Variant report

Variant	nsv904267
Chromosome Location	chr15:58699010-58769583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1857)
CpG islands
(count:674)
Chromatin interactive
region (count:60)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58707734-58708189	K562	blood:	n/a	n/a
2	ARID3A	chr15:58747156-58747675	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:58723845-58724674	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:58767778-58769308	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:58702198-58702395	K562	blood:	n/a	n/a
6	ARID3A	chr15:58734368-58734618	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:58717507-58717628	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:58712314-58712545	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:58761980-58762558	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:58749976-58750707	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:58722084-58722767	K562	blood:	n/a	n/a
12	ARID3A	chr15:58755905-58756780	HepG2	liver:	n/a	n/a
13	ARID3A	chr15:58731190-58731493	HepG2	liver:	n/a	n/a
14	ARID3A	chr15:58759096-58761393	HepG2	liver:	n/a	n/a
15	ARID3A	chr15:58733286-58733314	K562	blood:	n/a	n/a
16	ARID3A	chr15:58704468-58704476	K562	blood:	n/a	n/a
17	ATF1	chr15:58749705-58749952	K562	blood:	n/a	n/a
18	ATF1	chr15:58760148-58760226	K562	blood:	n/a	n/a
19	ATF1	chr15:58759466-58759852	K562	blood:	n/a	n/a
20	ATF1	chr15:58722141-58722665	K562	blood:	n/a	n/a
21	ATF1	chr15:58705605-58705761	K562	blood:	n/a	n/a
22	ATF1	chr15:58763625-58763852	K562	blood:	n/a	n/a
23	ATF1	chr15:58762340-58762460	K562	blood:	n/a	n/a
24	ATF2	chr15:58712602-58713391	GM12878	blood:	n/a	n/a
25	ATF2	chr15:58765953-58766459	GM12878	blood:	n/a	n/a
26	ATF2	chr15:58746518-58747031	GM12878	blood:	n/a	n/a
27	ATF2	chr15:58765955-58766385	GM12878	blood:	n/a	n/a
28	ATF2	chr15:58749604-58750667	GM12878	blood:	n/a	n/a
29	ATF2	chr15:58746536-58747070	GM12878	blood:	n/a	n/a
30	ATF2	chr15:58749559-58750757	GM12878	blood:	n/a	n/a
31	ATF3	chr15:58707834-58708186	K562	blood:	n/a	n/a
32	ATF3	chr15:58732140-58732968	A549	lung:	n/a	n/a
33	ATF3	chr15:58762213-58762548	K562	blood:	n/a	n/a
34	ATF3	chr15:58761860-58762588	A549	lung:	n/a	n/a
35	ATF3	chr15:58762307-58762508	K562	blood:	n/a	n/a
36	ATF3	chr15:58761953-58762623	A549	lung:	n/a	n/a
37	ATF3	chr15:58732131-58733054	A549	lung:	n/a	n/a
38	ATF3	chr15:58722156-58722424	K562	blood:	n/a	n/a
39	BACH1	chr15:58759449-58759476	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr15:58734064-58734133	H1-hESC	embryonic stem cell:	n/a	n/a
41	BATF	chr15:58713001-58713255	GM12878	blood:	n/a	n/a
42	BATF	chr15:58749613-58750100	GM12878	blood:	n/a	chr15:58749825-58749836
43	BATF	chr15:58712678-58713320	GM12878	blood:	n/a	n/a
44	BATF	chr15:58749589-58750157	GM12878	blood:	n/a	chr15:58749825-58749836
45	BATF	chr15:58765883-58766370	GM12878	blood:	n/a	n/a
46	BATF	chr15:58746405-58747008	GM12878	blood:	n/a	n/a
47	BATF	chr15:58750356-58750651	GM12878	blood:	n/a	n/a
48	BATF	chr15:58765966-58766352	GM12878	blood:	n/a	n/a
49	BATF	chr15:58746555-58746975	GM12878	blood:	n/a	n/a
50	BCL11A	chr15:58746589-58747023	GM12878	blood:	n/a	n/a

