Variant report

Variant	nsv584713
Chromosome Location	chr2:235092011-235236611
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2258)
CpG islands
(count:673)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2258 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:235112044-235112281	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:235197634-235197961	HepG2	liver:	n/a	n/a
3	ATF1	chr2:235201222-235201469	K562	blood:	n/a	n/a
4	ATF1	chr2:235178494-235178686	K562	blood:	n/a	n/a
5	ATF2	chr2:235199350-235199649	GM12878	blood:	n/a	n/a
6	ATF2	chr2:235197519-235197948	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:235217354-235217846	GM12878	blood:	n/a	n/a
8	ATF2	chr2:235199289-235199616	GM12878	blood:	n/a	n/a
9	ATF2	chr2:235201131-235201431	GM12878	blood:	n/a	n/a
10	ATF3	chr2:235166614-235167343	A549	lung:	n/a	n/a
11	ATF3	chr2:235102614-235103010	A549	lung:	n/a	n/a
12	ATF3	chr2:235216428-235217982	A549	lung:	n/a	chr2:235217621-235217632 chr2:235217622-235217629 chr2:235217619-235217630
13	ATF3	chr2:235197610-235197973	HepG2	liver:	n/a	chr2:235197634-235197643
14	ATF3	chr2:235111728-235112365	A549	lung:	n/a	n/a
15	ATF3	chr2:235160267-235161051	A549	lung:	n/a	chr2:235160786-235160800
16	ATF3	chr2:235197594-235198131	HepG2	liver:	n/a	chr2:235197634-235197643
17	ATF3	chr2:235166568-235167404	A549	lung:	n/a	n/a
18	ATF3	chr2:235111780-235112403	A549	lung:	n/a	n/a
19	ATF3	chr2:235111623-235112462	HCT-116	colon:	n/a	n/a
20	ATF3	chr2:235216851-235217873	A549	lung:	n/a	chr2:235217621-235217632 chr2:235217622-235217629 chr2:235217619-235217630
21	BACH1	chr2:235097894-235098271	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr2:235213660-235214009	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr2:235197566-235197884	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr2:235166846-235167057	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr2:235201125-235201414	GM12878	blood:	n/a	chr2:235201247-235201258
26	BATF	chr2:235199316-235199658	GM12878	blood:	n/a	chr2:235199444-235199455
27	BATF	chr2:235201052-235201409	GM12878	blood:	n/a	chr2:235201247-235201258
28	BATF	chr2:235217414-235217721	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:235201137-235201386	GM12878	blood:	n/a	chr2:235201247-235201256 chr2:235201246-235201255
30	BCL11A	chr2:235199312-235199713	GM12878	blood:	n/a	chr2:235199528-235199537
31	BCL11A	chr2:235199361-235199690	GM12878	blood:	n/a	chr2:235199528-235199537
32	BCL11A	chr2:235217485-235217854	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:235217431-235217805	GM12878	blood:	n/a	n/a
34	BCL3	chr2:235160234-235161056	A549	lung:	n/a	n/a
35	BCL3	chr2:235111522-235112384	A549	lung:	n/a	n/a
36	BCL3	chr2:235154356-235155191	A549	lung:	n/a	n/a
37	BCL3	chr2:235152427-235153105	A549	lung:	n/a	n/a
38	BCL3	chr2:235102582-235103072	A549	lung:	n/a	n/a
39	BCL3	chr2:235150498-235151272	A549	lung:	n/a	n/a
40	BCL3	chr2:235213251-235213962	A549	lung:	n/a	n/a
41	BCL3	chr2:235166648-235167630	A549	lung:	n/a	chr2:235167519-235167526
42	BCL3	chr2:235154234-235154955	A549	lung:	n/a	n/a
43	BCL3	chr2:235216741-235217971	A549	lung:	n/a	chr2:235216848-235216857
44	BCL3	chr2:235209515-235210077	GM12878	blood:	n/a	chr2:235209707-235209716
45	BCL3	chr2:235112956-235113644	A549	lung:	n/a	chr2:235113038-235113045
46	BCL3	chr2:235209574-235209991	GM12878	blood:	n/a	chr2:235209707-235209716
47	BCL3	chr2:235213465-235214205	A549	lung:	n/a	n/a
48	BCL3	chr2:235166533-235167756	A549	lung:	n/a	chr2:235167519-235167526
49	BCL3	chr2:235216504-235217943	A549	lung:	n/a	chr2:235216848-235216857
50	BCL3	chr2:235111639-235112398	A549	lung:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:235156663-235156713	HCPEpiC	choroid plexus:	n/a
2	chr2:235166931-235166981	HRE	kidney:	n/a
3	chr2:235156663-235156713	HCPEpiC	choroid plexus:	n/a
4	chr2:235166931-235166981	HRE	kidney:	n/a
5	chr2:235216719-235216769	SKMC	muscle:	n/a
6	chr2:235156415-235156465	HepG2	liver:	n/a
7	chr2:235156663-235156713	LNCaP	prostate:	n/a
8	chr2:235210313-235210363	HL-60	blood:	n/a
9	chr2:235160451-235160501	HCF	heart:	n/a
