Variant report

Variant	nsv834003
Chromosome Location	chr2:49131673-49312273
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	chr2:49173731-49173967	K562	blood:	n/a	n/a
2	ARID3A	chr2:49173646-49173953	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:49154095-49154817	HepG2	liver:	n/a	n/a
4	ATF2	chr2:49173687-49173977	GM12878	blood:	n/a	n/a
5	BACH1	chr2:49164205-49164317	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr2:49255280-49255569	GM12878	blood:	n/a	n/a
7	BATF	chr2:49255320-49255581	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:49307852-49308039	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr2:49255222-49255584	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:49255252-49255620	GM12878	blood:	n/a	n/a
11	BCL3	chr2:49168897-49169140	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:49255201-49255748	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:49173756-49173890	K562	blood:	n/a	n/a
14	BRCA1	chr2:49307903-49308246	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr2:49221271-49221604	A549	lung:	n/a	chr2:49221430-49221441 chr2:49221432-49221443
16	CEBPB	chr2:49154521-49154838	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:49221253-49221611	HepG2	liver:	n/a	chr2:49221430-49221441 chr2:49221432-49221443
18	CEBPB	chr2:49214105-49214319	HepG2	liver:	n/a	chr2:49214256-49214267
19	CEBPB	chr2:49214096-49214408	IMR90	lung:	n/a	chr2:49214256-49214267
20	CEBPB	chr2:49176679-49176903	HepG2	liver:	n/a	chr2:49176759-49176770
21	CEBPB	chr2:49173671-49174047	H1-hESC	embryonic stem cell:	n/a	chr2:49173907-49173918 chr2:49173906-49173919
22	CEBPB	chr2:49189056-49189087	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:49221268-49221566	IMR90	lung:	n/a	chr2:49221430-49221441 chr2:49221432-49221443
24	CEBPB	chr2:49173707-49174065	HepG2	liver:	n/a	chr2:49173907-49173918 chr2:49173906-49173919
25	CEBPB	chr2:49176607-49176832	K562	blood:	n/a	chr2:49176759-49176770
26	CEBPB	chr2:49173699-49174045	K562	blood:	n/a	chr2:49173907-49173918 chr2:49173906-49173919
27	CHD2	chr2:49255215-49255580	GM12878	blood:	n/a	n/a
28	CHD2	chr2:49269894-49269946	GM12878	blood:	n/a	n/a
29	CTCF	chr2:49271860-49272010	HRE	kidney:	n/a	n/a
30	CTCF	chr2:49139358-49139498	HepG2	liver:	n/a	n/a
31	CTCF	chr2:49173677-49173944	ECC-1	luminal epithelium:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
32	CTCF	chr2:49173556-49174115	HCT-116	colon:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
33	CTCF	chr2:49173680-49173830	HRE	kidney:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173791-49173807
34	CTCF	chr2:49271955-49272021	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr2:49173700-49173850	GM12875	blood:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173791-49173807
36	CTCF	chr2:49139331-49139491	HepG2	liver:	n/a	n/a
37	CTCF	chr2:49173760-49173910	A549	lung:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
38	CTCF	chr2:49173680-49173830	GM12870	blood:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173791-49173807
39	CTCF	chr2:49271948-49272031	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr2:49142476-49142668	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:49139360-49139510	HFF	foreskin:	n/a	n/a
42	CTCF	chr2:49271860-49272010	HFF	foreskin:	n/a	n/a
43	CTCF	chr2:49173720-49173870	Caco-2	colon:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
44	CTCF	chr2:49173740-49173890	BJ	skin:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
45	CTCF	chr2:49271920-49272070	HepG2	liver:	n/a	n/a
46	CTCF	chr2:49271880-49272030	GM12871	blood:	n/a	n/a
47	CTCF	chr2:49173720-49173870	AG10803	skin:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
48	CTCF	chr2:49183120-49183270	GM12873	blood:	n/a	n/a
49	CTCF	chr2:49139360-49139510	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr2:49182720-49182870	GM12868	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:49143238-49143288	HEEpiC	esophagus:	n/a
2	chr2:49143238-49143288	K562	blood:	n/a
3	chr2:49143238-49143288	AG09319	gingival:	n/a
4	chr2:49143238-49143288	BJ	skin:	n/a
