Variant report

Variant	nsv900481
Chromosome Location	chr13:70147851-70560731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1355)
CpG islands
(count:183)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1355 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:70485011-70485172	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:70431391-70431702	HepG2	liver:	n/a	n/a
3	ATF2	chr13:70522070-70522685	GM12878	blood:	n/a	n/a
4	ATF2	chr13:70258281-70258806	GM12878	blood:	n/a	n/a
5	ATF2	chr13:70522087-70522569	GM12878	blood:	n/a	n/a
6	BACH1	chr13:70250741-70250952	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr13:70251604-70251776	GM12878	blood:	n/a	chr13:70251694-70251705
8	BATF	chr13:70522173-70522484	GM12878	blood:	n/a	n/a
9	BATF	chr13:70522186-70522497	GM12878	blood:	n/a	n/a
10	BCL11A	chr13:70522218-70522397	GM12878	blood:	n/a	n/a
11	BCL11A	chr13:70522097-70522470	GM12878	blood:	n/a	n/a
12	BCL3	chr13:70522223-70522462	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:70522153-70522647	GM12878	blood:	n/a	n/a
14	BHLHE40	chr13:70275529-70275573	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:70430533-70430835	HepG2	liver:	n/a	chr13:70430691-70430700 chr13:70430688-70430701
16	BHLHE40	chr13:70251405-70251582	GM12878	blood:	n/a	n/a
17	BRCA1	chr13:70212779-70212821	GM12878	blood:	n/a	n/a
18	BRCA1	chr13:70531000-70531545	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr13:70431439-70431586	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr13:70513090-70513098	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr13:70325178-70325338	GM12878	blood:	n/a	n/a
22	CBX3	chr13:70351107-70351445	K562	blood:	n/a	n/a
23	CEBPB	chr13:70530428-70531479	Hela-S3	cervix:	n/a	chr13:70531465-70531476 chr13:70531460-70531477
24	CEBPB	chr13:70190558-70190930	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:70514453-70514782	HepG2	liver:	n/a	chr13:70514640-70514651 chr13:70514639-70514650
26	CEBPB	chr13:70171142-70171588	HepG2	liver:	n/a	chr13:70171344-70171355
27	CEBPB	chr13:70430376-70430903	Hela-S3	cervix:	n/a	chr13:70430726-70430738
28	CEBPB	chr13:70222228-70222409	HepG2	liver:	n/a	chr13:70222250-70222261
29	CEBPB	chr13:70368078-70368276	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr13:70483441-70483636	HepG2	liver:	n/a	chr13:70483610-70483621 chr13:70483611-70483622
31	CEBPB	chr13:70296495-70296604	HepG2	liver:	n/a	n/a
32	CEBPB	chr13:70295769-70296068	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr13:70230999-70231245	HepG2	liver:	n/a	chr13:70231088-70231099
34	CEBPB	chr13:70228711-70228846	K562	blood:	n/a	n/a
35	CEBPB	chr13:70308944-70309274	HepG2	liver:	n/a	chr13:70309100-70309111 chr13:70309099-70309112
36	CEBPB	chr13:70533146-70533558	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr13:70483573-70483710	H1-hESC	embryonic stem cell:	n/a	chr13:70483610-70483621 chr13:70483611-70483622
38	CEBPB	chr13:70511461-70512334	Hela-S3	cervix:	n/a	chr13:70512061-70512072 chr13:70512060-70512073
39	CEBPB	chr13:70556481-70556681	HepG2	liver:	n/a	chr13:70556518-70556529
40	CEBPB	chr13:70228603-70228905	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr13:70511933-70512191	HepG2	liver:	n/a	chr13:70512061-70512072 chr13:70512060-70512073
42	CEBPB	chr13:70502181-70502988	Hela-S3	cervix:	n/a	chr13:70502713-70502724
43	CEBPB	chr13:70556319-70556690	Hela-S3	cervix:	n/a	chr13:70556518-70556529
44	CEBPB	chr13:70524138-70524795	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr13:70502588-70503057	HepG2	liver:	n/a	chr13:70502713-70502724
46	CEBPB	chr13:70440679-70441116	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:70431436-70431605	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr13:70161792-70161803	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr13:70231021-70231199	A549	lung:	n/a	chr13:70231088-70231099
50	CEBPB	chr13:70300298-70300460	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:70369137-70369187	HCF	heart:	n/a
2	chr13:70369137-70369187	AG04449	skin:	fetal
3	chr13:70369137-70369187	GM12878	blood:	n/a
4	chr13:70369137-70369187	Caco-2	colon:	n/a
5	chr13:70154624-70154674	HRPEpiC	eye:	n/a
6	chr13:70431522-70431572	GM12892	blood:	n/a
7	chr13:70369137-70369187	HRE	kidney:	n/a
