Variant report

Variant	nsv830004
Chromosome Location	chr1:62242944-62382228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:830)
CpG islands
(count:244)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:62303430-62303834	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:62380411-62381209	HepG2	liver:	n/a	n/a
3	ATF1	chr1:62246872-62247150	K562	blood:	n/a	n/a
4	ATF1	chr1:62253065-62253068	K562	blood:	n/a	n/a
5	BACH1	chr1:62279461-62279505	K562	blood:	n/a	n/a
6	BACH1	chr1:62310570-62310571	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr1:62310447-62310604	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr1:62256638-62256741	GM12878	blood:	n/a	n/a
9	BRCA1	chr1:62317809-62318111	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr1:62339211-62339555	K562	blood:	n/a	n/a
11	CBX3	chr1:62303297-62303849	HCT-116	colon:	n/a	n/a
12	CCNT2	chr1:62339289-62339502	K562	blood:	n/a	n/a
13	CEBPB	chr1:62262855-62263175	A549	lung:	n/a	n/a
14	CEBPB	chr1:62304963-62305198	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:62303319-62303710	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:62305355-62305743	Hela-S3	cervix:	n/a	chr1:62305500-62305511
17	CEBPB	chr1:62262852-62263193	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:62305316-62305731	HCT-116	colon:	n/a	chr1:62305500-62305511
19	CEBPB	chr1:62305274-62305889	HCT-116	colon:	n/a	chr1:62305500-62305511
20	CEBPB	chr1:62243151-62243416	HepG2	liver:	n/a	chr1:62243292-62243303
21	CEBPB	chr1:62303296-62303871	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr1:62310615-62310629	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr1:62303295-62303838	HCT-116	colon:	n/a	n/a
24	CEBPB	chr1:62243226-62243314	A549	lung:	n/a	chr1:62243292-62243303
25	CEBPB	chr1:62262961-62263156	K562	blood:	n/a	n/a
26	CEBPB	chr1:62299687-62299918	K562	blood:	n/a	n/a
27	CEBPB	chr1:62262900-62263170	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:62303372-62303583	K562	blood:	n/a	n/a
29	CEBPB	chr1:62304907-62305678	IMR90	lung:	n/a	chr1:62305500-62305511
30	CEBPB	chr1:62303113-62303923	HCT-116	colon:	n/a	n/a
31	CEBPB	chr1:62303363-62303750	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:62262997-62263027	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:62262837-62263205	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:62303341-62303578	HepG2	liver:	n/a	n/a
35	CHD1	chr1:62305872-62305917	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr1:62362417-62362485	K562	blood:	n/a	n/a
37	CTCF	chr1:62317920-62318070	AG04449	skin:	n/a	chr1:62317980-62317996 chr1:62317974-62317995 chr1:62317979-62317997
38	CTCF	chr1:62308700-62308850	HUVEC	blood vessel:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
39	CTCF	chr1:62308680-62308830	AG04449	skin:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
40	CTCF	chr1:62317920-62318070	HUVEC	blood vessel:	n/a	chr1:62317980-62317996 chr1:62317974-62317995 chr1:62317979-62317997
41	CTCF	chr1:62319285-62319518	GM12878	blood:	n/a	chr1:62319448-62319461 chr1:62319441-62319462
42	CTCF	chr1:62317793-62318194	GM12878	blood:	n/a	chr1:62317980-62317996 chr1:62317974-62317995 chr1:62317979-62317997
43	CTCF	chr1:62319400-62319550	HUVEC	blood vessel:	n/a	chr1:62319448-62319461 chr1:62319441-62319462
44	CTCF	chr1:62317810-62318166	H1-hESC	embryonic stem cell:	n/a	chr1:62317980-62317996 chr1:62317974-62317995 chr1:62317979-62317997
45	CTCF	chr1:62318260-62318410	GM06990	blood:	n/a	n/a
46	CTCF	chr1:62300438-62300528	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr1:62317920-62318070	HVMF	connective:	n/a	chr1:62317980-62317996 chr1:62317974-62317995 chr1:62317979-62317997
48	CTCF	chr1:62317940-62318090	GM12872	blood:	n/a	chr1:62317980-62317996 chr1:62317974-62317995 chr1:62317979-62317997
49	CTCF	chr1:62319120-62319410	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr1:62317900-62318050	GM12878	blood:	n/a	chr1:62317980-62317996 chr1:62317974-62317995 chr1:62317979-62317997

