Variant report

Variant	nsv883271
Chromosome Location	chr5:178955046-179031595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1777)
CpG islands
(count:2934)
Chromatin interactive
region (count:127)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178977115-178977357	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178977590-178977818	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178985842-178986538	HepG2	liver:	n/a	n/a
4	ATF2	chr5:178960873-178961287	GM12878	blood:	n/a	n/a
5	ATF2	chr5:178971356-178971893	GM12878	blood:	n/a	n/a
6	ATF2	chr5:178971353-178972009	GM12878	blood:	n/a	n/a
7	ATF2	chr5:178986020-178986776	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:178977014-178977777	GM12878	blood:	n/a	n/a
9	ATF2	chr5:178985934-178986763	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:178976968-178977468	GM12878	blood:	n/a	n/a
11	BACH1	chr5:178957142-178957774	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:178976363-178976432	K562	blood:	n/a	n/a
13	BACH1	chr5:178977696-178978347	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr5:178971440-178971812	GM12878	blood:	n/a	chr5:178971650-178971659
15	BCL11A	chr5:178971422-178971880	GM12878	blood:	n/a	chr5:178971650-178971659
16	BCL3	chr5:178999749-179000029	GM12878	blood:	n/a	n/a
17	BCL3	chr5:179020516-179020812	GM12878	blood:	n/a	n/a
18	BCL3	chr5:178985836-178986998	A549	lung:	n/a	n/a
19	BCL3	chr5:178995617-178995986	GM12878	blood:	n/a	n/a
20	BCL3	chr5:179031106-179031606	A549	lung:	n/a	n/a
21	BCL3	chr5:179020495-179020879	GM12878	blood:	n/a	n/a
22	BCL3	chr5:178986050-178987128	A549	lung:	n/a	n/a
23	BCL3	chr5:178995361-178995595	GM12878	blood:	n/a	n/a
24	BCLAF1	chr5:178971380-178972055	GM12878	blood:	n/a	chr5:178971650-178971659
25	BCLAF1	chr5:178977094-178977496	GM12878	blood:	n/a	chr5:178977430-178977439
26	BCLAF1	chr5:178977522-178978403	GM12878	blood:	n/a	chr5:178978060-178978073 chr5:178978272-178978285 chr5:178978064-178978077
27	BHLHE40	chr5:178971425-178971980	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:179012837-179013284	K562	blood:	n/a	n/a
29	BHLHE40	chr5:178976912-178978367	GM12878	blood:	n/a	chr5:178978066-178978082 chr5:178978012-178978028 chr5:178978259-178978275
30	BHLHE40	chr5:178977555-178978270	HepG2	liver:	n/a	chr5:178978066-178978082 chr5:178978012-178978028
31	BHLHE40	chr5:178960996-178961233	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:178977025-178978380	K562	blood:	n/a	chr5:178978066-178978082 chr5:178978012-178978028 chr5:178978259-178978275
33	BHLHE40	chr5:178967579-178967940	HepG2	liver:	n/a	n/a
34	BRCA1	chr5:178985953-178986744	H1-hESC	embryonic stem cell:	n/a	n/a
35	CBX3	chr5:178985780-178986131	K562	blood:	n/a	n/a
36	CBX3	chr5:178957621-178958014	K562	blood:	n/a	n/a
37	CCNT2	chr5:178977542-178978403	K562	blood:	n/a	n/a
38	CCNT2	chr5:178957677-178957915	K562	blood:	n/a	n/a
39	CEBPB	chr5:178980904-178981262	IMR90	lung:	n/a	n/a
40	CEBPB	chr5:178976200-178976292	K562	blood:	n/a	n/a
41	CEBPB	chr5:178985390-178985674	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr5:178986395-178987118	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:178976139-178976344	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:178985906-178986047	K562	blood:	n/a	n/a
45	CEBPB	chr5:178971323-178971992	GM12878	blood:	n/a	n/a
46	CEBPB	chr5:178985889-178987010	A549	lung:	n/a	n/a
47	CEBPB	chr5:178961512-178961808	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:178973964-178974161	HepG2	liver:	n/a	chr5:178974017-178974028
49	CEBPB	chr5:178969797-178970128	HCT-116	colon:	n/a	chr5:178969816-178969827
50	CEBPB	chr5:179010198-179010347	K562	blood:	n/a	chr5:179010330-179010341

(count:2934 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178977641-178977691	HAEpiC	amniotic membrane:	n/a
2	chr5:179004707-179004757	HL-60	blood:	n/a
3	chr5:179004739-179004789	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:178977377-178977427	HCT-116	colon:	n/a