8	chr13:70431522-70431572	Jurkat	blood:	n/a
9	chr13:70369137-70369187	SK-N-SH_RA	brain:	n/a
10	chr13:70154624-70154674	NB4	blood:	n/a
11	chr13:70431522-70431572	A549	lung:	n/a
12	chr13:70431522-70431572	PANC-1	pancreas:	n/a
13	chr13:70431522-70431572	GM19239	blood:	n/a
14	chr13:70369137-70369187	PANC-1	pancreas:	n/a
15	chr13:70369137-70369187	PrEC	prostate:	n/a
16	chr13:70369137-70369187	HMEC	breast:	n/a
17	chr13:70431522-70431572	HEEpiC	esophagus:	n/a
18	chr13:70154624-70154674	ECC-1	luminal epithelium:	n/a
19	chr13:70369137-70369187	HEK293	kidney:	embryo
20	chr13:70154624-70154674	SK-N-SH_RA	brain:	n/a
21	chr13:70369137-70369187	NHBE	bronchial:	n/a
22	chr13:70154624-70154674	BE2_C	brain:	n/a
23	chr13:70154624-70154674	HCF	heart:	n/a
24	chr13:70431522-70431572	NH-A	brain:	n/a
25	chr13:70154624-70154674	AG09309	skin:	n/a
26	chr13:70369137-70369187	ovcar-3	ovarian:	n/a
27	chr13:70431522-70431572	NT2-D1	testis:	n/a
28	chr13:70369137-70369187	SK-N-MC	brain:	n/a
29	chr13:70369137-70369187	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:70154624-70154674	AG04450	lung:	fetal
31	chr13:70154624-70154674	IMR90	lung:	fetal
32	chr13:70431522-70431572	SK-N-SH	brain:	n/a
33	chr13:70431522-70431572	HCM	heart:	n/a
34	chr13:70154624-70154674	HAEpiC	amniotic membrane:	n/a
35	chr13:70369137-70369187	AG04450	lung:	fetal
36	chr13:70154624-70154674	Caco-2	colon:	n/a
37	chr13:70369137-70369187	HNPCEpiC	eye:	n/a
38	chr13:70431522-70431572	AG04450	lung:	fetal
39	chr13:70154624-70154674	HRCEpiC	kidney:	n/a
40	chr13:70154624-70154674	ovcar-3	ovarian:	n/a
41	chr13:70431522-70431572	T-47D	breast:	n/a
42	chr13:70431522-70431572	NB4	blood:	n/a
43	chr13:70431522-70431572	AoSMC	blood vessel:	n/a
44	chr13:70369137-70369187	HCM	heart:	n/a
45	chr13:70154624-70154674	NHDF-neo	bronchial:	n/a
46	chr13:70369137-70369187	NH-A	brain:	n/a
47	chr13:70431522-70431572	ECC-1	luminal epithelium:	n/a
48	chr13:70431522-70431572	MCF-7	breast:	n/a
49	chr13:70369137-70369187	CMK	blood:	n/a
50	chr13:70154624-70154674	A549	lung:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:70249631..70251882-chr13:70253333..70255746,2	K562	blood:
2	chr13:70271603..70273702-chr13:70276559..70278431,2	K562	blood:
3	chr13:70138280..70140328-chr13:70148714..70150548,2	MCF-7	breast:
4	chr13:70207003..70207565-chr6:110796356..110796874,2	MCF-7	breast:
5	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
6	chr13:70281102..70281979-chr16:2731851..2732580,2	MCF-7	breast:
7	chr13:70249631..70251882-chr13:70253333..70255746,2	K562	blood:
8	chr13:70456586..70458210-chr13:70462433..70464245,2	K562	blood:
9	chr13:70192216..70195164-chr13:70199916..70202276,2	MCF-7	breast:
10	chr13:70139358..70139986-chr13:70431208..70431784,2	MCF-7	breast:
11	chr13:70159894..70160626-chr13:70431095..70431958,2	MCF-7	breast:
12	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
13	chr13:70456586..70458210-chr13:70462433..70464245,2	K562	blood:
14	chr13:70153553..70154097-chr13:70431151..70432026,2	MCF-7	breast:
15	chr13:70508852..70509449-chr13:70884586..70885490,2	MCF-7	breast:
16	chr13:70192216..70195164-chr13:70199916..70202276,2	MCF-7	breast:
17	chr13:70159737..70160485-chr3:63899719..63900444,2	MCF-7	breast:
18	chr13:70111760..70112275-chr13:70431222..70431945,2	K562	blood:
19	chr13:70145786..70147691-chr13:70150305..70153180,2	K562	blood:
20	chr13:70521896..70524416-chr13:70526463..70528042,2	MCF-7	breast:
21	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
22	chr11:65198093..65198776-chr13:70273636..70274136,2	Hela-S3	cervix:
23	chr13:70159894..70160626-chr13:70431095..70431958,2	MCF-7	breast:
24	chr13:70111047..70112123-chr13:70431019..70432110,4	MCF-7	breast:
25	chr13:70508992..70509506-chr20:33082627..33083129,2	MCF-7	breast:
26	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
27	chr13:70444676..70447495-chr17:57919486..57921075,2	MCF-7	breast:
28	chr13:70153553..70154097-chr13:70431151..70432026,2	MCF-7	breast:
29	chr13:70271603..70273702-chr13:70276559..70278431,2	K562	blood:
30	chr13:70343892..70346345-chr13:113863086..113865250,2	MCF-7	breast:
31	chr13:70521896..70524416-chr13:70526463..70528042,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BORA-23	chr13:70487274-70487381	NONHSAT034249

