Variant report

Variant	esv1824154
Chromosome Location	chr1:211565640-211614280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:427)
Chromatin interactive
region (count:22)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:211589207-211589407	HepG2	liver:	n/a	n/a
2	ATF1	chr1:211593836-211594062	K562	blood:	n/a	n/a
3	BACH1	chr1:211590179-211590180	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:211589569-211589903	HepG2	liver:	n/a	n/a
5	BHLHE40	chr1:211590267-211590632	GM12878	blood:	n/a	n/a
6	CEBPB	chr1:211594312-211594788	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:211590377-211590785	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:211584978-211585573	K562	blood:	n/a	chr1:211585440-211585451
9	CEBPB	chr1:211613868-211614122	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr1:211584973-211585276	K562	blood:	n/a	n/a
11	CEBPB	chr1:211613790-211614156	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr1:211613773-211614031	K562	blood:	n/a	n/a
13	CEBPB	chr1:211585098-211585548	HepG2	liver:	n/a	chr1:211585440-211585451
14	CEBPB	chr1:211589066-211589316	A549	lung:	n/a	chr1:211589153-211589164
15	CEBPB	chr1:211589119-211589336	HepG2	liver:	n/a	chr1:211589153-211589164
16	CEBPB	chr1:211597451-211597626	A549	lung:	n/a	chr1:211597546-211597557
17	CEBPB	chr1:211589018-211589339	Hela-S3	cervix:	n/a	chr1:211589153-211589164
18	CEBPB	chr1:211597459-211597635	HepG2	liver:	n/a	chr1:211597546-211597557
19	CEBPB	chr1:211585029-211585456	IMR90	lung:	n/a	chr1:211585440-211585451
20	CEBPB	chr1:211589167-211589168	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:211583697-211584002	K562	blood:	n/a	n/a
22	CEBPB	chr1:211597443-211597645	IMR90	lung:	n/a	chr1:211597546-211597557
23	CEBPB	chr1:211597372-211597736	HepG2	liver:	n/a	chr1:211597546-211597557
24	CEBPB	chr1:211613890-211613986	K562	blood:	n/a	n/a
25	CEBPB	chr1:211585369-211585437	A549	lung:	n/a	n/a
26	CEBPB	chr1:211594350-211594714	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:211597489-211597663	Hela-S3	cervix:	n/a	chr1:211597546-211597557
28	CEBPB	chr1:211597452-211597652	K562	blood:	n/a	chr1:211597546-211597557
29	CEBPB	chr1:211597474-211597644	H1-hESC	embryonic stem cell:	n/a	chr1:211597546-211597557
30	CEBPB	chr1:211613887-211614013	A549	lung:	n/a	n/a
31	CEBPB	chr1:211581307-211581309	A549	lung:	n/a	n/a
32	CEBPB	chr1:211565417-211565700	A549	lung:	n/a	n/a
33	CHD1	chr1:211590045-211590186	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr1:211605902-211605926	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr1:211589611-211589955	A549	lung:	n/a	n/a
36	CTCF	chr1:211598298-211598355	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr1:211583370-211583402	GM12891	blood:	n/a	n/a
38	CTCF	chr1:211589586-211589928	A549	lung:	n/a	chr1:211589803-211589816
39	CTCF	chr1:211589740-211589890	GM12865	blood:	n/a	chr1:211589803-211589816
40	CTCF	chr1:211589604-211589957	H1-hESC	embryonic stem cell:	n/a	chr1:211589803-211589816
41	CTCF	chr1:211597767-211597803	GM20000	blood:	n/a	n/a
42	CTCF	chr1:211589630-211589862	GM13977	blood:	n/a	chr1:211589803-211589816
43	CTCF	chr1:211589619-211589842	Gliobla	brain:	n/a	chr1:211589803-211589816
44	CTCF	chr1:211590151-211590237	GM12892	blood:	n/a	chr1:211590182-211590195
45	CTCF	chr1:211590080-211590230	GM12872	blood:	n/a	chr1:211590182-211590195
46	CTCF	chr1:211589606-211589922	MCF-7	breast:	n/a	chr1:211589803-211589816
47	CTCF	chr1:211589600-211589750	GM12872	blood:	n/a	n/a
48	CTCF	chr1:211589580-211589730	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr1:211589589-211589890	H1-hESC	embryonic stem cell:	n/a	chr1:211589803-211589816
50	CTCF	chr1:211589680-211589830	HEK293	kidney:	n/a	chr1:211589803-211589816

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:211589139-211589189	HEEpiC	esophagus:	n/a
2	chr1:211589139-211589189	U87	brain:	n/a
3	chr1:211572722-211572772	HRPEpiC	eye:	n/a
4	chr1:211589678-211589728	ovcar-3	ovarian:	n/a
5	chr1:211591896-211591946	BE2_C	brain:	n/a
6	chr1:211590128-211590178	IMR90	lung:	fetal
7	chr1:211590292-211590342	H1-hESC	embryonic stem cell:	embryo
8	chr1:211591896-211591946	H1-hESC	embryonic stem cell:	embryo
9	chr1:211589139-211589189	AG04449	skin:	fetal
10	chr1:211590128-211590178	AG09319	gingival:	n/a
11	chr1:211590128-211590178	CMK	blood:	n/a
12	chr1:211586719-211586769	SK-N-MC	brain:	n/a
13	chr1:211589139-211589189	NHDF-neo	bronchial:	n/a
