Variant report

Variant	nsv430258
Chromosome Location	chr10:92770145-92817973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:92803080-92803373	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:92794410-92794433	HepG2	liver:	n/a	n/a
3	BATF	chr10:92776965-92777256	GM12878	blood:	n/a	chr10:92777094-92777104 chr10:92777190-92777199 chr10:92777097-92777108 chr10:92777170-92777179 chr10:92777098-92777108
4	BRCA1	chr10:92796883-92796939	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr10:92814080-92814420	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr10:92792526-92792583	A549	lung:	n/a	chr10:92792568-92792581
7	CEBPB	chr10:92814176-92814377	IMR90	lung:	n/a	n/a
8	CEBPB	chr10:92814066-92814440	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr10:92808858-92808914	HepG2	liver:	n/a	chr10:92808883-92808896
10	CTCF	chr10:92803120-92803270	GM06990	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
11	CTCF	chr10:92803069-92803365	A549	lung:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
12	CTCF	chr10:92803140-92803290	Caco-2	colon:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
13	CTCF	chr10:92803060-92803210	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr10:92803120-92803270	NHDF-neo	bronchial:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
15	CTCF	chr10:92806880-92807030	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr10:92803142-92803280	GM13977	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
17	CTCF	chr10:92790120-92790270	GM12875	blood:	n/a	n/a
18	CTCF	chr10:92803120-92803270	HBMEC	blood vessel:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
19	CTCF	chr10:92802971-92803300	K562	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
20	CTCF	chr10:92803088-92803262	GM19239	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
21	CTCF	chr10:92803140-92803290	AG10803	skin:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
22	CTCF	chr10:92803113-92803283	GM10266	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
23	CTCF	chr10:92803140-92803290	HCT-116	colon:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
24	CTCF	chr10:92803240-92803390	GM12867	blood:	n/a	n/a
25	CTCF	chr10:92803120-92803270	GM12875	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
26	CTCF	chr10:92791740-92791890	GM12871	blood:	n/a	n/a
27	CTCF	chr10:92803160-92803310	AG04449	skin:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
28	CTCF	chr10:92803160-92803310	HA-sp	spinal cord:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
29	CTCF	chr10:92802969-92803448	HCT-116	colon:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
30	CTCF	chr10:92803060-92803210	GM12868	blood:	n/a	n/a
31	CTCF	chr10:92803100-92803250	GM12873	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
32	CTCF	chr10:92803140-92803290	WERI-Rb-1	eye:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
33	CTCF	chr10:92776640-92776790	GM12873	blood:	n/a	n/a
34	CTCF	chr10:92803068-92803267	A549	lung:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
35	CTCF	chr10:92803021-92803342	H1-hESC	embryonic stem cell:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
36	CTCF	chr10:92803095-92803275	SK-N-SH_RA	brain:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
37	CTCF	chr10:92776580-92776730	GM12865	blood:	n/a	n/a
38	CTCF	chr10:92803120-92803270	GM12878	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
39	CTCF	chr10:92803100-92803250	NHDF-neo	bronchial:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
40	CTCF	chr10:92803140-92803290	HAc	cerebellar:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
41	CTCF	chr10:92803200-92803350	GM06990	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
42	CTCF	chr10:92803120-92803270	GM12872	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
43	CTCF	chr10:92803098-92803311	HepG2	liver:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
44	CTCF	chr10:92803066-92803323	MCF-7	breast:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
45	CTCF	chr10:92803180-92803330	AG09309	skin:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
46	CTCF	chr10:92803180-92803330	GM12864	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
47	CTCF	chr10:92803092-92803223	GM12892	blood:	n/a	chr10:92803215-92803223
48	CTCF	chr10:92803120-92803270	HRPEpiC	eye:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
49	CTCF	chr10:92803120-92803270	GM12870	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
50	CTCF	chr10:92803096-92803329	K562	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:92810359-92810409	HCF	heart:	n/a
2	chr10:92794806-92794856	HAEpiC	amniotic membrane:	n/a
3	chr10:92783852-92783902	HCPEpiC	choroid plexus:	n/a
4	chr10:92794806-92794856	SK-N-SH_RA	brain:	n/a
5	chr10:92783852-92783902	SKMC	muscle:	n/a
6	chr10:92794806-92794856	HUVEC	blood vessel:	n/a
7	chr10:92810359-92810409	SAEC	small airway:	n/a
8	chr10:92783852-92783902	ProgFib	skin:	n/a
9	chr10:92783852-92783902	HIPEpiC	eye:	n/a
10	chr10:92794806-92794856	HRPEpiC	eye:	n/a
11	chr10:92794806-92794856	GM19239	blood:	n/a
12	chr10:92783852-92783902	BJ	skin:	n/a
13	chr10:92794806-92794856	GM12892	blood:	n/a
14	chr10:92810359-92810409	AG10803	skin:	n/a
15	chr10:92810359-92810409	ECC-1	luminal epithelium:	n/a
16	chr10:92794806-92794856	AoSMC	blood vessel:	n/a
