Variant report

Variant	nsv888516
Chromosome Location	chr7:79086317-79221707
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:79136530-79136804	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:79135879-79136195	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:79091709-79092003	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:79090760-79091411	HepG2	liver:	n/a	n/a
5	ATF1	chr7:79155465-79155511	K562	blood:	n/a	n/a
6	ATF1	chr7:79168827-79168925	K562	blood:	n/a	n/a
7	ATF3	chr7:79136418-79136929	A549	lung:	n/a	n/a
8	BCL3	chr7:79136419-79136964	A549	lung:	n/a	n/a
9	BCL3	chr7:79135704-79136201	A549	lung:	n/a	n/a
10	BCL3	chr7:79135674-79136308	A549	lung:	n/a	n/a
11	BCL3	chr7:79136354-79136969	A549	lung:	n/a	n/a
12	BCL3	chr7:79090906-79091522	A549	lung:	n/a	n/a
13	BHLHE40	chr7:79154489-79154768	HepG2	liver:	n/a	n/a
14	CCNT2	chr7:79109715-79109825	K562	blood:	n/a	n/a
15	CEBPB	chr7:79177974-79178565	IMR90	lung:	n/a	chr7:79178066-79178077 chr7:79178142-79178153 chr7:79178525-79178536 chr7:79178523-79178536
16	CEBPB	chr7:79220629-79220866	H1-hESC	embryonic stem cell:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
17	CEBPB	chr7:79176617-79176808	H1-hESC	embryonic stem cell:	n/a	chr7:79176648-79176659
18	CEBPB	chr7:79089670-79089963	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:79091024-79091356	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:79176528-79176817	K562	blood:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
21	CEBPB	chr7:79091091-79091277	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:79161261-79161581	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:79212174-79212446	IMR90	lung:	n/a	chr7:79212322-79212333
24	CEBPB	chr7:79154457-79154741	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:79220570-79220924	HepG2	liver:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
26	CEBPB	chr7:79183216-79183696	A549	lung:	n/a	n/a
27	CEBPB	chr7:79201511-79201650	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:79090904-79091503	A549	lung:	n/a	n/a
29	CEBPB	chr7:79176477-79176825	HepG2	liver:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
30	CEBPB	chr7:79152801-79153095	IMR90	lung:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
31	CEBPB	chr7:79154408-79154729	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:79136335-79136839	A549	lung:	n/a	n/a
33	CEBPB	chr7:79220574-79220912	Hela-S3	cervix:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
34	CEBPB	chr7:79176480-79176829	IMR90	lung:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
35	CEBPB	chr7:79220593-79220881	A549	lung:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
36	CEBPB	chr7:79152796-79153050	A549	lung:	n/a	chr7:79152948-79152959 chr7:79152974-79152985
37	CEBPB	chr7:79176485-79176822	A549	lung:	n/a	chr7:79176648-79176659 chr7:79176551-79176562
38	CEBPB	chr7:79088192-79088458	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:79177973-79178548	A549	lung:	n/a	chr7:79178066-79178077 chr7:79178142-79178153 chr7:79178525-79178536 chr7:79178523-79178536
40	CEBPB	chr7:79091081-79091377	MCF-7	breast:	n/a	n/a
41	CEBPB	chr7:79209272-79209522	HepG2	liver:	n/a	chr7:79209368-79209379 chr7:79209368-79209377 chr7:79209366-79209377
42	CEBPB	chr7:79157659-79158257	HCT-116	colon:	n/a	n/a
43	CEBPB	chr7:79124997-79125653	IMR90	lung:	n/a	n/a
44	CEBPB	chr7:79159144-79159624	IMR90	lung:	n/a	chr7:79159560-79159573
45	CEBPB	chr7:79220583-79220924	K562	blood:	n/a	chr7:79220770-79220781 chr7:79220733-79220744
46	CEBPB	chr7:79177985-79178595	HepG2	liver:	n/a	chr7:79178066-79178077 chr7:79178142-79178153 chr7:79178525-79178536 chr7:79178523-79178536
47	CEBPB	chr7:79090731-79091364	A549	lung:	n/a	n/a
48	CEBPB	chr7:79209289-79209502	IMR90	lung:	n/a	chr7:79209368-79209379 chr7:79209368-79209377 chr7:79209366-79209377
49	CEBPB	chr7:79090711-79091341	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:79220553-79220927	IMR90	lung:	n/a	chr7:79220770-79220781 chr7:79220733-79220744

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:79134707-79134757	Caco-2	colon:	n/a
2	chr7:79134707-79134757	HEEpiC	esophagus:	n/a
3	chr7:79166927-79166977	SK-N-SH_RA	brain:	n/a
4	chr7:79134707-79134757	SK-N-MC	brain:	n/a
5	chr7:79134707-79134757	NHBE	bronchial:	n/a
6	chr7:79134707-79134757	HMEC	breast:	n/a
7	chr7:79166927-79166977	AG04449	skin:	fetal