No data

Variant related genes	Relation type
PSMC1P13	TF binding region
RNY3P10	TF binding region
PSMC1P13	CpG island
RNY3P10	CpG island
ENSG00000167977	chromatin interactions
ENSG00000139842	chromatin interactions

Extended variants
information (count: 5941 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:5941 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191804780	chr13:70153623-70153624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183117514	chr13:70153649-70153650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559035918	chr13:70153714-70153715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187406855	chr13:70153733-70153734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191900634	chr13:70153769-70153770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114988333	chr13:70153770-70153771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182604907	chr13:70153783-70153784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556162441	chr13:70153817-70153818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187761122	chr13:70153850-70153851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs519190	chr13:70153907-70153908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192676989	chr13:70153933-70153934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536435986	chr13:70153948-70153949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546784559	chr13:70153950-70153951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566201657	chr13:70153951-70153952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184133590	chr13:70153968-70153969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149065524	chr13:70154000-70154001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577954357	chr13:70154040-70154041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143061973	chr13:70154064-70154065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572384669	chr13:70154109-70154110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541463144	chr13:70154119-70154120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190645025	chr13:70154126-70154127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368836322	chr13:70154150-70154151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs193042752	chr13:70154175-70154176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374299014	chr13:70154203-70154204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs151165936	chr13:70154204-70154205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572613953	chr13:70154212-70154213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377220280	chr13:70154220-70154221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544696134	chr13:70154264-70154265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564941765	chr13:70154307-70154308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75719714	chr13:70154324-70154325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550889178	chr13:70154374-70154375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550189257	chr13:70154432-70154433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561044645	chr13:70154439-70154440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529990307	chr13:70154454-70154455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115122288	chr13:70154455-70154456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566660514	chr13:70154463-70154464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568360145	chr13:70154488-70154489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551559142	chr13:70154564-70154565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571648720	chr13:70154585-70154586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140329628	chr13:70154654-70154655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551161421	chr13:70154657-70154658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150349159	chr13:70154662-70154663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554491568	chr13:70154674-70154675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116718100	chr13:70154677-70154678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571381085	chr13:70154714-70154715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188876017	chr13:70154737-70154738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545117257	chr13:70154740-70154741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572742504	chr13:70154748-70154749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564817758	chr13:70154751-70154752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138234211	chr13:70154764-70154765	Enhancers Weak transcription	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
Esophageal cancer	21851588	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70153600-70154600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr13:70153600-70155000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr13:70153600-70155200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr13:70153800-70154200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr13:70153800-70154200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr13:70153800-70154600	Enhancers	Liver	Liver
7	chr13:70153800-70154800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr13:70153800-70154800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr13:70153800-70155000	Enhancers	HMEC	breast
10	chr13:70153800-70155200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:70154000-70154200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:70154000-70154600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr13:70154000-70154800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr13:70154200-70154800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr13:70154200-70154800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr13:70154200-70154800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr13:70154200-70156000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr13:70154600-70155000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr13:70155000-70159600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr13:70155200-70159600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr13:70156000-70156600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr13:70156600-70159600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:70159600-70159800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:70159600-70160000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr13:70159600-70160200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr13:70160200-70163800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr13:70161200-70161400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr13:70162800-70163600	Enhancers	Liver	Liver
29	chr13:70163400-70164800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr13:70163600-70165000	Weak transcription	Liver	Liver
31	chr13:70163800-70164200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr13:70165000-70167400	Enhancers	Liver	Liver
33	chr13:70167400-70168600	Weak transcription	Liver	Liver
34	chr13:70168600-70171000	Enhancers	Liver	Liver
35	chr13:70169400-70169600	Enhancers	Pancreas	Pancrea
36	chr13:70169600-70177400	Weak transcription	Pancreas	Pancrea
37	chr13:70174000-70174200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr13:70174200-70176000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr13:70175200-70175400	Enhancers	Fetal Heart	heart
40	chr13:70175200-70176000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr13:70175400-70175800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr13:70175800-70183400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr13:70176000-70177800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:70177400-70177600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr13:70177400-70177600	Enhancers	Pancreas	Pancrea
46	chr13:70186600-70187400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr13:70190000-70190200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr13:70190200-70190800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr13:70190800-70191600	Enhancers	Liver	Liver
50	chr13:70191600-70192400	Flanking Active TSS	Liver	Liver

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