Variant report

Variant	nsv874008
Chromosome Location	chr2:49126802-49189921
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	BCL3	chr2:49168897-49169140	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:49173756-49173890	K562	blood:	n/a	n/a
8	CEBPB	chr2:49154521-49154838	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:49176607-49176832	K562	blood:	n/a	chr2:49176759-49176770
10	CEBPB	chr2:49176679-49176903	HepG2	liver:	n/a	chr2:49176759-49176770
11	CEBPB	chr2:49173699-49174045	K562	blood:	n/a	chr2:49173907-49173918 chr2:49173906-49173919
12	CEBPB	chr2:49173671-49174047	H1-hESC	embryonic stem cell:	n/a	chr2:49173907-49173918 chr2:49173906-49173919
13	CEBPB	chr2:49173707-49174065	HepG2	liver:	n/a	chr2:49173907-49173918 chr2:49173906-49173919
14	CEBPB	chr2:49189056-49189087	HepG2	liver:	n/a	n/a
15	CTCF	chr2:49129700-49129850	HepG2	liver:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
16	CTCF	chr2:49173681-49173907	GM10266	blood:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
17	CTCF	chr2:49139400-49139550	NB4	blood:	n/a	n/a
18	CTCF	chr2:49129780-49129930	K562	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
19	CTCF	chr2:49139200-49139350	GM06990	blood:	n/a	n/a
20	CTCF	chr2:49173720-49173870	GM12866	blood:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
21	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
22	CTCF	chr2:49183120-49183270	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr2:49139333-49139521	MCF-7	breast:	n/a	n/a
24	CTCF	chr2:49129720-49129870	WERI-Rb-1	eye:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
25	CTCF	chr2:49139340-49139490	HAc	cerebellar:	n/a	n/a
26	CTCF	chr2:49139318-49139592	K562	blood:	n/a	n/a
27	CTCF	chr2:49173646-49173906	A549	lung:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
28	CTCF	chr2:49173740-49173890	Caco-2	colon:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
29	CTCF	chr2:49139331-49139491	HepG2	liver:	n/a	n/a
30	CTCF	chr2:49173668-49173916	GM13977	blood:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
31	CTCF	chr2:49139280-49139430	BE2_C	brain:	n/a	n/a
32	CTCF	chr2:49173640-49173910	HCM	heart:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
33	CTCF	chr2:49173660-49173810	HVMF	connective:	n/a	chr2:49173790-49173808 chr2:49173795-49173803 chr2:49173791-49173807
34	CTCF	chr2:49139360-49139510	GM12872	blood:	n/a	n/a
35	CTCF	chr2:49129722-49129897	HepG2	liver:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
36	CTCF	chr2:49129760-49129910	GM12869	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
37	CTCF	chr2:49173743-49173875	MCF-7	breast:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
38	CTCF	chr2:49139400-49139550	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr2:49139360-49139510	Caco-2	colon:	n/a	n/a
40	CTCF	chr2:49129740-49129890	GM12866	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
41	CTCF	chr2:49173720-49173870	GM12869	blood:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
42	CTCF	chr2:49173740-49173890	HMEC	breast:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
43	CTCF	chr2:49139390-49139491	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr2:49139338-49139524	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:49173720-49173870	HEEpiC	esophagus:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
46	CTCF	chr2:49173603-49173932	A549	lung:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807
47	CTCF	chr2:49139300-49139450	HEK293	kidney:	n/a	n/a
48	CTCF	chr2:49173680-49173830	GM12870	blood:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173791-49173807
49	CTCF	chr2:49173700-49173850	HUVEC	blood vessel:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173791-49173807
50	CTCF	chr2:49173361-49174269	A549	lung:	n/a	chr2:49173790-49173808 chr2:49173792-49173813 chr2:49173795-49173803 chr2:49173858-49173866 chr2:49173791-49173807

