Variant report

Variant	nsv984092
Chromosome Location	chr15:75970252-76000687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1401)
CpG islands
(count:976)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1401 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:75986626-75987312	K562	blood:	n/a	n/a
2	ARID3A	chr15:75987000-75987105	HepG2	liver:	n/a	n/a
3	ATF1	chr15:75986586-75987209	K562	blood:	n/a	n/a
4	ATF2	chr15:75988549-75988945	GM12878	blood:	n/a	n/a
5	ATF3	chr15:75986573-75987269	K562	blood:	n/a	n/a
6	ATF3	chr15:75986648-75987248	K562	blood:	n/a	n/a
7	BACH1	chr15:75986754-75987068	K562	blood:	n/a	n/a
8	BCL11A	chr15:75995022-75995273	GM12878	blood:	n/a	chr15:75995230-75995243
9	BCL11A	chr15:75992456-75992745	GM12878	blood:	n/a	n/a
10	BCL3	chr15:75998090-75998447	GM12878	blood:	n/a	n/a
11	BCL3	chr15:75979972-75980353	GM12878	blood:	n/a	n/a
12	BCL3	chr15:75998593-75998914	GM12878	blood:	n/a	chr15:75998657-75998666
13	BCL3	chr15:75998653-75998924	GM12878	blood:	n/a	chr15:75998657-75998666
14	BCL3	chr15:75979999-75980412	GM12878	blood:	n/a	n/a
15	BCL3	chr15:75998102-75998419	GM12878	blood:	n/a	n/a
16	BCL3	chr15:75975984-75976323	A549	lung:	n/a	n/a
17	BCL3	chr15:75986721-75987254	A549	lung:	n/a	n/a
18	BCL3	chr15:75986788-75987358	K562	blood:	n/a	n/a
19	BCLAF1	chr15:75986700-75987309	K562	blood:	n/a	n/a
20	BHLHE40	chr15:75976192-75976335	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:75987645-75987751	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:75978629-75978835	K562	blood:	n/a	n/a
23	BHLHE40	chr15:75992472-75992688	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:75988709-75988744	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:75986597-75987360	K562	blood:	n/a	chr15:75987181-75987197
26	BRCA1	chr15:75976163-75976363	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr15:75978535-75978880	K562	blood:	n/a	n/a
28	CBX3	chr15:75986422-75987613	K562	blood:	n/a	n/a
29	CBX3	chr15:75986644-75987144	K562	blood:	n/a	n/a
30	CCNT2	chr15:75986671-75987331	K562	blood:	n/a	chr15:75987032-75987052 chr15:75986746-75986755 chr15:75987279-75987288
31	CEBPB	chr15:75988734-75988953	IMR90	lung:	n/a	n/a
32	CEBPB	chr15:75976194-75976289	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr15:75986618-75987302	K562	blood:	n/a	n/a
34	CEBPB	chr15:75976092-75976290	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr15:75986901-75987593	GM12878	blood:	n/a	n/a
36	CEBPB	chr15:75988829-75988877	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:75986547-75987285	K562	blood:	n/a	n/a
38	CEBPB	chr15:75978678-75978827	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPD	chr15:75986444-75987440	K562	blood:	n/a	n/a
40	CEBPD	chr15:75986550-75987425	K562	blood:	n/a	n/a
41	CHD1	chr15:75975711-75976483	IMR90	lung:	n/a	n/a
42	CHD2	chr15:75976076-75976343	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr15:75987547-75987820	GM12878	blood:	n/a	n/a
44	CHD2	chr15:75988065-75988103	GM12878	blood:	n/a	n/a
45	CHD2	chr15:75988644-75988827	GM12878	blood:	n/a	n/a
46	CHD2	chr15:75992763-75992840	GM12878	blood:	n/a	n/a
47	CREB1	chr15:75986562-75987415	K562	blood:	n/a	n/a
48	CREB1	chr15:75976164-75976472	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr15:75978600-75978750	GM12869	blood:	n/a	chr15:75978712-75978733 chr15:75978710-75978728 chr15:75978711-75978727
50	CTCF	chr15:75978600-75978750	AG09319	gingival:	n/a	chr15:75978712-75978733 chr15:75978710-75978728 chr15:75978711-75978727

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75976099-75976149	PANC-1	pancreas:	n/a
2	chr15:75974684-75974734	MCF10A-Er-Src	breast:	n/a
3	chr15:75980285-75980335	HRCEpiC	kidney:	n/a
4	chr15:75981489-75981539	AG09309	skin:	n/a
5	chr15:75975061-75975111	BE2_C	brain:	n/a
6	chr15:75986363-75986413	PANC-1	pancreas:	n/a
7	chr15:75981391-75981441	AG09319	gingival:	n/a
8	chr15:75975227-75975277	AG04450	lung:	fetal
9	chr15:75982408-75982458	ovcar-3	ovarian:	n/a
10	chr15:75982408-75982458	U87	brain:	n/a
11	chr15:75975227-75975277	NH-A	brain:	n/a
12	chr15:75982408-75982458	HEK293	kidney:	embryo
13	chr15:75978121-75978171	HAEpiC	amniotic membrane:	n/a
14	chr15:75972447-75972497	HEEpiC	esophagus:	n/a
15	chr15:75978121-75978171	HRE	kidney:	n/a
16	chr15:75980285-75980335	ProgFib	skin:	n/a
17	chr15:75981968-75982018	GM19239	blood:	n/a
18	chr15:75975061-75975111	PrEC	prostate:	n/a
19	chr15:75972447-75972497	NHDF-neo	bronchial:	n/a
20	chr15:75986581-75986631	SKMC	muscle:	n/a
21	chr15:75981391-75981441	NH-A	brain:	n/a
