr7:84117652-84117653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200634377	chr7:84117663-84117664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201699054	chr7:84117665-84117666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199842948	chr7:84117667-84117668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540964054	chr7:84117735-84117736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74723811	chr7:84117748-84117749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201712688	chr7:84117795-84117796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577592545	chr7:84117798-84117799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143847313	chr7:84117820-84117821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370761155	chr7:84117855-84117856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76338542	chr7:84117869-84117870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575015238	chr7:84117896-84117897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373385301	chr7:84117897-84117898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534665754	chr7:84117967-84117968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542267267	chr7:84117974-84117975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181863452	chr7:84118058-84118059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76043265	chr7:84118089-84118090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528262748	chr7:84118160-84118161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546918307	chr7:84118164-84118165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563450207	chr7:84118194-84118195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565019238	chr7:84118201-84118202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532414077	chr7:84118204-84118205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551017282	chr7:84118229-84118230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148614273	chr7:84118231-84118232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536755061	chr7:84118240-84118241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144273433	chr7:84118300-84118301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374582818	chr7:84118350-84118351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186422052	chr7:84118365-84118366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147384962	chr7:84118405-84118406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559235559	chr7:84118412-84118413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116577092	chr7:84118446-84118447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538117861	chr7:84118554-84118555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139590164	chr7:84118566-84118567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369798550	chr7:84118584-84118585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552994610	chr7:84118616-84118617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189357154	chr7:84118628-84118629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560815918	chr7:84118709-84118710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573030019	chr7:84118724-84118725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540071246	chr7:84118740-84118741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2706898	chr7:84118743-84118744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs181443721	chr7:84118797-84118798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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

Chromatin state (count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84109200-84120000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr7:84114000-84130600	Weak transcription	Rectal Smooth Muscle	rectum
3	chr7:84116800-84118200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:84116800-84119600	Weak transcription	NHDF-Ad	bronchial
5	chr7:84117800-84118400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:84118400-84121600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:84119600-84122200	Active TSS	NHDF-Ad	bronchial
8	chr7:84120000-84120200	Enhancers	Osteobl	bone
9	chr7:84120000-84120400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:84120000-84120600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:84120000-84120800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:84120000-84121800	Active TSS	Adipose Nuclei	Adipose
13	chr7:84120000-84121800	Active TSS	Fetal Muscle Leg	muscle
14	chr7:84120000-84122200	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr7:84120000-84122200	Active TSS	Fetal Muscle Trunk	muscle
16	chr7:84120400-84120600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
17	chr7:84120600-84121200	Enhancers	Muscle Satellite Cultured Cells	--
18	chr7:84120600-84121600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:84120800-84121000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:84120800-84121600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:84121000-84122000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:84121600-84121800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:84121600-84121800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:84121600-84122000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:84121600-84122000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr7:84121800-84122200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:84121800-84122200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:84121800-84122200	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr7:84121800-84122200	Flanking Active TSS	Fetal Muscle Leg	muscle
30	chr7:84122000-84122600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:84122000-84125400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:84122200-84122400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr7:84122200-84122400	Flanking Active TSS	Fetal Muscle Trunk	muscle
34	chr7:84122200-84122400	Enhancers	Fetal Muscle Leg	muscle
35	chr7:84122200-84122600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:84122200-84122800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:84122200-84122800	Enhancers	Adipose Nuclei	Adipose
38	chr7:84122200-84122800	Enhancers	NHDF-Ad	bronchial
39	chr7:84122400-84123000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr7:84122600-84127200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:84122800-84126800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:84122800-84131400	Weak transcription	Adipose Nuclei	Adipose
43	chr7:84124200-84125000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:84126800-84127600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:84127000-84127400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:84127200-84127600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:84127200-84127600	Enhancers	Colon Smooth Muscle	Colon
48	chr7:84127400-84127600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:84127600-84131400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:84127600-84131400	Weak transcription	Colon Smooth Muscle	Colon

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