Variant report

Variant	nsv900080
Chromosome Location	chr13:51711436-51754873
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:582)
CpG islands
(count:427)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:51723945-51723963	K562	blood:	n/a	n/a
2	ATF2	chr13:51752532-51753109	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr13:51722161-51723003	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr13:51722254-51722901	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr13:51727626-51728075	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr13:51743483-51743963	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr13:51749034-51750155	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr13:51749147-51749705	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr13:51727630-51728038	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr13:51752086-51755611	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr13:51743253-51744039	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr13:51753991-51755386	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr13:51750770-51752029	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr13:51727681-51728002	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr13:51727692-51727935	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr13:51728329-51728649	K562	blood:	n/a	n/a
17	BACH1	chr13:51728343-51728651	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr13:51722957-51723440	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr13:51733092-51733304	GM12878	blood:	n/a	chr13:51733241-51733251
20	BCL11A	chr13:51722508-51722750	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr13:51754582-51755193	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr13:51743827-51744018	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr13:51747463-51747648	K562	blood:	n/a	n/a
24	CEBPB	chr13:51747482-51747670	K562	blood:	n/a	n/a
25	CEBPB	chr13:51737403-51737623	IMR90	lung:	n/a	chr13:51737476-51737487
26	CEBPB	chr13:51727711-51728021	HepG2	liver:	n/a	chr13:51727831-51727842
27	CEBPB	chr13:51728247-51728599	K562	blood:	n/a	n/a
28	CEBPB	chr13:51743514-51744089	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr13:51752929-51753042	HepG2	liver:	n/a	n/a
30	CEBPB	chr13:51727746-51727992	K562	blood:	n/a	chr13:51727831-51727842
31	CEBPB	chr13:51727666-51727999	IMR90	lung:	n/a	chr13:51727831-51727842
32	CEBPB	chr13:51749262-51749552	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr13:51737353-51737603	HepG2	liver:	n/a	chr13:51737476-51737487
34	CEBPB	chr13:51730838-51731183	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr13:51727657-51728062	ECC-1	luminal epithelium:	n/a	chr13:51727831-51727842
36	CEBPB	chr13:51747468-51747696	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:51727754-51727994	A549	lung:	n/a	chr13:51727831-51727842
38	CEBPB	chr13:51727647-51728029	H1-hESC	embryonic stem cell:	n/a	chr13:51727831-51727842
39	CEBPB	chr13:51727654-51728023	ECC-1	luminal epithelium:	n/a	chr13:51727831-51727842
40	CHD1	chr13:51743195-51744022	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr13:51748233-51748429	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr13:51749130-51750108	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr13:51745207-51745422	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr13:51744326-51744475	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr13:51750336-51750728	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr13:51751739-51751850	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr13:51747602-51747703	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr13:51753082-51753814	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr13:51742657-51743126	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr13:51751341-51755520	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51753863-51753913	HL-60	blood:	n/a
