Variant report

Variant	nsv516915
Chromosome Location	chr2:133999831-134054662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:563)
CpG islands
(count:732)
Chromatin interactive
region (count:27)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:134022701-134024075	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:134005181-134005429	GM12878	blood:	n/a	n/a
3	BCL3	chr2:134023499-134024135	A549	lung:	n/a	n/a
4	BCL3	chr2:134023525-134024142	A549	lung:	n/a	n/a
5	BRCA1	chr2:134004476-134004492	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr2:134022507-134023986	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:134043889-134044238	A549	lung:	n/a	n/a
8	CEBPB	chr2:134043952-134044155	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:134000488-134000570	A549	lung:	n/a	n/a
10	CEBPB	chr2:134024047-134024339	IMR90	lung:	n/a	chr2:134024205-134024216
11	CEBPB	chr2:134044066-134044190	K562	blood:	n/a	n/a
12	CEBPB	chr2:134043877-134044226	MCF-7	breast:	n/a	n/a
13	CEBPB	chr2:134028771-134028886	A549	lung:	n/a	n/a
14	CEBPB	chr2:134043975-134044199	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr2:134043932-134044239	A549	lung:	n/a	n/a
16	CEBPB	chr2:134051161-134051752	IMR90	lung:	n/a	chr2:134051271-134051288
17	CEBPB	chr2:134043852-134044617	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:134054015-134054327	IMR90	lung:	n/a	chr2:134054150-134054163 chr2:134054152-134054163 chr2:134054150-134054163
19	CEBPB	chr2:134003410-134003684	IMR90	lung:	n/a	chr2:134003550-134003561
20	CEBPB	chr2:134022735-134025209	Hela-S3	cervix:	n/a	chr2:134024205-134024216
21	CEBPB	chr2:134043906-134044270	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:134011419-134011757	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:134045260-134045655	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:134053980-134054421	Hela-S3	cervix:	n/a	chr2:134054150-134054163 chr2:134054152-134054163 chr2:134054150-134054163
25	CEBPB	chr2:134003426-134003717	HepG2	liver:	n/a	chr2:134003550-134003561
26	CEBPB	chr2:134043848-134044248	MCF-7	breast:	n/a	n/a
27	CEBPB	chr2:134000355-134000651	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:134003450-134003684	A549	lung:	n/a	chr2:134003550-134003561
29	CHD2	chr2:134023798-134024368	H1-hESC	embryonic stem cell:	n/a	chr2:134024118-134024128
30	CHD2	chr2:134022615-134025069	Hela-S3	cervix:	n/a	chr2:134023449-134023456 chr2:134024118-134024128 chr2:134023183-134023193
31	CREB1	chr2:134022973-134023418	A549	lung:	n/a	n/a
32	CTBP2	chr2:134022993-134024496	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr2:134023768-134023976	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr2:134044066-134044184	Hela-S3	cervix:	n/a	chr2:134044135-134044144
35	CTCF	chr2:134020606-134020661	GM20000	blood:	n/a	n/a
36	CTCF	chr2:134023760-134023910	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr2:134043960-134044110	RPTEC	kidney:	n/a	n/a
38	CTCF	chr2:134024240-134024390	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr2:134023721-134023957	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:134020500-134020650	AG04450	lung:	n/a	n/a
41	CTCF	chr2:134023740-134023890	GM12873	blood:	n/a	n/a
42	CTCF	chr2:134023820-134023970	AG09319	gingival:	n/a	n/a
43	CTCF	chr2:134020460-134020610	GM12864	blood:	n/a	n/a
44	CTCF	chr2:134023697-134024032	IMR90	lung:	n/a	n/a
45	CTCF	chr2:134044060-134044210	AG09319	gingival:	n/a	chr2:134044135-134044144
46	CTCF	chr2:134023800-134023950	GM12869	blood:	n/a	n/a
47	CTCF	chr2:134023920-134024070	GM12868	blood:	n/a	chr2:134024038-134024051
48	CTCF	chr2:134044120-134044270	HCPEpiC	choroid plexus:	n/a	chr2:134044135-134044144
49	CTCF	chr2:134023700-134023850	HVMF	connective:	n/a	n/a
50	CTCF	chr2:134023781-134023961	MCF-7	breast:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134004614-134004664	HEEpiC	esophagus:	n/a
2	chr2:134023662-134023712	T-47D	breast:	n/a
3	chr2:134024618-134024668	HIPEpiC	eye:	n/a
4	chr2:134004614-134004664	PrEC	prostate:	n/a
5	chr2:134023662-134023712	HepG2	liver:	n/a
6	chr2:134024093-134024143	ovcar-3	ovarian:	n/a
7	chr2:134024093-134024143	CMK	blood:	n/a
8	chr2:134024618-134024668	AG04450	lung:	fetal
9	chr2:134028440-134028490	HEK293	kidney:	embryo
10	chr2:134020041-134020091	SKMC	muscle:	n/a
11	chr2:134024418-134024468	HRPEpiC	eye:	n/a
12	chr2:134010875-134010925	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:134024266-134024316	ECC-1	luminal epithelium:	n/a
