Variant report

Variant	nsv819520
Chromosome Location	chr15:75819453-75865881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:420)
CpG islands
(count:183)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:75824822-75825149	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:75857762-75858126	K562	blood:	n/a	n/a
3	ARID3A	chr15:75837428-75837557	K562	blood:	n/a	n/a
4	ATF1	chr15:75862639-75862664	K562	blood:	n/a	n/a
5	ATF1	chr15:75837337-75837610	K562	blood:	n/a	n/a
6	ATF1	chr15:75824867-75825158	K562	blood:	n/a	n/a
7	BACH1	chr15:75824813-75824969	K562	blood:	n/a	n/a
8	BHLHE40	chr15:75846026-75846125	K562	blood:	n/a	n/a
9	BRCA1	chr15:75824914-75825048	HepG2	liver:	n/a	n/a
10	CBX3	chr15:75851691-75852009	K562	blood:	n/a	n/a
11	CEBPB	chr15:75834604-75834964	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr15:75834613-75834972	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr15:75835683-75835995	A549	lung:	n/a	n/a
14	CEBPB	chr15:75834608-75834914	K562	blood:	n/a	n/a
15	CEBPB	chr15:75820264-75820294	K562	blood:	n/a	n/a
16	CEBPB	chr15:75845180-75845418	K562	blood:	n/a	n/a
17	CEBPB	chr15:75865367-75865705	A549	lung:	n/a	n/a
18	CEBPB	chr15:75858115-75858327	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr15:75843611-75843751	A549	lung:	n/a	n/a
20	CEBPB	chr15:75865356-75865705	IMR90	lung:	n/a	n/a
21	CEBPB	chr15:75823823-75824098	K562	blood:	n/a	n/a
22	CEBPB	chr15:75857998-75858390	IMR90	lung:	n/a	n/a
23	CEBPD	chr15:75834788-75835238	K562	blood:	n/a	n/a
24	CEBPD	chr15:75834696-75835215	K562	blood:	n/a	n/a
25	CREB1	chr15:75824847-75825109	A549	lung:	n/a	n/a
26	CTCF	chr15:75857780-75857930	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr15:75824701-75825135	HepG2	liver:	n/a	chr15:75825114-75825123 chr15:75824928-75824937
28	CTCF	chr15:75859420-75859570	HCT-116	colon:	n/a	n/a
29	CTCF	chr15:75824840-75824990	K562	blood:	n/a	chr15:75824928-75824937
30	CTCF	chr15:75857781-75857854	GM10248	blood:	n/a	n/a
31	CTCF	chr15:75824820-75824970	AG09309	skin:	n/a	chr15:75824928-75824937
32	CTCF	chr15:75824820-75824970	AG09319	gingival:	n/a	chr15:75824928-75824937
33	CTCF	chr15:75824818-75825050	HepG2	liver:	n/a	chr15:75824928-75824937
34	CTCF	chr15:75824653-75825147	K562	blood:	n/a	chr15:75825114-75825123 chr15:75824928-75824937
35	CTCF	chr15:75824880-75825030	BE2_C	brain:	n/a	chr15:75824928-75824937
36	CTCF	chr15:75824920-75825070	GM12874	blood:	n/a	chr15:75824928-75824937
37	CTCF	chr15:75824861-75825023	Kidney_OC	kidney:	n/a	chr15:75824928-75824937
38	CTCF	chr15:75824840-75824990	HEK293	kidney:	n/a	chr15:75824928-75824937
39	CTCF	chr15:75824840-75824990	GM12801	blood:	n/a	chr15:75824928-75824937
40	CTCF	chr15:75857760-75857910	HMF	breast:	n/a	n/a
41	CTCF	chr15:75824900-75825050	AG04449	skin:	n/a	chr15:75824928-75824937
42	CTCF	chr15:75824880-75825030	GM12878	blood:	n/a	chr15:75824928-75824937
43	CTCF	chr15:75842554-75842594	Medullo	brain:	n/a	n/a
44	CTCF	chr15:75824748-75825033	H1-hESC	embryonic stem cell:	n/a	chr15:75824928-75824937
45	CTCF	chr15:75824785-75825214	IMR90	lung:	n/a	chr15:75825114-75825123 chr15:75824928-75824937
46	CTCF	chr15:75824960-75825110	NHEK	skin:	n/a	n/a
47	CTCF	chr15:75824754-75825141	K562	blood:	n/a	chr15:75825114-75825123 chr15:75824928-75824937
48	CTCF	chr15:75824880-75825030	HPAF	blood vessel:	n/a	chr15:75824928-75824937
49	CTCF	chr15:75824800-75824950	HCM	heart:	n/a	chr15:75824928-75824937
50	CTCF	chr15:75824840-75824990	GM12871	blood:	n/a	chr15:75824928-75824937

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75851548-75851598	MCF-7	breast:	n/a
2	chr15:75865604-75865654	AG09319	gingival:	n/a
3	chr15:75851548-75851598	BJ	skin:	n/a
4	chr15:75865604-75865654	SK-N-SH	brain:	n/a
5	chr15:75851548-75851598	PFSK-1	brain:	n/a
6	chr15:75865604-75865654	Hepatocyte	liver:	n/a
7	chr15:75851548-75851598	SAEC	small airway:	n/a
8	chr15:75835738-75835788	Hela-S3	cervix:	n/a
9	chr15:75865604-75865654	HepG2	liver:	n/a
10	chr15:75851548-75851598	AG04450	lung:	fetal
11	chr15:75835738-75835788	AG10803	skin:	n/a
12	chr15:75835738-75835788	SK-N-SH_RA	brain:	n/a
13	chr15:75851548-75851598	HRPEpiC	eye:	n/a
14	chr15:75835738-75835788	Jurkat	blood:	n/a
15	chr15:75851548-75851598	HEEpiC	esophagus:	n/a
16	chr15:75835738-75835788	Caco-2	colon:	n/a
