Variant report

Variant	nsv834382
Chromosome Location	chr2:133728399-133891418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:437)
CpG islands
(count:305)
Chromatin interactive
region (count:24)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:437 , 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	BCL11A	chr2:133736400-133736844	GM12878	blood:	n/a	n/a
2	BHLHE40	chr2:133770871-133771272	GM12878	blood:	n/a	n/a
3	BHLHE40	chr2:133736509-133736513	GM12878	blood:	n/a	n/a
4	CEBPB	chr2:133752193-133752411	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:133808972-133809055	HepG2	liver:	n/a	chr2:133809011-133809022 chr2:133809010-133809023
6	CEBPB	chr2:133797903-133797994	H1-hESC	embryonic stem cell:	n/a	chr2:133797955-133797966
7	CEBPB	chr2:133797791-133798131	Hela-S3	cervix:	n/a	chr2:133797955-133797966
8	CEBPB	chr2:133792922-133793196	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:133862229-133862527	A549	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
10	CEBPB	chr2:133834945-133835142	IMR90	lung:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
11	CEBPB	chr2:133884617-133885020	HepG2	liver:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
12	CEBPB	chr2:133867421-133867772	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:133821434-133821709	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:133867453-133867754	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:133884649-133884917	IMR90	lung:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
16	CEBPB	chr2:133835003-133835062	HepG2	liver:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
17	CEBPB	chr2:133752159-133752432	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:133833598-133833686	HepG2	liver:	n/a	chr2:133833672-133833683 chr2:133833611-133833622
19	CEBPB	chr2:133836687-133836898	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:133819747-133820083	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:133748166-133748284	A549	lung:	n/a	chr2:133748232-133748243
22	CEBPB	chr2:133797830-133798092	HepG2	liver:	n/a	chr2:133797955-133797966
23	CEBPB	chr2:133862268-133862515	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:133819724-133820116	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:133797776-133798143	IMR90	lung:	n/a	chr2:133797955-133797966
26	CEBPB	chr2:133836703-133836940	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:133748918-133749459	HepG2	liver:	n/a	chr2:133749057-133749070 chr2:133749057-133749068 chr2:133749056-133749073 chr2:133749057-133749070 chr2:133749057-133749070
28	CEBPB	chr2:133792877-133793234	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:133752167-133752449	A549	lung:	n/a	n/a
30	CEBPB	chr2:133820511-133821222	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:133821472-133821768	MCF-7	breast:	n/a	n/a
32	CEBPB	chr2:133888455-133888729	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:133782590-133782918	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:133836739-133836849	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:133888428-133888781	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:133808875-133809161	IMR90	lung:	n/a	chr2:133809011-133809022 chr2:133809010-133809023
37	CEBPB	chr2:133792934-133793194	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:133797821-133798110	A549	lung:	n/a	chr2:133797955-133797966
39	CEBPB	chr2:133748145-133748354	HepG2	liver:	n/a	chr2:133748232-133748243
40	CEBPB	chr2:133735747-133736076	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:133792973-133793173	A549	lung:	n/a	n/a
42	CEBPB	chr2:133821436-133821710	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr2:133862217-133862515	IMR90	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
44	CEBPB	chr2:133821440-133821725	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:133748993-133749121	Hela-S3	cervix:	n/a	chr2:133749057-133749070 chr2:133749057-133749068 chr2:133749056-133749073 chr2:133749057-133749070 chr2:133749057-133749070
46	CHD2	chr2:133736475-133736717	GM12878	blood:	n/a	n/a
47	CHD2	chr2:133737450-133737503	GM12878	blood:	n/a	n/a
48	CTCF	chr2:133766740-133766890	AG09319	gingival:	n/a	n/a
49	CTCF	chr2:133749360-133749510	HMEC	breast:	n/a	n/a
50	CTCF	chr2:133854755-133854759	GM12892	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133855847-133855897	HEK293	kidney:	embryo
2	chr2:133834998-133835048	BE2_C	brain:	n/a
3	chr2:133855847-133855897	AG04450	lung:	fetal
4	chr2:133834998-133835048	GM19239	blood:	n/a
5	chr2:133733241-133733291	HIPEpiC	eye:	n/a
6	chr2:133855847-133855897	PrEC	prostate:	n/a
7	chr2:133855847-133855897	GM12892	blood:	n/a
8	chr2:133888263-133888313	GM12892	blood:	n/a
9	chr2:133868449-133868499	T-47D	breast:	n/a
10	chr2:133733241-133733291	AG04449	skin:	fetal
11	chr2:133733241-133733291	AG09309	skin:	n/a
12	chr2:133888263-133888313	NHBE	bronchial:	n/a
13	chr2:133733241-133733291	SK-N-SH	brain:	n/a
14	chr2:133868449-133868499	MCF-7	breast:	n/a
15	chr2:133868449-133868499	AG04450	lung:	fetal
16	chr2:133834998-133835048	AG09319	gingival:	n/a
17	chr2:133868449-133868499	HepG2	liver:	n/a
18	chr2:133888263-133888313	ProgFib	skin:	n/a
19	chr2:133733241-133733291	IMR90	lung:	fetal
20	chr2:133868449-133868499	RPTEC	kidney:	n/a
21	chr2:133733241-133733291	HEEpiC	esophagus:	n/a
22	chr2:133888263-133888313	HCT-116	colon:	n/a
23	chr2:133733241-133733291	HCM	heart:	n/a
24	chr2:133868449-133868499	HEK293	kidney:	embryo
25	chr2:133888263-133888313	GM12891	blood:	n/a
26	chr2:133888263-133888313	PFSK-1	brain:	n/a