5	chr5:178977181-178977231	HEEpiC	esophagus:	n/a
6	chr5:178973820-178973870	PFSK-1	brain:	n/a
7	chr5:178977641-178977691	HAEpiC	amniotic membrane:	n/a
8	chr5:179004707-179004757	HL-60	blood:	n/a
9	chr5:179004739-179004789	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:178977377-178977427	HCT-116	colon:	n/a
11	chr5:178977181-178977231	HEEpiC	esophagus:	n/a
12	chr5:178973820-178973870	PFSK-1	brain:	n/a
13	chr5:178977326-178977376	LNCaP	prostate:	n/a
14	chr5:178986726-178986776	NB4	blood:	n/a
15	chr5:178977123-178977173	K562	blood:	n/a
16	chr5:178987429-178987479	PrEC	prostate:	n/a
17	chr5:179004757-179004807	HepG2	liver:	n/a
18	chr5:179008603-179008653	HEEpiC	esophagus:	n/a
19	chr5:178986906-178986956	SK-N-MC	brain:	n/a
20	chr5:179003843-179003893	GM19239	blood:	n/a
21	chr5:179004707-179004757	MCF10A-Er-Src	breast:	n/a
22	chr5:178978460-178978510	NB4	blood:	n/a
23	chr5:179030634-179030684	AG09309	skin:	n/a
24	chr5:178990055-178990105	SK-N-SH_RA	brain:	n/a
25	chr5:178986131-178986181	NHBE	bronchial:	n/a
26	chr5:178956838-178956888	K562	blood:	n/a
27	chr5:179004739-179004789	GM12878	blood:	n/a
28	chr5:178986728-178986778	HCT-116	colon:	n/a
29	chr5:178977641-178977691	HCPEpiC	choroid plexus:	n/a
30	chr5:178977326-178977376	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:179030634-179030684	GM12892	blood:	n/a
32	chr5:178986291-178986341	HCF	heart:	n/a
33	chr5:178960377-178960427	SAEC	small airway:	n/a
34	chr5:178960377-178960427	PrEC	prostate:	n/a
35	chr5:178977375-178977425	AG04450	lung:	fetal
36	chr5:178977326-178977376	Hela-S3	cervix:	n/a
37	chr5:178956931-178956981	PrEC	prostate:	n/a
38	chr5:178956874-178956924	AoSMC	blood vessel:	n/a
39	chr5:178977377-178977427	Jurkat	blood:	n/a
40	chr5:178957434-178957484	PrEC	prostate:	n/a
41	chr5:178977377-178977427	MCF-7	breast:	n/a
42	chr5:179008603-179008653	AoSMC	blood vessel:	n/a
43	chr5:178977406-178977456	HAEpiC	amniotic membrane:	n/a
44	chr5:179029719-179029769	T-47D	breast:	n/a
45	chr5:179006403-179006453	RPTEC	kidney:	n/a
46	chr5:178977236-178977286	HNPCEpiC	eye:	n/a
47	chr5:178986412-178986462	HCPEpiC	choroid plexus:	n/a
48	chr5:178986728-178986778	HRPEpiC	eye:	n/a
49	chr5:178957880-178957930	SK-N-SH	brain:	n/a
50	chr5:179004535-179004585	HAEpiC	amniotic membrane:	n/a

(count:127 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:178979685..178981490-chr5:178983248..178984975,2	K562	blood:
2	chr5:178971437..178973246-chr5:178974311..178976700,2	K562	blood:
3	chr5:178999030..179001028-chr5:179028298..179031172,2	MCF-7	breast:
4	chr5:178972300..178975805-chr5:178975972..178979443,5	MCF-7	breast:
5	chr5:178975871..178983601-chr5:179047224..179052413,15	K562	blood:
6	chr5:178979685..178981490-chr5:178983248..178984975,2	K562	blood:
7	chr5:178966233..178969209-chr5:178970782..178972509,2	MCF-7	breast:
8	chr5:179011326..179015421-chr5:179015501..179018945,4	MCF-7	breast:
9	chr5:178975690..178977861-chr5:179029775..179032308,2	K562	blood:
10	chr5:178976288..178979908-chr5:179158372..179161228,3	MCF-7	breast:
11	chr5:178972500..178975262-chr5:178977445..178979874,2	K562	blood:
12	chr5:178976591..178978128-chr5:179049452..179051597,2	MCF-7	breast:
13	chr5:178967564..178969306-chr5:178978047..178979581,2	K562	blood:
14	chr5:178979685..178981544-chr5:178981841..178984975,3	K562	blood:
15	chr5:179020501..179022389-chr5:179025199..179026893,2	K562	blood:
16	chr5:178975440..178984076-chr5:179047224..179053131,17	K562	blood:
17	chr5:178999030..179001028-chr5:179028298..179031172,2	MCF-7	breast:
18	chr5:178966269..178968602-chr5:178984458..178986550,2	MCF-7	breast:
19	chr5:178975751..178978306-chr5:178993914..178996502,2	MCF-7	breast:
20	chr5:178959529..178962397-chr5:178966368..178968696,2	K562	blood:
21	chr5:178951884..178954426-chr5:179031332..179033126,2	MCF-7	breast:
22	chr5:178986818..178988892-chr5:179105129..179106638,2	K562	blood:
23	chr5:179004969..179007855-chr5:179049122..179050815,2	MCF-7	breast:
24	chr5:178977809..178978321-chr5:178985908..178986661,2	MCF-7	breast:
25	chr5:179020501..179022389-chr5:179025199..179026893,2	K562	blood:
26	chr5:178991096..178994000-chr5:178994365..178996408,2	K562	blood:
27	chr5:178975690..178977861-chr5:179029775..179032308,2	K562	blood:
28	chr5:178971437..178973246-chr5:178974311..178976700,2	K562	blood:
29	chr5:179017199..179019587-chr5:179035470..179037928,2	MCF-7	breast:
30	chr5:179015557..179018325-chr5:179025854..179028795,2	K562	blood:
31	chr5:178975801..178977799-chr5:178987617..178990258,3	K562	blood:
32	chr5:179008184..179011132-chr5:179049089..179051840,4	MCF-7	breast:
33	chr5:179023716..179025532-chr5:179027753..179029789,2	K562	blood:
34	chr5:179003044..179005228-chr5:179048934..179051877,3	K562	blood:
35	chr5:178979685..178981544-chr5:178981841..178984975,3	K562	blood:
36	chr1:110881782..110882370-chr5:178977392..178978012,2	Hela-S3	cervix:
37	chr5:178977295..178978049-chrX:153718720..153719639,2	Hela-S3	cervix:
38	chr15:101835145..101835812-chr5:178986003..178986591,2	HCT-116	colon:
39	chr5:178976850..178979581-chr5:179125172..179127163,2	K562	blood:
40	chr5:178993088..178996882-chr5:179048174..179052059,4	K562	blood:
41	chr5:178955819..178957353-chr5:179123603..179125281,2	MCF-7	breast:
42	chr5:178961944..178964885-chr5:178975318..178977306,2	MCF-7	breast:
43	chr5:178976811..178980871-chr5:179039605..179043375,3	K562	blood:
44	chr5:178973738..178976008-chr5:178976265..178978073,2	K562	blood:
45	chr5:178964680..178966401-chr5:178977965..178979894,2	K562	blood:
46	chr5:178976757..178979190-chr5:180687275..180690244,2	K562	blood:
47	chr5:178989508..178991362-chr5:179048413..179051335,2	MCF-7	breast:
48	chr5:178967735..178971439-chr5:178974886..178978659,7	MCF-7	breast:
49	chr5:178964185..178968820-chr5:178974807..178977846,4	K562	blood:
50	chr5:179023883..179026184-chr5:179031149..179032775,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPH1-4	chr5:178975273-178975507	expReg_chr5_10798_-
2	lnc-HNRNPH1-1	chr5:179029065-179029267	ENSG00000244945.1
3	lnc-HNRNPH1-1	chr5:179026269-179026390	ENSG00000244945.1
4	lnc-HNRNPH1-1	chr5:179030608-179030742	ENSG00000244945.1
5	lnc-HNRNPH1-1	chr5:179029378-179029773	ENSG00000244945.1
6	lnc-HNRNPH1-1	chr5:179025254-179025356	ENSG00000244945.1
7	lnc-RUFY1-3	chr5:178971224-178972983	NONHSAT105589
8	lnc-HNRNPH1-1	chr5:179027074-179027099	ENSG00000244945.1
9	lnc-HNRNPH1-1	chr5:179026486-179026636	ENSG00000244945.1
10	lnc-HNRNPH1-1	chr5:179023823-179023962	ENSG00000244945.1
11	lnc-AC136604.1-5	chr5:178999157-178999742	NONHSAT105590
12	lnc-HNRNPH1-1	chr5:179022905-179023594	ENSG00000244945.1

No data

Variant related genes	Relation type
PRDX2P3	TF binding region
ENSG00000244945	TF binding region
ENSG00000253520	TF binding region
RUFY1	TF binding region
PRDX2P3	CpG island
ENSG00000244945	CpG island
ENSG00000253520	CpG island
RUFY1	CpG island
ENSG00000176783	chromatin interactions
ENSG00000126903	chromatin interactions
ENSG00000253520	chromatin interactions
ENSG00000248275	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000131876	chromatin interactions
ENSG00000183718	chromatin interactions
ENSG00000244945	chromatin interactions
ENSG00000251545	chromatin interactions
ENSG00000161021	chromatin interactions
ENSG00000259172	chromatin interactions
ENSG00000162775	chromatin interactions
ENSG00000249140	chromatin interactions
ENSG00000167716	chromatin interactions
ENSG00000225051	chromatin interactions
ENSG00000161011	chromatin interactions
ENSG00000227963	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000153575	chromatin interactions
ENSG00000186594	chromatin interactions
ENSG00000221394	chromatin interactions

Extended variants
