Variant report

Variant	nsv427963
Chromosome Location	chr1:241718799-241832833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2404)
CpG islands
(count:1590)
Chromatin interactive
region (count:159)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2404 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:241773416-241773835	K562	blood:	n/a	n/a
2	ARID3A	chr1:241806015-241806374	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:241778349-241779228	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:241800842-241801482	K562	blood:	n/a	n/a
5	ARID3A	chr1:241774315-241774675	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:241790662-241791173	K562	blood:	n/a	n/a
7	ARID3A	chr1:241804647-241805695	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:241774231-241774743	K562	blood:	n/a	n/a
9	ARID3A	chr1:241776447-241776455	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:241803591-241804098	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:241803551-241803704	K562	blood:	n/a	n/a
12	ARID3A	chr1:241801745-241802837	K562	blood:	n/a	n/a
13	ATF1	chr1:241790840-241791139	K562	blood:	n/a	n/a
14	ATF1	chr1:241759920-241760248	K562	blood:	n/a	n/a
15	ATF1	chr1:241772036-241772262	K562	blood:	n/a	n/a
16	ATF1	chr1:241775886-241776245	K562	blood:	n/a	n/a
17	ATF1	chr1:241773419-241773824	K562	blood:	n/a	n/a
18	ATF1	chr1:241774340-241774808	K562	blood:	n/a	n/a
19	ATF2	chr1:241755465-241756007	GM12878	blood:	n/a	n/a
20	ATF3	chr1:241804904-241805548	A549	lung:	n/a	n/a
21	ATF3	chr1:241803464-241803926	K562	blood:	n/a	chr1:241803839-241803848
22	ATF3	chr1:241773283-241773869	A549	lung:	n/a	n/a
23	BACH1	chr1:241824764-241824777	K562	blood:	n/a	n/a
24	BACH1	chr1:241830959-241830963	K562	blood:	n/a	n/a
25	BACH1	chr1:241768508-241768738	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr1:241817312-241817525	GM12878	blood:	n/a	n/a
27	BATF	chr1:241807290-241807486	GM12878	blood:	n/a	n/a
28	BATF	chr1:241755578-241755936	GM12878	blood:	n/a	n/a
29	BATF	chr1:241763845-241764061	GM12878	blood:	n/a	chr1:241763938-241763948 chr1:241763942-241763952 chr1:241763937-241763948
30	BATF	chr1:241755595-241755842	GM12878	blood:	n/a	n/a
31	BATF	chr1:241763771-241764096	GM12878	blood:	n/a	chr1:241763938-241763948 chr1:241763942-241763952 chr1:241763937-241763948
32	BCL3	chr1:241804258-241805505	A549	lung:	n/a	n/a
33	BCL3	chr1:241803712-241804889	A549	lung:	n/a	n/a
34	BCL3	chr1:241773285-241773860	A549	lung:	n/a	n/a
35	BCL3	chr1:241778459-241779575	A549	lung:	n/a	chr1:241778550-241778559
36	BCL3	chr1:241754516-241755236	A549	lung:	n/a	chr1:241755098-241755105
37	BCL3	chr1:241754549-241755017	A549	lung:	n/a	n/a
38	BCL3	chr1:241773177-241773961	A549	lung:	n/a	chr1:241773203-241773212
39	BCL3	chr1:241778696-241779448	A549	lung:	n/a	n/a
40	BCLAF1	chr1:241763760-241764173	GM12878	blood:	n/a	n/a
41	BCLAF1	chr1:241790728-241791458	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:241807465-241807468	GM12878	blood:	n/a	n/a
43	BHLHE40	chr1:241800775-241801276	K562	blood:	n/a	n/a
44	BHLHE40	chr1:241760223-241760415	K562	blood:	n/a	n/a
45	BHLHE40	chr1:241773414-241773779	K562	blood:	n/a	n/a
46	BHLHE40	chr1:241751273-241751358	K562	blood:	n/a	n/a
47	BHLHE40	chr1:241777804-241777817	K562	blood:	n/a	n/a
48	BHLHE40	chr1:241774196-241775013	K562	blood:	n/a	n/a
49	BHLHE40	chr1:241802446-241802705	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:241803571-241803575	GM12878	blood:	n/a	n/a

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:241795170-241795220	SK-N-SH_RA	brain:	n/a
2	chr1:241802961-241803011	HRE	kidney:	n/a
3	chr1:241803298-241803348	CMK	blood:	n/a
4	chr1:241803680-241803730	ECC-1	luminal epithelium:	n/a
5	chr1:241795170-241795220	SK-N-SH_RA	brain:	n/a
6	chr1:241802961-241803011	HRE	kidney:	n/a
7	chr1:241803298-241803348	CMK	blood:	n/a
8	chr1:241803680-241803730	ECC-1	luminal epithelium:	n/a
9	chr1:241791729-241791779	GM06990	blood:	n/a
10	chr1:241791729-241791779	HRE	kidney:	n/a
11	chr1:241790950-241791000	HepG2	liver:	n/a
12	chr1:241804128-241804178	GM06990	blood:	n/a
13	chr1:241804175-241804225	AG04449	skin:	fetal
14	chr1:241803298-241803348	HEK293	kidney:	embryo
15	chr1:241803367-241803417	HNPCEpiC	eye:	n/a
16	chr1:241804175-241804225	HEEpiC	esophagus:	n/a
17	chr1:241803367-241803417	MCF10A-Er-Src	breast:	n/a
18	chr1:241803682-241803732	GM19239	blood:	n/a
19	chr1:241803820-241803870	AG10803	skin:	n/a
20	chr1:241795170-241795220	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:241757027-241757077	HCM	heart:	n/a
22	chr1:241799063-241799113	BE2_C	brain:	n/a
23	chr1:241802556-241802606	Hepatocyte	liver:	n/a
24	chr1:241757027-241757077	T-47D	breast:	n/a
25	chr1:241803298-241803348	SK-N-SH	brain:	n/a
