Variant report

Variant	nsv900465
Chromosome Location	chr13:69568612-69812252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:244)
Chromatin interactive
region (count:38)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:69796023-69796174	K562	blood:	n/a	n/a
2	ARID3A	chr13:69584667-69584945	K562	blood:	n/a	n/a
3	BCL3	chr13:69713198-69713412	GM12878	blood:	n/a	n/a
4	CEBPB	chr13:69621157-69621357	K562	blood:	n/a	n/a
5	CEBPB	chr13:69643875-69643893	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr13:69720588-69720825	HepG2	liver:	n/a	chr13:69720689-69720700
7	CEBPB	chr13:69795365-69795601	HepG2	liver:	n/a	n/a
8	CEBPB	chr13:69680041-69680394	HepG2	liver:	n/a	chr13:69680205-69680216
9	CEBPB	chr13:69659461-69660073	HepG2	liver:	n/a	n/a
10	CEBPB	chr13:69744343-69744543	HepG2	liver:	n/a	chr13:69744403-69744416 chr13:69744414-69744427 chr13:69744414-69744425
11	CEBPB	chr13:69768102-69768453	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr13:69795373-69795654	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr13:69733575-69733858	HepG2	liver:	n/a	chr13:69733710-69733721
14	CEBPB	chr13:69795374-69795674	K562	blood:	n/a	n/a
15	CEBPB	chr13:69603498-69603621	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr13:69659890-69660227	A549	lung:	n/a	n/a
17	CEBPB	chr13:69639602-69639802	HepG2	liver:	n/a	chr13:69639729-69639742 chr13:69639730-69639741
18	CEBPD	chr13:69795817-69796165	K562	blood:	n/a	n/a
19	CHD1	chr13:69808687-69808760	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr13:69808828-69809721	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr13:69599796-69599859	A549	lung:	n/a	n/a
22	CTCF	chr13:69667220-69667370	RPTEC	kidney:	n/a	n/a
23	CTCF	chr13:69749083-69749169	K562	blood:	n/a	n/a
24	CTCF	chr13:69659697-69659702	K562	blood:	n/a	n/a
25	CTCF	chr13:69667163-69667287	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr13:69797040-69797102	LNCaP	prostate:	n/a	n/a
27	CTCF	chr13:69667214-69667298	K562	blood:	n/a	n/a
28	CTCF	chr13:69667010-69667385	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr13:69667197-69667299	GM12878	blood:	n/a	n/a
30	CTCF	chr13:69667160-69667305	Gliobla	brain:	n/a	n/a
31	CTCF	chr13:69667160-69667310	GM06990	blood:	n/a	n/a
32	CTCF	chr13:69667237-69667243	Medullo	brain:	n/a	n/a
33	CTCF	chr13:69680623-69680682	Fibrobl	skin:	n/a	n/a
34	CTCF	chr13:69638168-69638246	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr13:69757894-69757968	Gliobla	brain:	n/a	n/a
36	CTCF	chr13:69667180-69667330	BE2_C	brain:	n/a	n/a
37	CTCF	chr13:69667128-69667390	GM12878	blood:	n/a	n/a
38	CTCF	chr13:69667222-69667225	Medullo	brain:	n/a	n/a
39	CTCF	chr13:69667160-69667310	HRE	kidney:	n/a	n/a
40	CTCF	chr13:69667040-69667190	A549	lung:	n/a	n/a
41	CTCF	chr13:69667160-69667310	HEK293	kidney:	n/a	n/a
42	CTCF	chr13:69800977-69800998	GM20000	blood:	n/a	n/a
43	CTCF	chr13:69666540-69666690	BE2_C	brain:	n/a	n/a
44	CTCF	chr13:69667140-69667290	GM12878	blood:	n/a	n/a
45	CTCF	chr13:69667060-69667210	HCT-116	colon:	n/a	n/a
46	CTCF	chr13:69667200-69667350	HepG2	liver:	n/a	n/a
47	CTCF	chr13:69732120-69732177	ProgFib	skin:	n/a	n/a
48	CTCF	chr13:69667160-69667310	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr13:69680320-69680470	WI-38	lung:	n/a	n/a
50	CTCF	chr13:69575186-69575268	GM10248	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:69809293-69809343	MCF-7	breast:	n/a
2	chr13:69587760-69587810	MCF10A-Er-Src	breast:	n/a
3	chr13:69809293-69809343	MCF10A-Er-Src	breast:	n/a
4	chr13:69809293-69809343	Hela-S3	cervix:	n/a
5	chr13:69796857-69796907	AG04449	skin:	fetal
6	chr13:69587760-69587810	HNPCEpiC	eye:	n/a
7	chr13:69796872-69796922	HPAEpiC	pulmonary alveolar:	n/a
8	chr13:69587760-69587810	ovcar-3	ovarian:	n/a
9	chr13:69796857-69796907	AoSMC	blood vessel:	n/a
10	chr13:69809293-69809343	ECC-1	luminal epithelium:	n/a
11	chr13:69796857-69796907	SK-N-SH	brain:	n/a
12	chr13:69796857-69796907	NHBE	bronchial:	n/a
13	chr13:69809293-69809343	NB4	blood:	n/a
14	chr13:69796857-69796907	BE2_C	brain:	n/a
15	chr13:69809293-69809343	HCT-116	colon:	n/a
16	chr13:69796872-69796922	HRCEpiC	kidney:	n/a
17	chr13:69587760-69587810	Caco-2	colon:	n/a
18	chr13:69587760-69587810	BE2_C	brain:	n/a
19	chr13:69796872-69796922	SK-N-MC	brain:	n/a
20	chr13:69587760-69587810	SK-N-SH_RA	brain:	n/a
21	chr13:69809293-69809343	BJ	skin:	n/a
22	chr13:69796857-69796907	SAEC	small airway:	n/a
23	chr13:69796872-69796922	GM06990	blood:	n/a
24	chr13:69809293-69809343	AoSMC	blood vessel:	n/a
25	chr13:69587760-69587810	PFSK-1	brain:	n/a
26	chr13:69796872-69796922	PANC-1	pancreas:	n/a
27	chr13:69587760-69587810	NHBE	bronchial:	n/a
28	chr13:69587760-69587810	AG04450	lung:	fetal
29	chr13:69796857-69796907	Hela-S3	cervix:	n/a
30	chr13:69809293-69809343	HAEpiC	amniotic membrane:	n/a
31	chr13:69796872-69796922	SK-N-SH	brain:	n/a
32	chr13:69587760-69587810	RPTEC	kidney:	n/a
33	chr13:69809293-69809343	HNPCEpiC	eye:	n/a
34	chr13:69587760-69587810	AG09309	skin:	n/a
35	chr13:69796857-69796907	MCF-7	breast:	n/a
36	chr13:69809293-69809343	SK-N-SH_RA	brain:	n/a
37	chr13:69809293-69809343	HMEC	breast:	n/a
38	chr13:69796872-69796922	HNPCEpiC	eye:	n/a
39	chr13:69809293-69809343	U87	brain:	n/a
40	chr13:69809293-69809343	AG10803	skin:	n/a
41	chr13:69796872-69796922	CMK	blood:	n/a
42	chr13:69796857-69796907	K562	blood:	n/a
43	chr13:69796857-69796907	HEK293	kidney:	embryo
44	chr13:69809293-69809343	BE2_C	brain:	n/a
45	chr13:69587760-69587810	NH-A	brain:	n/a
46	chr13:69796872-69796922	AG09309	skin:	n/a
47	chr13:69587760-69587810	HCPEpiC	choroid plexus:	n/a
48	chr13:69796872-69796922	AG09319	gingival:	n/a
49	chr13:69587760-69587810	HUVEC	blood vessel:	n/a
