Variant report

Variant	nsv591961
Chromosome Location	chr3:146394094-146725217
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	chr3:146422930-146423336	GM12878	blood:	n/a	n/a
2	ATF2	chr3:146423016-146423351	GM12878	blood:	n/a	n/a
3	ATF3	chr3:146513944-146514174	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:146399305-146399357	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:146498718-146499236	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:146423014-146423296	GM12878	blood:	n/a	n/a
7	BATF	chr3:146423040-146423275	GM12878	blood:	n/a	n/a
8	BRCA1	chr3:146614791-146614794	GM12878	blood:	n/a	n/a
9	CBX3	chr3:146685849-146686581	HCT-116	colon:	n/a	n/a
10	CBX3	chr3:146685751-146686637	HCT-116	colon:	n/a	n/a
11	CEBPB	chr3:146614578-146614858	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:146410117-146410434	A549	lung:	n/a	chr3:146410255-146410264 chr3:146410255-146410264 chr3:146410255-146410264 chr3:146410255-146410264 chr3:146410254-146410265
13	CEBPB	chr3:146685570-146686464	HCT-116	colon:	n/a	n/a
14	CEBPB	chr3:146666819-146667156	MCF-7	breast:	n/a	chr3:146666948-146666959
15	CEBPB	chr3:146500701-146500953	HepG2	liver:	n/a	chr3:146500786-146500797 chr3:146500839-146500850
16	CEBPB	chr3:146592582-146592634	HepG2	liver:	n/a	chr3:146592596-146592607
17	CEBPB	chr3:146626783-146627078	IMR90	lung:	n/a	chr3:146626928-146626939 chr3:146626929-146626938 chr3:146626927-146626938
18	CEBPB	chr3:146626801-146627083	HepG2	liver:	n/a	chr3:146626928-146626939 chr3:146626929-146626938 chr3:146626927-146626938
19	CEBPB	chr3:146605165-146605465	HepG2	liver:	n/a	chr3:146605290-146605301
20	CEBPB	chr3:146619744-146619883	HepG2	liver:	n/a	chr3:146619796-146619807 chr3:146619794-146619811 chr3:146619795-146619808 chr3:146619795-146619808
21	CEBPB	chr3:146605148-146605460	IMR90	lung:	n/a	chr3:146605290-146605301
22	CEBPB	chr3:146637184-146637457	HepG2	liver:	n/a	chr3:146637326-146637337
23	CEBPB	chr3:146637291-146637349	K562	blood:	n/a	chr3:146637326-146637337
24	CEBPB	chr3:146410103-146410437	HepG2	liver:	n/a	chr3:146410255-146410264 chr3:146410255-146410264 chr3:146410255-146410264 chr3:146410255-146410264 chr3:146410254-146410265
25	CEBPB	chr3:146685602-146686183	IMR90	lung:	n/a	n/a
26	CEBPB	chr3:146666800-146667132	Hela-S3	cervix:	n/a	chr3:146666948-146666959
27	CEBPB	chr3:146423085-146423301	HepG2	liver:	n/a	chr3:146423224-146423235 chr3:146423223-146423234 chr3:146423223-146423236
28	CEBPB	chr3:146494736-146494911	HepG2	liver:	n/a	chr3:146494776-146494787
29	CEBPB	chr3:146436512-146436746	A549	lung:	n/a	chr3:146436647-146436658
30	CEBPB	chr3:146666764-146667147	H1-hESC	embryonic stem cell:	n/a	chr3:146666948-146666959
31	CEBPB	chr3:146607136-146607259	K562	blood:	n/a	chr3:146607178-146607189
32	CEBPB	chr3:146694613-146694842	HepG2	liver:	n/a	chr3:146694708-146694719 chr3:146694708-146694721
33	CEBPB	chr3:146637236-146637407	Hela-S3	cervix:	n/a	chr3:146637326-146637337
34	CEBPB	chr3:146686339-146686461	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr3:146666865-146667078	ECC-1	luminal epithelium:	n/a	chr3:146666948-146666959
36	CEBPB	chr3:146485828-146486016	A549	lung:	n/a	chr3:146485921-146485930 chr3:146485919-146485930
37	CEBPB	chr3:146666777-146667143	K562	blood:	n/a	chr3:146666948-146666959
38	CEBPB	chr3:146498833-146499006	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr3:146666856-146667157	MCF-7	breast:	n/a	chr3:146666948-146666959
40	CEBPB	chr3:146500703-146500955	A549	lung:	n/a	chr3:146500786-146500797 chr3:146500839-146500850
41	CEBPB	chr3:146723680-146723890	HepG2	liver:	n/a	chr3:146723818-146723829
42	CEBPB	chr3:146605252-146605373	K562	blood:	n/a	chr3:146605290-146605301
43	CEBPB	chr3:146687179-146687451	IMR90	lung:	n/a	n/a
44	CEBPB	chr3:146666799-146667103	ECC-1	luminal epithelium:	n/a	chr3:146666948-146666959
45	CEBPB	chr3:146666869-146667104	A549	lung:	n/a	chr3:146666948-146666959
46	CEBPB	chr3:146436607-146436753	H1-hESC	embryonic stem cell:	n/a	chr3:146436647-146436658
47	CEBPB	chr3:146666824-146667006	HepG2	liver:	n/a	chr3:146666948-146666959
48	CEBPB	chr3:146687962-146688145	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:146605363-146605409	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr3:146423182-146423312	A549	lung:	n/a	chr3:146423224-146423235 chr3:146423223-146423234 chr3:146423223-146423236

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:146491153-146491203	NH-A	brain:	n/a