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58723851-58723901	HCM	heart:	n/a
2	chr15:58699976-58700026	Hela-S3	cervix:	n/a
3	chr15:58724225-58724275	AG04449	skin:	fetal
4	chr15:58723851-58723901	HCM	heart:	n/a
5	chr15:58699976-58700026	Hela-S3	cervix:	n/a
6	chr15:58724225-58724275	AG04449	skin:	fetal
7	chr15:58735214-58735264	GM12891	blood:	n/a
8	chr15:58723879-58723929	ovcar-3	ovarian:	n/a
9	chr15:58766885-58766935	PANC-1	pancreas:	n/a
10	chr15:58732754-58732804	K562	blood:	n/a
11	chr15:58723879-58723929	AG04450	lung:	fetal
12	chr15:58724041-58724091	GM19239	blood:	n/a
13	chr15:58724225-58724275	NHDF-neo	bronchial:	n/a
14	chr15:58758468-58758518	HCPEpiC	choroid plexus:	n/a
15	chr15:58732754-58732804	LNCaP	prostate:	n/a
16	chr15:58732754-58732804	ovcar-3	ovarian:	n/a
17	chr15:58723657-58723707	LNCaP	prostate:	n/a
18	chr15:58732754-58732804	AG04450	lung:	fetal
19	chr15:58732754-58732804	HRPEpiC	eye:	n/a
20	chr15:58699976-58700026	HEK293	kidney:	embryo
21	chr15:58735214-58735264	U87	brain:	n/a
22	chr15:58733736-58733786	ovcar-3	ovarian:	n/a
23	chr15:58766885-58766935	PrEC	prostate:	n/a
24	chr15:58758468-58758518	H1-hESC	embryonic stem cell:	embryo
25	chr15:58766885-58766935	NT2-D1	testis:	n/a
26	chr15:58724041-58724091	SKMC	muscle:	n/a
27	chr15:58732754-58732804	HepG2	liver:	n/a
28	chr15:58766885-58766935	HCT-116	colon:	n/a
29	chr15:58723879-58723929	RPTEC	kidney:	n/a
30	chr15:58735214-58735264	NH-A	brain:	n/a
31	chr15:58723851-58723901	HPAEpiC	pulmonary alveolar:	n/a
32	chr15:58733736-58733786	SAEC	small airway:	n/a
33	chr15:58724225-58724275	SKMC	muscle:	n/a
34	chr15:58735214-58735264	T-47D	breast:	n/a
35	chr15:58758468-58758518	AG04450	lung:	fetal
36	chr15:58733736-58733786	CMK	blood:	n/a
37	chr15:58699976-58700026	BE2_C	brain:	n/a
38	chr15:58758468-58758518	HepG2	liver:	n/a
39	chr15:58723879-58723929	HMEC	breast:	n/a
40	chr15:58723851-58723901	HRCEpiC	kidney:	n/a
41	chr15:58699976-58700026	Hepatocyte	liver:	n/a
42	chr15:58735214-58735264	HUVEC	blood vessel:	n/a
43	chr15:58723879-58723929	NH-A	brain:	n/a
44	chr15:58732754-58732804	U87	brain:	n/a
45	chr15:58766885-58766935	LNCaP	prostate:	n/a
46	chr15:58732754-58732804	HEK293	kidney:	embryo
47	chr15:58724225-58724275	MCF10A-Er-Src	breast:	n/a
48	chr15:58699976-58700026	GM12878	blood:	n/a
49	chr15:58723851-58723901	HRE	kidney:	n/a
50	chr15:58735214-58735264	HEK293	kidney:	embryo

