Variant report

Variant	nsv528015
Chromosome Location	chr1:241865219-242070731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2737)
CpG islands
(count:1589)
Chromatin interactive
region (count:326)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2737 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:241992816-241992894	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:242004667-242004671	K562	blood:	n/a	n/a
3	ARID3A	chr1:241897828-241898364	K562	blood:	n/a	n/a
4	ARID3A	chr1:241877940-241878906	K562	blood:	n/a	n/a
5	ARID3A	chr1:241996568-241997431	K562	blood:	n/a	n/a
6	ARID3A	chr1:241998023-241998408	K562	blood:	n/a	n/a
7	ARID3A	chr1:241969803-241970700	K562	blood:	n/a	n/a
8	ARID3A	chr1:242010974-242011703	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:242010326-242012219	K562	blood:	n/a	n/a
10	ARID3A	chr1:242059728-242060038	K562	blood:	n/a	n/a
11	ARID3A	chr1:241933495-241933817	K562	blood:	n/a	n/a
12	ARID3A	chr1:241884824-241885093	K562	blood:	n/a	n/a
13	ARID3A	chr1:241937342-241937877	K562	blood:	n/a	n/a
14	ARID3A	chr1:241898598-241898935	K562	blood:	n/a	n/a
15	ARID3A	chr1:242059677-242060049	HepG2	liver:	n/a	n/a
16	ARID3A	chr1:241938087-241938302	K562	blood:	n/a	n/a
17	ATF1	chr1:241913628-241913891	K562	blood:	n/a	n/a
18	ATF1	chr1:241970180-241970577	K562	blood:	n/a	n/a
19	ATF1	chr1:242010197-242012251	K562	blood:	n/a	n/a
20	ATF1	chr1:241897953-241898264	K562	blood:	n/a	n/a
21	ATF1	chr1:242059628-242059975	K562	blood:	n/a	n/a
22	ATF1	chr1:241878068-241878448	K562	blood:	n/a	n/a
23	ATF1	chr1:241869696-241869877	K562	blood:	n/a	n/a
24	ATF1	chr1:241998147-241998402	K562	blood:	n/a	n/a
25	ATF1	chr1:241973285-241973421	K562	blood:	n/a	n/a
26	ATF1	chr1:242058327-242058480	K562	blood:	n/a	n/a
27	ATF2	chr1:242010887-242011878	H1-hESC	embryonic stem cell:	n/a	chr1:242011450-242011461
28	ATF2	chr1:242011039-242011638	H1-hESC	embryonic stem cell:	n/a	chr1:242011450-242011461
29	ATF2	chr1:242010898-242011694	GM12878	blood:	n/a	chr1:242011450-242011461
30	ATF2	chr1:242010933-242011644	GM12878	blood:	n/a	chr1:242011450-242011461
31	ATF3	chr1:242010776-242011665	K562	blood:	n/a	chr1:242011449-242011462 chr1:242011449-242011460 chr1:242011448-242011463 chr1:242011452-242011459 chr1:242011449-242011462 chr1:242011452-242011460 chr1:242011450-242011461 chr1:242011449-242011459 chr1:242011450-242011463
32	ATF3	chr1:242010908-242011404	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr1:242011029-242011390	K562	blood:	n/a	n/a
34	ATF3	chr1:242010936-242011373	GM12878	blood:	n/a	n/a
35	ATF3	chr1:242010961-242011660	K562	blood:	n/a	chr1:242011449-242011462 chr1:242011449-242011460 chr1:242011448-242011463 chr1:242011452-242011459 chr1:242011449-242011462 chr1:242011452-242011460 chr1:242011450-242011461 chr1:242011449-242011459 chr1:242011450-242011463
36	ATF3	chr1:242010940-242011667	A549	lung:	n/a	chr1:242011449-242011462 chr1:242011449-242011460 chr1:242011448-242011463 chr1:242011452-242011459 chr1:242011449-242011462 chr1:242011452-242011460 chr1:242011450-242011461 chr1:242011449-242011459 chr1:242011450-242011463
37	ATF3	chr1:241970153-241970622	K562	blood:	n/a	n/a
38	BACH1	chr1:241969963-241970827	K562	blood:	n/a	n/a
39	BACH1	chr1:241997054-241997314	K562	blood:	n/a	n/a
40	BACH1	chr1:241943245-241943552	K562	blood:	n/a	n/a
41	BACH1	chr1:241930500-241930532	K562	blood:	n/a	n/a
42	BACH1	chr1:242009793-242010186	K562	blood:	n/a	n/a
43	BACH1	chr1:241898456-241898654	K562	blood:	n/a	n/a
44	BACH1	chr1:242011361-242011674	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr1:241866558-241866559	K562	blood:	n/a	n/a
46	BACH1	chr1:242044778-242045267	K562	blood:	n/a	n/a
47	BACH1	chr1:242003527-242003565	K562	blood:	n/a	n/a
48	BACH1	chr1:242010553-242011829	K562	blood:	n/a	n/a
49	BATF	chr1:242002153-242002378	GM12878	blood:	n/a	chr1:242002248-242002259
50	BATF	chr1:241970239-241970482	GM12878	blood:	n/a	chr1:241970356-241970367

