Variant report

Variant	nsv1018720
Chromosome Location	chr7:111172317-111337169
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1452)
CpG islands
(count:916)
Chromatin interactive
region (count:106)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1452 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
2	ARID3A	chr7:111202247-111202264	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:111202492-111202797	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:111202485-111202878	K562	blood:	n/a	n/a
5	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
6	ARID3A	chr7:111290764-111291175	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:111290526-111290531	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
9	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
10	ATF1	chr7:111335575-111335722	K562	blood:	n/a	n/a
11	ATF1	chr7:111319096-111319299	K562	blood:	n/a	n/a
12	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
13	ATF2	chr7:111201787-111202190	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr7:111290708-111291147	A549	lung:	n/a	n/a
15	ATF3	chr7:111201918-111202678	K562	blood:	n/a	n/a
16	BACH1	chr7:111202015-111202410	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:111188905-111189076	K562	blood:	n/a	n/a
18	BACH1	chr7:111201779-111202839	K562	blood:	n/a	n/a
19	BACH1	chr7:111312247-111312255	K562	blood:	n/a	n/a
20	BACH1	chr7:111172186-111172416	K562	blood:	n/a	n/a
21	BATF	chr7:111228155-111228552	GM12878	blood:	n/a	chr7:111228280-111228290 chr7:111228384-111228394 chr7:111228383-111228394
22	BCL3	chr7:111201738-111202909	A549	lung:	n/a	chr7:111202581-111202590 chr7:111202620-111202629 chr7:111202514-111202527 chr7:111202540-111202549
23	BCLAF1	chr7:111201762-111202357	GM12878	blood:	n/a	n/a
24	BCLAF1	chr7:111202426-111202931	GM12878	blood:	n/a	chr7:111202581-111202590 chr7:111202620-111202629 chr7:111202514-111202527 chr7:111202540-111202549
25	BHLHE40	chr7:111201850-111202859	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:111198942-111199292	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:111202134-111202334	A549	lung:	n/a	n/a
28	BHLHE40	chr7:111201889-111202773	HepG2	liver:	n/a	n/a
29	BHLHE40	chr7:111200634-111202933	K562	blood:	n/a	n/a
30	BHLHE40	chr7:111172180-111172524	K562	blood:	n/a	n/a
31	BRCA1	chr7:111202039-111202441	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr7:111201100-111201803	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr7:111202645-111202975	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr7:111172126-111172326	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr7:111262088-111262588	K562	blood:	n/a	n/a
36	CBX3	chr7:111202484-111202951	K562	blood:	n/a	n/a
37	CBX3	chr7:111211688-111212363	K562	blood:	n/a	n/a
38	CBX3	chr7:111262117-111262448	K562	blood:	n/a	n/a
39	CBX3	chr7:111211729-111212168	K562	blood:	n/a	n/a
40	CBX3	chr7:111200954-111203145	K562	blood:	n/a	chr7:111201281-111201292
41	CBX3	chr7:111284633-111285081	K562	blood:	n/a	n/a
42	CBX3	chr7:111284643-111285027	K562	blood:	n/a	n/a
43	CCNT2	chr7:111182271-111182423	K562	blood:	n/a	n/a
44	CCNT2	chr7:111201524-111202824	K562	blood:	n/a	n/a
45	CCNT2	chr7:111172127-111172375	K562	blood:	n/a	n/a
46	CCNT2	chr7:111262060-111262457	K562	blood:	n/a	n/a
47	CCNT2	chr7:111296594-111296630	K562	blood:	n/a	n/a
48	CEBPB	chr7:111198483-111198623	A549	lung:	n/a	n/a
49	CEBPB	chr7:111175787-111175840	A549	lung:	n/a	n/a
50	CEBPB	chr7:111219525-111219571	HepG2	liver:	n/a	chr7:111219536-111219547

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111202666-111202716	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:111202666-111202716	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:111249576-111249626	PFSK-1	brain:	n/a
4	chr7:111249576-111249626	AG10803	skin:	n/a
5	chr7:111203008-111203058	HEK293	kidney:	embryo
6	chr7:111249576-111249626	U87	brain:	n/a
7	chr7:111249924-111249974	CMK	blood:	n/a
8	chr7:111202679-111202729	SKMC	muscle:	n/a
9	chr7:111203008-111203058	MCF-7	breast:	n/a
10	chr7:111202222-111202272	SAEC	small airway:	n/a
11	chr7:111202389-111202439	HCF	heart:	n/a
12	chr7:111202395-111202445	HCF	heart:	n/a
13	chr7:111202395-111202445	Hepatocyte	liver:	n/a
14	chr7:111202679-111202729	U87	brain:	n/a
15	chr7:111202222-111202272	HCF	heart:	n/a
16	chr7:111204826-111204876	MCF-7	breast:	n/a
17	chr7:111198163-111198213	HUVEC	blood vessel:	n/a
18	chr7:111202450-111202500	T-47D	breast:	n/a
19	chr7:111204826-111204876	GM19239	blood:	n/a