17	chr15:75851548-75851598	HCPEpiC	choroid plexus:	n/a
18	chr15:75835738-75835788	NH-A	brain:	n/a
19	chr15:75865604-75865654	HEEpiC	esophagus:	n/a
20	chr15:75851548-75851598	HRCEpiC	kidney:	n/a
21	chr15:75835738-75835788	PrEC	prostate:	n/a
22	chr15:75865604-75865654	PrEC	prostate:	n/a
23	chr15:75865604-75865654	BE2_C	brain:	n/a
24	chr15:75851548-75851598	Jurkat	blood:	n/a
25	chr15:75835738-75835788	A549	lung:	n/a
26	chr15:75865604-75865654	PANC-1	pancreas:	n/a
27	chr15:75851548-75851598	ECC-1	luminal epithelium:	n/a
28	chr15:75851548-75851598	AoSMC	blood vessel:	n/a
29	chr15:75851548-75851598	ProgFib	skin:	n/a
30	chr15:75851548-75851598	HAEpiC	amniotic membrane:	n/a
31	chr15:75835738-75835788	AG09309	skin:	n/a
32	chr15:75851548-75851598	NH-A	brain:	n/a
33	chr15:75851548-75851598	Hepatocyte	liver:	n/a
34	chr15:75865604-75865654	ovcar-3	ovarian:	n/a
35	chr15:75851548-75851598	GM12892	blood:	n/a
36	chr15:75835738-75835788	HMEC	breast:	n/a
37	chr15:75851548-75851598	HRE	kidney:	n/a
38	chr15:75851548-75851598	IMR90	lung:	fetal
39	chr15:75835738-75835788	SK-N-SH	brain:	n/a
40	chr15:75851548-75851598	ovcar-3	ovarian:	n/a
41	chr15:75851548-75851598	PrEC	prostate:	n/a
42	chr15:75865604-75865654	HNPCEpiC	eye:	n/a
43	chr15:75865604-75865654	HMEC	breast:	n/a
44	chr15:75835738-75835788	HL-60	blood:	n/a
45	chr15:75851548-75851598	GM12891	blood:	n/a
46	chr15:75835738-75835788	GM12891	blood:	n/a
47	chr15:75865604-75865654	SAEC	small airway:	n/a
48	chr15:75835738-75835788	IMR90	lung:	fetal
49	chr15:75851548-75851598	HUVEC	blood vessel:	n/a
50	chr15:75865604-75865654	NHBE	bronchial:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:75859984..75863258-chr15:75866377..75869193,4	K562	blood:
2	chr15:75851394..75853425-chr15:75868272..75871108,2	K562	blood:
3	chr15:75856629..75858738-chr15:75865984..75868280,2	K562	blood:
4	chr15:75842828..75845197-chr15:75930996..75932704,2	K562	blood:
5	chr15:75743022..75744794-chr15:75864546..75866192,2	MCF-7	breast:
6	chr15:75860740..75863258-chr15:75866377..75868431,2	K562	blood:
7	chr15:75843940..75845891-chr15:75930880..75933630,3	MCF-7	breast:
8	chr15:75828987..75830600-chr15:75834894..75837866,2	MCF-7	breast:
9	chr15:75852657..75854166-chr15:75870160..75871943,2	MCF-7	breast:
10	chr15:75835718..75837782-chr15:75838863..75841785,2	K562	blood:
11	chr15:75823461..75825727-chr15:75832256..75834760,2	K562	blood:
12	chr15:75860084..75867497-chr15:75867809..75873787,11	MCF-7	breast:
13	chr15:75858252..75862761-chr15:75869329..75871763,6	K562	blood:
14	chr15:75835718..75837782-chr15:75838863..75841785,2	K562	blood:
15	chr15:75847388..75849839-chr15:75869858..75872339,2	MCF-7	breast:
16	chr15:75865359..75867704-chr15:75932021..75934061,2	MCF-7	breast:
17	chr15:75860072..75862994-chr15:75870067..75872547,2	K562	blood:
18	chr15:75823394..75827667-chr15:75930118..75933171,4	MCF-7	breast:
19	chr15:75824690..75826344-chr15:75835953..75838472,2	K562	blood:
20	chr15:75745002..75747584-chr15:75825328..75827934,2	K562	blood:
21	chr15:75853761..75856722-chr15:75869091..75870929,2	K562	blood:
22	chr15:75829509..75831948-chr15:75932181..75934351,2	MCF-7	breast:
23	chr15:75823461..75825727-chr15:75832256..75834760,2	K562	blood:
24	chr15:75863315..75865200-chr15:75868911..75871447,2	K562	blood:
25	chr15:75816718..75819055-chr15:75823449..75825405,3	MCF-7	breast:
26	chr15:75840878..75843615-chr15:75844264..75846206,2	K562	blood:
27	chr15:75853862..75856764-chr15:75868169..75871693,4	MCF-7	breast:
28	chr15:75854504..75856363-chr15:75868779..75870922,2	MCF-7	breast:
29	chr15:75817321..75818967-chr15:75847702..75849379,2	K562	blood:
30	chr15:75847269..75849470-chr15:75869744..75871872,2	MCF-7	breast:
31	chr15:75830608..75832951-chr15:75924851..75928314,3	MCF-7	breast:
32	chr15:75824690..75826344-chr15:75835953..75838472,2	K562	blood:
33	chr15:75814778..75817471-chr15:75819035..75821931,2	K562	blood:
34	chr15:75745273..75747975-chr15:75823616..75825294,2	MCF-7	breast:
35	chr15:75846082..75849079-chr15:75867653..75869638,2	K562	blood:
36	chr15:75862791..75867744-chr15:75868149..75872408,7	MCF-7	breast:
37	chr15:75864375..75868073-chr15:75869193..75873820,11	K562	blood:
38	chr15:75840878..75843615-chr15:75844264..75846206,2	K562	blood:
39	chr15:75851394..75854536-chr15:75867744..75871108,3	K562	blood:
40	chr15:75808443..75810760-chr15:75862466..75865367,2	K562	blood:

No data

Variant related genes	Relation type
PTPN9	TF binding region
ENSG00000203473	TF binding region
PTPN9	CpG island
ENSG00000203473	CpG island
ENSG00000203473	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000169410	chromatin interactions
ENSG00000177971	chromatin interactions

Extended variants
information (count: 1585 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1585 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146997520	chr15:75819463-75819464	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs538521905	chr15:75819487-75819488	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs114183309	chr15:75819488-75819489	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs375533645	chr15:75819584-75819585	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs113854779	chr15:75819585-75819586	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs114063444	chr15:75819594-75819595	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs369859591	chr15:75819601-75819602	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144732987	chr15:75819609-75819610	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs534176146	chr15:75819619-75819620	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs74026512	chr15:75819645-75819646	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369433612	chr15:75819646-75819647	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544753221	chr15:75819688-75819689	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563040065	chr15:75819698-75819699	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs184140006	chr15:75819723-75819724	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545328086	chr15:75819799-75819800	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76312251	chr15:75819811-75819812	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs528013236	chr15:75819817-75819818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs148545076	chr15:75819861-75819862	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117665130	chr15:75819864-75819865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs117301369	chr15:75819865-75819866	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529840916	chr15:75819891-75819892	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs549479465	chr15:75819925-75819926	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111549089	chr15:75819932-75819933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532346132	chr15:75819971-75819972	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542106534	chr15:75820054-75820055	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142915712	chr15:75820065-75820066	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561179545	chr15:75820066-75820067	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536581429	chr15:75820069-75820070	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs146132057	chr15:75820074-75820075	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370710421	chr15:75820103-75820104	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs140141325	chr15:75820184-75820185	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541275769	chr15:75820195-75820196	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs538316069	chr15:75820215-75820216	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs556619517	chr15:75820248-75820249	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544158238	chr15:75820256-75820257	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs550807754	chr15:75820296-75820297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370994350	chr15:75820325-75820326	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554115910	chr15:75820375-75820376	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115641276	chr15:75820409-75820410	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs572676777	chr15:75820439-75820440	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564520222	chr15:75820455-75820456	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542948229	chr15:75820473-75820474	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533240175	chr15:75820476-75820477	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs76551311	