Variant report

Variant	nsv460857
Chromosome Location	chr3:133101390-133122216
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:442)
CpG islands
(count:551)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:133103254-133103611	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr3:133103236-133103592	GM12878	blood:	n/a	chr3:133103412-133103421
3	BHLHE40	chr3:133103360-133103618	GM12878	blood:	n/a	n/a
4	BHLHE40	chr3:133103299-133103602	HepG2	liver:	n/a	n/a
5	BRCA1	chr3:133103533-133103635	GM12878	blood:	n/a	n/a
6	CBX3	chr3:133101922-133102523	HCT-116	colon:	n/a	n/a
7	CEBPB	chr3:133112105-133112305	K562	blood:	n/a	chr3:133112176-133112187
8	CEBPB	chr3:133112044-133112436	MCF-7	breast:	n/a	chr3:133112176-133112187
9	CEBPB	chr3:133112029-133112321	IMR90	lung:	n/a	chr3:133112176-133112187
10	CEBPB	chr3:133112050-133112311	HepG2	liver:	n/a	chr3:133112176-133112187
11	CEBPB	chr3:133112120-133112256	Hela-S3	cervix:	n/a	chr3:133112176-133112187
12	CEBPB	chr3:133111950-133112444	MCF-7	breast:	n/a	chr3:133112176-133112187
13	CHD1	chr3:133103423-133103521	GM12878	blood:	n/a	n/a
14	CHD2	chr3:133103341-133103610	HepG2	liver:	n/a	n/a
15	CHD2	chr3:133113097-133113213	GM12878	blood:	n/a	n/a
16	CHD2	chr3:133103313-133103669	GM12878	blood:	n/a	n/a
17	CTCF	chr3:133103440-133103590	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr3:133103357-133103646	LNCaP	prostate:	n/a	n/a
19	CTCF	chr3:133105900-133106050	HAc	cerebellar:	n/a	n/a
20	CTCF	chr3:133103480-133103630	K562	blood:	n/a	n/a
21	CTCF	chr3:133105880-133106030	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr3:133103420-133103570	RPTEC	kidney:	n/a	n/a
23	CTCF	chr3:133103760-133103910	WERI-Rb-1	eye:	n/a	chr3:133103801-133103819 chr3:133103803-133103824
24	CTCF	chr3:133106800-133106950	GM12873	blood:	n/a	n/a
25	CTCF	chr3:133105840-133105990	K562	blood:	n/a	n/a
26	CTCF	chr3:133120620-133120770	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr3:133106160-133106310	BE2_C	brain:	n/a	n/a
28	CTCF	chr3:133103420-133103570	GM12869	blood:	n/a	n/a
29	CTCF	chr3:133103400-133103550	AG09309	skin:	n/a	n/a
30	CTCF	chr3:133103234-133103694	HepG2	liver:	n/a	n/a
31	CTCF	chr3:133103380-133103530	WI-38	lung:	n/a	n/a
32	CTCF	chr3:133103368-133103635	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr3:133103400-133103550	HepG2	liver:	n/a	n/a
34	CTCF	chr3:133105839-133105966	K562	blood:	n/a	n/a
35	CTCF	chr3:133103500-133103650	AG04450	lung:	n/a	n/a
36	CTCF	chr3:133103440-133103590	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr3:133103330-133103557	A549	lung:	n/a	n/a
38	CTCF	chr3:133103420-133103570	Caco-2	colon:	n/a	n/a
39	CTCF	chr3:133105840-133105990	GM12868	blood:	n/a	n/a
40	CTCF	chr3:133103400-133103550	GM06990	blood:	n/a	n/a
41	CTCF	chr3:133103420-133103570	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr3:133103400-133103550	GM12873	blood:	n/a	n/a
43	CTCF	chr3:133103404-133103620	GM10248	blood:	n/a	n/a
44	CTCF	chr3:133105860-133106010	GM06990	blood:	n/a	n/a
45	CTCF	chr3:133103400-133103550	WI-38	lung:	n/a	n/a
46	CTCF	chr3:133106800-133106950	HAc	cerebellar:	n/a	n/a
47	CTCF	chr3:133103380-133103530	GM12864	blood:	n/a	n/a
48	CTCF	chr3:133103420-133103570	GM12867	blood:	n/a	n/a
49	CTCF	chr3:133105920-133106070	NB4	blood:	n/a	n/a
50	CTCF	chr3:133103359-133103634	HUVEC	blood vessel:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:133117569-133117619	HCT-116	colon:	n/a
2	chr3:133118114-133118164	AG09319	gingival:	n/a
3	chr3:133117569-133117619	HCT-116	colon:	n/a
4	chr3:133118114-133118164	AG09319	gingival:	n/a
5	chr3:133118114-133118164	NHBE	bronchial:	n/a
6	chr3:133121913-133121963	HNPCEpiC	eye:	n/a
7	chr3:133118940-133118990	GM19239	blood:	n/a
8	chr3:133121913-133121963	LNCaP	prostate:	n/a
9	chr3:133118940-133118990	SAEC	small airway:	n/a
10	chr3:133117420-133117470	NHDF-neo	bronchial:	n/a
11	chr3:133117420-133117470	GM12878	blood:	n/a
12	chr3:133115942-133115992	Caco-2	colon:	n/a
13	chr3:133117420-133117470	K562	blood:	n/a