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:49143534-49143584	IMR90	lung:	fetal
2	chr2:49143534-49143584	HEK293	kidney:	embryo
3	chr2:49143238-49143288	A549	lung:	n/a
4	chr2:49143238-49143288	CMK	blood:	n/a
5	chr2:49143238-49143288	SK-N-SH_RA	brain:	n/a
6	chr2:49143238-49143288	HEK293	kidney:	embryo
7	chr2:49143334-49143384	IMR90	lung:	fetal
8	chr2:49143238-49143288	PFSK-1	brain:	n/a
9	chr2:49143334-49143384	PrEC	prostate:	n/a
10	chr2:49143334-49143384	SK-N-MC	brain:	n/a
11	chr2:49143534-49143584	HCPEpiC	choroid plexus:	n/a
12	chr2:49143238-49143288	NT2-D1	testis:	n/a
13	chr2:49143238-49143288	HRE	kidney:	n/a
14	chr2:49143334-49143384	AG09319	gingival:	n/a
15	chr2:49143334-49143384	PANC-1	pancreas:	n/a
16	chr2:49143534-49143584	AG09319	gingival:	n/a
17	chr2:49143334-49143384	MCF-7	breast:	n/a
18	chr2:49143534-49143584	GM19239	blood:	n/a
19	chr2:49143238-49143288	MCF-7	breast:	n/a
20	chr2:49143534-49143584	Caco-2	colon:	n/a
21	chr2:49143334-49143384	NB4	blood:	n/a
22	chr2:49143238-49143288	NB4	blood:	n/a
23	chr2:49143534-49143584	HCT-116	colon:	n/a
24	chr2:49143238-49143288	HNPCEpiC	eye:	n/a
25	chr2:49143334-49143384	NHBE	bronchial:	n/a
26	chr2:49143238-49143288	K562	blood:	n/a
27	chr2:49143534-49143584	HIPEpiC	eye:	n/a
28	chr2:49143534-49143584	HRE	kidney:	n/a
29	chr2:49143238-49143288	HL-60	blood:	n/a
30	chr2:49143334-49143384	HUVEC	blood vessel:	n/a
31	chr2:49143534-49143584	SKMC	muscle:	n/a
32	chr2:49143534-49143584	HNPCEpiC	eye:	n/a
33	chr2:49143534-49143584	HL-60	blood:	n/a
34	chr2:49143238-49143288	PANC-1	pancreas:	n/a
35	chr2:49143534-49143584	K562	blood:	n/a
36	chr2:49143534-49143584	AG10803	skin:	n/a
37	chr2:49143534-49143584	PANC-1	pancreas:	n/a
38	chr2:49143334-49143384	HRPEpiC	eye:	n/a
39	chr2:49143238-49143288	ProgFib	skin:	n/a
40	chr2:49143534-49143584	AG04449	skin:	fetal
41	chr2:49143334-49143384	SK-N-SH	brain:	n/a
42	chr2:49143334-49143384	RPTEC	kidney:	n/a
43	chr2:49143334-49143384	SAEC	small airway:	n/a
44	chr2:49143534-49143584	PFSK-1	brain:	n/a
45	chr2:49143334-49143384	K562	blood:	n/a
46	chr2:49143238-49143288	HCM	heart:	n/a
47	chr2:49143238-49143288	AoSMC	blood vessel:	n/a
48	chr2:49143534-49143584	A549	lung:	n/a
49	chr2:49143238-49143288	NH-A	brain:	n/a
50	chr2:49143534-49143584	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:49139634..49141993-chr2:49154425..49156573,2	K562	blood:
2	chr2:48827557..48828940-chr2:49173265..49174447,4	MCF-7	breast:
3	chr2:49164670..49166344-chr2:49166473..49169459,2	MCF-7	breast:
4	chr2:49164670..49166344-chr2:49166473..49169459,2	MCF-7	breast:
5	chr2:49186669..49188869-chr2:49189204..49191153,2	K562	blood:
6	chr2:49139634..49141993-chr2:49154425..49156573,2	K562	blood:
7	chr2:49163249..49165235-chr2:49165442..49167974,2	K562	blood:
8	chr2:49127535..49130275-chr2:49154381..49157152,2	MCF-7	breast:
9	chr2:49121216..49123118-chr2:49126253..49127804,2	MCF-7	breast:
10	chr2:49173283..49174235-chr2:49717706..49718797,6	MCF-7	breast:
11	chr2:49127535..49130275-chr2:49154381..49157152,2	MCF-7	breast:
12	chr2:49163249..49165235-chr2:49165442..49167974,2	K562	blood:
13	chr2:48993937..48996711-chr2:49125527..49127927,2	MCF-7	breast:
14	chr2:49182201..49184078-chr2:49187654..49190318,2	K562	blood:
15	chr2:49173374..49174210-chr2:49199575..49200403,3	MCF-7	breast:
16	chr2:49173523..49174048-chr2:50629252..50630106,2	MCF-7	breast:
17	chr2:49186669..49188869-chr2:49189204..49191153,2	K562	blood:
18	chr2:49182201..49184078-chr2:49187654..49190318,2	K562	blood:
19	chr2:49173436..49174023-chr2:50371199..50372057,2	MCF-7	breast:

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

Variant related genes	Relation type
CTBP2P5	TF binding region
CTBP2P5	CpG island
ENSG00000068781	chromatin interactions