17	chr10:92794806-92794856	T-47D	breast:	n/a
18	chr10:92794806-92794856	LNCaP	prostate:	n/a
19	chr10:92794806-92794856	SK-N-SH	brain:	n/a
20	chr10:92810359-92810409	AG09309	skin:	n/a
21	chr10:92810359-92810409	NB4	blood:	n/a
22	chr10:92783852-92783902	A549	lung:	n/a
23	chr10:92794806-92794856	IMR90	lung:	fetal
24	chr10:92810359-92810409	RPTEC	kidney:	n/a
25	chr10:92794806-92794856	NT2-D1	testis:	n/a
26	chr10:92810359-92810409	CMK	blood:	n/a
27	chr10:92810359-92810409	AoSMC	blood vessel:	n/a
28	chr10:92794806-92794856	HL-60	blood:	n/a
29	chr10:92783852-92783902	PANC-1	pancreas:	n/a
30	chr10:92810359-92810409	SK-N-SH	brain:	n/a
31	chr10:92783852-92783902	HRCEpiC	kidney:	n/a
32	chr10:92783852-92783902	ovcar-3	ovarian:	n/a
33	chr10:92810359-92810409	HAEpiC	amniotic membrane:	n/a
34	chr10:92794806-92794856	BJ	skin:	n/a
35	chr10:92810359-92810409	SKMC	muscle:	n/a
36	chr10:92810359-92810409	HEEpiC	esophagus:	n/a
37	chr10:92794806-92794856	U87	brain:	n/a
38	chr10:92810359-92810409	GM12878	blood:	n/a
39	chr10:92810359-92810409	A549	lung:	n/a
40	chr10:92810359-92810409	HRPEpiC	eye:	n/a
41	chr10:92794806-92794856	HEK293	kidney:	embryo
42	chr10:92794806-92794856	ovcar-3	ovarian:	n/a
43	chr10:92810359-92810409	PFSK-1	brain:	n/a
44	chr10:92783852-92783902	NB4	blood:	n/a
45	chr10:92794806-92794856	H1-hESC	embryonic stem cell:	embryo
46	chr10:92794806-92794856	HRCEpiC	kidney:	n/a
47	chr10:92794806-92794856	Hela-S3	cervix:	n/a
48	chr10:92794806-92794856	A549	lung:	n/a
49	chr10:92783852-92783902	CMK	blood:	n/a
50	chr10:92783852-92783902	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:92791172..92794052-chr10:92801075..92803431,2	MCF-7	breast:
2	chr10:92665895..92668775-chr10:92778505..92780416,2	K562	blood:
3	chr10:92791172..92794052-chr10:92801075..92803431,2	MCF-7	breast:
4	chr10:92802747..92803726-chr10:93010975..93011501,3	K562	blood:
5	chr10:92802749..92803570-chr10:93008473..93009291,2	MCF-7	breast:
6	chr10:92805073..92806604-chr10:92807653..92810163,2	K562	blood:
7	chr10:92768647..92770927-chr10:92793984..92796644,2	MCF-7	breast:
8	chr10:92768647..92770927-chr10:92793984..92796644,2	MCF-7	breast:
9	chr10:92805073..92806604-chr10:92807653..92810163,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD1-2	chr10:92795970-92796139	XLOC_008903
2	lnc-ANKRD1-2	chr10:92796888-92796960	XLOC_008903
3	lnc-RPP30-4	chr10:92807658-92807786	NONHSAT015618
4	lnc-RPP30-4	chr10:92806923-92807057	ENSG00000224851.1
5	lnc-ANKRD1-2	chr10:92793811-92794238	XLOC_008903
6	lnc-RPP30-4	chr10:92807658-92807786	ENSG00000224851.1
7	lnc-RPP30-4	chr10:92806769-92806875	NONHSAT015618
8	lnc-RPP30-4	chr10:92805565-92805687	NONHSAT015618

Variant related genes	Relation type
LINC00502	TF binding region
DDX18P6	TF binding region
LINC00502	CpG island
DDX18P6	CpG island

Extended variants
information (count: 1958 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7087402	chr10:92770145-92770146	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185702258	chr10:92770161-92770162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572108169	chr10:92770171-92770172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116333129	chr10:92770182-92770183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190232278	chr10:92770263-92770264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs199821070	chr10:92770266-92770267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377521242	chr10:92770308-92770309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376024427	chr10:92770316-92770317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138898319	chr10:92770319-92770320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140495840	chr10:92770361-92770362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563859230	chr10:92770395-92770396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531317815	chr10:92770397-92770398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545079877	chr10:92770417-92770418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28662270	chr10:92770422-92770423	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs527256186	chr10:92770476-92770477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76983888	chr10:92770485-92770486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182159757	chr10:92770490-92770491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112002656	chr10:92770536-92770537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549710660	chr10:92770541-92770542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569789994	chr10:92770596-92770597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538794844	chr10:92770617-92770618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558989201	chr10:92770657-92770658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149551363	chr10:92770715-92770716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374185860	chr10:92770717-92770718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542472271	chr10:92770718-92770719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565772544	chr10:92770750-92770751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11812810	chr10:92770755-92770756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75814387	