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:58726222..58728488-chr15:58751000..58752953,2	K562	blood:
2	chr15:58762234..58763977-chr15:59040711..59042531,2	K562	blood:
3	chr15:58624699..58626357-chr15:58758259..58760422,2	MCF-7	breast:
4	chr15:58709732..58712579-chr15:58730855..58732681,2	K562	blood:
5	chr15:58728810..58730578-chr15:58760180..58761799,2	MCF-7	breast:
6	chr15:58758492..58760005-chr15:58885829..58888502,2	MCF-7	breast:
7	chr15:58623609..58625282-chr15:58727962..58730632,2	MCF-7	breast:
8	chr15:58726654..58728474-chr15:58730449..58733344,2	MCF-7	breast:
9	chr15:58706598..58709949-chr15:58711625..58715312,3	K562	blood:
10	chr15:58720668..58723820-chr15:58759148..58762580,3	K562	blood:
11	chr15:58729567..58734283-chr15:58741092..58746394,5	K562	blood:
12	chr15:58750305..58752654-chr15:58755983..58757859,3	K562	blood:
13	chr15:58762574..58764554-chr15:58812167..58813777,2	K562	blood:
14	chr15:58685871..58690225-chr15:58716411..58720519,4	K562	blood:
15	chr15:58698100..58699843-chr15:58703706..58705363,2	K562	blood:
16	chr15:58714110..58717947-chr15:58718129..58721624,4	K562	blood:
17	chr15:58767133..58770014-chr15:58770584..58772843,2	MCF-7	breast:
18	chr15:58623181..58625459-chr15:58764481..58766715,2	MCF-7	breast:
19	chr15:58731963..58734945-chr15:58743116..58746394,3	K562	blood:
20	chr15:58706598..58709949-chr15:58711625..58715312,3	K562	blood:
21	chr15:58730575..58732285-chr15:58839559..58842370,2	K562	blood:
22	chr15:58728810..58730578-chr15:58760180..58761799,2	MCF-7	breast:
23	chr15:58754820..58757599-chr15:58758355..58762013,3	K562	blood:
24	chr15:58731963..58734945-chr15:58743116..58746394,3	K562	blood:
25	chr15:58739121..58741793-chr15:58746543..58749268,3	K562	blood:
26	chr15:58519770..58521503-chr15:58715577..58717727,2	K562	blood:
27	chr15:58681878..58684869-chr15:58759181..58760747,2	MCF-7	breast:
28	chr15:58739121..58741793-chr15:58746543..58749268,3	K562	blood:
29	chr15:58758547..58760128-chr15:58777523..58780209,2	MCF-7	breast:
30	chr15:58695539..58698492-chr15:58699127..58701058,3	K562	blood:
31	chr15:58742210..58745056-chr15:58745443..58748993,3	K562	blood:
32	chr15:58737118..58738691-chr15:58740817..58742511,2	K562	blood:
33	chr15:58731261..58732919-chr15:58735065..58738026,2	K562	blood:
34	chr15:58726654..58728474-chr15:58730449..58733344,2	MCF-7	breast:
35	chr15:58750305..58752654-chr15:58755983..58757859,3	K562	blood:
36	chr15:58713103..58715507-chr15:58716251..58718186,2	MCF-7	breast:
37	chr15:58623588..58626439-chr15:58697018..58699779,2	K562	blood:
38	chr15:58758655..58760808-chr15:58812229..58814183,2	MCF-7	breast:
39	chr15:58714110..58717947-chr15:58718129..58721624,4	K562	blood:
40	chr15:58732540..58734705-chr15:58743392..58745682,2	MCF-7	breast:
41	chr15:58730817..58731598-chr22:22510997..22511880,2	HCT-116	colon:
42	chr15:58623889..58626326-chr15:58704441..58709164,4	K562	blood:
43	chr15:58623562..58626994-chr15:58730618..58733502,3	MCF-7	breast:
44	chr15:58767751..58769658-chr15:58771265..58773299,2	MCF-7	breast:
45	chr15:58726222..58728488-chr15:58751000..58752953,2	K562	blood:
46	chr15:58729567..58734283-chr15:58741092..58746394,5	K562	blood:
47	chr15:58624527..58626111-chr15:58750898..58753049,2	K562	blood:
48	chr15:58720668..58723820-chr15:58759148..58762580,3	K562	blood:
49	chr15:58684651..58686772-chr15:58697716..58700224,2	K562	blood:
50	chr15:58723370..58725024-chr15:58732776..58734366,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-9	chr15:58765830-58765959	NONHSAT044093
2	lnc-ADAM10-9	chr15:58712170-58712304	NONHSAT044093
3	lnc-AQP9-5	chr15:58723026-58723350	NONHSAT044110
4	lnc-ALDH1A2-1	chr15:58727089-58729111	ENSG00000259293.1
5	lnc-AQP9-5	chr15:58702780-58703017	NONHSAT044110
6	lnc-AQP9-5	chr15:58724192-58724562	NONHSAT044110

No data

Variant related genes	Relation type
LIPC	TF binding region
ALDH1A2	TF binding region
LIPC	CpG island
ALDH1A2	CpG island
ENSG00000259476	chromatin interactions
ENSG00000166035	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000233720	chromatin interactions
ENSG00000137845	chromatin interactions