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:241912510-241912560	PrEC	prostate:	n/a
2	chr1:241912768-241912818	BE2_C	brain:	n/a
3	chr1:242012044-242012094	K562	blood:	n/a
4	chr1:241912510-241912560	PrEC	prostate:	n/a
5	chr1:241912768-241912818	BE2_C	brain:	n/a
6	chr1:242012044-242012094	K562	blood:	n/a
7	chr1:241981543-241981593	HCT-116	colon:	n/a
8	chr1:242011382-242011432	NHBE	bronchial:	n/a
9	chr1:241912510-241912560	SK-N-MC	brain:	n/a
10	chr1:242011513-242011563	HCT-116	colon:	n/a
11	chr1:242011513-242011563	Caco-2	colon:	n/a
12	chr1:242011396-242011446	HL-60	blood:	n/a
13	chr1:242011743-242011793	AG04450	lung:	fetal
14	chr1:242012049-242012099	NT2-D1	testis:	n/a
15	chr1:241992272-241992322	H1-hESC	embryonic stem cell:	embryo
16	chr1:242052841-242052891	HCT-116	colon:	n/a
17	chr1:242011587-242011637	T-47D	breast:	n/a
18	chr1:242011587-242011637	ECC-1	luminal epithelium:	n/a
19	chr1:242011743-242011793	GM19239	blood:	n/a
20	chr1:242011447-242011497	Caco-2	colon:	n/a
21	chr1:242011513-242011563	AG09309	skin:	n/a
22	chr1:242044107-242044157	CMK	blood:	n/a
23	chr1:242007710-242007760	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:241912768-241912818	HRE	kidney:	n/a
25	chr1:242011587-242011637	AG10803	skin:	n/a
26	chr1:242012044-242012094	HRE	kidney:	n/a
27	chr1:242011447-242011497	NT2-D1	testis:	n/a
28	chr1:242011396-242011446	IMR90	lung:	fetal
29	chr1:242011104-242011154	AG04450	lung:	fetal
30	chr1:242044107-242044157	U87	brain:	n/a
31	chr1:241981543-241981593	PFSK-1	brain:	n/a
32	chr1:242011743-242011793	HAEpiC	amniotic membrane:	n/a
33	chr1:242007710-242007760	K562	blood:	n/a
34	chr1:242011513-242011563	SK-N-MC	brain:	n/a
35	chr1:242010305-242010355	AG09319	gingival:	n/a
36	chr1:242011396-242011446	HUVEC	blood vessel:	n/a
37	chr1:242011587-242011637	SK-N-MC	brain:	n/a
38	chr1:241964727-241964777	HepG2	liver:	n/a
39	chr1:242011513-242011563	HMEC	breast:	n/a
40	chr1:242010305-242010355	GM06990	blood:	n/a
41	chr1:242011104-242011154	HEK293	kidney:	embryo
42	chr1:242002464-242002514	GM06990	blood:	n/a
43	chr1:242011256-242011306	A549	lung:	n/a
44	chr1:242030232-242030282	HUVEC	blood vessel:	n/a
45	chr1:242044107-242044157	MCF10A-Er-Src	breast:	n/a
46	chr1:241912764-241912814	GM06990	blood:	n/a
47	chr1:242011447-242011497	NH-A	brain:	n/a
48	chr1:242011256-242011306	GM19239	blood:	n/a
49	chr1:242011057-242011107	HRPEpiC	eye:	n/a
50	chr1:242011898-242011948	GM06990	blood:	n/a

