Variant report

Variant	nsv1040257
Chromosome Location	chr14:67634585-67762806
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1408)
CpG islands
(count:1650)
Chromatin interactive
region (count:90)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1408 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:67752600-67752882	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:67752645-67752887	K562	blood:	n/a	n/a
3	ARID3A	chr14:67707890-67709331	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:67708722-67709610	K562	blood:	n/a	n/a
5	ATF2	chr14:67708095-67708783	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr14:67707601-67708011	GM12878	blood:	n/a	n/a
7	ATF2	chr14:67707487-67707860	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr14:67708083-67708286	K562	blood:	n/a	n/a
9	ATF3	chr14:67653804-67654380	HCT-116	colon:	n/a	n/a
10	BACH1	chr14:67735003-67735180	K562	blood:	n/a	n/a
11	BACH1	chr14:67653942-67654252	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr14:67707621-67708891	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:67707713-67707824	K562	blood:	n/a	n/a
14	BACH1	chr14:67708636-67708994	K562	blood:	n/a	n/a
15	BCL3	chr14:67708193-67708916	A549	lung:	n/a	chr14:67708552-67708561 chr14:67708550-67708563 chr14:67708264-67708277
16	BCLAF1	chr14:67708228-67708842	GM12878	blood:	n/a	chr14:67708552-67708561 chr14:67708550-67708563 chr14:67708264-67708277
17	BCLAF1	chr14:67708176-67708819	GM12878	blood:	n/a	chr14:67708552-67708561 chr14:67708550-67708563 chr14:67708264-67708277
18	BHLHE40	chr14:67707027-67708525	K562	blood:	n/a	chr14:67708011-67708027 chr14:67708016-67708032 chr14:67708008-67708024
19	BHLHE40	chr14:67707510-67708965	GM12878	blood:	n/a	chr14:67708011-67708027 chr14:67708016-67708032 chr14:67708008-67708024
20	BHLHE40	chr14:67707706-67708209	HepG2	liver:	n/a	chr14:67708011-67708027 chr14:67708016-67708032 chr14:67708008-67708024
21	BRCA1	chr14:67653450-67654283	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr14:67707226-67709600	Hela-S3	cervix:	n/a	chr14:67708921-67708928
23	BRCA1	chr14:67707553-67708189	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr14:67707565-67708198	GM12878	blood:	n/a	n/a
25	BRCA1	chr14:67687730-67688804	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr14:67707861-67708128	HepG2	liver:	n/a	n/a
27	CBX3	chr14:67653814-67654476	HCT-116	colon:	n/a	n/a
28	CBX3	chr14:67640488-67640777	K562	blood:	n/a	n/a
29	CBX3	chr14:67653506-67655062	HCT-116	colon:	n/a	n/a
30	CBX3	chr14:67640533-67640784	K562	blood:	n/a	n/a
31	CCNT2	chr14:67707712-67708759	K562	blood:	n/a	n/a
32	CEBPB	chr14:67708633-67709420	A549	lung:	n/a	chr14:67709085-67709097 chr14:67709108-67709121 chr14:67709242-67709253 chr14:67709242-67709255 chr14:67709243-67709254 chr14:67709242-67709253 chr14:67709242-67709255
33	CEBPB	chr14:67707726-67708102	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:67708759-67709450	K562	blood:	n/a	chr14:67709085-67709097 chr14:67709108-67709121 chr14:67709242-67709253 chr14:67709242-67709255 chr14:67709243-67709254 chr14:67709242-67709253 chr14:67709242-67709255
35	CEBPB	chr14:67751154-67751499	HepG2	liver:	n/a	chr14:67751306-67751317
36	CEBPB	chr14:67707592-67708113	K562	blood:	n/a	n/a
37	CEBPB	chr14:67751224-67751506	A549	lung:	n/a	chr14:67751306-67751317
38	CEBPB	chr14:67709156-67709411	HepG2	liver:	n/a	chr14:67709242-67709253 chr14:67709242-67709255 chr14:67709243-67709254 chr14:67709242-67709253 chr14:67709242-67709255
39	CEBPB	chr14:67743779-67744027	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr14:67637361-67637805	IMR90	lung:	n/a	n/a
41	CEBPB	chr14:67707679-67708113	A549	lung:	n/a	n/a
42	CEBPB	chr14:67675991-67676233	K562	blood:	n/a	chr14:67676155-67676166
43	CEBPB	chr14:67707780-67707998	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:67751103-67751598	A549	lung:	n/a	chr14:67751306-67751317
45	CEBPB	chr14:67751061-67751618	MCF-7	breast:	n/a	chr14:67751306-67751317
