Variant report

Variant	esv3379138
Chromosome Location	chr1:84531980-84545128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:499)
CpG islands
(count:733)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:499 , 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	chr1:84539139-84539400	K562	blood:	n/a	n/a
2	ARID3A	chr1:84544449-84544500	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:84543380-84543588	HepG2	liver:	n/a	n/a
4	ATF3	chr1:84543471-84543757	K562	blood:	n/a	chr1:84543641-84543650 chr1:84543645-84543654 chr1:84543690-84543699 chr1:84543605-84543614 chr1:84543554-84543574
5	ATF3	chr1:84543513-84543717	H1-hESC	embryonic stem cell:	n/a	chr1:84543641-84543650 chr1:84543645-84543654 chr1:84543690-84543699 chr1:84543605-84543614 chr1:84543554-84543574
6	BACH1	chr1:84543125-84543656	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:84544537-84544708	K562	blood:	n/a	n/a
8	BCL3	chr1:84543200-84543635	A549	lung:	n/a	chr1:84543570-84543579
9	BCL3	chr1:84543469-84543767	GM12878	blood:	n/a	chr1:84543694-84543707 chr1:84543570-84543579 chr1:84543635-84543644
10	BCLAF1	chr1:84543128-84543608	GM12878	blood:	n/a	chr1:84543570-84543579
11	BHLHE40	chr1:84543041-84543667	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:84543122-84543669	K562	blood:	n/a	n/a
13	BHLHE40	chr1:84543976-84544360	K562	blood:	n/a	n/a
14	BRCA1	chr1:84543387-84543473	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr1:84542671-84544001	Hela-S3	cervix:	n/a	chr1:84543052-84543059
16	CBX3	chr1:84534959-84535365	HCT-116	colon:	n/a	n/a
17	CBX3	chr1:84543011-84543657	K562	blood:	n/a	n/a
18	CCNT2	chr1:84543165-84544195	K562	blood:	n/a	chr1:84543960-84543969
19	CEBPB	chr1:84538762-84539056	K562	blood:	n/a	chr1:84538926-84538939 chr1:84538928-84538939
20	CEBPB	chr1:84542988-84544028	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:84538833-84539272	IMR90	lung:	n/a	chr1:84538926-84538939 chr1:84538928-84538939
22	CEBPB	chr1:84538789-84539299	Hela-S3	cervix:	n/a	chr1:84538926-84538939 chr1:84538928-84538939
23	CEBPD	chr1:84543330-84543772	HepG2	liver:	n/a	n/a
24	CHD1	chr1:84542946-84543127	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr1:84543918-84544576	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr1:84543358-84543587	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:84543121-84543425	K562	blood:	n/a	n/a
28	CHD2	chr1:84543339-84543660	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr1:84543323-84543545	HepG2	liver:	n/a	n/a
30	CHD2	chr1:84543084-84544560	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr1:84543442-84543722	A549	lung:	n/a	n/a
32	CREB1	chr1:84543007-84544063	GM12878	blood:	n/a	n/a
33	CREB1	chr1:84543360-84543852	ECC-1	luminal epithelium:	n/a	n/a
34	CREB1	chr1:84543083-84543993	HepG2	liver:	n/a	n/a
35	CREB1	chr1:84543166-84543932	K562	blood:	n/a	n/a
36	CREB1	chr1:84542957-84543966	K562	blood:	n/a	n/a
37	CREB1	chr1:84543082-84544252	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr1:84543042-84544114	HepG2	liver:	n/a	n/a
39	CREB1	chr1:84543023-84544014	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr1:84543215-84543897	A549	lung:	n/a	n/a
41	CTBP2	chr1:84543178-84544544	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr1:84543347-84543440	GM19240	blood:	n/a	n/a
43	CTCF	chr1:84543140-84543290	AG04450	lung:	n/a	n/a
44	CTCF	chr1:84543461-84543703	H1-hESC	embryonic stem cell:	n/a	chr1:84543585-84543598
45	CTCF	chr1:84543380-84543530	NHLF	lung:	n/a	n/a
46	CTCF	chr1:84543380-84543530	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr1:84544712-84544767	K562	blood:	n/a	n/a
48	CTCF	chr1:84543340-84543490	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:84543280-84543430	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr1:84543120-84543270	HVMF	connective:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:84544284-84544334	PANC-1	pancreas:	n/a
2	chr1:84544284-84544334	PANC-1	pancreas:	n/a
3	chr1:84543369-84543419	SK-N-SH	brain:	n/a
4	chr1:84544097-84544147	MCF10A-Er-Src	breast:	n/a
5	chr1:84543551-84543601	GM06990	blood:	n/a
6	chr1:84544220-84544270	SK-N-SH_RA	brain:	n/a
7	chr1:84543951-84544001	Hepatocyte	liver:	n/a
