Variant report

Variant	nsv482521
Chromosome Location	chr7:101604002-101718950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1750)
CpG islands
(count:2017)
Chromatin interactive
region (count:208)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1750 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101612988-101613093	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:101667927-101668675	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101663659-101663683	K562	blood:	n/a	n/a
4	ARID3A	chr7:101685684-101685947	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:101656159-101656653	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:101663221-101663249	K562	blood:	n/a	n/a
7	ARID3A	chr7:101618979-101619111	HepG2	liver:	n/a	n/a
8	ATF2	chr7:101624772-101625788	GM12878	blood:	n/a	n/a
9	ATF2	chr7:101698816-101699190	GM12878	blood:	n/a	n/a
10	ATF2	chr7:101632792-101633565	GM12878	blood:	n/a	n/a
11	ATF2	chr7:101705065-101705763	GM12878	blood:	n/a	n/a
12	ATF2	chr7:101633931-101634825	GM12878	blood:	n/a	n/a
13	ATF2	chr7:101705008-101705884	GM12878	blood:	n/a	n/a
14	ATF2	chr7:101673858-101674327	GM12878	blood:	n/a	n/a
15	ATF2	chr7:101628267-101628688	GM12878	blood:	n/a	n/a
16	ATF2	chr7:101633969-101634812	GM12878	blood:	n/a	n/a
17	ATF2	chr7:101624950-101625759	GM12878	blood:	n/a	n/a
18	ATF2	chr7:101628184-101628802	GM12878	blood:	n/a	n/a
19	ATF2	chr7:101689235-101689601	GM12878	blood:	n/a	n/a
20	ATF3	chr7:101639638-101639846	K562	blood:	n/a	n/a
21	BACH1	chr7:101707125-101707347	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:101630664-101630794	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr7:101628334-101628672	GM12878	blood:	n/a	n/a
24	BATF	chr7:101634223-101634678	GM12878	blood:	n/a	n/a
25	BATF	chr7:101705126-101705709	GM12878	blood:	n/a	chr7:101705696-101705704
26	BATF	chr7:101634322-101634547	GM12878	blood:	n/a	n/a
27	BATF	chr7:101698772-101699268	GM12878	blood:	n/a	n/a
28	BATF	chr7:101625154-101625513	GM12878	blood:	n/a	chr7:101625422-101625432
29	BATF	chr7:101689231-101689611	GM12878	blood:	n/a	chr7:101689378-101689389
30	BATF	chr7:101715275-101715515	GM12878	blood:	n/a	n/a
31	BATF	chr7:101628342-101628615	GM12878	blood:	n/a	n/a
32	BATF	chr7:101698849-101699202	GM12878	blood:	n/a	n/a
33	BATF	chr7:101625043-101625639	GM12878	blood:	n/a	chr7:101625422-101625432
34	BATF	chr7:101689187-101689511	GM12878	blood:	n/a	chr7:101689378-101689389
35	BATF	chr7:101626666-101626987	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:101625103-101625646	GM12878	blood:	n/a	chr7:101625475-101625484
37	BCL11A	chr7:101673950-101674296	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:101634172-101634647	GM12878	blood:	n/a	chr7:101634448-101634457
39	BCL11A	chr7:101628387-101628604	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:101625024-101625540	GM12878	blood:	n/a	chr7:101625475-101625484
41	BCL11A	chr7:101673906-101674298	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:101705249-101705669	GM12878	blood:	n/a	chr7:101705578-101705591
43	BCL11A	chr7:101628337-101628624	GM12878	blood:	n/a	chr7:101628338-101628347
44	BCL11A	chr7:101633053-101633481	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:101689283-101689435	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:101705243-101705706	GM12878	blood:	n/a	chr7:101705578-101705591
47	BCL11A	chr7:101634158-101634684	GM12878	blood:	n/a	chr7:101634448-101634457
48	BCL3	chr7:101618769-101619264	A549	lung:	n/a	n/a
49	BCL3	chr7:101689217-101689578	GM12878	blood:	n/a	chr7:101689491-101689500 chr7:101689513-101689522
50	BCL3	chr7:101705133-101705731	GM12878	blood:	n/a	chr7:101705578-101705591