50	chr13:69587760-69587810	HAEpiC	amniotic membrane:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:69583714..69586393-chr13:69587871..69590253,3	K562	blood:
2	chr13:69794151..69795814-chr13:69798376..69800690,2	K562	blood:
3	chr13:69714056..69716276-chr13:69718003..69720076,2	K562	blood:
4	chr13:69676877..69679728-chr13:69680148..69683095,2	K562	blood:
5	chr13:69794151..69795814-chr13:69798376..69800690,2	K562	blood:
6	chr13:69577123..69579403-chr13:69580839..69583998,3	K562	blood:
7	chr13:69803907..69806465-chr13:69811377..69814161,2	K562	blood:
8	chr13:69745232..69748502-chr13:69749716..69752165,3	K562	blood:
9	chr13:69794008..69796830-chr13:69806883..69809682,2	K562	blood:
10	chr13:69761351..69764047-chr13:69765452..69767697,2	K562	blood:
11	chr13:69803907..69806465-chr13:69811377..69814161,2	K562	blood:
12	chr13:69584341..69586393-chr13:69588333..69590253,2	K562	blood:
13	chr13:69788123..69789818-chr13:69791504..69794154,2	K562	blood:
14	chr13:69591603..69593208-chr13:69593619..69596259,2	K562	blood:
15	chr13:69795398..69798188-chr13:69884200..69887047,2	K562	blood:
16	chr13:69584341..69586393-chr13:69588333..69590253,2	K562	blood:
17	chr13:69588937..69591463-chr13:69592795..69594701,2	MCF-7	breast:
18	chr13:69745779..69747312-chr13:69749716..69751908,2	K562	blood:
19	chr13:69682184..69685154-chr13:69690217..69692966,2	MCF-7	breast:
20	chr13:69788123..69789818-chr13:69791504..69794154,2	K562	blood:
21	chr13:52026657..52027294-chr13:69594051..69594992,2	Hela-S3	cervix:
22	chr13:69761351..69764047-chr13:69765452..69767697,2	K562	blood:
23	chr13:69588937..69591463-chr13:69592795..69594701,2	MCF-7	breast:
24	chr13:69745232..69748502-chr13:69749716..69752165,3	K562	blood:
25	chr13:69792364..69793914-chr13:69801146..69804044,2	K562	blood:
26	chr13:69613880..69614380-chr3:73159953..73160630,2	HCT-116	colon:
27	chr13:69792364..69793914-chr13:69801146..69804044,2	K562	blood:
28	chr13:69745779..69747312-chr13:69749716..69751908,2	K562	blood:
29	chr13:69577123..69579403-chr13:69580839..69583998,3	K562	blood:
30	chr13:69682184..69685154-chr13:69690217..69692966,2	MCF-7	breast:
31	chr13:69583714..69586393-chr13:69587871..69590253,3	K562	blood:
32	chr13:69577914..69580803-chr13:69584083..69586306,2	K562	blood:
33	chr13:69799858..69802118-chr13:69802729..69806556,4	K562	blood:
34	chr13:69676877..69679728-chr13:69680148..69683095,2	K562	blood:
35	chr13:69591603..69593208-chr13:69593619..69596259,2	K562	blood:
36	chr13:69799858..69802118-chr13:69802729..69806556,4	K562	blood:
37	chr13:69577914..69580803-chr13:69584083..69586306,2	K562	blood:
38	chr13:69714056..69716276-chr13:69718003..69720076,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BORA-6	chr13:69795972-69796802	NONHSAT034241
2	lnc-BORA-6	chr13:69796478-69796580	XLOC_010420
3	lnc-KLHL1-7	chr13:69675964-69676188	NONHSAT034240

No data

Variant related genes	Relation type
LINC00383	TF binding region
SNRPFP3	TF binding region
LINC00383	CpG island
SNRPFP3	CpG island
ENSG00000223247	chromatin interactions
ENSG00000237534	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000235221	chromatin interactions
EIF4G2	miRNA target sites

Extended variants
information (count: 3822 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3822 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9541684	chr13:69568612-69568613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543448907	chr13:69568619-69568620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73521917	chr13:69568640-69568641	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs187591741	chr13:69568725-69568726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199932543	chr13:69568785-69568786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548869457	chr13:69568927-69568928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146999175	chr13:69568929-69568930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528323937	chr13:69568931-69568932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547862183	chr13:69568962-69568963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570623679	chr13:69569000-69569001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570637812	chr13:69569015-69569016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71427691	chr13:69569048-69569049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs550261192	chr13:69569083-69569084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370195327	chr13:69569132-69569133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116648532	chr13:69569142-69569143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76968224	chr13:69569144-69569145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536132490	chr13:69569150-69569151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138082033	chr13:69569207-69569208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116281787	chr13:69569209-69569210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192037285	chr13:69569276-69569277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113589953	chr13:69569284-69569285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs66659233	chr13:69569285-69569286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75038664	chr13:69569287-69569288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9646062	chr13:69569288-69569289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9541685	chr13:69569329-69569330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9541686	chr13:69569350-69569351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9541687	chr13:69569353-69569354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs9541688	chr13:69569375-69569376	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs183914839	