Variant report

Variant	esv2759942
Chromosome Location	chr13:66164294-66394450
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	chr13:66212820-66213067	GM12878	blood:	n/a	n/a
2	CBX3	chr13:66212653-66213113	HCT-116	colon:	n/a	n/a
3	CEBPB	chr13:66212723-66213083	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr13:66252032-66252574	HCT-116	colon:	n/a	n/a
5	CEBPB	chr13:66357410-66357610	HepG2	liver:	n/a	n/a
6	CEBPB	chr13:66302712-66302983	HepG2	liver:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
7	CEBPB	chr13:66172567-66172901	A549	lung:	n/a	n/a
8	CEBPB	chr13:66179445-66179793	IMR90	lung:	n/a	chr13:66179676-66179689 chr13:66179676-66179689 chr13:66179504-66179517 chr13:66179506-66179517 chr13:66179504-66179517 chr13:66179506-66179517 chr13:66179504-66179517 chr13:66179678-66179689
9	CEBPB	chr13:66302696-66303002	IMR90	lung:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
10	CEBPB	chr13:66300708-66300953	IMR90	lung:	n/a	chr13:66300832-66300845
11	CEBPB	chr13:66269557-66269900	IMR90	lung:	n/a	chr13:66269714-66269727 chr13:66269716-66269727 chr13:66269714-66269725
12	CEBPB	chr13:66180730-66181006	IMR90	lung:	n/a	n/a
13	CEBPB	chr13:66302788-66302938	A549	lung:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
14	CEBPB	chr13:66343051-66343372	IMR90	lung:	n/a	n/a
15	CEBPB	chr13:66252152-66252392	K562	blood:	n/a	n/a
16	CEBPB	chr13:66172480-66172999	A549	lung:	n/a	chr13:66172550-66172561
17	CEBPB	chr13:66348781-66349093	A549	lung:	n/a	chr13:66348913-66348924
18	CEBPB	chr13:66172507-66172920	IMR90	lung:	n/a	chr13:66172550-66172561
19	CEBPB	chr13:66252098-66252418	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:66252087-66252372	A549	lung:	n/a	n/a
21	CEBPB	chr13:66252010-66252510	HCT-116	colon:	n/a	n/a
22	CEBPB	chr13:66252056-66252395	A549	lung:	n/a	n/a
23	CEBPB	chr13:66252079-66252396	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr13:66252073-66252455	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:66281605-66281903	HepG2	liver:	n/a	chr13:66281750-66281763 chr13:66281752-66281761 chr13:66281750-66281763 chr13:66281752-66281761 chr13:66281751-66281762 chr13:66281752-66281761 chr13:66281752-66281761 chr13:66281750-66281761
26	CEBPB	chr13:66269598-66269845	A549	lung:	n/a	chr13:66269714-66269727 chr13:66269716-66269727 chr13:66269714-66269725
27	CEBPB	chr13:66348742-66349098	IMR90	lung:	n/a	chr13:66348913-66348924
28	CEBPB	chr13:66172469-66172941	Hela-S3	cervix:	n/a	chr13:66172550-66172561
29	CEBPB	chr13:66252041-66252457	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr13:66284785-66285094	IMR90	lung:	n/a	chr13:66284953-66284964 chr13:66285014-66285031 chr13:66284954-66284963
31	CEBPB	chr13:66252168-66252428	MCF-7	breast:	n/a	n/a
32	CEBPB	chr13:66284808-66285037	K562	blood:	n/a	chr13:66284953-66284964 chr13:66285014-66285031 chr13:66284954-66284963
33	CEBPB	chr13:66281643-66281912	IMR90	lung:	n/a	chr13:66281750-66281763 chr13:66281752-66281761 chr13:66281750-66281763 chr13:66281752-66281761 chr13:66281751-66281762 chr13:66281752-66281761 chr13:66281752-66281761 chr13:66281750-66281761
34	CEBPB	chr13:66172575-66172866	A549	lung:	n/a	n/a
35	CEBPB	chr13:66343067-66343334	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr13:66174859-66175241	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:66348740-66349098	HepG2	liver:	n/a	chr13:66348913-66348924
38	CEBPB	chr13:66302768-66302924	H1-hESC	embryonic stem cell:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
39	CEBPB	chr13:66367393-66367619	IMR90	lung:	n/a	n/a
40	CEBPB	chr13:66269575-66269889	HepG2	liver:	n/a	chr13:66269716-66269727 chr13:66269714-66269727 chr13:66269714-66269725
41	CEBPB	chr13:66252078-66252417	IMR90	lung:	n/a	n/a
42	CEBPB	chr13:66302716-66302972	K562	blood:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
43	CEBPB	chr13:66252054-66252437	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr13:66284791-66285143	HepG2	liver:	n/a	chr13:66284953-66284964 chr13:66285014-66285031 chr13:66284954-66284963
45	CHD1	chr13:66175000-66175048	GM12878	blood:	n/a	n/a
46	CTCF	chr13:66212860-66213010	GM12870	blood:	n/a	n/a
47	CTCF	chr13:66212820-66212970	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr13:66212781-66213029	GM12878	blood:	n/a	n/a
49	CTCF	chr13:66212800-66212950	A549	lung:	n/a	n/a
50	CTCF	chr13:66212880-66213030	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66322551-66322601	ECC-1	luminal epithelium:	n/a
2	chr13:66322551-66322601	NHDF-neo	bronchial:	n/a
3	chr13:66252177-66252227	HUVEC	blood vessel:	n/a
4	chr13:66322551-66322601	SK-N-SH_RA	brain:	n/a
5	chr13:66322551-66322601	Jurkat	blood:	n/a
6	chr13:66322551-66322601	HL-60	blood:	n/a
7	chr13:66322551-66322601	HIPEpiC	eye:	n/a
8	chr13:66322551-66322601	Hela-S3	cervix:	n/a
9	chr13:66322551-66322601	Hepatocyte	liver:	n/a
10	chr13:66322551-66322601	MCF10A-Er-Src	breast:	n/a
11	chr13:66252177-66252227	SK-N-SH_RA	brain:	n/a
12	chr13:66322551-66322601	AoSMC	blood vessel:	n/a
13	chr13:66252177-66252227	HRCEpiC	kidney:	n/a
14	chr13:66322551-66322601	PrEC	prostate:	n/a
15	chr13:66252177-66252227	AG04450	lung:	fetal
16	chr13:66322551-66322601	AG04450	lung:	fetal
