Variant report

Variant	nsv1042671
Chromosome Location	chr14:66010886-66399888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2183)
CpG islands
(count:671)
Chromatin interactive
region (count:140)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2183 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:66060978-66061178	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:66071728-66072103	K562	blood:	n/a	n/a
3	ARID3A	chr14:66219662-66220354	HepG2	liver:	n/a	n/a
4	ATF1	chr14:66239784-66239891	K562	blood:	n/a	n/a
5	ATF1	chr14:66320115-66320484	K562	blood:	n/a	n/a
6	ATF1	chr14:66255615-66255868	K562	blood:	n/a	n/a
7	ATF1	chr14:66317185-66317521	K562	blood:	n/a	n/a
8	ATF1	chr14:66282878-66282933	K562	blood:	n/a	n/a
9	ATF1	chr14:66242946-66243226	K562	blood:	n/a	n/a
10	ATF1	chr14:66314008-66314464	K562	blood:	n/a	n/a
11	ATF2	chr14:66271831-66272216	GM12878	blood:	n/a	n/a
12	ATF2	chr14:66258206-66258469	GM12878	blood:	n/a	n/a
13	ATF2	chr14:66271721-66272266	GM12878	blood:	n/a	n/a
14	ATF2	chr14:66190002-66190441	GM12878	blood:	n/a	n/a
15	ATF2	chr14:66104367-66104999	GM12878	blood:	n/a	n/a
16	ATF2	chr14:66258109-66258595	GM12878	blood:	n/a	n/a
17	ATF2	chr14:66104327-66104964	GM12878	blood:	n/a	n/a
18	ATF3	chr14:66067517-66067789	HepG2	liver:	n/a	n/a
19	ATF3	chr14:66320157-66320475	K562	blood:	n/a	chr14:66320296-66320307 chr14:66320298-66320305 chr14:66320298-66320308 chr14:66320294-66320309 chr14:66320295-66320306 chr14:66320295-66320308 chr14:66320296-66320307 chr14:66320296-66320309 chr14:66320298-66320306
20	BACH1	chr14:66170506-66170838	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr14:66148425-66148528	K562	blood:	n/a	n/a
22	BATF	chr14:66171543-66171876	GM12878	blood:	n/a	n/a
23	BATF	chr14:66271796-66272282	GM12878	blood:	n/a	n/a
24	BATF	chr14:66104430-66104869	GM12878	blood:	n/a	n/a
25	BATF	chr14:66171598-66171870	GM12878	blood:	n/a	n/a
26	BATF	chr14:66198844-66199129	GM12878	blood:	n/a	n/a
27	BATF	chr14:66271809-66272191	GM12878	blood:	n/a	n/a
28	BATF	chr14:66230151-66230442	GM12878	blood:	n/a	n/a
29	BATF	chr14:66104377-66104890	GM12878	blood:	n/a	n/a
30	BATF	chr14:66248660-66248894	GM12878	blood:	n/a	n/a
31	BCL11A	chr14:66190053-66190442	GM12878	blood:	n/a	n/a
32	BCL11A	chr14:66104468-66104896	GM12878	blood:	n/a	n/a
33	BCL11A	chr14:66104363-66104972	GM12878	blood:	n/a	n/a
34	BCL11A	chr14:66271844-66272110	GM12878	blood:	n/a	n/a
35	BCL3	chr14:66143757-66143941	GM12878	blood:	n/a	n/a
36	BCL3	chr14:66258214-66258533	GM12878	blood:	n/a	n/a
37	BCL3	chr14:66143700-66143997	GM12878	blood:	n/a	n/a
38	BCL3	chr14:66272517-66272812	GM12878	blood:	n/a	n/a
39	BCL3	chr14:66104394-66104855	GM12878	blood:	n/a	n/a
40	BCLAF1	chr14:66104385-66104951	GM12878	blood:	n/a	n/a
41	BCLAF1	chr14:66104342-66104906	GM12878	blood:	n/a	n/a
42	BHLHE40	chr14:66271969-66272070	GM12878	blood:	n/a	n/a
43	BHLHE40	chr14:66239698-66239956	K562	blood:	n/a	n/a
44	BHLHE40	chr14:66313859-66314064	GM12878	blood:	n/a	n/a
45	BHLHE40	chr14:66143428-66143628	HepG2	liver:	n/a	n/a
46	BHLHE40	chr14:66104506-66104910	GM12878	blood:	n/a	n/a
47	BHLHE40	chr14:66219884-66220155	HepG2	liver:	n/a	n/a
48	BHLHE40	chr14:66256192-66256474	K562	blood:	n/a	n/a
49	BHLHE40	chr14:66258121-66258529	GM12878	blood:	n/a	n/a
50	BHLHE40	chr14:66256169-66256555	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:66100719-66100769	PANC-1	pancreas:	n/a
2	chr14:66288146-66288196	HEEpiC	esophagus:	n/a
3	chr14:66135379-66135429	NHBE	bronchial:	n/a
4	chr14:66294715-66294765	HEEpiC	esophagus:	n/a
5	chr14:66301166-66301216	HUVEC	blood vessel:	n/a
6	chr14:66171222-66171272	T-47D	breast:	n/a
7	chr14:66058810-66058860	AG09319	gingival:	n/a
8	chr14:66294715-66294765	PrEC	prostate:	n/a
9	chr14:66100719-66100769	MCF10A-Er-Src	breast:	n/a
10	chr14:66058810-66058860	NB4	blood:	n/a
11	chr14:66301166-66301216	Jurkat	blood:	n/a
