Variant report

Variant	nsv895887
Chromosome Location	chr10:92791516-92836763
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	BRCA1	chr10:92796883-92796939	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr10:92833105-92833317	A549	lung:	n/a	n/a
5	CEBPB	chr10:92792526-92792583	A549	lung:	n/a	chr10:92792568-92792581
6	CEBPB	chr10:92814176-92814377	IMR90	lung:	n/a	n/a
7	CEBPB	chr10:92814066-92814440	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr10:92833051-92833338	HepG2	liver:	n/a	n/a
9	CEBPB	chr10:92808858-92808914	HepG2	liver:	n/a	chr10:92808883-92808896
10	CEBPB	chr10:92828987-92829164	K562	blood:	n/a	chr10:92829126-92829137
11	CEBPB	chr10:92833034-92833260	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:92822408-92822689	A549	lung:	n/a	chr10:92822612-92822625
13	CEBPB	chr10:92814080-92814420	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr10:92829102-92829180	HepG2	liver:	n/a	chr10:92829126-92829137
15	CTCF	chr10:92803120-92803270	AoAF	blood vessel:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
16	CTCF	chr10:92803140-92803290	SK-N-SH_RA	brain:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
17	CTCF	chr10:92803086-92803308	Gliobla	brain:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
18	CTCF	chr10:92803120-92803270	HepG2	liver:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
19	CTCF	chr10:92803100-92803250	AG09319	gingival:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
20	CTCF	chr10:92802986-92803391	HCT-116	colon:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
21	CTCF	chr10:92803140-92803290	HCT-116	colon:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
22	CTCF	chr10:92803180-92803330	GM12864	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
23	CTCF	chr10:92803040-92803190	GM12867	blood:	n/a	n/a
24	CTCF	chr10:92803120-92803270	GM12875	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
25	CTCF	chr10:92802995-92803419	A549	lung:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
26	CTCF	chr10:92803160-92803310	HMF	breast:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
27	CTCF	chr10:92803080-92803230	GM12866	blood:	n/a	chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
28	CTCF	chr10:92803115-92803227	MCF-7	breast:	n/a	chr10:92803211-92803227 chr10:92803215-92803223
29	CTCF	chr10:92793780-92793930	BE2_C	brain:	n/a	chr10:92793867-92793883 chr10:92793866-92793884 chr10:92793868-92793889
30	CTCF	chr10:92803100-92803250	GM12873	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
31	CTCF	chr10:92803100-92803250	MCF-7	breast:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
32	CTCF	chr10:92793960-92794110	BE2_C	brain:	n/a	n/a
33	CTCF	chr10:92803140-92803290	WERI-Rb-1	eye:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
34	CTCF	chr10:92803080-92803349	HUVEC	blood vessel:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
35	CTCF	chr10:92803120-92803270	GM12864	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
36	CTCF	chr10:92803120-92803270	GM12865	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
37	CTCF	chr10:92802969-92803448	HCT-116	colon:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
38	CTCF	chr10:92803160-92803310	HPF	lung:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
39	CTCF	chr10:92803140-92803290	HPAF	blood vessel:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
40	CTCF	chr10:92803068-92803390	MCF-7	breast:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
41	CTCF	chr10:92803112-92803215	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:92803140-92803290	HEK293	kidney:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
43	CTCF	chr10:92803080-92803337	Hela-S3	cervix:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
44	CTCF	chr10:92791740-92791890	GM12871	blood:	n/a	n/a
45	CTCF	chr10:92803120-92803270	NB4	blood:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
46	CTCF	chr10:92803069-92803365	A549	lung:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
47	CTCF	chr10:92803120-92803270	HFF-Myc	foreskin:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
48	CTCF	chr10:92803140-92803290	RPTEC	kidney:	n/a	chr10:92803212-92803233 chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
49	CTCF	chr10:92803080-92803230	BJ	skin:	n/a	chr10:92803211-92803227 chr10:92803210-92803228 chr10:92803215-92803223
50	CTCF	chr10:92803100-92803250	SAEC	small airway:	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	HCPEpiC	choroid plexus:	n/a
2	chr10:92810359-92810409	SK-N-MC	brain:	n/a
3	chr10:92794806-92794856	HepG2	liver:	n/a
4	chr10:92794806-92794856	SK-N-SH_RA	brain:	n/a
5	chr10:92810359-92810409	RPTEC	kidney:	n/a
6	chr10:92794806-92794856	HIPEpiC	eye:	n/a
7	chr10:92794806-92794856	SK-N-SH	brain:	n/a
8	chr10:92810359-92810409	HMEC	breast:	n/a
9	chr10:92794806-92794856	SAEC	small airway:	n/a
10	chr10:92810359-92810409	IMR90	lung:	fetal
11	chr10:92794806-92794856	HCM	heart:	n/a
12	chr10:92794806-92794856	AoSMC	blood vessel:	n/a
13	chr10:92794806-92794856	PANC-1	pancreas:	n/a
14	chr10:92794806-92794856	AG04449	skin:	fetal
15	chr10:92810359-92810409	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:92810359-92810409	MCF-7	breast:	n/a
17	chr10:92794806-92794856	GM12878	blood:	n/a
18	chr10:92794806-92794856	HCPEpiC	choroid plexus:	n/a
19	chr10:92794806-92794856	A549	lung:	n/a
20	chr10:92794806-92794856	T-47D	breast:	n/a
