Variant report

Variant	nsv831080
Chromosome Location	chr7:101629121-101718950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1362)
CpG islands
(count:1772)
Chromatin interactive
region (count:132)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101663659-101663683	K562	blood:	n/a	n/a
2	ARID3A	chr7:101667927-101668675	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101685684-101685947	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:101656159-101656653	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:101663221-101663249	K562	blood:	n/a	n/a
6	ATF2	chr7:101705065-101705763	GM12878	blood:	n/a	n/a
7	ATF2	chr7:101689235-101689601	GM12878	blood:	n/a	n/a
8	ATF2	chr7:101632792-101633565	GM12878	blood:	n/a	n/a
9	ATF2	chr7:101705008-101705884	GM12878	blood:	n/a	n/a
10	ATF2	chr7:101633931-101634825	GM12878	blood:	n/a	n/a
11	ATF2	chr7:101633969-101634812	GM12878	blood:	n/a	n/a
12	ATF2	chr7:101673858-101674327	GM12878	blood:	n/a	n/a
13	ATF2	chr7:101698816-101699190	GM12878	blood:	n/a	n/a
14	ATF3	chr7:101639638-101639846	K562	blood:	n/a	n/a
15	BACH1	chr7:101630664-101630794	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:101707125-101707347	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr7:101705126-101705709	GM12878	blood:	n/a	chr7:101705696-101705704
18	BATF	chr7:101698849-101699202	GM12878	blood:	n/a	n/a
19	BATF	chr7:101689187-101689511	GM12878	blood:	n/a	chr7:101689378-101689389
20	BATF	chr7:101698772-101699268	GM12878	blood:	n/a	n/a
21	BATF	chr7:101715275-101715515	GM12878	blood:	n/a	n/a
22	BATF	chr7:101634322-101634547	GM12878	blood:	n/a	n/a
23	BATF	chr7:101689231-101689611	GM12878	blood:	n/a	chr7:101689378-101689389
24	BATF	chr7:101634223-101634678	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:101673950-101674296	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:101633053-101633481	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:101689283-101689435	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:101705249-101705669	GM12878	blood:	n/a	chr7:101705578-101705591
29	BCL11A	chr7:101705243-101705706	GM12878	blood:	n/a	chr7:101705578-101705591
30	BCL11A	chr7:101634172-101634647	GM12878	blood:	n/a	chr7:101634448-101634457
31	BCL11A	chr7:101634158-101634684	GM12878	blood:	n/a	chr7:101634448-101634457
32	BCL11A	chr7:101673906-101674298	GM12878	blood:	n/a	n/a
33	BCL3	chr7:101689217-101689578	GM12878	blood:	n/a	chr7:101689491-101689500 chr7:101689513-101689522
34	BCL3	chr7:101705133-101705731	GM12878	blood:	n/a	chr7:101705578-101705591
35	BCL3	chr7:101691164-101691591	GM12878	blood:	n/a	n/a
36	BCL3	chr7:101683991-101684228	GM12878	blood:	n/a	n/a
37	BCL3	chr7:101656036-101656645	A549	lung:	n/a	chr7:101656111-101656120
38	BCLAF1	chr7:101698783-101699172	GM12878	blood:	n/a	n/a
39	BCLAF1	chr7:101683749-101684275	GM12878	blood:	n/a	n/a
40	BCLAF1	chr7:101673836-101674435	GM12878	blood:	n/a	n/a
41	BCLAF1	chr7:101632950-101633501	GM12878	blood:	n/a	n/a
42	BCLAF1	chr7:101634036-101634885	GM12878	blood:	n/a	chr7:101634448-101634457
43	BCLAF1	chr7:101705157-101705795	GM12878	blood:	n/a	chr7:101705578-101705591
44	BHLHE40	chr7:101698953-101699166	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:101705269-101705746	GM12878	blood:	n/a	chr7:101705517-101705530
46	BHLHE40	chr7:101634015-101634840	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:101673824-101674323	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:101667963-101668509	HepG2	liver:	n/a	n/a
49	BHLHE40	chr7:101688413-101688423	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:101630603-101631182	K562	blood:	n/a	chr7:101630972-101630981 chr7:101630973-101630982 chr7:101630974-101630983 chr7:101630973-101630982

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101656975-101657025	HRCEpiC	kidney:	n/a
2	chr7:101632568-101632618	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:101680927-101680977	HCM	heart:	n/a
4	chr7:101656975-101657025	HRCEpiC	kidney:	n/a
5	chr7:101632568-101632618	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:101680927-101680977	HCM	heart:	n/a
7	chr7:101712363-101712413	AG04450	lung:	fetal
8	chr7:101662332-101662382	AoSMC	blood vessel:	n/a
9	chr7:101656975-101657025	AG04449	skin:	fetal
10	chr7:101712087-101712137	HRE	kidney:	n/a
11	chr7:101671556-101671606	HRE	kidney:	n/a
12	chr7:101632645-101632695	AG04450	lung:	fetal
13	chr7:101632568-101632618	IMR90	lung:	fetal
14	chr7:101630546-101630596	SK-N-SH_RA	brain:	n/a
15	chr7:101680429-101680479	AG09309	skin:	n/a