14	chr2:134024093-134024143	HAEpiC	amniotic membrane:	n/a
15	chr2:134024459-134024509	HRCEpiC	kidney:	n/a
16	chr2:134024459-134024509	HL-60	blood:	n/a
17	chr2:134024618-134024668	ECC-1	luminal epithelium:	n/a
18	chr2:134024459-134024509	K562	blood:	n/a
19	chr2:134023210-134023260	A549	lung:	n/a
20	chr2:134028440-134028490	HCF	heart:	n/a
21	chr2:134023662-134023712	NT2-D1	testis:	n/a
22	chr2:134024418-134024468	K562	blood:	n/a
23	chr2:134028440-134028490	H1-hESC	embryonic stem cell:	embryo
24	chr2:134024093-134024143	NB4	blood:	n/a
25	chr2:134020041-134020091	HL-60	blood:	n/a
26	chr2:134028440-134028490	Jurkat	blood:	n/a
27	chr2:134020041-134020091	HCT-116	colon:	n/a
28	chr2:134024093-134024143	PrEC	prostate:	n/a
29	chr2:134023662-134023712	HL-60	blood:	n/a
30	chr2:134024618-134024668	HUVEC	blood vessel:	n/a
31	chr2:134052012-134052062	MCF-7	breast:	n/a
32	chr2:134024266-134024316	LNCaP	prostate:	n/a
33	chr2:134010875-134010925	Jurkat	blood:	n/a
34	chr2:134024093-134024143	AG04449	skin:	fetal
35	chr2:134010875-134010925	K562	blood:	n/a
36	chr2:134024418-134024468	GM12892	blood:	n/a
37	chr2:134028440-134028490	HMEC	breast:	n/a
38	chr2:134010875-134010925	NT2-D1	testis:	n/a
39	chr2:134024266-134024316	SKMC	muscle:	n/a
40	chr2:134024266-134024316	HEK293	kidney:	embryo
41	chr2:134024618-134024668	LNCaP	prostate:	n/a
42	chr2:134020041-134020091	HRCEpiC	kidney:	n/a
43	chr2:134004614-134004664	HRPEpiC	eye:	n/a
44	chr2:134024266-134024316	HCT-116	colon:	n/a
45	chr2:134028440-134028490	HIPEpiC	eye:	n/a
46	chr2:134004614-134004664	T-47D	breast:	n/a
47	chr2:134020041-134020091	SK-N-MC	brain:	n/a
48	chr2:134024418-134024468	U87	brain:	n/a
49	chr2:134010875-134010925	HRPEpiC	eye:	n/a
50	chr2:134028440-134028490	IMR90	lung:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:134020208..134021163-chr2:134537454..134538295,5	MCF-7	breast:
2	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
3	chr2:134003474..134006247-chr2:134007339..134011249,3	MCF-7	breast:
4	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
5	chr2:134020041..134020759-chr2:134398921..134399467,2	MCF-7	breast:
6	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
7	chr2:134003474..134006247-chr2:134007339..134011249,3	MCF-7	breast:
8	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:
9	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
10	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
11	chr2:134020179..134020906-chr2:134601878..134602419,2	MCF-7	breast:
12	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:
13	chr2:134020255..134021142-chr2:134318343..134319277,2	MCF-7	breast:
14	chr19:18793804..18794673-chr2:134023005..134023895,2	Hela-S3	cervix:
15	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
16	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
17	chr2:134033733..134036491-chr2:134192911..134194605,2	MCF-7	breast:
18	chr16:30709997..30710818-chr2:134023319..134023932,2	Hela-S3	cervix:
19	chr2:134020760..134021325-chr2:134537400..134538161,2	K562	blood:
20	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
21	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
22	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
23	chr2:134019056..134021492-chr2:134262374..134264487,2	MCF-7	breast:
24	chr2:134020528..134022424-chr2:134324632..134327514,2	MCF-7	breast:
25	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
26	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
27	chr1:154946346..154946996-chr2:134023337..134024323,2	Hela-S3	cervix:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-4	chr2:134023767-134023868	NR_110294
2	lnc-GPR39-4	chr2:134024845-134024996	NR_110294
3	lnc-GPR39-4	chr2:134023767-134023868	ENSG00000226953
4	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953
5	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953.3
6	lnc-GPR39-4	chr2:134026488-134026613	NR_110294
7	lnc-GPR39-4	chr2:134042267-134042330	NR_110294
8	lnc-GPR39-4	chr2:134026488-134026582	ENSG00000226953
9	lnc-GPR39-4	chr2:134022540-134022674	ENSG00000226953
10	lnc-GPR39-4	chr2:134026488-134026613	ENSG00000226953
11	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953
12	lnc-GPR39-4	chr2:134042267-134042334	ENSG00000226953
13	lnc-GPR39-4	chr2:134026488-134026613	ENSG00000226953.3
14	lnc-GPR39-4	chr2:134025928-134026014	NR_110294