46	CEBPB	chr14:67708629-67709472	A549	lung:	n/a	chr14:67709085-67709097 chr14:67709108-67709121 chr14:67709242-67709253 chr14:67709242-67709255 chr14:67709243-67709254 chr14:67709242-67709253 chr14:67709242-67709255
47	CEBPB	chr14:67751229-67751486	H1-hESC	embryonic stem cell:	n/a	chr14:67751306-67751317
48	CEBPB	chr14:67735531-67735815	A549	lung:	n/a	chr14:67735670-67735681
49	CEBPB	chr14:67634157-67634903	Hela-S3	cervix:	n/a	chr14:67634338-67634349
50	CEBPB	chr14:67637360-67637762	Hela-S3	cervix:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67688261-67688311	HCPEpiC	choroid plexus:	n/a
2	chr14:67708212-67708262	LNCaP	prostate:	n/a
3	chr14:67707359-67707409	NH-A	brain:	n/a
4	chr14:67688261-67688311	HCPEpiC	choroid plexus:	n/a
5	chr14:67708212-67708262	LNCaP	prostate:	n/a
6	chr14:67707359-67707409	NH-A	brain:	n/a
7	chr14:67707462-67707512	PFSK-1	brain:	n/a
8	chr14:67656082-67656132	AoSMC	blood vessel:	n/a
9	chr14:67707442-67707492	PANC-1	pancreas:	n/a
10	chr14:67647740-67647790	Jurkat	blood:	n/a
11	chr14:67736448-67736498	GM12892	blood:	n/a
12	chr14:67692701-67692751	HPAEpiC	pulmonary alveolar:	n/a
13	chr14:67707756-67707806	HMEC	breast:	n/a
14	chr14:67708212-67708262	AG04449	skin:	fetal
15	chr14:67752711-67752761	MCF10A-Er-Src	breast:	n/a
16	chr14:67707462-67707512	GM12878	blood:	n/a
17	chr14:67708950-67709000	MCF-7	breast:	n/a
18	chr14:67707442-67707492	U87	brain:	n/a
19	chr14:67656082-67656132	HRPEpiC	eye:	n/a
20	chr14:67708212-67708262	A549	lung:	n/a
21	chr14:67729501-67729551	ProgFib	skin:	n/a
22	chr14:67736448-67736498	HCPEpiC	choroid plexus:	n/a
23	chr14:67656241-67656291	ovcar-3	ovarian:	n/a
24	chr14:67656029-67656079	HUVEC	blood vessel:	n/a
25	chr14:67647740-67647790	HNPCEpiC	eye:	n/a
26	chr14:67707442-67707492	HNPCEpiC	eye:	n/a
27	chr14:67688261-67688311	GM19239	blood:	n/a
28	chr14:67655478-67655528	LNCaP	prostate:	n/a
29	chr14:67708475-67708525	HRCEpiC	kidney:	n/a
30	chr14:67656241-67656291	SAEC	small airway:	n/a
31	chr14:67692701-67692751	SK-N-MC	brain:	n/a
32	chr14:67688261-67688311	Jurkat	blood:	n/a
33	chr14:67707462-67707512	HCPEpiC	choroid plexus:	n/a
34	chr14:67665364-67665414	MCF-7	breast:	n/a
35	chr14:67752711-67752761	HPAEpiC	pulmonary alveolar:	n/a
36	chr14:67654854-67654904	GM12892	blood:	n/a
37	chr14:67736448-67736498	HEK293	kidney:	embryo
38	chr14:67708950-67709000	H1-hESC	embryonic stem cell:	embryo
39	chr14:67665364-67665414	AG04449	skin:	fetal
40	chr14:67707706-67707756	PANC-1	pancreas:	n/a
41	chr14:67736448-67736498	PrEC	prostate:	n/a
42	chr14:67708475-67708525	GM12891	blood:	n/a
43	chr14:67707306-67707356	HAEpiC	amniotic membrane:	n/a
44	chr14:67688261-67688311	HUVEC	blood vessel:	n/a
45	chr14:67729501-67729551	HEEpiC	esophagus:	n/a
46	chr14:67707442-67707492	AG10803	skin:	n/a
47	chr14:67656082-67656132	AG10803	skin:	n/a
48	chr14:67707706-67707756	PFSK-1	brain:	n/a
49	chr14:67736448-67736498	PANC-1	pancreas:	n/a
50	chr14:67688261-67688311	AG04450	lung:	fetal

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:67687798..67690741-chr14:67704286..67706160,2	K562	blood:
2	chr14:67684726..67688779-chr14:67706181..67709859,3	K562	blood:
3	chr14:67707960..67708596-chr22:29196481..29197205,2	Hela-S3	cervix:
4	chr14:67634777..67636512-chr14:67650337..67652354,2	MCF-7	breast:
5	chr14:67694347..67697306-chr14:67698938..67704022,4	K562	blood:
6	chr14:67708184..67709973-chr14:67753641..67755758,3	MCF-7	breast:
7	chr14:67708016..67710004-chr14:67804973..67807646,2	MCF-7	breast:
8	chr14:67632850..67634159-chr14:67752109..67753244,6	MCF-7	breast:
9	chr14:67707691..67708267-chr8:144363492..144364061,2	Hela-S3	cervix:
10	chr14:67708428..67708936-chr7:155436811..155437523,2	Hela-S3	cervix:
11	chr14:67705323..67710204-chr14:67712445..67718210,9	MCF-7	breast:
12	chr14:67605438..67607246-chr14:67649867..67652399,2	K562	blood:
13	chr14:67701131..67704543-chr14:67705188..67709170,5	MCF-7	breast:
14	chr14:67670737..67673131-chr14:67673684..67677270,3	K562	blood:
15	chr14:67707644..67708448-chr6:36561991..36562788,2	Hela-S3	cervix:
16	chr14:67632611..67633531-chr14:67749102..67749903,3	MCF-7	breast:
17	chr14:67722215..67724352-chr14:67724413..67726414,2	MCF-7	breast:
18	chr14:67738987..67741215-chr14:67751343..67753337,2	MCF-7	breast:
19	chr14:67674549..67677391-chr14:67814114..67816733,2	K562	blood:
20	chr14:67693784..67695307-chr14:67706692..67708259,2	MCF-7	breast:
21	chr14:67634777..67636512-chr14:67650337..67652354,2	MCF-7	breast:
22	chr14:67632272..67633959-chr14:67750952..67752534,2	MCF-7	breast:
23	chr14:67717694..67719444-chr14:67723330..67725776,2	MCF-7	breast:
24	chr14:67707666..67709746-chr14:67710366..67712436,2	K562	blood:
25	chr14:67707832..67708382-chr17:33914542..33915288,2	Hela-S3	cervix:
26	chr14:67747069..67749404-chr14:67756666..67758453,2	MCF-7	breast:
27	chr14:67681892..67685441-chr14:67688163..67690297,3	MCF-7	breast:
28	chr14:67663302..67666275-chr14:67670215..67672411,3	K562	blood:
29	chr14:67700811..67702650-chr14:67710191..67712644,2	K562	blood:
30	chr14:67665237..67668000-chr14:67705488..67708368,2	MCF-7	breast:
31	chr14:67729051..67730762-chr14:67734620..67736969,2	MCF-7	breast:
32	chr14:67707885..67709803-chr14:67710291..67712170,4	MCF-7	breast:
33	chr14:67718314..67720012-chr14:67725841..67728702,2	K562	blood:
34	chr14:67706036..67709545-chr14:67826326..67828458,4	MCF-7	breast:
35	chr14:67726872..67728842-chr14:67731326..67733317,2	K562	blood:
36	chr14:67752656..67754395-chr14:67757275..67759401,2	K562	blood:
37	chr14:67694347..67697310-chr14:67698732..67700438,2	K562	blood:
38	chr14:67707695..67708382-chr16:58426045..58426842,2	Hela-S3	cervix:
39	chr14:67726872..67728842-chr14:67731326..67733317,2	K562	blood:
40	chr14:67697366..67699727-chr14:67704401..67707161,2	MCF-7	breast:
41	chr14:67717953..67720005-chr14:67723957..67726126,2	K562	blood:
42	chr14:67717694..67719444-chr14:67723330..67725776,2	MCF-7	breast:
43	chr14:67710745..67713299-chr14:67720642..67722378,2	MCF-7	breast:
44	chr14:67722215..67724352-chr14:67724413..67726414,2	MCF-7	breast:
45	chr14:67687798..67690741-chr14:67704286..67706160,2	K562	blood:
46	chr14:67692344..67694125-chr14:67702855..67704369,2	MCF-7	breast:
47	chr14:67707264..67709261-chr14:67712534..67714050,2	MCF-7	breast:
48	chr14:67752656..67754395-chr14:67757275..67759401,2	K562	blood:
49	chr14:67733714..67736125-chr14:67745424..67748088,2	K562	blood:
50	chr14:67737210..67739382-chr14:67748000..67750840,3	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71D-1	chr14:67736418-67738776	NONHSAT037435
2	lnc-ATP6V1D-1	chr14:67652258-67652438	XLOC_011057
3	lnc-MPP5-1	chr14:67694188-67694451	NONHSAT037432
4	lnc-FAM71D-1	chr14:67708152-67708250	NONHSAT037435
5	lnc-ATP6V1D-4	chr14:67706007-67706180	NONHSAT037433
6	lnc-FAM71D-1	chr14:67708059-67708250	NONHSAT037434
7	lnc-ATP6V1D-1	chr14:67649711-67649740	XLOC_011057
8	lnc-GPHN-2	chr14:67669885-67670004	NONHSAT037431
9	lnc-ATP6V1D-4	chr14:67697621-67697844	NONHSAT037433
10	lnc-GPHN-2	chr14:67664853-67665037	NONHSAT037431
11	lnc-GPHN-2	chr14:67664006-67664074	NONHSAT037431
12	lnc-MPP5-1	chr14:67695105-67695261	NONHSAT037432
13	lnc-ATP6V1D-3	chr14:67726938-67727164	NONHSAT037436
14	lnc-FAM71D-1	chr14:67720921-67721027	NONHSAT037434
15	lnc-FAM71D-1	chr14:67736418-67736481	NONHSAT037434

No data

Variant related genes	Relation type
MPP5	TF binding region
FAM71D	TF binding region
GPHN	TF binding region
ENSG00000258988	TF binding region
MPP5	CpG island
FAM71D	CpG island
GPHN	CpG island
ENSG00000258988	CpG island
ENSG00000258988	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000199755	chromatin interactions
ENSG00000240972	chromatin interactions
ENSG00000100554	chromatin interactions
ENSG00000072415	chromatin interactions
ENSG00000184863	chromatin interactions
ENSG00000216895	chromatin interactions
ENSG00000253716	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000181938	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000134001	chromatin interactions
ENSG00000171723	chromatin interactions
ENSG00000172717	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000100219	chromatin interactions

Extended variants