5	chr2:49271470-49271520	AoSMC	blood vessel:	n/a
6	chr2:49143334-49143384	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:49143534-49143584	HRCEpiC	kidney:	n/a
8	chr2:49143534-49143584	HRPEpiC	eye:	n/a
9	chr2:49143534-49143584	A549	lung:	n/a
10	chr2:49143534-49143584	H1-hESC	embryonic stem cell:	embryo
11	chr2:49143534-49143584	ProgFib	skin:	n/a
12	chr2:49143238-49143288	T-47D	breast:	n/a
13	chr2:49143238-49143288	HCPEpiC	choroid plexus:	n/a
14	chr2:49143334-49143384	HRE	kidney:	n/a
15	chr2:49271470-49271520	SAEC	small airway:	n/a
16	chr2:49143238-49143288	GM12892	blood:	n/a
17	chr2:49143534-49143584	PrEC	prostate:	n/a
18	chr2:49143238-49143288	AG04450	lung:	fetal
19	chr2:49271470-49271520	ProgFib	skin:	n/a
20	chr2:49143334-49143384	HRCEpiC	kidney:	n/a
21	chr2:49143334-49143384	HepG2	liver:	n/a
22	chr2:49143238-49143288	SK-N-SH	brain:	n/a
23	chr2:49143238-49143288	Hela-S3	cervix:	n/a
24	chr2:49271470-49271520	PANC-1	pancreas:	n/a
25	chr2:49143334-49143384	IMR90	lung:	fetal
26	chr2:49271470-49271520	MCF-7	breast:	n/a
27	chr2:49143238-49143288	HCF	heart:	n/a
28	chr2:49143238-49143288	ECC-1	luminal epithelium:	n/a
29	chr2:49143534-49143584	HMEC	breast:	n/a
30	chr2:49143238-49143288	HL-60	blood:	n/a
31	chr2:49143238-49143288	HRE	kidney:	n/a
32	chr2:49143334-49143384	GM06990	blood:	n/a
33	chr2:49143238-49143288	NT2-D1	testis:	n/a
34	chr2:49143534-49143584	SAEC	small airway:	n/a
35	chr2:49143334-49143384	BJ	skin:	n/a
36	chr2:49143534-49143584	AG04450	lung:	fetal
37	chr2:49143534-49143584	PANC-1	pancreas:	n/a
38	chr2:49143334-49143384	K562	blood:	n/a
39	chr2:49143334-49143384	NHBE	bronchial:	n/a
40	chr2:49143238-49143288	HNPCEpiC	eye:	n/a
41	chr2:49143534-49143584	GM06990	blood:	n/a
42	chr2:49143534-49143584	AoSMC	blood vessel:	n/a
43	chr2:49143334-49143384	Jurkat	blood:	n/a
44	chr2:49143334-49143384	GM19239	blood:	n/a
45	chr2:49143334-49143384	AG09319	gingival:	n/a
46	chr2:49143334-49143384	HRPEpiC	eye:	n/a
47	chr2:49143334-49143384	GM12878	blood:	n/a
48	chr2:49143534-49143584	NHDF-neo	bronchial:	n/a
49	chr2:49143334-49143384	MCF-7	breast:	n/a
50	chr2:49143534-49143584	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:49226004..49228152-chr2:49232900..49234588,2	MCF-7	breast:
2	chr2:49139634..49141993-chr2:49154425..49156573,2	K562	blood:
3	chr2:49209751..49211732-chr2:49248932..49250816,2	K562	blood:
4	chr2:49232587..49234128-chr2:49242964..49245708,2	K562	blood:
5	chr2:49139634..49141993-chr2:49154425..49156573,2	K562	blood:
6	chr2:49199332..49202324-chr2:49209255..49211522,2	K562	blood:
7	chr2:49199332..49202324-chr2:49209255..49211522,2	K562	blood:
8	chr2:49209751..49211732-chr2:49248932..49250816,2	K562	blood:
9	chr2:49232587..49234128-chr2:49242964..49245708,2	K562	blood:
10	chr2:49173374..49174210-chr2:49199575..49200403,3	MCF-7	breast:
11	chr2:49182201..49184078-chr2:49187654..49190318,2	K562	blood:
12	chr2:49164670..49166344-chr2:49166473..49169459,2	MCF-7	breast:
13	chr2:49173374..49174210-chr2:49199575..49200403,3	MCF-7	breast:
14	chr2:49271536..49272486-chr2:49717616..49718379,2	MCF-7	breast:
15	chr2:49163249..49165235-chr2:49165442..49167974,2	K562	blood:
16	chr2:49173436..49174023-chr2:50371199..50372057,2	MCF-7	breast:
17	chr2:49164670..49166344-chr2:49166473..49169459,2	MCF-7	breast:
18	chr2:49260442..49262914-chr2:49263129..49265285,2	K562	blood:
19	chr2:49226004..49228152-chr2:49232900..49234588,2	MCF-7	breast:
20	chr2:48827557..48828940-chr2:49173265..49174447,4	MCF-7	breast:
21	chr2:49260442..49262914-chr2:49263129..49265285,2	K562	blood:
22	chr2:49163249..49165235-chr2:49165442..49167974,2	K562	blood:
23	chr2:49173283..49174235-chr2:49717706..49718797,6	MCF-7	breast:
24	chr2:49186669..49188869-chr2:49189204..49191153,2	K562	blood:
25	chr2:49173523..49174048-chr2:50629252..50630106,2	MCF-7	breast:
26	chr2:49186669..49188869-chr2:49189204..49191153,2	K562	blood:
27	chr2:49127535..49130275-chr2:49154381..49157152,2	MCF-7	breast:
28	chr2:49216778..49218351-chr2:49224131..49226334,2	MCF-7	breast:
29	chr2:49182201..49184078-chr2:49187654..49190318,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSHR-1	chr2:49179431-49179679	NONHSAT070635