22	chr15:75981968-75982018	GM12878	blood:	n/a
23	chr15:75981489-75981539	GM06990	blood:	n/a
24	chr15:75986380-75986430	HepG2	liver:	n/a
25	chr15:75978121-75978171	HL-60	blood:	n/a
26	chr15:75974684-75974734	HepG2	liver:	n/a
27	chr15:75981391-75981441	HCM	heart:	n/a
28	chr15:75980037-75980087	H1-hESC	embryonic stem cell:	embryo
29	chr15:75981968-75982018	AG10803	skin:	n/a
30	chr15:75981968-75982018	HL-60	blood:	n/a
31	chr15:75986380-75986430	NH-A	brain:	n/a
32	chr15:75986363-75986413	GM12892	blood:	n/a
33	chr15:75980037-75980087	AG09309	skin:	n/a
34	chr15:75980285-75980335	HCPEpiC	choroid plexus:	n/a
35	chr15:75975041-75975091	A549	lung:	n/a
36	chr15:75975041-75975091	ProgFib	skin:	n/a
37	chr15:75982408-75982458	AG09309	skin:	n/a
38	chr15:75981968-75982018	HAEpiC	amniotic membrane:	n/a
39	chr15:75980037-75980087	HIPEpiC	eye:	n/a
40	chr15:75975041-75975091	BJ	skin:	n/a
41	chr15:75975061-75975111	GM12891	blood:	n/a
42	chr15:75980285-75980335	HL-60	blood:	n/a
43	chr15:75975061-75975111	SK-N-SH_RA	brain:	n/a
44	chr15:75986380-75986430	SK-N-MC	brain:	n/a
45	chr15:75981391-75981441	HAEpiC	amniotic membrane:	n/a
46	chr15:75980037-75980087	HPAEpiC	pulmonary alveolar:	n/a
47	chr15:75981968-75982018	HRCEpiC	kidney:	n/a
48	chr15:75981489-75981539	SK-N-MC	brain:	n/a
49	chr15:75972447-75972497	BJ	skin:	n/a
50	chr15:75981968-75982018	IMR90	lung:	fetal

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:75939888..75940630-chr15:75974609..75975564,2	MCF-7	breast:
2	chr15:75978056..75979175-chr15:76013173..76013818,3	MCF-7	breast:
3	chr15:75870147..75872073-chr15:75974509..75976090,2	MCF-7	breast:
4	chr15:75504489..75506524-chr15:75971584..75974058,2	K562	blood:
5	chr15:75971018..75973050-chr15:75976828..75979527,2	K562	blood:
6	chr15:75868253..75872057-chr15:75972710..75976290,5	MCF-7	breast:
7	chr15:75963026..75964801-chr15:75971008..75973448,2	K562	blood:
8	chr15:75965361..75969270-chr15:75970035..75973000,4	K562	blood:
9	chr15:75973092..75975055-chr15:75975527..75978110,2	MCF-7	breast:
10	chr15:75988253..75990634-chr15:75998621..76001353,2	MCF-7	breast:
11	chr15:75917916..75920303-chr15:75970982..75973343,2	K562	blood:
12	chr15:75975803..75976315-chr15:78195454..78196010,2	K562	blood:
13	chr15:75929555..75932491-chr15:75973247..75974868,2	MCF-7	breast:
14	chr15:75978354..75979242-chr15:76013198..76014075,3	MCF-7	breast:
15	chr15:75680619..75682756-chr15:75973372..75975411,2	MCF-7	breast:
16	chr15:75889918..75890742-chr15:75975684..75976291,2	K562	blood:
17	chr15:75890174..75890978-chr15:75976106..75976698,2	MCF-7	breast:
18	chr15:75931756..75934593-chr15:75971947..75973695,3	K562	blood:
19	chr15:75967780..75970635-chr15:75975258..75976965,2	K562	blood:
20	chr15:75659585..75661797-chr15:75985686..75987280,3	K562	blood:
21	chr15:75969135..75972026-chr15:75974754..75976965,2	K562	blood:
22	chr15:75985273..75987777-chr15:76025449..76027210,2	K562	blood:
23	chr15:75985353..75988154-chr15:76080946..76082859,2	K562	blood:
24	chr15:75971018..75973050-chr15:75976828..75979527,2	K562	blood:
25	chr15:75988253..75990634-chr15:75998621..76001353,2	MCF-7	breast:
26	chr15:75746353..75748635-chr15:75987744..75989992,2	K562	blood:
27	chr15:75660217..75660799-chr15:75975793..75976725,5	K562	blood:
28	chr15:75930877..75932818-chr15:75977424..75979818,2	MCF-7	breast:
29	chr15:75916584..75920303-chr15:75971619..75973343,3	K562	blood:
30	chr15:75658228..75661982-chr15:75967267..75971746,4	K562	blood:
31	chr15:75658746..75661779-chr15:75974591..75977413,4	MCF-7	breast:
32	chr15:75976428..75978953-chr4:105982186..105984226,2	MCF-7	breast:
33	chr15:75967021..75968742-chr15:75972614..75974874,2	K562	blood:
34	chr15:75659345..75662146-chr15:75971665..75975217,4	MCF-7	breast:
35	chr15:75746464..75749152-chr15:75974484..75977471,5	MCF-7	breast:
36	chr15:75973092..75975055-chr15:75975527..75978110,2	MCF-7	breast:
37	chr15:75745181..75746690-chr15:75968871..75970441,2	MCF-7	breast:
38	chr15:75978476..75979174-chr15:78192448..78193224,3	MCF-7	breast:
39	chr15:75932588..75933144-chr15:75974522..75975361,2	MCF-7	breast:
40	chr15:75977113..75977773-chr15:76094531..76095051,2	MCF-7	breast:
41	chr15:75978548..75980308-chr15:76018385..76020892,2	K562	blood:
42	chr15:75931027..75932851-chr15:75970430..75972051,3	MCF-7	breast:
43	chr15:75937337..75939364-chr15:75984333..75987165,2	MCF-7	breast:
44	chr15:75978451..75979139-chr15:78192424..78193254,5	MCF-7	breast:
45	chr15:75978647..75979179-chr15:76094246..76094786,2	MCF-7	breast:
46	chr15:75743029..75745161-chr15:75973200..75975375,2	K562	blood:
47	chr15:75985843..75987761-chr15:76194772..76196422,2	K562	blood:
48	chr15:75987941..75988697-chr15:76013170..76014036,2	MCF-7	breast:
49	chr15:75986266..75989100-chr15:76049527..76052289,2	MCF-7	breast:
50	chr15:75799442..75801004-chr15:75975056..75976624,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000203392	TF binding region
ENSG00000203392	CpG island
ENSG00000140400	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000169371	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000167196	chromatin interactions
ENSG00000169410	chromatin interactions
ENSG00000261779	chromatin interactions
ENSG00000260892	chromatin interactions
ENSG00000260274	chromatin interactions
ENSG00000260288	chromatin interactions
ENSG00000173548	chromatin interactions
ENSG00000260235	chromatin interactions
ENSG00000203392	chromatin interactions

Extended variants
information (count: 1415 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75696622	chr15:75970267-75970268	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs188051535	chr15:75970300-75970301	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs117555715	chr15:75970327-75970328	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs113692091	chr15:75970354-75970355	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs190925327	chr15:75970376-75970377	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs373925473	chr15:75970421-75970422	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs138967830	chr15:75970451-75970452	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs540759129	chr15:75970452-75970453	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs369505675	chr15:75970476-75970477	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs562252118	chr15:75970480-75970481	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs529532615	chr15:75970552-75970553	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs550989768	chr15:75970570-75970571	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs78164991	chr15:75970616-75970617	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs182491502	chr15:75970617-75970618	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs372755334	chr15:75970625-75970626	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs532753681	chr15:75970633-75970634	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs146407279	chr15:75970655-75970656	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs377167580	chr15:75970672-75970673	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs71941668	chr15:75970685-75970686	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs372666061	chr15:75970691-75970692	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs57332159	chr15:75970692-75970693	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs188003805	chr15:75970755-75970756	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs555080071	chr15:75970799-75970800	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs567343954	chr15:75970835-75970836	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs78061890	chr15:75970860-75970861	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs113233015	chr15:75970885-75970886	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs192492154	chr15:75970924-75970925	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs368370366	chr15:75970926-75970927	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs371786826	chr15:75970932-75970933	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs546190712	chr15:75970933-75970934	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs184923522	chr15:75970962-75970963	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs187382316	chr15:75970997-75970998	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs540720453	chr15:75971046-75971047	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs192213244	chr15:75971084-75971085	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs184774897	chr15:75971087-75971088	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs376845947	chr15:75971105-75971106	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs142528793	chr15:75971114-75971115	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs559553965	chr15:75971177-75971178	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs573183394	chr15:75971199-75971200	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs370322872	chr15:75971225-75971226	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs551687880	