27	chr2:133733241-133733291	NT2-D1	testis:	n/a
28	chr2:133868449-133868499	GM19239	blood:	n/a
29	chr2:133868449-133868499	AoSMC	blood vessel:	n/a
30	chr2:133868449-133868499	HCM	heart:	n/a
31	chr2:133855847-133855897	GM12891	blood:	n/a
32	chr2:133834998-133835048	LNCaP	prostate:	n/a
33	chr2:133855847-133855897	NH-A	brain:	n/a
34	chr2:133868449-133868499	GM12892	blood:	n/a
35	chr2:133888263-133888313	ovcar-3	ovarian:	n/a
36	chr2:133733241-133733291	HNPCEpiC	eye:	n/a
37	chr2:133733241-133733291	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:133855847-133855897	AG09309	skin:	n/a
39	chr2:133888263-133888313	Caco-2	colon:	n/a
40	chr2:133834998-133835048	HCT-116	colon:	n/a
41	chr2:133888263-133888313	T-47D	breast:	n/a
42	chr2:133834998-133835048	HEEpiC	esophagus:	n/a
43	chr2:133733241-133733291	HL-60	blood:	n/a
44	chr2:133733241-133733291	H1-hESC	embryonic stem cell:	embryo
45	chr2:133733241-133733291	AG10803	skin:	n/a
46	chr2:133834998-133835048	NHBE	bronchial:	n/a
47	chr2:133733241-133733291	K562	blood:	n/a
48	chr2:133888263-133888313	HMEC	breast:	n/a
49	chr2:133868449-133868499	ovcar-3	ovarian:	n/a
50	chr2:133855847-133855897	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
2	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
3	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
4	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
5	chr2:133737097..133739714-chr2:133742077..133743742,2	MCF-7	breast:
6	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
7	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
8	chr2:133427195..133430167-chr2:133854644..133856509,2	MCF-7	breast:
9	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
10	chr2:133737230..133740275-chr2:133741296..133743711,3	K562	blood:
11	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
12	chr2:133737230..133740275-chr2:133741296..133743711,3	K562	blood:
13	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
14	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
15	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:
16	chr2:133427399..133430167-chr2:133804238..133806785,2	MCF-7	breast:
17	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
18	chr2:133831745..133832436-chr8:97637034..97637925,2	MCF-7	breast:
19	chr2:133737097..133739714-chr2:133742077..133743742,2	MCF-7	breast:
20	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:
21	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
22	chr2:133795860..133798019-chr2:133803076..133805297,2	MCF-7	breast:
23	chr2:133722484..133724496-chr2:133727279..133729057,2	K562	blood:
24	chr2:133795860..133798019-chr2:133803076..133805297,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-12	chr2:133741315-133741466	ucscGeneNc_uc002ttu_1
2	lnc-GPR39-12	chr2:133740284-133740478	ucscGeneNc_uc002ttu_1
3	lnc-GPR39-12	chr2:133742398-133742484	ucscGeneNc_uc002ttu_1
4	lnc-GPR39-12	chr2:133742958-133743083	ucscGeneNc_uc002ttu_1

No data

Variant related genes	Relation type
ENSG00000269686	TF binding region
ENSG00000269686	CpG island
ENSG00000150551	chromatin interactions

Extended variants
information (count: 6161 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:6161 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572767483	chr2:133728401-133728402	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189567385	chr2:133728515-133728516	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181297091	chr2:133728532-133728533	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554974504	chr2:133728536-133728537	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573297127	chr2:133728542-133728543	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148789936	chr2:133728561-133728562	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564775340	chr2:133728577-133728578	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76911606	chr2:133728587-133728588	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185816743	chr2:133728616-133728617	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545158111	chr2:133728649-133728650	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560468975	chr2:133728666-133728667	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545260643	chr2:133728669-133728670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116239381	chr2:133728672-133728673	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565061695	chr2:133728682-133728683	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79920550	chr2:133728731-133728732	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562107574	chr2:133728733-133728734	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529249274	chr2:133728739-133728740	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550801855	chr2:133728760-133728761	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs151295922	chr2:133728767-133728768	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7556707	chr2:133728774-133728775	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551594758	chr2:133728788-133728789	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111997750	chr2:133728827-133728828	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375592629	chr2:133728970-133728971	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs367560000	chr2:133729006-133729007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534266723	chr2:133729031-133729032	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544045246	chr2:133729180-133729181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144288867	chr2:133729181-133729182	