chr10:92770833-92770834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138118471	chr10:92770847-92770848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185866526	chr10:92770855-92770856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200151288	chr10:92770879-92770880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111422318	chr10:92770912-92770913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369060313	chr10:92770922-92770923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557313552	chr10:92770931-92770932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78380122	chr10:92770938-92770939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545918132	chr10:92770979-92770980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17103739	chr10:92771038-92771039	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs4520505	chr10:92771109-92771110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111385216	chr10:92771111-92771112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527346869	chr10:92771123-92771124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541049195	chr10:92771125-92771126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149643710	chr10:92771142-92771143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530022908	chr10:92771198-92771199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550037836	chr10:92771202-92771203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569781280	chr10:92771224-92771225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144375390	chr10:92771245-92771246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139324958	chr10:92771247-92771248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377668814	chr10:92771248-92771249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551746902	chr10:92771256-92771257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369561674	chr10:92771296-92771297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:92761800-92782800	Weak transcription	Aorta	Aorta
2	chr10:92767200-92770600	Weak transcription	Osteobl	bone
3	chr10:92767400-92781400	Weak transcription	HSMM	muscle
4	chr10:92769600-92770200	Enhancers	GM12878-XiMat	blood
5	chr10:92769600-92770800	Weak transcription	Brain Anterior Caudate	brain
6	chr10:92769800-92770200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr10:92770000-92772000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr10:92770000-92772000	Weak transcription	Fetal Thymus	thymus
9	chr10:92770000-92772000	Weak transcription	Dnd41	blood
10	chr10:92770200-92771400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr10:92770400-92771400	Enhancers	A549	lung
12	chr10:92770600-92771200	Enhancers	Osteobl	bone
13	chr10:92770800-92771200	Enhancers	Brain Anterior Caudate	brain
14	chr10:92771200-92777200	Weak transcription	Brain Anterior Caudate	brain
15	chr10:92772000-92772200	Enhancers	Fetal Thymus	thymus
16	chr10:92772000-92772200	Enhancers	Dnd41	blood
17	chr10:92772000-92772200	ZNF genes & repeats	GM12878-XiMat	blood
18	chr10:92772000-92772400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
19	chr10:92772200-92776200	Weak transcription	GM12878-XiMat	blood
20	chr10:92772400-92780200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr10:92773200-92773800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr10:92773600-92774400	Enhancers	HepG2	liver
23	chr10:92773800-92774000	Enhancers	A549	lung
24	chr10:92774200-92775000	Weak transcription	HSMMtube	muscle
25	chr10:92775000-92775200	Enhancers	HSMMtube	muscle
26	chr10:92775200-92777000	Weak transcription	HSMMtube	muscle
27	chr10:92775400-92775600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr10:92775600-92783000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr10:92776200-92776400	Flanking Active TSS	GM12878-XiMat	blood
30	chr10:92776400-92777200	Active TSS	GM12878-XiMat	blood
31	chr10:92776600-92776800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr10:92776800-92777200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr10:92776800-92777200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr10:92776800-92777200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr10:92777000-92777200	Enhancers	HSMMtube	muscle
36	chr10:92777000-92777400	Enhancers	Brain Hippocampus Middle	brain
37	chr10:92777200-92777600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr10:92777200-92777600	Enhancers	GM12878-XiMat	blood
39	chr10:92777200-92778200	Enhancers	Brain Substantia Nigra	brain
40	chr10:92777200-92778400	Enhancers	Brain Anterior Caudate	brain
41	chr10:92777200-92782000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr10:92777200-92782200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr10:92777400-92781000	Weak transcription	Brain Hippocampus Middle	brain
44	chr10:92777600-92782400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr10:92778200-92781200	Weak transcription	Brain Substantia Nigra	brain
46	chr10:92778400-92781000	Weak transcription	Brain Anterior Caudate	brain
47	chr10:92778400-92781400	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr10:92780200-92780400	Enhancers	Ovary	ovary
49	chr10:92780200-92784800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr10:92780200-92784800	Enhancers	Fetal Muscle Leg	muscle

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