Variant report

Variant	nsv1732
Chromosome Location	chr1:84499098-84544635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:549)
CpG islands
(count:795)
Chromatin interactive
region (count:41)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:84544449-84544500	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:84539139-84539400	K562	blood:	n/a	n/a
3	ARID3A	chr1:84543380-84543588	HepG2	liver:	n/a	n/a
4	ATF1	chr1:84526663-84526766	K562	blood:	n/a	n/a
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	ATF3	chr1:84543471-84543757	K562	blood:	n/a	chr1:84543641-84543650 chr1:84543645-84543654 chr1:84543690-84543699 chr1:84543605-84543614 chr1:84543554-84543574
7	BACH1	chr1:84543125-84543656	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:84514555-84514849	K562	blood:	n/a	n/a
9	BACH1	chr1:84544537-84544708	K562	blood:	n/a	n/a
10	BCL3	chr1:84543200-84543635	A549	lung:	n/a	chr1:84543570-84543579
11	BCL3	chr1:84543469-84543767	GM12878	blood:	n/a	chr1:84543694-84543707 chr1:84543570-84543579 chr1:84543635-84543644
12	BCLAF1	chr1:84543128-84543608	GM12878	blood:	n/a	chr1:84543570-84543579
13	BHLHE40	chr1:84543976-84544360	K562	blood:	n/a	n/a
14	BHLHE40	chr1:84543041-84543667	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:84543122-84543669	K562	blood:	n/a	n/a
16	BRCA1	chr1:84506395-84506501	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr1:84542671-84544001	Hela-S3	cervix:	n/a	chr1:84543052-84543059
18	BRCA1	chr1:84543387-84543473	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr1:84543011-84543657	K562	blood:	n/a	n/a
20	CBX3	chr1:84534959-84535365	HCT-116	colon:	n/a	n/a
21	CCNT2	chr1:84543165-84544195	K562	blood:	n/a	chr1:84543960-84543969
22	CEBPB	chr1:84528187-84528531	MCF-7	breast:	n/a	n/a
23	CEBPB	chr1:84538762-84539056	K562	blood:	n/a	chr1:84538926-84538939 chr1:84538928-84538939
24	CEBPB	chr1:84511477-84511661	K562	blood:	n/a	n/a
25	CEBPB	chr1:84542988-84544028	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr1:84538789-84539299	Hela-S3	cervix:	n/a	chr1:84538926-84538939 chr1:84538928-84538939
27	CEBPB	chr1:84528215-84528572	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:84538833-84539272	IMR90	lung:	n/a	chr1:84538926-84538939 chr1:84538928-84538939
29	CEBPD	chr1:84543330-84543772	HepG2	liver:	n/a	n/a
30	CHD1	chr1:84543918-84544576	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr1:84543358-84543587	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr1:84542946-84543127	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr1:84543323-84543545	HepG2	liver:	n/a	n/a
34	CHD2	chr1:84543084-84544560	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr1:84543339-84543660	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr1:84543121-84543425	K562	blood:	n/a	n/a
37	CREB1	chr1:84543215-84543897	A549	lung:	n/a	n/a
38	CREB1	chr1:84543442-84543722	A549	lung:	n/a	n/a
39	CREB1	chr1:84543023-84544014	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr1:84543042-84544114	HepG2	liver:	n/a	n/a
41	CREB1	chr1:84543166-84543932	K562	blood:	n/a	n/a
42	CREB1	chr1:84542957-84543966	K562	blood:	n/a	n/a
43	CREB1	chr1:84543007-84544063	GM12878	blood:	n/a	n/a
44	CREB1	chr1:84543083-84543993	HepG2	liver:	n/a	n/a
45	CREB1	chr1:84543360-84543852	ECC-1	luminal epithelium:	n/a	n/a
46	CREB1	chr1:84543082-84544252	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTBP2	chr1:84543178-84544544	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr1:84543320-84543470	HMF	breast:	n/a	n/a
49	CTCF	chr1:84543340-84543490	RPTEC	kidney:	n/a	n/a
50	CTCF	chr1:84543294-84543522	Fibrobl	skin:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:84543558-84543608	PFSK-1	brain:	n/a
2	chr1:84543951-84544001	HepG2	liver:	n/a
3	chr1:84543558-84543608	PFSK-1	brain:	n/a
4	chr1:84543951-84544001	HepG2	liver:	n/a
5	chr1:84543558-84543608	T-47D	breast:	n/a
6	chr1:84524127-84524177	HCM	heart:	n/a
7	chr1:84544284-84544334	GM06990	blood:	n/a
8	chr1:84543558-84543608	HCPEpiC	choroid plexus:	n/a
9	chr1:84543374-84543424	BJ	skin:	n/a
10	chr1:84543551-84543601	GM12892	blood:	n/a
11	chr1:84544220-84544270	GM19239	blood:	n/a
12	chr1:84543156-84543206	ProgFib	skin:	n/a
13	chr1:84542225-84542275	BJ	skin:	n/a
14	chr1:84544097-84544147	HL-60	blood:	n/a
15	chr1:84544097-84544147	HRE	kidney:	n/a
16	chr1:84543156-84543206	SAEC	small airway:	n/a