16	chr7:101712212-101712262	SKMC	muscle:	n/a
17	chr7:101630650-101630700	BE2_C	brain:	n/a
18	chr7:101650989-101651039	GM19239	blood:	n/a
19	chr7:101630546-101630596	NHBE	bronchial:	n/a
20	chr7:101688730-101688780	HRCEpiC	kidney:	n/a
21	chr7:101630948-101630998	HEEpiC	esophagus:	n/a
22	chr7:101630888-101630938	PrEC	prostate:	n/a
23	chr7:101632568-101632618	AoSMC	blood vessel:	n/a
24	chr7:101707668-101707718	PrEC	prostate:	n/a
25	chr7:101629430-101629480	CMK	blood:	n/a
26	chr7:101630888-101630938	AoSMC	blood vessel:	n/a
27	chr7:101662182-101662232	AG09319	gingival:	n/a
28	chr7:101630620-101630670	AG09319	gingival:	n/a
29	chr7:101629430-101629480	PrEC	prostate:	n/a
30	chr7:101630839-101630889	HRE	kidney:	n/a
31	chr7:101688648-101688698	HIPEpiC	eye:	n/a
32	chr7:101630650-101630700	H1-hESC	embryonic stem cell:	embryo
33	chr7:101688730-101688780	A549	lung:	n/a
34	chr7:101630839-101630889	U87	brain:	n/a
35	chr7:101688675-101688725	IMR90	lung:	fetal
36	chr7:101712212-101712262	RPTEC	kidney:	n/a
37	chr7:101641453-101641503	SK-N-SH	brain:	n/a
38	chr7:101712308-101712358	GM12891	blood:	n/a
39	chr7:101662116-101662166	GM12878	blood:	n/a
40	chr7:101688675-101688725	HepG2	liver:	n/a
41	chr7:101632568-101632618	RPTEC	kidney:	n/a
42	chr7:101647464-101647514	HNPCEpiC	eye:	n/a
43	chr7:101712308-101712358	NT2-D1	testis:	n/a
44	chr7:101680429-101680479	HMEC	breast:	n/a
45	chr7:101688730-101688780	HNPCEpiC	eye:	n/a
46	chr7:101671556-101671606	AG04450	lung:	fetal
47	chr7:101630839-101630889	SAEC	small airway:	n/a
48	chr7:101707668-101707718	GM06990	blood:	n/a
49	chr7:101707668-101707718	SK-N-SH_RA	brain:	n/a
50	chr7:101688648-101688698	PrEC	prostate:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:101656842..101659859-chr7:101660301..101664311,4	K562	blood:
2	chr7:101631872..101634524-chr7:101635259..101637821,2	MCF-7	breast:
3	chr7:101611685..101612677-chr7:101647099..101648113,5	MCF-7	breast:
4	chr7:101459872..101462595-chr7:101643871..101645866,3	MCF-7	breast:
5	chr7:101652466..101655257-chr7:101700349..101702104,2	MCF-7	breast:
6	chr7:101582848..101590446-chr7:101646237..101653992,20	MCF-7	breast:
7	chr7:101635581..101637536-chr7:101644954..101647593,3	MCF-7	breast:
8	chr7:101513034..101514774-chr7:101650619..101652950,2	MCF-7	breast:
9	chr7:101677836..101679461-chr7:101681645..101683380,2	K562	blood:
10	chr7:101524415..101527254-chr7:101635329..101637588,2	MCF-7	breast:
11	chr7:101634157..101637054-chr7:101638722..101641195,2	MCF-7	breast:
12	chr7:101627337..101631221-chr7:101631346..101635612,7	MCF-7	breast:
13	chr7:101635855..101638805-chr7:101640285..101643011,2	K562	blood:
14	chr7:101652466..101655257-chr7:101700349..101702104,2	MCF-7	breast:
15	chr7:101634157..101637054-chr7:101638722..101641195,2	MCF-7	breast:
16	chr7:101635409..101637242-chr7:101637513..101639320,2	MCF-7	breast:
17	chr7:101711827..101713959-chr7:101721934..101723640,2	MCF-7	breast:
18	chr7:101458855..101462085-chr7:101664015..101667033,4	MCF-7	breast:
19	chr7:101554525..101555243-chr7:101647231..101647936,2	MCF-7	breast:
20	chr7:101459264..101462006-chr7:101705742..101707719,3	MCF-7	breast:
21	chr7:101628172..101630666-chr7:101646616..101649464,3	MCF-7	breast:
22	chr7:101717039..101718587-chr7:101722028..101724096,2	K562	blood:
23	chr20:52278044..52278974-chr7:101647121..101648013,2	MCF-7	breast:
24	chr7:101627966..101630739-chr7:101669621..101671157,2	MCF-7	breast:
25	chr20:60640319..60642125-chr7:101687169..101688689,2	K562	blood:
26	chr7:101642133..101644445-chr7:101650974..101653254,2	MCF-7	breast:
27	chr7:101554223..101556621-chr7:101646115..101648996,2	MCF-7	breast:
28	chr7:101602326..101606469-chr7:101646129..101649808,3	MCF-7	breast:
29	chr7:101657254..101660021-chr7:101660679..101662867,2	MCF-7	breast:
30	chr7:101341451..101343777-chr7:101646171..101649307,3	MCF-7	breast:
31	chr7:101677836..101679461-chr7:101681645..101683380,2	K562	blood:
32	chr7:101587675..101589304-chr7:101641856..101645951,3	MCF-7	breast:
33	chr7:101647260..101647782-chr7:101656357..101656872,2	MCF-7	breast:
34	chr7:101714618..101716441-chr7:101723476..101725531,2	K562	blood:
35	chr7:101460537..101463033-chr7:101654903..101656505,2	MCF-7	breast:
36	chr7:101688104..101690930-chr7:101693641..101697108,3	MCF-7	breast:
37	chr7:101628339..101629982-chr7:101630689..101633025,2	MCF-7	breast:
38	chr7:101635581..101637536-chr7:101644954..101647593,3	MCF-7	breast:
39	chr7:101526018..101527121-chr7:101647260..101648089,3	MCF-7	breast:
40	chr7:101625094..101626938-chr7:101639657..101641295,2	MCF-7	breast:
41	chr7:101525260..101527111-chr7:101652933..101654478,2	MCF-7	breast:
42	chr7:101587608..101588933-chr7:101647131..101648172,27	MCF-7	breast:
43	chr7:101629646..101631231-chr7:101651146..101653804,2	MCF-7	breast:
44	chr7:101705153..101708097-chr7:101711212..101713863,3	K562	blood:
45	chr7:101647260..101647782-chr7:101656357..101656872,2	MCF-7	breast:
46	chr7:101647287..101648033-chr7:101957510..101958354,3	MCF-7	breast:
47	chr7:101525676..101527121-chr7:101647199..101648097,5	MCF-7	breast:
48	chr7:101656842..101659859-chr7:101660301..101664311,4	K562	blood:
49	chr7:101715723..101719126-chr7:101720326..101723914,4	K562	blood:
50	chr20:60640086..60642079-chr7:101687169..101688689,3	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 3639 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3639 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116758938	chr7:101629150-101629151	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs561212576	chr7:101629235-101629236	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs528543042	chr7:101629279-101629280	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568113567	chr7:101629338-101629339	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184802698	chr7:101629391-101629392	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550770335	chr7:101629401-101629402	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569205586	chr7:101629419-101629420	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373397599	chr7:101629491-101629492	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528055501	chr7:101629492-101629493	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539339633	chr7:101629495-101629496	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138924424	chr7:101629498-101629499	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570756074	chr7:101629503-101629504	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534972317	chr7:101629505-101629506	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113991780	chr7:101629529-101629530	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370533444	chr7:101629535-101629536	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553061809	chr7:101629573-101629574	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11975995	chr7:101629577-101629578	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs188351519	chr7:101629622-101629623	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs180710078	chr7:101629625-101629626	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs10953355	chr7:101629629-101629630	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs546167224	chr7:101629767-101629768	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs564152795	chr7:101629817-101629818	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs528075237	chr7:101629840-101629841	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs116028201	chr7:101629904-101629905	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs568923608	chr7:101629911-101629912	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs142146595	chr7:101629935-101629936	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs550831458	chr7:101629939-101629940	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs112789694	chr7:101629951-101629952	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs569063883	chr7:101629992-101629993	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs145968612	chr7:101629994-101629995	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs186354345	chr7:101630009-101630010	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566719616	chr7:101630016-101630017	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115018673	chr7:101630059-101630060	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546560119	chr7:101630148-101630149	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191409017	chr7:101630154-101630155	Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535539095	chr7:101630216-101630217	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs34253202	chr7:101630217-101630218	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs557170689	chr7:101630226-101630227	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs117342143	chr7:101630227-101630228	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs35478196	chr7:101630249-101630250	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs558175436	chr7:101630292-101630293	