Variant report

Variant	nsv870185
Chromosome Location	chr3:140265153-140395673
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	chr3:140282147-140282294	HepG2	liver:	n/a	n/a
2	ATF1	chr3:140336242-140336250	K562	blood:	n/a	n/a
3	BACH1	chr3:140318453-140318653	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:140367452-140367456	K562	blood:	n/a	n/a
5	BATF	chr3:140374547-140374771	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:140329685-140329713	K562	blood:	n/a	n/a
7	BHLHE40	chr3:140347642-140347676	GM12878	blood:	n/a	n/a
8	CCNT2	chr3:140312647-140312920	K562	blood:	n/a	n/a
9	CCNT2	chr3:140314146-140314500	K562	blood:	n/a	chr3:140314351-140314371
10	CEBPB	chr3:140282056-140282429	HepG2	liver:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
11	CEBPB	chr3:140282059-140282352	HepG2	liver:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
12	CEBPB	chr3:140282076-140282385	A549	lung:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
13	CEBPB	chr3:140348716-140349002	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:140267102-140267390	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:140282113-140282318	HepG2	liver:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
16	CEBPB	chr3:140282075-140282408	K562	blood:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
17	CEBPB	chr3:140282125-140282367	H1-hESC	embryonic stem cell:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
18	CEBPB	chr3:140324409-140324596	HepG2	liver:	n/a	chr3:140324518-140324529
19	CEBPB	chr3:140272491-140272712	K562	blood:	n/a	chr3:140272503-140272520
20	CEBPB	chr3:140354064-140354201	HepG2	liver:	n/a	chr3:140354175-140354186
21	CEBPB	chr3:140282075-140282398	IMR90	lung:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
22	CEBPB	chr3:140282054-140282416	Hela-S3	cervix:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
23	CEBPB	chr3:140348639-140349072	MCF-7	breast:	n/a	n/a
24	CEBPB	chr3:140282070-140282481	MCF-7	breast:	n/a	chr3:140282237-140282250 chr3:140282239-140282248 chr3:140282239-140282248 chr3:140282236-140282253 chr3:140282238-140282249 chr3:140282239-140282248
25	CEBPB	chr3:140348665-140348999	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr3:140307456-140307691	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr3:140306728-140306917	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr3:140271820-140271970	HVMF	connective:	n/a	n/a
29	CTCF	chr3:140265670-140265797	LNCaP	prostate:	n/a	chr3:140265708-140265729
30	CTCF	chr3:140271246-140271627	H1-hESC	embryonic stem cell:	n/a	chr3:140271439-140271457 chr3:140271434-140271455
31	CTCF	chr3:140271340-140271490	GM12871	blood:	n/a	chr3:140271439-140271457 chr3:140271434-140271455
32	CTCF	chr3:140291262-140291437	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr3:140271300-140271450	AG09309	skin:	n/a	n/a
34	CTCF	chr3:140265620-140265770	HMF	breast:	n/a	chr3:140265708-140265729
35	CTCF	chr3:140271420-140271570	GM12864	blood:	n/a	chr3:140271439-140271457 chr3:140271434-140271455
36	CTCF	chr3:140291313-140291434	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:140354220-140354370	GM12873	blood:	n/a	n/a
38	CTCF	chr3:140271833-140272064	HepG2	liver:	n/a	chr3:140271958-140271976 chr3:140271963-140271984 chr3:140271964-140271977
39	CTCF	chr3:140271360-140271510	HEEpiC	esophagus:	n/a	chr3:140271439-140271457 chr3:140271434-140271455
40	CTCF	chr3:140271887-140272036	GM19238	blood:	n/a	chr3:140271958-140271976 chr3:140271963-140271984 chr3:140271964-140271977
41	CTCF	chr3:140298320-140298470	NHEK	skin:	n/a	n/a
42	CTCF	chr3:140354080-140354230	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:140271440-140271590	HepG2	liver:	n/a	n/a
44	CTCF	chr3:140298180-140298330	HMF	breast:	n/a	n/a
45	CTCF	chr3:140291329-140291426	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:140271880-140272030	HCPEpiC	choroid plexus:	n/a	chr3:140271958-140271976 chr3:140271963-140271984 chr3:140271964-140271977
47	CTCF	chr3:140271940-140272090	K562	blood:	n/a	chr3:140271958-140271976 chr3:140271963-140271984 chr3:140271964-140271977
48	CTCF	chr3:140291339-140291437	GM12891	blood:	n/a	n/a
49	CTCF	chr3:140265620-140265770	HBMEC	blood vessel:	n/a	chr3:140265708-140265729