(count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101630620-101630670	SK-N-MC	brain:	n/a
2	chr7:101630650-101630700	PANC-1	pancreas:	n/a
3	chr7:101632618-101632668	Hepatocyte	liver:	n/a
4	chr7:101688675-101688725	SK-N-SH	brain:	n/a
5	chr7:101630620-101630670	SK-N-MC	brain:	n/a
6	chr7:101630650-101630700	PANC-1	pancreas:	n/a
7	chr7:101632618-101632668	Hepatocyte	liver:	n/a
8	chr7:101688675-101688725	SK-N-SH	brain:	n/a
9	chr7:101707668-101707718	HepG2	liver:	n/a
10	chr7:101656975-101657025	SK-N-SH	brain:	n/a
11	chr7:101647464-101647514	AG04450	lung:	fetal
12	chr7:101616020-101616070	HUVEC	blood vessel:	n/a
13	chr7:101647464-101647514	Hepatocyte	liver:	n/a
14	chr7:101688730-101688780	AG04450	lung:	fetal
15	chr7:101632645-101632695	HAEpiC	amniotic membrane:	n/a
16	chr7:101688730-101688780	HRPEpiC	eye:	n/a
17	chr7:101630839-101630889	HCM	heart:	n/a
18	chr7:101712308-101712358	Jurkat	blood:	n/a
19	chr7:101680429-101680479	GM12891	blood:	n/a
20	chr7:101662332-101662382	PANC-1	pancreas:	n/a
21	chr7:101688675-101688725	PANC-1	pancreas:	n/a
22	chr7:101662182-101662232	SK-N-SH_RA	brain:	n/a
23	chr7:101667129-101667179	GM12892	blood:	n/a
24	chr7:101632568-101632618	HCF	heart:	n/a
25	chr7:101630948-101630998	IMR90	lung:	fetal
26	chr7:101630948-101630998	SK-N-SH_RA	brain:	n/a
27	chr7:101662182-101662232	AG09319	gingival:	n/a
28	chr7:101630650-101630700	HNPCEpiC	eye:	n/a
29	chr7:101615743-101615793	NH-A	brain:	n/a
30	chr7:101630650-101630700	HIPEpiC	eye:	n/a
31	chr7:101707668-101707718	GM12892	blood:	n/a
32	chr7:101656975-101657025	PANC-1	pancreas:	n/a
33	chr7:101630888-101630938	CMK	blood:	n/a
34	chr7:101680429-101680479	HRPEpiC	eye:	n/a
35	chr7:101671556-101671606	Jurkat	blood:	n/a
36	chr7:101632568-101632618	HCPEpiC	choroid plexus:	n/a
37	chr7:101608014-101608064	HUVEC	blood vessel:	n/a
38	chr7:101671556-101671606	GM12892	blood:	n/a
39	chr7:101712212-101712262	NT2-D1	testis:	n/a
40	chr7:101629430-101629480	PANC-1	pancreas:	n/a
41	chr7:101707668-101707718	PANC-1	pancreas:	n/a
42	chr7:101630650-101630700	HRCEpiC	kidney:	n/a
43	chr7:101632568-101632618	HUVEC	blood vessel:	n/a
44	chr7:101616020-101616070	Jurkat	blood:	n/a
45	chr7:101630888-101630938	A549	lung:	n/a
46	chr7:101680927-101680977	HRPEpiC	eye:	n/a
47	chr7:101680429-101680479	MCF10A-Er-Src	breast:	n/a
48	chr7:101629430-101629480	NH-A	brain:	n/a
49	chr7:101630888-101630938	U87	brain:	n/a
50	chr7:101680429-101680479	GM19239	blood:	n/a

