Variant report

Variant	nsv900389
Chromosome Location	chr13:66867794-66961006
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	chr13:66886857-66887028	HepG2	liver:	n/a	n/a
2	ATF3	chr13:66886740-66887227	A549	lung:	n/a	n/a
3	BCL3	chr13:66886752-66887345	A549	lung:	n/a	n/a
4	BCL3	chr13:66886608-66887994	A549	lung:	n/a	n/a
5	BHLHE40	chr13:66902776-66902779	K562	blood:	n/a	n/a
6	BHLHE40	chr13:66917482-66917943	K562	blood:	n/a	n/a
7	BRCA1	chr13:66878245-66878246	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr13:66948076-66948370	HepG2	liver:	n/a	chr13:66948242-66948255 chr13:66948244-66948253 chr13:66948242-66948255 chr13:66948244-66948253 chr13:66948244-66948255 chr13:66948244-66948253 chr13:66948244-66948253 chr13:66948242-66948253
9	CEBPB	chr13:66888682-66888899	HepG2	liver:	n/a	n/a
10	CEBPB	chr13:66887496-66887884	A549	lung:	n/a	n/a
11	CEBPB	chr13:66872470-66872807	IMR90	lung:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
12	CEBPB	chr13:66872525-66872807	Hela-S3	cervix:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
13	CEBPB	chr13:66932688-66932916	HepG2	liver:	n/a	chr13:66932747-66932758
14	CEBPB	chr13:66891929-66892183	HepG2	liver:	n/a	chr13:66892052-66892065 chr13:66892041-66892052
15	CEBPB	chr13:66872481-66872820	HepG2	liver:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
16	CEBPB	chr13:66906331-66906484	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr13:66887551-66887864	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:66935066-66935291	HepG2	liver:	n/a	n/a
19	CEBPB	chr13:66946973-66947173	HepG2	liver:	n/a	chr13:66947077-66947088
20	CEBPB	chr13:66887553-66887871	IMR90	lung:	n/a	n/a
21	CEBPB	chr13:66887481-66887890	A549	lung:	n/a	n/a
22	CEBPB	chr13:66886928-66887166	A549	lung:	n/a	n/a
23	CEBPB	chr13:66872539-66872758	H1-hESC	embryonic stem cell:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
24	CEBPB	chr13:66898105-66898199	HepG2	liver:	n/a	chr13:66898111-66898122
25	CEBPB	chr13:66886648-66888000	A549	lung:	n/a	n/a
26	CEBPB	chr13:66872489-66872826	K562	blood:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
27	CEBPB	chr13:66930900-66931157	A549	lung:	n/a	n/a
28	CEBPB	chr13:66954916-66955129	HepG2	liver:	n/a	n/a
29	CEBPB	chr13:66923133-66923414	A549	lung:	n/a	n/a
30	CEBPB	chr13:66886797-66887222	A549	lung:	n/a	n/a
31	CEBPB	chr13:66948118-66948402	IMR90	lung:	n/a	chr13:66948242-66948255 chr13:66948244-66948253 chr13:66948242-66948255 chr13:66948244-66948253 chr13:66948244-66948255 chr13:66948244-66948253 chr13:66948244-66948253 chr13:66948242-66948253
32	CEBPB	chr13:66872466-66872822	A549	lung:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
33	CEBPB	chr13:66930894-66931208	HepG2	liver:	n/a	n/a
34	CEBPB	chr13:66888568-66888896	A549	lung:	n/a	n/a
35	CEBPD	chr13:66872704-66873142	K562	blood:	n/a	n/a
36	CHD2	chr13:66898349-66898352	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr13:66886531-66886751	A549	lung:	n/a	n/a
38	CREB1	chr13:66887558-66887926	A549	lung:	n/a	n/a
39	CREB1	chr13:66923338-66923523	A549	lung:	n/a	n/a
40	CREB1	chr13:66887670-66887940	A549	lung:	n/a	n/a
41	CTCF	chr13:66927839-66928175	K562	blood:	n/a	chr13:66928040-66928061 chr13:66928042-66928049
42	CTCF	chr13:66925777-66925865	K562	blood:	n/a	n/a
43	CTCF	chr13:66927960-66928110	HBMEC	blood vessel:	n/a	chr13:66928040-66928061 chr13:66928042-66928049
44	CTCF	chr13:66928000-66928150	HPAF	blood vessel:	n/a	chr13:66928040-66928061 chr13:66928042-66928049
45	CTCF	chr13:66908162-66908197	Lung_OC	lung:	n/a	n/a
46	CTCF	chr13:66927920-66928070	SK-N-SH_RA	brain:	n/a	chr13:66928040-66928061 chr13:66928042-66928049
47	CTCF	chr13:66927960-66928110	HCPEpiC	choroid plexus:	n/a	chr13:66928040-66928061 chr13:66928042-66928049
48	CTCF	chr13:66888880-66889030	BE2_C	brain:	n/a	n/a
49	CTCF	chr13:66877471-66877527	GM10248	blood:	n/a	n/a
50	CTCF	chr13:66951360-66951510	AG09309	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66929165-66929215	Jurkat	blood:	n/a
2	chr13:66929165-66929215	Jurkat	blood:	n/a
3	chr13:66878738-66878788	NB4	blood:	n/a
4	chr13:66929165-66929215	HCM	heart:	n/a
5	chr13:66919912-66919962	Hela-S3	cervix:	n/a
6	chr13:66878738-66878788	AG10803	skin:	n/a
7	chr13:66878738-66878788	SK-N-MC	brain:	n/a
8	chr13:66929165-66929215	K562	blood:	n/a
9	chr13:66919912-66919962	NH-A	brain:	n/a
10	chr13:66929165-66929215	ECC-1	luminal epithelium:	n/a
11	chr13:66878738-66878788	HUVEC	blood vessel:	n/a
12	chr13:66929165-66929215	Hela-S3	cervix:	n/a
13	chr13:66878738-66878788	NHBE	bronchial:	n/a
14	chr13:66878738-66878788	ProgFib	skin:	n/a
15	chr13:66919912-66919962	AG04450	lung:	fetal
16	chr13:66929165-66929215	HepG2	liver:	n/a
17	chr13:66929165-66929215	SK-N-SH	brain:	n/a
18	chr13:66878738-66878788	PFSK-1	brain:	n/a
19	chr13:66878738-66878788	HIPEpiC	eye:	n/a
20	chr13:66929165-66929215	BJ	skin:	n/a
21	chr13:66878738-66878788	U87	brain:	n/a
22	chr13:66878738-66878788	PrEC	prostate:	n/a
23	chr13:66878738-66878788	HNPCEpiC	eye:	n/a
