Variant report

Variant	nsv877517
Chromosome Location	chr3:134709951-134805581
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	ATF2	chr3:134737365-134737784	GM12878	blood:	n/a	n/a
2	BACH1	chr3:134786215-134786398	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr3:134737385-134737727	GM12878	blood:	n/a	n/a
4	BHLHE40	chr3:134737060-134737736	GM12878	blood:	n/a	n/a
5	BHLHE40	chr3:134742787-134743472	GM12878	blood:	n/a	n/a
6	BRCA1	chr3:134736236-134736333	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:134772757-134772802	HepG2	liver:	n/a	chr3:134772784-134772795
8	CEBPB	chr3:134719348-134719620	K562	blood:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
9	CEBPB	chr3:134739116-134739316	HepG2	liver:	n/a	chr3:134739181-134739192
10	CEBPB	chr3:134719376-134719636	Hela-S3	cervix:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
11	CEBPB	chr3:134719386-134719664	IMR90	lung:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
12	CEBPB	chr3:134719324-134719734	ECC-1	luminal epithelium:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
13	CEBPB	chr3:134719355-134719684	HepG2	liver:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
14	CEBPB	chr3:134739094-134739293	K562	blood:	n/a	chr3:134739181-134739192
15	CEBPB	chr3:134719337-134719724	ECC-1	luminal epithelium:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
16	CEBPB	chr3:134719404-134719632	A549	lung:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
17	CHD1	chr3:134742803-134743033	GM12878	blood:	n/a	n/a
18	CHD2	chr3:134786193-134786329	GM12878	blood:	n/a	n/a
19	CHD2	chr3:134742841-134743502	GM12878	blood:	n/a	n/a
20	CHD2	chr3:134737429-134737855	GM12878	blood:	n/a	n/a
21	CTCF	chr3:134797275-134797418	GM12892	blood:	n/a	chr3:134797316-134797324
22	CTCF	chr3:134797273-134797404	GM19239	blood:	n/a	chr3:134797316-134797324
23	CTCF	chr3:134751800-134751950	AG09309	skin:	n/a	n/a
24	CTCF	chr3:134797160-134797310	RPTEC	kidney:	n/a	n/a
25	CTCF	chr3:134797320-134797470	GM12873	blood:	n/a	n/a
26	CTCF	chr3:134797220-134797370	MCF-7	breast:	n/a	chr3:134797316-134797324
27	CTCF	chr3:134797160-134797310	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr3:134797240-134797390	HepG2	liver:	n/a	chr3:134797316-134797324
29	CTCF	chr3:134797161-134797431	H1-hESC	embryonic stem cell:	n/a	chr3:134797316-134797324
30	CTCF	chr3:134797257-134797421	MCF-7	breast:	n/a	chr3:134797316-134797324
31	CTCF	chr3:134717818-134717940	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr3:134797300-134797388	K562	blood:	n/a	chr3:134797316-134797324
33	CTCF	chr3:134797300-134797450	HepG2	liver:	n/a	chr3:134797316-134797324
34	CTCF	chr3:134797288-134797415	MCF-7	breast:	n/a	chr3:134797316-134797324
35	CTCF	chr3:134734311-134734361	LNCaP	prostate:	n/a	n/a
36	CTCF	chr3:134797220-134797370	GM12869	blood:	n/a	chr3:134797316-134797324
37	CTCF	chr3:134765476-134765509	GM20000	blood:	n/a	n/a
38	CTCF	chr3:134797200-134797350	GM12878	blood:	n/a	chr3:134797316-134797324
39	CTCF	chr3:134797309-134797365	GM12878	blood:	n/a	chr3:134797316-134797324
40	CTCF	chr3:134797344-134797351	HepG2	liver:	n/a	n/a
41	CTCF	chr3:134765138-134765239	LNCaP	prostate:	n/a	n/a
42	CTCF	chr3:134797278-134797424	MCF-7	breast:	n/a	chr3:134797316-134797324
43	CTCF	chr3:134797245-134797420	MCF-7	breast:	n/a	chr3:134797316-134797324
44	CTCF	chr3:134797220-134797370	RPTEC	kidney:	n/a	chr3:134797316-134797324
45	CTCF	chr3:134802747-134802982	GM12878	blood:	n/a	n/a
46	CTCF	chr3:134797283-134797430	GM12878	blood:	n/a	chr3:134797316-134797324
47	CTCF	chr3:134797233-134797433	H1-hESC	embryonic stem cell:	n/a	chr3:134797316-134797324
48	CTCF	chr3:134719978-134720058	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:134719984-134720050	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:134797260-134797410	Caco-2	colon:	n/a	chr3:134797316-134797324

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:134798947-134798997	HCF	heart:	n/a
2	chr3:134801915-134801965	T-47D	breast:	n/a
3	chr3:134710864-134710914	HEK293	kidney:	embryo
4	chr3:134801915-134801965	NHDF-neo	bronchial:	n/a
5	chr3:134798947-134798997	HCM	heart:	n/a
6	chr3:134710864-134710914	HIPEpiC	eye:	n/a
7	chr3:134758333-134758383	GM12892	blood:	n/a
8	chr3:134798947-134798997	NH-A	brain:	n/a
9	chr3:134798947-134798997	HepG2	liver:	n/a
10	chr3:134798947-134798997	U87	brain:	n/a
11	chr3:134798947-134798997	SK-N-MC	brain:	n/a
12	chr3:134758333-134758383	CMK	blood:	n/a
13	chr3:134798947-134798997	HL-60	blood:	n/a
14	chr3:134710864-134710914	GM12892	blood:	n/a
15	chr3:134758333-134758383	PANC-1	pancreas:	n/a
16	chr3:134798947-134798997	NHBE	bronchial:	n/a
17	chr3:134758333-134758383	Caco-2	colon:	n/a
18	chr3:134801915-134801965	HepG2	liver:	n/a
19	chr3:134798947-134798997	AG10803	skin:	n/a
20	chr3:134798947-134798997	Hela-S3	cervix:	n/a
21	chr3:134801915-134801965	AG09309	skin:	n/a
22	chr3:134758333-134758383	AG09319	gingival:	n/a
23	chr3:134798947-134798997	Caco-2	colon:	n/a
24	chr3:134758333-134758383	U87	brain:	n/a
25	chr3:134758333-134758383	ovcar-3	ovarian:	n/a