2	chr3:146491153-146491203	NHBE	bronchial:	n/a
3	chr3:146498234-146498284	HCM	heart:	n/a
4	chr3:146498234-146498284	HAEpiC	amniotic membrane:	n/a
5	chr3:146491153-146491203	SKMC	muscle:	n/a
6	chr3:146498234-146498284	RPTEC	kidney:	n/a
7	chr3:146491153-146491203	NB4	blood:	n/a
8	chr3:146490184-146490234	PrEC	prostate:	n/a
9	chr3:146490370-146490420	AG04450	lung:	fetal
10	chr3:146490370-146490420	HRPEpiC	eye:	n/a
11	chr3:146491153-146491203	SAEC	small airway:	n/a
12	chr3:146490370-146490420	CMK	blood:	n/a
13	chr3:146490370-146490420	A549	lung:	n/a
14	chr3:146490370-146490420	MCF-7	breast:	n/a
15	chr3:146490370-146490420	GM12878	blood:	n/a
16	chr3:146491153-146491203	HEEpiC	esophagus:	n/a
17	chr3:146490184-146490234	Hela-S3	cervix:	n/a
18	chr3:146490184-146490234	MCF10A-Er-Src	breast:	n/a
19	chr3:146490370-146490420	NHDF-neo	bronchial:	n/a
20	chr3:146490184-146490234	HCF	heart:	n/a
21	chr3:146490184-146490234	HIPEpiC	eye:	n/a
22	chr3:146498234-146498284	SK-N-SH	brain:	n/a
23	chr3:146490370-146490420	Jurkat	blood:	n/a
24	chr3:146490184-146490234	NT2-D1	testis:	n/a
25	chr3:146490184-146490234	SK-N-SH	brain:	n/a
26	chr3:146490184-146490234	T-47D	breast:	n/a
27	chr3:146490184-146490234	K562	blood:	n/a
28	chr3:146490184-146490234	SK-N-MC	brain:	n/a
29	chr3:146490370-146490420	GM12891	blood:	n/a
30	chr3:146498234-146498284	HCF	heart:	n/a
31	chr3:146491153-146491203	PANC-1	pancreas:	n/a
32	chr3:146498234-146498284	ovcar-3	ovarian:	n/a
33	chr3:146491153-146491203	A549	lung:	n/a
34	chr3:146490184-146490234	AG09319	gingival:	n/a
35	chr3:146490370-146490420	Hela-S3	cervix:	n/a
36	chr3:146490184-146490234	SAEC	small airway:	n/a
37	chr3:146491153-146491203	LNCaP	prostate:	n/a
38	chr3:146490370-146490420	HNPCEpiC	eye:	n/a
39	chr3:146490370-146490420	BE2_C	brain:	n/a
40	chr3:146491153-146491203	GM06990	blood:	n/a
41	chr3:146498234-146498284	NHDF-neo	bronchial:	n/a
42	chr3:146490370-146490420	AG09319	gingival:	n/a
43	chr3:146498234-146498284	PANC-1	pancreas:	n/a
44	chr3:146490370-146490420	HepG2	liver:	n/a
45	chr3:146491153-146491203	ProgFib	skin:	n/a
46	chr3:146490184-146490234	AG04450	lung:	fetal
47	chr3:146490370-146490420	PANC-1	pancreas:	n/a
48	chr3:146498234-146498284	HRPEpiC	eye:	n/a
49	chr3:146491153-146491203	HL-60	blood:	n/a
50	chr3:146490370-146490420	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:146453782..146456764-chr3:146457731..146459904,2	K562	blood:
2	chr3:146477908..146479521-chr3:146482688..146484661,2	K562	blood:
3	chr3:146568702..146571051-chr3:146573084..146575725,2	K562	blood:
4	chr3:146535264..146535780-chr3:146909367..146910281,2	MCF-7	breast:
5	chr3:146636773..146638616-chr3:146643446..146646080,2	K562	blood:
6	chr3:146535974..146536861-chr3:146909343..146910183,2	MCF-7	breast:
7	chr3:146523515..146525331-chr3:147109923..147112497,2	MCF-7	breast:
8	chr3:146570466..146572566-chr3:146575792..146578256,3	K562	blood:
9	chr3:146477908..146479521-chr3:146482688..146484661,2	K562	blood:
10	chr3:146698311..146701060-chr3:146701293..146703528,2	MCF-7	breast:
11	chr3:146543043..146545819-chr3:146575097..146577219,2	MCF-7	breast:
12	chr12:52448335..52448943-chr3:146400166..146400666,2	Hela-S3	cervix:
13	chr3:146534888..146535944-chr3:147793502..147794515,3	MCF-7	breast:
14	chr3:146535184..146535986-chr3:147334472..147335106,2	MCF-7	breast:
15	chr3:146543043..146545819-chr3:146575097..146577219,2	MCF-7	breast:
16	chr3:146715446..146717460-chr3:146722255..146724620,2	K562	blood:
17	chr3:146698311..146701060-chr3:146701293..146703528,2	MCF-7	breast:
18	chr3:146465618..146466350-chr3:146909313..146909963,2	MCF-7	breast:
19	chr3:146715446..146717460-chr3:146722255..146724620,2	K562	blood:
20	chr3:146540807..146541687-chr3:146910591..146911284,2	MCF-7	breast:
21	chr3:146636773..146638616-chr3:146643446..146646080,2	K562	blood:
22	chr3:146544997..146545778-chr7:73597769..73598409,2	MCF-7	breast:
23	chr3:146724156..146724656-chr7:158811116..158812074,2	MCF-7	breast:
24	chr3:146568702..146571051-chr3:146573084..146575725,2	K562	blood:
25	chr3:146453782..146456764-chr3:146457731..146459904,2	K562	blood:
26	chr3:146535595..146536102-chr3:147133508..147134222,2	MCF-7	breast:
27	chr3:146570466..146572566-chr3:146575792..146578256,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZIC1-4	chr3:146639710-146639961	XLOC_002856
2	lnc-ZIC1-4	chr3:146641088-146641111	XLOC_002856