2	chr13:51723181-51723231	Caco-2	colon:	n/a
3	chr13:51742569-51742619	HL-60	blood:	n/a
4	chr13:51733079-51733129	HepG2	liver:	n/a
5	chr13:51733079-51733129	HCT-116	colon:	n/a
6	chr13:51753863-51753913	HPAEpiC	pulmonary alveolar:	n/a
7	chr13:51733079-51733129	AG04449	skin:	fetal
8	chr13:51724467-51724517	T-47D	breast:	n/a
9	chr13:51744542-51744592	SK-N-SH	brain:	n/a
10	chr13:51742569-51742619	SAEC	small airway:	n/a
11	chr13:51724467-51724517	HPAEpiC	pulmonary alveolar:	n/a
12	chr13:51724467-51724517	LNCaP	prostate:	n/a
13	chr13:51753863-51753913	HIPEpiC	eye:	n/a
14	chr13:51733079-51733129	SK-N-SH	brain:	n/a
15	chr13:51742569-51742619	Jurkat	blood:	n/a
16	chr13:51744561-51744611	HEK293	kidney:	embryo
17	chr13:51742569-51742619	SK-N-MC	brain:	n/a
18	chr13:51742569-51742619	NHDF-neo	bronchial:	n/a
19	chr13:51744542-51744592	AoSMC	blood vessel:	n/a
20	chr13:51733079-51733129	PFSK-1	brain:	n/a
21	chr13:51744542-51744592	HIPEpiC	eye:	n/a
22	chr13:51724467-51724517	MCF10A-Er-Src	breast:	n/a
23	chr13:51744561-51744611	MCF-7	breast:	n/a
24	chr13:51744542-51744592	HCT-116	colon:	n/a
25	chr13:51744561-51744611	NB4	blood:	n/a
26	chr13:51753863-51753913	SK-N-MC	brain:	n/a
27	chr13:51723181-51723231	AoSMC	blood vessel:	n/a
28	chr13:51723181-51723231	HEK293	kidney:	embryo
29	chr13:51724467-51724517	PANC-1	pancreas:	n/a
30	chr13:51742569-51742619	HPAEpiC	pulmonary alveolar:	n/a
31	chr13:51724467-51724517	NHDF-neo	bronchial:	n/a
32	chr13:51733079-51733129	HEK293	kidney:	embryo
33	chr13:51744561-51744611	SAEC	small airway:	n/a
34	chr13:51742569-51742619	BE2_C	brain:	n/a
35	chr13:51744561-51744611	LNCaP	prostate:	n/a
36	chr13:51733079-51733129	K562	blood:	n/a
37	chr13:51753863-51753913	SK-N-SH	brain:	n/a
38	chr13:51733079-51733129	ovcar-3	ovarian:	n/a
39	chr13:51744542-51744592	ECC-1	luminal epithelium:	n/a
40	chr13:51723181-51723231	HCF	heart:	n/a
41	chr13:51742569-51742619	IMR90	lung:	fetal
42	chr13:51744561-51744611	H1-hESC	embryonic stem cell:	embryo
43	chr13:51723181-51723231	PANC-1	pancreas:	n/a
44	chr13:51742569-51742619	HCM	heart:	n/a
45	chr13:51723181-51723231	NT2-D1	testis:	n/a
46	chr13:51744561-51744611	U87	brain:	n/a
47	chr13:51742569-51742619	Hepatocyte	liver:	n/a
48	chr13:51744561-51744611	PrEC	prostate:	n/a
49	chr13:51733079-51733129	PrEC	prostate:	n/a
50	chr13:51744542-51744592	HCF	heart:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:51721200..51723188-chr13:51728041..51731012,2	MCF-7	breast:
2	chr13:51699580..51700109-chr13:51722979..51723590,2	MCF-7	breast:
3	chr13:51730986..51733604-chr13:52024721..52026662,2	K562	blood:
4	chr13:51698016..51700737-chr13:51726914..51729156,2	K562	blood:
5	chr13:51722837..51724133-chr13:51860193..51861210,11	MCF-7	breast:
6	chr13:51721200..51723188-chr13:51728041..51731012,2	MCF-7	breast:
7	chr13:51722919..51723811-chr13:51860090..51861195,8	MCF-7	breast:
8	chr13:51722852..51723780-chr13:51858091..51858924,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM124A-2	chr13:51754413-51755574	NONHSAT033887
2	lnc-INTS6-7	chr13:51729392-51729919	NONHSAT033886
3	lnc-INTS6-7	chr13:51730022-51730186	NONHSAT033886
4	lnc-FAM124A-2	chr13:51744127-51744792	NONHSAT033887
5	lnc-FAM124A-2	chr13:51749072-51750179	NONHSAT033887
6	lnc-FAM124A-2	chr13:51746440-51746737	NONHSAT033887