8	chr1:84543369-84543419	AG10803	skin:	n/a
9	chr1:84544220-84544270	MCF10A-Er-Src	breast:	n/a
10	chr1:84544097-84544147	HEK293	kidney:	embryo
11	chr1:84544284-84544334	HL-60	blood:	n/a
12	chr1:84544220-84544270	ECC-1	luminal epithelium:	n/a
13	chr1:84542225-84542275	NT2-D1	testis:	n/a
14	chr1:84543551-84543601	LNCaP	prostate:	n/a
15	chr1:84543369-84543419	HNPCEpiC	eye:	n/a
16	chr1:84544220-84544270	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:84541035-84541085	HEK293	kidney:	embryo
18	chr1:84544220-84544270	MCF-7	breast:	n/a
19	chr1:84543369-84543419	HUVEC	blood vessel:	n/a
20	chr1:84543951-84544001	NT2-D1	testis:	n/a
21	chr1:84543539-84543589	ovcar-3	ovarian:	n/a
22	chr1:84544097-84544147	AG09309	skin:	n/a
23	chr1:84544097-84544147	HCM	heart:	n/a
24	chr1:84543374-84543424	AG04449	skin:	fetal
25	chr1:84544097-84544147	GM19239	blood:	n/a
26	chr1:84542225-84542275	HL-60	blood:	n/a
27	chr1:84544097-84544147	NHDF-neo	bronchial:	n/a
28	chr1:84543369-84543419	GM12891	blood:	n/a
29	chr1:84543539-84543589	PFSK-1	brain:	n/a
30	chr1:84543374-84543424	GM12892	blood:	n/a
31	chr1:84543369-84543419	K562	blood:	n/a
32	chr1:84543369-84543419	HRE	kidney:	n/a
33	chr1:84543951-84544001	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:84543551-84543601	K562	blood:	n/a
35	chr1:84544097-84544147	AoSMC	blood vessel:	n/a
36	chr1:84544284-84544334	T-47D	breast:	n/a
37	chr1:84544284-84544334	HEK293	kidney:	embryo
38	chr1:84543374-84543424	AG09309	skin:	n/a
39	chr1:84543156-84543206	K562	blood:	n/a
40	chr1:84541035-84541085	T-47D	breast:	n/a
41	chr1:84544220-84544270	ovcar-3	ovarian:	n/a
42	chr1:84543369-84543419	Hela-S3	cervix:	n/a
43	chr1:84541035-84541085	GM12891	blood:	n/a
44	chr1:84543539-84543589	T-47D	breast:	n/a
45	chr1:84543156-84543206	BJ	skin:	n/a
46	chr1:84543558-84543608	HEEpiC	esophagus:	n/a
47	chr1:84543951-84544001	HCF	heart:	n/a
48	chr1:84544220-84544270	PrEC	prostate:	n/a
49	chr1:84544284-84544334	HRE	kidney:	n/a
50	chr1:84542225-84542275	HPAEpiC	pulmonary alveolar:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84539639..84541968-chr1:84547734..84550751,3	K562	blood:
2	chr1:84542242..84543745-chr1:85154770..85157524,2	K562	blood:
3	chr1:84530745..84533538-chr1:84541261..84543799,3	K562	blood:
4	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:
5	chr1:84542977..84543701-chr9:140135375..140136244,2	Hela-S3	cervix:
6	chr1:84463410..84466364-chr1:84542152..84546505,5	K562	blood:
7	chr1:84539350..84542065-chr1:84568304..84570726,2	K562	blood:
8	chr1:84543599..84544134-chr11:62648019..62648854,2	Hela-S3	cervix:
9	chr1:84541371..84543109-chr1:84583953..84586517,2	K562	blood:
10	chr1:84528524..84531344-chr1:84538975..84541375,2	MCF-7	breast:
11	chr1:84387778..84389882-chr1:84541236..84543359,2	K562	blood:
12	chr1:84543103..84544767-chr1:84969541..84972530,2	K562	blood:
13	chr1:84542759..84543477-chr10:17272146..17272948,2	Hela-S3	cervix:
14	chr1:84541598..84548799-chr1:84549003..84554628,15	K562	blood:
15	chr1:84377090..84379247-chr1:84542414..84544902,2	K562	blood:
16	chr1:84536131..84538617-chr1:84567747..84570815,3	K562	blood:
17	chr1:84543365..84543953-chr2:136633448..136634387,2	Hela-S3	cervix:
18	chr1:84543517..84544097-chr5:34915086..34915845,2	Hela-S3	cervix:
19	chr1:84413047..84415136-chr1:84540240..84542127,2	K562	blood:
20	chr1:84540590..84543508-chr1:84558962..84560991,2	K562	blood:
21	chr1:84525894..84527456-chr1:84531489..84533439,2	K562	blood:
22	chr1:84543429..84544009-chr3:122233490..122234112,2	Hela-S3	cervix:
23	chr1:84543836..84545852-chr1:84545884..84547709,2	K562	blood:
24	chr1:84371561..84374304-chr1:84536819..84538453,2	K562	blood:
25	chr1:84411907..84414547-chr1:84539636..84541740,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTLL7-3	chr1:84542014-84543655	NONHSAT004184
2	lnc-TTLL7-3	chr1:84542014-84543614	ENSG00000271576.1
3	lnc-TTLL7-3	chr1:84542062-84543325	XLOC_000889
4	lnc-TTLL7-3	chr1:84543564-84543595	XLOC_000889

No data

Variant related genes	Relation type
PRKACB	TF binding region
ENSG00000271576	TF binding region
PRKACB	CpG island
ENSG00000271576	CpG island
ENSG00000026025	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000174021	chromatin interactions
