Variant report

Variant	nsv901963
Chromosome Location	chr14:55871452-56085130
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4221)
CpG islands
(count:3235)
Chromatin interactive
region (count:159)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4221 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:55886501-55886594	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:56059242-56059676	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:56065676-56067238	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:56039327-56039726	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:55896954-55897161	K562	blood:	n/a	n/a
6	ARID3A	chr14:56046597-56046900	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:55967006-55967310	K562	blood:	n/a	n/a
8	ARID3A	chr14:55901366-55901865	HepG2	liver:	n/a	chr14:55901771-55901787
9	ARID3A	chr14:56046048-56046085	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:56072303-56073086	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:56045690-56045890	K562	blood:	n/a	n/a
12	ARID3A	chr14:56049811-56049826	K562	blood:	n/a	n/a
13	ARID3A	chr14:55897005-55897180	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:55878445-55878842	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:56066266-56066272	K562	blood:	n/a	n/a
16	ARID3A	chr14:55884839-55884914	K562	blood:	n/a	n/a
17	ARID3A	chr14:55912933-55913378	K562	blood:	n/a	n/a
18	ARID3A	chr14:55912857-55913179	HepG2	liver:	n/a	n/a
19	ATF1	chr14:55936899-55937089	K562	blood:	n/a	n/a
20	ATF1	chr14:55921337-55921668	K562	blood:	n/a	n/a
21	ATF1	chr14:55966919-55967426	K562	blood:	n/a	n/a
22	ATF2	chr14:55896755-55897141	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr14:55878289-55878963	GM12878	blood:	n/a	n/a
24	ATF2	chr14:55917669-55918218	GM12878	blood:	n/a	n/a
25	ATF2	chr14:55878330-55878770	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr14:55925395-55925997	GM12878	blood:	n/a	n/a
27	ATF2	chr14:55878444-55878902	GM12878	blood:	n/a	n/a
28	ATF2	chr14:55925406-55926072	GM12878	blood:	n/a	n/a
29	ATF2	chr14:55917640-55918105	GM12878	blood:	n/a	n/a
30	ATF2	chr14:55878367-55878784	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr14:55878392-55878727	HepG2	liver:	n/a	n/a
32	ATF3	chr14:55878236-55878771	GM12878	blood:	n/a	n/a
33	ATF3	chr14:55878386-55878648	K562	blood:	n/a	n/a
34	ATF3	chr14:55878343-55878649	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF3	chr14:56065984-56066673	A549	lung:	n/a	n/a
36	ATF3	chr14:55878254-55878821	A549	lung:	n/a	n/a
37	ATF3	chr14:55878444-55878620	GM12878	blood:	n/a	n/a
38	ATF3	chr14:55878356-55878801	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr14:56060350-56060550	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr14:55896818-55897008	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr14:56078661-56078956	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr14:56078606-56078951	K562	blood:	n/a	n/a
43	BACH1	chr14:56045735-56046148	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr14:56046476-56046887	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr14:56067550-56067798	H1-hESC	embryonic stem cell:	n/a	n/a
46	BATF	chr14:55917712-55918018	GM12878	blood:	n/a	n/a
47	BATF	chr14:55925499-55926006	GM12878	blood:	n/a	n/a
48	BATF	chr14:55925457-55926073	GM12878	blood:	n/a	n/a
49	BATF	chr14:56012977-56013309	GM12878	blood:	n/a	chr14:56013151-56013162
50	BATF	chr14:56043978-56044311	GM12878	blood:	n/a	n/a

(count:3235 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55875634-55875684	HEEpiC	esophagus:	n/a
2	chr14:56046098-56046148	NB4	blood:	n/a
3	chr14:55875634-55875684	HEEpiC	esophagus:	n/a
4	chr14:56046098-56046148	NB4	blood:	n/a
5	chr14:56042963-56043013	Jurkat	blood:	n/a
6	chr14:55878799-55878849	U87	brain:	n/a
7	chr14:55878641-55878691	AG04450	lung:	fetal
8	chr14:55878535-55878585	BJ	skin:	n/a
9	chr14:56053654-56053704	A549	lung:	n/a
10	chr14:55895678-55895728	PFSK-1	brain:	n/a
11	chr14:56053654-56053704	AoSMC	blood vessel:	n/a
12	chr14:56042963-56043013	HEEpiC	esophagus:	n/a
13	chr14:55999890-55999940	HEEpiC	esophagus:	n/a
14	chr14:56048454-56048504	AG04450	lung:	fetal
