Variant report

Variant	nsv1014236
Chromosome Location	chr2:34571948-34761890
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	ATF2	chr2:34590863-34591498	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:34626250-34626627	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
3	BATF	chr2:34626271-34626588	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
4	BCL11A	chr2:34591088-34591422	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr2:34626351-34626529	GM12878	blood:	n/a	chr2:34626400-34626409 chr2:34626401-34626410
6	BCL3	chr2:34633202-34633571	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
7	BCL3	chr2:34633212-34633509	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
8	BHLHE40	chr2:34633159-34633448	GM12878	blood:	n/a	n/a
9	CBX3	chr2:34744823-34745018	K562	blood:	n/a	n/a
10	CCNT2	chr2:34623370-34623530	K562	blood:	n/a	n/a
11	CEBPB	chr2:34706730-34706928	H1-hESC	embryonic stem cell:	n/a	chr2:34706794-34706805
12	CEBPB	chr2:34651788-34652080	HepG2	liver:	n/a	chr2:34651953-34651964
13	CEBPB	chr2:34634613-34634777	A549	lung:	n/a	n/a
14	CEBPB	chr2:34637712-34637983	ECC-1	luminal epithelium:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
15	CEBPB	chr2:34637703-34637950	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
16	CEBPB	chr2:34651781-34652060	IMR90	lung:	n/a	chr2:34651953-34651964
17	CEBPB	chr2:34637625-34637979	A549	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
18	CEBPB	chr2:34608697-34608972	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:34759886-34760188	MCF-7	breast:	n/a	chr2:34759972-34759985
20	CEBPB	chr2:34651784-34652054	A549	lung:	n/a	chr2:34651953-34651964
21	CEBPB	chr2:34759033-34759047	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:34706655-34707006	MCF-7	breast:	n/a	chr2:34706794-34706805
23	CEBPB	chr2:34651786-34652048	K562	blood:	n/a	chr2:34651953-34651964
24	CEBPB	chr2:34637607-34637980	HepG2	liver:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
25	CEBPB	chr2:34610815-34611181	A549	lung:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
26	CEBPB	chr2:34717914-34718139	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:34637613-34637978	K562	blood:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
28	CEBPB	chr2:34590884-34591363	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr2:34651815-34652025	H1-hESC	embryonic stem cell:	n/a	chr2:34651953-34651964
30	CEBPB	chr2:34637693-34638019	A549	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
31	CEBPB	chr2:34610798-34611191	HepG2	liver:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
32	CEBPB	chr2:34637636-34637968	Hela-S3	cervix:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
33	CEBPB	chr2:34736004-34736033	HepG2	liver:	n/a	chr2:34736017-34736028
34	CEBPB	chr2:34706608-34706989	HepG2	liver:	n/a	chr2:34706794-34706805
35	CEBPB	chr2:34706676-34706941	A549	lung:	n/a	chr2:34706794-34706805
36	CEBPB	chr2:34637621-34637979	H1-hESC	embryonic stem cell:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
37	CEBPB	chr2:34759749-34759988	HepG2	liver:	n/a	chr2:34759832-34759845 chr2:34759832-34759843 chr2:34759972-34759985
38	CEBPB	chr2:34637610-34637983	IMR90	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
39	CEBPB	chr2:34637705-34637966	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
40	CEBPB	chr2:34706625-34706972	K562	blood:	n/a	chr2:34706794-34706805
41	CEBPB	chr2:34759877-34760165	K562	blood:	n/a	chr2:34759972-34759985
42	CEBPB	chr2:34633823-34633989	A549	lung:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
43	CEBPB	chr2:34575982-34576211	HepG2	liver:	n/a	chr2:34576118-34576129
44	CEBPB	chr2:34633778-34633979	HepG2	liver:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
45	CEBPB	chr2:34610824-34611131	Hela-S3	cervix:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
46	CEBPB	chr2:34610823-34611180	IMR90	lung:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
47	CEBPB	chr2:34661633-34661923	HepG2	liver:	n/a	chr2:34661857-34661869
48	CEBPB	chr2:34706631-34706981	IMR90	lung:	n/a	chr2:34706794-34706805
49	CEBPB	chr2:34717910-34718155	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:34610850-34611138	MCF-7	breast:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34719565-34719615	NHDF-neo	bronchial:	n/a
2	chr2:34719565-34719615	NHDF-neo	bronchial:	n/a
3	chr2:34720275-34720325	NHBE	bronchial:	n/a
4	chr2:34633637-34633687	ProgFib	skin:	n/a
5	chr2:34633637-34633687	HNPCEpiC	eye:	n/a
6	chr2:34590591-34590641	HepG2	liver:	n/a
7	chr2:34633637-34633687	NHBE	bronchial:	n/a
8	chr2:34719719-34719769	PANC-1	pancreas:	n/a
9	chr2:34720275-34720325	HL-60	blood:	n/a
10	chr2:34720275-34720325	MCF10A-Er-Src	breast:	n/a
11	chr2:34720275-34720325	Jurkat	blood:	n/a
12	chr2:34719719-34719769	GM12892	blood:	n/a
13	chr2:34720275-34720325	HUVEC	blood vessel:	n/a
14	chr2:34590591-34590641	LNCaP	prostate:	n/a
15	chr2:34719565-34719615	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:34720275-34720325	AG10803	skin:	n/a
17	chr2:34719719-34719769	HCF	heart:	n/a
18	chr2:34633637-34633687	HEK293	kidney:	embryo
19	chr2:34590591-34590641	MCF-7	breast:	n/a
20	chr2:34590591-34590641	PANC-1	pancreas:	n/a
21	chr2:34719719-34719769	GM19239	blood:	n/a
22	chr2:34633637-34633687	CMK	blood:	n/a
23	chr2:34719565-34719615	ECC-1	luminal epithelium:	n/a
