Variant report

Variant	nsv2
Chromosome Location	chr1:144874979-144913548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:424)
CpG islands
(count:183)
Chromatin interactive
region (count:46)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:144893871-144894101	K562	blood:	n/a	n/a
2	ARID3A	chr1:144887242-144887658	K562	blood:	n/a	n/a
3	ATF1	chr1:144893850-144893916	K562	blood:	n/a	n/a
4	ATF2	chr1:144908048-144908805	GM12878	blood:	n/a	n/a
5	ATF2	chr1:144908134-144908746	GM12878	blood:	n/a	n/a
6	BACH1	chr1:144887336-144887619	K562	blood:	n/a	chr1:144887457-144887471
7	BACH1	chr1:144887269-144887748	H1-hESC	embryonic stem cell:	n/a	chr1:144887457-144887471
8	BATF	chr1:144908200-144908921	GM12878	blood:	n/a	n/a
9	BATF	chr1:144908154-144908914	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:144908211-144908941	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:144908224-144908540	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:144887736-144887832	K562	blood:	n/a	n/a
13	BHLHE40	chr1:144881409-144881640	K562	blood:	n/a	n/a
14	BHLHE40	chr1:144907946-144908684	GM12878	blood:	n/a	n/a
15	BRCA1	chr1:144912899-144912910	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr1:144881456-144881641	K562	blood:	n/a	n/a
17	CCNT2	chr1:144881870-144882070	K562	blood:	n/a	n/a
18	CEBPB	chr1:144884908-144885062	IMR90	lung:	n/a	chr1:144884984-144884995
19	CEBPB	chr1:144884889-144885111	Hela-S3	cervix:	n/a	chr1:144884984-144884995
20	CEBPB	chr1:144886646-144886811	K562	blood:	n/a	n/a
21	CEBPB	chr1:144893700-144894047	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:144884857-144885106	K562	blood:	n/a	chr1:144884984-144884995
23	CEBPB	chr1:144888845-144889029	A549	lung:	n/a	chr1:144888868-144888881 chr1:144888889-144888900 chr1:144888889-144888902
24	CEBPB	chr1:144888759-144889027	HepG2	liver:	n/a	chr1:144888868-144888881 chr1:144888889-144888900 chr1:144888889-144888902
25	CEBPB	chr1:144875361-144875648	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:144891851-144892054	A549	lung:	n/a	n/a
27	CEBPB	chr1:144893745-144893973	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:144891727-144892119	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:144888855-144888901	K562	blood:	n/a	chr1:144888868-144888881 chr1:144888889-144888900
30	CEBPB	chr1:144893629-144894043	K562	blood:	n/a	n/a
31	CEBPB	chr1:144884893-144885058	HepG2	liver:	n/a	chr1:144884984-144884995
32	CEBPB	chr1:144908669-144909024	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:144891731-144892054	MCF-7	breast:	n/a	n/a
34	CEBPB	chr1:144893729-144893974	K562	blood:	n/a	n/a
35	CEBPB	chr1:144891560-144892204	IMR90	lung:	n/a	n/a
36	CEBPD	chr1:144886542-144887059	K562	blood:	n/a	n/a
37	CEBPD	chr1:144881243-144881740	K562	blood:	n/a	n/a
38	CEBPD	chr1:144876854-144877446	K562	blood:	n/a	n/a
39	CHD1	chr1:144908052-144908165	GM12878	blood:	n/a	n/a
40	CHD2	chr1:144908428-144908865	GM12878	blood:	n/a	n/a
41	CHD2	chr1:144887438-144887454	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr1:144876880-144877030	BE2_C	brain:	n/a	chr1:144876971-144876989 chr1:144876974-144876983
43	CTCF	chr1:144893860-144894010	Caco-2	colon:	n/a	n/a
44	CTCF	chr1:144882700-144882850	GM12872	blood:	n/a	n/a
45	CTCF	chr1:144876840-144876990	AG09309	skin:	n/a	chr1:144876971-144876989 chr1:144876974-144876983
46	CTCF	chr1:144876800-144876950	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr1:144876847-144877080	K562	blood:	n/a	chr1:144876971-144876989 chr1:144876974-144876983
48	CTCF	chr1:144876860-144877010	Caco-2	colon:	n/a	chr1:144876971-144876989 chr1:144876974-144876983
49	CTCF	chr1:144876860-144877010	HCPEpiC	choroid plexus:	n/a	chr1:144876971-144876989 chr1:144876974-144876983
50	CTCF	chr1:144876840-144876990	HBMEC	blood vessel:	n/a	chr1:144876971-144876989 chr1:144876974-144876983