17	chr1:84524127-84524177	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:84543539-84543589	A549	lung:	n/a
19	chr1:84543558-84543608	GM12892	blood:	n/a
20	chr1:84542225-84542275	AG04449	skin:	fetal
21	chr1:84541035-84541085	HCM	heart:	n/a
22	chr1:84543156-84543206	AG04450	lung:	fetal
23	chr1:84544220-84544270	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:84544220-84544270	PrEC	prostate:	n/a
25	chr1:84541035-84541085	IMR90	lung:	fetal
26	chr1:84543951-84544001	HEK293	kidney:	embryo
27	chr1:84544220-84544270	NH-A	brain:	n/a
28	chr1:84542225-84542275	NH-A	brain:	n/a
29	chr1:84543551-84543601	HIPEpiC	eye:	n/a
30	chr1:84541035-84541085	GM12878	blood:	n/a
31	chr1:84524127-84524177	HL-60	blood:	n/a
32	chr1:84543558-84543608	AG04450	lung:	fetal
33	chr1:84543558-84543608	Caco-2	colon:	n/a
34	chr1:84543951-84544001	HEEpiC	esophagus:	n/a
35	chr1:84543539-84543589	HEEpiC	esophagus:	n/a
36	chr1:84543951-84544001	GM12878	blood:	n/a
37	chr1:84542225-84542275	HUVEC	blood vessel:	n/a
38	chr1:84544220-84544270	GM12878	blood:	n/a
39	chr1:84543551-84543601	NHDF-neo	bronchial:	n/a
40	chr1:84543369-84543419	ECC-1	luminal epithelium:	n/a
41	chr1:84541035-84541085	HNPCEpiC	eye:	n/a
42	chr1:84544220-84544270	AG10803	skin:	n/a
43	chr1:84543551-84543601	SKMC	muscle:	n/a
44	chr1:84541035-84541085	Hela-S3	cervix:	n/a
45	chr1:84541035-84541085	PANC-1	pancreas:	n/a
46	chr1:84544220-84544270	NT2-D1	testis:	n/a
47	chr1:84544097-84544147	SKMC	muscle:	n/a
48	chr1:84544097-84544147	AG04450	lung:	fetal
49	chr1:84543369-84543419	Hela-S3	cervix:	n/a
50	chr1:84543369-84543419	PrEC	prostate:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84539350..84542065-chr1:84568304..84570726,2	K562	blood:
2	chr1:84507393..84510373-chr17:41380299..41381957,2	MCF-7	breast:
3	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:
4	chr1:84387778..84389882-chr1:84541236..84543359,2	K562	blood:
5	chr1:84543103..84544767-chr1:84969541..84972530,2	K562	blood:
6	chr1:84506312..84509081-chr1:84514938..84517601,2	MCF-7	breast:
7	chr1:84543517..84544097-chr5:34915086..34915845,2	Hela-S3	cervix:
8	chr1:84542759..84543477-chr10:17272146..17272948,2	Hela-S3	cervix:
9	chr1:84543836..84545852-chr1:84545884..84547709,2	K562	blood:
10	chr1:84543365..84543953-chr2:136633448..136634387,2	Hela-S3	cervix:
11	chr1:84377090..84379247-chr1:84542414..84544902,2	K562	blood:
12	chr1:84507131..84508951-chr1:84514289..84516421,2	K562	blood:
13	chr1:84543429..84544009-chr3:122233490..122234112,2	Hela-S3	cervix:
14	chr1:84528524..84531344-chr1:84538975..84541375,2	MCF-7	breast:
15	chr1:84515190..84517358-chr1:84542033..84543983,2	K562	blood:
16	chr1:84413047..84415136-chr1:84540240..84542127,2	K562	blood:
17	chr1:84524044..84526029-chr1:84541192..84543741,2	K562	blood:
18	chr1:84524529..84526369-chr1:84540016..84543741,3	K562	blood:
19	chr1:84493894..84496229-chr1:84499298..84501973,3	K562	blood:
20	chr1:84411907..84414547-chr1:84539636..84541740,2	K562	blood:
21	chr1:84528524..84531344-chr1:84538975..84541375,2	MCF-7	breast:
22	chr1:84541598..84548799-chr1:84549003..84554628,15	K562	blood:
23	chr1:84540590..84543508-chr1:84558962..84560991,2	K562	blood:
24	chr1:84542977..84543701-chr9:140135375..140136244,2	Hela-S3	cervix:
25	chr1:84371561..84374304-chr1:84536819..84538453,2	K562	blood:
26	chr1:84507131..84508951-chr1:84514289..84516421,2	K562	blood:
27	chr1:84543599..84544134-chr11:62648019..62648854,2	Hela-S3	cervix:
28	chr1:84525894..84527456-chr1:84531489..84533439,2	K562	blood:
29	chr1:84508873..84510393-chr17:41398425..41400518,3	K562	blood:
30	chr1:84542242..84543745-chr1:85154770..85157524,2	K562	blood:
31	chr1:84525894..84527456-chr1:84531489..84533439,2	K562	blood:
32	chr1:84539639..84541968-chr1:84547734..84550751,3	K562	blood:
33	chr1:84541371..84543109-chr1:84583953..84586517,2	K562	blood:
34	chr1:84536131..84538617-chr1:84567747..84570815,3	K562	blood:
35	chr1:84530745..84533538-chr1:84541261..84543799,3	K562	blood:
36	chr1:84490870..84492577-chr1:84505542..84507269,2	K562	blood:
37	chr1:84516996..84518865-chr1:84523452..84525021,2	MCF-7	breast:
38	chr1:84516996..84518865-chr1:84523452..84525021,2	MCF-7	breast:
39	chr1:84463410..84466364-chr1:84542152..84546505,5	K562	blood:
40	chr1:84508873..84510373-chr17:41380522..41383401,3	K562	blood:
41	chr1:84506312..84509081-chr1:84514938..84517601,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
PRKACB	TF binding region
ENSG00000271576	TF binding region
PRKACB	CpG island
ENSG00000271576	CpG island
ENSG00000174021	chromatin interactions
ENSG00000137941	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000213540	chromatin interactions
ENSG00000113460	chromatin interactions
ENSG00000271576	chromatin interactions
ENSG00000114030	chromatin interactions
ENSG00000076003	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000117155	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000113456	chromatin interactions
ENSG00000142875	chromatin interactions
ENSG00000026025	chromatin interactions
ENSG00000122432	chromatin interactions
ARHGAP12	miRNA target sites
FBXO28	miRNA target sites

Extended variants
information (count: 903 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148760751	chr1:84499106-84499107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12034540	chr1:84499157-84499158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528362406	chr1:84501001-84501002	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs146057289	chr1:84501020-84501021	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs561089758	chr1:84501089-84501090	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs530218188	chr1:84501121-84501122	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs546639741	chr1:84501127-84501128	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs76444635	chr1:84501136-84501137	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs627712	chr1:84501140-84501141	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116788711	chr1:84501147-84501148	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs569232672	chr1:84501155-84501156	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs627658	chr1:84501182-84501183	Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs530607441	chr1:84501208-84501209	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs550796560	chr1:84501247-84501248	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs570428769	chr1:84501259-84501260	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs554560544	chr1:84501260-84501261	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs367941941	chr1:84501285-84501286	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs371814183	chr1:84501289-84501290	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs553894795	chr1:84501323-84501324	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs77350646	chr1:84501344-84501345	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs556659110	chr1:84501387-84501388	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs576721860	chr1:84503508-84503509	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs74561699	chr1:84503521-84503522	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs528985743	chr1:84503526-84503527	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs549059898	chr1:84503590-84503591	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs565580168	chr1:84503665-84503666	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs189426157	chr1:84503692-84503693	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs528257409	chr1:84503708-84503709	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs551291329	chr1:84503749-84503750	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs181263354	chr1:84503781-84503782	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs1602999	chr1:84503782-84503783	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556292849	chr1:84503787-84503788	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs184880459	chr1:84503829-84503830	ZNF genes & repeats Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535619542	chr1:84503843-84503844	ZNF genes & repeats Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78731366	chr1:84504026-84504027	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs72721436	chr1:84504052-84504053	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs541614532	chr1:84504062-84504063	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs117364282	chr1:84504107-84504108	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs566830	chr1:84504109-84504110	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs558036692	