24	chr2:34720275-34720325	ECC-1	luminal epithelium:	n/a
25	chr2:34590591-34590641	HUVEC	blood vessel:	n/a
26	chr2:34720275-34720325	Hela-S3	cervix:	n/a
27	chr2:34719719-34719769	ECC-1	luminal epithelium:	n/a
28	chr2:34720275-34720325	AG09309	skin:	n/a
29	chr2:34719719-34719769	HNPCEpiC	eye:	n/a
30	chr2:34719719-34719769	AG04449	skin:	fetal
31	chr2:34633637-34633687	HRCEpiC	kidney:	n/a
32	chr2:34590591-34590641	SK-N-MC	brain:	n/a
33	chr2:34590591-34590641	IMR90	lung:	fetal
34	chr2:34590591-34590641	HCPEpiC	choroid plexus:	n/a
35	chr2:34720275-34720325	PANC-1	pancreas:	n/a
36	chr2:34719565-34719615	GM12891	blood:	n/a
37	chr2:34633637-34633687	HUVEC	blood vessel:	n/a
38	chr2:34720275-34720325	ovcar-3	ovarian:	n/a
39	chr2:34719565-34719615	ProgFib	skin:	n/a
40	chr2:34719565-34719615	Jurkat	blood:	n/a
41	chr2:34590591-34590641	SK-N-SH	brain:	n/a
42	chr2:34719719-34719769	HepG2	liver:	n/a
43	chr2:34719565-34719615	SKMC	muscle:	n/a
44	chr2:34633637-34633687	GM19239	blood:	n/a
45	chr2:34719565-34719615	CMK	blood:	n/a
46	chr2:34590591-34590641	AG04450	lung:	fetal
47	chr2:34720275-34720325	HPAEpiC	pulmonary alveolar:	n/a
48	chr2:34590591-34590641	U87	brain:	n/a
49	chr2:34719565-34719615	BJ	skin:	n/a
50	chr2:34590591-34590641	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
2	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
3	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
4	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
5	chr12:46765173..46767943-chr2:34590937..34593382,2	MCF-7	breast:
6	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
7	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
8	chr17:41466170..41467868-chr2:34623111..34624611,2	MCF-7	breast:
9	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
10	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
11	chr17:57969237..57970939-chr2:34675539..34678526,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-14	chr2:34756150-34756498	NONHSAT070037
2	lnc-RASGRP3-3	chr2:34608855-34609276	ENSG00000226785
3	lnc-RASGRP3-13	chr2:34713820-34713911	NONHSAT070033
4	lnc-RASGRP3-3	chr2:34609584-34609796	NONHSAT070034
5	lnc-RASGRP3-3	chr2:34609584-34609636	ENSG00000226785

Variant related genes	Relation type
ENSG00000212025	TF binding region
ENSG00000226785	TF binding region
ENSG00000212025	CpG island
ENSG00000226785	CpG island
ENSG00000188825	chromatin interactions
ENSG00000258096	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000134294	chromatin interactions

Extended variants
information (count: 3775 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3775 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146495654	chr2:34573426-34573427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs201419113	chr2:34573435-34573436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550172622	chr2:34573436-34573437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139155960	chr2:34573465-34573466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530179020	chr2:34573472-34573473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375240469	chr2:34573478-34573479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541663688	chr2:34573486-34573487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548716649	chr2:34573490-34573491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs71409699	chr2:34573495-34573496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs386354909	chr2:34573503-34573504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538749770	chr2:34573520-34573521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558326242	chr2:34573527-34573528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531563326	chr2:34573541-34573542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549793190	chr2:34573542-34573543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369577190	chr2:34573545-34573546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571949727	chr2:34573563-34573564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114563926	chr2:34573581-34573582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554592567	chr2:34573584-34573585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541382441	chr2:34573604-34573605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543014607	chr2:34573615-34573616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563306586	chr2:34573629-34573630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142952889	chr2:34573657-34573658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62163235	chr2:34573714-34573715	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs10204052	chr2:34573723-34573724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6543825	chr2:34573754-34573755	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112618301	chr2:34573815-34573816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72786857	chr2:34573846-34573847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530438617	chr2:34573863-34573864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554671041	chr2:34573885-34573886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569760788	chr2:34573900-34573901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188837916	chr2:34573927-34573928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552288003	