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144887235-144887285	GM06990	blood:	n/a
2	chr1:144892111-144892161	NT2-D1	testis:	n/a
3	chr1:144887235-144887285	Caco-2	colon:	n/a
4	chr1:144887235-144887285	NB4	blood:	n/a
5	chr1:144892111-144892161	AG04449	skin:	fetal
6	chr1:144892566-144892616	GM19239	blood:	n/a
7	chr1:144892111-144892161	HEEpiC	esophagus:	n/a
8	chr1:144892566-144892616	A549	lung:	n/a
9	chr1:144887235-144887285	HNPCEpiC	eye:	n/a
10	chr1:144892111-144892161	HRPEpiC	eye:	n/a
11	chr1:144892566-144892616	ProgFib	skin:	n/a
12	chr1:144892111-144892161	AG04450	lung:	fetal
13	chr1:144887235-144887285	AG09319	gingival:	n/a
14	chr1:144892111-144892161	H1-hESC	embryonic stem cell:	embryo
15	chr1:144892111-144892161	ProgFib	skin:	n/a
16	chr1:144892111-144892161	ECC-1	luminal epithelium:	n/a
17	chr1:144887235-144887285	SAEC	small airway:	n/a
18	chr1:144892111-144892161	A549	lung:	n/a
19	chr1:144892111-144892161	Hepatocyte	liver:	n/a
20	chr1:144887235-144887285	LNCaP	prostate:	n/a
21	chr1:144887235-144887285	CMK	blood:	n/a
22	chr1:144887235-144887285	HUVEC	blood vessel:	n/a
23	chr1:144887235-144887285	HCF	heart:	n/a
24	chr1:144887235-144887285	HL-60	blood:	n/a
25	chr1:144892566-144892616	NT2-D1	testis:	n/a
26	chr1:144887235-144887285	AG09309	skin:	n/a
27	chr1:144892111-144892161	HEK293	kidney:	embryo
28	chr1:144887235-144887285	HEEpiC	esophagus:	n/a
29	chr1:144887235-144887285	NH-A	brain:	n/a
30	chr1:144892111-144892161	LNCaP	prostate:	n/a
31	chr1:144887235-144887285	HAEpiC	amniotic membrane:	n/a
32	chr1:144887235-144887285	K562	blood:	n/a
33	chr1:144892111-144892161	GM12892	blood:	n/a
34	chr1:144887235-144887285	AoSMC	blood vessel:	n/a
35	chr1:144892111-144892161	NB4	blood:	n/a
36	chr1:144892111-144892161	HRCEpiC	kidney:	n/a
37	chr1:144892566-144892616	HUVEC	blood vessel:	n/a
38	chr1:144887235-144887285	PFSK-1	brain:	n/a
39	chr1:144887235-144887285	NHDF-neo	bronchial:	n/a
40	chr1:144892566-144892616	HepG2	liver:	n/a
41	chr1:144892111-144892161	SKMC	muscle:	n/a
42	chr1:144892566-144892616	K562	blood:	n/a
43	chr1:144887235-144887285	MCF10A-Er-Src	breast:	n/a
44	chr1:144892566-144892616	Jurkat	blood:	n/a
45	chr1:144892566-144892616	HAEpiC	amniotic membrane:	n/a
46	chr1:144892566-144892616	ovcar-3	ovarian:	n/a
47	chr1:144887235-144887285	H1-hESC	embryonic stem cell:	embryo
48	chr1:144892111-144892161	GM19239	blood:	n/a
49	chr1:144892566-144892616	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:144892566-144892616	PrEC	prostate:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144877869..144879998-chr1:144892579..144894748,2	MCF-7	breast:
2	chr1:144891214..144893695-chr1:144896100..144898968,2	MCF-7	breast:
3	chr1:144894819..144897241-chr1:144898698..144901682,2	K562	blood:
4	chr1:144895341..144897404-chr1:144905462..144906982,2	MCF-7	breast:
5	chr1:144895702..144897735-chr1:144904870..144906981,2	MCF-7	breast:
6	chr1:17046027..17047625-chr1:144886603..144888109,2	MCF-7	breast:
7	chr1:144906087..144908086-chr1:144911253..144912912,2	K562	blood:
8	chr1:144878185..144879777-chr1:144881889..144884530,2	MCF-7	breast:
9	chr1:144891174..144892693-chr1:144930887..144933429,2	MCF-7	breast:
10	chr1:144886541..144889030-chr1:144932018..144933743,3	MCF-7	breast:
11	chr1:17045982..17048017-chr1:144885102..144888081,2	K562	blood:
12	chr1:144881667..144883836-chr1:144885018..144890367,4	K562	blood:
13	chr1:144887488..144889062-chr1:144895977..144898603,2	MCF-7	breast:
14	chr1:144873625..144876777-chr1:144880154..144883711,4	MCF-7	breast:
15	chr1:144889740..144892703-chr1:146500075..146502138,3	MCF-7	breast:
16	chr1:144893909..144894771-chr8:51229590..51230343,2	MCF-7	breast:
17	chr1:144906087..144908086-chr1:144911253..144912912,2	K562	blood:
18	chr1:144891214..144893695-chr1:144896100..144898968,2	MCF-7	breast:
19	chr1:144894819..144897241-chr1:144898698..144901682,2	K562	blood:
20	chr1:144912771..144915909-chr1:144922533..144924963,5	MCF-7	breast:
21	chr1:144891445..144893339-chr1:146502271..146504240,2	MCF-7	breast:
22	chr1:144913341..144914857-chr1:144914948..144916749,2	K562	blood:
23	chr1:144879410..144881863-chr1:144882763..144884923,2	K562	blood:
24	chr1:144888141..144890870-chr1:145070504..145072082,2	K562	blood:
25	chr1:144893446..144895237-chr1:144930953..144933183,2	MCF-7	breast:
26	chr1:144895341..144897404-chr1:144905462..144906982,2	MCF-7	breast:
27	chr1:144895504..144897115-chr1:144905432..144907751,3	K562	blood:
28	chr1:144891477..144893654-chr1:144895299..144897580,2	K562	blood:
29	chr1:144879410..144881863-chr1:144882763..144884923,2	K562	blood:
30	chr1:144883229..144886021-chr1:146495313..146498284,2	MCF-7	breast:
31	chr1:144855730..144858367-chr1:144880531..144882326,2	MCF-7	breast:
32	chr1:144892597..144895392-chr11:118795022..118797131,2	MCF-7	breast:
33	chr1:144873625..144876777-chr1:144880154..144883711,4	MCF-7	breast:
34	chr1:144890884..144894068-chr1:146500995..146504405,3	K562	blood:
35	chr1:144895702..144897735-chr1:144904870..144906981,2	MCF-7	breast:
36	chr1:144895504..144897115-chr1:144905432..144907751,3	K562	blood:
37	chr1:144873922..144875453-chr1:144885951..144887655,2	MCF-7	breast:
38	chr1:144887488..144889062-chr1:144895977..144898603,2	MCF-7	breast:
39	chr1:144877869..144879998-chr1:144892579..144894748,2	MCF-7	breast:
40	chr1:144891477..144893654-chr1:144895299..144897580,2	K562	blood:
41	chr1:144911399..144913167-chr1:144914593..144916227,2	MCF-7	breast:
42	chr1:144874282..144876288-chr1:144878980..144880964,2	K562	blood:
43	chr1:144861814..144863936-chr1:144885385..144887357,2	MCF-7	breast:
44	chr1:144856713..144858353-chr1:144872499..144875477,2	K562	blood:
45	chr1:144912685..144914252-chr1:144947438..144950034,2	K562	blood:
46	chr1:144892599..144896749-chr1:144930798..144933879,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBPF9-2	chr1:144874945-144874987	ENSG00000254913.1
2	lnc-NBPF9-2	chr1:144877226-144877296	ENSG00000254913.1
3	lnc-NBPF9-2	chr1:144877872-144878163	ENSG00000254913.1