No data

Variant related genes	Relation type
RPL5P31	TF binding region
LINC00371	TF binding region
RPL5P31	CpG island
LINC00371	CpG island
ENSG00000236778	chromatin interactions
ENSG00000102786	chromatin interactions

Extended variants
information (count: 1870 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs927863	chr13:51711436-51711437	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557745836	chr13:51711449-51711450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183369033	chr13:51711534-51711535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533924477	chr13:51711561-51711562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554001855	chr13:51711598-51711599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573917109	chr13:51711650-51711651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542885465	chr13:51711686-51711687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556157928	chr13:51711717-51711718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186457182	chr13:51711724-51711725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576302246	chr13:51711730-51711731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545027284	chr13:51711731-51711732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564983157	chr13:51711818-51711819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547132076	chr13:51711819-51711820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7320501	chr13:51711858-51711859	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs541161201	chr13:51711896-51711897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7320544	chr13:51711961-51711962	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs530200909	chr13:51711979-51711980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550363720	chr13:51711980-51711981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191305928	chr13:51712018-51712019	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532845397	chr13:51712033-51712034	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs151096615	chr13:51712084-51712085	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571307613	chr13:51712087-51712088	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533860362	chr13:51712090-51712091	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574046258	chr13:51712145-51712146	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35362741	chr13:51712149-51712150	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542740725	chr13:51712196-51712197	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556333524	chr13:51712275-51712276	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568382288	chr13:51712310-51712311	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576254409	chr13:51712318-51712319	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545326289	chr13:51712320-51712321	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371597454	chr13:51712322-51712323	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6561616	chr13:51712383-51712384	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs572136253	chr13:51712401-51712402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141054443	chr13:51712464-51712465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74992380	chr13:51712489-51712490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530220091	chr13:51712497-51712498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543607043	chr13:51712527-51712528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563956736	chr13:51712561-51712562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532687515	chr13:51712563-51712564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184843413	chr13:51712566-51712567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559724764	chr13:51712578-51712579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371350693	chr13:51712586-51712587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564852701	chr13:51712587-51712588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs36043013	chr13:51712644-51712645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs56183773	chr13:51712655-51712656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs7327944	chr13:51712665-51712666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs116861442	chr13:51712682-51712683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536391973	chr13:51712692-51712693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552681582	chr13:51712721-51712722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370879159	chr13:51712750-51712751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51700400-51721200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr13:51707800-51717400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr13:51708000-51714400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr13:51708200-51715800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr13:51708200-51720400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr13:51710200-51711600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr13:51711200-51712000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr13:51711400-51712400	Enhancers	Spleen	Spleen
9	chr13:51711600-51720400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr13:51712000-51712400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:51712400-51714400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:51713600-51714600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr13:51714400-51715000	Enhancers	H9 Cell Line	embryonic stem cell
14	chr13:51714400-51715000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr13:51717000-51720000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:51717400-51719600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
17	chr13:51718000-51719200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr13:51718600-51720000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
19	chr13:51719200-51720600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr13:51719600-51720000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr13:51719800-51725200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr13:51720000-51720200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
23	chr13:51720000-51720600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:51720000-51722200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr13:51720200-51720400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr13:51720400-51720600	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr13:51720400-51722200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr13:51720400-51722200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr13:51720400-51722600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr13:51720400-51722800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr13:51720400-51723200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr13:51720400-51724000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr13:51720600-51723600	Weak transcription	Right Atrium	heart
34	chr13:51720600-51724000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr13:51720600-51724400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:51720600-51724600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr13:51720600-51725200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr13:51720600-51731600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr13:51720800-51724600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr13:51721000-51721600	Enhancers	Spleen	Spleen
41	chr13:51721000-51722400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr13:51721200-51721400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr13:51721400-51722000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr13:51721600-51728600	Weak transcription	Spleen	Spleen
45	chr13:51722000-51724000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr13:51722200-51722400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr13:51722200-51722600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr13:51722200-51722800	Enhancers	Adipose Nuclei	Adipose
49	chr13:51722200-51723000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr13:51722200-51723200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived

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