20	chr7:111202457-111202507	HCM	heart:	n/a
21	chr7:111202457-111202507	AG04450	lung:	fetal
22	chr7:111249924-111249974	PANC-1	pancreas:	n/a
23	chr7:111202222-111202272	NH-A	brain:	n/a
24	chr7:111202666-111202716	AG09319	gingival:	n/a
25	chr7:111202457-111202507	SKMC	muscle:	n/a
26	chr7:111202395-111202445	HRPEpiC	eye:	n/a
27	chr7:111204826-111204876	CMK	blood:	n/a
28	chr7:111202755-111202805	HUVEC	blood vessel:	n/a
29	chr7:111200944-111200994	HCPEpiC	choroid plexus:	n/a
30	chr7:111202755-111202805	GM19239	blood:	n/a
31	chr7:111202389-111202439	ovcar-3	ovarian:	n/a
32	chr7:111204826-111204876	ProgFib	skin:	n/a
33	chr7:111198163-111198213	SK-N-SH	brain:	n/a
34	chr7:111204826-111204876	PANC-1	pancreas:	n/a
35	chr7:111202457-111202507	ECC-1	luminal epithelium:	n/a
36	chr7:111198163-111198213	U87	brain:	n/a
37	chr7:111202457-111202507	SAEC	small airway:	n/a
38	chr7:111249576-111249626	HEEpiC	esophagus:	n/a
39	chr7:111202450-111202500	BJ	skin:	n/a
40	chr7:111249576-111249626	IMR90	lung:	fetal
41	chr7:111202395-111202445	HL-60	blood:	n/a
42	chr7:111249576-111249626	RPTEC	kidney:	n/a
43	chr7:111202222-111202272	ovcar-3	ovarian:	n/a
44	chr7:111203008-111203058	NB4	blood:	n/a
45	chr7:111202222-111202272	AoSMC	blood vessel:	n/a
46	chr7:111200944-111200994	AG10803	skin:	n/a
47	chr7:111202222-111202272	HepG2	liver:	n/a
48	chr7:111202450-111202500	AG04449	skin:	fetal
49	chr7:111204826-111204876	HAEpiC	amniotic membrane:	n/a
50	chr7:111249924-111249974	SK-N-SH	brain:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:111238331..111240393-chr7:111247235..111250162,2	K562	blood:
2	chr7:111201205..111204064-chr7:111204287..111207408,3	K562	blood:
3	chr7:111296753..111298671-chr7:111300525..111303326,2	K562	blood:
4	chr7:111201977..111202695-chrX:48754562..48755511,2	Hela-S3	cervix:
5	chr7:111310577..111313223-chr7:111316574..111319309,2	K562	blood:
6	chr7:111182436..111184713-chr7:111201121..111202847,2	MCF-7	breast:
7	chr7:111299093..111300961-chr7:111312313..111315147,2	K562	blood:
8	chr7:111173111..111178494-chr7:111200645..111202653,4	MCF-7	breast:
9	chr7:111304451..111306356-chr7:111315376..111317800,2	MCF-7	breast:
10	chr7:111186407..111189009-chr7:111189104..111191721,2	K562	blood:
11	chr7:111180162..111182327-chr7:111200913..111202538,2	MCF-7	breast:
12	chr7:111176200..111178839-chr7:111180322..111182875,3	K562	blood:
13	chr7:111252421..111255385-chr7:111257912..111259805,2	MCF-7	breast:
14	chr7:111265016..111267943-chr7:111268536..111270636,2	MCF-7	breast:
15	chr7:111226016..111229076-chr7:111232229..111235664,3	K562	blood:
16	chr7:111178493..111181177-chr7:111184776..111187564,2	K562	blood:
17	chr7:111199186..111200731-chr7:111244724..111246694,2	K562	blood:
18	chr7:111227327..111229119-chr7:111232502..111234968,2	K562	blood:
19	chr7:111172655..111174823-chr7:111200872..111202478,2	MCF-7	breast:
20	chr5:39074237..39075141-chr7:111201699..111202501,2	Hela-S3	cervix:
21	chr7:111284627..111287307-chr7:111300910..111302600,2	K562	blood:
22	chr7:111199186..111200731-chr7:111244724..111246694,2	K562	blood:
23	chr7:111293955..111295853-chr7:111296098..111298925,2	K562	blood:
24	chr19:16738439..16739222-chr7:111202426..111202989,2	HCT-116	colon:
25	chr7:111178053..111179952-chr7:111201249..111203327,2	MCF-7	breast:
26	chr7:111204432..111206292-chr7:111209030..111211645,2	K562	blood:
27	chr7:111299147..111302092-chr7:111316986..111318533,2	K562	blood:
28	chr7:111183053..111185306-chr7:111210487..111212870,2	K562	blood:
29	chr7:111252721..111255749-chr7:111259045..111261451,3	K562	blood:
30	chr7:111166819..111169168-chr7:111191445..111193799,2	K562	blood:
31	chr6:31639869..31641695-chr7:111180406..111182806,2	MCF-7	breast:
32	chr7:111252421..111255385-chr7:111257912..111259805,2	MCF-7	breast:
33	chr7:111321825..111324162-chr7:111332702..111335171,2	K562	blood:
34	chr7:111265016..111267943-chr7:111268536..111270636,2	MCF-7	breast:
35	chr7:111176200..111178839-chr7:111180322..111182875,3	K562	blood:
36	chr7:111181285..111183708-chr7:111185192..111188559,3	K562	blood:
37	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
38	chr7:111201240..111203723-chr7:111208743..111211882,3	K562	blood:
39	chr7:111323962..111326043-chr7:111330961..111333909,2	MCF-7	breast:
40	chr7:111201180..111203639-chr7:116596222..116597858,2	MCF-7	breast:
41	chr7:111299093..111300961-chr7:111312313..111315147,2	K562	blood:
42	chr7:111328919..111331695-chr7:111335640..111337914,2	MCF-7	breast:
43	chr1:231114585..231115155-chr7:111179137..111179637,2	NB4	blood:
44	chr7:111198400..111201071-chr7:111297443..111299093,2	K562	blood:
45	chr7:111222849..111225723-chr7:111230601..111232352,2	K562	blood:
46	chr7:111310577..111313223-chr7:111316574..111319309,2	K562	blood:
47	chr7:111204432..111206292-chr7:111209030..111211645,2	K562	blood:
48	chr7:111284627..111287307-chr7:111300910..111302600,2	K562	blood:
49	chr7:111226200..111228452-chr7:111228554..111231372,2	K562	blood:
50	chr7:111165046..111167501-chr7:111171827..111173680,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRN3-2	chr7:111235830-111235905	ucscGeneNc_uc003vfz_2
2	lnc-LRRN3-2	chr7:111246670-111249064	ucscGeneNc_uc003vfz_2

No data

Variant related genes	Relation type
IMMP2L	TF binding region
IMMP2L	CpG island
ENSG00000240053	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000178951	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000143643	chromatin interactions

Extended variants
information (count: 3951 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3951 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148691334	chr7:111172379-111172380	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs545317772	chr7:111172396-111172397	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs189827561	chr7:111172423-111172424	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs144380166	chr7:111172435-111172436	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs181727986	chr7:111172454-111172455	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs115122285	chr7:111172535-111172536	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147827859	chr7:111172544-111172545	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs115954420	chr7:111172564-111172565	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs185698748	chr7:111172569-111172570	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs556171631	chr7:111172597-111172598	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs139699677	chr7:111172619-111172620	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs2529491	chr7:111172634-111172635	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs145105464	chr7:111172648-111172649	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369031741	chr7:111172686-111172687	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs150969462	chr7:111172687-111172688	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs35360547	chr7:111172695-111172696	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs564167515	chr7:111172723-111172724	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs376430451	chr7:111172740-111172741	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs576283729	chr7:111172784-111172785	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368963744	chr7:111172855-111172856	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543340270	chr7:111172863-111172864	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189376309	chr7:111172879-111172880	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs78809932	chr7:111172971-111172972	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs79981472	chr7:111172997-111172998	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140694039	chr7:111173041-111173042	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561015643	chr7:111173054-111173055	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs36004365	chr7:111173117-111173118	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs139546227	chr7:111173124-111173125	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533303985	chr7:111173131-111173132	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140532421	chr7:111173145-111173146	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs118053810	chr7:111173149-111173150	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115683139	chr7:111173152-111173153	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs150089539	chr7:111173172-111173173	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537737403	chr7:111173249-111173250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549666393	chr7:111173266-111173267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs117730563	chr7:111173276-111173277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181784271	chr7:111173304-111173305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113915833	chr7:111173308-111173309	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370358737	chr7:111173315-111173316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs73203030	