information (count: 4349 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4349 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536870034	chr14:67634620-67634621	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554068681	chr14:67634635-67634636	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572387278	chr14:67634644-67634645	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546151125	chr14:67634654-67634655	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555491236	chr14:67634668-67634669	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576466485	chr14:67634701-67634702	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543592539	chr14:67634743-67634744	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573861970	chr14:67634797-67634798	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117382735	chr14:67634823-67634824	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181372042	chr14:67634839-67634840	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547592183	chr14:67634881-67634882	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73276986	chr14:67634907-67634908	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs533475408	chr14:67634934-67634935	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185555117	chr14:67634960-67634961	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570395234	chr14:67634984-67634985	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559220627	chr14:67635079-67635080	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577644975	chr14:67635086-67635087	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189966505	chr14:67635104-67635105	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148727909	chr14:67635109-67635110	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180951359	chr14:67635134-67635135	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566546893	chr14:67635136-67635137	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544986282	chr14:67635166-67635167	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554032156	chr14:67635191-67635192	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572348674	chr14:67635194-67635195	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185945615	chr14:67635220-67635221	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192471399	chr14:67635231-67635232	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576404905	chr14:67635308-67635309	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183923080	chr14:67635320-67635321	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561804368	chr14:67635366-67635367	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368995393	chr14:67635397-67635398	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531009265	chr14:67635410-67635411	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573809977	chr14:67635411-67635412	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541195593	chr14:67635428-67635429	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559557924	chr14:67635435-67635436	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371885459	chr14:67635457-67635458	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551836501	chr14:67635480-67635481	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188880571	chr14:67635486-67635487	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531169275	chr14:67635538-67635539	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549818757	chr14:67635590-67635591	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111969334	chr14:67635613-67635614	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565205810	chr14:67635643-67635644	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374685366	chr14:67635647-67635648	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529026517	chr14:67635663-67635664	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142963402	chr14:67635666-67635667	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79377176	chr14:67635668-67635669	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368951901	chr14:67635777-67635778	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200658858	chr14:67635790-67635791	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116568307	chr14:67635809-67635810	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs41285536	chr14:67635835-67635836	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs142271501	chr14:67635841-67635842	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2481 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67584200-67637400	Weak transcription	Pancreas	Pancrea