17	chr13:66252177-66252227	AG10803	skin:	n/a
18	chr13:66322551-66322601	HEEpiC	esophagus:	n/a
19	chr13:66252177-66252227	K562	blood:	n/a
20	chr13:66252177-66252227	SAEC	small airway:	n/a
21	chr13:66252177-66252227	NHBE	bronchial:	n/a
22	chr13:66322551-66322601	HRPEpiC	eye:	n/a
23	chr13:66252177-66252227	GM12891	blood:	n/a
24	chr13:66252177-66252227	HL-60	blood:	n/a
25	chr13:66322551-66322601	GM12892	blood:	n/a
26	chr13:66322551-66322601	PANC-1	pancreas:	n/a
27	chr13:66322551-66322601	GM12891	blood:	n/a
28	chr13:66252177-66252227	HEK293	kidney:	embryo
29	chr13:66252177-66252227	GM19239	blood:	n/a
30	chr13:66322551-66322601	NH-A	brain:	n/a
31	chr13:66252177-66252227	Hepatocyte	liver:	n/a
32	chr13:66322551-66322601	GM06990	blood:	n/a
33	chr13:66322551-66322601	SKMC	muscle:	n/a
34	chr13:66252177-66252227	HCPEpiC	choroid plexus:	n/a
35	chr13:66252177-66252227	Jurkat	blood:	n/a
36	chr13:66322551-66322601	HCPEpiC	choroid plexus:	n/a
37	chr13:66252177-66252227	AG09309	skin:	n/a
38	chr13:66322551-66322601	GM19239	blood:	n/a
39	chr13:66252177-66252227	HIPEpiC	eye:	n/a
40	chr13:66322551-66322601	NHBE	bronchial:	n/a
41	chr13:66322551-66322601	IMR90	lung:	fetal
42	chr13:66252177-66252227	Hela-S3	cervix:	n/a
43	chr13:66322551-66322601	PFSK-1	brain:	n/a
44	chr13:66322551-66322601	AG09319	gingival:	n/a
45	chr13:66322551-66322601	ProgFib	skin:	n/a
46	chr13:66322551-66322601	SK-N-MC	brain:	n/a
47	chr13:66252177-66252227	SKMC	muscle:	n/a
48	chr13:66252177-66252227	NH-A	brain:	n/a
49	chr13:66322551-66322601	HEK293	kidney:	embryo
50	chr13:66252177-66252227	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:65045929..65046727-chr13:66212514..66213321,2	MCF-7	breast:
2	chr13:66355137..66357196-chr13:66362374..66364366,2	K562	blood:
3	chr13:65020257..65021157-chr13:66212532..66213123,2	MCF-7	breast:
4	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:
5	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
6	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
7	chr13:66363582..66364363-chr21:32786060..32786817,2	MCF-7	breast:
8	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
9	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
10	chr13:66377468..66378968-chr8:43092929..43094908,2	MCF-7	breast:
11	chr13:66358245..66360880-chr16:71346372..71347872,2	MCF-7	breast:

Variant related genes	Relation type
HNRNPA3P5	TF binding region
HNRNPA3P5	CpG island
ENSG00000236565	chromatin interactions

Extended variants
information (count: 2779 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2779 , 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	rs374121182	chr13:66166816-66166817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556341921	chr13:66166836-66166837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112451008	chr13:66167000-66167001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7319348	chr13:66167039-66167040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574254573	chr13:66167115-66167116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191884279	chr13:66167127-66167128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542001829	chr13:66167195-66167196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561722993	chr13:66167267-66167268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535258176	chr13:66167351-66167352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9528946	chr13:66167356-66167357	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs146783047	chr13:66167464-66167465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533320564	chr13:66167474-66167475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550361708	chr13:66167504-66167505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9540481	chr13:66167561-66167562	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531431891	chr13:66167571-66167572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184178745	chr13:66167588-66167589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186590024	chr13:66167597-66167598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533790714	chr13:66167617-66167618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547664620	chr13:66167619-66167620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570769400	chr13:66167690-66167691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9599006	chr13:66167699-66167700	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs563881424	chr13:66167728-66167729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556317154	chr13:66167801-66167802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576183699	chr13:66167830-66167831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141155098	chr13:66167836-66167837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555459018	chr13:66167837-66167838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368341264	chr13:66167845-66167846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572081843	chr13:66167850-66167851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9599007	chr13:66167865-66167866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541032645	