Variant report

Variant	nsv877617
Chromosome Location	chr3:146096182-146172109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:244)
Chromatin interactive
region (count:24)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr3:146130211-146130634	K562	blood:	n/a	n/a
2	CBX3	chr3:146121518-146121906	HCT-116	colon:	n/a	n/a
3	CBX3	chr3:146130261-146130561	K562	blood:	n/a	n/a
4	CBX3	chr3:146163490-146163843	HCT-116	colon:	n/a	n/a
5	CEBPB	chr3:146112954-146113374	K562	blood:	n/a	chr3:146113140-146113151
6	CEBPB	chr3:146140168-146140455	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:146112957-146113329	IMR90	lung:	n/a	chr3:146113140-146113151
8	CEBPB	chr3:146140161-146140507	MCF-7	breast:	n/a	n/a
9	CEBPB	chr3:146139531-146140133	A549	lung:	n/a	n/a
10	CEBPB	chr3:146112976-146113336	Hela-S3	cervix:	n/a	chr3:146113140-146113151
11	CEBPB	chr3:146112894-146113347	A549	lung:	n/a	chr3:146113140-146113151
12	CEBPB	chr3:146112955-146113338	H1-hESC	embryonic stem cell:	n/a	chr3:146113140-146113151
13	CEBPB	chr3:146120425-146120469	A549	lung:	n/a	n/a
14	CEBPB	chr3:146112962-146113334	HepG2	liver:	n/a	chr3:146113140-146113151
15	CEBPB	chr3:146113057-146113226	ECC-1	luminal epithelium:	n/a	chr3:146113140-146113151
16	CEBPB	chr3:146108873-146109145	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:146139507-146139992	MCF-7	breast:	n/a	n/a
18	CEBPB	chr3:146113046-146113339	A549	lung:	n/a	chr3:146113140-146113151
19	CEBPB	chr3:146113007-146113331	A549	lung:	n/a	chr3:146113140-146113151
20	CHD2	chr3:146145207-146145271	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr3:146128660-146128810	HepG2	liver:	n/a	n/a
22	CTCF	chr3:146100320-146100470	GM12869	blood:	n/a	n/a
23	CTCF	chr3:146158363-146158401	Fibrobl	skin:	n/a	n/a
24	CTCF	chr3:146100280-146100430	NHEK	skin:	n/a	n/a
25	CTCF	chr3:146100287-146100490	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:146100320-146100470	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr3:146099959-146100723	A549	lung:	n/a	n/a
28	CTCF	chr3:146100244-146100440	HepG2	liver:	n/a	n/a
29	CTCF	chr3:146100280-146100430	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr3:146100301-146100460	Fibrobl	skin:	n/a	n/a
31	CTCF	chr3:146140280-146140430	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr3:146100324-146100424	GM19239	blood:	n/a	n/a
33	CTCF	chr3:146100280-146100430	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr3:146100320-146100470	BJ	skin:	n/a	n/a
35	CTCF	chr3:146140300-146140450	HPF	lung:	n/a	n/a
36	CTCF	chr3:146100320-146100470	AG10803	skin:	n/a	n/a
37	CTCF	chr3:146100300-146100450	HFF	foreskin:	n/a	n/a
38	CTCF	chr3:146100280-146100430	AG09319	gingival:	n/a	n/a
39	CTCF	chr3:146100258-146100465	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr3:146100260-146100410	AG04450	lung:	n/a	n/a
41	CTCF	chr3:146150089-146150147	LNCaP	prostate:	n/a	n/a
42	CTCF	chr3:146100180-146100330	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr3:146140280-146140430	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr3:146100320-146100470	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr3:146100260-146100410	RPTEC	kidney:	n/a	n/a
46	CTCF	chr3:146100260-146100410	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr3:146100340-146100490	AG04450	lung:	n/a	n/a
48	CTCF	chr3:146100240-146100390	HepG2	liver:	n/a	n/a
49	CTCF	chr3:146100286-146100471	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr3:146136520-146136670	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:146129360-146129410	HCPEpiC	choroid plexus:	n/a
2	chr3:146129360-146129410	SK-N-SH	brain:	n/a
3	chr3:146129360-146129410	HCM	heart:	n/a
4	chr3:146129264-146129314	HAEpiC	amniotic membrane:	n/a
5	chr3:146129420-146129470	HCT-116	colon:	n/a
6	chr3:146129420-146129470	BJ	skin:	n/a
7	chr3:146129264-146129314	SK-N-SH_RA	brain:	n/a
8	chr3:146129360-146129410	HMEC	breast:	n/a
9	chr3:146129420-146129470	HRCEpiC	kidney:	n/a
10	chr3:146129264-146129314	HCT-116	colon:	n/a
11	chr3:146157056-146157106	GM12892	blood:	n/a
12	chr3:146129360-146129410	NB4	blood:	n/a
13	chr3:146129264-146129314	BJ	skin:	n/a
14	chr3:146157056-146157106	T-47D	breast:	n/a
15	chr3:146129264-146129314	K562	blood:	n/a
16	chr3:146129360-146129410	HAEpiC	amniotic membrane:	n/a
17	chr3:146129420-146129470	HEEpiC	esophagus:	n/a
18	chr3:146157056-146157106	PrEC	prostate:	n/a
19	chr3:146129264-146129314	GM12892	blood:	n/a
20	chr3:146157056-146157106	HNPCEpiC	eye:	n/a
21	chr3:146157056-146157106	HEK293	kidney:	embryo
22	chr3:146129360-146129410	SAEC	small airway:	n/a
23	chr3:146129420-146129470	LNCaP	prostate:	n/a
24	chr3:146129264-146129314	HPAEpiC	pulmonary alveolar:	n/a
25	chr3:146129264-146129314	LNCaP	prostate:	n/a
26	chr3:146129420-146129470	HNPCEpiC	eye:	n/a
27	chr3:146129420-146129470	SK-N-MC	brain:	n/a
28	chr3:146157056-146157106	AG04449	skin:	fetal
29	chr3:146157056-146157106	AG04450	lung:	fetal
30	chr3:146129360-146129410	AG09319	gingival:	n/a
31	chr3:146129420-146129470	HAEpiC	amniotic membrane:	n/a
32	chr3:146129264-146129314	HCPEpiC	choroid plexus:	n/a
33	chr3:146129264-146129314	NT2-D1	testis:	n/a
34	chr3:146129420-146129470	ECC-1	luminal epithelium:	n/a
35	chr3:146129420-146129470	RPTEC	kidney:	n/a
36	chr3:146129420-146129470	HIPEpiC	eye:	n/a
37	chr3:146129360-146129410	AG04450	lung:	fetal
38	chr3:146129264-146129314	Caco-2	colon:	n/a
39	chr3:146129264-146129314	AG10803	skin:	n/a
40	chr3:146129264-146129314	AG09319	gingival:	n/a
41	chr3:146129420-146129470	SAEC	small airway:	n/a