14	chr3:133118114-133118164	PFSK-1	brain:	n/a
15	chr3:133118114-133118164	Hela-S3	cervix:	n/a
16	chr3:133115942-133115992	IMR90	lung:	fetal
17	chr3:133118839-133118889	HRCEpiC	kidney:	n/a
18	chr3:133117569-133117619	PANC-1	pancreas:	n/a
19	chr3:133117569-133117619	RPTEC	kidney:	n/a
20	chr3:133112774-133112824	U87	brain:	n/a
21	chr3:133118940-133118990	HL-60	blood:	n/a
22	chr3:133117420-133117470	A549	lung:	n/a
23	chr3:133118114-133118164	SK-N-SH_RA	brain:	n/a
24	chr3:133121913-133121963	PFSK-1	brain:	n/a
25	chr3:133121913-133121963	HMEC	breast:	n/a
26	chr3:133117569-133117619	H1-hESC	embryonic stem cell:	embryo
27	chr3:133118114-133118164	LNCaP	prostate:	n/a
28	chr3:133103339-133103389	Hepatocyte	liver:	n/a
29	chr3:133118114-133118164	HRPEpiC	eye:	n/a
30	chr3:133117569-133117619	SK-N-SH	brain:	n/a
31	chr3:133117569-133117619	AG09319	gingival:	n/a
32	chr3:133115942-133115992	HRE	kidney:	n/a
33	chr3:133118940-133118990	HRE	kidney:	n/a
34	chr3:133103339-133103389	BJ	skin:	n/a
35	chr3:133118114-133118164	BJ	skin:	n/a
36	chr3:133103339-133103389	MCF-7	breast:	n/a
37	chr3:133118839-133118889	HAEpiC	amniotic membrane:	n/a
38	chr3:133118940-133118990	HCM	heart:	n/a
39	chr3:133112774-133112824	CMK	blood:	n/a
40	chr3:133117569-133117619	CMK	blood:	n/a
41	chr3:133118114-133118164	HCF	heart:	n/a
42	chr3:133117420-133117470	SK-N-MC	brain:	n/a
43	chr3:133117420-133117470	HRPEpiC	eye:	n/a
44	chr3:133118114-133118164	NHDF-neo	bronchial:	n/a
45	chr3:133103339-133103389	HCM	heart:	n/a
46	chr3:133103339-133103389	HUVEC	blood vessel:	n/a
47	chr3:133117569-133117619	MCF-7	breast:	n/a
48	chr3:133118940-133118990	Hepatocyte	liver:	n/a
49	chr3:133117420-133117470	Caco-2	colon:	n/a
50	chr3:133117569-133117619	SKMC	muscle:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:133112630..133114708-chr3:133139610..133142045,2	MCF-7	breast:
2	chr3:133103081..133103646-chr3:133142086..133142975,2	MCF-7	breast:
3	chr3:132450083..132450589-chr3:133103033..133103593,2	K562	blood:
4	chr3:133078806..133080710-chr3:133106761..133108268,2	K562	blood:
5	chr3:133110660..133112809-chr3:133115300..133117323,2	K562	blood:
6	chr3:133100831..133103449-chr3:133112603..133115144,2	K562	blood:
7	chr3:133100753..133103511-chr3:133104610..133107430,2	K562	blood:
8	chr3:133103166..133105237-chr3:133107966..133110867,2	MCF-7	breast:
9	chr3:133101161..133103236-chr3:133110708..133113387,2	MCF-7	breast:
10	chr3:133103166..133105237-chr3:133107966..133110867,2	MCF-7	breast:
11	chr3:133105415..133106537-chr3:133142074..133142947,6	MCF-7	breast:
12	chr3:132759780..132760619-chr3:133102965..133103930,4	MCF-7	breast:
13	chr3:132449680..132450196-chr3:133103197..133103913,2	MCF-7	breast:
14	chr3:132451003..132451965-chr3:133102656..133103518,2	K562	blood:
15	chr3:133105226..133106115-chr3:133142183..133142702,2	MCF-7	breast:
16	chr3:133100831..133103449-chr3:133112603..133115144,2	K562	blood:
17	chr3:132522337..132523099-chr3:133103066..133103802,4	MCF-7	breast:
18	chr3:132759895..132760704-chr3:133103022..133103783,2	K562	blood:
19	chr3:133101161..133103236-chr3:133110708..133113387,2	MCF-7	breast:
20	chr3:133110660..133112809-chr3:133115300..133117323,2	K562	blood:
21	chr3:133116761..133118281-chr3:133121220..133123369,2	MCF-7	breast:
22	chr3:133103700..133105206-chr3:133145260..133147537,2	MCF-7	breast:
23	chr3:132449516..132450612-chr3:133102788..133103978,6	MCF-7	breast:
24	chr3:133116761..133118281-chr3:133121220..133123369,2	MCF-7	breast:
25	chr3:133100753..133103511-chr3:133104610..133107430,2	K562	blood:
26	chr3:132445194..132445751-chr3:133103395..133104219,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOPBP1-6	chr3:133103148-133103256	NONHSAT092182

No data

Variant related genes	Relation type
BFSP2	TF binding region
BFSP2	CpG island
ENSG00000144868	chromatin interactions

Extended variants
