Variant report

Variant	nsv832624
Chromosome Location	chr13:61383648-61553974
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	BHLHE40	chr13:61412918-61413046	K562	blood:	n/a	n/a
2	CEBPB	chr13:61540891-61541011	HepG2	liver:	n/a	chr13:61540921-61540932
3	CEBPB	chr13:61427254-61427512	H1-hESC	embryonic stem cell:	n/a	chr13:61427383-61427394
4	CEBPB	chr13:61443537-61443723	HepG2	liver:	n/a	n/a
5	CEBPB	chr13:61427252-61427487	HepG2	liver:	n/a	chr13:61427383-61427394
6	CEBPB	chr13:61455745-61455946	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr13:61427298-61427498	A549	lung:	n/a	chr13:61427383-61427394
8	CEBPB	chr13:61397061-61397243	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr13:61540764-61541094	H1-hESC	embryonic stem cell:	n/a	chr13:61540921-61540932
10	CEBPB	chr13:61434828-61435014	A549	lung:	n/a	n/a
11	CTCF	chr13:61532100-61532250	HEEpiC	esophagus:	n/a	n/a
12	CTCF	chr13:61442396-61442456	GM20000	blood:	n/a	n/a
13	CTCF	chr13:61475140-61475290	HepG2	liver:	n/a	n/a
14	CTCF	chr13:61545604-61545655	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr13:61532080-61532230	RPTEC	kidney:	n/a	n/a
16	CTCF	chr13:61390140-61390290	GM06990	blood:	n/a	n/a
17	CTCF	chr13:61406736-61406749	MCF-7	breast:	n/a	n/a
18	CTCF	chr13:61534617-61534730	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr13:61502220-61502370	NHEK	skin:	n/a	n/a
20	CTCF	chr13:61478820-61478854	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr13:61538820-61538970	BJ	skin:	n/a	n/a
22	CTCF	chr13:61438408-61438506	GM10248	blood:	n/a	n/a
23	CTCF	chr13:61406690-61406801	MCF-7	breast:	n/a	n/a
24	CTCF	chr13:61406755-61406777	MCF-7	breast:	n/a	n/a
25	CTCF	chr13:61474215-61474271	GM13976	blood:	n/a	n/a
26	CTCF	chr13:61531984-61532310	GM12878	blood:	n/a	n/a
27	CTCF	chr13:61426259-61426302	GM20000	blood:	n/a	n/a
28	E2F4	chr13:61384742-61384941	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr13:61507582-61507872	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr13:61506471-61506724	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr13:61495751-61496036	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr13:61446952-61447152	GM12878	blood:	n/a	chr13:61447042-61447053
33	ELK1	chr13:61420053-61420188	Hela-S3	cervix:	n/a	n/a
34	FOS	chr13:61519068-61519174	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr13:61427388-61427403	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr13:61430164-61430497	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr13:61506016-61506369	MCF10A-Er-Src	breast:	n/a	chr13:61506179-61506188 chr13:61506178-61506189 chr13:61506180-61506189
38	FOS	chr13:61430164-61430496	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr13:61430156-61430477	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr13:61412080-61412322	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr13:61399523-61399598	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr13:61507799-61508116	MCF10A-Er-Src	breast:	n/a	chr13:61507967-61507974 chr13:61507967-61507975 chr13:61507811-61507820 chr13:61507967-61507975 chr13:61507966-61507976
43	FOS	chr13:61384734-61385062	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr13:61412038-61412263	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr13:61507785-61508155	MCF10A-Er-Src	breast:	n/a	chr13:61507967-61507974 chr13:61507967-61507975 chr13:61507811-61507820 chr13:61507967-61507975 chr13:61507966-61507976
46	FOS	chr13:61507764-61508131	MCF10A-Er-Src	breast:	n/a	chr13:61507967-61507974 chr13:61507967-61507975 chr13:61507811-61507820 chr13:61507967-61507975 chr13:61507966-61507976
47	FOS	chr13:61505993-61506419	MCF10A-Er-Src	breast:	n/a	chr13:61506179-61506188 chr13:61506178-61506189 chr13:61506180-61506189
48	FOS	chr13:61396955-61397086	MCF10A-Er-Src	breast:	n/a	chr13:61396987-61396999 chr13:61396989-61396997 chr13:61396988-61396997 chr13:61396989-61396996 chr13:61396992-61396999 chr13:61396990-61397001
49	FOS	chr13:61507798-61508116	MCF10A-Er-Src	breast:	n/a	chr13:61507967-61507974 chr13:61507967-61507975 chr13:61507811-61507820 chr13:61507967-61507975 chr13:61507966-61507976
50	FOS	chr13:61412063-61412272	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:61455634-61455684	H1-hESC	embryonic stem cell:	embryo
2	chr13:61490935-61490985	GM19239	blood:	n/a
3	chr13:61490935-61490985	HCM	heart:	n/a
4	chr13:61491000-61491050	HPAEpiC	pulmonary alveolar:	n/a
5	chr13:61455634-61455684	Jurkat	blood:	n/a
6	chr13:61455634-61455684	ECC-1	luminal epithelium:	n/a
7	chr13:61491000-61491050	HRCEpiC	kidney:	n/a
8	chr13:61490935-61490985	SAEC	small airway:	n/a
9	chr13:61491000-61491050	HAEpiC	amniotic membrane:	n/a
10	chr13:61491000-61491050	AG09309	skin:	n/a
11	chr13:61490822-61490872	ProgFib	skin:	n/a
12	chr13:61490822-61490872	HCM	heart:	n/a
13	chr13:61490935-61490985	U87	brain:	n/a
14	chr13:61490935-61490985	AG04450	lung:	fetal
15	chr13:61455634-61455684	HRE	kidney:	n/a
16	chr13:61455634-61455684	IMR90	lung:	fetal
17	chr13:61490822-61490872	HEK293	kidney:	embryo
18	chr13:61455634-61455684	HCM	heart:	n/a
19	chr13:61491000-61491050	NB4	blood:	n/a
20	chr13:61455634-61455684	SK-N-SH	brain:	n/a