(count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr1:241964291..241965013-chr1:241980298..241981106,4	MCF-7	breast:
2	chr1:241973745..241976603-chr1:241996523..241998163,2	K562	blood:
3	chr1:241888976..241891584-chr1:241891842..241893961,2	K562	blood:
4	chr1:241994931..241996990-chr1:242009652..242011355,2	K562	blood:
5	chr1:241965187..241967417-chr1:241968927..241971834,2	K562	blood:
6	chr1:242022063..242023665-chr1:242035192..242037679,2	K562	blood:
7	chr1:241868961..241870541-chr1:241927631..241929626,2	K562	blood:
8	chr1:241973745..241976603-chr1:241996523..241998163,2	K562	blood:
9	chr1:241960036..241962650-chr1:241969067..241971965,2	K562	blood:
10	chr1:241913661..241915313-chr1:242019528..242022307,2	K562	blood:
11	chr1:241992525..241994073-chr1:242002310..242004336,2	K562	blood:
12	chr1:241795192..241798178-chr1:241987807..241989667,2	K562	blood:
13	chr1:242019573..242021986-chr1:242042304..242045116,2	K562	blood:
14	chr1:241802379..241805328-chr1:241946088..241947643,2	MCF-7	breast:
15	chr1:241972366..241975039-chr1:241979342..241982449,3	MCF-7	breast:
16	chr1:241964225..241965074-chr1:241980473..241981109,2	MCF-7	breast:
17	chr1:241930047..241932478-chr1:241986893..241988841,2	K562	blood:
18	chr1:241961947..241964736-chr1:241977926..241980630,2	MCF-7	breast:
19	chr1:241861393..241865984-chr1:241866809..241872029,8	K562	blood:
20	chr1:242010595..242011154-chr22:36781613..36782133,2	Hela-S3	cervix:
21	chr1:241930047..241932478-chr1:241986893..241988841,2	K562	blood:
22	chr1:241888976..241891584-chr1:241891842..241893961,2	K562	blood:
23	chr1:241871855..241872397-chr1:241980123..241980733,2	MCF-7	breast:
24	chr1:241681862..241683903-chr1:242032872..242034945,2	K562	blood:
25	chr1:241799844..241805446-chr1:241909864..241915090,9	MCF-7	breast:
26	chr1:241913661..241915313-chr1:242019528..242022307,2	K562	blood:
27	chr1:241796724..241805103-chr1:242008052..242013159,15	K562	blood:
28	chr1:241892280..241894949-chr1:241897684..241899477,2	MCF-7	breast:
29	chr1:241930910..241933191-chr1:241964518..241967044,2	MCF-7	breast:
30	chr1:241942422..241944758-chr1:241945834..241947773,2	K562	blood:
31	chr1:241802184..241804306-chr1:241865232..241867576,2	MCF-7	breast:
32	chr1:242063118..242065688-chr1:242068745..242071369,2	K562	blood:
33	chr1:241792727..241796800-chr1:241998323..242001938,3	K562	blood:
34	chr1:241801647..241805071-chr1:241978967..241982321,4	MCF-7	breast:
35	chr1:241803368..241804887-chr1:241968226..241970324,2	MCF-7	breast:
36	chr1:241961688..241963195-chr1:241963373..241965136,2	K562	blood:
37	chr1:241970555..241972246-chr1:241972959..241974560,2	K562	blood:
38	chr1:241789486..241791019-chr1:241984145..241986452,2	K562	blood:
39	chr1:241988238..241990297-chr1:241995533..241997207,2	K562	blood:
40	chr1:241884855..241887577-chr1:241896978..241898586,2	MCF-7	breast:
41	chr1:241868172..241869866-chr1:241906945..241909756,2	MCF-7	breast:
42	chr1:241800789..241803579-chr1:241920453..241923115,2	K562	blood:
43	chr1:241911789..241914316-chr1:241924318..241925966,2	MCF-7	breast:
44	chr1:241898426..241900599-chr1:241930292..241934977,4	K562	blood:
45	chr1:242034639..242037217-chr1:242050358..242052283,2	K562	blood:
46	chr1:241950020..241951757-chr1:241963779..241966195,2	MCF-7	breast:
47	chr1:241980403..241982619-chr1:241984891..241986981,2	K562	blood:
48	chr1:242001512..242004311-chr1:242010064..242012333,2	MCF-7	breast:
49	chr1:241868961..241870541-chr1:241927631..241929626,2	K562	blood:
50	chr1:242037775..242040488-chr1:242043413..242045224,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OPN3-3	chr1:241962658-241962914	uc_43_-
2	lnc-EXO1-1	chr1:242061356-242061975	NONHSAT010556
3	lnc-EXO1-6	chr1:241962658-241962914	uc_43_+

No data

Variant related genes	Relation type
EXO1	TF binding region
ENSG00000229022	TF binding region
WDR64	TF binding region
EXO1	CpG island
ENSG00000229022	CpG island
WDR64	CpG island
ENSG00000140598	chromatin interactions
ENSG00000134884	chromatin interactions
ENSG00000171522	chromatin interactions
ENSG00000157456	chromatin interactions
ENSG00000091483	chromatin interactions
ENSG00000229022	chromatin interactions
ENSG00000054277	chromatin interactions
ENSG00000117009	chromatin interactions
ENSG00000162843	chromatin interactions
ENSG00000093000	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000153187	chromatin interactions
ENSG00000203668	chromatin interactions
ENSG00000140682	chromatin interactions