15	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953.3
16	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953
17	lnc-GPR39-4	chr2:134023814-134024008	ENSG00000226953.3
18	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953

No data

Variant related genes	Relation type
ENSG00000226953	TF binding region
ENSG00000226953	CpG island
ENSG00000080603	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000105662	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000176771	chromatin interactions
ATOX1	miRNA target sites
FNTA	miRNA target sites
NFKB1	miRNA target sites
CALU	miRNA target sites
SMCR7L	miRNA target sites
LRIG1	miRNA target sites
KIF23	miRNA target sites
IQCB1	miRNA target sites
TNFSF10	miRNA target sites

Extended variants
information (count: 1958 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77343807	chr2:133999831-133999832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149629845	chr2:133999855-133999856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189179180	chr2:133999868-133999869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144339643	chr2:133999919-133999920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181894132	chr2:133999936-133999937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530113983	chr2:133999956-133999957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184977768	chr2:134000009-134000010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188281005	chr2:134000014-134000015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6749561	chr2:134000064-134000065	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552390616	chr2:134000092-134000093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547282364	chr2:134000099-134000100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs57010177	chr2:134000136-134000137	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs113123333	chr2:134000137-134000138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553635067	chr2:134000154-134000155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574994297	chr2:134000183-134000184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535448900	chr2:134000209-134000210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556655395	chr2:134000253-134000254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181206844	chr2:134000302-134000303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186519690	chr2:134000317-134000318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144737779	chr2:134000320-134000321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535105859	chr2:134000378-134000379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111461684	chr2:134000420-134000421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573076285	chr2:134000457-134000458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371995733	chr2:134000465-134000466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77858104	chr2:134000544-134000545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562029785	chr2:134000615-134000616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529145260	chr2:134000632-134000633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548588681	chr2:134000648-134000649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563515461	chr2:134000660-134000661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144348686	chr2:134000662-134000663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113296498	chr2:134000680-134000681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113999819	chr2:134000691-134000692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1549740	chr2:134000694-134000695	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568609057	chr2:134000700-134000701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs16822540	chr2:134000738-134000739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs116052232	chr2:134000818-134000819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546845153	chr2:134000819-134000820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs13426705	chr2:134000822-134000823	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs79922651	chr2:134000876-134000877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557590677	chr2:134000917-134000918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569207597	chr2:134001026-134001027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556956834	