26	chr1:241807529-241807579	SK-N-MC	brain:	n/a
27	chr1:241815640-241815690	GM06990	blood:	n/a
28	chr1:241803820-241803870	HMEC	breast:	n/a
29	chr1:241804036-241804086	NB4	blood:	n/a
30	chr1:241799063-241799113	HCM	heart:	n/a
31	chr1:241804036-241804086	SKMC	muscle:	n/a
32	chr1:241803680-241803730	NT2-D1	testis:	n/a
33	chr1:241757027-241757077	NH-A	brain:	n/a
34	chr1:241804939-241804989	NH-A	brain:	n/a
35	chr1:241791729-241791779	ProgFib	skin:	n/a
36	chr1:241804939-241804989	BJ	skin:	n/a
37	chr1:241804175-241804225	Hela-S3	cervix:	n/a
38	chr1:241804421-241804471	HepG2	liver:	n/a
39	chr1:241814413-241814463	Caco-2	colon:	n/a
40	chr1:241757027-241757077	LNCaP	prostate:	n/a
41	chr1:241804175-241804225	Jurkat	blood:	n/a
42	chr1:241803367-241803417	ECC-1	luminal epithelium:	n/a
43	chr1:241800323-241800373	Caco-2	colon:	n/a
44	chr1:241803682-241803732	CMK	blood:	n/a
45	chr1:241757027-241757077	NHBE	bronchial:	n/a
46	chr1:241803757-241803807	Hepatocyte	liver:	n/a
47	chr1:241815640-241815690	HepG2	liver:	n/a
48	chr1:241801700-241801750	HEK293	kidney:	embryo
49	chr1:241790950-241791000	ECC-1	luminal epithelium:	n/a
50	chr1:241757027-241757077	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:241792727..241796800-chr1:241998323..242001938,3	K562	blood:
2	chr1:241804722..241806985-chr1:241808766..241812200,3	MCF-7	breast:
3	chr1:241803496..241804225-chr2:38978064..38978860,2	HCT-116	colon:
4	chr1:241788460..241791197-chr1:241796744..241798499,2	MCF-7	breast:
5	chr1:241758385..241760120-chr1:241802525..241804678,2	K562	blood:
6	chr1:241750197..241751935-chr1:241752579..241755133,2	MCF-7	breast:
7	chr1:241773941..241774653-chr1:241997834..241998681,3	MCF-7	breast:
8	chr1:241692640..241698484-chr1:241752819..241757508,7	MCF-7	breast:
9	chr1:241803858..241804682-chr20:35723932..35724595,2	Hela-S3	cervix:
10	chr1:241730497..241733176-chr1:241756519..241759419,2	K562	blood:
11	chr1:241720513..241722973-chr1:241723576..241726554,2	K562	blood:
12	chr1:241694376..241696393-chr1:241777138..241779245,2	MCF-7	breast:
13	chr1:241803211..241803846-chr17:8338934..8339755,2	Hela-S3	cervix:
14	chr1:241697913..241700856-chr1:241791206..241793471,2	MCF-7	breast:
15	chr1:241798094..241801033-chr1:242010173..242012572,2	MCF-7	breast:
16	chr1:241745082..241748095-chr1:241752482..241756598,4	MCF-7	breast:
17	chr1:241802003..241803890-chr1:241818719..241820872,2	K562	blood:
18	chr1:241794861..241797433-chr1:241996680..241998541,2	K562	blood:
19	chr1:241774394..241774939-chr1:242180635..242181533,2	K562	blood:
20	chr1:241774151..241775699-chr1:242004811..242007727,2	K562	blood:
21	chr1:241760186..241764464-chr1:241765135..241770087,5	K562	blood:
22	chr1:241777588..241780548-chr1:241795040..241796800,2	MCF-7	breast:
23	chr1:241799429..241802453-chr1:241804405..241808572,4	MCF-7	breast:
24	chr1:241693395..241696373-chr1:241788082..241790840,3	K562	blood:
25	chr1:241801200..241805205-chr1:241910998..241914529,7	MCF-7	breast:
26	chr1:241703983..241707059-chr1:241753583..241756935,3	MCF-7	breast:
27	chr1:241719444..241722973-chr1:241723572..241727553,5	K562	blood:
28	chr1:241787070..241789418-chr1:242025979..242027637,2	K562	blood:
29	chr1:241789367..241790948-chr1:241857642..241860164,2	K562	blood:
30	chr1:241800930..241802917-chr1:241824611..241827597,2	K562	blood:
31	chr1:241767091..241768658-chr1:242019786..242021766,2	K562	blood:
32	chr1:241768518..241769062-chr1:242180915..242181517,2	MCF-7	breast:
33	chr1:241778937..241781849-chr1:241955297..241957609,2	K562	blood:
34	chr1:241752654..241756956-chr1:241801862..241804156,4	MCF-7	breast:
35	chr1:241796344..241797874-chr1:241911347..241912847,2	K562	blood:
36	chr1:241715297..241717214-chr1:241721647..241724093,2	K562	blood:
37	chr1:241797614..241799339-chr1:241801296..241804255,2	MCF-7	breast:
38	chr1:241717431..241720398-chr1:241722976..241725386,2	K562	blood:
39	chr1:241778921..241781913-chr1:242009994..242011882,2	K562	blood:
40	chr1:241745713..241748645-chr1:241790250..241792527,2	K562	blood:
41	chr1:35324929..35325577-chr1:241803103..241803897,2	Hela-S3	cervix:
42	chr1:241773131..241776077-chr1:241996871..241998567,3	K562	blood:
43	chr1:241795192..241798178-chr1:241987807..241989667,2	K562	blood:
44	chr1:241801309..241803243-chr1:241980186..241981798,2	MCF-7	breast:
45	chr1:241801957..241807032-chr1:241808533..241817679,11	K562	blood:
46	chr1:241799844..241805446-chr1:241909864..241915090,9	MCF-7	breast:
47	chr1:241772854..241774502-chr1:242014133..242017108,2	K562	blood:
48	chr1:241692675..241699772-chr1:241751334..241757827,9	MCF-7	breast:
49	chr1:241800887..241803348-chr1:241881120..241884579,4	K562	blood:
50	chr1:241802310..241805173-chr1:241993132..241995327,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHML-1	chr1:241792155-241794724	NONHSAT010550