50	CTCF	chr3:140271380-140271530	MCF-7	breast:	n/a	chr3:140271439-140271457 chr3:140271434-140271455

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140271994-140272044	NHDF-neo	bronchial:	n/a
2	chr3:140271994-140272044	HNPCEpiC	eye:	n/a
3	chr3:140306730-140306780	RPTEC	kidney:	n/a
4	chr3:140306730-140306780	HRCEpiC	kidney:	n/a
5	chr3:140286910-140286960	SAEC	small airway:	n/a
6	chr3:140271994-140272044	U87	brain:	n/a
7	chr3:140271994-140272044	AG09309	skin:	n/a
8	chr3:140306730-140306780	HCPEpiC	choroid plexus:	n/a
9	chr3:140306730-140306780	Hela-S3	cervix:	n/a
10	chr3:140271994-140272044	HepG2	liver:	n/a
11	chr3:140286910-140286960	BJ	skin:	n/a
12	chr3:140306730-140306780	GM12891	blood:	n/a
13	chr3:140271994-140272044	AG04450	lung:	fetal
14	chr3:140306730-140306780	HRE	kidney:	n/a
15	chr3:140286910-140286960	T-47D	breast:	n/a
16	chr3:140306730-140306780	IMR90	lung:	fetal
17	chr3:140271994-140272044	Caco-2	colon:	n/a
18	chr3:140286910-140286960	HepG2	liver:	n/a
19	chr3:140286910-140286960	MCF-7	breast:	n/a
20	chr3:140271994-140272044	HCF	heart:	n/a
21	chr3:140286910-140286960	AG09319	gingival:	n/a
22	chr3:140306730-140306780	NHDF-neo	bronchial:	n/a
23	chr3:140271994-140272044	Hepatocyte	liver:	n/a
24	chr3:140306730-140306780	U87	brain:	n/a
25	chr3:140271994-140272044	AG04449	skin:	fetal
26	chr3:140286910-140286960	GM12891	blood:	n/a
27	chr3:140306730-140306780	ovcar-3	ovarian:	n/a
28	chr3:140306730-140306780	ProgFib	skin:	n/a
29	chr3:140271994-140272044	H1-hESC	embryonic stem cell:	embryo
30	chr3:140306730-140306780	MCF10A-Er-Src	breast:	n/a
31	chr3:140306730-140306780	GM19239	blood:	n/a
32	chr3:140286910-140286960	H1-hESC	embryonic stem cell:	embryo
33	chr3:140286910-140286960	AG09309	skin:	n/a
34	chr3:140306730-140306780	GM06990	blood:	n/a
35	chr3:140271994-140272044	HRCEpiC	kidney:	n/a
36	chr3:140306730-140306780	ECC-1	luminal epithelium:	n/a
37	chr3:140271994-140272044	HUVEC	blood vessel:	n/a
38	chr3:140286910-140286960	SK-N-SH	brain:	n/a
39	chr3:140286910-140286960	GM12892	blood:	n/a
40	chr3:140286910-140286960	NHBE	bronchial:	n/a
41	chr3:140286910-140286960	HRE	kidney:	n/a
42	chr3:140306730-140306780	HCM	heart:	n/a
43	chr3:140306730-140306780	BE2_C	brain:	n/a
44	chr3:140286910-140286960	SK-N-SH_RA	brain:	n/a
45	chr3:140271994-140272044	NHBE	bronchial:	n/a
46	chr3:140286910-140286960	GM19239	blood:	n/a
47	chr3:140306730-140306780	AG10803	skin:	n/a
48	chr3:140286910-140286960	SK-N-MC	brain:	n/a
49	chr3:140286910-140286960	HCPEpiC	choroid plexus:	n/a
50	chr3:140271994-140272044	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:140354121..140354796-chr3:140455695..140456494,2	MCF-7	breast:
2	chr3:140265369..140267923-chr3:140268388..140271022,3	K562	blood:
3	chr3:140294766..140296496-chr3:140304376..140305951,2	MCF-7	breast:
4	chr3:140313745..140316717-chr3:140320885..140322798,2	K562	blood:
5	chr17:48156766..48157639-chr3:140271390..140272077,2	MCF-7	breast:
6	chr3:140279088..140280998-chr3:140285629..140287681,2	K562	blood:
7	chr3:140272136..140274047-chr3:140274410..140276420,2	MCF-7	breast:
8	chr3:139656565..139657391-chr3:140271192..140271914,2	MCF-7	breast:
9	chr3:140279088..140280998-chr3:140285629..140287681,2	K562	blood:
10	chr3:140286202..140288218-chr3:140290822..140292470,2	MCF-7	breast:
11	chr3:140272136..140274047-chr3:140274410..140276420,2	MCF-7	breast:
12	chr3:140284899..140286878-chr3:140297066..140299043,2	K562	blood:
13	chr3:140314929..140317518-chr3:140320988..140323953,2	K562	blood:
14	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
15	chr3:140271350..140272024-chr3:140455669..140456272,2	MCF-7	breast:
16	chr3:140313745..140316717-chr3:140320885..140322798,2	K562	blood:
17	chr3:140284899..140286878-chr3:140297066..140299043,2	K562	blood:
18	chr3:140314929..140317518-chr3:140320988..140323953,2	K562	blood:
19	chr3:140294766..140296496-chr3:140304376..140305951,2	MCF-7	breast:
20	chr3:140265369..140267923-chr3:140268388..140271022,3	K562	blood:
21	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
22	chr3:140286202..140288218-chr3:140290822..140292470,2	MCF-7	breast:
23	chr3:140271820..140272427-chr3:140582348..140582959,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLSTN2-1	chr3:140290548-140294071	NONHSAT092403