chr1:84504234-84504235	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs374150328	chr1:84504325-84504326	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs189739576	chr1:84504326-84504327	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs563184268	chr1:84504331-84504332	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs578230879	chr1:84504364-84504365	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs375910554	chr1:84504365-84504366	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs181846080	chr1:84504382-84504383	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs527701493	chr1:84505359-84505360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552057156	chr1:84507447-84507448	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs143052190	chr1:84507471-84507472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111986579	chr1:84507517-84507518	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84499000-84499200	Enhancers	Pancreas	Pancrea
2	chr1:84501000-84501200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
3	chr1:84501200-84501400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr1:84503400-84504000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:84503400-84504400	Active TSS	HepG2	liver
6	chr1:84503600-84504000	Enhancers	Pancreas	Pancrea
7	chr1:84503800-84504400	Active TSS	Liver	Liver
8	chr1:84504000-84504400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:84505200-84505400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:84507800-84508800	Enhancers	Fetal Brain Female	brain
11	chr1:84508600-84509000	Enhancers	Fetal Brain Male	brain
12	chr1:84516200-84517800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:84525600-84526800	Enhancers	Brain Substantia Nigra	brain
14	chr1:84525800-84526600	Enhancers	Brain Cingulate Gyrus	brain
15	chr1:84525800-84527000	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr1:84526400-84526600	Active TSS	Brain Hippocampus Middle	brain
17	chr1:84526400-84526800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr1:84526600-84526800	Flanking Active TSS	Brain Hippocampus Middle	brain
19	chr1:84526600-84528600	Enhancers	NHEK	skin
20	chr1:84526800-84528200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr1:84526800-84528400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:84528400-84532600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:84531400-84532000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:84531400-84532200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:84532600-84533600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:84532800-84533600	Enhancers	Brain Hippocampus Middle	brain
27	chr1:84533000-84533400	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr1:84533200-84533600	Enhancers	Brain Substantia Nigra	brain
29	chr1:84533400-84534600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr1:84533600-84534400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:84534200-84535000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:84534400-84534600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:84536600-84537600	Enhancers	K562	blood
34	chr1:84536600-84542400	Weak transcription	Fetal Lung	lung
35	chr1:84537600-84541000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr1:84537600-84541000	Weak transcription	K562	blood
37	chr1:84538000-84538200	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr1:84538000-84541200	Weak transcription	Liver	Liver
39	chr1:84538000-84542000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:84538400-84542400	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr1:84538400-84542800	Weak transcription	HSMM	muscle
42	chr1:84538600-84542000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr1:84538600-84542400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:84538600-84542400	Weak transcription	Osteobl	bone
45	chr1:84538800-84542200	Weak transcription	Fetal Brain Male	brain
46	chr1:84539200-84542000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:84539200-84542400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:84540200-84542400	Weak transcription	Colon Smooth Muscle	Colon
49	chr1:84540800-84541000	Enhancers	A549	lung
50	chr1:84541000-84541200	Enhancers	Brain Inferior Temporal Lobe	brain

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