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs573456807	chr7:101630313-101630314	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs141142648	chr7:101630329-101630330	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs561652853	chr7:101630330-101630331	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs573820866	chr7:101630387-101630388	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs554509629	chr7:101630391-101630392	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs181878946	chr7:101630455-101630456	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs150726546	chr7:101630465-101630466	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs532993387	chr7:101630473-101630474	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551521574	chr7:101630512-101630513	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	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:2380 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101578200-101671200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:101592400-101629200	Weak transcription	Aorta	Aorta
3	chr7:101597000-101642000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:101598200-101631600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:101604800-101629600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:101614400-101646400	Weak transcription	Fetal Brain Female	brain
7	chr7:101616400-101633000	Weak transcription	Gastric	stomach
8	chr7:101616600-101630200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr7:101617000-101634000	Weak transcription	Liver	Liver
10	chr7:101619600-101630800	Weak transcription	HepG2	liver
11	chr7:101620200-101642000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr7:101622200-101635600	Weak transcription	Pancreas	Pancrea
13	chr7:101623000-101631800	Weak transcription	Fetal Intestine Large	intestine
14	chr7:101623600-101630200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr7:101624600-101630000	Enhancers	Stomach Mucosa	stomach
16	chr7:101625000-101630200	Weak transcription	Spleen	Spleen
17	chr7:101625600-101630200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:101625600-101635400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:101625600-101635400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr7:101625800-101629200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:101625800-101634200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:101626800-101631200	Weak transcription	Primary B cells from cord blood	blood
23	chr7:101626800-101631600	Weak transcription	Hela-S3	cervix
24	chr7:101627000-101629800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr7:101627000-101629800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr7:101627000-101630200	Enhancers	Fetal Thymus	thymus
27	chr7:101627000-101632800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr7:101627000-101633400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:101627000-101633800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr7:101627000-101647400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:101627000-101671200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr7:101627200-101630600	Weak transcription	Primary B cells from peripheral blood	blood
33	chr7:101627400-101630200	Enhancers	Thymus	Thymus
34	chr7:101627600-101630600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:101627800-101629200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr7:101627800-101629200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:101627800-101629400	Enhancers	Primary hematopoietic stem cells	blood
38	chr7:101627800-101630000	Enhancers	Fetal Muscle Trunk	muscle
39	chr7:101627800-101630200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr7:101627800-101630400	Enhancers	Right Atrium	heart
41	chr7:101627800-101630400	Enhancers	Dnd41	blood
42	chr7:101627800-101630600	Enhancers	Left Ventricle	heart
43	chr7:101627800-101630600	Enhancers	Psoas Muscle	Psoas
44	chr7:101627800-101631000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:101627800-101634400	Strong transcription	Fetal Intestine Small	intestine
46	chr7:101628000-101629400	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr7:101628000-101651600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr7:101628200-101630000	Enhancers	Fetal Lung	lung
49	chr7:101628200-101630400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr7:101628200-101630600	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

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