12	chr14:66171222-66171272	HRCEpiC	kidney:	n/a
13	chr14:66100719-66100769	AG10803	skin:	n/a
14	chr14:66136078-66136128	PrEC	prostate:	n/a
15	chr14:66301166-66301216	IMR90	lung:	fetal
16	chr14:66058810-66058860	HEK293	kidney:	embryo
17	chr14:66212404-66212454	A549	lung:	n/a
18	chr14:66288146-66288196	LNCaP	prostate:	n/a
19	chr14:66212404-66212454	HRE	kidney:	n/a
20	chr14:66209523-66209573	HCPEpiC	choroid plexus:	n/a
21	chr14:66301166-66301216	AG09319	gingival:	n/a
22	chr14:66135379-66135429	PANC-1	pancreas:	n/a
23	chr14:66212404-66212454	AG04449	skin:	fetal
24	chr14:66026095-66026145	GM06990	blood:	n/a
25	chr14:66100719-66100769	HAEpiC	amniotic membrane:	n/a
26	chr14:66136078-66136128	GM12891	blood:	n/a
27	chr14:66212404-66212454	HCM	heart:	n/a
28	chr14:66301166-66301216	HNPCEpiC	eye:	n/a
29	chr14:66135379-66135429	SKMC	muscle:	n/a
30	chr14:66026095-66026145	HRCEpiC	kidney:	n/a
31	chr14:66026095-66026145	HIPEpiC	eye:	n/a
32	chr14:66136078-66136128	SK-N-SH	brain:	n/a
33	chr14:66026095-66026145	HRPEpiC	eye:	n/a
34	chr14:66136078-66136128	HEEpiC	esophagus:	n/a
35	chr14:66136078-66136128	K562	blood:	n/a
36	chr14:66212404-66212454	LNCaP	prostate:	n/a
37	chr14:66171222-66171272	GM12878	blood:	n/a
38	chr14:66212404-66212454	SK-N-SH_RA	brain:	n/a
39	chr14:66288146-66288196	HNPCEpiC	eye:	n/a
40	chr14:66058810-66058860	NH-A	brain:	n/a
41	chr14:66301166-66301216	PFSK-1	brain:	n/a
42	chr14:66100719-66100769	BJ	skin:	n/a
43	chr14:66212404-66212454	ovcar-3	ovarian:	n/a
44	chr14:66135379-66135429	HCPEpiC	choroid plexus:	n/a
45	chr14:66136078-66136128	HRPEpiC	eye:	n/a
46	chr14:66294715-66294765	MCF10A-Er-Src	breast:	n/a
47	chr14:66171222-66171272	HAEpiC	amniotic membrane:	n/a
48	chr14:66026095-66026145	ovcar-3	ovarian:	n/a
49	chr14:66136078-66136128	HCF	heart:	n/a
50	chr14:66100719-66100769	A549	lung:	n/a

(count:140 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:66376945..66378491-chr14:66381580..66383559,2	K562	blood:
2	chr14:66021842..66025531-chr14:66028043..66031703,3	MCF-7	breast:
3	chr14:66270049..66272588-chr14:66272600..66274303,2	MCF-7	breast:
4	chr14:66013723..66015373-chr14:66016823..66019100,2	K562	blood:
5	chr14:66055552..66057835-chr14:66062107..66064874,2	MCF-7	breast:
6	chr14:65882552..65883151-chr14:66291137..66291691,2	MCF-7	breast:
7	chr14:65878384..65879993-chr14:66335426..66337174,2	MCF-7	breast:
8	chr13:49549946..49550625-chr14:66379146..66379906,2	NB4	blood:
9	chr14:66072945..66075543-chr14:66078088..66081039,2	MCF-7	breast:
10	chr14:66277703..66280018-chr14:66286044..66288348,2	K562	blood:
11	chr14:66136933..66139072-chr14:66142582..66145379,2	MCF-7	breast:
12	chr14:66136933..66139072-chr14:66142582..66145379,2	MCF-7	breast:
13	chr14:66376945..66378491-chr14:66381580..66383559,2	K562	blood:
14	chr14:66051562..66054296-chr14:66056670..66058762,2	MCF-7	breast:
15	chr14:65878097..65879607-chr14:66264869..66267520,2	MCF-7	breast:
16	chr14:66268768..66270797-chr14:66283972..66286335,2	MCF-7	breast:
17	chr14:66314305..66316649-chr14:66316764..66318880,2	MCF-7	breast:
18	chr13:31681394..31681914-chr14:66291283..66291835,2	MCF-7	breast:
19	chr14:66109125..66110872-chr14:66135151..66136835,2	MCF-7	breast:
20	chr14:66221986..66224383-chr14:66256586..66258647,2	MCF-7	breast:
21	chr14:66062925..66064543-chr14:66085225..66086774,2	MCF-7	breast:
22	chr14:65996757..65998904-chr14:66010555..66012729,2	MCF-7	breast:
23	chr14:66013895..66016507-chr14:66016557..66019347,2	MCF-7	breast:
24	chr14:66306305..66308376-chr14:66309339..66311609,2	MCF-7	breast:
25	chr14:66002294..66004964-chr14:66020886..66023654,2	MCF-7	breast:
26	chr14:66198099..66200739-chr14:66200960..66203371,2	MCF-7	breast:
27	chr14:66265298..66267312-chr14:66388199..66390774,2	K562	blood:
28	chr14:66125185..66127124-chr14:66130505..66132106,2	MCF-7	breast:
29	chr14:66033929..66036074-chr14:66039041..66041342,2	MCF-7	breast:
30	chr14:66353685..66356222-chr14:66365985..66367880,2	MCF-7	breast:
31	chr14:66284784..66288296-chr14:66289898..66292901,3	MCF-7	breast:
32	chr14:66082764..66084424-chr14:66084646..66087072,2	K562	blood:
33	chr14:65630573..65631232-chr14:66248277..66249054,2	MCF-7	breast:
34	chr14:66398944..66401924-chr2:88314871..88317108,2	MCF-7	breast:
35	chr14:66240279..66241916-chr14:66244186..66245969,2	MCF-7	breast:
36	chr14:66283306..66285455-chr14:66289070..66291693,2	MCF-7	breast:
37	chr14:66066380..66068212-chr14:66091661..66094526,2	MCF-7	breast:
38	chr14:66169539..66172058-chr14:66175074..66177504,2	K562	blood:
39	chr14:66306305..66308376-chr14:66309339..66311609,2	MCF-7	breast:
40	chr14:66332081..66334699-chr14:66335847..66337619,2	MCF-7	breast:
41	chr14:66281943..66282566-chr14:66537249..66538129,3	MCF-7	breast:
42	chr14:66396499..66397053-chr14:66425648..66426403,2	MCF-7	breast:
43	chr14:66284784..66288296-chr14:66289898..66292901,3	MCF-7	breast:
44	chr14:66332081..66334699-chr14:66335847..66337619,2	MCF-7	breast:
45	chr14:66186993..66189656-chr14:66205388..66207201,2	MCF-7	breast:
46	chr14:66263365..66266038-chr14:66272538..66274429,2	MCF-7	breast:
47	chr14:66066380..66068212-chr14:66091661..66094526,2	MCF-7	breast:
48	chr14:65881391..65882373-chr14:66299222..66299740,2	MCF-7	breast:
49	chr14:65878369..65881220-chr14:66065484..66068700,4	MCF-7	breast:
50	chr14:66025175..66028940-chr14:66031643..66034367,3	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHURC1-FNTB-4	chr14:66022842-66023023	ucscGeneNc_uc001xiv_2
2	lnc-FUT8-3	chr14:66287495-66287592	NONHSAT037398
3	lnc-FUT8-1	chr14:66219257-66219479	XLOC_010855
4	lnc-CHURC1-FNTB-4	chr14:66034824-66035024	ucscGeneNc_uc001xiv_2
5	lnc-CHURC1-FNTB-4	chr14:66027213-66027290	ucscGeneNc_uc001xiv_2
6	lnc-FUT8-3	chr14:66261740-66262033	NONHSAT037398
7	lnc-FUT8-1	chr14:66219256-66219479	NONHSAT037396
8	lnc-FUT8-1	chr14:66219895-66221396	NONHSAT037396
9	lnc-CHURC1-FNTB-4	chr14:66028078-66028156	ucscGeneNc_uc001xiv_2
10	lnc-CHURC1-FNTB-4	chr14:66024631-66024727	ucscGeneNc_uc001xiv_2
11	lnc-CHURC1-FNTB-4	chr14:66028524-66028665	ucscGeneNc_uc001xiv_2
12	lnc-CTD-2014B16.3.1-4	chr14:66213366-66213869	NONHSAT037395
13	lnc-FUT8-1	chr14:66220444-66220716	XLOC_010855
14	lnc-CHURC1-FNTB-4	chr14:66034580-66034638	ucscGeneNc_uc001xiv_2
15	lnc-CTD-2014B16.3.1-3	chr14:66346310-66347788	NONHSAT037399
16	lnc-CHURC1-FNTB-4	chr14:66033298-66033338	ucscGeneNc_uc001xiv_2
17	lnc-CHURC1-FNTB-4	chr14:66023128-66023280	ucscGeneNc_uc001xiv_2
18	lnc-CHURC1-FNTB-4	chr14:66025458-66025508	ucscGeneNc_uc001xiv_2
19	lnc-FUT8-3	chr14:66313476-66313886	NONHSAT037398

No data

Variant related genes	Relation type
ENSG00000258960	TF binding region
ENSG00000258629	TF binding region
FUT8	TF binding region
ENSG00000258960	CpG island
ENSG00000258629	CpG island
FUT8	CpG island
ENSG00000033170	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000255002	chromatin interactions
ENSG00000102531	chromatin interactions
WWC2	miRNA target sites
WWC1	miRNA target sites

Extended variants
information (count: 13747 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:13747 , 50 per page) page: 1 2 3 4 5 6 7 ... 275

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560423198	chr14:66010889-66010890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548880243	chr14:66010907-66010908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143208460	chr14:66010975-66010976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549280374	chr14:66011053-66011054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71420502	chr14:66011084-66011085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531344766	chr14:66011110-66011111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548271406	chr14:66011168-66011169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551128637	