Variant report

Variant	nsv1016271
Chromosome Location	chr5:118836891-119487982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2455)
CpG islands
(count:1220)
Chromatin interactive
region (count:73)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2455 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118868088-118868866	K562	blood:	n/a	n/a
2	ARID3A	chr5:118858510-118859076	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:119079705-119079979	K562	blood:	n/a	n/a
4	ARID3A	chr5:119079791-119079975	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:118848063-118848258	K562	blood:	n/a	n/a
6	ARID3A	chr5:118860192-118860556	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:119474632-119475168	HepG2	liver:	n/a	n/a
8	ATF1	chr5:119474813-119475088	K562	blood:	n/a	n/a
9	ATF1	chr5:119393482-119393828	K562	blood:	n/a	n/a
10	ATF1	chr5:119198294-119198382	K562	blood:	n/a	n/a
11	ATF1	chr5:119160125-119160178	K562	blood:	n/a	n/a
12	ATF1	chr5:119318458-119318658	K562	blood:	n/a	n/a
13	ATF1	chr5:118868403-118868934	K562	blood:	n/a	n/a
14	ATF2	chr5:118914677-118915033	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:119285237-119285699	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:118873197-118874032	GM12878	blood:	n/a	n/a
17	ATF2	chr5:118873223-118873968	GM12878	blood:	n/a	n/a
18	BACH1	chr5:119370023-119370074	K562	blood:	n/a	n/a
19	BACH1	chr5:119309649-119309722	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:119318639-119318660	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr5:119030048-119030274	GM12878	blood:	n/a	n/a
22	BATF	chr5:118873364-118873881	GM12878	blood:	n/a	n/a
23	BATF	chr5:118873272-118873908	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:118873461-118873945	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
25	BCL11A	chr5:118873315-118873926	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
26	BCL3	chr5:118873342-118873895	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
27	BCL3	chr5:119474650-119475185	A549	lung:	n/a	chr5:119474911-119474920
28	BCLAF1	chr5:118873198-118873942	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
29	BCLAF1	chr5:118873277-118873927	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
30	BHLHE40	chr5:118873360-118873825	GM12878	blood:	n/a	n/a
31	BHLHE40	chr5:118868487-118868714	K562	blood:	n/a	n/a
32	BHLHE40	chr5:118967365-118967634	GM12878	blood:	n/a	n/a
33	BRCA1	chr5:118905293-118905295	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr5:119214598-119214714	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr5:118990797-118991092	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr5:118839585-118839997	K562	blood:	n/a	n/a
37	CBX3	chr5:118914624-118915116	HCT-116	colon:	n/a	n/a
38	CBX3	chr5:118840630-118841009	HCT-116	colon:	n/a	n/a
39	CBX3	chr5:118839564-118839934	K562	blood:	n/a	n/a
40	CBX3	chr5:118840652-118840899	K562	blood:	n/a	n/a
41	CBX3	chr5:119002384-119002525	K562	blood:	n/a	n/a
42	CBX3	chr5:119002274-119002565	HCT-116	colon:	n/a	n/a
43	CBX3	chr5:118848014-118848343	K562	blood:	n/a	n/a
44	CBX3	chr5:119087374-119087627	K562	blood:	n/a	n/a
45	CBX3	chr5:119322801-119323073	K562	blood:	n/a	n/a
46	CBX3	chr5:119143704-119143991	HCT-116	colon:	n/a	n/a
47	CBX3	chr5:118848039-118848282	K562	blood:	n/a	n/a
48	CCNT2	chr5:118868541-118868579	K562	blood:	n/a	n/a
49	CEBPB	chr5:118950558-118950922	HepG2	liver:	n/a	chr5:118950732-118950743
50	CEBPB	chr5:118881941-118881942	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118964760-118964810	HUVEC	blood vessel:	n/a
2	chr5:118852883-118852933	HEEpiC	esophagus:	n/a
3	chr5:118964330-118964380	PANC-1	pancreas:	n/a
4	chr5:118965199-118965249	PrEC	prostate:	n/a
5	chr5:118852883-118852933	HRE	kidney:	n/a
6	chr5:119285514-119285564	NHDF-neo	bronchial:	n/a
7	chr5:119116179-119116229	MCF-7	breast:	n/a
8	chr5:118965347-118965397	NB4	blood:	n/a
9	chr5:118852883-118852933	AG09309	skin:	n/a
10	chr5:118971490-118971540	HUVEC	blood vessel:	n/a
11	chr5:118943582-118943632	AG04450	lung:	fetal
12	chr5:118965202-118965252	Jurkat	blood:	n/a
13	chr5:118853005-118853055	SK-N-MC	brain:	n/a
14	chr5:118964760-118964810	AG04449	skin:	fetal
15	chr5:118964760-118964810	PFSK-1	brain:	n/a
16	chr5:118964330-118964380	HRPEpiC	eye:	n/a
17	chr5:118943582-118943632	MCF-7	breast:	n/a
18	chr5:119214672-119214722	Jurkat	blood:	n/a
19	chr5:118966450-118966500	MCF-7	breast:	n/a
20	chr5:118965199-118965249	ovcar-3	ovarian:	n/a
21	chr5:118965202-118965252	NHBE	bronchial:	n/a
22	chr5:119285514-119285564	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:119116329-119116379	AG04450	lung:	fetal
24	chr5:119214672-119214722	NT2-D1	testis:	n/a