8	chr7:79166927-79166977	Jurkat	blood:	n/a
9	chr7:79166927-79166977	HAEpiC	amniotic membrane:	n/a
10	chr7:79166927-79166977	GM06990	blood:	n/a
11	chr7:79134707-79134757	ProgFib	skin:	n/a
12	chr7:79134707-79134757	SKMC	muscle:	n/a
13	chr7:79134707-79134757	IMR90	lung:	fetal
14	chr7:79166927-79166977	SK-N-SH	brain:	n/a
15	chr7:79166927-79166977	GM19239	blood:	n/a
16	chr7:79134707-79134757	RPTEC	kidney:	n/a
17	chr7:79134707-79134757	HUVEC	blood vessel:	n/a
18	chr7:79134707-79134757	GM19239	blood:	n/a
19	chr7:79166927-79166977	PrEC	prostate:	n/a
20	chr7:79166927-79166977	SAEC	small airway:	n/a
21	chr7:79134707-79134757	HAEpiC	amniotic membrane:	n/a
22	chr7:79134707-79134757	HRPEpiC	eye:	n/a
23	chr7:79166927-79166977	HNPCEpiC	eye:	n/a
24	chr7:79166927-79166977	GM12878	blood:	n/a
25	chr7:79134707-79134757	GM12878	blood:	n/a
26	chr7:79134707-79134757	MCF-7	breast:	n/a
27	chr7:79134707-79134757	HCF	heart:	n/a
28	chr7:79134707-79134757	HNPCEpiC	eye:	n/a
29	chr7:79166927-79166977	HCF	heart:	n/a
30	chr7:79134707-79134757	HCT-116	colon:	n/a
31	chr7:79166927-79166977	AoSMC	blood vessel:	n/a
32	chr7:79134707-79134757	BE2_C	brain:	n/a
33	chr7:79166927-79166977	HCM	heart:	n/a
34	chr7:79134707-79134757	HCM	heart:	n/a
35	chr7:79166927-79166977	PFSK-1	brain:	n/a
36	chr7:79166927-79166977	HCPEpiC	choroid plexus:	n/a
37	chr7:79166927-79166977	RPTEC	kidney:	n/a
38	chr7:79166927-79166977	IMR90	lung:	fetal
39	chr7:79166927-79166977	ECC-1	luminal epithelium:	n/a
40	chr7:79166927-79166977	AG04450	lung:	fetal
41	chr7:79166927-79166977	Hela-S3	cervix:	n/a
42	chr7:79134707-79134757	AG09309	skin:	n/a
43	chr7:79166927-79166977	HRE	kidney:	n/a
44	chr7:79166927-79166977	T-47D	breast:	n/a
45	chr7:79134707-79134757	Hepatocyte	liver:	n/a
46	chr7:79134707-79134757	U87	brain:	n/a
47	chr7:79134707-79134757	AG04449	skin:	fetal
48	chr7:79166927-79166977	HRCEpiC	kidney:	n/a
49	chr7:79166927-79166977	Hepatocyte	liver:	n/a
50	chr7:79166927-79166977	AG10803	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:79095989..79098582-chr7:79174957..79177392,2	K562	blood:
2	chr7:79095989..79098582-chr7:79174957..79177392,2	K562	blood:
3	chr13:75245963..75246703-chr7:79210691..79211521,2	MCF-7	breast:
4	chr5:150846511..150848831-chr7:79188913..79190608,2	MCF-7	breast:
5	chr7:79171467..79174385-chr7:79176496..79179081,2	K562	blood:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-2	chr7:79100099-79100452	NONHSAT121725
2	lnc-GNAI1-2	chr7:79088852-79093061	ENSG00000234456.2
3	lnc-GNAI1-2	chr7:79088163-79088315	ENSG00000234456.2
4	lnc-GNAI1-2	chr7:79088852-79089916	NONHSAT121716
5	lnc-MAGI2-1	chr7:79088353-79093892	ENSG00000249657
6	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121718
7	lnc-GNAI1-2	chr7:79100099-79100524	ENSG00000234456.2
8	lnc-GNAI1-2	chr7:79088852-79089155	ENSG00000234456.2
9	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121723
10	lnc-GNAI1-2	chr7:79100099-79100512	ENSG00000234456.2
11	lnc-GNAI1-2	chr7:79100099-79100185	NONHSAT121703
12	lnc-GNAI1-2	chr7:79088163-79088315	ENSG00000234456.2
13	lnc-GNAI1-2	chr7:79100099-79100431	NONHSAT121719
14	lnc-GNAI1-2	chr7:79088163-79088315	ENSG00000234456.2
15	lnc-GNAI1-2	chr7:79088852-79096786	ENSG00000234456.3
16	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121719
17	lnc-GNAI1-2	chr7:79088120-79088315	NONHSAT121723
18	lnc-GNAI1-2	chr7:79098343-79098762	NONHSAT121725
19	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121725
20	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121717
21	lnc-GNAI1-2	chr7:79088852-79090496	NONHSAT121718
22	lnc-GNAI1-2	chr7:79088021-79088315	ENSG00000234456.3
23	lnc-GNAI1-2	chr7:79100099-79100170	NONHSAT121723
24	lnc-GNAI1-2	chr7:79099743-79099995	ENSG00000234456.2
25	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121719
26	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121703
27	lnc-MAGI2-1	chr7:79093975-79096779	ENSG00000249657
28	lnc-GNAI1-2	chr7:79088852-79089022	ENSG00000234456.2
29	lnc-GNAI1-2	chr7:79099907-79099997	NONHSAT121718
30	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121717
31	lnc-GNAI1-2	chr7:79088021-79088315	ENSG00000234456.2
32	lnc-GNAI1-2	chr7:79100099-79100516	ENSG00000234456.2
33	lnc-GNAI1-2	chr7:79099910-79099995	ENSG00000234456.2
34	lnc-GNAI1-2	chr7:79091029-79091950	NONHSAT121718
35	lnc-GNAI1-2	chr7:79100099-79100515	NONHSAT121718