21	chr13:61491000-61491050	HUVEC	blood vessel:	n/a
22	chr13:61490822-61490872	BE2_C	brain:	n/a
23	chr13:61455634-61455684	GM12878	blood:	n/a
24	chr13:61490935-61490985	AoSMC	blood vessel:	n/a
25	chr13:61491000-61491050	T-47D	breast:	n/a
26	chr13:61490935-61490985	HRCEpiC	kidney:	n/a
27	chr13:61490935-61490985	BJ	skin:	n/a
28	chr13:61455634-61455684	Caco-2	colon:	n/a
29	chr13:61490822-61490872	HCPEpiC	choroid plexus:	n/a
30	chr13:61491000-61491050	HMEC	breast:	n/a
31	chr13:61490822-61490872	NB4	blood:	n/a
32	chr13:61490822-61490872	NHDF-neo	bronchial:	n/a
33	chr13:61491000-61491050	HEEpiC	esophagus:	n/a
34	chr13:61491000-61491050	ovcar-3	ovarian:	n/a
35	chr13:61455634-61455684	HEK293	kidney:	embryo
36	chr13:61490822-61490872	HCT-116	colon:	n/a
37	chr13:61490935-61490985	HNPCEpiC	eye:	n/a
38	chr13:61490935-61490985	GM12891	blood:	n/a
39	chr13:61455634-61455684	HepG2	liver:	n/a
40	chr13:61491000-61491050	PANC-1	pancreas:	n/a
41	chr13:61490935-61490985	Hepatocyte	liver:	n/a
42	chr13:61455634-61455684	HCT-116	colon:	n/a
43	chr13:61490822-61490872	NT2-D1	testis:	n/a
44	chr13:61455634-61455684	NH-A	brain:	n/a
45	chr13:61455634-61455684	RPTEC	kidney:	n/a
46	chr13:61490935-61490985	HRPEpiC	eye:	n/a
47	chr13:61490935-61490985	HepG2	liver:	n/a
48	chr13:61455634-61455684	NHBE	bronchial:	n/a
49	chr13:61490935-61490985	SK-N-SH	brain:	n/a
50	chr13:61455634-61455684	T-47D	breast:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-13	chr13:61476227-61476644	NONHSAT034119
2	lnc-PCDH20-13	chr13:61476225-61476644	l_860_chr13:61476224-61497619_testes
3	lnc-TDRD3-3	chr13:61493947-61494141	ENSG00000227510.2
4	lnc-TDRD3-3	chr13:61491934-61492139	ENSG00000227510
5	lnc-PCDH20-13	chr13:61497518-61497619	l_860_chr13:61476224-61497619_testes
6	lnc-TDRD3-3	chr13:61491135-61491372	NONHSAT034120
7	lnc-TDRD3-3	chr13:61514541-61515902	NONHSAT034120
8	lnc-TDRD3-3	chr13:61491176-61491372	ENSG00000227510
9	lnc-PCDH20-13	chr13:61501393-61501682	NONHSAT034119
10	lnc-TDRD3-3	chr13:61491176-61491372	ENSG00000227510.2

Variant related genes	Relation type
RNY4P31	TF binding region
ENSG00000227510	TF binding region
RNY4P31	CpG island
ENSG00000227510	CpG island

Extended variants
information (count: 2787 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2787 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370050345	chr13:61384043-61384044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs3119878	chr13:61384056-61384057	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs137916186	chr13:61384061-61384062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538203122	chr13:61384076-61384077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575635952	chr13:61384129-61384130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542281870	chr13:61384159-61384160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550387232	chr13:61384164-61384165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568679054	chr13:61384194-61384195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544563468	chr13:61384259-61384260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181392348	chr13:61384326-61384327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375355774	chr13:61384341-61384342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9538939	chr13:61384399-61384400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201966089	chr13:61384415-61384416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572482739	chr13:61384418-61384419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539799886	chr13:61384421-61384422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140910284	chr13:61384424-61384425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114903411	chr13:61384429-61384430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544111179	chr13:61384440-61384441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1399150	chr13:61384486-61384487	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs371056437	chr13:61384489-61384490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531527515	chr13:61384521-61384522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1399151	chr13:61384530-61384531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574311909	chr13:61384580-61384581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117445269	chr13:61384593-61384594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560174206	chr13:61384615-61384616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527420544	chr13:61384674-61384675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545779812	chr13:61384675-61384676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564435873	chr13:61384719-61384720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs925641	chr13:61384766-61384767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs186764676	chr13:61384796-61384797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143104685	chr13:61384802-61384803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529495772	chr13:61384837-61384838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76727101	chr13:61384840-61384841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566162403	