14	chr1:211590292-211590342	AG04450	lung:	fetal
15	chr1:211590292-211590342	NHBE	bronchial:	n/a
16	chr1:211572722-211572772	PFSK-1	brain:	n/a
17	chr1:211591896-211591946	PANC-1	pancreas:	n/a
18	chr1:211589678-211589728	NT2-D1	testis:	n/a
19	chr1:211572722-211572772	AG04450	lung:	fetal
20	chr1:211589678-211589728	AG09319	gingival:	n/a
21	chr1:211572722-211572772	GM12878	blood:	n/a
22	chr1:211589139-211589189	BE2_C	brain:	n/a
23	chr1:211572722-211572772	H1-hESC	embryonic stem cell:	embryo
24	chr1:211591896-211591946	AG04449	skin:	fetal
25	chr1:211590292-211590342	HRE	kidney:	n/a
26	chr1:211590292-211590342	NB4	blood:	n/a
27	chr1:211591896-211591946	HCT-116	colon:	n/a
28	chr1:211586719-211586769	HCF	heart:	n/a
29	chr1:211589139-211589189	AG09319	gingival:	n/a
30	chr1:211590128-211590178	HCT-116	colon:	n/a
31	chr1:211590128-211590178	MCF-7	breast:	n/a
32	chr1:211586719-211586769	SK-N-SH_RA	brain:	n/a
33	chr1:211590292-211590342	NT2-D1	testis:	n/a
34	chr1:211589678-211589728	BE2_C	brain:	n/a
35	chr1:211589139-211589189	HIPEpiC	eye:	n/a
36	chr1:211586719-211586769	SKMC	muscle:	n/a
37	chr1:211590292-211590342	HIPEpiC	eye:	n/a
38	chr1:211590128-211590178	U87	brain:	n/a
39	chr1:211586719-211586769	Hela-S3	cervix:	n/a
40	chr1:211589678-211589728	NHBE	bronchial:	n/a
41	chr1:211586719-211586769	MCF-7	breast:	n/a
42	chr1:211589678-211589728	PrEC	prostate:	n/a
43	chr1:211590292-211590342	Caco-2	colon:	n/a
44	chr1:211590292-211590342	HUVEC	blood vessel:	n/a
45	chr1:211591896-211591946	HepG2	liver:	n/a
46	chr1:211589678-211589728	IMR90	lung:	fetal
47	chr1:211590292-211590342	HEK293	kidney:	embryo
48	chr1:211586719-211586769	GM12891	blood:	n/a
49	chr1:211591896-211591946	A549	lung:	n/a
50	chr1:211590128-211590178	NT2-D1	testis:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:211556090..211557781-chr1:211604466..211606047,2	K562	blood:
2	chr1:211591294..211593237-chr1:211594620..211596952,2	K562	blood:
3	chr1:211582791..211587024-chr1:211588072..211591351,4	MCF-7	breast:
4	chr1:211565192..211566756-chr1:211567269..211570151,2	K562	blood:
5	chr1:211546344..211548686-chr1:211564910..211567315,2	K562	blood:
6	chr1:211504123..211506416-chr1:211604400..211606288,2	K562	blood:
7	chr1:211431599..211434301-chr1:211581665..211583556,2	MCF-7	breast:
8	chr1:211592567..211595477-chr1:211598046..211600040,2	K562	blood:
9	chr1:211554866..211557592-chr1:211571886..211574017,3	K562	blood:
10	chr1:211599016..211601630-chr1:211604235..211606553,2	K562	blood:
11	chr1:211565192..211566756-chr1:211567269..211570151,2	K562	blood:
12	chr1:211565165..211567494-chr1:211569278..211571043,2	K562	blood:
13	chr1:211565208..211568165-chr1:211585336..211586905,2	K562	blood:
14	chr1:211554768..211559509-chr1:211560606..211570007,12	MCF-7	breast:
15	chr1:211565208..211568165-chr1:211585336..211586905,2	K562	blood:
16	chr1:211599016..211601630-chr1:211604235..211606553,2	K562	blood:
17	chr1:211581760..211583766-chr1:211585922..211587874,2	MCF-7	breast:
18	chr1:211592567..211595477-chr1:211598046..211600040,2	K562	blood:
19	chr1:211591294..211593237-chr1:211594620..211596952,2	K562	blood:
20	chr1:211597928..211598767-chr1:211649263..211649948,2	MCF-7	breast:
21	chr1:211581760..211583766-chr1:211585922..211587874,2	MCF-7	breast:
22	chr1:211565165..211567494-chr1:211569278..211571043,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RD3-5	chr1:211570109-211570174	NONHSAT009295
2	lnc-TRAF5-1	chr1:211605661-211605877	NONHSAT009289
3	lnc-TRAF5-1	chr1:211605661-211605911	NONHSAT009292
4	lnc-TRAF5-1	chr1:211599553-211599625	ENSG00000153363
5	lnc-RD3-5	chr1:211572618-211572779	NONHSAT009295
6	lnc-TRAF5-1	chr1:211572502-211572779	NONHSAT009292
7	lnc-TRAF5-2	chr1:211608414-211608675	ENSG00000261252.1
8	lnc-TRAF5-1	chr1:211599553-211599625	NONHSAT009289
9	lnc-RD3-4	chr1:211597757-211598038	NONHSAT009297
10	lnc-TRAF5-1	chr1:211570109-211570173	NONHSAT009292
11	lnc-TRAF5-1	chr1:211605661-211606029	NONHSAT009294
12	lnc-TRAF5-1	chr1:211599553-211599625	NONHSAT009294
13	lnc-TRAF5-1	chr1:211570109-211570173	ENSG00000153363
14	lnc-TRAF5-2	chr1:211608238-211608784	NONHSAT009298
15	lnc-TRAF5-1	chr1:211570109-211570173	NONHSAT009289
16	lnc-TRAF5-1	chr1:211570109-211570173	NONHSAT009291
17	lnc-TRAF5-1	chr1:211571378-211572206	NONHSAT009291
18	lnc-TRAF5-1	chr1:211570198-211570206	ENSG00000153363
19	lnc-TRAF5-1	chr1:211570109-211570173	ENSG00000153363