Extended variants
information (count: 7923 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:7923 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12117802	chr1:241865219-241865220	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186442404	chr1:241865245-241865246	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534249367	chr1:241865273-241865274	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376981600	chr1:241865277-241865278	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs56034445	chr1:241865284-241865285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555700617	chr1:241865294-241865295	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs150060609	chr1:241865307-241865308	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs540159170	chr1:241865315-241865316	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs146430761	chr1:241865323-241865324	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs575243016	chr1:241865393-241865394	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs9428514	chr1:241865435-241865436	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs554509545	chr1:241865534-241865535	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs144405315	chr1:241865597-241865598	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs76507089	chr1:241865601-241865602	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139803948	chr1:241865607-241865608	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs539915077	chr1:241865624-241865625	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs545027104	chr1:241865636-241865637	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559947423	chr1:241865655-241865656	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs143282927	chr1:241865656-241865657	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371958174	chr1:241865692-241865693	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs77147803	chr1:241865694-241865695	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs562641981	chr1:241865728-241865729	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs531592587	chr1:241865736-241865737	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs548305056	chr1:241865777-241865778	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs11338254	chr1:241865824-241865825	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562031651	chr1:241865872-241865873	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs6698986	chr1:241865877-241865878	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547895059	chr1:241865900-241865901	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs146686188	chr1:241865957-241865958	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs74150366	chr1:241865958-241865959	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11586891	chr1:241865979-241865980	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs570263025	chr1:241865983-241865984	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs537112885	chr1:241866028-241866029	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577213211	chr1:241866046-241866047	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536113457	chr1:241866119-241866120	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs554167719	chr1:241866166-241866167	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs182708219	chr1:241866190-241866191	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs533678018	chr1:241866205-241866206	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs188178359	chr1:241866218-241866219	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs576481319	chr1:241866223-241866224	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs61825801	chr1:241866254-241866255	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533162456	chr1:241866272-241866273	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs563003094	chr1:241866280-241866281	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556288198	chr1:241866290-241866291	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576278955	chr1:241866294-241866295	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs530535035	chr1:241866305-241866306	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs76859108	chr1:241866333-241866334	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143573434	chr1:241866334-241866335	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs150983459	chr1:241866344-241866345	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs541585611	chr1:241866346-241866347	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
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
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1694 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241860400-241869400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:241864400-241865400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:241864400-241866800	Enhancers	NHDF-Ad	bronchial
4	chr1:241864600-241866800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:241864800-241865600	Enhancers	K562	blood
6	chr1:241864800-241866200	Enhancers	NHEK	skin
7	chr1:241864800-241866800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:241864800-241866800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr1:241864800-241867000	Enhancers	HMEC	breast
10	chr1:241865000-241866800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:241865000-241866800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:241865000-241866800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:241865000-241866800	Enhancers	Hela-S3	cervix
14	chr1:241865000-241866800	Enhancers	Osteobl	bone
15	chr1:241865000-241867200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:241865000-241870200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:241865200-241866800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:241865400-241866200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:241865600-241866600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:241865800-241866400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:241866200-241866600	Enhancers	HSMM	muscle
22	chr1:241866200-241866600	Flanking Active TSS	NHEK	skin
23	chr1:241866200-241866800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:241866400-241866600	Enhancers	Esophagus	oesophagus
25	chr1:241866600-241866800	Enhancers	Placenta	Placenta
26	chr1:241866600-241867400	Weak transcription	Esophagus	oesophagus
27	chr1:241866600-241869600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:241866600-241869600	Weak transcription	HSMM	muscle
29	chr1:241866600-241870200	Enhancers	NHEK	skin
30	chr1:241866800-241869000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:241866800-241869000	Weak transcription	Hela-S3	cervix
32	chr1:241866800-241869200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr1:241866800-241869200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:241866800-241869400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:241866800-241869400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:241866800-241869400	Weak transcription	NHDF-Ad	bronchial
37	chr1:241866800-241869400	Weak transcription	Osteobl	bone
38	chr1:241866800-241869600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:241867000-241868000	Weak transcription	HMEC	breast
40	chr1:241867200-241868200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:241867400-241867600	Enhancers	Esophagus	oesophagus
42	chr1:241867400-241867600	Weak transcription	K562	blood
43	chr1:241867600-241869400	Weak transcription	Esophagus	oesophagus
44	chr1:241868000-241871600	Enhancers	HMEC	breast
45	chr1:241868200-241868400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:241868400-241868800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:241868800-241871800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:241869000-241869400	Weak transcription	Placenta	Placenta
49	chr1:241869000-241870600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:241869000-241871200	Enhancers	Primary T killer memory cells from peripheral blood	blood

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