Variant report

Variant	nsv1046455
Chromosome Location	chr14:66345369-66848234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2784)
CpG islands
(count:856)
Chromatin interactive
region (count:139)
LncRNA
region (count:59)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2784 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:66426007-66426319	HepG2	liver:	n/a	n/a
2	ATF1	chr14:66695088-66695283	K562	blood:	n/a	n/a
3	ATF1	chr14:66568597-66568782	K562	blood:	n/a	n/a
4	ATF1	chr14:66406754-66407439	K562	blood:	n/a	n/a
5	ATF2	chr14:66416443-66416942	GM12878	blood:	n/a	n/a
6	ATF2	chr14:66406804-66407134	GM12878	blood:	n/a	n/a
7	ATF2	chr14:66406799-66407200	GM12878	blood:	n/a	n/a
8	ATF2	chr14:66416553-66416889	GM12878	blood:	n/a	n/a
9	ATF3	chr14:66406887-66407028	K562	blood:	n/a	chr14:66406994-66407009
10	ATF3	chr14:66406819-66407108	K562	blood:	n/a	chr14:66406994-66407009
11	BACH1	chr14:66797780-66797883	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr14:66427748-66428001	H1-hESC	embryonic stem cell:	n/a	chr14:66427851-66427865
13	BACH1	chr14:66584318-66584693	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr14:66619034-66619332	H1-hESC	embryonic stem cell:	n/a	chr14:66619184-66619198
15	BACH1	chr14:66475865-66476150	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr14:66619055-66619335	K562	blood:	n/a	chr14:66619184-66619198
17	BACH1	chr14:66477452-66477707	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr14:66429715-66430007	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr14:66416572-66416914	GM12878	blood:	n/a	chr14:66416732-66416743 chr14:66416729-66416739 chr14:66416733-66416743
20	BATF	chr14:66423566-66424023	GM12878	blood:	n/a	n/a
21	BATF	chr14:66416599-66416852	GM12878	blood:	n/a	chr14:66416732-66416743 chr14:66416729-66416739 chr14:66416733-66416743
22	BATF	chr14:66566631-66567016	GM12878	blood:	n/a	chr14:66566808-66566818 chr14:66566811-66566822
23	BATF	chr14:66832110-66832442	GM12878	blood:	n/a	chr14:66832271-66832282
24	BATF	chr14:66566765-66567028	GM12878	blood:	n/a	chr14:66566808-66566818 chr14:66566811-66566822
25	BATF	chr14:66423646-66423990	GM12878	blood:	n/a	n/a
26	BATF	chr14:66832132-66832355	GM12878	blood:	n/a	chr14:66832271-66832282
27	BATF	chr14:66694978-66695280	GM12878	blood:	n/a	n/a
28	BCL11A	chr14:66423678-66423854	GM12878	blood:	n/a	n/a
29	BCL11A	chr14:66416613-66416916	GM12878	blood:	n/a	chr14:66416732-66416741
30	BCL11A	chr14:66423650-66423982	GM12878	blood:	n/a	n/a
31	BCL3	chr14:66453277-66453522	GM12878	blood:	n/a	n/a
32	BCLAF1	chr14:66606864-66607318	GM12878	blood:	n/a	n/a
33	BHLHE40	chr14:66546923-66546985	K562	blood:	n/a	n/a
34	BHLHE40	chr14:66566759-66566997	GM12878	blood:	n/a	n/a
35	BHLHE40	chr14:66404636-66404668	K562	blood:	n/a	n/a
36	BHLHE40	chr14:66512369-66512589	K562	blood:	n/a	n/a
37	BHLHE40	chr14:66537498-66537809	GM12878	blood:	n/a	n/a
38	BHLHE40	chr14:66607026-66607291	GM12878	blood:	n/a	n/a
39	BHLHE40	chr14:66456846-66456918	A549	lung:	n/a	n/a
40	BRCA1	chr14:66449179-66449188	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr14:66426109-66426309	H1-hESC	embryonic stem cell:	n/a	n/a
42	CBX3	chr14:66673352-66673534	K562	blood:	n/a	n/a
43	CBX3	chr14:66584326-66584820	HCT-116	colon:	n/a	n/a
44	CBX3	chr14:66466574-66467004	HCT-116	colon:	n/a	n/a
45	CBX3	chr14:66683492-66683903	HCT-116	colon:	n/a	n/a
46	CCNT2	chr14:66427330-66427977	K562	blood:	n/a	n/a
47	CCNT2	chr14:66808991-66809191	K562	blood:	n/a	n/a
48	CEBPB	chr14:66552523-66552694	K562	blood:	n/a	n/a
49	CEBPB	chr14:66468152-66468475	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:66797876-66798072	A549	lung:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:66560996-66561046	NHDF-neo	bronchial:	n/a
2	chr14:66460413-66460463	Hepatocyte	liver:	n/a
3	chr14:66560996-66561046	NHDF-neo	bronchial:	n/a
4	chr14:66460413-66460463	Hepatocyte	liver:	n/a
5	chr14:66460413-66460463	IMR90	lung:	fetal
6	chr14:66532279-66532329	A549	lung:	n/a
7	chr14:66532279-66532329	BJ	skin:	n/a
8	chr14:66480309-66480359	Caco-2	colon:	n/a
9	chr14:66560996-66561046	Caco-2	colon:	n/a
10	chr14:66481512-66481562	SKMC	muscle:	n/a
11	chr14:66560781-66560831	SKMC	muscle:	n/a
12	chr14:66532279-66532329	NHBE	bronchial:	n/a
13	chr14:66560996-66561046	PFSK-1	brain:	n/a