15	chr14:55878535-55878585	A549	lung:	n/a
16	chr14:56042963-56043013	SKMC	muscle:	n/a
17	chr14:56046001-56046051	SAEC	small airway:	n/a
18	chr14:55895678-55895728	HCM	heart:	n/a
19	chr14:56048454-56048504	U87	brain:	n/a
20	chr14:55907374-55907424	HCT-116	colon:	n/a
21	chr14:55878758-55878808	AG04450	lung:	fetal
22	chr14:55875634-55875684	HCM	heart:	n/a
23	chr14:56047764-56047814	NH-A	brain:	n/a
24	chr14:56046001-56046051	AoSMC	blood vessel:	n/a
25	chr14:56072740-56072790	Caco-2	colon:	n/a
26	chr14:56046685-56046735	AG04449	skin:	fetal
27	chr14:56047764-56047814	AG04450	lung:	fetal
28	chr14:55907427-55907477	AG09309	skin:	n/a
29	chr14:55905105-55905155	CMK	blood:	n/a
30	chr14:55878758-55878808	PFSK-1	brain:	n/a
31	chr14:55907299-55907349	SKMC	muscle:	n/a
32	chr14:56077052-56077102	Hepatocyte	liver:	n/a
33	chr14:55878649-55878699	ProgFib	skin:	n/a
34	chr14:55999890-55999940	SKMC	muscle:	n/a
35	chr14:56046098-56046148	ProgFib	skin:	n/a
36	chr14:55905105-55905155	Jurkat	blood:	n/a
37	chr14:56047964-56048014	HCT-116	colon:	n/a
38	chr14:55907501-55907551	HIPEpiC	eye:	n/a
39	chr14:55908365-55908415	SK-N-MC	brain:	n/a
40	chr14:56023591-56023641	SAEC	small airway:	n/a
41	chr14:55907460-55907510	HEK293	kidney:	embryo
42	chr14:55878680-55878730	K562	blood:	n/a
43	chr14:55923136-55923186	PANC-1	pancreas:	n/a
44	chr14:55907007-55907057	HRCEpiC	kidney:	n/a
45	chr14:56007778-56007828	IMR90	lung:	fetal
46	chr14:56072740-56072790	IMR90	lung:	fetal
47	chr14:56050164-56050214	RPTEC	kidney:	n/a
48	chr14:55914753-55914803	NHBE	bronchial:	n/a
49	chr14:55910650-55910700	HUVEC	blood vessel:	n/a
50	chr14:56060624-56060674	A549	lung:	n/a

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr14:55888467..55890762-chr14:55899523..55901753,2	K562	blood:
2	chr14:56057726..56060571-chr14:56061645..56063881,2	K562	blood:
3	chr14:55930242..55933239-chr14:55934431..55937260,2	MCF-7	breast:
4	chr14:56057179..56059764-chr14:56063889..56065411,2	K562	blood:
5	chr14:55912884..55915003-chr14:55916118..55918746,2	K562	blood:
6	chr14:55882209..55883793-chr14:55889649..55891588,2	K562	blood:
7	chr14:56012207..56014964-chr14:56021875..56024671,2	MCF-7	breast:
8	chr14:56052261..56055376-chr14:56058166..56061190,4	K562	blood:
9	chr14:56064719..56067198-chr14:56076951..56079697,2	K562	blood:
10	chr14:55888467..55890762-chr14:55899523..55901753,2	K562	blood:
11	chr14:55995958..55999191-chr14:56000283..56002949,4	MCF-7	breast:
12	chr14:55947632..55950014-chr14:55951455..55953042,2	K562	blood:
13	chr14:55873181..55876141-chr14:55896106..55898564,2	K562	blood:
14	chr14:55911475..55914836-chr14:55916178..55919121,4	MCF-7	breast:
15	chr14:55873181..55876141-chr14:55896106..55898564,2	K562	blood:
16	chr14:56046559..56049206-chr14:56078372..56080917,2	MCF-7	breast:
17	chr14:56007987..56009584-chr14:56010088..56012589,2	MCF-7	breast:
18	chr14:55936925..55938790-chr14:55938821..55940391,2	K562	blood:
19	chr14:56032572..56034215-chr14:56037864..56039579,2	MCF-7	breast:
20	chr14:55878684..55880292-chr14:55881926..55883661,2	K562	blood:
21	chr14:55870951..55872840-chr14:55874953..55876700,2	K562	blood:
22	chr14:55875694..55878426-chr14:55879816..55881880,2	MCF-7	breast:
23	chr14:55882209..55883793-chr14:55889649..55891588,2	K562	blood:
24	chr14:56014631..56016749-chr14:56021571..56023338,2	MCF-7	breast:
25	chr14:55889778..55893394-chr14:55894134..55896526,3	K562	blood:
26	chr14:56008500..56010380-chr14:56023755..56025494,2	MCF-7	breast:
27	chr12:21654164..21654736-chr14:56046727..56047402,2	Hela-S3	cervix:
28	chr14:56032572..56034215-chr14:56037864..56039579,2	MCF-7	breast:
29	chr14:56053518..56055259-chr14:56070896..56073206,2	MCF-7	breast:
30	chr14:55863036..55866300-chr14:55870450..55873492,4	K562	blood:
31	chr14:56063086..56065940-chr14:56074647..56076603,2	K562	blood:
32	chr14:56060669..56063373-chr14:56064902..56067658,2	K562	blood:
33	chr14:56072488..56077213-chr14:56077351..56081424,5	MCF-7	breast:
34	chr14:55913503..55916476-chr14:55916660..55918746,2	K562	blood:
35	chr14:55932703..55935495-chr14:55937792..55940291,2	MCF-7	breast:
36	chr14:56046168..56050032-chr14:56060605..56067298,7	K562	blood:
37	chr14:55832090..55833883-chr14:55878712..55880700,2	MCF-7	breast:
38	chr14:56046884..56048461-chr14:56110849..56113567,2	K562	blood:
39	chr14:55967592..55969824-chr14:55972621..55974139,2	K562	blood:
40	chr14:55913503..55916476-chr14:55916660..55918746,2	K562	blood:
41	chr14:55883538..55884193-chr14:55896578..55897445,2	MCF-7	breast:
42	chr14:55870132..55872485-chr14:55876302..55878951,2	MCF-7	breast:
43	chr14:55934279..55936415-chr14:55944398..55946379,2	K562	blood:
44	chr14:55889778..55893394-chr14:55894134..55896526,3	K562	blood:
45	chr14:56035971..56038143-chr14:56044533..56046893,2	K562	blood:
46	chr14:56053879..56055533-chr14:56070490..56072513,2	K562	blood:
47	chr14:55946573..55948131-chr14:56047906..56049458,2	K562	blood:
48	chr14:55872877..55874681-chr14:55877005..55878622,2	MCF-7	breast:
49	chr14:55737206..55739469-chr14:55885262..55887168,2	K562	blood:
50	chr14:56044147..56045759-chr14:56045883..56047408,2	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBPL2-1	chr14:56046654-56046792	ENSG00000186615.6
2	lnc-FBXO34-1	chr14:56032792-56032968	l_989_chr14:56031091-56033068_testes
3	lnc-TBPL2-3	chr14:56016058-56016636	NONHSAT037012
4	lnc-TBPL2-1	chr14:56027807-56027881	ENSG00000186615
5	lnc-FBXO34-1	chr14:56032982-56033096	l_989_chr14:56031091-56033068_testes
6	lnc-TBPL2-1	chr14:56046654-56046810	ENSG00000186615.6
7	lnc-TBPL2-1	chr14:56042875-56044097	ENSG00000186615
8	lnc-TBPL2-1	chr14:56027807-56027881	XLOC_011036
9	lnc-TBPL2-1	chr14:55965996-55966211	ENSG00000186615.6
10	lnc-TBPL2-1	chr14:56046654-56046814	ENSG00000186615
11	lnc-TBPL2-1	chr14:56024690-56026492	ENSG00000186615
12	lnc-TBPL2-1	chr14:56042905-56044097	ENSG00000186615
13	lnc-FBXO34-2	chr14:56050822-56050988	ucscGeneNc_uc001xci_2
14	lnc-TBPL2-1	chr14:56046654-56046810	ENSG00000186615
15	lnc-TBPL2-1	chr14:56045324-56045455	ENSG00000186615
16	lnc-TBPL2-1	chr14:56027865-56027881	XLOC_011036
17	lnc-TBPL2-1	chr14:56027807-56027881	ENSG00000186615.6
18	lnc-TBPL2-1	chr14:56042904-56044097	ENSG00000186615.6
19	lnc-TBPL2-1	chr14:56045324-56045455	ENSG00000186615
20	lnc-TBPL2-1	chr14:56045324-56045455	XLOC_011036
21	lnc-TBPL2-1	chr14:56046654-56046828	ENSG00000186615
22	lnc-ATG14-2	chr14:55880274-55880777	NONHSAT037009
23	lnc-FBXO34-1	chr14:56031092-56031396	l_989_chr14:56031091-56033068_testes
24	lnc-TBPL2-1	chr14:56045324-56045455	ENSG00000186615.6
25	lnc-TBPL2-1	chr14:56045324-56045769	XLOC_011036
26	lnc-TBPL2-1	chr14:56045324-56045455	ENSG00000186615.6
27	lnc-TBPL2-1	chr14:56046654-56046810	XLOC_011036
28	lnc-TBPL2-1	chr14:56042876-56044097	XLOC_011036
29	lnc-TBPL2-1	chr14:56046654-56046810	XLOC_011036
30	lnc-KTN1-3	chr14:55964856-55966219	NONHSAT037010
31	lnc-FBXO34-1	chr14:56040028-56040285	l_989_chr14:56031091-56033068_testes
32	lnc-TBPL2-1	chr14:56024690-56026492	XLOC_011036

No data

Variant related genes	Relation type
ATG14	TF binding region
ENSG00000271484	TF binding region
KTN1-AS1	TF binding region
TBPL2	TF binding region
RPL21P6	TF binding region
KTN1	TF binding region
RPL7AP4	TF binding region
ATG14	CpG island
ENSG00000271484	CpG island
KTN1-AS1	CpG island
TBPL2	CpG island
RPL21P6	CpG island
KTN1	CpG island
RPL7AP4	CpG island
ENSG00000273270	chromatin interactions
ENSG00000213641	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000111711	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000123810	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000260170	chromatin interactions
ENSG00000271484	chromatin interactions
ENSG00000004700	chromatin interactions
ENSG00000197568	chromatin interactions
ENSG00000170631	chromatin interactions
ENSG00000104164	chromatin interactions
ENSG00000197747	chromatin interactions
ENSG00000182521	chromatin interactions
ENSG00000126775	chromatin interactions
ENSG00000142046	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000186615	chromatin interactions
ENSG00000239199	chromatin interactions
ENSG00000118454	chromatin interactions
SRRM1	miRNA target sites
TRRAP	miRNA target sites
CDK19	miRNA target sites
GPATCH8	miRNA target sites
NLK	miRNA target sites
INTS6	miRNA target sites
SFXN1	miRNA target sites

Extended variants
