Variant report

Variant	esv2830429
Chromosome Location	chr2:183300759-183545378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1701)
CpG islands
(count:1100)
Chromatin interactive
region (count:59)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1701 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183460601-183460670	K562	blood:	n/a	n/a
2	ARID3A	chr2:183481518-183482276	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:183514101-183514302	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:183515581-183515755	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:183483411-183483533	K562	blood:	n/a	n/a
6	ATF1	chr2:183507090-183507423	K562	blood:	n/a	n/a
7	BACH1	chr2:183413092-183413127	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:183490541-183490891	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:183515561-183515598	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:183460356-183460628	GM12878	blood:	n/a	n/a
11	BATF	chr2:183471691-183471996	GM12878	blood:	n/a	chr2:183471798-183471809
12	BCL11A	chr2:183471694-183472024	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:183471755-183471955	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:183483428-183483594	K562	blood:	n/a	n/a
15	BHLHE40	chr2:183481919-183482224	HepG2	liver:	n/a	n/a
16	BHLHE40	chr2:183475883-183475985	K562	blood:	n/a	n/a
17	BHLHE40	chr2:183507102-183507339	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:183511689-183511769	K562	blood:	n/a	n/a
19	BRCA1	chr2:183515566-183515708	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr2:183515397-183515792	Hela-S3	cervix:	n/a	n/a
21	CCNT2	chr2:183503497-183503741	K562	blood:	n/a	n/a
22	CCNT2	chr2:183410365-183410490	K562	blood:	n/a	n/a
23	CCNT2	chr2:183483419-183483635	K562	blood:	n/a	n/a
24	CEBPB	chr2:183419504-183420125	Hela-S3	cervix:	n/a	chr2:183419569-183419580 chr2:183419645-183419656
25	CEBPB	chr2:183437502-183437657	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:183352357-183352555	IMR90	lung:	n/a	chr2:183352441-183352452
27	CEBPB	chr2:183301089-183301298	K562	blood:	n/a	chr2:183301184-183301195
28	CEBPB	chr2:183462330-183462663	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:183515403-183515763	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:183306717-183307024	IMR90	lung:	n/a	chr2:183306851-183306862
31	CEBPB	chr2:183422590-183422627	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:183437450-183437650	K562	blood:	n/a	n/a
33	CEBPB	chr2:183462338-183462651	A549	lung:	n/a	n/a
34	CEBPB	chr2:183494019-183494120	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:183368379-183368671	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:183301066-183301332	A549	lung:	n/a	chr2:183301184-183301195
37	CEBPB	chr2:183310193-183310620	Hela-S3	cervix:	n/a	chr2:183310406-183310418
38	CEBPB	chr2:183456106-183456513	MCF-7	breast:	n/a	n/a
39	CEBPB	chr2:183368414-183368614	A549	lung:	n/a	n/a
40	CEBPB	chr2:183507061-183507545	MCF-7	breast:	n/a	n/a
41	CEBPB	chr2:183306725-183306989	HepG2	liver:	n/a	chr2:183306851-183306862
42	CEBPB	chr2:183456206-183456413	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:183449945-183449968	K562	blood:	n/a	n/a
44	CEBPB	chr2:183515326-183515830	HCT-116	colon:	n/a	n/a
45	CEBPB	chr2:183352393-183352490	HepG2	liver:	n/a	chr2:183352441-183352452
46	CEBPB	chr2:183481552-183482235	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr2:183371321-183371665	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:183309586-183309939	Hela-S3	cervix:	n/a	chr2:183309774-183309786
49	CEBPB	chr2:183533497-183533760	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:183301036-183301362	IMR90	lung:	n/a	chr2:183301184-183301195

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183409471-183409521	HCF	heart:	n/a
2	chr2:183489804-183489854	GM12892	blood:	n/a
3	chr2:183409471-183409521	HCF	heart:	n/a
4	chr2:183489804-183489854	GM12892	blood:	n/a
5	chr2:183312755-183312805	PrEC	prostate:	n/a
6	chr2:183458286-183458336	HUVEC	blood vessel:	n/a
7	chr2:183457634-183457684	GM19239	blood:	n/a
8	chr2:183473236-183473286	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:183458286-183458336	NHBE	bronchial:	n/a
10	chr2:183387885-183387935	HUVEC	blood vessel:	n/a
11	chr2:183473236-183473286	GM06990	blood:	n/a
12	chr2:183473088-183473138	GM12892	blood:	n/a
13	chr2:183312755-183312805	NB4	blood:	n/a
14	chr2:183473088-183473138	HepG2	liver:	n/a
15	chr2:183473236-183473286	HRPEpiC	eye:	n/a
16	chr2:183489804-183489854	GM12878	blood:	n/a
17	chr2:183387392-183387442	SAEC	small airway:	n/a
18	chr2:183386928-183386978	U87	brain:	n/a