chr15:75971239-75971240	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs566118628	chr15:75971272-75971273	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs569269881	chr15:75971280-75971281	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs527330229	chr15:75971297-75971298	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs548620113	chr15:75971325-75971326	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs567362580	chr15:75971362-75971363	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs573429806	chr15:75971415-75971416	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs189475238	chr15:75971423-75971424	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs35351373	chr15:75971424-75971425	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs571379922	chr15:75971435-75971436	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
XY gonadal dysgenesis	20685758	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75965600-75978400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr15:75965800-75986000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:75966000-75972400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr15:75966200-75971000	Weak transcription	NHEK	skin
5	chr15:75966200-75971200	Genic enhancers	Fetal Intestine Small	intestine
6	chr15:75966200-75974400	Weak transcription	Pancreas	Pancrea
7	chr15:75966400-75972600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr15:75966400-75972800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr15:75966400-75979000	Weak transcription	HMEC	breast
10	chr15:75966400-75993200	Weak transcription	Hela-S3	cervix
11	chr15:75966600-75986000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr15:75966800-75970400	Genic enhancers	Fetal Muscle Trunk	muscle
13	chr15:75966800-75971000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:75966800-75973600	Weak transcription	Fetal Lung	lung
15	chr15:75966800-75985600	Weak transcription	Osteobl	bone
16	chr15:75967000-75970400	Genic enhancers	Fetal Muscle Leg	muscle
17	chr15:75967200-75970400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr15:75967400-75976600	Weak transcription	NH-A	brain
19	chr15:75967600-75975400	Strong transcription	Colon Smooth Muscle	Colon
20	chr15:75968000-75985600	Strong transcription	Fetal Stomach	stomach
21	chr15:75968200-75971000	Weak transcription	NHDF-Ad	bronchial
22	chr15:75968200-75974600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:75968200-75974600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr15:75968200-75975000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr15:75968200-75985800	Weak transcription	Left Ventricle	heart
26	chr15:75968400-75971800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr15:75968400-75972800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr15:75968400-75976800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:75968400-75984600	Strong transcription	NHLF	lung
30	chr15:75968400-75985000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr15:75968400-75985600	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr15:75968600-75971200	Strong transcription	Stomach Smooth Muscle	stomach
33	chr15:75968600-75975800	Strong transcription	Duodenum Smooth Muscle	Duodenum
34	chr15:75968600-75976000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr15:75968600-75978000	Strong transcription	Aorta	Aorta
36	chr15:75968800-75970600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:75968800-75970600	Genic enhancers	Fetal Intestine Large	intestine
38	chr15:75968800-75972000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr15:75968800-75974800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr15:75968800-75975800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr15:75968800-75980400	Weak transcription	Brain Substantia Nigra	brain
42	chr15:75968800-75985600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr15:75969000-75970600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr15:75969200-75974600	Weak transcription	Gastric	stomach
45	chr15:75969200-75975800	Weak transcription	Colonic Mucosa	Colon
46	chr15:75969200-75980000	Weak transcription	Lung	lung
47	chr15:75969200-75985800	Weak transcription	Right Atrium	heart
48	chr15:75969600-75970400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr15:75969600-75970400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr15:75969600-75970400	Genic enhancers	Skeletal Muscle Female	skeletal muscle

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