2	lnc-CLSTN2-3	chr3:140325513-140326693	l_2484_NR_026783
3	lnc-CLSTN2-3	chr3:140305717-140307953	l_2484_NR_026783
4	lnc-CLSTN2-3	chr3:140310744-140310837	l_2484_NR_026783
5	lnc-CLSTN2-1	chr3:140290548-140296239	ENSG00000261179.1

Variant related genes	Relation type
TRIM42	TF binding region
ENSG00000249305	TF binding region
TRIM42	CpG island
ENSG00000249305	CpG island

Extended variants
information (count: 3307 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3307 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149812390	chr3:140265165-140265166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192191691	chr3:140265186-140265187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs55856137	chr3:140265187-140265188	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs555636480	chr3:140265231-140265232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573811777	chr3:140265256-140265257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541437865	chr3:140265257-140265258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559517424	chr3:140265292-140265293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146338703	chr3:140265332-140265333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371757465	chr3:140265337-140265338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146589649	chr3:140265353-140265354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201488984	chr3:140265385-140265386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139725728	chr3:140265397-140265398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374836443	chr3:140265418-140265419	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs202013971	chr3:140265423-140265424	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200822657	chr3:140265448-140265449	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145299723	chr3:140265463-140265464	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369160182	chr3:140265467-140265468	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147654181	chr3:140265497-140265498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374306883	chr3:140265505-140265506	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs377757913	chr3:140265538-140265539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369567661	chr3:140265551-140265552	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549271912	chr3:140265577-140265578	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59364093	chr3:140265587-140265588	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs139582664	chr3:140265596-140265597	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144221765	chr3:140265597-140265598	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549886465	chr3:140265598-140265599	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565710271	chr3:140265601-140265602	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532945755	chr3:140265660-140265661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563408262	chr3:140265673-140265674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551546969	chr3:140265681-140265682	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569720956	chr3:140265687-140265688	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537250741	chr3:140265694-140265695	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555235813	chr3:140265779-140265780	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532380556	chr3:140265784-140265785	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567434125	chr3:140265793-140265794	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184030247	chr3:140265838-140265839	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553222969	chr3:140265892-140265893	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186037254	chr3:140265928-140265929	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550368334	chr3:140265945-140265946	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557048097	chr3:140265946-140265947	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369160727	chr3:140265978-140265979	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572681246	chr3:140266034-140266035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190021299	