25	chr5:118943582-118943632	GM19239	blood:	n/a
26	chr5:119285772-119285822	HCT-116	colon:	n/a
27	chr5:119116179-119116229	PANC-1	pancreas:	n/a
28	chr5:119285772-119285822	HEK293	kidney:	embryo
29	chr5:118943582-118943632	HCF	heart:	n/a
30	chr5:118971490-118971540	BE2_C	brain:	n/a
31	chr5:118943582-118943632	K562	blood:	n/a
32	chr5:118964760-118964810	AG10803	skin:	n/a
33	chr5:119116179-119116229	GM06990	blood:	n/a
34	chr5:118852883-118852933	MCF10A-Er-Src	breast:	n/a
35	chr5:118964330-118964380	MCF-7	breast:	n/a
36	chr5:118918353-118918403	AG04450	lung:	fetal
37	chr5:118965233-118965283	PFSK-1	brain:	n/a
38	chr5:118964760-118964810	PANC-1	pancreas:	n/a
39	chr5:119116329-119116379	HCT-116	colon:	n/a
40	chr5:119116329-119116379	AoSMC	blood vessel:	n/a
41	chr5:118964311-118964361	HRE	kidney:	n/a
42	chr5:118971490-118971540	RPTEC	kidney:	n/a
43	chr5:119285514-119285564	LNCaP	prostate:	n/a
44	chr5:119214672-119214722	IMR90	lung:	fetal
45	chr5:118852883-118852933	T-47D	breast:	n/a
46	chr5:118965347-118965397	H1-hESC	embryonic stem cell:	embryo
47	chr5:119116179-119116229	HRE	kidney:	n/a
48	chr5:119285514-119285564	GM12878	blood:	n/a
49	chr5:119116179-119116229	HCT-116	colon:	n/a
50	chr5:118945798-118945848	GM12891	blood:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:119315165..119317093-chr5:119319183..119320996,2	K562	blood:
2	chr5:119311184..119313460-chr5:119315140..119318048,2	K562	blood:
3	chr5:118872062..118875418-chr5:118875456..118880778,4	K562	blood:
4	chr5:118991005..118992570-chr5:118993778..118996554,2	K562	blood:
5	chr18:65208157..65208941-chr5:119229771..119230382,2	MCF-7	breast:
6	chr5:118983880..118986442-chr5:118987297..118989127,2	K562	blood:
7	chr5:118825394..118827286-chr5:118834797..118837688,2	K562	blood:
8	chr5:118844240..118846924-chr5:118848133..118851535,3	K562	blood:
9	chr5:118806209..118806753-chr5:119079435..119080027,2	K562	blood:
10	chr5:118891974..118894099-chr5:118898157..118900146,2	K562	blood:
11	chr5:119093091..119095460-chr5:119099041..119101933,3	K562	blood:
12	chr5:118828423..118830428-chr5:118858768..118861011,2	K562	blood:
13	chr5:118863717..118866521-chr5:118868164..118871056,3	K562	blood:
14	chr5:118872062..118875418-chr5:118875456..118880778,4	K562	blood:
15	chr5:119093091..119095460-chr5:119099041..119101933,3	K562	blood:
16	chr5:119042499..119044624-chr5:119047745..119049345,2	K562	blood:
17	chr5:118872062..118874467-chr5:118875456..118877548,2	K562	blood:
18	chr5:119457407..119460056-chr5:119489321..119491015,2	K562	blood:
19	chr5:118894367..118897199-chr5:119080311..119081964,2	K562	blood:
20	chr5:119082500..119084067-chr5:119086307..119088713,2	K562	blood:
21	chr5:118969350..118971172-chr5:118976054..118978224,2	K562	blood:
22	chr5:119398548..119400773-chr5:119411952..119413721,2	K562	blood:
23	chr3:99997776..99998276-chr5:119383981..119384507,2	MCF-7	breast:
24	chr5:118969123..118972666-chr5:118973811..118977554,4	K562	blood:
25	chr5:119126307..119128529-chr5:119131393..119133622,2	K562	blood:
26	chr5:119425445..119427707-chr5:119431108..119433766,2	MCF-7	breast:
27	chr5:119007680..119010019-chr5:119012077..119014040,2	K562	blood:
28	chr5:118987303..118989018-chr5:118989601..118992459,2	K562	blood:
29	chr5:118868196..118870095-chr5:118875556..118878228,2	K562	blood:
30	chr5:119339357..119341886-chr5:119342360..119344963,3	MCF-7	breast:
31	chr5:119311184..119313460-chr5:119315140..119318048,2	K562	blood:
32	chr5:118991005..118992570-chr5:118993778..118996554,2	K562	blood:
33	chr10:7991136..7992090-chr5:119132393..119133207,2	MCF-7	breast:
34	chr5:119390926..119393461-chr5:119405366..119407503,2	K562	blood:
35	chr5:118806455..118807257-chr5:119079374..119080361,4	MCF-7	breast:
36	chr5:119082500..119084067-chr5:119086307..119088713,2	K562	blood:
37	chr5:119322458..119322958-chr8:143315608..143316280,2	MCF-7	breast:
38	chr5:118856782..118858975-chr5:118859993..118862585,2	K562	blood:
39	chr5:119339357..119341886-chr5:119342360..119344963,3	MCF-7	breast:
40	chr5:119164632..119167610-chr5:119169967..119171530,2	K562	blood:
41	chr5:118866950..118868481-chr5:118871752..118873914,2	K562	blood:
42	chr5:119042499..119044624-chr5:119047745..119049345,2	K562	blood:
43	chr5:118806276..118807504-chr5:119079301..119080297,7	MCF-7	breast:
44	chr5:118973233..118975098-chr5:118976996..118979393,2	K562	blood:
45	chr5:118868196..118870095-chr5:118875556..118878228,2	K562	blood:
46	chr5:118969123..118972666-chr5:118973811..118977554,4	K562	blood:
47	chr5:118831350..118835449-chr5:118835713..118839843,3	MCF-7	breast:
48	chr5:118891974..118894099-chr5:118898157..118900146,2	K562	blood:
49	chr5:118806633..118808561-chr5:119073564..119075972,2	MCF-7	breast:
50	chr5:118914344..118915154-chr5:119079337..119079948,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM170A-2	chr5:119375212-119375297	l_3004_chr5:119198853-119375297_testes
2	lnc-FAM170A-2	chr5:119341293-119341390	l_3004_chr5:119198853-119375297_testes
3	lnc-DTWD2-11	chr5:118890945-118891353	NONHSAT103440
4	lnc-FAM170A-2	chr5:119198854-119198913	l_3004_chr5:119198853-119375297_testes
5	lnc-FAM170A-2	chr5:119328116-119328211	l_3004_chr5:119198853-119375297_testes

No data

Variant related genes	Relation type
HSD17B4	TF binding region
ENSG00000250895	TF binding region
FAM170A	TF binding region
FABP5P6	TF binding region
ENSG00000234259	TF binding region
ENSG00000213663	TF binding region
ENSG00000239067	TF binding region
HSD17B4	CpG island
ENSG00000250895	CpG island
FAM170A	CpG island
FABP5P6	CpG island
ENSG00000234259	CpG island
ENSG00000213663	CpG island
ENSG00000239067	CpG island
ENSG00000239084	chromatin interactions
ENSG00000133835	chromatin interactions
ENSG00000250895	chromatin interactions

Extended variants
information (count: 14822 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:14822 , 50 per page) page: 1 2 3 4 5 6 7 ... 297

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529585246	chr5:118836939-118836940	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs3797363	chr5:118836954-118836955	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs185037834	chr5:118836979-118836980	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538287250	chr5:118836981-118836982	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146784412	chr5:118836996-118836997	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112856975	chr5:118837025-118837026	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571674826	chr5:118837049-118837050	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534036528	chr5:118837060-118837061	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs548601511	chr5:118837067-118837068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs147076881	chr5:118837187-118837188	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553902635	chr5:118837227-118837228	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138485389	chr5:118837280-118837281	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs542499822	chr5:118837296-118837297	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs556068403	chr5:118837356-118837357	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs575629740	chr5:118837381-118837382	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs144059507	chr5:118837438-118837439	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs189032891	chr5:118837459-118837460	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs572062488	chr5:118837466-118837467	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs73790877	chr5:118837495-118837496	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560704283	chr5:118837579-118837580	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs181750711	chr5:118837585-118837586	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs111758000	chr5:118837652-118837653	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563713386	chr5:118837654-118837655	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs257969	chr5:118837658-118837659	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs34840516	chr5:118837661-118837662	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs185291937	chr5:118837671-118837672	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373107613	chr5:118837677-118837678	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs111676146	chr5:118837679-118837680	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs199502857	chr5:118837686-118837687	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs529746859	chr5:118837726-118837727	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs34254740	chr5:118837728-118837729	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs371585154	chr5:118837742-118837743	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs150536709	chr5:118837763-118837764	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371682983	chr5:118837801-118837802	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs547608499	chr5:118837812-118837813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567104008	chr5:118837819-118837820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs460945	chr5:118837833-118837834	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377024389	chr5:118837834-118837835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138961791	