10	chr2:235156415-235156465	GM06990	blood:	n/a
11	chr2:235178208-235178258	NH-A	brain:	n/a
12	chr2:235166931-235166981	HL-60	blood:	n/a
13	chr2:235213874-235213924	HNPCEpiC	eye:	n/a
14	chr2:235200560-235200610	PFSK-1	brain:	n/a
15	chr2:235160451-235160501	GM12878	blood:	n/a
16	chr2:235200560-235200610	NH-A	brain:	n/a
17	chr2:235216719-235216769	HCT-116	colon:	n/a
18	chr2:235210313-235210363	SK-N-SH	brain:	n/a
19	chr2:235210313-235210363	Jurkat	blood:	n/a
20	chr2:235160451-235160501	HIPEpiC	eye:	n/a
21	chr2:235213874-235213924	GM06990	blood:	n/a
22	chr2:235156663-235156713	PANC-1	pancreas:	n/a
23	chr2:235166931-235166981	Hela-S3	cervix:	n/a
24	chr2:235213874-235213924	HEEpiC	esophagus:	n/a
25	chr2:235166931-235166981	K562	blood:	n/a
26	chr2:235098156-235098206	ovcar-3	ovarian:	n/a
27	chr2:235156663-235156713	AoSMC	blood vessel:	n/a
28	chr2:235098156-235098206	SK-N-SH	brain:	n/a
29	chr2:235210313-235210363	HRPEpiC	eye:	n/a
30	chr2:235098156-235098206	U87	brain:	n/a
31	chr2:235216719-235216769	SAEC	small airway:	n/a
32	chr2:235160451-235160501	U87	brain:	n/a
33	chr2:235156663-235156713	ovcar-3	ovarian:	n/a
34	chr2:235156663-235156713	Caco-2	colon:	n/a
35	chr2:235210313-235210363	HEK293	kidney:	embryo
36	chr2:235178208-235178258	MCF-7	breast:	n/a
37	chr2:235166931-235166981	RPTEC	kidney:	n/a
38	chr2:235156415-235156465	AG10803	skin:	n/a
39	chr2:235200560-235200610	HL-60	blood:	n/a
40	chr2:235178208-235178258	HMEC	breast:	n/a
41	chr2:235216719-235216769	HEK293	kidney:	embryo
42	chr2:235156415-235156465	GM12891	blood:	n/a
43	chr2:235210313-235210363	IMR90	lung:	fetal
44	chr2:235156509-235156559	SK-N-SH_RA	brain:	n/a
45	chr2:235216719-235216769	T-47D	breast:	n/a
46	chr2:235216719-235216769	HCPEpiC	choroid plexus:	n/a
47	chr2:235098156-235098206	AoSMC	blood vessel:	n/a
48	chr2:235166931-235166981	AoSMC	blood vessel:	n/a
49	chr2:235098156-235098206	PANC-1	pancreas:	n/a
50	chr2:235178208-235178258	AG04449	skin:	fetal

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:235197567..235199398-chr2:235404539..235407014,2	MCF-7	breast:
2	chr2:235198144..235199087-chr2:235301414..235302273,2	MCF-7	breast:
3	chr2:235197644..235198199-chr2:235453526..235454186,2	MCF-7	breast:
4	chr2:235235018..235236605-chr2:235238040..235239669,2	K562	blood:
5	chr2:235134989..235136667-chr2:235136969..235139077,2	MCF-7	breast:
6	chr2:235197396..235198049-chr3:12430421..12431137,2	MCF-7	breast:
7	chr2:235079344..235080200-chr2:235166670..235167350,3	MCF-7	breast:
8	chr12:61782102..61782969-chr2:235157951..235158503,2	MCF-7	breast:
9	chr2:235044193..235044936-chr2:235166707..235167413,3	MCF-7	breast:
10	chr2:235043979..235044965-chr2:235166466..235167435,6	MCF-7	breast:
11	chr12:122235892..122238477-chr2:235091344..235092959,2	MCF-7	breast:
12	chr2:234885292..234886125-chr2:235166874..235167410,2	MCF-7	breast:
13	chr2:235201767..235203347-chr2:235209023..235210724,2	MCF-7	breast:
14	chr2:235206539..235209460-chr2:235391484..235393644,2	K562	blood:
15	chr2:235197507..235198142-chr2:235314505..235315353,4	MCF-7	breast:
16	chr2:235189626..235191968-chr2:235200515..235202999,2	K562	blood:
17	chr2:235198086..235200981-chr2:235203016..235204860,2	MCF-7	breast:
18	chr2:235196853..235198165-chr2:235314416..235315341,7	MCF-7	breast:
19	chr2:235134989..235136667-chr2:235136969..235139077,2	MCF-7	breast:
20	chr2:235044065..235044622-chr2:235157381..235158015,2	MCF-7	breast:
21	chr2:235201767..235203347-chr2:235209023..235210724,2	MCF-7	breast:
22	chr2:235233335..235235300-chr2:235237162..235239539,2	K562	blood:
23	chr2:235198086..235200981-chr2:235203016..235204860,2	MCF-7	breast:
24	chr2:235189626..235191968-chr2:235200515..235202999,2	K562	blood:
25	chr2:235197413..235198142-chr2:235409239..235409759,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPP2-2	chr2:235131958-235133158	ENSG00000261298.1
2	lnc-SPP2-2	chr2:235131482-235132585	ENSG00000261298.1
3	lnc-ARL4C-9	chr2:235111682-235111954	NONHSAT077528
4	lnc-ARL4C-9	chr2:235107918-235107987	NONHSAT077528

No data

Variant related genes	Relation type
ENSG00000237784	TF binding region
