Variant report

Variant	nsv569522
Chromosome Location	chr15:55532211-55611126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2190)
CpG islands
(count:1770)
Chromatin interactive
region (count:135)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2190 , 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	chr15:55582683-55582974	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:55542686-55542931	K562	blood:	n/a	n/a
3	ARID3A	chr15:55574357-55574917	K562	blood:	n/a	n/a
4	ARID3A	chr15:55582501-55582999	K562	blood:	n/a	n/a
5	ARID3A	chr15:55611067-55611566	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:55550744-55550788	K562	blood:	n/a	n/a
7	ARID3A	chr15:55576575-55577009	K562	blood:	n/a	n/a
8	ARID3A	chr15:55530654-55532559	K562	blood:	n/a	n/a
9	ARID3A	chr15:55552870-55553285	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:55547675-55547685	K562	blood:	n/a	n/a
11	ARID3A	chr15:55542492-55543043	HepG2	liver:	n/a	n/a
12	ARID3A	chr15:55571700-55572175	HepG2	liver:	n/a	n/a
13	ARID3A	chr15:55571287-55572489	K562	blood:	n/a	n/a
14	ARID3A	chr15:55578355-55578439	K562	blood:	n/a	n/a
15	ARID3A	chr15:55559634-55560031	K562	blood:	n/a	n/a
16	ATF1	chr15:55571782-55572252	K562	blood:	n/a	n/a
17	ATF1	chr15:55531712-55532710	K562	blood:	n/a	n/a
18	ATF1	chr15:55611017-55611627	K562	blood:	n/a	n/a
19	ATF1	chr15:55547268-55547416	K562	blood:	n/a	n/a
20	ATF1	chr15:55574440-55574824	K562	blood:	n/a	n/a
21	ATF1	chr15:55578747-55579084	K562	blood:	n/a	n/a
22	ATF2	chr15:55610860-55611517	GM12878	blood:	n/a	n/a
23	ATF2	chr15:55582700-55583050	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr15:55581834-55583029	GM12878	blood:	n/a	n/a
25	ATF2	chr15:55571619-55572737	GM12878	blood:	n/a	n/a
26	ATF2	chr15:55571687-55572736	GM12878	blood:	n/a	n/a
27	ATF2	chr15:55582132-55582686	GM12878	blood:	n/a	n/a
28	ATF2	chr15:55547721-55548440	GM12878	blood:	n/a	n/a
29	ATF2	chr15:55610849-55611625	GM12878	blood:	n/a	n/a
30	ATF2	chr15:55568824-55569817	GM12878	blood:	n/a	n/a
31	ATF2	chr15:55569066-55569831	GM12878	blood:	n/a	n/a
32	ATF3	chr15:55611075-55611605	A549	lung:	n/a	n/a
33	ATF3	chr15:55571938-55572177	K562	blood:	n/a	n/a
34	ATF3	chr15:55574419-55574817	K562	blood:	n/a	n/a
35	ATF3	chr15:55611094-55611636	A549	lung:	n/a	n/a
36	ATF3	chr15:55571773-55572313	K562	blood:	n/a	n/a
37	ATF3	chr15:55582555-55583026	A549	lung:	n/a	n/a
38	ATF3	chr15:55559648-55559988	K562	blood:	n/a	n/a
39	BACH1	chr15:55582872-55582986	K562	blood:	n/a	n/a
40	BACH1	chr15:55582697-55583094	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr15:55571797-55572568	K562	blood:	n/a	chr15:55572032-55572046
42	BATF	chr15:55548428-55548851	GM12878	blood:	n/a	n/a
43	BATF	chr15:55571856-55572580	GM12878	blood:	n/a	chr15:55572036-55572046
44	BATF	chr15:55569207-55569657	GM12878	blood:	n/a	n/a
45	BATF	chr15:55569137-55569735	GM12878	blood:	n/a	n/a
46	BATF	chr15:55571852-55572569	GM12878	blood:	n/a	chr15:55572036-55572046
47	BATF	chr15:55610929-55611200	GM12878	blood:	n/a	n/a
48	BCL11A	chr15:55571804-55572354	GM12878	blood:	n/a	chr15:55572035-55572044 chr15:55572034-55572043
49	BCL11A	chr15:55569282-55569581	GM12878	blood:	n/a	n/a
50	BCL11A	chr15:55569181-55569757	GM12878	blood:	n/a	n/a

(count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55582248-55582298	ProgFib	skin:	n/a
2	chr15:55582248-55582298	ProgFib	skin:	n/a
3	chr15:55582808-55582858	NT2-D1	testis:	n/a
4	chr15:55562773-55562823	A549	lung:	n/a
5	chr15:55582570-55582620	AG09319	gingival:	n/a
6	chr15:55582159-55582209	HAEpiC	amniotic membrane:	n/a
7	chr15:55581420-55581470	HCF	heart:	n/a
8	chr15:55611086-55611136	HUVEC	blood vessel:	n/a
9	chr15:55582570-55582620	HEK293	kidney:	embryo
10	chr15:55582494-55582544	SK-N-SH_RA	brain:	n/a
11	chr15:55583094-55583144	PFSK-1	brain:	n/a
12	chr15:55610624-55610674	GM06990	blood:	n/a
13	chr15:55604363-55604413	NHDF-neo	bronchial:	n/a
14	chr15:55562773-55562823	MCF10A-Er-Src	breast:	n/a
15	chr15:55604363-55604413	HRCEpiC	kidney:	n/a
16	chr15:55583094-55583144	HCF	heart:	n/a
17	chr15:55582808-55582858	GM19239	blood:	n/a
18	chr15:55582165-55582215	ovcar-3	ovarian:	n/a
19	chr15:55559759-55559809	NHBE	bronchial:	n/a
20	chr15:55582808-55582858	HCF	heart:	n/a
21	chr15:55543264-55543314	GM06990	blood:	n/a
22	chr15:55594433-55594483	HepG2	liver:	n/a
23	chr15:55581420-55581470	AoSMC	blood vessel:	n/a
24	chr15:55563985-55564035	HRE	kidney:	n/a
25	chr15:55562699-55562749	AG04450	lung:	fetal
26	chr15:55563985-55564035	GM06990	blood:	n/a
27	chr15:55582248-55582298	NHDF-neo	bronchial:	n/a
28	chr15:55582808-55582858	MCF-7	breast:	n/a
29	chr15:55543264-55543314	NHDF-neo	bronchial:	n/a