36	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121716
37	lnc-MAGI2-2	chr7:79173227-79174169	NONHSAT121727
38	lnc-MAGI2-1	chr7:79092173-79093984	XLOC_006507
39	lnc-GNAI1-2	chr7:79088163-79088256	ENSG00000234456.2
40	lnc-GNAI1-2	chr7:79088163-79088315	ENSG00000234456.2
41	lnc-GNAI1-2	chr7:79100099-79100447	NONHSAT121717
42	lnc-MAGI2-1	chr7:79088787-79091858	XLOC_006507
43	lnc-GNAI1-2	chr7:79087967-79088046	ENSG00000234456.2

No data

Variant related genes	Relation type
ENSG00000226285	TF binding region
MAGI2-AS3	TF binding region
MAGI2	TF binding region
ENSG00000226285	CpG island
MAGI2-AS3	CpG island
MAGI2	CpG island
ENSG00000226285	chromatin interactions
USP38	miRNA target sites
TNRC6A	miRNA target sites
B4GALT1	miRNA target sites

Extended variants
information (count: 3658 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3658 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6964700	chr7:79086317-79086318	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141665769	chr7:79086319-79086320	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138260880	chr7:79086373-79086374	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528894776	chr7:79086393-79086394	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs185157850	chr7:79086436-79086437	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs386715014	chr7:79086438-79086439	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs181760400	chr7:79086439-79086440	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs551730367	chr7:79086515-79086516	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs186434549	chr7:79086517-79086518	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs10258595	chr7:79086534-79086535	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs374334092	chr7:79086537-79086538	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs534526625	chr7:79086546-79086547	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs572366845	chr7:79086573-79086574	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs554528531	chr7:79086576-79086577	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs567926500	chr7:79086630-79086631	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs189708316	chr7:79086638-79086639	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs545171169	chr7:79086680-79086681	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs368437304	chr7:79086754-79086755	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs536261511	chr7:79086823-79086824	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs137869918	chr7:79086828-79086829	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180957022	chr7:79086891-79086892	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545467605	chr7:79086904-79086905	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs33988738	chr7:79086908-79086909	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557559106	chr7:79086917-79086918	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77137568	chr7:79086918-79086919	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6970599	chr7:79086964-79086965	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531071854	chr7:79086967-79086968	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560824095	chr7:79086985-79086986	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560023538	chr7:79086988-79086989	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111331826	chr7:79087002-79087003	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544584276	chr7:79087027-79087028	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529137364	chr7:79087037-79087038	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529715309	chr7:79087105-79087106	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150578985	chr7:79087111-79087112	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576224640	chr7:79087125-79087126	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369425601	chr7:79087151-79087152	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372898665	chr7:79087173-79087174	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6970901	chr7:79087189-79087190	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs531342082	chr7:79087204-79087205	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551481514	chr7:79087211-79087212	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571337875	