3	lnc-ZIC1-4	chr3:146639750-146639961	XLOC_002856
4	lnc-ZIC4-3	chr3:146636855-146636972	ENSG00000243620.1
5	lnc-ZIC4-3	chr3:146644242-146644437	ENSG00000243620.1
6	lnc-ZIC4-3	chr3:146627472-146627498	ENSG00000243620.1
7	lnc-ZIC1-4	chr3:146641389-146641628	XLOC_002856
8	lnc-ZIC1-4	chr3:146641389-146643005	XLOC_002856

Variant related genes	Relation type
ENSG00000242671	TF binding region
RNU6-505P	TF binding region
ENSG00000251800	TF binding region
ENSG00000242671	CpG island
RNU6-505P	CpG island
ENSG00000251800	CpG island
ENSG00000174963	chromatin interactions
ENSG00000152977	chromatin interactions
ENSG00000106682	chromatin interactions
PHF19	miRNA target sites

Extended variants
information (count: 7397 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:7397 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566284809	chr3:146395021-146395022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183105335	chr3:146395077-146395078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116143440	chr3:146395166-146395167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114967768	chr3:146395167-146395168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150494154	chr3:146395169-146395170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138792695	chr3:146395197-146395198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs578214071	chr3:146395208-146395209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141949986	chr3:146395215-146395216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77935303	chr3:146395221-146395222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs118181812	chr3:146395248-146395249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545503245	chr3:146395276-146395277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187400588	chr3:146395312-146395313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146316850	chr3:146395330-146395331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10935639	chr3:146395398-146395399	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs79428541	chr3:146395446-146395447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564389730	chr3:146395510-146395511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533102963	chr3:146395546-146395547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557855560	chr3:146395550-146395551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11709433	chr3:146395563-146395564	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs11713544	chr3:146395589-146395590	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs11709435	chr3:146395611-146395612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs115852647	chr3:146395629-146395630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566220219	chr3:146395655-146395656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116237513	chr3:146395700-146395701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191220346	chr3:146395708-146395709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35416181	chr3:146395721-146395722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183074260	chr3:146395752-146395753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571884626	chr3:146395760-146395761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148581347	chr3:146395793-146395794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546910850	chr3:146395799-146395800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556085287	chr3:146395814-146395815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575952187	chr3:146395977-146395978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11718101	chr3:146396006-146396007	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs538878485	chr3:146396083-146396084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79779484	chr3:146396140-146396141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142982091	chr3:146396173-146396174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187969069	chr3:146396177-146396178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557686586	chr3:146396183-146396184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201521328	chr3:146396187-146396188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374297110	chr3:146396190-146396191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377735358	chr3:146396220-146396221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192797861	