24	chr13:66919912-66919962	HRE	kidney:	n/a
25	chr13:66929165-66929215	HAEpiC	amniotic membrane:	n/a
26	chr13:66929165-66929215	HEK293	kidney:	embryo
27	chr13:66919912-66919962	HIPEpiC	eye:	n/a
28	chr13:66929165-66929215	ProgFib	skin:	n/a
29	chr13:66929165-66929215	AG10803	skin:	n/a
30	chr13:66878738-66878788	ovcar-3	ovarian:	n/a
31	chr13:66878738-66878788	SKMC	muscle:	n/a
32	chr13:66919912-66919962	Jurkat	blood:	n/a
33	chr13:66878738-66878788	Hela-S3	cervix:	n/a
34	chr13:66919912-66919962	IMR90	lung:	fetal
35	chr13:66929165-66929215	A549	lung:	n/a
36	chr13:66929165-66929215	PrEC	prostate:	n/a
37	chr13:66878738-66878788	AG04450	lung:	fetal
38	chr13:66878738-66878788	GM12892	blood:	n/a
39	chr13:66929165-66929215	T-47D	breast:	n/a
40	chr13:66919912-66919962	GM12892	blood:	n/a
41	chr13:66919912-66919962	HNPCEpiC	eye:	n/a
42	chr13:66878738-66878788	HEK293	kidney:	embryo
43	chr13:66919912-66919962	SAEC	small airway:	n/a
44	chr13:66919912-66919962	HEEpiC	esophagus:	n/a
45	chr13:66919912-66919962	PANC-1	pancreas:	n/a
46	chr13:66919912-66919962	SK-N-SH_RA	brain:	n/a
47	chr13:66929165-66929215	MCF-7	breast:	n/a
48	chr13:66919912-66919962	LNCaP	prostate:	n/a
49	chr13:66929165-66929215	HEEpiC	esophagus:	n/a
50	chr13:66878738-66878788	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
2	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
3	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
4	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
5	chr13:66918574..66921439-chr13:66945401..66948264,2	MCF-7	breast:
6	chr13:66918574..66921439-chr13:66945401..66948264,2	MCF-7	breast:
7	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
8	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-13	chr13:66878003-66878146	ENSG00000234527.1
2	lnc-AL445989.1-13	chr13:66897306-66897693	ENSG00000234527.1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PCDH9	hsa-miR-155-5p	chr13:66877756-66877779
2	PCDH9	hsa-miR-155-5p	chr13:66878327-66878320
3	PCDH9	hsa-miR-155-5p	chr13:66878321-66878343

Variant related genes	Relation type
PCDH9-AS1	TF binding region
PCDH9-AS1	CpG island

Extended variants
information (count: 2687 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2687 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117268717	chr13:66872650-66872651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs578097856	chr13:66872653-66872654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79592149	chr13:66872690-66872691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182991247	chr13:66872766-66872767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34002613	chr13:66872777-66872778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9571570	chr13:66872809-66872810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556740523	chr13:66872832-66872833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143395849	chr13:66872877-66872878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573663470	chr13:66872908-66872909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115832952	chr13:66872910-66872911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201314554	chr13:66872923-66872924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375361157	chr13:66872930-66872931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200858931	chr13:66872931-66872932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541005905	chr13:66872938-66872939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561302663	chr13:66872951-66872952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199577125	chr13:66872963-66872964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74409107	chr13:66873001-66873002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142692115	chr13:66873070-66873071	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs373294969	chr13:66873142-66873143	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs113405426	chr13:66873181-66873182	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs372760129	chr13:66873186-66873187	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539600692	chr13:66873187-66873188	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs112453988	chr13:66873201-66873202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188789081	chr13:66873218-66873219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77145094	chr13:66873219-66873220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113792012	chr13:66873242-66873243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146942958	chr13:66873261-66873262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551998230	chr13:66873272-66873273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563686207	chr13:66873294-66873295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535021687	chr13:66873359-66873360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4883772	chr13:66873409-66873410	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs74618086	