Variant report

Variant	esv3434233
Chromosome Location	chr13:67872454-68265687
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	chr13:68128670-68128870	K562	blood:	n/a	n/a
2	ARID3A	chr13:67957650-67957867	HepG2	liver:	n/a	n/a
3	ATF1	chr13:68129258-68129434	K562	blood:	n/a	n/a
4	ATF1	chr13:68014427-68014642	K562	blood:	n/a	n/a
5	ATF2	chr13:67990402-67990747	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr13:67877967-67878020	A549	lung:	n/a	n/a
7	BHLHE40	chr13:67914600-67914697	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:67981208-67981213	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:67957539-67957853	HepG2	liver:	n/a	n/a
10	BHLHE40	chr13:67914536-67914710	K562	blood:	n/a	n/a
11	BHLHE40	chr13:68090082-68090364	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:67940874-67940875	GM12878	blood:	n/a	n/a
13	BRCA1	chr13:68213539-68213621	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:67941712-67941854	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr13:68094107-68094138	GM12878	blood:	n/a	n/a
16	CBX3	chr13:68131868-68132121	K562	blood:	n/a	n/a
17	CBX3	chr13:68131811-68132172	K562	blood:	n/a	n/a
18	CBX3	chr13:68131870-68132186	HCT-116	colon:	n/a	n/a
19	CCNT2	chr13:68217486-68217843	K562	blood:	n/a	n/a
20	CEBPB	chr13:68144258-68144556	IMR90	lung:	n/a	chr13:68144409-68144420
21	CEBPB	chr13:68006413-68006613	A549	lung:	n/a	n/a
22	CEBPB	chr13:68206698-68207165	IMR90	lung:	n/a	n/a
23	CEBPB	chr13:67925283-67925549	A549	lung:	n/a	chr13:67925441-67925450 chr13:67925439-67925450 chr13:67925441-67925450 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925377-67925388
24	CEBPB	chr13:67983041-67983303	ECC-1	luminal epithelium:	n/a	chr13:67983192-67983203
25	CEBPB	chr13:67917699-67917847	K562	blood:	n/a	chr13:67917760-67917771
26	CEBPB	chr13:67957573-67957884	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr13:68131362-68131630	H1-hESC	embryonic stem cell:	n/a	chr13:68131452-68131463
28	CEBPB	chr13:68131299-68131641	K562	blood:	n/a	chr13:68131452-68131463
29	CEBPB	chr13:67882143-67882491	Hela-S3	cervix:	n/a	chr13:67882281-67882294
30	CEBPB	chr13:67982954-67983392	ECC-1	luminal epithelium:	n/a	chr13:67983192-67983203
31	CEBPB	chr13:68128500-68129266	IMR90	lung:	n/a	chr13:68128559-68128571
32	CEBPB	chr13:67925346-67925624	HepG2	liver:	n/a	chr13:67925441-67925450 chr13:67925439-67925450 chr13:67925441-67925450 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925377-67925388
33	CEBPB	chr13:68162141-68162341	HepG2	liver:	n/a	chr13:68162250-68162261 chr13:68162249-68162260 chr13:68162249-68162262 chr13:68162248-68162265
34	CEBPB	chr13:68128519-68128802	K562	blood:	n/a	chr13:68128559-68128571
35	CEBPB	chr13:67957646-67957798	IMR90	lung:	n/a	n/a
36	CEBPB	chr13:67925266-67925623	IMR90	lung:	n/a	chr13:67925441-67925450 chr13:67925439-67925450 chr13:67925441-67925450 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925377-67925388
37	CEBPB	chr13:67983010-67983379	HepG2	liver:	n/a	chr13:67983192-67983203
38	CEBPB	chr13:68060708-68060924	K562	blood:	n/a	chr13:68060761-68060772 chr13:68060763-68060772 chr13:68060763-68060774
39	CEBPB	chr13:67886478-67886731	K562	blood:	n/a	chr13:67886624-67886635
40	CEBPB	chr13:67917602-67917928	HepG2	liver:	n/a	chr13:67917760-67917771
41	CEBPB	chr13:68060645-68060905	A549	lung:	n/a	chr13:68060761-68060772 chr13:68060763-68060772 chr13:68060763-68060774
42	CEBPB	chr13:67933047-67933298	HepG2	liver:	n/a	chr13:67933196-67933205 chr13:67933194-67933205
43	CEBPB	chr13:67900201-67900450	A549	lung:	n/a	chr13:67900293-67900304
44	CEBPB	chr13:67952124-67952426	Hela-S3	cervix:	n/a	chr13:67952260-67952271
45	CEBPB	chr13:68135776-68135872	K562	blood:	n/a	n/a
46	CEBPB	chr13:68218637-68218912	HepG2	liver:	n/a	n/a
47	CEBPB	chr13:67900192-67900488	IMR90	lung:	n/a	chr13:67900293-67900304
48	CEBPB	chr13:67917618-67917912	Hela-S3	cervix:	n/a	chr13:67917760-67917771
49	CEBPB	chr13:68033581-68033863	HepG2	liver:	n/a	chr13:68033747-68033760 chr13:68033747-68033758