2	chr14:67588000-67639400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr14:67588400-67639200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr14:67588600-67638400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:67590200-67637400	Weak transcription	Aorta	Aorta
6	chr14:67590200-67638000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr14:67590800-67637600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr14:67591400-67640000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr14:67600800-67647400	Weak transcription	Fetal Kidney	kidney
10	chr14:67610600-67634600	Weak transcription	Ovary	ovary
11	chr14:67610800-67638400	Weak transcription	Left Ventricle	heart
12	chr14:67613000-67640200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr14:67613200-67637400	Weak transcription	Adipose Nuclei	Adipose
14	chr14:67614400-67653200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:67615000-67634600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr14:67618400-67639200	Weak transcription	Brain Hippocampus Middle	brain
17	chr14:67618400-67658200	Weak transcription	Brain Angular Gyrus	brain
18	chr14:67625400-67638800	Weak transcription	GM12878-XiMat	blood
19	chr14:67626000-67638600	Weak transcription	Esophagus	oesophagus
20	chr14:67626400-67639800	Weak transcription	Primary T cells from cord blood	blood
21	chr14:67627000-67637400	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr14:67627000-67638400	Weak transcription	Fetal Stomach	stomach
23	chr14:67629800-67637400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr14:67630000-67645600	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:67630400-67637200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr14:67631600-67637600	Weak transcription	Fetal Intestine Small	intestine
27	chr14:67631600-67645800	Weak transcription	Psoas Muscle	Psoas
28	chr14:67631800-67638600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:67632400-67634600	Weak transcription	Liver	Liver
30	chr14:67632400-67640000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr14:67632600-67638800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr14:67632800-67636000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:67633200-67637200	Weak transcription	Right Ventricle	heart
34	chr14:67633200-67640000	Weak transcription	Brain Anterior Caudate	brain
35	chr14:67633200-67640000	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr14:67633200-67645400	Weak transcription	Rectal Smooth Muscle	rectum
37	chr14:67633400-67637400	Weak transcription	Gastric	stomach
38	chr14:67633400-67639800	Weak transcription	Dnd41	blood
39	chr14:67633600-67636000	Enhancers	A549	lung
40	chr14:67633600-67637200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr14:67633600-67637200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr14:67633600-67637600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr14:67633600-67640000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr14:67633600-67640200	Weak transcription	Colon Smooth Muscle	Colon
45	chr14:67633800-67638200	Weak transcription	Fetal Muscle Leg	muscle
46	chr14:67634200-67635000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr14:67634200-67635000	Enhancers	NH-A	brain
48	chr14:67634200-67635000	Enhancers	NHEK	skin
49	chr14:67634200-67635200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr14:67634200-67635200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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