chr7:111173337-111173338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs572099559	chr7:111173345-111173346	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs571495159	chr7:111173395-111173396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs145852450	chr7:111173427-111173428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs186159019	chr7:111173485-111173486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs76055729	chr7:111173642-111173643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561601261	chr7:111173656-111173657	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573605798	chr7:111173683-111173684	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541016068	chr7:111173781-111173782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559533495	chr7:111173782-111173783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs17158599	chr7:111173930-111173931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111151000-111180600	Weak transcription	Pancreas	Pancrea
2	chr7:111157800-111178000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:111159200-111172800	Weak transcription	Aorta	Aorta
4	chr7:111159200-111175600	Weak transcription	Small Intestine	intestine
5	chr7:111161200-111195600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr7:111162200-111200800	Weak transcription	Brain Anterior Caudate	brain
7	chr7:111162400-111172600	Weak transcription	Psoas Muscle	Psoas
8	chr7:111162400-111178000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:111162600-111175200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:111162800-111177800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr7:111162800-111192800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr7:111168000-111201200	Weak transcription	Left Ventricle	heart
13	chr7:111168400-111200400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr7:111168600-111190200	Weak transcription	Primary T cells from cord blood	blood
15	chr7:111168600-111190400	Weak transcription	Primary B cells from cord blood	blood
16	chr7:111168800-111188800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr7:111168800-111199600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:111170200-111172800	Weak transcription	Osteobl	bone
19	chr7:111170200-111189600	Weak transcription	Ovary	ovary
20	chr7:111170200-111200800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr7:111170200-111201600	Weak transcription	Esophagus	oesophagus
22	chr7:111170600-111180400	Weak transcription	Stomach Mucosa	stomach
23	chr7:111171000-111183600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr7:111171600-111172400	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr7:111171600-111172600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr7:111171600-111172800	Enhancers	GM12878-XiMat	blood
27	chr7:111171600-111173000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:111171800-111172800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:111171800-111173200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr7:111171800-111173600	Enhancers	Fetal Heart	heart
31	chr7:111172000-111173600	Enhancers	Colon Smooth Muscle	Colon
32	chr7:111172000-111173600	Enhancers	Hela-S3	cervix
33	chr7:111172000-111176200	Enhancers	A549	lung
34	chr7:111172200-111172600	Enhancers	K562	blood
35	chr7:111172200-111172800	Enhancers	Primary B cells from peripheral blood	blood
36	chr7:111172200-111173000	Enhancers	Right Atrium	heart
37	chr7:111172200-111173000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr7:111172200-111173200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:111172200-111173400	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr7:111172200-111173600	Enhancers	Rectal Smooth Muscle	rectum
41	chr7:111172400-111172800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr7:111172400-111173000	Enhancers	Brain Hippocampus Middle	brain
43	chr7:111172600-111173000	Enhancers	Psoas Muscle	Psoas
44	chr7:111172600-111173000	Enhancers	Stomach Smooth Muscle	stomach
45	chr7:111172600-111173400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:111172600-111180800	Weak transcription	K562	blood
47	chr7:111172800-111173000	Enhancers	Right Ventricle	heart
48	chr7:111172800-111173000	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr7:111172800-111173200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr7:111172800-111173200	Enhancers	Aorta	Aorta

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