chr14:66011181-66011182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7147636	chr14:66011184-66011185	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543409412	chr14:66011204-66011205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188751863	chr14:66011209-66011210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181079351	chr14:66011210-66011211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566747503	chr14:66011260-66011261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375723433	chr14:66011294-66011295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185360848	chr14:66011359-66011360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575889895	chr14:66011391-66011392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140458997	chr14:66011405-66011406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561774077	chr14:66011412-66011413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34751176	chr14:66011481-66011482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538529354	chr14:66011520-66011521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557895462	chr14:66011537-66011538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190021099	chr14:66011548-66011549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529313786	chr14:66011558-66011559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541149159	chr14:66011565-66011566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78587427	chr14:66011597-66011598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573882179	chr14:66011657-66011658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559475772	chr14:66011777-66011778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542415370	chr14:66011783-66011784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532081858	chr14:66011785-66011786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562692646	chr14:66011811-66011812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531551227	chr14:66011817-66011818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147494211	chr14:66011860-66011861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180852617	chr14:66011876-66011877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527267225	chr14:66011892-66011893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138381427	chr14:66011923-66011924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551730266	chr14:66011971-66011972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149570357	chr14:66012029-66012030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536338703	chr14:66012041-66012042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570327163	chr14:66012089-66012090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571416982	chr14:66012097-66012098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569412325	chr14:66012098-66012099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538190639	chr14:66012118-66012119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558395312	chr14:66012152-66012153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs578084986	chr14:66012165-66012166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534135316	chr14:66012247-66012248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554315656	chr14:66012287-66012288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574224059	chr14:66012297-66012298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77468637	chr14:66012301-66012302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76538794	chr14:66012302-66012303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76440703	chr14:66012331-66012332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Non-syndromic sensorineural hearing loss	18496225	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	23393157	CNVD
Schizophrenia	23393157	CNVD
Seizures	23393157	CNVD