chr2:34573950-34573951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565514263	chr2:34573959-34573960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142002027	chr2:34573961-34573962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554762936	chr2:34573983-34573984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373486246	chr2:34573984-34573985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537357182	chr2:34573990-34573991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs193207416	chr2:34573994-34573995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560210916	chr2:34573995-34573996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6543826	chr2:34574034-34574035	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553132372	chr2:34574050-34574051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs13411686	chr2:34574054-34574055	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs541232417	chr2:34574111-34574112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373273708	chr2:34574126-34574127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183652447	chr2:34574158-34574159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs62163236	chr2:34574179-34574180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34534265	chr2:34574180-34574181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs79826726	chr2:34574215-34574216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs58847425	chr2:34574216-34574217	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs186625902	chr2:34574220-34574221	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Incontinentia Pigmenti	22033527	CNVD
Alcoholism	22295116	CNVD
small cell lung cancer	20016488	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34573400-34575400	Enhancers	Fetal Heart	heart
2	chr2:34578200-34579000	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr2:34578400-34579200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr2:34578600-34579000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:34578600-34579400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:34578800-34579200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:34578800-34579200	Enhancers	Liver	Liver
8	chr2:34581600-34582000	Enhancers	Fetal Heart	heart
9	chr2:34584200-34584800	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr2:34587400-34591400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:34587800-34590000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:34587800-34590800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:34588000-34588600	Enhancers	Fetal Kidney	kidney
14	chr2:34588000-34590600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr2:34588000-34590800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr2:34588200-34588400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:34588200-34590800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:34588400-34589200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:34588600-34589000	Weak transcription	Fetal Kidney	kidney
20	chr2:34588800-34589000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:34588800-34589400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr2:34588800-34590800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:34589000-34589200	Enhancers	Fetal Kidney	kidney
24	chr2:34589000-34589600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr2:34589000-34589800	Enhancers	Colon Smooth Muscle	Colon
26	chr2:34589000-34590200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr2:34589000-34590800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:34589000-34592400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr2:34589200-34589400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr2:34589200-34589400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:34589200-34589600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:34589200-34590800	Weak transcription	Fetal Kidney	kidney
33	chr2:34589200-34591200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:34589400-34590800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr2:34589400-34590800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr2:34589600-34590000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:34589600-34590400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:34589600-34590800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:34590000-34590400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr2:34590000-34592600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:34590200-34591400	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr2:34590400-34590800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:34590400-34592200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr2:34590600-34590800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr2:34590800-34591000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr2:34590800-34591000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr2:34590800-34591000	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr2:34590800-34591200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr2:34590800-34591200	Enhancers	Fetal Intestine Small	intestine
50	chr2:34590800-34591400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links