50	CEBPB	chr13:67926113-67926355	Hela-S3	cervix:	n/a	chr13:67926245-67926256

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:68260105-68260155	HMEC	breast:	n/a
2	chr13:68260105-68260155	HMEC	breast:	n/a
3	chr13:68093157-68093207	SK-N-SH_RA	brain:	n/a
4	chr13:68261695-68261745	HCPEpiC	choroid plexus:	n/a
5	chr13:68093157-68093207	HCF	heart:	n/a
6	chr13:68194226-68194276	AoSMC	blood vessel:	n/a
7	chr13:67872416-67872466	IMR90	lung:	fetal
8	chr13:68218088-68218138	A549	lung:	n/a
9	chr13:68260105-68260155	ECC-1	luminal epithelium:	n/a
10	chr13:68194226-68194276	IMR90	lung:	fetal
11	chr13:68093157-68093207	ovcar-3	ovarian:	n/a
12	chr13:68260105-68260155	U87	brain:	n/a
13	chr13:67872416-67872466	MCF10A-Er-Src	breast:	n/a
14	chr13:68220805-68220855	HEK293	kidney:	embryo
15	chr13:68194226-68194276	HIPEpiC	eye:	n/a
16	chr13:68194226-68194276	HCF	heart:	n/a
17	chr13:68218088-68218138	NH-A	brain:	n/a
18	chr13:68218088-68218138	HAEpiC	amniotic membrane:	n/a
19	chr13:68260105-68260155	HCPEpiC	choroid plexus:	n/a
20	chr13:68218088-68218138	U87	brain:	n/a
21	chr13:67872416-67872466	PrEC	prostate:	n/a
22	chr13:68220805-68220855	SK-N-SH_RA	brain:	n/a
23	chr13:68260105-68260155	AG09309	skin:	n/a
24	chr13:68194226-68194276	ovcar-3	ovarian:	n/a
25	chr13:68093157-68093207	AoSMC	blood vessel:	n/a
26	chr13:67872416-67872466	K562	blood:	n/a
27	chr13:68218088-68218138	ovcar-3	ovarian:	n/a
28	chr13:68093157-68093207	HIPEpiC	eye:	n/a
29	chr13:68093157-68093207	SK-N-MC	brain:	n/a
30	chr13:68093157-68093207	AG04449	skin:	fetal
31	chr13:68093157-68093207	CMK	blood:	n/a
32	chr13:68093157-68093207	HEK293	kidney:	embryo
33	chr13:68093157-68093207	GM12892	blood:	n/a
34	chr13:68261695-68261745	AG04449	skin:	fetal
35	chr13:68093157-68093207	GM19239	blood:	n/a
36	chr13:68220805-68220855	PrEC	prostate:	n/a
37	chr13:68093157-68093207	BE2_C	brain:	n/a
38	chr13:68218088-68218138	HRE	kidney:	n/a
39	chr13:68194226-68194276	MCF-7	breast:	n/a
40	chr13:68220805-68220855	LNCaP	prostate:	n/a
41	chr13:68218088-68218138	AG09309	skin:	n/a
42	chr13:68194226-68194276	HCT-116	colon:	n/a
43	chr13:68260105-68260155	NB4	blood:	n/a
44	chr13:68194226-68194276	HRE	kidney:	n/a
45	chr13:67872416-67872466	T-47D	breast:	n/a
46	chr13:67872416-67872466	HCF	heart:	n/a
47	chr13:68218088-68218138	GM19239	blood:	n/a
48	chr13:68093157-68093207	IMR90	lung:	fetal
49	chr13:68261695-68261745	RPTEC	kidney:	n/a
50	chr13:68093157-68093207	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:68105208..68107775-chr13:68119944..68122394,2	K562	blood:
2	chr13:68060280..68061789-chr13:68065167..68067699,2	K562	blood:
3	chr13:68141533..68143284-chr13:68158186..68161018,2	MCF-7	breast:
4	chr13:67896040..67897805-chr13:67907096..67909108,2	K562	blood:
5	chr13:68176298..68176798-chr18:12308206..12308971,2	Hela-S3	cervix:
6	chr13:68141533..68143284-chr13:68158186..68161018,2	MCF-7	breast:
7	chr13:68060280..68061789-chr13:68065167..68067699,2	K562	blood:
8	chr13:67896040..67897805-chr13:67907096..67909108,2	K562	blood:
9	chr13:68215746..68218310-chr4:161981929..161984752,2	MCF-7	breast:
10	chr12:113839422..113840262-chr13:68011903..68012677,2	MCF-7	breast:
11	chr13:68105208..68107775-chr13:68119944..68122394,2	K562	blood:
12	chr13:68241658..68242183-chr6:114561063..114561674,2	MCF-7	breast:
13	chr13:67649311..67650094-chr13:67990535..67991084,2	MCF-7	breast:
14	chr13:67919389..67921263-chr13:67925624..67927193,2	MCF-7	breast:
15	chr13:68112593..68114688-chr13:68118915..68121186,2	K562	blood:
16	chr11:405424..407455-chr13:68082317..68085316,2	K562	blood:
17	chr13:68112593..68114688-chr13:68118915..68121186,2	K562	blood:
18	chr13:67919389..67921263-chr13:67925624..67927193,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH9-2	chr13:68157228-68157361	XLOC_010648
2	lnc-AL445989.1-18	chr13:68170509-68170530	XLOC_010418
3	lnc-AL445989.1-18	chr13:68172858-68173105	XLOC_010418
4	lnc-PCDH9-8	chr13:68222217-68222724	NONHSAT034223
5	lnc-PCDH9-2	chr13:68155305-68155476	XLOC_010648