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548ba	chr2:49286742-49286763	MIMAT0031175

Variant related genes	Relation type
FSHR	TF binding region
CTBP2P5	TF binding region
FSHR	CpG island
CTBP2P5	CpG island
ENSG00000170820	chromatin interactions

Extended variants
information (count: 5009 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5009 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576462709	chr2:49131674-49131675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78549045	chr2:49131687-49131688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs45524931	chr2:49131696-49131697	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs537514088	chr2:49131723-49131724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139707267	chr2:49131778-49131779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10490121	chr2:49131781-49131782	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs577693242	chr2:49131802-49131803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541456504	chr2:49131803-49131804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557273235	chr2:49131823-49131824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182186985	chr2:49131852-49131853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560950408	chr2:49131854-49131855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546547979	chr2:49131888-49131889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149794553	chr2:49131920-49131921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549575663	chr2:49131931-49131932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565011637	chr2:49131934-49131935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532106394	chr2:49131951-49131952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547459638	chr2:49131966-49131967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79079616	chr2:49131998-49131999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140639458	chr2:49131999-49132000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558486132	chr2:49132000-49132001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570116921	chr2:49132002-49132003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537673795	chr2:49132046-49132047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558735757	chr2:49132062-49132063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576931906	chr2:49132069-49132070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576645705	chr2:49132078-49132079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186662878	chr2:49132082-49132083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552996319	chr2:49132099-49132100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571986449	chr2:49132112-49132113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573516590	chr2:49132120-49132121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542587364	chr2:49132121-49132122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554861333	chr2:49132159-49132160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569326403	chr2:49132161-49132162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576126494	chr2:49132162-49132163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543604423	chr2:49132177-49132178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145805100	chr2:49132192-49132193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74263479	chr2:49132194-49132195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562095870	chr2:49132206-49132207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559428038	chr2:49132209-49132210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114753309	chr2:49132277-49132278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191471236	chr2:49132381-49132382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565495454	chr2:49132403-49132404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146625431	chr2:49132409-49132410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149223718	