21	chr10:92810359-92810409	AG09319	gingival:	n/a
22	chr10:92794806-92794856	ovcar-3	ovarian:	n/a
23	chr10:92810359-92810409	PANC-1	pancreas:	n/a
24	chr10:92794806-92794856	PrEC	prostate:	n/a
25	chr10:92810359-92810409	HEEpiC	esophagus:	n/a
26	chr10:92794806-92794856	HCT-116	colon:	n/a
27	chr10:92794806-92794856	Hela-S3	cervix:	n/a
28	chr10:92810359-92810409	HIPEpiC	eye:	n/a
29	chr10:92810359-92810409	ovcar-3	ovarian:	n/a
30	chr10:92794806-92794856	NHDF-neo	bronchial:	n/a
31	chr10:92810359-92810409	HRPEpiC	eye:	n/a
32	chr10:92794806-92794856	NT2-D1	testis:	n/a
33	chr10:92794806-92794856	HMEC	breast:	n/a
34	chr10:92794806-92794856	SK-N-MC	brain:	n/a
35	chr10:92794806-92794856	HAEpiC	amniotic membrane:	n/a
36	chr10:92794806-92794856	Hepatocyte	liver:	n/a
37	chr10:92794806-92794856	Caco-2	colon:	n/a
38	chr10:92810359-92810409	HRE	kidney:	n/a
39	chr10:92794806-92794856	BE2_C	brain:	n/a
40	chr10:92810359-92810409	A549	lung:	n/a
41	chr10:92794806-92794856	ECC-1	luminal epithelium:	n/a
42	chr10:92794806-92794856	GM12892	blood:	n/a
43	chr10:92810359-92810409	HUVEC	blood vessel:	n/a
44	chr10:92810359-92810409	Hepatocyte	liver:	n/a
45	chr10:92794806-92794856	HCF	heart:	n/a
46	chr10:92810359-92810409	T-47D	breast:	n/a
47	chr10:92810359-92810409	GM12892	blood:	n/a
48	chr10:92810359-92810409	H1-hESC	embryonic stem cell:	embryo
49	chr10:92794806-92794856	HEEpiC	esophagus:	n/a
50	chr10:92794806-92794856	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr10:92791172..92794052-chr10:92801075..92803431,2	MCF-7	breast:
2	chr10:92768647..92770927-chr10:92793984..92796644,2	MCF-7	breast:
3	chr10:92805073..92806604-chr10:92807653..92810163,2	K562	blood:
4	chr10:92820344..92822180-chr10:92825701..92827282,2	K562	blood:
5	chr10:92827544..92830506-chr10:92832665..92835426,2	K562	blood:
6	chr10:92802749..92803570-chr10:93008473..93009291,2	MCF-7	breast:
7	chr10:92791172..92794052-chr10:92801075..92803431,2	MCF-7	breast:
8	chr10:92827544..92830506-chr10:92832665..92835426,2	K562	blood:
9	chr10:92805073..92806604-chr10:92807653..92810163,2	K562	blood:
10	chr10:92820344..92822180-chr10:92825701..92827282,2	K562	blood:
11	chr10:92802747..92803726-chr10:93010975..93011501,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD1-2	chr10:92793811-92794238	XLOC_008903
2	lnc-RPP30-4	chr10:92821736-92821916	NONHSAT015618
3	lnc-RPP30-4	chr10:92806923-92807057	ENSG00000224851.1
4	lnc-RPP30-4	chr10:92805565-92805687	NONHSAT015618
5	lnc-ANKRD1-2	chr10:92795970-92796139	XLOC_008903
6	lnc-RPP30-4	chr10:92821736-92821916	ENSG00000224851.1
7	lnc-ANKRD1-2	chr10:92796888-92796960	XLOC_008903
8	lnc-RPP30-4	chr10:92807658-92807786	ENSG00000224851.1
9	lnc-RPP30-4	chr10:92806769-92806875	NONHSAT015618
10	lnc-RPP30-4	chr10:92807658-92807786	NONHSAT015618

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

Extended variants
information (count: 1825 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10509615	chr10:92791516-92791517	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549515263	chr10:92791529-92791530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187474820	chr10:92791545-92791546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550023566	chr10:92791550-92791551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149306371	chr10:92791565-92791566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563454028	chr10:92791601-92791602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143545141	chr10:92791607-92791608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112580506	chr10:92791660-92791661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553978352	chr10:92791675-92791676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192030142	chr10:92791684-92791685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542782706	chr10:92791699-92791700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148336945	chr10:92791810-92791811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182764328	chr10:92791850-92791851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544238897	chr10:92791870-92791871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563925832	chr10:92791893-92791894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533287651	chr10:92791903-92791904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375394831	chr10:92791958-92791959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529235599	chr10:92791959-92791960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145699179	chr10:92791961-92791962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546903326	chr10:92792035-92792036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560455902	chr10:92792040-92792041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529125404	chr10:92792045-92792046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186983498	chr10:92792171-92792172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569344222	chr10:92792188-92792189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531708386	chr10:92792196-92792197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368974545	chr10:92792210-92792211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141443222	chr10:92792285-92792286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7907658	chr10:92792388-92792389	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs533895900	chr10:92792395-92792396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146304549	