No data

Variant related genes	Relation type
CHML	TF binding region
KMO	TF binding region
WDR64	TF binding region
OPN3	TF binding region
CHML	CpG island
KMO	CpG island
WDR64	CpG island
OPN3	CpG island
ENSG00000163866	chromatin interactions
ENSG00000229022	chromatin interactions
ENSG00000121274	chromatin interactions
ENSG00000166579	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000091483	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000075711	chromatin interactions
ENSG00000203668	chromatin interactions
ENSG00000117009	chromatin interactions
ENSG00000184254	chromatin interactions
ENSG00000271885	chromatin interactions
ENSG00000076344	chromatin interactions
ENSG00000080839	chromatin interactions
ENSG00000054277	chromatin interactions
ENSG00000162843	chromatin interactions
ENSG00000269846	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000136261	chromatin interactions
ENSG00000227375	chromatin interactions

Extended variants
information (count: 4331 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:4331 , 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	rs182903142	chr1:241718804-241718805	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs377482502	chr1:241718936-241718937	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs76387396	chr1:241718954-241718955	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374180915	chr1:241718968-241718969	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs74150322	chr1:241719062-241719063	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144955502	chr1:241719153-241719154	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs561344287	chr1:241719157-241719158	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560196663	chr1:241719165-241719166	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187753396	chr1:241719166-241719167	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs6429279	chr1:241719173-241719174	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs149048642	chr1:241719184-241719185	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs531528657	chr1:241719211-241719212	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs548064287	chr1:241719253-241719254	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs561611639	chr1:241719254-241719255	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143077179	chr1:241719265-241719266	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs540645375	chr1:241719382-241719383	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs148257331	chr1:241719398-241719399	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs371772915	chr1:241719414-241719415	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141249468	chr1:241719459-241719460	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550380190	chr1:241719518-241719519	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570249988	chr1:241719529-241719530	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374854477	chr1:241719535-241719536	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs147017197	chr1:241719539-241719540	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549450326	chr1:241719558-241719559	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572732148	chr1:241719559-241719560	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs533793948	chr1:241719609-241719610	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369300911	chr1:241719618-241719619	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553480120	chr1:241719649-241719650	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576916913	chr1:241719662-241719663	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545557447	chr1:241719691-241719692	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs193143412	chr1:241719735-241719736	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182774712	chr1:241719744-241719745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs187693185	chr1:241719754-241719755	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561648397	chr1:241719784-241719785	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs527550114	chr1:241719798-241719799	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541454085	chr1:241719817-241719818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs12086193	chr1:241719837-241719838	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs12089621	chr1:241719841-241719842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs550315849	chr1:241719845-241719846	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368976500	chr1:241719867-241719868	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558950549	