20	lnc-TRAF5-1	chr1:211605661-211605878	ENSG00000153363
21	lnc-TRAF5-1	chr1:211599553-211599625	NONHSAT009292

No data

Variant related genes	Relation type
ENSG00000261252	TF binding region
ARPC3P2	TF binding region
SNX25P1	TF binding region
ENSG00000261252	CpG island
ARPC3P2	CpG island
SNX25P1	CpG island
ENSG00000117625	chromatin interactions
ENSG00000153363	chromatin interactions
ENSG00000236809	chromatin interactions
CCNE2	miRNA target sites
MSN	miRNA target sites

Extended variants
information (count: 1826 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1826 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs784377	chr1:211565640-211565641	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373339902	chr1:211565667-211565668	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs148787900	chr1:211565677-211565678	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369148122	chr1:211565695-211565696	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185238204	chr1:211565716-211565717	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376831426	chr1:211565719-211565720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189646008	chr1:211565746-211565747	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12406356	chr1:211565797-211565798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs34897475	chr1:211565817-211565818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530763898	chr1:211565836-211565837	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs549378452	chr1:211565842-211565843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76013857	chr1:211565845-211565846	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
13	rs183111409	chr1:211565888-211565889	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553133197	chr1:211565915-211565916	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs76639491	chr1:211565931-211565932	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
16	rs186388340	chr1:211566001-211566002	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs60100179	chr1:211566023-211566024	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs557331604	chr1:211566043-211566044	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs151235986	chr1:211566074-211566075	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376995673	chr1:211566165-211566166	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545824420	chr1:211566166-211566167	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542231372	chr1:211566178-211566179	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs11119733	chr1:211566185-211566186	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs191635728	chr1:211566203-211566204	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183494892	chr1:211566221-211566222	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12563239	chr1:211566227-211566228	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75510331	chr1:211566287-211566288	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187906717	chr1:211566356-211566357	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544397269	chr1:211566361-211566362	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs784378	chr1:211566366-211566367	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs530019429	chr1:211566474-211566475	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs80062020	chr1:211566480-211566481	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs567353496	chr1:211566481-211566482	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535520951	chr1:211566537-211566538	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs140030889	chr1:211566589-211566590	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs571418393	chr1:211566686-211566687	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192682728	chr1:211566692-211566693	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145441823	chr1:211566701-211566702	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183334433	chr1:211566719-211566720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536980538	chr1:211566756-211566757	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs784379	chr1:211566760-211566761	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs572915969	chr1:211566841-211566842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533776348	chr1:211566848-211566849	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs376934202	chr1:211566874-211566875	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576890550	chr1:211566912-211566913	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544040760	chr1:211566923-211566924	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs562739219	chr1:211566955-211566956	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186906988	chr1:211566980-211566981	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541771343	chr1:211566995-211566996	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192623833	chr1:211567019-211567020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD

Chromatin state (count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211556800-211585800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:211556800-211589800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:211557000-211568000	Weak transcription	Psoas Muscle	Psoas
4	chr1:211557000-211568400	Weak transcription	Placenta	Placenta
5	chr1:211557000-211569800	Weak transcription	Ovary	ovary
6	chr1:211557000-211571400	Weak transcription	Fetal Muscle Leg	muscle
7	chr1:211557000-211572400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr1:211557000-211573200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:211557000-211575000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr1:211557000-211576600	Weak transcription	Left Ventricle	heart
11	chr1:211557000-211580600	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr1:211557000-211581000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr1:211557000-211581800	Weak transcription	Fetal Kidney	kidney
14	chr1:211557200-211566400	Weak transcription	Duodenum Mucosa	Duodenum
15	chr1:211557200-211568000	Weak transcription	Colon Smooth Muscle	Colon
16	chr1:211557200-211568400	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr1:211557200-211569600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:211557200-211571000	Weak transcription	Fetal Lung	lung
19	chr1:211557200-211572800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr1:211557200-211573400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr1:211557400-211565800	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr1:211557400-211568000	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr1:211557400-211569600	Weak transcription	Primary hematopoietic stem cells	blood
24	chr1:211557400-211569600	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr1:211557400-211570000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr1:211557400-211570600	Weak transcription	Primary B cells from peripheral blood	blood
27	chr1:211557400-211570600	Weak transcription	Osteobl	bone
28	chr1:211557400-211571400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr1:211557400-211571400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:211557400-211571600	Weak transcription	Fetal Heart	heart
31	chr1:211557400-211572800	Weak transcription	Fetal Intestine Large	intestine
32	chr1:211557400-211572800	Weak transcription	K562	blood
33	chr1:211557400-211574400	Weak transcription	Brain Substantia Nigra	brain
34	chr1:211557400-211574400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr1:211557400-211575600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:211557400-211576000	Weak transcription	Fetal Intestine Small	intestine
37	chr1:211557600-211571400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr1:211557600-211573400	Weak transcription	GM12878-XiMat	blood
39	chr1:211557600-211573400	Weak transcription	Hela-S3	cervix
40	chr1:211557600-211576200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:211560800-211569600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr1:211560800-211569800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:211560800-211571000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr1:211560800-211571400	Weak transcription	HSMMtube	muscle
45	chr1:211561600-211573000	Weak transcription	Right Ventricle	heart
46	chr1:211563400-211572000	Weak transcription	Primary T cells from cord blood	blood
47	chr1:211564400-211571400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:211564800-211570800	Weak transcription	Primary B cells from cord blood	blood
49	chr1:211565000-211565800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr1:211565200-211566000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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