ENSG00000261298	TF binding region
ENSG00000237784	CpG island
ENSG00000261298	CpG island
ENSG00000237784	chromatin interactions
ENSG00000188042	chromatin interactions

Extended variants
information (count: 5978 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5978 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6753274	chr2:235092011-235092012	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139475378	chr2:235092057-235092058	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191004196	chr2:235092094-235092095	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548096551	chr2:235092125-235092126	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545000293	chr2:235092136-235092137	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2885704	chr2:235092144-235092145	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142229086	chr2:235092244-235092245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6431236	chr2:235092268-235092269	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs563469902	chr2:235092269-235092270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553764689	chr2:235092295-235092296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs59151757	chr2:235092304-235092305	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs539489559	chr2:235092307-235092308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114389615	chr2:235092319-235092320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567203950	chr2:235092328-235092329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534650489	chr2:235092345-235092346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551383559	chr2:235092426-235092427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs5839506	chr2:235092475-235092476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571273688	chr2:235092482-235092483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537124036	chr2:235092484-235092485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372623316	chr2:235092485-235092486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200475757	chr2:235092486-235092487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201691354	chr2:235092488-235092489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376326297	chr2:235092525-235092526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536440029	chr2:235092529-235092530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553300833	chr2:235092538-235092539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573177793	chr2:235092543-235092544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148812788	chr2:235092557-235092558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs180711037	chr2:235092576-235092577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185098401	chr2:235092585-235092586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375989518	chr2:235092590-235092591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200448072	chr2:235092609-235092610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201878265	chr2:235092646-235092647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371251330	chr2:235092648-235092649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190003882	chr2:235092649-235092650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544644212	chr2:235092652-235092653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563344692	chr2:235092698-235092699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529125130	chr2:235092740-235092741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs62184331	chr2:235092811-235092812	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145588842	chr2:235092833-235092834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528362425	chr2:235092845-235092846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551420627	chr2:235092852-235092853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73121207	chr2:235092873-235092874	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536756540	chr2:235092883-235092884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550692330	