Variant related genes	Relation type
LINC00364	TF binding region
LINC00364	CpG island
ENSG00000176014	chromatin interactions
ENSG00000185187	chromatin interactions

Extended variants
information (count: 5435 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:5435 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537663413	chr13:67872509-67872510	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572695594	chr13:67872553-67872554	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541590842	chr13:67872582-67872583	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114187410	chr13:67872599-67872600	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191985683	chr13:67872648-67872649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531466245	chr13:67872703-67872704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543529665	chr13:67872718-67872719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563293189	chr13:67872726-67872727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529295910	chr13:67872795-67872796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574475304	chr13:67872806-67872807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535240142	chr13:67872820-67872821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17082334	chr13:67872850-67872851	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs145077033	chr13:67872867-67872868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148349700	chr13:67872869-67872870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540022999	chr13:67872873-67872874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183117380	chr13:67872893-67872894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533012724	chr13:67872915-67872916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140552956	chr13:67872938-67872939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569692075	chr13:67872998-67872999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543644664	chr13:67873015-67873016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12873821	chr13:67873031-67873032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12873835	chr13:67873054-67873055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187089461	chr13:67873061-67873062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555094886	chr13:67873063-67873064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202208073	chr13:67873089-67873090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72521100	chr13:67873090-67873091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs5804318	chr13:67873091-67873092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78600242	chr13:67873092-67873093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192779024	chr13:67873125-67873126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113060086	chr13:67873134-67873135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535000697	chr13:67873135-67873136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376805898	chr13:67873139-67873140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557900500	chr13:67873156-67873157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1360717	chr13:67873157-67873158	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs75118031	chr13:67873165-67873166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557023697	chr13:67873170-67873171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574080433	chr13:67873181-67873182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542993798	chr13:67873188-67873189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1360718	chr13:67873202-67873203	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs533030686	chr13:67873217-67873218	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs150472217	chr13:67873260-67873261	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs541336569	chr13:67873289-67873290	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs564233314	chr13:67873351-67873352	