19	chr2:183387885-183387935	K562	blood:	n/a
20	chr2:183321813-183321863	GM12891	blood:	n/a
21	chr2:183312755-183312805	ECC-1	luminal epithelium:	n/a
22	chr2:183458286-183458336	H1-hESC	embryonic stem cell:	embryo
23	chr2:183312755-183312805	HNPCEpiC	eye:	n/a
24	chr2:183387516-183387566	HRE	kidney:	n/a
25	chr2:183473088-183473138	MCF10A-Er-Src	breast:	n/a
26	chr2:183387516-183387566	GM12891	blood:	n/a
27	chr2:183457634-183457684	HAEpiC	amniotic membrane:	n/a
28	chr2:183370084-183370134	HUVEC	blood vessel:	n/a
29	chr2:183458286-183458336	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:183321813-183321863	HCPEpiC	choroid plexus:	n/a
31	chr2:183409471-183409521	NHBE	bronchial:	n/a
32	chr2:183370084-183370134	SK-N-SH	brain:	n/a
33	chr2:183473411-183473461	MCF-7	breast:	n/a
34	chr2:183482086-183482136	Jurkat	blood:	n/a
35	chr2:183473236-183473286	NT2-D1	testis:	n/a
36	chr2:183387885-183387935	HMEC	breast:	n/a
37	chr2:183482086-183482136	HCT-116	colon:	n/a
38	chr2:183387015-183387065	NH-A	brain:	n/a
39	chr2:183473411-183473461	T-47D	breast:	n/a
40	chr2:183387516-183387566	ovcar-3	ovarian:	n/a
41	chr2:183387015-183387065	GM12891	blood:	n/a
42	chr2:183387885-183387935	AG04450	lung:	fetal
43	chr2:183312755-183312805	GM12878	blood:	n/a
44	chr2:183387885-183387935	HAEpiC	amniotic membrane:	n/a
45	chr2:183370084-183370134	HCT-116	colon:	n/a
46	chr2:183387501-183387551	HUVEC	blood vessel:	n/a
47	chr2:183387885-183387935	CMK	blood:	n/a
48	chr2:183473411-183473461	GM12891	blood:	n/a
49	chr2:183386928-183386978	HNPCEpiC	eye:	n/a
50	chr2:183409471-183409521	HMEC	breast:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:183444746..183446283-chr2:183447847..183449772,2	K562	blood:
2	chr2:183484463..183486734-chr2:183489147..183491693,3	K562	blood:
3	chr2:183165936..183166478-chr2:183451147..183451888,2	MCF-7	breast:
4	chr2:183497857..183499568-chr2:183500564..183503369,2	K562	blood:
5	chr2:183050662..183051405-chr2:183513747..183514396,3	MCF-7	breast:
6	chr2:183165658..183166473-chr2:183513729..183514661,3	MCF-7	breast:
7	chr2:183050932..183051609-chr2:183514883..183516080,4	MCF-7	breast:
8	chr2:183050946..183051551-chr2:183517788..183518340,2	MCF-7	breast:
9	chr2:183525253..183526981-chr2:183533807..183535350,2	K562	blood:
10	chr2:183462276..183465034-chr2:183470042..183471619,2	K562	blood:
11	chr2:183409611..183411975-chr2:183412414..183414560,2	K562	blood:
12	chr2:183410632..183412807-chr2:183450091..183453006,2	K562	blood:
13	chr2:183410632..183412807-chr2:183450091..183453006,2	K562	blood:
14	chr2:183485446..183488008-chr2:183493899..183496895,2	K562	blood:
15	chr2:183415450..183417641-chr2:183419320..183421411,2	K562	blood:
16	chr2:183472950..183474900-chr2:183475047..183476914,2	K562	blood:
17	chr2:183381297..183382810-chr2:183385812..183388467,2	K562	blood:
18	chr2:183523433..183526191-chr2:183577944..183579909,2	MCF-7	breast:
19	chr2:183492322..183494288-chr2:183495772..183497912,2	K562	blood:
20	chr2:183325057..183326924-chr2:183328449..183330084,2	K562	blood:
21	chr2:183297531..183299912-chr2:183299956..183302678,2	K562	blood:
22	chr2:183407157..183409269-chr2:183412477..183414356,2	K562	blood:
23	chr2:183105157..183107059-chr2:183513716..183516271,10	MCF-7	breast:
24	chr2:183485234..183486908-chr2:183488749..183490647,2	K562	blood:
25	chr2:183497857..183499568-chr2:183500564..183503369,2	K562	blood:
26	chr2:183344989..183346517-chr2:183352874..183355064,2	MCF-7	breast:
27	chr2:183462276..183465034-chr2:183470042..183471619,2	K562	blood:
28	chr2:183409611..183411975-chr2:183412414..183414560,2	K562	blood:
29	chr2:183105303..183105848-chr2:183450937..183451448,2	MCF-7	breast:
30	chr2:183050633..183051569-chr2:183514775..183515804,6	K562	blood:
31	chr2:183335532..183337618-chr2:183340373..183342974,2	K562	blood:
32	chr2:183530500..183533463-chr2:183581172..183582687,2	MCF-7	breast:
33	chr2:183335532..183337618-chr2:183340373..183342974,2	K562	blood:
34	chr2:183407157..183409269-chr2:183412477..183414356,2	K562	blood:
35	chr2:183515898..183518111-chr2:183519211..183521393,2	MCF-7	breast:
36	chr2:183398225..183399816-chr2:183400215..183403060,2	MCF-7	breast:
37	chr2:183516388..183518623-chr2:183519704..183522732,3	K562	blood:
38	chr2:183415450..183417641-chr2:183419320..183421411,2	K562	blood:
39	chr2:183398225..183399816-chr2:183400215..183403060,2	MCF-7	breast:
40	chr2:183051017..183051535-chr2:183513719..183514634,2	K562	blood:
41	chr2:183533406..183536291-chr2:183538994..183541514,2	MCF-7	breast:
42	chr2:183485234..183486908-chr2:183488749..183490647,2	K562	blood:
43	chr2:183344989..183346517-chr2:183352874..183355064,2	MCF-7	breast:
44	chr2:183406601..183409032-chr2:183409704..183411675,2	K562	blood:
45	chr2:183515898..183518111-chr2:183519211..183521393,2	MCF-7	breast:
46	chr2:183291063..183292586-chr2:183298159..183300836,2	MCF-7	breast:
47	chr2:183533406..183536291-chr2:183538994..183541514,2	MCF-7	breast:
48	chr2:183502276..183505154-chr2:183507754..183509508,2	K562	blood:
49	chr2:183296401..183298106-chr2:183311342..183313093,2	K562	blood:
50	chr2:183472950..183474900-chr2:183475047..183476914,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE1A-1	chr2:183537627-183537875	NONHSAT075909
2	lnc-DNAJC10-3	chr2:183510878-183510968	NONHSAT075908
3	lnc-PDE1A-1	chr2:183539151-183539242	XLOC_002420
4	lnc-PDE1A-1	chr2:183539150-183539242	NONHSAT075911
5	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
6	lnc-DNAJC10-3	chr2:183513193-183513418	NONHSAT075908
7	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
8	lnc-PDE1A-1	chr2:183538117-183538135	XLOC_002420
9	lnc-PDE1A-1	chr2:183537628-183537875	XLOC_002420
10	lnc-PDE1A-1	chr2:183537302-183537749	NONHSAT075911
11	lnc-PDE1A-1	chr2:183536803-183536945	NONHSAT075909
12	lnc-PDE1A-1	chr2:183536804-183536945	XLOC_002420

No data

Variant related genes	Relation type
PDE1A	TF binding region
PDE1A	CpG island
ENSG00000115252	chromatin interactions

Extended variants
information (count: 7434 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7434 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17356166	chr2:183300759-183300760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192558176	chr2:183300823-183300824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs114312874	chr2:183300915-183300916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531815067	chr2:183300936-183300937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542544554	chr2:183301021-183301022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143445288	chr2:183301049-183301050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533621081	chr2:183301067-183301068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146794430	chr2:183301096-183301097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570103463	chr2:183301165-183301166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577958835	chr2:183301166-183301167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114721876	chr2:183301210-183301211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140422928	chr2:183301291-183301292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201690538	chr2:183301294-183301295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183678888	chr2:183301295-183301296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535307725	chr2:183301318-183301319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555587760	chr2:183301343-183301344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560608343	chr2:183301367-183301368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575012063	chr2:183301455-183301456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540726146	chr2:183301488-183301489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576159899	chr2:183301505-183301506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560508422	chr2:183301531-183301532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577175792	chr2:183301536-183301537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546130885	chr2:183301592-183301593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544984165	chr2:183301603-183301604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150432209	chr2:183301612-183301613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561168255	chr2:183301632-183301633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188191222	chr2:183301699-183301700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527578655	chr2:183301751-183301752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561943611	chr2:183301754-183301755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181000679	chr2:183301756-183301757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547100125	chr2:183301760-183301761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570483052	chr2:183301762-183301763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184145105	chr2:183301782-183301783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549717835	chr2:183301899-183301900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138242033	chr2:183301903-183301904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149164408	chr2:183301919-183301920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199749366	