chr2:235092894-235092895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148870601	chr2:235092900-235092901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143727736	chr2:235092936-235092937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553133670	chr2:235092946-235092947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566838077	chr2:235093003-235093004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538917122	chr2:235093044-235093045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182646837	chr2:235093096-235093097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Wilms tumour	21544195	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1735 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:235078600-235098000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:235091400-235092200	Genic enhancers	Dnd41	blood
3	chr2:235091600-235092400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:235092200-235094000	Enhancers	Dnd41	blood
5	chr2:235093800-235094000	Enhancers	NHEK	skin
6	chr2:235094000-235094800	Weak transcription	Dnd41	blood
7	chr2:235094000-235097800	Weak transcription	NHEK	skin
8	chr2:235094800-235096000	Genic enhancers	Dnd41	blood
9	chr2:235095000-235096400	Weak transcription	A549	lung
10	chr2:235095600-235097200	Enhancers	Fetal Thymus	thymus
11	chr2:235096000-235097000	Enhancers	Pancreas	Pancrea
12	chr2:235096000-235097000	Transcr. at gene 5' and 3'	Dnd41	blood
13	chr2:235096400-235096600	Enhancers	A549	lung
14	chr2:235096400-235097000	Enhancers	Thymus	Thymus
15	chr2:235096400-235098400	Enhancers	Primary B cells from peripheral blood	blood
16	chr2:235096600-235099000	Weak transcription	A549	lung
17	chr2:235096800-235097000	Enhancers	Esophagus	oesophagus
18	chr2:235096800-235097400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr2:235096800-235097600	Bivalent Enhancer	Primary B cells from cord blood	blood
20	chr2:235097000-235097600	Weak transcription	Esophagus	oesophagus
21	chr2:235097000-235097800	Weak transcription	Pancreas	Pancrea
22	chr2:235097000-235098200	Flanking Active TSS	Dnd41	blood
23	chr2:235097200-235097600	Weak transcription	Fetal Thymus	thymus
24	chr2:235097400-235100200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:235097600-235098000	Enhancers	Primary B cells from cord blood	blood
26	chr2:235097600-235098400	Enhancers	Fetal Thymus	thymus
27	chr2:235097600-235098800	Enhancers	Esophagus	oesophagus
28	chr2:235097800-235098000	Enhancers	NHEK	skin
29	chr2:235097800-235098400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr2:235097800-235098400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:235097800-235098400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr2:235097800-235098600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:235097800-235098800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr2:235098000-235098200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr2:235098000-235098400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr2:235098000-235098400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:235098000-235098400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:235098000-235098600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr2:235098000-235098800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:235098000-235098800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:235098000-235099000	Enhancers	HMEC	breast
42	chr2:235098000-235099000	Flanking Active TSS	NHEK	skin
43	chr2:235098200-235098800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:235098200-235098800	Transcr. at gene 5' and 3'	Dnd41	blood
45	chr2:235098200-235100600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:235098400-235098600	Enhancers	HSMMtube	muscle
47	chr2:235098400-235100600	Weak transcription	Fetal Thymus	thymus
48	chr2:235098600-235098800	Enhancers	Thymus	Thymus
49	chr2:235098600-235098800	Flanking Active TSS	HSMMtube	muscle
50	chr2:235098800-235099000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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