14	chr14:66439955-66440005	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:66460413-66460463	GM12878	blood:	n/a
16	chr14:66480625-66480675	U87	brain:	n/a
17	chr14:66439955-66440005	T-47D	breast:	n/a
18	chr14:66480641-66480691	H1-hESC	embryonic stem cell:	embryo
19	chr14:66480625-66480675	NB4	blood:	n/a
20	chr14:66439955-66440005	HEEpiC	esophagus:	n/a
21	chr14:66425226-66425276	HMEC	breast:	n/a
22	chr14:66480641-66480691	MCF10A-Er-Src	breast:	n/a
23	chr14:66560996-66561046	A549	lung:	n/a
24	chr14:66480528-66480578	SK-N-SH_RA	brain:	n/a
25	chr14:66460413-66460463	U87	brain:	n/a
26	chr14:66560996-66561046	NH-A	brain:	n/a
27	chr14:66480492-66480542	GM06990	blood:	n/a
28	chr14:66439955-66440005	PANC-1	pancreas:	n/a
29	chr14:66481512-66481562	HCF	heart:	n/a
30	chr14:66480492-66480542	HCM	heart:	n/a
31	chr14:66480641-66480691	K562	blood:	n/a
32	chr14:66480625-66480675	BJ	skin:	n/a
33	chr14:66481512-66481562	Hela-S3	cervix:	n/a
34	chr14:66480641-66480691	T-47D	breast:	n/a
35	chr14:66481512-66481562	SAEC	small airway:	n/a
36	chr14:66583879-66583929	BE2_C	brain:	n/a
37	chr14:66480641-66480691	HL-60	blood:	n/a
38	chr14:66560781-66560831	GM19239	blood:	n/a
39	chr14:66425226-66425276	T-47D	breast:	n/a
40	chr14:66583879-66583929	GM12891	blood:	n/a
41	chr14:66532279-66532329	MCF10A-Er-Src	breast:	n/a
42	chr14:66480641-66480691	U87	brain:	n/a
43	chr14:66460413-66460463	AG09309	skin:	n/a
44	chr14:66481512-66481562	PFSK-1	brain:	n/a
45	chr14:66532279-66532329	PANC-1	pancreas:	n/a
46	chr14:66460413-66460463	Hela-S3	cervix:	n/a
47	chr14:66560781-66560831	A549	lung:	n/a
48	chr14:66480528-66480578	Hepatocyte	liver:	n/a
49	chr14:66480309-66480359	MCF-7	breast:	n/a
50	chr14:66480492-66480542	AG10803	skin:	n/a

(count:139 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:66450401..66452102-chr14:66461586..66464258,3	MCF-7	breast:
2	chr14:66658198..66660216-chr14:66664121..66666312,2	MCF-7	breast:
3	chr14:66825542..66826429-chr14:66862069..66862684,3	MCF-7	breast:
4	chr14:66407663..66410306-chr14:66414738..66417001,2	K562	blood:
5	chr14:66725117..66725617-chr3:38044558..38045262,2	MCF-7	breast:
6	chr14:66428978..66429819-chr14:66537577..66538194,2	K562	blood:
7	chr14:66521475..66523379-chr14:66526729..66528546,2	MCF-7	breast:
8	chr14:66735910..66737746-chr14:66747875..66749421,2	MCF-7	breast:
9	chr14:66635957..66638319-chr14:66640527..66643392,2	K562	blood:
10	chr14:66554115..66555793-chr14:66584396..66586785,2	MCF-7	breast:
11	chr14:66559402..66562010-chr14:66563540..66565836,2	MCF-7	breast:
12	chr14:66709204..66711912-chr14:66719252..66721670,2	MCF-7	breast:
13	chr14:66594602..66596794-chr14:66597135..66599693,2	MCF-7	breast:
14	chr14:66826294..66826807-chr14:66869300..66870066,2	NB4	blood:
15	chr13:49549946..49550625-chr14:66379146..66379906,2	NB4	blood:
16	chr14:66459974..66462191-chr14:66465058..66467335,2	MCF-7	breast:
17	chr14:66504509..66507103-chr14:66519083..66521992,2	MCF-7	breast:
18	chr14:66588235..66589171-chr14:66861977..66862698,2	MCF-7	breast:
19	chr14:66618901..66621881-chr14:66631890..66633961,2	MCF-7	breast:
20	chr14:66588446..66589156-chr14:66844160..66844957,2	MCF-7	breast:
21	chr14:66594842..66597809-chr14:66597917..66600910,2	MCF-7	breast:
22	chr14:66518135..66520658-chr14:66522408..66524792,2	K562	blood:
23	chr14:66696991..66699499-chr14:66704656..66706344,2	MCF-7	breast:
24	chr14:66465630..66467339-chr14:66491272..66492864,2	MCF-7	breast:
25	chr14:66572868..66574441-chr14:66581197..66583523,2	MCF-7	breast:
26	chr14:66425926..66426823-chr14:66537370..66538030,2	MCF-7	breast:
27	chr14:66547263..66549999-chr14:66562087..66564818,2	MCF-7	breast:
28	chr14:66826252..66826789-chr14:66844012..66844547,2	MCF-7	breast:
29	chr14:66404813..66406809-chr14:66413591..66416552,2	MCF-7	breast:
30	chr14:66526556..66528838-chr14:66531153..66533621,2	MCF-7	breast:
31	chr14:66547263..66549999-chr14:66562087..66564818,2	MCF-7	breast:
32	chr14:66594842..66597809-chr14:66597917..66600910,2	MCF-7	breast:
33	chr14:66281810..66282561-chr14:66425521..66426262,2	MCF-7	breast:
34	chr14:66691660..66694411-chr14:66704319..66706775,2	MCF-7	breast:
35	chr14:66451472..66453019-chr14:66480410..66482560,2	MCF-7	breast:
36	chr14:66433052..66435993-chr14:66437879..66439711,3	K562	blood:
37	chr14:66427325..66428411-chr14:66537144..66538123,6	MCF-7	breast:
38	chr14:66526556..66528838-chr14:66531153..66533621,2	MCF-7	breast:
39	chr14:66469138..66471712-chr14:66485442..66488243,2	MCF-7	breast:
40	chr14:66353685..66356222-chr14:66365985..66367880,2	MCF-7	breast:
41	chr14:65628473..65630943-chr14:66425441..66427693,2	MCF-7	breast:
42	chr14:66425922..66427142-chr14:66536724..66537891,6	MCF-7	breast:
43	chr14:66497882..66501051-chr14:66504960..66506958,3	MCF-7	breast:
44	chr14:66396337..66398949-chr14:66400737..66403632,3	MCF-7	breast:
45	chr14:66566662..66568953-chr14:66571284..66573051,2	MCF-7	breast:
46	chr14:66635957..66638319-chr14:66640527..66643392,2	K562	blood:
47	chr14:66416957..66418575-chr14:66539864..66542721,2	MCF-7	breast:
48	chr14:66487758..66489942-chr14:66489951..66492637,2	MCF-7	breast:
49	chr14:66353685..66356222-chr14:66365985..66367880,2	MCF-7	breast:
50	chr14:66427325..66428411-chr14:66537144..66538123,6	MCF-7	breast:

(count:59 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FUT8-2	chr14:66584626-66584772	ENSG00000258502
2	lnc-FUT8-2	chr14:66593680-66593804	XLOC_010856
3	lnc-FUT8-2	chr14:66578349-66578489	ENSG00000258502
4	lnc-FUT8-2	chr14:66589860-66590031	XLOC_010856
5	lnc-FUT8-2	chr14:66584626-66584843	XLOC_010856
6	lnc-CTD-2014B16.3.1-2	chr14:66697051-66697613	ENSG00000258561
7	lnc-FUT8-2	chr14:66578349-66578489	ENSG00000258502
8	lnc-FUT8-2	chr14:66584626-66584772	ENSG00000258502
9	lnc-FUT8-2	chr14:66593891-66593920	XLOC_010856
10	lnc-FUT8-2	chr14:66589358-66589596	XLOC_010856
11	lnc-FUT8-2	chr14:66589860-66590031	XLOC_010856
12	lnc-FUT8-2	chr14:66590379-66590542	ENSG00000258502
13	lnc-FUT8-2	chr14:66590379-66590542	XLOC_010856
14	lnc-FUT8-2	chr14:66578260-66578489	XLOC_010856
15	lnc-GPHN-3	chr14:66734293-66734727	NONHSAT037416
16	lnc-FUT8-2	chr14:66578260-66578489	XLOC_010856
17	lnc-FUT8-2	chr14:66592487-66592607	XLOC_010856
18	lnc-FUT8-2	chr14:66578349-66578489	ENSG00000258502
19	lnc-FUT8-2	chr14:66594473-66595534	XLOC_010856
20	lnc-CTD-2014B16.3.1-2	chr14:66680617-66680669	ENSG00000258561
21	lnc-FUT8-2	chr14:66584626-66584772	XLOC_010856
22	lnc-FUT8-2	chr14:66589862-66590031	ENSG00000258502
23	lnc-FUT8-2	chr14:66584626-66584772	XLOC_010856
24	lnc-FUT8-2	chr14:66593185-66593227	XLOC_010856
25	lnc-FUT8-2	chr14:66589358-66589733	XLOC_010856
26	lnc-FUT8-2	chr14:66578299-66578713	ENSG00000258502
27	lnc-FUT8-2	chr14:66589862-66590031	XLOC_010856
28	lnc-FUT8-2	chr14:66578585-66578713	XLOC_010856
29	lnc-FUT8-2	chr14:66594473-66596708	XLOC_010856
30	lnc-FUT8-2	chr14:66592487-66592607	XLOC_010856
31	lnc-FUT8-2	chr14:66584626-66584772	ENSG00000258502
32	lnc-FUT8-2	chr14:66593185-66593227	XLOC_010856
33	lnc-FUT8-2	chr14:66584626-66584772	ENSG00000258502
34	lnc-FUT8-2	chr14:66589862-66589917	ENSG00000258502
35	lnc-FUT8-2	chr14:66589358-66589596	ENSG00000258502
36	lnc-FUT8-2	chr14:66589862-66589911	ENSG00000258502
37	lnc-FUT8-2	chr14:66593684-66593920	XLOC_010856
38	lnc-FUT8-2	chr14:66590379-66590542	XLOC_010856
39	lnc-FUT8-2	chr14:66592487-66592565	ENSG00000258502
40	lnc-FUT8-2	chr14:66592483-66592607	XLOC_010856
41	lnc-FUT8-2	chr14:66584626-66584772	ENSG00000258502
42	lnc-FUT8-2	chr14:66590379-66590424	ENSG00000258502
43	lnc-GPHN-3	chr14:66830511-66830686	NONHSAT037416
44	lnc-FUT8-2	chr14:66592487-66592609	XLOC_010856
45	lnc-FUT8-2	chr14:66593684-66593873	XLOC_010856
46	lnc-FUT8-2	chr14:66594473-66595534	XLOC_010856
47	lnc-FUT8-2	chr14:66578250-66578489	XLOC_010856
48	lnc-FUT8-2	chr14:66584626-66584772	XLOC_010856
49	lnc-FUT8-2	chr14:66589358-66589596	XLOC_010856
50	lnc-CTD-2014B16.3.1-2	chr14:66715924-66715952	ENSG00000258561

No data

Variant related genes	Relation type
ENSG00000258960	TF binding region
ENSG00000258502	TF binding region
ENSG00000238876	TF binding region
ENSG00000258847	TF binding region
YBX1P1	TF binding region
ENSG00000200860	TF binding region
ENSG00000258629	TF binding region
ENSG00000258960	CpG island
ENSG00000258502	CpG island
ENSG00000238876	CpG island
ENSG00000258847	CpG island
YBX1P1	CpG island
ENSG00000200860	CpG island
ENSG00000258629	CpG island
ENSG00000258847	chromatin interactions
ENSG00000033170	chromatin interactions
ENSG00000115648	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000102531	chromatin interactions
ENSG00000224861	chromatin interactions
CDK9	miRNA target sites