chr2:183301945-183301946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555645227	chr2:183301960-183301961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79061046	chr2:183301997-183301998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146828148	chr2:183302008-183302009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561573305	chr2:183302068-183302069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189793032	chr2:183302077-183302078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577240358	chr2:183302078-183302079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11899588	chr2:183302100-183302101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181620832	chr2:183302110-183302111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576712414	chr2:183302127-183302128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139228175	chr2:183302169-183302170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372990350	chr2:183302179-183302180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs13407156	chr2:183302191-183302192	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs527884192	chr2:183302276-183302277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1157 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183298800-183320800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:183300000-183301000	Enhancers	Brain Hippocampus Middle	brain
3	chr2:183300000-183301000	Enhancers	Osteobl	bone
4	chr2:183300000-183301200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:183300000-183301200	Enhancers	NHDF-Ad	bronchial
6	chr2:183300000-183301400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:183300200-183301400	Enhancers	Hela-S3	cervix
8	chr2:183300200-183301600	Enhancers	A549	lung
9	chr2:183300400-183301000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr2:183300600-183302600	Weak transcription	Fetal Heart	heart
11	chr2:183300600-183302800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:183301000-183308200	Weak transcription	Brain Hippocampus Middle	brain
13	chr2:183301200-183309200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr2:183301400-183309800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr2:183302800-183306400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:183305600-183306000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:183306400-183307200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:183307200-183309800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:183308200-183308400	ZNF genes & repeats	Brain Hippocampus Middle	brain
20	chr2:183308400-183311000	Weak transcription	Brain Hippocampus Middle	brain
21	chr2:183308400-183312000	Weak transcription	Left Ventricle	heart
22	chr2:183308800-183310600	Enhancers	HSMMtube	muscle
23	chr2:183309000-183311400	Enhancers	HSMM	muscle
24	chr2:183309200-183309800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr2:183309200-183311200	Enhancers	Hela-S3	cervix
26	chr2:183309200-183311400	Enhancers	Osteobl	bone
27	chr2:183309200-183313800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:183309400-183309600	Weak transcription	Fetal Heart	heart
29	chr2:183309600-183310400	Active TSS	Aorta	Aorta
30	chr2:183309600-183310800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:183309600-183311400	Enhancers	Fetal Heart	heart
32	chr2:183309800-183310000	Enhancers	Fetal Brain Female	brain
33	chr2:183309800-183310200	Enhancers	NHDF-Ad	bronchial
34	chr2:183309800-183310400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr2:183309800-183310400	Enhancers	HUVEC	blood vessel
36	chr2:183309800-183310800	Enhancers	NHLF	lung
37	chr2:183309800-183311000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr2:183309800-183313800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:183310000-183310600	Weak transcription	Fetal Brain Female	brain
40	chr2:183310000-183310600	Enhancers	Fetal Lung	lung
41	chr2:183310200-183312200	Weak transcription	NHDF-Ad	bronchial
42	chr2:183310400-183311400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr2:183310400-183312000	Weak transcription	Aorta	Aorta
44	chr2:183310600-183311000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr2:183310600-183311000	Weak transcription	HSMMtube	muscle
46	chr2:183310600-183311200	Enhancers	Fetal Brain Female	brain
47	chr2:183310800-183312200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:183310800-183312200	Weak transcription	NHLF	lung
49	chr2:183311000-183311200	Enhancers	Brain Angular Gyrus	brain
50	chr2:183311000-183311200	Enhancers	HSMMtube	muscle

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