chr13:69569391-69569392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573587802	chr13:69569432-69569433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9564515	chr13:69569442-69569443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559431514	chr13:69569480-69569481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528252627	chr13:69569488-69569489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375648563	chr13:69569505-69569506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557960365	chr13:69569556-69569557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544806822	chr13:69569557-69569558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576217688	chr13:69569563-69569564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564214950	chr13:69569667-69569668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377760209	chr13:69569668-69569669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114914843	chr13:69569721-69569722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190485332	chr13:69569761-69569762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149362483	chr13:69569784-69569785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569691526	chr13:69569819-69569820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1572464	chr13:69569832-69569833	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs549642254	chr13:69569839-69569840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9564516	chr13:69569875-69569876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373769454	chr13:69569886-69569887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73521926	chr13:69569893-69569894	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116505584	chr13:69569923-69569924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367774301	chr13:69569924-69569925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22737080	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69558000-69570200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr13:69563800-69569800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr13:69564200-69569400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr13:69569400-69571200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr13:69569400-69571800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:69569600-69571800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:69569800-69570200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr13:69569800-69571200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr13:69570200-69570400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr13:69570200-69570600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr13:69570200-69570600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr13:69570200-69571200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr13:69570400-69571000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr13:69570400-69571000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr13:69570600-69571000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr13:69570600-69571200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr13:69571000-69571200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr13:69583600-69585800	Active TSS	K562	blood
19	chr13:69584400-69584600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr13:69584600-69587600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr13:69587600-69588400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr13:69587600-69590200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr13:69587800-69588800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr13:69588000-69588400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr13:69590200-69590400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr13:69601000-69601600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr13:69620200-69620600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr13:69620200-69620600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr13:69620600-69624600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr13:69623800-69625600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr13:69624000-69625800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr13:69624000-69625800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr13:69624200-69625200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr13:69624600-69625800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr13:69625000-69625200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr13:69625000-69625400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr13:69625200-69628800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr13:69625600-69627600	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr13:69627600-69627800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr13:69628800-69629000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr13:69638200-69639000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr13:69638400-69638600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr13:69638400-69638800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr13:69638400-69638800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr13:69638400-69638800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr13:69638400-69639000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr13:69638600-69639400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr13:69638800-69643800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr13:69638800-69643800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr13:69639000-69643800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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