26	chr3:134710864-134710914	HCF	heart:	n/a
27	chr3:134758333-134758383	BJ	skin:	n/a
28	chr3:134801915-134801965	GM19239	blood:	n/a
29	chr3:134710864-134710914	HEEpiC	esophagus:	n/a
30	chr3:134798947-134798997	HAEpiC	amniotic membrane:	n/a
31	chr3:134710864-134710914	SKMC	muscle:	n/a
32	chr3:134710864-134710914	CMK	blood:	n/a
33	chr3:134798947-134798997	GM06990	blood:	n/a
34	chr3:134710864-134710914	SK-N-SH	brain:	n/a
35	chr3:134710864-134710914	U87	brain:	n/a
36	chr3:134798947-134798997	AoSMC	blood vessel:	n/a
37	chr3:134801915-134801965	HAEpiC	amniotic membrane:	n/a
38	chr3:134758333-134758383	AG04450	lung:	fetal
39	chr3:134801915-134801965	MCF-7	breast:	n/a
40	chr3:134798947-134798997	Hepatocyte	liver:	n/a
41	chr3:134710864-134710914	IMR90	lung:	fetal
42	chr3:134798947-134798997	AG04450	lung:	fetal
43	chr3:134758333-134758383	NHDF-neo	bronchial:	n/a
44	chr3:134798947-134798997	RPTEC	kidney:	n/a
45	chr3:134710864-134710914	HCPEpiC	choroid plexus:	n/a
46	chr3:134758333-134758383	IMR90	lung:	fetal
47	chr3:134710864-134710914	H1-hESC	embryonic stem cell:	embryo
48	chr3:134758333-134758383	HL-60	blood:	n/a
49	chr3:134801915-134801965	ProgFib	skin:	n/a
50	chr3:134758333-134758383	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:134725899..134728503-chr3:134730689..134733347,3	MCF-7	breast:
2	chr3:134795759..134797342-chr3:134802255..134804359,2	MCF-7	breast:
3	chr3:134711495..134714035-chr3:134895700..134897544,2	K562	blood:
4	chr3:134513827..134514378-chr3:134719808..134720327,2	MCF-7	breast:
5	chr3:134725899..134728503-chr3:134730689..134733347,3	MCF-7	breast:
6	chr3:134769674..134771857-chr3:134772148..134774562,2	K562	blood:
7	chr3:134795759..134797342-chr3:134802255..134804359,2	MCF-7	breast:
8	chr3:134769674..134771857-chr3:134772148..134774562,2	K562	blood:

Variant related genes	Relation type
EPHB1	TF binding region
EPHB1	CpG island
ENSG00000154928	chromatin interactions

Extended variants
information (count: 3473 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3473 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7613213	chr3:134709951-134709952	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181951311	chr3:134710010-134710011	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538736176	chr3:134710058-134710059	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552343889	chr3:134710060-134710061	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs36096	chr3:134710112-134710113	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535262957	chr3:134710138-134710139	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140359597	chr3:134710215-134710216	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187469335	chr3:134710222-134710223	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369855493	chr3:134710232-134710233	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573046900	chr3:134710270-134710271	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9289488	chr3:134710304-134710305	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs191477055	chr3:134710330-134710331	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577214253	chr3:134710333-134710334	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs72973600	chr3:134710337-134710338	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs553084574	chr3:134710343-134710344	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561548693	chr3:134710387-134710388	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1993503	chr3:134710418-134710419	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs36095	chr3:134710460-134710461	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183784094	chr3:134710461-134710462	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35659794	chr3:134710492-134710493	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs1993502	chr3:134710494-134710495	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186306210	chr3:134710525-134710526	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190275290	chr3:134710553-134710554	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563287940	chr3:134710566-134710567	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372945774	chr3:134710581-134710582	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539570345	chr3:134710584-134710585	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145469839	chr3:134710600-134710601	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182184847	chr3:134710623-134710624	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs36094	chr3:134710656-134710657	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs369187202	chr3:134710688-134710689	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186462601	chr3:134710718-134710719	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537745587	chr3:134710735-134710736	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374165942	chr3:134710750-134710751	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570496770	chr3:134710822-134710823	