30	chr15:55563294-55563344	NHDF-neo	bronchial:	n/a
31	chr15:55582165-55582215	HRPEpiC	eye:	n/a
32	chr15:55562699-55562749	AG09309	skin:	n/a
33	chr15:55582159-55582209	HEK293	kidney:	embryo
34	chr15:55610624-55610674	BJ	skin:	n/a
35	chr15:55582165-55582215	GM06990	blood:	n/a
36	chr15:55562773-55562823	GM12878	blood:	n/a
37	chr15:55579397-55579447	HCM	heart:	n/a
38	chr15:55582248-55582298	AG09309	skin:	n/a
39	chr15:55563985-55564035	HNPCEpiC	eye:	n/a
40	chr15:55585235-55585285	SKMC	muscle:	n/a
41	chr15:55604363-55604413	AG09309	skin:	n/a
42	chr15:55582494-55582544	HUVEC	blood vessel:	n/a
43	chr15:55574912-55574962	HMEC	breast:	n/a
44	chr15:55564203-55564253	AG09319	gingival:	n/a
45	chr15:55594433-55594483	Jurkat	blood:	n/a
46	chr15:55581420-55581470	T-47D	breast:	n/a
47	chr15:55559759-55559809	GM12878	blood:	n/a
48	chr15:55579397-55579447	GM12891	blood:	n/a
49	chr15:55562773-55562823	SK-N-SH_RA	brain:	n/a
50	chr15:55581420-55581470	PANC-1	pancreas:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:55607682..55613892-chr15:55697623..55703247,7	K562	blood:
2	chr15:55530634..55534857-chr15:55538048..55543600,7	K562	blood:
3	chr15:55582045..55582784-chr17:41392767..41393534,2	Hela-S3	cervix:
4	chr15:55538847..55540639-chr15:55576116..55578035,2	MCF-7	breast:
5	chr15:55532146..55535139-chr15:55535159..55539232,4	K562	blood:
6	chr15:55540071..55542542-chr15:55580150..55582152,2	K562	blood:
7	chr15:55609847..55611398-chr15:55646178..55648636,2	K562	blood:
8	chr15:55531824..55534011-chr15:55559781..55562269,2	K562	blood:
9	chr15:55607488..55610247-chr15:55633602..55635929,2	K562	blood:
10	chr15:55542658..55546534-chr15:55547557..55552018,8	K562	blood:
11	chr15:55542912..55546349-chr15:55547649..55552018,4	K562	blood:
12	chr15:55531291..55533361-chr15:55609048..55611784,2	K562	blood:
13	chr15:55520021..55524159-chr15:55571941..55574919,3	K562	blood:
14	chr15:55546620..55548726-chr15:55579934..55582507,2	K562	blood:
15	chr15:55532208..55534403-chr15:55539105..55541114,2	MCF-7	breast:
16	chr15:55556814..55559793-chr15:55572719..55574257,2	K562	blood:
17	chr15:55576187..55578993-chr15:55609821..55611472,2	MCF-7	breast:
18	chr15:55509415..55510514-chr15:55582030..55583628,14	K562	blood:
19	chr15:55533451..55535034-chr15:55546175..55548758,2	K562	blood:
20	chr15:55545068..55547245-chr15:55548982..55551880,2	MCF-7	breast:
21	chr15:55556814..55559793-chr15:55572719..55574257,2	K562	blood:
22	chr15:55610027..55612992-chr15:55688713..55692198,3	K562	blood:
23	chr15:55579894..55582757-chr15:55689915..55691723,2	K562	blood:
24	chr15:55572408..55575581-chr15:55726220..55729674,3	K562	blood:
25	chr15:55553510..55555776-chr15:55556679..55558459,2	MCF-7	breast:
26	chr15:55579295..55584870-chr15:55607881..55612970,10	K562	blood:
27	chr15:55531824..55534011-chr15:55559781..55562269,2	K562	blood:
28	chr15:55529753..55531504-chr15:55533201..55534943,2	K562	blood:
29	chr15:55563023..55565322-chr15:55568988..55571105,2	K562	blood:
30	chr15:55523751..55526514-chr15:55535362..55537475,2	K562	blood:
31	chr15:55485173..55489207-chr15:55609824..55611374,3	K562	blood:
32	chr15:55528685..55531049-chr15:55537192..55539121,2	MCF-7	breast:
33	chr15:55542912..55546349-chr15:55547649..55552018,4	K562	blood:
34	chr15:55529177..55531366-chr15:55559639..55562184,2	K562	blood:
35	chr15:55499772..55503303-chr15:55582922..55584824,3	K562	blood:
36	chr15:55563892..55565494-chr15:55566396..55568632,2	K562	blood:
37	chr15:55611060..55611901-chr3:128968118..128968744,2	Hela-S3	cervix:
38	chr15:55549763..55552169-chr15:55552285..55555168,2	K562	blood:
39	chr15:55511874..55516207-chr15:55570260..55572623,4	K562	blood:
40	chr15:55558293..55561051-chr15:55570591..55574257,3	K562	blood:
41	chr15:55579295..55584870-chr15:55607881..55612970,10	K562	blood:
42	chr15:55462838..55463684-chr15:55582353..55582908,2	K562	blood:
43	chr15:55582304..55584506-chr15:55726191..55728043,2	MCF-7	breast:
44	chr15:55536038..55538985-chr15:55542222..55544123,2	K562	blood:
45	chr15:55485508..55492313-chr15:55579801..55583590,12	K562	blood:
46	chr15:55542658..55546534-chr15:55547557..55552018,8	K562	blood:
47	chr15:55509907..55510441-chr15:55581136..55581807,2	MCF-7	breast:
48	chr15:55575274..55577450-chr15:55698113..55700653,2	K562	blood:
49	chr15:55538847..55540639-chr15:55576116..55578035,2	MCF-7	breast:
50	chr15:55488197..55490619-chr15:55563570..55565134,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCPG1-1	chr15:55606218-55606358	NONHSAT043986
2	lnc-CCPG1-1	chr15:55582086-55582594	NONHSAT043986
3	lnc-RSL24D1-2	chr15:55581914-55581989	NONHSAT043985
4	lnc-RSL24D1-2	chr15:55562363-55562482	NONHSAT043984