information (count: 814 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6807356	chr3:133101390-133101391	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77146833	chr3:133101406-133101407	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs183996323	chr3:133101413-133101414	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs114071775	chr3:133101432-133101433	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs527668210	chr3:133101464-133101465	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs547777824	chr3:133101507-133101508	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs571622932	chr3:133101526-133101527	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs189853619	chr3:133101555-133101556	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs554682697	chr3:133101585-133101586	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs570147851	chr3:133101663-133101664	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs114588950	chr3:133101675-133101676	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs111338654	chr3:133101681-133101682	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs572369623	chr3:133101687-133101688	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs541351087	chr3:133101688-133101689	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs553445181	chr3:133101746-133101747	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs113509723	chr3:133101792-133101793	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs76473763	chr3:133101825-133101826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565313424	chr3:133101842-133101843	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35887281	chr3:133101843-133101844	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73209855	chr3:133101891-133101892	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs180761425	chr3:133101900-133101901	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1197307	chr3:133101933-133101934	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs150483251	chr3:133101960-133101961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548025542	chr3:133101998-133101999	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545255389	chr3:133102013-133102014	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs7631459	chr3:133102019-133102020	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs111603804	chr3:133102040-133102041	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs547671851	chr3:133102110-133102111	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs561083750	chr3:133102176-133102177	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs530156765	chr3:133102309-133102310	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs549985413	chr3:133102314-133102315	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs550420235	chr3:133102341-133102342	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs367556576	chr3:133102345-133102346	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs186141655	chr3:133102347-133102348	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs189314565	chr3:133102371-133102372	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs1201673	chr3:133102409-133102410	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs374224954	chr3:133102413-133102414	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527998201	chr3:133102469-133102470	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534947520	chr3:133102513-133102514	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1197306	chr3:133102534-133102535	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs182301595	chr3:133102549-133102550	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138119318	chr3:133102602-133102603	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79719860	chr3:133102630-133102631	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186446133	chr3:133102635-133102636	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545146888	chr3:133102685-133102686	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1197305	chr3:133102687-133102688	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572278502	