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:101643865..101645968-chr7:101646120..101648774,2	K562	blood:
2	chr7:101619566..101621139-chr7:101625025..101626768,2	K562	blood:
3	chr7:101616036..101617995-chr7:101623779..101626539,2	MCF-7	breast:
4	chr7:101587675..101589304-chr7:101641856..101645951,3	MCF-7	breast:
5	chr7:101458855..101462085-chr7:101664015..101667033,4	MCF-7	breast:
6	chr7:101617978..101621240-chr7:101621803..101623926,3	K562	blood:
7	chr7:101628339..101629982-chr7:101630689..101633025,2	MCF-7	breast:
8	chr7:101677836..101679461-chr7:101681645..101683380,2	K562	blood:
9	chr7:101647120..101647995-chr7:101957457..101958324,5	MCF-7	breast:
10	chr7:101625094..101626938-chr7:101639657..101641295,2	MCF-7	breast:
11	chr7:101654464..101657712-chr7:101662423..101666684,4	MCF-7	breast:
12	chr7:101527665..101530418-chr7:101615760..101617815,3	MCF-7	breast:
13	chr7:101619172..101621456-chr7:101707365..101710139,2	MCF-7	breast:
14	chr7:101584833..101587634-chr7:101667426..101668972,2	MCF-7	breast:
15	chr20:60640319..60642125-chr7:101687169..101688689,2	K562	blood:
16	chr7:101529626..101530204-chr7:101647546..101648051,2	MCF-7	breast:
17	chr7:101616108..101616642-chr7:101957466..101958066,2	MCF-7	breast:
18	chr7:101698449..101701130-chr7:101703905..101706013,2	MCF-7	breast:
19	chr7:101615283..101617064-chr7:101647091..101648139,67	MCF-7	breast:
20	chr7:101647226..101647995-chr7:101957457..101958324,3	MCF-7	breast:
21	chr7:101645872..101649176-chr7:101651087..101654410,4	MCF-7	breast:
22	chr7:101591380..101593397-chr7:101609992..101611735,2	K562	blood:
23	chr7:101528092..101529388-chr7:101615803..101616659,3	MCF-7	breast:
24	chr7:101523069..101525610-chr7:101617549..101619285,2	MCF-7	breast:
25	chr7:101705153..101708097-chr7:101711212..101713863,3	K562	blood:
26	chr7:101642133..101644445-chr7:101650974..101653254,2	MCF-7	breast:
27	chr7:101657254..101660021-chr7:101660679..101662867,2	MCF-7	breast:
28	chr7:101704873..101706493-chr7:101731658..101734496,2	K562	blood:
29	chr7:101497931..101500798-chr7:101614587..101617565,2	MCF-7	breast:
30	chr7:101611841..101614545-chr7:101629314..101633135,4	MCF-7	breast:
31	chr7:101635097..101635843-chr7:101647196..101647966,2	MCF-7	breast:
32	chr7:101554397..101555333-chr7:101616192..101617002,4	MCF-7	breast:
33	chr7:101714618..101716538-chr7:101724031..101725533,2	K562	blood:
34	chr7:101715723..101719126-chr7:101720326..101723914,4	K562	blood:
35	chr7:101628172..101630666-chr7:101646616..101649464,3	MCF-7	breast:
36	chr7:101635581..101637536-chr7:101644954..101647593,3	MCF-7	breast:
37	chr7:101627337..101631221-chr7:101631346..101635612,7	MCF-7	breast:
38	chr7:101586382..101587949-chr7:101645381..101648210,2	MCF-7	breast:
39	chr7:101615765..101617035-chr7:101647115..101648119,24	MCF-7	breast:
40	chr7:101456365..101464966-chr7:101609986..101627610,39	MCF-7	breast:
41	chr20:60641089..60641822-chr7:101688169..101689168,2	MCF-7	breast:
42	chr7:101585316..101588407-chr7:101614430..101618418,4	MCF-7	breast:
43	chr7:101647260..101647782-chr7:101656357..101656872,2	MCF-7	breast:
44	chr7:101619477..101622792-chr7:101626038..101627957,3	MCF-7	breast:
45	chr7:101627337..101631221-chr7:101631346..101635612,7	MCF-7	breast:
46	chr7:101602922..101605689-chr7:101609271..101612139,2	MCF-7	breast:
47	chr7:101525260..101527111-chr7:101652933..101654478,2	MCF-7	breast:
48	chr7:101654464..101657712-chr7:101662423..101666684,4	MCF-7	breast:
49	chr7:101343414..101344257-chr7:101647212..101647964,4	MCF-7	breast:
50	chr7:101647287..101648033-chr7:101957510..101958354,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH2B2-6	chr7:101676303-101677447	ENSG00000272544.1
2	lnc-SH2B2-7	chr7:101603396-101605174	ENSG00000272219.1
3	lnc-SH2B2-5	chr7:101685040-101688225	ucscGeneNc_uc003uyy_2

No data

Variant related genes	Relation type
ENSG00000272544	TF binding region
ENSG00000272544	CpG island
ENSG00000130699	chromatin interactions
ENSG00000265306	chromatin interactions
ENSG00000257923	chromatin interactions
ENSG00000272219	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000272544	chromatin interactions