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537801055	chr2:133729187-133729188	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146558701	chr2:133729252-133729253	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76287443	chr2:133729302-133729303	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141224773	chr2:133729313-133729314	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77816684	chr2:133729315-133729316	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144935963	chr2:133729341-133729342	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542955635	chr2:133729344-133729345	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561122061	chr2:133729360-133729361	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548348196	chr2:133729408-133729409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190378066	chr2:133729416-133729417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544560504	chr2:133729417-133729418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530091230	chr2:133729459-133729460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562724130	chr2:133729464-133729465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75125421	chr2:133729491-133729492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551460682	chr2:133729496-133729497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73956088	chr2:133729503-133729504	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs527838060	chr2:133729507-133729508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181555888	chr2:133729629-133729630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567918082	chr2:133729637-133729638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565718824	chr2:133729660-133729661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536573524	chr2:133729702-133729703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549781381	chr2:133729741-133729742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6738269	chr2:133729748-133729749	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133714600-133735400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:133721400-133732200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:133725800-133732600	Weak transcription	Brain Hippocampus Middle	brain
4	chr2:133726400-133734800	Weak transcription	Brain Anterior Caudate	brain
5	chr2:133727400-133728400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:133727400-133728800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr2:133727400-133729200	Weak transcription	NHEK	skin
8	chr2:133727400-133732000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:133728200-133729400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:133728400-133729000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:133728400-133730200	Enhancers	Stomach Mucosa	stomach
12	chr2:133728800-133730000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr2:133729200-133730000	Enhancers	NHEK	skin
14	chr2:133729400-133730000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr2:133729400-133733000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:133730000-133732200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:133730000-133732200	Weak transcription	NHEK	skin
18	chr2:133730000-133735400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:133731800-133732400	Enhancers	Colon Smooth Muscle	Colon
20	chr2:133732000-133732600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr2:133732000-133732600	Enhancers	Fetal Stomach	stomach
22	chr2:133732000-133733400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:133732000-133733400	Enhancers	Fetal Kidney	kidney
24	chr2:133732000-133733600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:133732200-133732400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:133732200-133732400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr2:133732200-133732600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr2:133732200-133732600	Enhancers	Fetal Muscle Leg	muscle
29	chr2:133732200-133732600	Enhancers	Rectal Smooth Muscle	rectum
30	chr2:133732200-133732600	Enhancers	NHEK	skin
31	chr2:133732200-133732800	Enhancers	Fetal Lung	lung
32	chr2:133732200-133733000	Enhancers	Fetal Brain Female	brain
33	chr2:133732200-133733200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr2:133732200-133733800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr2:133732200-133734000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:133732400-133732800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:133732400-133732800	Flanking Active TSS	Colon Smooth Muscle	Colon
38	chr2:133732400-133733600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr2:133732400-133733800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:133732400-133733800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr2:133732400-133735600	Weak transcription	NH-A	brain
42	chr2:133732600-133733000	Enhancers	Brain Hippocampus Middle	brain
43	chr2:133732600-133733400	Weak transcription	Fetal Stomach	stomach
44	chr2:133732600-133734800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr2:133732600-133735600	Weak transcription	NHEK	skin
46	chr2:133732800-133733000	Enhancers	Fetal Brain Male	brain
47	chr2:133732800-133733200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:133732800-133733200	Enhancers	Colon Smooth Muscle	Colon
49	chr2:133732800-133733800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:133733000-133734000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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