ENSG00000271576	chromatin interactions
ENSG00000114030	chromatin interactions
ENSG00000213540	chromatin interactions
ENSG00000113456	chromatin interactions
ENSG00000113460	chromatin interactions
ENSG00000117155	chromatin interactions
ENSG00000142875	chromatin interactions
ENSG00000137941	chromatin interactions
ENSG00000122432	chromatin interactions
ENSG00000076003	chromatin interactions
FBXO28	miRNA target sites
ARHGAP12	miRNA target sites

Extended variants
information (count: 404 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372353320	chr1:84532043-84532044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs617568	chr1:84532056-84532057	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs72938456	chr1:84532077-84532078	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs552504412	chr1:84532105-84532106	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576778508	chr1:84532134-84532135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs182219437	chr1:84532143-84532144	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555018452	chr1:84532270-84532271	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs559550241	chr1:84532297-84532298	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs528266559	chr1:84532319-84532320	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs548414510	chr1:84532325-84532326	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs562024877	chr1:84532391-84532392	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs572154044	chr1:84532422-84532423	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs368102319	chr1:84532430-84532431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375314904	chr1:84532443-84532444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532939432	chr1:84532518-84532519	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs140527394	chr1:84532624-84532625	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs563251607	chr1:84532669-84532670	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549211181	chr1:84532738-84532739	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs548609270	chr1:84532742-84532743	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186788577	chr1:84532744-84532745	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs527818921	chr1:84532749-84532750	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190787049	chr1:84532753-84532754	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570928339	chr1:84532758-84532759	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75493233	chr1:84532770-84532771	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs112343138	chr1:84532794-84532795	Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs541343477	chr1:84532801-84532802	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs556757104	chr1:84532803-84532804	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs367693315	chr1:84532805-84532806	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs570334983	chr1:84532824-84532825	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs147100877	chr1:84532861-84532862	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555383455	chr1:84532969-84532970	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs114301172	chr1:84532976-84532977	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs375452211	chr1:84533020-84533021	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540756456	chr1:84533021-84533022	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs557453433	chr1:84533059-84533060	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114845524	chr1:84533111-84533112	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs543216064	chr1:84533124-84533125	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs10874427	chr1:84533132-84533133	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs535924503	chr1:84533154-84533155	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs75740768	chr1:84533176-84533177	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs397806970	chr1:84533178-84533179	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs550275967	