information (count: 3365 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3365 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10035797	chr5:178955046-178955047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561907208	chr5:178955086-178955087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568666607	chr5:178955105-178955106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534421279	chr5:178955110-178955111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371933458	chr5:178955114-178955115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs116738400	chr5:178955301-178955302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551148923	chr5:178955326-178955327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568597703	chr5:178955331-178955332	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs536733657	chr5:178955337-178955338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs192310584	chr5:178955344-178955345	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113864913	chr5:178955354-178955355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533933832	chr5:178955404-178955405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs558570264	chr5:178955411-178955412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190403918	chr5:178955424-178955425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537779367	chr5:178955425-178955426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556308756	chr5:178955444-178955445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574563977	chr5:178955445-178955446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181717458	chr5:178955467-178955468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560294591	chr5:178955487-178955488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs185017213	chr5:178955530-178955531	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs149535920	chr5:178955545-178955546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs111671678	chr5:178955548-178955549	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532829464	chr5:178955556-178955557	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs144081193	chr5:178955611-178955612	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140464122	chr5:178955642-178955643	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188539505	chr5:178955643-178955644	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548615327	chr5:178955661-178955662	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs370589976	chr5:178955684-178955685	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs540576953	chr5:178955696-178955697	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs566634325	chr5:178955714-178955715	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143113289	chr5:178955728-178955729	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs552132836	chr5:178955744-178955745	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570547069	chr5:178955755-178955756	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115736671	chr5:178955814-178955815	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556209124	chr5:178955912-178955913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574530718	chr5:178955914-178955915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535301506	chr5:178955944-178955945	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571139495	chr5:178955977-178955978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539404740	chr5:178955989-178955990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554052606	chr5:178956117-178956118	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs572165826	chr5:178956158-178956159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs77645217	chr5:178956172-178956173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375905424	chr5:178956194-178956195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149085564	chr5:178956275-178956276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113961089	chr5:178956279-178956280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200279201	chr5:178956285-178956286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567363632	