chr1:241719878-241719879	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529514437	chr1:241719881-241719882	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs549559771	chr1:241719882-241719883	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566404267	chr1:241719890-241719891	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs138177096	chr1:241719893-241719894	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553757630	chr1:241719906-241719907	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs570336590	chr1:241719917-241719918	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539384131	chr1:241719918-241719919	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs555858796	chr1:241719928-241719929	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs575683246	chr1:241719954-241719955	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	17989066	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma	18772890	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Brain overgrowth syndrome	24179207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2038 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241714600-241722000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:241714600-241732600	Weak transcription	Spleen	Spleen
3	chr1:241715400-241719200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:241715800-241739400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr1:241716200-241746200	Weak transcription	GM12878-XiMat	blood
6	chr1:241716600-241718800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr1:241717400-241721800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr1:241717800-241720000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr1:241717800-241720800	Strong transcription	Primary B cells from peripheral blood	blood
10	chr1:241718400-241720000	Strong transcription	Placenta	Placenta
11	chr1:241718400-241721000	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr1:241718400-241723200	Strong transcription	Primary B cells from cord blood	blood
13	chr1:241718600-241719000	Weak transcription	Liver	Liver
14	chr1:241718800-241719600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:241718800-241719800	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr1:241719000-241719400	Enhancers	Fetal Intestine Large	intestine
17	chr1:241719000-241719800	Strong transcription	Liver	Liver
18	chr1:241719200-241719600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:241719600-241725600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:241719800-241720400	Weak transcription	Liver	Liver
21	chr1:241719800-241722800	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr1:241720000-241724000	Weak transcription	Placenta	Placenta
23	chr1:241720400-241723400	Enhancers	Liver	Liver
24	chr1:241720600-241721400	Enhancers	A549	lung
25	chr1:241720800-241721200	Genic enhancers	Primary B cells from peripheral blood	blood
26	chr1:241721000-241721800	Enhancers	HSMM	muscle
27	chr1:241721000-241722600	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr1:241721200-241722000	Enhancers	Fetal Kidney	kidney
29	chr1:241721200-241722000	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr1:241721200-241723400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr1:241721200-241739400	Strong transcription	Primary B cells from peripheral blood	blood
32	chr1:241721400-241722200	Flanking Active TSS	A549	lung
33	chr1:241721600-241721800	Enhancers	HepG2	liver
34	chr1:241721600-241722000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:241721600-241723200	Enhancers	HSMMtube	muscle
36	chr1:241721800-241723600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr1:241722000-241722200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:241722000-241725800	Weak transcription	Fetal Kidney	kidney
39	chr1:241722600-241722800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr1:241722800-241723200	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr1:241722800-241723400	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr1:241723200-241723600	Weak transcription	HSMMtube	muscle
43	chr1:241723200-241724400	Genic enhancers	Primary B cells from cord blood	blood
44	chr1:241723200-241725000	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr1:241723400-241723800	Flanking Active TSS	Liver	Liver
46	chr1:241723400-241724400	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr1:241723400-241724800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr1:241723600-241724200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr1:241723600-241724400	Enhancers	HepG2	liver
50	chr1:241723600-241724400	Enhancers	HSMMtube	muscle

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