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs533152565	chr13:67873410-67873411	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs550048831	chr13:67873416-67873417	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs138336166	chr13:67873467-67873468	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs141388984	chr13:67873481-67873482	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs184445622	chr13:67873485-67873486	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs372303730	chr13:67873496-67873497	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs189362547	chr13:67873531-67873532	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67870600-67873200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr13:67870800-67874600	Enhancers	HSMM	muscle
3	chr13:67871000-67873800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr13:67871400-67872600	Active TSS	Brain Cingulate Gyrus	brain
5	chr13:67871400-67873400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr13:67872000-67872600	Enhancers	Fetal Brain Male	brain
7	chr13:67872400-67872600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr13:67872400-67872600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr13:67872400-67872800	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr13:67872400-67873200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr13:67872400-67873200	Weak transcription	Brain Substantia Nigra	brain
12	chr13:67872600-67873600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr13:67872600-67873800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr13:67872800-67874400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:67873000-67873200	Enhancers	Osteobl	bone
16	chr13:67873200-67873400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr13:67873200-67873400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr13:67873200-67873600	Enhancers	HSMMtube	muscle
19	chr13:67873200-67873600	Enhancers	NH-A	brain
20	chr13:67873200-67873800	Enhancers	Brain Substantia Nigra	brain
21	chr13:67873200-67873800	Enhancers	HUVEC	blood vessel
22	chr13:67873200-67874200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr13:67873200-67874200	Enhancers	NHDF-Ad	bronchial
24	chr13:67873200-67874200	Flanking Active TSS	Osteobl	bone
25	chr13:67873200-67874400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr13:67873200-67874600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr13:67873200-67874600	Enhancers	HMEC	breast
28	chr13:67873400-67873600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr13:67873400-67873600	Enhancers	Brain Cingulate Gyrus	brain
30	chr13:67873400-67873800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr13:67873600-67874000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr13:67873600-67874000	Flanking Active TSS	HSMMtube	muscle
33	chr13:67873600-67874200	Flanking Active TSS	NH-A	brain
34	chr13:67873600-67874400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr13:67873800-67874000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr13:67874000-67874400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr13:67874000-67874600	Enhancers	HSMMtube	muscle
38	chr13:67874200-67874400	Enhancers	Osteobl	bone
39	chr13:67874400-67874800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr13:67874600-67882400	Weak transcription	HMEC	breast
41	chr13:67882200-67882400	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr13:67882400-67882600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr13:67882400-67882800	Enhancers	HMEC	breast
44	chr13:67882600-67883000	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr13:67888400-67888800	Enhancers	Fetal Heart	heart
46	chr13:67888600-67889600	Enhancers	Left Ventricle	heart
47	chr13:67898400-67898600	Enhancers	Fetal Heart	heart
48	chr13:67898600-67900200	Weak transcription	Fetal Heart	heart
49	chr13:67900200-67901000	Enhancers	Fetal Heart	heart
50	chr13:67901000-67905600	Weak transcription	Fetal Heart	heart

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