chr10:92792398-92792399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535398464	chr10:92792488-92792489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567570747	chr10:92792490-92792491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554008813	chr10:92792586-92792587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139478528	chr10:92792626-92792627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575347498	chr10:92792749-92792750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543951888	chr10:92792768-92792769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564392086	chr10:92792769-92792770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557770478	chr10:92792801-92792802	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577582590	chr10:92792829-92792830	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192348967	chr10:92792864-92792865	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116387219	chr10:92792935-92792936	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529161553	chr10:92792992-92792993	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184426873	chr10:92792996-92792997	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542890248	chr10:92793012-92793013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562520738	chr10:92793018-92793019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12415456	chr10:92793040-92793041	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs551599774	chr10:92793072-92793073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188955127	chr10:92793075-92793076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547919701	chr10:92793171-92793172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs193230617	chr10:92793194-92793195	Enhancers Weak transcription	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:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:92784400-92797800	Weak transcription	Aorta	Aorta
2	chr10:92784600-92796600	Weak transcription	Left Ventricle	heart
3	chr10:92784800-92792200	Weak transcription	Fetal Muscle Leg	muscle
4	chr10:92785800-92793000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr10:92790000-92793600	Enhancers	Dnd41	blood
6	chr10:92790200-92792200	Weak transcription	Brain Angular Gyrus	brain
7	chr10:92790200-92794800	Enhancers	Fetal Thymus	thymus
8	chr10:92790800-92794800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr10:92791200-92793200	Weak transcription	Primary T cells from cord blood	blood
10	chr10:92791400-92793200	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr10:92792000-92792800	Enhancers	Placenta	Placenta
12	chr10:92792000-92792800	Enhancers	Lung	lung
13	chr10:92792000-92795400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:92792200-92792800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr10:92792200-92792800	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr10:92792200-92793200	Enhancers	Brain Angular Gyrus	brain
17	chr10:92792200-92793200	Enhancers	Fetal Lung	lung
18	chr10:92792200-92794400	Enhancers	Brain Anterior Caudate	brain
19	chr10:92792200-92794800	Enhancers	Fetal Brain Male	brain
20	chr10:92792200-92795200	Enhancers	Brain Cingulate Gyrus	brain
21	chr10:92792200-92795200	Enhancers	Brain Hippocampus Middle	brain
22	chr10:92792200-92795400	Enhancers	Brain Substantia Nigra	brain
23	chr10:92792200-92795600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:92792200-92795600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr10:92792200-92796600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr10:92792200-92797200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr10:92792200-92798000	Enhancers	Fetal Muscle Leg	muscle
28	chr10:92792400-92792600	Weak transcription	Fetal Muscle Trunk	muscle
29	chr10:92792400-92792800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr10:92792400-92793400	Enhancers	Brain Germinal Matrix	brain
31	chr10:92792400-92793400	Enhancers	Osteobl	bone
32	chr10:92792400-92794600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr10:92792400-92795200	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr10:92792600-92792800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr10:92792600-92792800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr10:92792600-92792800	Enhancers	Adipose Nuclei	Adipose
37	chr10:92792600-92792800	Enhancers	Fetal Muscle Trunk	muscle
38	chr10:92792600-92793000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr10:92792600-92793200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:92792600-92793200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr10:92792600-92793400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:92792600-92794600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr10:92792600-92795400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr10:92792800-92793000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr10:92792800-92793400	Weak transcription	Fetal Muscle Trunk	muscle
46	chr10:92792800-92793800	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr10:92792800-92794200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr10:92792800-92794200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr10:92792800-92794400	Weak transcription	Adipose Nuclei	Adipose
50	chr10:92792800-92794800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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