Extended variants
information (count: 2422 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2422 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4953640	chr2:49126802-49126803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537407945	chr2:49126803-49126804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs72889188	chr2:49126816-49126817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531113340	chr2:49126834-49126835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs578184761	chr2:49126845-49126846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545710322	chr2:49126867-49126868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552743973	chr2:49126945-49126946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572563332	chr2:49126957-49126958	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543263358	chr2:49126959-49126960	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561315784	chr2:49126961-49126962	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375354842	chr2:49126962-49126963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143936367	chr2:49126985-49126986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535071356	chr2:49127040-49127041	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141019868	chr2:49127077-49127078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs114233254	chr2:49127091-49127092	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553424393	chr2:49127130-49127131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181971940	chr2:49127133-49127134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs533064222	chr2:49127193-49127194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs551619803	chr2:49127260-49127261	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566675511	chr2:49127263-49127264	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs533694431	chr2:49127268-49127269	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150247919	chr2:49127303-49127304	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138998278	chr2:49127426-49127427	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568404382	chr2:49127454-49127455	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537594597	chr2:49127482-49127483	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555863653	chr2:49127496-49127497	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534870999	chr2:49127506-49127507	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2192614	chr2:49127549-49127550	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs557197029	chr2:49127562-49127563	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142268154	chr2:49127615-49127616	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146401603	chr2:49127621-49127622	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370890552	chr2:49127622-49127623	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs77996416	chr2:49127650-49127651	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs77697227	chr2:49127705-49127706	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576586125	chr2:49127767-49127768	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543971010	chr2:49127805-49127806	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565251428	chr2:49127806-49127807	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187429781	chr2:49127835-49127836	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532510484	chr2:49127838-49127839	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs190599212	chr2:49127848-49127849	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375387966	chr2:49127883-49127884	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs149257195	chr2:49127899-49127900	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs35456987	chr2:49127921-49127922	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs111644086	chr2:49128006-49128007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553519194	chr2:49128025-49128026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531290100	chr2:49128045-49128046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549811789	chr2:49128056-49128057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571274151	chr2:49128088-49128089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538579963	chr2:49128095-49128096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73928343	chr2:49128098-49128099	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

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

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:49120200-49127200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:49126400-49128400	Enhancers	HSMMtube	muscle
3	chr2:49127000-49128200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:49127000-49128200	Enhancers	Brain Germinal Matrix	brain
5	chr2:49127000-49128400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:49127000-49128400	Enhancers	Brain Hippocampus Middle	brain
7	chr2:49127200-49127800	Enhancers	Lung	lung
8	chr2:49127200-49128000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:49127200-49128000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr2:49127200-49128000	Enhancers	Brain Angular Gyrus	brain
11	chr2:49127200-49128000	Enhancers	Placenta Amnion	Placenta Amnion
12	chr2:49127200-49128200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:49127200-49128200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:49127200-49128200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr2:49127200-49128200	Enhancers	Brain Substantia Nigra	brain
16	chr2:49127200-49128200	Enhancers	Fetal Muscle Leg	muscle
17	chr2:49127200-49128200	Enhancers	Placenta	Placenta
18	chr2:49127200-49128400	Enhancers	Brain Anterior Caudate	brain
19	chr2:49127200-49128400	Enhancers	Brain Cingulate Gyrus	brain
20	chr2:49127200-49128400	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr2:49127200-49128800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:49127200-49128800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:49127400-49127800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:49127400-49127800	Enhancers	Fetal Muscle Trunk	muscle
25	chr2:49127400-49128400	Enhancers	Osteobl	bone
26	chr2:49127400-49128600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr2:49127400-49128600	Enhancers	HSMM	muscle
28	chr2:49127600-49128000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:49127600-49128200	Enhancers	Adipose Nuclei	Adipose
30	chr2:49127800-49128000	Enhancers	HMEC	breast
31	chr2:49128000-49132400	Weak transcription	Brain Angular Gyrus	brain
32	chr2:49128200-49129600	Weak transcription	Placenta	Placenta
33	chr2:49128200-49132200	Weak transcription	Brain Substantia Nigra	brain
34	chr2:49128200-49132400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr2:49128200-49133200	Weak transcription	Adipose Nuclei	Adipose
36	chr2:49128400-49132200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr2:49128400-49132400	Weak transcription	Brain Anterior Caudate	brain
38	chr2:49128400-49132400	Weak transcription	Brain Hippocampus Middle	brain
39	chr2:49128400-49132400	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr2:49129600-49129800	Enhancers	Placenta	Placenta
41	chr2:49131600-49131800	Enhancers	Fetal Stomach	stomach
42	chr2:49131800-49133200	Weak transcription	Fetal Stomach	stomach
43	chr2:49132200-49132600	Enhancers	Brain Cingulate Gyrus	brain
44	chr2:49132200-49132600	Enhancers	Brain Substantia Nigra	brain
45	chr2:49132400-49132600	Enhancers	Brain Angular Gyrus	brain
46	chr2:49132400-49132600	Enhancers	Brain Hippocampus Middle	brain
47	chr2:49132400-49132600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr2:49132400-49133600	Enhancers	Brain Anterior Caudate	brain
49	chr2:49132400-49134200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr2:49132600-49132800	Flanking Active TSS	Brain Cingulate Gyrus	brain

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