chr2:134001067-134001068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369381849	chr2:134001071-134001072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575309055	chr2:134001092-134001093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191792709	chr2:134001110-134001111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372770951	chr2:134001114-134001115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183256893	chr2:134001130-134001131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116913410	chr2:134001140-134001141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572937994	chr2:134001156-134001157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs115044243	chr2:134001188-134001189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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

Chromatin state (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133991600-134005400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:133994000-134023600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:133997800-134000400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:133998400-134005000	Weak transcription	Psoas Muscle	Psoas
5	chr2:133998400-134005800	Weak transcription	Left Ventricle	heart
6	chr2:133998600-134003800	Weak transcription	Brain Angular Gyrus	brain
7	chr2:133998800-134004600	Weak transcription	Fetal Heart	heart
8	chr2:133998800-134013000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:133998800-134014800	Weak transcription	Fetal Stomach	stomach
10	chr2:133999000-134000600	Enhancers	Brain Substantia Nigra	brain
11	chr2:133999000-134005000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:133999200-134001200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr2:133999200-134003200	Weak transcription	Fetal Brain Male	brain
14	chr2:133999200-134003400	Weak transcription	Brain Hippocampus Middle	brain
15	chr2:133999200-134003600	Weak transcription	Fetal Brain Female	brain
16	chr2:133999200-134003600	Weak transcription	Fetal Lung	lung
17	chr2:133999200-134005400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:133999200-134007800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr2:133999400-134000000	Weak transcription	NHLF	lung
20	chr2:133999400-134000200	Enhancers	Hela-S3	cervix
21	chr2:133999400-134000600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:133999400-134001000	Weak transcription	Brain Anterior Caudate	brain
23	chr2:133999400-134003800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:133999400-134005200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr2:133999400-134005200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr2:133999400-134005200	Weak transcription	Fetal Muscle Leg	muscle
27	chr2:133999400-134005400	Weak transcription	Ovary	ovary
28	chr2:133999400-134005800	Weak transcription	Lung	lung
29	chr2:133999600-134001000	Weak transcription	Right Ventricle	heart
30	chr2:134000000-134000200	Enhancers	NHLF	lung
31	chr2:134000200-134000400	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr2:134000200-134005400	Weak transcription	NHLF	lung
33	chr2:134000600-134001000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:134000600-134003600	Weak transcription	Brain Substantia Nigra	brain
35	chr2:134000800-134001400	Enhancers	Fetal Intestine Large	intestine
36	chr2:134001000-134001200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:134001000-134001400	Enhancers	Brain Anterior Caudate	brain
38	chr2:134001200-134005200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:134001200-134005800	Weak transcription	Right Ventricle	heart
40	chr2:134001400-134003600	Weak transcription	Brain Anterior Caudate	brain
41	chr2:134002200-134004800	Weak transcription	HMEC	breast
42	chr2:134003200-134004600	Enhancers	Fetal Brain Male	brain
43	chr2:134003400-134003800	Enhancers	Brain Hippocampus Middle	brain
44	chr2:134003600-134003800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:134003600-134003800	Enhancers	Brain Anterior Caudate	brain
46	chr2:134003600-134004600	Enhancers	Fetal Brain Female	brain
47	chr2:134003600-134006000	Enhancers	Fetal Lung	lung
48	chr2:134003600-134006400	Enhancers	Brain Substantia Nigra	brain
49	chr2:134003800-134004000	Enhancers	Brain Angular Gyrus	brain
50	chr2:134003800-134004200	Weak transcription	Brain Anterior Caudate	brain

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