chr13:66167870-66167871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74091267	chr13:66167889-66167890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1538814	chr13:66167897-66167898	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs74452966	chr13:66167944-66167945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543808246	chr13:66167961-66167962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563885910	chr13:66167978-66167979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529498640	chr13:66167993-66167994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541917575	chr13:66167996-66167997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543080968	chr13:66168040-66168041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141874163	chr13:66168045-66168046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191956657	chr13:66168046-66168047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527242568	chr13:66168108-66168109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547406628	chr13:66168145-66168146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570397033	chr13:66168186-66168187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370392055	chr13:66168188-66168189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116575604	chr13:66168200-66168201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549839976	chr13:66168207-66168208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569796127	chr13:66168214-66168215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182502331	chr13:66168291-66168292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555397110	chr13:66168326-66168327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142218443	chr13:66168361-66168362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66166800-66167800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:66166800-66169200	Enhancers	Fetal Lung	lung
3	chr13:66166800-66171200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:66167000-66167200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr13:66167000-66167400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr13:66167000-66167400	Enhancers	Fetal Heart	heart
7	chr13:66167000-66167400	Enhancers	Fetal Stomach	stomach
8	chr13:66167000-66167600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr13:66167000-66169200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr13:66167000-66169400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr13:66167000-66169400	Enhancers	NH-A	brain
12	chr13:66167400-66167600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr13:66167400-66167600	Weak transcription	Fetal Stomach	stomach
14	chr13:66167400-66167800	Weak transcription	Fetal Heart	heart
15	chr13:66167400-66168400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr13:66167600-66168000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr13:66167600-66168000	Enhancers	Fetal Stomach	stomach
18	chr13:66167600-66172000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr13:66167800-66168000	Enhancers	Fetal Heart	heart
20	chr13:66167800-66169000	Enhancers	Fetal Brain Male	brain
21	chr13:66167800-66169200	Enhancers	Osteobl	bone
22	chr13:66167800-66169600	Enhancers	Brain Germinal Matrix	brain
23	chr13:66168000-66168800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr13:66168000-66169400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr13:66168000-66169800	Weak transcription	Fetal Stomach	stomach
26	chr13:66168000-66171800	Weak transcription	Fetal Heart	heart
27	chr13:66168400-66169200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr13:66168400-66169200	Enhancers	Adipose Nuclei	Adipose
29	chr13:66168800-66169400	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr13:66169000-66170600	Enhancers	NHDF-Ad	bronchial
31	chr13:66169200-66171800	Weak transcription	Fetal Lung	lung
32	chr13:66169200-66172200	Weak transcription	Adipose Nuclei	Adipose
33	chr13:66169200-66172200	Weak transcription	Osteobl	bone
34	chr13:66169400-66169800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr13:66169400-66169800	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr13:66169400-66170000	Weak transcription	NH-A	brain
37	chr13:66169800-66170000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr13:66169800-66170000	Enhancers	Fetal Stomach	stomach
39	chr13:66169800-66170600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr13:66170000-66170600	Enhancers	NH-A	brain
41	chr13:66170000-66171800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr13:66170600-66171800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr13:66170600-66172200	Weak transcription	NHDF-Ad	bronchial
44	chr13:66170600-66172400	Weak transcription	NH-A	brain
45	chr13:66171200-66171600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr13:66171600-66172600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr13:66171800-66172000	Flanking Active TSS	Fetal Lung	lung
48	chr13:66171800-66172600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr13:66171800-66172800	Enhancers	Fetal Heart	heart
50	chr13:66171800-66173400	Enhancers	Muscle Satellite Cultured Cells	--

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