chr5:118837892-118837893	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs538562783	chr5:118837945-118837946	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558500814	chr5:118837994-118837995	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs571964647	chr5:118838049-118838050	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189405757	chr5:118838052-118838053	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560864294	chr5:118838053-118838054	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs149346720	chr5:118838064-118838065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543199996	chr5:118838067-118838068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2636968	chr5:118838068-118838069	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs535213612	chr5:118838098-118838099	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532015115	chr5:118838104-118838105	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs377021719	chr5:118838119-118838120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2128 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118791800-118846600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:118794800-118861200	Weak transcription	HSMM	muscle
3	chr5:118804200-118879600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr5:118804800-118837000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr5:118805200-118839400	Weak transcription	NHEK	skin
6	chr5:118806000-118846400	Weak transcription	Esophagus	oesophagus
7	chr5:118806000-118846400	Weak transcription	Spleen	Spleen
8	chr5:118806200-118844800	Weak transcription	Thymus	Thymus
9	chr5:118806200-118846400	Weak transcription	Pancreas	Pancrea
10	chr5:118806200-118855600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr5:118806400-118845000	Weak transcription	Fetal Stomach	stomach
12	chr5:118806400-118846400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr5:118806800-118845400	Weak transcription	Fetal Heart	heart
14	chr5:118808000-118839600	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr5:118808000-118839800	Weak transcription	Psoas Muscle	Psoas
16	chr5:118809600-118838000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr5:118811200-118839600	Weak transcription	Brain Germinal Matrix	brain
18	chr5:118812000-118846400	Weak transcription	NHLF	lung
19	chr5:118814000-118838200	Weak transcription	Fetal Intestine Small	intestine
20	chr5:118814000-118845000	Weak transcription	Gastric	stomach
21	chr5:118814000-118845200	Weak transcription	Aorta	Aorta
22	chr5:118814800-118839400	Weak transcription	Right Ventricle	heart
23	chr5:118814800-118844800	Weak transcription	Lung	lung
24	chr5:118815400-118839000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr5:118815800-118839000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr5:118815800-118845400	Weak transcription	HMEC	breast
27	chr5:118816000-118844000	Weak transcription	Hela-S3	cervix
28	chr5:118816000-118847000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr5:118816800-118837800	Strong transcription	Dnd41	blood
30	chr5:118816800-118839600	Strong transcription	Adipose Nuclei	Adipose
31	chr5:118817000-118837800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr5:118817000-118846400	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr5:118817200-118839600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:118818400-118839600	Weak transcription	Fetal Kidney	kidney
35	chr5:118819000-118839200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr5:118819600-118844400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:118820000-118839000	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr5:118820000-118839600	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr5:118820200-118838600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr5:118820200-118846400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr5:118820400-118838800	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr5:118821000-118839600	Strong transcription	Liver	Liver
43	chr5:118821000-118843800	Weak transcription	NHDF-Ad	bronchial
44	chr5:118822000-118837200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:118823600-118837000	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr5:118823800-118837400	Strong transcription	Primary B cells from peripheral blood	blood
47	chr5:118824200-118838400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:118824400-118837000	Strong transcription	Placenta	Placenta
49	chr5:118827600-118847800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr5:118828000-118840400	Weak transcription	Osteobl	bone

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