42	chr3:146129360-146129410	PrEC	prostate:	n/a
43	chr3:146157056-146157106	RPTEC	kidney:	n/a
44	chr3:146157056-146157106	HCM	heart:	n/a
45	chr3:146129420-146129470	MCF-7	breast:	n/a
46	chr3:146129264-146129314	NB4	blood:	n/a
47	chr3:146129420-146129470	A549	lung:	n/a
48	chr3:146129420-146129470	HPAEpiC	pulmonary alveolar:	n/a
49	chr3:146157056-146157106	U87	brain:	n/a
50	chr3:146129420-146129470	AG09309	skin:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:146139609..146141816-chr3:146146728..146148840,3	MCF-7	breast:
2	chr3:146051931..146052494-chr3:146139879..146140654,2	MCF-7	breast:
3	chr3:145879440..145881243-chr3:146138706..146140785,2	MCF-7	breast:
4	chr3:146137952..146139503-chr3:146261134..146263708,2	MCF-7	breast:
5	chr3:146142625..146144505-chr3:146147964..146150004,2	K562	blood:
6	chr3:146044568..146045746-chr3:146099870..146100750,3	MCF-7	breast:
7	chr3:146137722..146139477-chr3:146142959..146145248,2	MCF-7	breast:
8	chr3:146100063..146100757-chr3:146220788..146221766,2	MCF-7	breast:
9	chr3:146158889..146161569-chr3:146161974..146164517,2	MCF-7	breast:
10	chr3:146155934..146158732-chr3:146162320..146163882,2	MCF-7	breast:
11	chr3:146169890..146171748-chr3:146177366..146178910,2	K562	blood:
12	chr3:146139398..146141443-chr3:146220518..146223634,3	MCF-7	breast:
13	chr3:146090461..146092431-chr3:146097019..146099426,2	MCF-7	breast:
14	chr3:146137722..146139477-chr3:146142959..146145248,2	MCF-7	breast:
15	chr3:146139318..146141303-chr3:146183434..146185764,2	MCF-7	breast:
16	chr3:146158889..146161569-chr3:146161974..146164517,2	MCF-7	breast:
17	chr3:146139609..146141816-chr3:146146728..146148840,3	MCF-7	breast:
18	chr3:146158561..146161277-chr3:146161473..146163225,2	K562	blood:
19	chr3:146158561..146161277-chr3:146161473..146163225,2	K562	blood:
20	chr3:146133340..146136821-chr3:146137357..146140210,3	MCF-7	breast:
21	chr3:146155934..146158732-chr3:146162320..146163882,2	MCF-7	breast:
22	chr3:146168876..146171592-chr3:146171883..146173684,2	K562	blood:
23	chr3:146168876..146171592-chr3:146171883..146173684,2	K562	blood:
24	chr3:146142625..146144505-chr3:146147964..146150004,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLSCR2-1	chr3:146119142-146119363	NONHSAT092557
2	lnc-PLSCR2-1	chr3:146116444-146116610	NONHSAT092557
3	lnc-PLSCR2-1	chr3:146113547-146113708	NONHSAT092556
4	lnc-PLSCR2-1	chr3:146109150-146109349	NONHSAT092556
5	lnc-PLSCR2-1	chr3:146134293-146134364	NONHSAT092557
6	lnc-PLSCR2-1	chr3:146119147-146119346	NONHSAT092556
7	lnc-PLSCR2-1	chr3:146113527-146113702	NONHSAT092557
8	lnc-PLSCR2-1	chr3:146134291-146134390	NONHSAT092556
9	lnc-PLSCR2-1	chr3:146132912-146132954	NONHSAT092556

No data

Variant related genes	Relation type
ENSG00000241358	TF binding region
ENSG00000241358	CpG island
ENSG00000188313	chromatin interactions
ENSG00000163746	chromatin interactions
ENSG00000241358	chromatin interactions

Extended variants
information (count: 2517 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2517 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1018271	chr3:146096182-146096183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530324401	chr3:146096204-146096205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111496650	chr3:146096230-146096231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1033115	chr3:146096241-146096242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184702411	chr3:146096273-146096274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115496026	chr3:146096292-146096293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534289771	chr3:146096323-146096324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7432259	chr3:146096369-146096370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs151160175	chr3:146096372-146096373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538270294	chr3:146096376-146096377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140207522	chr3:146096423-146096424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574724929	chr3:146096436-146096437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145192884	chr3:146096496-146096497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376892060	chr3:146096548-146096549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111736526	chr3:146096602-146096603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548498034	chr3:146096660-146096661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2063525	chr3:146096673-146096674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs187993618	chr3:146096716-146096717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs137882175	chr3:146096761-146096762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376019573	chr3:146096762-146096763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538049508	chr3:146096778-146096779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552972602	chr3:146096812-146096813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34765812	chr3:146096822-146096823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191329304	chr3:146096828-146096829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78816603	chr3:146096913-146096914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143642764	chr3:146096963-146096964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561517061	chr3:146097013-146097014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75863413	chr3:146097025-146097026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115013001	