chr5:178956286-178956287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575960535	chr5:178956288-178956289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs58280534	chr5:178956291-178956292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374862584	chr5:178956295-178956296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2947 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178949400-178956600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr5:178951000-178957000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:178953200-178956600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:178953600-178956400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:178953600-178956600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr5:178954600-178956600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr5:178954600-178956800	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr5:178954600-178957200	Weak transcription	Spleen	Spleen
9	chr5:178954800-178956600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr5:178954800-178956600	Weak transcription	Thymus	Thymus
11	chr5:178954800-178957400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:178955000-178955200	Enhancers	Dnd41	blood
13	chr5:178955000-178956800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr5:178955200-178955400	Enhancers	Colon Smooth Muscle	Colon
15	chr5:178955200-178956600	Weak transcription	Dnd41	blood
16	chr5:178955400-178956600	Weak transcription	Colon Smooth Muscle	Colon
17	chr5:178955800-178956400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr5:178956400-178958800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:178956600-178956800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr5:178956600-178956800	Enhancers	Adipose Nuclei	Adipose
21	chr5:178956600-178956800	Enhancers	Duodenum Mucosa	Duodenum
22	chr5:178956600-178957000	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr5:178956600-178957000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr5:178956600-178957000	Enhancers	Colon Smooth Muscle	Colon
25	chr5:178956600-178957000	Enhancers	Thymus	Thymus
26	chr5:178956600-178957400	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr5:178956600-178957400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr5:178956600-178957800	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr5:178956600-178958200	Active TSS	GM12878-XiMat	blood
30	chr5:178956600-178958800	Flanking Active TSS	Dnd41	blood
31	chr5:178956800-178957000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr5:178956800-178957000	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr5:178956800-178957000	Enhancers	Primary B cells from peripheral blood	blood
34	chr5:178956800-178957000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr5:178956800-178957000	Enhancers	Fetal Thymus	thymus
36	chr5:178956800-178957000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr5:178956800-178957200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr5:178956800-178957200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr5:178956800-178957200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
40	chr5:178956800-178957400	Flanking Active TSS	Duodenum Mucosa	Duodenum
41	chr5:178956800-178957800	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr5:178956800-178957800	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr5:178956800-178957800	Active TSS	Rectal Mucosa Donor 29	rectum
44	chr5:178956800-178958000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr5:178956800-178958000	Active TSS	Brain Anterior Caudate	brain
46	chr5:178956800-178958000	Active TSS	Fetal Lung	lung
47	chr5:178956800-178958000	Active TSS	Osteobl	bone
48	chr5:178956800-178958200	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr5:178957000-178957200	Active TSS	H1 Cell Line	embryonic stem cell
50	chr5:178957000-178957200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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