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191308058	chr3:134710864-134710865	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73214188	chr3:134710865-134710866	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368141172	chr3:134710890-134710891	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111781607	chr3:134710894-134710895	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183699461	chr3:134710896-134710897	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6775338	chr3:134710929-134710930	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189138502	chr3:134710952-134710953	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543687810	chr3:134710987-134710988	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563466166	chr3:134711009-134711010	Enhancers Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs137994055	chr3:134711011-134711012	Enhancers Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545778960	chr3:134711084-134711085	Enhancers Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528774272	chr3:134711127-134711128	Enhancers Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142794431	chr3:134711134-134711135	Enhancers Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559397326	chr3:134711173-134711174	Enhancers Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528143898	chr3:134711220-134711221	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548850379	chr3:134711223-134711224	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134707200-134711000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:134708000-134717800	Weak transcription	Psoas Muscle	Psoas
3	chr3:134708200-134710000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:134708200-134710000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:134708200-134710000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:134708400-134710200	Weak transcription	Fetal Brain Male	brain
7	chr3:134709400-134711000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr3:134709600-134710200	Enhancers	Fetal Brain Female	brain
9	chr3:134709600-134711800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:134709600-134712000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:134709600-134712800	Enhancers	GM12878-XiMat	blood
12	chr3:134709800-134710800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr3:134709800-134710800	Enhancers	Brain Germinal Matrix	brain
14	chr3:134709800-134711400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr3:134709800-134711600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr3:134710000-134710200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr3:134710000-134710600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:134710000-134711000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr3:134710000-134711200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:134710000-134711200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:134710000-134711400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr3:134710000-134711400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:134710000-134711400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:134710000-134711600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr3:134710000-134711600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr3:134710000-134711600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr3:134710000-134711600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:134710000-134712000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:134710000-134712400	Enhancers	Brain Anterior Caudate	brain
30	chr3:134710200-134710600	Enhancers	Fetal Brain Male	brain
31	chr3:134710200-134710800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr3:134710200-134711000	Weak transcription	Fetal Brain Female	brain
33	chr3:134710600-134711600	Weak transcription	Fetal Brain Male	brain
34	chr3:134710800-134711200	Weak transcription	Brain Germinal Matrix	brain
35	chr3:134710800-134711600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr3:134711000-134712200	Enhancers	Fetal Brain Female	brain
37	chr3:134711000-134713400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr3:134711200-134712000	Enhancers	Brain Germinal Matrix	brain
39	chr3:134711200-134712000	Enhancers	Dnd41	blood
40	chr3:134711200-134712200	Enhancers	Adipose Nuclei	Adipose
41	chr3:134711400-134711600	Enhancers	Brain Cingulate Gyrus	brain
42	chr3:134711400-134712200	Enhancers	Brain Hippocampus Middle	brain
43	chr3:134711600-134712200	Enhancers	Fetal Brain Male	brain
44	chr3:134712000-134716800	Weak transcription	Dnd41	blood
45	chr3:134712800-134716800	Weak transcription	GM12878-XiMat	blood
46	chr3:134713400-134718400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:134716800-134717200	Enhancers	Dnd41	blood
48	chr3:134716800-134717800	Enhancers	GM12878-XiMat	blood
49	chr3:134717800-134718400	Enhancers	Psoas Muscle	Psoas
50	chr3:134718400-134720800	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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