chr7:79087222-79087223	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7802400	chr7:79087223-79087224	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs547969949	chr7:79087304-79087305	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139658548	chr7:79087324-79087325	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536941903	chr7:79087328-79087329	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369036647	chr7:79087341-79087342	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34200927	chr7:79087354-79087355	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570009341	chr7:79087385-79087386	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538628025	chr7:79087402-79087403	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs558639171	chr7:79087422-79087423	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Cancer	20164920	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79084200-79091200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:79084400-79088200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:79084400-79089000	Weak transcription	NH-A	brain
4	chr7:79084400-79095000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:79084400-79102200	Weak transcription	Left Ventricle	heart
6	chr7:79084600-79101000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr7:79084800-79086600	Enhancers	Brain Cingulate Gyrus	brain
8	chr7:79084800-79087000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:79084800-79087600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:79084800-79091000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:79084800-79100800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr7:79084800-79102800	Weak transcription	HSMM	muscle
13	chr7:79085000-79086400	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:79085000-79086600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:79085000-79086600	Enhancers	Brain Angular Gyrus	brain
16	chr7:79085000-79086600	Enhancers	Brain Anterior Caudate	brain
17	chr7:79085000-79086600	Enhancers	Brain Hippocampus Middle	brain
18	chr7:79085000-79086600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:79085000-79087000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:79085000-79087400	Weak transcription	HSMMtube	muscle
21	chr7:79085000-79087800	Weak transcription	Right Ventricle	heart
22	chr7:79085000-79087800	Enhancers	HepG2	liver
23	chr7:79085000-79088800	Weak transcription	Fetal Brain Female	brain
24	chr7:79085000-79089000	Weak transcription	Fetal Heart	heart
25	chr7:79085000-79090400	Weak transcription	Lung	lung
26	chr7:79085000-79098600	Weak transcription	Fetal Muscle Leg	muscle
27	chr7:79085000-79099600	Weak transcription	Fetal Stomach	stomach
28	chr7:79085200-79088000	Genic enhancers	Osteobl	bone
29	chr7:79085200-79089000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr7:79085200-79091800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:79085400-79086400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:79085400-79086600	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr7:79085400-79087600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:79085400-79088000	Genic enhancers	Ovary	ovary
35	chr7:79085600-79086600	Genic enhancers	Colon Smooth Muscle	Colon
36	chr7:79085600-79088200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr7:79085800-79086600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr7:79085800-79087400	Weak transcription	Aorta	Aorta
39	chr7:79085800-79087400	Weak transcription	Fetal Lung	lung
40	chr7:79085800-79087400	Weak transcription	Fetal Muscle Trunk	muscle
41	chr7:79085800-79087600	Weak transcription	NHDF-Ad	bronchial
42	chr7:79085800-79088000	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr7:79085800-79088200	Enhancers	Adipose Nuclei	Adipose
44	chr7:79085800-79089000	Weak transcription	Liver	Liver
45	chr7:79085800-79089800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:79085800-79090800	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr7:79085800-79095400	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr7:79085800-79098000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr7:79086000-79086600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:79086000-79087400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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