Extended variants
information (count: 3170 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3170 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11856159	chr15:58699010-58699011	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541342599	chr15:58699012-58699013	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150174166	chr15:58699028-58699029	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs561019980	chr15:58699048-58699049	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs76220778	chr15:58699128-58699129	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs150630774	chr15:58699136-58699137	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188318055	chr15:58699181-58699182	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs193169519	chr15:58699193-58699194	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs60808669	chr15:58699199-58699200	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs571602274	chr15:58699238-58699239	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184791973	chr15:58699248-58699249	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534172732	chr15:58699273-58699274	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554063414	chr15:58699365-58699366	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567483949	chr15:58699396-58699397	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536478834	chr15:58699426-58699427	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559591161	chr15:58699453-58699454	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556597129	chr15:58699461-58699462	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139926150	chr15:58699533-58699534	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189478556	chr15:58699587-58699588	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545375130	chr15:58699589-58699590	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116920812	chr15:58699590-58699591	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs180701424	chr15:58699624-58699625	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs541305736	chr15:58699678-58699679	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs541986462	chr15:58699699-58699700	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs561183360	chr15:58699701-58699702	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529900478	chr15:58699717-58699718	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs183739899	chr15:58699774-58699775	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561518571	chr15:58699842-58699843	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs563396288	chr15:58699921-58699922	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs189632807	chr15:58699934-58699935	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs13329672	chr15:58699937-58699938	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs79254571	chr15:58699985-58699986	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs181195642	chr15:58699999-58700000	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs547667268	chr15:58700011-58700012	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs564286884	chr15:58700034-58700035	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs79497281	chr15:58700039-58700040	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs550147221	chr15:58700083-58700084	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs73420510	chr15:58700088-58700089	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186701232	chr15:58700113-58700114	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs191476980	chr15:58700126-58700127	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs13329681	chr15:58700128-58700129	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs13329676	chr15:58700132-58700133	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554886736	chr15:58700207-58700208	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs181565949	chr15:58700219-58700220	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs543598128	chr15:58700250-58700251	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs186109205	chr15:58700286-58700287	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs17240869	chr15:58700311-58700312	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs140708441	chr15:58700315-58700316	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs559052432	chr15:58700330-58700331	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs190864340	chr15:58700332-58700333	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1799 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58690800-58702400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr15:58694800-58702600	Weak transcription	HepG2	liver
3	chr15:58694800-58716000	Weak transcription	Esophagus	oesophagus
4	chr15:58695000-58699400	Weak transcription	Fetal Thymus	thymus
5	chr15:58697400-58701200	Weak transcription	K562	blood
6	chr15:58698200-58699600	Weak transcription	Right Atrium	heart
7	chr15:58698800-58700400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:58698800-58700600	Enhancers	Brain Substantia Nigra	brain
9	chr15:58699000-58699600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr15:58699000-58699800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr15:58699000-58699800	Enhancers	Brain Hippocampus Middle	brain
12	chr15:58699000-58700000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr15:58699000-58700400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr15:58699000-58700400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr15:58699000-58700400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr15:58699000-58700400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr15:58699000-58700400	Enhancers	Brain Cingulate Gyrus	brain
18	chr15:58699000-58700400	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr15:58699000-58700600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:58699000-58700600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr15:58699000-58700600	Enhancers	Brain Angular Gyrus	brain
22	chr15:58699200-58700400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr15:58699200-58700600	Enhancers	Brain Anterior Caudate	brain
24	chr15:58699400-58700400	Enhancers	Fetal Thymus	thymus
25	chr15:58699600-58699800	Enhancers	Right Atrium	heart
26	chr15:58699600-58700000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr15:58699600-58700400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr15:58699800-58700200	Flanking Active TSS	Brain Hippocampus Middle	brain
29	chr15:58699800-58700400	Enhancers	Thymus	Thymus
30	chr15:58700000-58700200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr15:58700200-58700400	Enhancers	Brain Hippocampus Middle	brain
32	chr15:58700200-58702600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr15:58700400-58700600	Enhancers	GM12878-XiMat	blood
34	chr15:58700400-58702000	Weak transcription	Fetal Thymus	thymus
35	chr15:58700400-58702200	Weak transcription	Thymus	Thymus
36	chr15:58700400-58702400	Weak transcription	Brain Hippocampus Middle	brain
37	chr15:58700400-58702600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr15:58700400-58702600	Weak transcription	Brain Cingulate Gyrus	brain
39	chr15:58700400-58702600	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr15:58700400-58702800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr15:58700600-58702000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:58700600-58702400	Weak transcription	Brain Angular Gyrus	brain
43	chr15:58700600-58702600	Weak transcription	Brain Anterior Caudate	brain
44	chr15:58700600-58702600	Weak transcription	Brain Substantia Nigra	brain
45	chr15:58701200-58702200	Weak transcription	GM12878-XiMat	blood
46	chr15:58701200-58702400	Enhancers	K562	blood
47	chr15:58701800-58702000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr15:58701800-58702200	Enhancers	Dnd41	blood
49	chr15:58701800-58702400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr15:58701800-58703000	Enhancers	Left Ventricle	heart

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