Extended variants
information (count: 4618 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4618 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545406140	chr7:101604056-101604057	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs571403062	chr7:101604109-101604110	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs538582520	chr7:101604149-101604150	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs554029076	chr7:101604229-101604230	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs112011038	chr7:101604249-101604250	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs540240949	chr7:101604292-101604293	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs555294842	chr7:101604320-101604321	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs185707116	chr7:101604326-101604327	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs544266602	chr7:101604327-101604328	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs562974989	chr7:101604385-101604386	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs533548829	chr7:101604390-101604391	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs141634994	chr7:101604400-101604401	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs190223509	chr7:101604417-101604418	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs573930978	chr7:101604420-101604421	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs183588647	chr7:101604456-101604457	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs150154917	chr7:101604467-101604468	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs373930617	chr7:101604475-101604476	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs427039	chr7:101604526-101604527	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs549877914	chr7:101604563-101604564	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs544769479	chr7:101604570-101604571	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs188586530	chr7:101604604-101604605	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs138674216	chr7:101604605-101604606	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs407366	chr7:101604646-101604647	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs192853089	chr7:101604655-101604656	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs76877503	chr7:101604737-101604738	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs573683742	chr7:101604823-101604824	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs6954798	chr7:101604886-101604887	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs556616464	chr7:101604888-101604889	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs578141915	chr7:101604926-101604927	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs11461485	chr7:101604928-101604929	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs397822722	chr7:101604929-101604930	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs373613270	chr7:101605087-101605088	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs11409394	chr7:101605155-101605156	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs74325553	chr7:101605173-101605174	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs545595635	chr7:101605240-101605241	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs35293683	chr7:101605241-101605242	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs111352885	chr7:101605243-101605244	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs373073637	chr7:101605244-101605245	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs546643292	chr7:101605338-101605339	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs184118420	chr7:101605445-101605446	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs572801083	chr7:101605461-101605462	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs543326625	chr7:101605466-101605467	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs560893496	chr7:101605496-101605497	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs531327080	chr7:101605518-101605519	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs10276057	chr7:101605522-101605523	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs149295305	chr7:101605545-101605546	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs146254255	chr7:101605554-101605555	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562911514	chr7:101605555-101605556	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs433736	chr7:101605558-101605559	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs187572114	chr7:101605560-101605561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2908 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101578200-101612000	Weak transcription	HepG2	liver
2	chr7:101578200-101671200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:101583400-101608000	Weak transcription	Primary B cells from cord blood	blood
4	chr7:101586400-101615800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:101586400-101620600	Weak transcription	Adipose Nuclei	Adipose
6	chr7:101591400-101628200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:101591600-101607800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr7:101592400-101629200	Weak transcription	Aorta	Aorta
9	chr7:101594800-101612400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:101596200-101606200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:101596200-101606400	Weak transcription	Thymus	Thymus
12	chr7:101596200-101615400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:101596400-101606400	Weak transcription	Pancreas	Pancrea
14	chr7:101596400-101608000	Weak transcription	Spleen	Spleen
15	chr7:101596400-101615800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr7:101596800-101614200	Weak transcription	K562	blood
17	chr7:101597000-101608400	Weak transcription	Small Intestine	intestine
18	chr7:101597000-101642000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr7:101597200-101621200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:101597400-101604200	Weak transcription	Liver	Liver
21	chr7:101597400-101608000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:101597400-101616400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:101597400-101624800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr7:101597400-101625400	Weak transcription	NHLF	lung
25	chr7:101597600-101615800	Weak transcription	Primary T cells from cord blood	blood
26	chr7:101597600-101624600	Weak transcription	Hela-S3	cervix
27	chr7:101598000-101608600	Weak transcription	Ovary	ovary
28	chr7:101598200-101631600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr7:101598400-101606400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:101598600-101606400	Weak transcription	Lung	lung
31	chr7:101598600-101608000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr7:101598600-101612800	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr7:101598800-101604200	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr7:101598800-101608000	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr7:101598800-101615800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr7:101599000-101607800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr7:101599000-101612800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr7:101599200-101626200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr7:101600200-101604200	Weak transcription	Fetal Muscle Trunk	muscle
40	chr7:101600800-101608200	Weak transcription	Right Atrium	heart
41	chr7:101601200-101604400	Strong transcription	Fetal Intestine Small	intestine
42	chr7:101601600-101606800	Weak transcription	Fetal Thymus	thymus
43	chr7:101601600-101607800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:101601600-101626600	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr7:101601800-101604400	Weak transcription	Fetal Stomach	stomach
46	chr7:101601800-101607000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr7:101601800-101607800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:101601800-101613600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr7:101601800-101615600	Weak transcription	Fetal Muscle Leg	muscle
50	chr7:101601800-101624400	Weak transcription	Primary B cells from peripheral blood	blood

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