chr13:66873496-66873497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112205635	chr13:66873526-66873527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192629640	chr13:66873530-66873531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569425887	chr13:66873544-66873545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575736936	chr13:66873545-66873546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183144495	chr13:66873554-66873555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561361307	chr13:66873562-66873563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35097955	chr13:66873579-66873580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527249714	chr13:66873604-66873605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540993040	chr13:66873623-66873624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75897275	chr13:66873644-66873645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1200532	chr13:66873657-66873658	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs143977199	chr13:66873672-66873673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs67358141	chr13:66873673-66873674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs71750468	chr13:66873674-66873675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs3223251	chr13:66873675-66873676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201934138	chr13:66873680-66873681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191111197	chr13:66873694-66873695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61955829	chr13:66873699-66873700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66872600-66886400	Weak transcription	HSMM	muscle
2	chr13:66872800-66875000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr13:66873200-66874200	Enhancers	Dnd41	blood
4	chr13:66874200-66878600	Weak transcription	Dnd41	blood
5	chr13:66875000-66875600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr13:66875200-66875400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:66875200-66875400	Enhancers	Brain Hippocampus Middle	brain
8	chr13:66875200-66875400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr13:66875200-66875600	Enhancers	Fetal Kidney	kidney
10	chr13:66875200-66876000	Enhancers	Brain Cingulate Gyrus	brain
11	chr13:66875200-66876000	Enhancers	Brain Substantia Nigra	brain
12	chr13:66875200-66876400	Enhancers	A549	lung
13	chr13:66875400-66876000	Weak transcription	Brain Hippocampus Middle	brain
14	chr13:66875400-66878800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr13:66876000-66876200	Enhancers	Brain Hippocampus Middle	brain
16	chr13:66876000-66887000	Weak transcription	Brain Substantia Nigra	brain
17	chr13:66876200-66882800	Weak transcription	Brain Hippocampus Middle	brain
18	chr13:66876400-66876600	Enhancers	Brain Anterior Caudate	brain
19	chr13:66876400-66884400	Weak transcription	A549	lung
20	chr13:66876800-66879800	Weak transcription	Brain Anterior Caudate	brain
21	chr13:66878600-66879800	Enhancers	Dnd41	blood
22	chr13:66878800-66879000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr13:66878800-66879000	ZNF genes & repeats	Pancreas	Pancrea
24	chr13:66878800-66879200	Enhancers	Primary B cells from peripheral blood	blood
25	chr13:66879000-66879800	Enhancers	Primary B cells from cord blood	blood
26	chr13:66879000-66886400	Weak transcription	Pancreas	Pancrea
27	chr13:66879000-66889200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:66879800-66880400	Flanking Active TSS	Dnd41	blood
29	chr13:66879800-66880600	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr13:66879800-66880800	Enhancers	Primary hematopoietic stem cells	blood
31	chr13:66880000-66880800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr13:66880400-66881400	Enhancers	Dnd41	blood
33	chr13:66880600-66881400	Enhancers	Primary B cells from cord blood	blood
34	chr13:66882600-66883000	Enhancers	Brain Cingulate Gyrus	brain
35	chr13:66882800-66883400	Enhancers	Brain Hippocampus Middle	brain
36	chr13:66883000-66889000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr13:66883400-66887400	Weak transcription	Brain Hippocampus Middle	brain
38	chr13:66884400-66885600	Enhancers	A549	lung
39	chr13:66884400-66887600	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr13:66885000-66885200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr13:66885200-66886200	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr13:66885600-66886400	Flanking Active TSS	A549	lung
43	chr13:66886000-66887400	Enhancers	Stomach Mucosa	stomach
44	chr13:66886200-66886600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr13:66886200-66888400	Enhancers	Osteobl	bone
46	chr13:66886400-66886600	Enhancers	HSMM	muscle
47	chr13:66886400-66886800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr13:66886400-66886800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr13:66886400-66886800	Enhancers	Ovary	ovary
50	chr13:66886400-66886800	Enhancers	Pancreas	Pancrea

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