chr2:49132412-49132413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375941690	chr2:49132452-49132453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552775876	chr2:49132459-49132460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7600883	chr2:49132470-49132471	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs78130017	chr2:49132488-49132489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552933228	chr2:49132508-49132509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs13410096	chr2:49132516-49132517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7574561	chr2:49132550-49132551	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:49128000-49132400	Weak transcription	Brain Angular Gyrus	brain
2	chr2:49128200-49132200	Weak transcription	Brain Substantia Nigra	brain
3	chr2:49128200-49132400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr2:49128200-49133200	Weak transcription	Adipose Nuclei	Adipose
5	chr2:49128400-49132200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr2:49128400-49132400	Weak transcription	Brain Anterior Caudate	brain
7	chr2:49128400-49132400	Weak transcription	Brain Hippocampus Middle	brain
8	chr2:49128400-49132400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:49131600-49131800	Enhancers	Fetal Stomach	stomach
10	chr2:49131800-49133200	Weak transcription	Fetal Stomach	stomach
11	chr2:49132200-49132600	Enhancers	Brain Cingulate Gyrus	brain
12	chr2:49132200-49132600	Enhancers	Brain Substantia Nigra	brain
13	chr2:49132400-49132600	Enhancers	Brain Angular Gyrus	brain
14	chr2:49132400-49132600	Enhancers	Brain Hippocampus Middle	brain
15	chr2:49132400-49132600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr2:49132400-49133600	Enhancers	Brain Anterior Caudate	brain
17	chr2:49132400-49134200	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:49132600-49132800	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr2:49132600-49132800	Flanking Active TSS	Brain Hippocampus Middle	brain
20	chr2:49132600-49132800	Flanking Active TSS	Brain Substantia Nigra	brain
21	chr2:49132600-49133000	Weak transcription	Brain Angular Gyrus	brain
22	chr2:49132600-49133400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr2:49132800-49133000	Enhancers	Brain Hippocampus Middle	brain
24	chr2:49132800-49133000	Enhancers	Brain Substantia Nigra	brain
25	chr2:49132800-49133200	Enhancers	Brain Cingulate Gyrus	brain
26	chr2:49133000-49133200	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr2:49133000-49133200	Flanking Active TSS	Brain Substantia Nigra	brain
28	chr2:49133000-49133600	Enhancers	Fetal Lung	lung
29	chr2:49133000-49134200	Enhancers	Fetal Muscle Leg	muscle
30	chr2:49133000-49134400	Enhancers	Brain Angular Gyrus	brain
31	chr2:49133200-49133400	Flanking Active TSS	Brain Cingulate Gyrus	brain
32	chr2:49133200-49133600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:49133200-49134000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:49133200-49134000	Enhancers	Adipose Nuclei	Adipose
35	chr2:49133200-49134200	Enhancers	Fetal Kidney	kidney
36	chr2:49133200-49134200	Enhancers	Fetal Stomach	stomach
37	chr2:49133200-49134400	Enhancers	Brain Substantia Nigra	brain
38	chr2:49133200-49134800	Enhancers	Brain Hippocampus Middle	brain
39	chr2:49133400-49133600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr2:49133400-49134000	Enhancers	Brain Cingulate Gyrus	brain
41	chr2:49133600-49134200	Weak transcription	Brain Anterior Caudate	brain
42	chr2:49134200-49134400	Enhancers	Brain Anterior Caudate	brain
43	chr2:49141800-49142600	Enhancers	GM12878-XiMat	blood
44	chr2:49143200-49148600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:49147400-49147800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:49148600-49149000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:49153600-49155600	Enhancers	HepG2	liver
48	chr2:49154200-49154600	Enhancers	A549	lung
49	chr2:49155600-49156000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr2:49156200-49157600	Enhancers	Fetal Brain Male	brain

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