information (count: 7981 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:7981 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6573020	chr14:55871452-55871453	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529058777	chr14:55871469-55871470	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546353633	chr14:55871505-55871506	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567947610	chr14:55871530-55871531	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs61975446	chr14:55871532-55871533	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550899509	chr14:55871542-55871543	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs190474461	chr14:55871572-55871573	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs539377960	chr14:55871619-55871620	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557474373	chr14:55871746-55871747	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs566546875	chr14:55871791-55871792	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs115745438	chr14:55871801-55871802	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs192937071	chr14:55871821-55871822	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113990779	chr14:55871838-55871839	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs544567830	chr14:55871857-55871858	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs546264888	chr14:55871868-55871869	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs556772967	chr14:55871905-55871906	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs578187883	chr14:55871970-55871971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs545358899	chr14:55871989-55871990	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs143685748	chr14:55872031-55872032	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185173992	chr14:55872073-55872074	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370518058	chr14:55872139-55872140	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs542739769	chr14:55872183-55872184	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs117428809	chr14:55872190-55872191	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201022109	chr14:55872235-55872236	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs148113503	chr14:55872260-55872261	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569849963	chr14:55872335-55872336	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs550512377	chr14:55872372-55872373	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs189899276	chr14:55872392-55872393	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533100728	chr14:55872420-55872421	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs181528959	chr14:55872448-55872449	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs185666579	chr14:55872490-55872491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs188465577	chr14:55872492-55872493	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555538881	chr14:55872534-55872535	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567375663	chr14:55872607-55872608	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs8020065	chr14:55872610-55872611	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs578170615	chr14:55872612-55872613	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs545410334	chr14:55872616-55872617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs180673210	chr14:55872668-55872669	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs562380048	chr14:55872704-55872705	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs186456817	chr14:55872720-55872721	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs374844327	chr14:55872738-55872739	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529602561	chr14:55872815-55872816	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs561007348	chr14:55872855-55872856	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373892277	chr14:55872904-55872905	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs368148402	chr14:55872913-55872914	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs146338498	chr14:55872915-55872916	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201672848	