5	lnc-CCPG1-1	chr15:55609902-55610065	ENSG00000225973.3
6	lnc-RSL24D1-2	chr15:55581914-55582011	NONHSAT043984
7	lnc-RSL24D1-2	chr15:55561992-55562482	NONHSAT043985
8	lnc-CCPG1-1	chr15:55611099-55611305	ENSG00000225973.3

No data

Variant related genes	Relation type
PIGB	TF binding region
RAB27A	TF binding region
PIGB	CpG island
RAB27A	CpG island
ENSG00000199347	chromatin interactions
ENSG00000225973	chromatin interactions
ENSG00000069974	chromatin interactions
ENSG00000138279	chromatin interactions
ENSG00000261652	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000181789	chromatin interactions
ENSG00000256061	chromatin interactions
ENSG00000260916	chromatin interactions
ENSG00000124795	chromatin interactions
ENSG00000069943	chromatin interactions
ENSG00000137876	chromatin interactions
ENSG00000261771	chromatin interactions
ENSG00000167565	chromatin interactions

Extended variants
information (count: 3349 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3349 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2444039	chr15:55532211-55532212	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74015534	chr15:55532216-55532217	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs569704614	chr15:55532222-55532223	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs539308345	chr15:55532228-55532229	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs184327074	chr15:55532230-55532231	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs58797842	chr15:55532294-55532295	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs534912599	chr15:55532320-55532321	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs554609241	chr15:55532348-55532349	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs74015535	chr15:55532369-55532370	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs537175940	chr15:55532389-55532390	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs571766064	chr15:55532398-55532399	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs570180181	chr15:55532446-55532447	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs188306353	chr15:55532447-55532448	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs545242246	chr15:55532460-55532461	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs180869226	chr15:55532486-55532487	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs532725240	chr15:55532647-55532648	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs7170936	chr15:55532655-55532656	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572172198	chr15:55532685-55532686	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs540893069	chr15:55532741-55532742	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs530032907	chr15:55532752-55532753	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs8030426	chr15:55532782-55532783	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs529801078	chr15:55532800-55532801	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs543584937	chr15:55532811-55532812	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs563268621	chr15:55532938-55532939	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs532012415	chr15:55532958-55532959	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs566386232	chr15:55532982-55532983	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs566175949	chr15:55533002-55533003	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566256809	chr15:55533058-55533059	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs535316878	chr15:55533140-55533141	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs528656201	chr15:55533194-55533195	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs141901601	chr15:55533215-55533216	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs61585844	chr15:55533237-55533238	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73409884	chr15:55533255-55533256	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557039889	chr15:55533307-55533308	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs570785371	chr15:55533344-55533345	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs186069083	chr15:55533346-55533347	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs558790383	chr15:55533352-55533353	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs572227852	chr15:55533441-55533442	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs475104	chr15:55533449-55533450	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554796727	chr15:55533516-55533517	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555010100	chr15:55533614-55533615	