chr15:75820496-75820497	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531227361	chr15:75820499-75820500	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143867121	chr15:75820510-75820511	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs543444062	chr15:75820514-75820515	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562478463	chr15:75820536-75820537	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564983530	chr15:75820678-75820679	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs564332235	chr15:75820723-75820724	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75797800-75819600	Strong transcription	HUES6 Cell Line	embryonic stem cell
2	chr15:75797800-75819600	Strong transcription	Fetal Stomach	stomach
3	chr15:75797800-75820000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr15:75798400-75824800	Weak transcription	Stomach Mucosa	stomach
5	chr15:75798400-75825000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr15:75798800-75820400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:75799400-75821800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr15:75800600-75819800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:75801400-75820800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr15:75802400-75820000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr15:75802800-75819600	Strong transcription	Liver	Liver
12	chr15:75802800-75820000	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr15:75803200-75819800	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr15:75803200-75828000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr15:75803400-75819600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr15:75803400-75820200	Strong transcription	Fetal Intestine Small	intestine
17	chr15:75804400-75820000	Strong transcription	Fetal Muscle Leg	muscle
18	chr15:75804600-75819600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr15:75804600-75819600	Strong transcription	Lung	lung
20	chr15:75804800-75820000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr15:75805200-75819800	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr15:75808400-75819800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr15:75808600-75819600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:75808800-75819800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr15:75809000-75819800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr15:75809200-75819600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr15:75809200-75819600	Strong transcription	Fetal Muscle Trunk	muscle
28	chr15:75809200-75819800	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr15:75809400-75819600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr15:75809400-75819600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr15:75809400-75819600	Strong transcription	Adipose Nuclei	Adipose
32	chr15:75809400-75819800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr15:75809600-75819600	Strong transcription	Duodenum Mucosa	Duodenum
34	chr15:75809600-75819600	Strong transcription	Fetal Intestine Large	intestine
35	chr15:75809600-75819800	Strong transcription	Dnd41	blood
36	chr15:75809800-75821400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr15:75810000-75819600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr15:75810000-75820800	Strong transcription	A549	lung
39	chr15:75810000-75823400	Weak transcription	Right Atrium	heart
40	chr15:75811600-75819800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr15:75811800-75819600	Strong transcription	Thymus	Thymus
42	chr15:75812000-75819600	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr15:75812200-75819600	Strong transcription	Fetal Lung	lung
44	chr15:75812200-75819800	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr15:75812200-75820200	Strong transcription	Fetal Thymus	thymus
46	chr15:75814200-75819600	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr15:75814600-75826400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr15:75815000-75823400	Weak transcription	Psoas Muscle	Psoas
49	chr15:75816000-75823000	Weak transcription	Brain Germinal Matrix	brain
50	chr15:75816000-75823400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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