chr13:61384909-61384910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539591056	chr13:61384925-61384926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543090744	chr13:61384968-61384969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558094466	chr13:61384969-61384970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1399152	chr13:61384973-61384974	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537717891	chr13:61385014-61385015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556052398	chr13:61385039-61385040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192152743	chr13:61385113-61385114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541600492	chr13:61385133-61385134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551798438	chr13:61385180-61385181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs80207738	chr13:61385194-61385195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572097663	chr13:61385206-61385207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545588130	chr13:61385247-61385248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148191691	chr13:61385295-61385296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183810896	chr13:61385337-61385338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543478724	chr13:61385352-61385353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141169138	chr13:61385358-61385359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
small cell lung cancer	20016488	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	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
Esophageal squamous carcinoma	20200074	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Obesity	20950786	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61384000-61384400	Enhancers	Aorta	Aorta
2	chr13:61384400-61386200	Weak transcription	Aorta	Aorta
3	chr13:61384400-61386400	Enhancers	HUVEC	blood vessel
4	chr13:61385200-61385800	Enhancers	NH-A	brain
5	chr13:61386200-61386400	Enhancers	Aorta	Aorta
6	chr13:61406800-61407400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr13:61411200-61412000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr13:61411200-61412200	Enhancers	Aorta	Aorta
9	chr13:61411200-61412200	Enhancers	NHEK	skin
10	chr13:61411600-61412200	Enhancers	Fetal Brain Male	brain
11	chr13:61411800-61413200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr13:61412000-61413200	Enhancers	Fetal Kidney	kidney
13	chr13:61412200-61412600	Weak transcription	Fetal Brain Male	brain
14	chr13:61412600-61413000	Enhancers	Fetal Brain Male	brain
15	chr13:61413200-61418800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr13:61418800-61420200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:61419400-61420200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr13:61424400-61425000	Enhancers	Fetal Lung	lung
19	chr13:61427000-61427200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr13:61443400-61444200	ZNF genes & repeats	Pancreas	Pancrea
21	chr13:61443600-61444400	Enhancers	Esophagus	oesophagus
22	chr13:61443600-61444800	Enhancers	Right Ventricle	heart
23	chr13:61443800-61444400	Enhancers	Left Ventricle	heart
24	chr13:61443800-61444800	Enhancers	Right Atrium	heart
25	chr13:61444000-61444400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr13:61444000-61445200	Enhancers	Fetal Heart	heart
27	chr13:61447000-61447600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr13:61447000-61447600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr13:61447600-61448000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr13:61447600-61448200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr13:61447800-61448200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr13:61448000-61448800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr13:61451000-61459000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr13:61454600-61456400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr13:61455200-61456600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr13:61455400-61456400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr13:61455400-61456400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr13:61455600-61456400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr13:61455600-61456600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr13:61455800-61456400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr13:61456000-61456400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr13:61456000-61456400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr13:61456000-61456600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr13:61456000-61456600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr13:61456600-61459200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr13:61459000-61459800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr13:61466800-61467400	Enhancers	Fetal Heart	heart
48	chr13:61467400-61467600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr13:61467800-61468200	Enhancers	Fetal Lung	lung
50	chr13:61468200-61468400	Enhancers	HUES64 Cell Line	embryonic stem cell

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