chr3:133102722-133102723	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112327458	chr3:133102725-133102726	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528167720	chr3:133102731-133102732	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540956450	chr3:133102781-133102782	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Hailey-hailey disease	17597066	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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133093000-133102400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:133094000-133109000	Weak transcription	HSMM	muscle
3	chr3:133094400-133102800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:133094800-133102000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:133094800-133110400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:133095200-133103200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr3:133095800-133103200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr3:133096000-133107800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:133096400-133103200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:133097800-133102400	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr3:133098800-133101400	Enhancers	Pancreas	Pancrea
12	chr3:133098800-133103600	Weak transcription	Spleen	Spleen
13	chr3:133098800-133103800	Enhancers	Fetal Brain Male	brain
14	chr3:133099000-133101600	Genic enhancers	Fetal Brain Female	brain
15	chr3:133099000-133117000	Weak transcription	Placenta	Placenta
16	chr3:133099600-133122600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr3:133099800-133103000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr3:133100000-133101400	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr3:133100000-133101600	Enhancers	Fetal Muscle Leg	muscle
20	chr3:133100200-133103200	Weak transcription	Brain Hippocampus Middle	brain
21	chr3:133100200-133103600	Weak transcription	Brain Germinal Matrix	brain
22	chr3:133100400-133102800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr3:133100400-133103000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr3:133100400-133103200	Weak transcription	Brain Angular Gyrus	brain
25	chr3:133100800-133101800	Genic enhancers	Fetal Lung	lung
26	chr3:133100800-133102800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:133100800-133111600	Weak transcription	HSMMtube	muscle
28	chr3:133101000-133103000	Weak transcription	Liver	Liver
29	chr3:133101000-133103800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr3:133101200-133103200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr3:133101200-133103400	Enhancers	Lung	lung
32	chr3:133101400-133101800	Enhancers	Fetal Thymus	thymus
33	chr3:133101400-133101800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
34	chr3:133101400-133103000	Weak transcription	Pancreas	Pancrea
35	chr3:133101600-133102200	Weak transcription	Fetal Brain Female	brain
36	chr3:133101600-133102400	Weak transcription	Fetal Muscle Leg	muscle
37	chr3:133101600-133104000	Enhancers	HMEC	breast
38	chr3:133101800-133102000	Weak transcription	Fetal Lung	lung
39	chr3:133101800-133103200	Weak transcription	Fetal Thymus	thymus
40	chr3:133101800-133103800	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr3:133102000-133102400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:133102000-133102800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr3:133102000-133102800	Strong transcription	Fetal Lung	lung
44	chr3:133102000-133104200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:133102000-133104200	Enhancers	NHEK	skin
46	chr3:133102200-133102600	Enhancers	Fetal Brain Female	brain
47	chr3:133102200-133103400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr3:133102200-133103400	Enhancers	Stomach Mucosa	stomach
49	chr3:133102200-133103600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:133102200-133103800	Enhancers	HUVEC	blood vessel

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