YAP1	miRNA target sites
ATP2B4	miRNA target sites
CDKN1A	miRNA target sites
ATP5G2	miRNA target sites
KEAP1	miRNA target sites
ATP6AP2	miRNA target sites
TP53INP1	miRNA target sites
ZEB1	miRNA target sites
ZEB2	miRNA target sites
RAB30	miRNA target sites

Extended variants
information (count: 13652 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:13652 , 50 per page) page: 1 2 3 4 5 6 7 ... 274

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17103072	chr14:66345369-66345370	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs111990525	chr14:66345397-66345398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564701176	chr14:66345404-66345405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs180729037	chr14:66345413-66345414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570815737	chr14:66345449-66345450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532195099	chr14:66345450-66345451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550386687	chr14:66345504-66345505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111408092	chr14:66345511-66345512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112996050	chr14:66345514-66345515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566722610	chr14:66345629-66345630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113503790	chr14:66345650-66345651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548244231	chr14:66345688-66345689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535971464	chr14:66345761-66345762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555881438	chr14:66345762-66345763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186031254	chr14:66345771-66345772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574678539	chr14:66345791-66345792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2318304	chr14:66345807-66345808	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs143902532	chr14:66345838-66345839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190506394	chr14:66345841-66345842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182391451	chr14:66345861-66345862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540129025	chr14:66345891-66345892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534003779	chr14:66345912-66345913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371172678	chr14:66345913-66345914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573541995	chr14:66345916-66345917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542356793	chr14:66346009-66346010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10144744	chr14:66346035-66346036	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186943844	chr14:66346039-66346040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191670823	chr14:66346054-66346055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533069281	chr14:66346060-66346061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533697222	chr14:66346063-66346064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546953534	chr14:66346084-66346085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182691613	chr14:66346095-66346096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146381624	chr14:66346173-66346174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529261091	chr14:66346180-66346181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549545509	chr14:66346234-66346235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569376878	chr14:66346235-66346236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17753596	chr14:66346271-66346272	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs113978780	chr14:66346275-66346276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139753354	chr14:66346366-66346367	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs116196916	chr14:66346371-66346372	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs556836579	chr14:66346387-66346388	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs72716491	chr14:66346398-66346399	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs142948087	chr14:66346399-66346400	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs367574602	chr14:66346414-66346415	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs4902430	chr14:66346446-66346447	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs151084186	chr14:66346497-66346498	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs555703090	chr14:66346535-66346536	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs575745154	chr14:66346569-66346570	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs544673788	chr14:66346621-66346622	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs185568935	chr14:66346636-66346637	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Breast cancer	17603634	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