chr3:146097032-146097033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560688434	chr3:146097054-146097055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531064837	chr3:146097086-146097087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200114184	chr3:146097140-146097141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184983257	chr3:146097168-146097169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556706961	chr3:146097179-146097180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189314694	chr3:146097197-146097198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570950303	chr3:146097216-146097217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566520062	chr3:146097226-146097227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13075926	chr3:146097229-146097230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531711887	chr3:146097249-146097250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181613503	chr3:146097295-146097296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73867579	chr3:146097308-146097309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs371735819	chr3:146097320-146097321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1512070	chr3:146097330-146097331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs184717109	chr3:146097339-146097340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553623868	chr3:146097415-146097416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189953113	chr3:146097423-146097424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539282797	chr3:146097442-146097443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557645758	chr3:146097461-146097462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56162947	chr3:146097466-146097467	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs575098030	chr3:146097550-146097551	Weak transcription	n/a	n/a	Overlapped CNVs	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
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146093000-146098400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:146093000-146104800	Weak transcription	Fetal Lung	lung
3	chr3:146097600-146098800	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr3:146097800-146098600	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr3:146097800-146099000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr3:146098400-146098800	Enhancers	Colonic Mucosa	Colon
7	chr3:146098400-146098800	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr3:146099000-146100600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr3:146100400-146101200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:146100400-146101600	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr3:146100600-146100800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr3:146100600-146101000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr3:146100600-146101200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:146100600-146101200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr3:146100800-146101600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr3:146100800-146112600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:146101200-146101600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:146101600-146111800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:146104600-146104800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr3:146104600-146105000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:146104800-146105000	Enhancers	Fetal Lung	lung
22	chr3:146104800-146106800	Enhancers	A549	lung
23	chr3:146105000-146105400	Weak transcription	Fetal Lung	lung
24	chr3:146105200-146106000	Weak transcription	Ovary	ovary
25	chr3:146105400-146105600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr3:146105400-146106200	Enhancers	Fetal Lung	lung
27	chr3:146106000-146106200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:146106000-146106200	Enhancers	Ovary	ovary
29	chr3:146106200-146107200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:146106200-146107200	Weak transcription	Fetal Lung	lung
31	chr3:146106200-146107200	Weak transcription	Ovary	ovary
32	chr3:146106800-146107200	Weak transcription	A549	lung
33	chr3:146107200-146107400	Enhancers	Ovary	ovary
34	chr3:146107200-146107400	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
35	chr3:146107200-146108800	Enhancers	Fetal Stomach	stomach
36	chr3:146107200-146109600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr3:146107200-146110000	Enhancers	Fetal Lung	lung
38	chr3:146107600-146108600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr3:146107800-146108400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:146108000-146109400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr3:146108000-146109600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr3:146108000-146109600	Enhancers	Osteobl	bone
43	chr3:146108200-146108400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr3:146108200-146108600	Enhancers	Colon Smooth Muscle	Colon
45	chr3:146108400-146108800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:146108400-146108800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:146108400-146108800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr3:146108400-146109000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:146108400-146109000	Enhancers	NHLF	lung
50	chr3:146108400-146109200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links