chr14:55872947-55872948	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544370251	chr14:55872995-55872996	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562559435	chr14:55873018-55873019	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs564033628	chr14:55873093-55873094	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Medulloblastoma	21163964	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4268 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55818200-55877600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:55836800-55877800	Weak transcription	Esophagus	oesophagus
3	chr14:55848600-55876600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr14:55849200-55876600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr14:55849200-55878000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:55852000-55877200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr14:55853000-55877200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr14:55854800-55878000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr14:55856200-55876200	Weak transcription	Fetal Brain Male	brain
10	chr14:55856200-55878000	Weak transcription	Spleen	Spleen
11	chr14:55856400-55876800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr14:55856400-55877600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:55856600-55876600	Weak transcription	Fetal Brain Female	brain
14	chr14:55856800-55875600	Weak transcription	Dnd41	blood
15	chr14:55856800-55877200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr14:55859200-55874200	Weak transcription	Fetal Stomach	stomach
17	chr14:55860600-55877800	Weak transcription	Lung	lung
18	chr14:55862000-55876000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr14:55862000-55876200	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr14:55862000-55876400	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr14:55862000-55876800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr14:55862200-55873600	Weak transcription	Fetal Intestine Small	intestine
23	chr14:55862200-55876200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr14:55862200-55876400	Weak transcription	Brain Germinal Matrix	brain
25	chr14:55862200-55877000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr14:55862200-55877600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:55862400-55876200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr14:55862400-55876200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr14:55862400-55877200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr14:55862600-55877400	Weak transcription	Fetal Thymus	thymus
31	chr14:55862800-55876000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr14:55862800-55876800	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr14:55862800-55877200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr14:55863400-55876600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:55863400-55876600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr14:55863400-55877600	Weak transcription	Placenta	Placenta
37	chr14:55863600-55877400	Weak transcription	Thymus	Thymus
38	chr14:55863800-55876600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr14:55864000-55874400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:55864000-55874600	Weak transcription	Fetal Muscle Trunk	muscle
41	chr14:55864000-55875800	Weak transcription	HepG2	liver
42	chr14:55864000-55876000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr14:55864000-55876400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr14:55864000-55876400	Weak transcription	Liver	Liver
45	chr14:55864000-55876400	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr14:55864000-55876600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr14:55864000-55876600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr14:55864000-55877200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr14:55864200-55874200	Weak transcription	Primary hematopoietic stem cells	blood
50	chr14:55864200-55877200	Weak transcription	Primary B cells from cord blood	blood

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