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	23393157	CNVD
Schizophrenia	23393157	CNVD
Seizures	23393157	CNVD
Cancer	20164919	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66342400-66346800	Enhancers	Dnd41	blood
2	chr14:66343200-66346800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
3	chr14:66343200-66347000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr14:66343400-66346400	Enhancers	Primary T cells from cord blood	blood
5	chr14:66343600-66345400	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr14:66343600-66347000	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr14:66343600-66348000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr14:66343800-66345400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr14:66344000-66346800	Weak transcription	Esophagus	oesophagus
10	chr14:66344000-66347200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr14:66344200-66346400	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr14:66344200-66346800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:66344200-66347800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr14:66344600-66347000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr14:66344600-66347600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr14:66344800-66346000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr14:66345000-66347600	Enhancers	Fetal Thymus	thymus
18	chr14:66345200-66346400	Enhancers	Thymus	Thymus
19	chr14:66345200-66347800	Enhancers	NHDF-Ad	bronchial
20	chr14:66345400-66346400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr14:66345400-66346600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr14:66345800-66347800	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr14:66345800-66348000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr14:66346000-66346400	Enhancers	HUVEC	blood vessel
25	chr14:66346000-66347000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr14:66346000-66347800	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr14:66346000-66347800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr14:66346200-66346600	Enhancers	A549	lung
29	chr14:66346200-66346600	Enhancers	HMEC	breast
30	chr14:66346200-66346600	Enhancers	NHEK	skin
31	chr14:66346200-66346600	Enhancers	Osteobl	bone
32	chr14:66346200-66347000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr14:66346200-66347200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr14:66346200-66347200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr14:66346200-66347600	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr14:66346400-66346800	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr14:66346400-66347000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr14:66346400-66347000	Enhancers	Primary hematopoietic stem cells	blood
39	chr14:66346400-66347000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr14:66346400-66347200	Enhancers	Primary T cells fromperipheralblood	blood
41	chr14:66346400-66347400	Weak transcription	Primary T cells from cord blood	blood
42	chr14:66346600-66348000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr14:66346800-66347000	Enhancers	Esophagus	oesophagus
44	chr14:66346800-66347200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr14:66346800-66347200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:66346800-66347200	Flanking Active TSS	Dnd41	blood
47	chr14:66346800-66347800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr14:66346800-66348400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr14:66347200-66348000	Enhancers	Dnd41	blood
50	chr14:66347400-66348000	Enhancers	Primary T cells from cord blood	blood

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