chr1:84533195-84533196	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs138387493	chr1:84533198-84533199	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143932133	chr1:84533224-84533225	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs7530801	chr1:84533343-84533344	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs11811024	chr1:84533382-84533383	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs182660642	chr1:84533387-84533388	Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570969504	chr1:84533437-84533438	Strong transcription Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs35105659	chr1:84533445-84533446	Strong transcription Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553241627	chr1:84533516-84533517	Strong transcription Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84528400-84532600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:84531400-84532000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:84531400-84532200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:84532600-84533600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:84532800-84533600	Enhancers	Brain Hippocampus Middle	brain
6	chr1:84533000-84533400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr1:84533200-84533600	Enhancers	Brain Substantia Nigra	brain
8	chr1:84533400-84534600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr1:84533600-84534400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:84534200-84535000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:84534400-84534600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:84536600-84537600	Enhancers	K562	blood
13	chr1:84536600-84542400	Weak transcription	Fetal Lung	lung
14	chr1:84537600-84541000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr1:84537600-84541000	Weak transcription	K562	blood
16	chr1:84538000-84538200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr1:84538000-84541200	Weak transcription	Liver	Liver
18	chr1:84538000-84542000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:84538400-84542400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr1:84538400-84542800	Weak transcription	HSMM	muscle
21	chr1:84538600-84542000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr1:84538600-84542400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr1:84538600-84542400	Weak transcription	Osteobl	bone
24	chr1:84538800-84542200	Weak transcription	Fetal Brain Male	brain
25	chr1:84539200-84542000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:84539200-84542400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:84540200-84542400	Weak transcription	Colon Smooth Muscle	Colon
28	chr1:84540800-84541000	Enhancers	A549	lung
29	chr1:84541000-84541200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr1:84541000-84541200	Weak transcription	Brain Substantia Nigra	brain
31	chr1:84541000-84541400	Enhancers	Brain Anterior Caudate	brain
32	chr1:84541000-84542000	Weak transcription	A549	lung
33	chr1:84541000-84542000	Enhancers	K562	blood
34	chr1:84541000-84542400	Enhancers	HepG2	liver
35	chr1:84541200-84541400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:84541200-84541400	Enhancers	Liver	Liver
37	chr1:84541200-84541400	Enhancers	Brain Substantia Nigra	brain
38	chr1:84541200-84541600	Enhancers	GM12878-XiMat	blood
39	chr1:84541200-84541800	Enhancers	Brain Cingulate Gyrus	brain
40	chr1:84541200-84542400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:84541200-84542400	Enhancers	Brain Hippocampus Middle	brain
42	chr1:84541200-84542400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr1:84541200-84542400	Enhancers	Dnd41	blood
44	chr1:84541400-84542000	Weak transcription	Liver	Liver
45	chr1:84541400-84542400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:84541400-84542400	Weak transcription	Brain Anterior Caudate	brain
47	chr1:84541400-84542600	Weak transcription	Brain Substantia Nigra	brain
48	chr1:84541600-84542000	Weak transcription	GM12878-XiMat	blood
49	chr1:84541800-84542200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr1:84542000-84542200	Enhancers	Hela-S3	cervix

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