Schizophrenia	23813976	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Cancer	20164919	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3189 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65985000-66025200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr14:65995200-66028000	Weak transcription	Dnd41	blood
3	chr14:65995400-66061000	Weak transcription	Gastric	stomach
4	chr14:66002400-66028000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr14:66003000-66028000	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr14:66003400-66028200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:66003800-66017800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr14:66003800-66041200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr14:66004000-66018000	Weak transcription	Brain Hippocampus Middle	brain
10	chr14:66005400-66028400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr14:66007600-66017600	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr14:66008600-66025800	Weak transcription	Primary T cells from cord blood	blood
13	chr14:66008600-66028000	Weak transcription	Primary B cells from cord blood	blood
14	chr14:66010400-66011000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr14:66010800-66011600	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr14:66011600-66014600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr14:66013200-66028200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr14:66014600-66014800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr14:66014600-66015200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr14:66014600-66015800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr14:66014800-66015200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr14:66014800-66015200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr14:66014800-66022000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr14:66015000-66015200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr14:66015200-66015600	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr14:66015200-66015600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr14:66015200-66033600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr14:66015400-66015800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr14:66015600-66015800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr14:66015600-66015800	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr14:66015600-66015800	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr14:66015600-66016000	Enhancers	Ovary	ovary
33	chr14:66015800-66016000	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr14:66015800-66016000	Enhancers	Small Intestine	intestine
35	chr14:66015800-66016600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr14:66015800-66017800	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr14:66015800-66021400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr14:66016000-66016400	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr14:66016000-66016600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr14:66016000-66032800	Weak transcription	Small Intestine	intestine
41	chr14:66016000-66041400	Weak transcription	Ovary	ovary
42	chr14:66016600-66028000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr14:66016600-66033800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr14:66017600-66018200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr14:66017800-66018000	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr14:66017800-66018400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr14:66017800-66018400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr14:66017800-66019000	Enhancers	Brain Cingulate Gyrus	brain
49	chr14:66018000-66018200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr14:66018000-66018800	Weak transcription	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links