No data

Variant related genes	Relation type
PDE4DIP	TF binding region
ENSG00000266739	TF binding region
PDE4DIP	CpG island
ENSG00000266739	CpG island
ENSG00000110375	chromatin interactions
ENSG00000254913	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000186174	chromatin interactions
ENSG00000268869	chromatin interactions
ENSG00000255148	chromatin interactions

Extended variants
information (count: 1570 )
Associated
traits (count: 166 )

Variant overlapped rSNPs/rCNVs (count:1570 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587727888	chr1:144874995-144874996	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs587629846	chr1:144875021-144875022	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587679221	chr1:144875341-144875342	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs587763332	chr1:144875344-144875345	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs587635617	chr1:144875402-144875403	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs587715287	chr1:144875455-144875456	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs587770768	chr1:144875458-144875459	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs587668671	chr1:144875484-144875485	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs1778153	chr1:144875485-144875486	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs587714722	chr1:144875501-144875502	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs587765170	chr1:144875514-144875515	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373741236	chr1:144875568-144875569	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs587646131	chr1:144875616-144875617	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs587718112	chr1:144875647-144875648	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs587601637	chr1:144875757-144875758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs111968804	chr1:144875787-144875788	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs764983	chr1:144875799-144875800	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201573746	chr1:144875815-144875816	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376819925	chr1:144875816-144875817	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371001668	chr1:144875828-144875829	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs368300414	chr1:144875856-144875857	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs587677598	chr1:144875879-144875880	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs587710491	chr1:144875915-144875916	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71664004	chr1:144875916-144875917	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374596259	chr1:144875939-144875940	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs79858727	chr1:144875940-144875941	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs372450870	chr1:144875947-144875948	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs71664005	chr1:144875979-144875980	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs587667941	chr1:144875985-144875986	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113953552	chr1:144875986-144875987	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587620924	chr1:144875987-144875988	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587660845	chr1:144875989-144875990	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587760559	chr1:144876016-144876017	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs587633796	chr1:144876045-144876046	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373212452	chr1:144876049-144876050	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs199514897	chr1:144876053-144876054	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs201174986	chr1:144876055-144876056	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200493038	chr1:144876061-144876062	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368722484	chr1:144876066-144876067	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs587655894	chr1:144876076-144876077	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587685333	chr1:144876082-144876083	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587768656	chr1:144876104-144876105	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587637172	chr1:144876113-144876114	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs587698683	chr1:144876119-144876120	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587757790	chr1:144876133-144876134	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587653190	chr1:144876144-144876145	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs587720714	chr1:144876153-144876154	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs587599746	chr1:144876161-144876162	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs587650607	chr1:144876167-144876168	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs587701550	chr1:144876191-144876192	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:166)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD

Chromatin state (count:1386 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144843800-144880600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:144850000-144875800	Strong transcription	Liver	Liver
3	chr1:144850000-144883200	Strong transcription	Rectal Mucosa Donor 31	rectum
4	chr1:144850000-144883600	Strong transcription	Duodenum Mucosa	Duodenum
5	chr1:144850000-144883800	Strong transcription	Muscle Satellite Cultured Cells	--
6	chr1:144850000-144885800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:144850000-144886200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:144850000-144886200	Strong transcription	Osteobl	bone
9	chr1:144850000-144886400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr1:144850000-144894000	Strong transcription	Stomach Smooth Muscle	stomach
11	chr1:144850400-144883400	Strong transcription	Fetal Brain Female	brain
12	chr1:144850400-144886200	Strong transcription	HSMMtube	muscle
13	chr1:144850400-144886600	Strong transcription	Adipose Nuclei	Adipose
14	chr1:144850400-144894200	Strong transcription	Brain Germinal Matrix	brain
15	chr1:144851200-144884400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr1:144851600-144884000	Strong transcription	Placenta	Placenta
17	chr1:144852200-144913200	Weak transcription	Stomach Mucosa	stomach
18	chr1:144854200-144886000	Weak transcription	Right Atrium	heart
19	chr1:144859800-144880600	Strong transcription	K562	blood
20	chr1:144860200-144886600	Strong transcription	HSMM	muscle
21	chr1:144860200-144888400	Strong transcription	Fetal Muscle Leg	muscle
22	chr1:144860400-144886000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr1:144860400-144886200	Strong transcription	Brain Substantia Nigra	brain
24	chr1:144860400-144887200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:144861200-144882000	Strong transcription	Primary T helper cells PMA-I stimulated	--
26	chr1:144861400-144876200	Strong transcription	Left Ventricle	heart
27	chr1:144861400-144883200	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr1:144861400-144884800	Strong transcription	NHDF-Ad	bronchial
29	chr1:144861400-144886800	Strong transcription	Brain Hippocampus Middle	brain
30	chr1:144861400-144887200	Strong transcription	Aorta	Aorta
31	chr1:144861800-144883000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:144861800-144883000	Strong transcription	Primary T cells from cord blood	blood
33	chr1:144861800-144883200	Strong transcription	Fetal Stomach	stomach
34	chr1:144861800-144883200	Strong transcription	Right Ventricle	heart
35	chr1:144861800-144883400	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr1:144861800-144884600	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr1:144861800-144885200	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr1:144862000-144875200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:144862200-144883600	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr1:144863000-144876800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr1:144863000-144877400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:144863000-144880200	Strong transcription	Fetal Intestine Large	intestine
43	chr1:144863200-144875200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr1:144863200-144879600	Strong transcription	Colon Smooth Muscle	Colon
45	chr1:144863200-144882200	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr1:144863600-144879600	Strong transcription	Pancreatic Islets	Pancreatic Islet
47	chr1:144863800-144877000	Strong transcription	Pancreas	Pancrea
48	chr1:144864400-144875000	Strong transcription	NH-A	brain
49	chr1:144864400-144883800	Strong transcription	Fetal Brain Male	brain
50	chr1:144866400-144886400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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