chr3:146396222-146396223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541403295	chr3:146396267-146396268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11718196	chr3:146396321-146396322	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs34327211	chr3:146396364-146396365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374147129	chr3:146396383-146396384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569777535	chr3:146396385-146396386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139884553	chr3:146396393-146396394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145088802	chr3:146396453-146396454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs62275443	chr3:146396547-146396548	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

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
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
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146395000-146397600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:146396600-146396800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:146397600-146399200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:146398400-146398600	Enhancers	Brain Germinal Matrix	brain
5	chr3:146398400-146399000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:146398400-146404200	Enhancers	Dnd41	blood
7	chr3:146398600-146399000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:146399200-146399600	Enhancers	Fetal Heart	heart
9	chr3:146399200-146401000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:146399600-146400600	Weak transcription	Fetal Heart	heart
11	chr3:146400800-146401000	Enhancers	Brain Germinal Matrix	brain
12	chr3:146400800-146401000	Enhancers	Fetal Heart	heart
13	chr3:146403800-146410000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:146408400-146408600	ZNF genes & repeats	Dnd41	blood
15	chr3:146409600-146422000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr3:146409800-146410400	ZNF genes & repeats	Dnd41	blood
17	chr3:146410000-146410200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:146410000-146410200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr3:146410200-146413200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:146414800-146415200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:146415200-146422800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:146420200-146432400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr3:146422800-146423200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:146422800-146424000	Enhancers	GM12878-XiMat	blood
25	chr3:146422800-146425600	Enhancers	Dnd41	blood
26	chr3:146423200-146424600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:146424600-146425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:146425000-146427200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:146425600-146426600	Weak transcription	Dnd41	blood
30	chr3:146425800-146426000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr3:146426000-146427200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr3:146426600-146427600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr3:146426600-146427600	Enhancers	Dnd41	blood
34	chr3:146427000-146427600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:146427200-146427800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr3:146427200-146427800	Enhancers	HSMM	muscle
37	chr3:146427200-146428000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:146427200-146428600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr3:146427400-146427600	Enhancers	NHDF-Ad	bronchial
40	chr3:146427600-146430000	Weak transcription	NHDF-Ad	bronchial
41	chr3:146427800-146432800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr3:146428600-146430000	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr3:146430000-146431000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr3:146430000-146431400	Enhancers	NHDF-Ad	bronchial
45	chr3:146430600-146431000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:146431400-146432600	Weak transcription	NHDF-Ad	bronchial
47	chr3:146432400-146433000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr3:146432600-146433000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr3:146432600-146433000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr3:146432600-146433200	Enhancers	NHDF-Ad	bronchial

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