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574731629	chr15:55533632-55533633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs145765297	chr15:55533677-55533678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147779158	chr15:55533682-55533683	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538081244	chr15:55533709-55533710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532095851	chr15:55533733-55533734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545503975	chr15:55533750-55533751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs7176528	chr15:55533756-55533757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs189407541	chr15:55533793-55533794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs58693379	chr15:55533799-55533800	Weak transcription Enhancers	Chromatin interactive 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
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	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
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:2587 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55489800-55540200	Weak transcription	Esophagus	oesophagus
2	chr15:55490000-55562800	Weak transcription	Ovary	ovary
3	chr15:55509400-55541600	Weak transcription	Small Intestine	intestine
4	chr15:55512800-55541600	Weak transcription	Colonic Mucosa	Colon
5	chr15:55513400-55532400	Weak transcription	Left Ventricle	heart
6	chr15:55514200-55532600	Weak transcription	Psoas Muscle	Psoas
7	chr15:55514200-55540400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr15:55514200-55545200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr15:55514400-55541200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr15:55514600-55534200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr15:55514600-55542600	Weak transcription	Hela-S3	cervix
12	chr15:55514600-55543200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr15:55514800-55532600	Weak transcription	Adipose Nuclei	Adipose
14	chr15:55514800-55539800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr15:55514800-55560400	Weak transcription	Spleen	Spleen
16	chr15:55516000-55559600	Weak transcription	Fetal Stomach	stomach
17	chr15:55517600-55542800	Weak transcription	Thymus	Thymus
18	chr15:55517800-55532400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr15:55517800-55539600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr15:55517800-55542200	Weak transcription	Fetal Thymus	thymus
21	chr15:55517800-55542800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr15:55518000-55539200	Weak transcription	Fetal Lung	lung
23	chr15:55518600-55533600	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr15:55518600-55539400	Weak transcription	Placenta	Placenta
25	chr15:55518800-55541200	Weak transcription	Aorta	Aorta
26	chr15:55520800-55574800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr15:55521000-55541400	Weak transcription	Fetal Intestine Large	intestine
28	chr15:55522400-55532400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr15:55522800-55532400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr15:55522800-55532600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr15:55522800-55534200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr15:55522800-55540600	Weak transcription	Liver	Liver
33	chr15:55522800-55543200	Weak transcription	Pancreas	Pancrea
34	chr15:55522800-55547000	Weak transcription	GM12878-XiMat	blood
35	chr15:55523200-55542600	Weak transcription	HMEC	breast
36	chr15:55523600-55533200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr15:55526800-55537200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr15:55526800-55543200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr15:55527000-55532400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr15:55527000-55534600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr15:55527000-55542400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:55527000-55544200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr15:55527200-55538800	Weak transcription	Primary B cells from cord blood	blood
44	chr15:55527200-55542800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr15:55529800-55533000	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr15:55530200-55532600	Flanking Active TSS	K562	blood
47	chr15:55530600-55532400	Enhancers	Stomach Mucosa	stomach
48	chr15:55531000-55532400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr15:55531400-55532600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr15:55531600-55533400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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