chr3:140266053-140266054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113504524	chr3:140266088-140266089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113584098	chr3:140266113-140266114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78764105	chr3:140266131-140266132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61138256	chr3:140266132-140266133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374330942	chr3:140266133-140266134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59920486	chr3:140266135-140266136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528666329	chr3:140266185-140266186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Lung cancer	16740712	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
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Schizophrenia	17989066	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140254000-140266400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:140262200-140265400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:140262600-140265800	Enhancers	Adipose Nuclei	Adipose
4	chr3:140263200-140265200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:140263400-140265800	Enhancers	Ovary	ovary
6	chr3:140264000-140265400	Enhancers	HSMMtube	muscle
7	chr3:140264000-140265600	Enhancers	Rectal Smooth Muscle	rectum
8	chr3:140264000-140265800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr3:140264200-140265200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:140264400-140265400	Enhancers	Placenta	Placenta
11	chr3:140264400-140265600	Enhancers	Pancreas	Pancrea
12	chr3:140264600-140265200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr3:140264600-140265400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr3:140265000-140265200	Enhancers	Stomach Smooth Muscle	stomach
15	chr3:140265000-140265400	Enhancers	Aorta	Aorta
16	chr3:140265200-140265800	Enhancers	Lung	lung
17	chr3:140265200-140266000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:140265200-140270400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr3:140265400-140267200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:140265400-140267400	Weak transcription	Aorta	Aorta
21	chr3:140265400-140267800	Strong transcription	HSMMtube	muscle
22	chr3:140265600-140287800	Weak transcription	Pancreas	Pancrea
23	chr3:140265800-140275200	Weak transcription	Ovary	ovary
24	chr3:140265800-140282000	Weak transcription	Adipose Nuclei	Adipose
25	chr3:140266400-140266800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr3:140266800-140280800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr3:140267200-140274800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:140267800-140270800	Weak transcription	HSMMtube	muscle
29	chr3:140270400-140272000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr3:140270800-140278200	Strong transcription	HSMMtube	muscle
31	chr3:140271200-140271800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr3:140271200-140272200	Enhancers	NHEK	skin
33	chr3:140271400-140271800	Enhancers	HMEC	breast
34	chr3:140271600-140272000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:140271600-140272000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr3:140271600-140272000	Enhancers	HSMM	muscle
37	chr3:140274200-140287600	Weak transcription	Brain Hippocampus Middle	brain
38	chr3:140274800-140275600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr3:140275200-140277600	Strong transcription	Ovary	ovary
40	chr3:140275600-140280800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr3:140277600-140280400	Weak transcription	Ovary	ovary
42	chr3:140278200-140279200	Weak transcription	HSMMtube	muscle
43	chr3:140279200-140288400	Strong transcription	HSMMtube	muscle
44	chr3:140279600-140289600	Weak transcription	Fetal Brain Female	brain
45	chr3:140280400-140286200	Strong transcription	Ovary	ovary
46	chr3:140280600-140281000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:140280800-140283200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr3:140280800-140286200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr3:140281000-140287800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr3:140282000-140282400	Enhancers	Adipose Nuclei	Adipose

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