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62319602-62319652	NT2-D1	testis:	n/a
2	chr1:62319602-62319652	MCF10A-Er-Src	breast:	n/a
3	chr1:62270278-62270328	GM19239	blood:	n/a
4	chr1:62372488-62372538	AG09319	gingival:	n/a
5	chr1:62270278-62270328	HAEpiC	amniotic membrane:	n/a
6	chr1:62270278-62270328	AG09319	gingival:	n/a
7	chr1:62319602-62319652	HEEpiC	esophagus:	n/a
8	chr1:62270278-62270328	ECC-1	luminal epithelium:	n/a
9	chr1:62319602-62319652	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:62311238-62311288	AG09319	gingival:	n/a
11	chr1:62311238-62311288	HCF	heart:	n/a
12	chr1:62372488-62372538	IMR90	lung:	fetal
13	chr1:62311238-62311288	HNPCEpiC	eye:	n/a
14	chr1:62319602-62319652	ProgFib	skin:	n/a
15	chr1:62270278-62270328	Hepatocyte	liver:	n/a
16	chr1:62270278-62270328	SAEC	small airway:	n/a
17	chr1:62372488-62372538	U87	brain:	n/a
18	chr1:62319602-62319652	NHDF-neo	bronchial:	n/a
19	chr1:62372488-62372538	SK-N-SH_RA	brain:	n/a
20	chr1:62319602-62319652	HCPEpiC	choroid plexus:	n/a
21	chr1:62372488-62372538	A549	lung:	n/a
22	chr1:62372488-62372538	HL-60	blood:	n/a
23	chr1:62311238-62311288	AoSMC	blood vessel:	n/a
24	chr1:62319602-62319652	MCF-7	breast:	n/a
25	chr1:62270278-62270328	HMEC	breast:	n/a
26	chr1:62372488-62372538	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:62311238-62311288	SK-N-SH_RA	brain:	n/a
28	chr1:62372488-62372538	PrEC	prostate:	n/a
29	chr1:62319602-62319652	CMK	blood:	n/a
30	chr1:62270278-62270328	T-47D	breast:	n/a
31	chr1:62311238-62311288	HEEpiC	esophagus:	n/a
32	chr1:62372488-62372538	SKMC	muscle:	n/a
33	chr1:62311238-62311288	AG10803	skin:	n/a
34	chr1:62311238-62311288	HUVEC	blood vessel:	n/a
35	chr1:62311238-62311288	HCT-116	colon:	n/a
36	chr1:62311238-62311288	ovcar-3	ovarian:	n/a
37	chr1:62311238-62311288	IMR90	lung:	fetal
38	chr1:62311238-62311288	MCF10A-Er-Src	breast:	n/a
39	chr1:62311238-62311288	GM06990	blood:	n/a
40	chr1:62311238-62311288	AG04449	skin:	fetal
41	chr1:62372488-62372538	PFSK-1	brain:	n/a
42	chr1:62372488-62372538	GM12891	blood:	n/a
43	chr1:62270278-62270328	HUVEC	blood vessel:	n/a
44	chr1:62270278-62270328	BE2_C	brain:	n/a
45	chr1:62319602-62319652	AG09319	gingival:	n/a
46	chr1:62372488-62372538	SK-N-MC	brain:	n/a
47	chr1:62311238-62311288	BJ	skin:	n/a
48	chr1:62319602-62319652	SK-N-SH	brain:	n/a
49	chr1:62311238-62311288	HCM	heart:	n/a
50	chr1:62372488-62372538	HMEC	breast:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:62268254..62269859-chr1:62281765..62283319,2	MCF-7	breast:
2	chr1:62288601..62290902-chr1:62291765..62293446,2	K562	blood:
3	chr1:62319433..62321663-chr1:62323711..62326271,2	K562	blood:
4	chr1:62188330..62190848-chr1:62304902..62307738,2	K562	blood:
5	chr1:62284465..62286145-chr1:62287888..62289486,2	K562	blood:
6	chr1:62288601..62290902-chr1:62291765..62293446,2	K562	blood:
7	chr1:62207401..62209297-chr1:62277222..62279728,2	MCF-7	breast:
8	chr1:62284465..62286145-chr1:62287888..62289486,2	K562	blood:
9	chr1:62313339..62316037-chr1:62320752..62322318,2	MCF-7	breast:
10	chr1:62294253..62296248-chr1:62299623..62302341,2	K562	blood:
11	chr1:62263282..62264953-chr1:62267149..62270089,2	MCF-7	breast:
12	chr1:62263282..62264953-chr1:62267149..62270089,2	MCF-7	breast:
13	chr1:62206940..62209583-chr1:62260283..62262996,3	MCF-7	breast:
14	chr1:62304428..62307569-chr1:62310144..62313240,3	MCF-7	breast:
15	chr1:62270101..62271801-chr1:62272747..62275462,2	MCF-7	breast:
16	chr1:62304428..62307569-chr1:62310144..62313240,3	MCF-7	breast:
17	chr1:62208685..62210922-chr1:62306053..62308101,2	MCF-7	breast:
18	chr1:62319433..62321663-chr1:62323711..62326271,2	K562	blood:
19	chr1:61546840..61548759-chr1:62318537..62320361,2	K562	blood:
20	chr1:62313339..62316037-chr1:62320752..62322318,2	MCF-7	breast:
21	chr1:60442169..60443081-chr1:62317566..62318142,2	K562	blood:
22	chr1:62294253..62296248-chr1:62299623..62302341,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-414P	TF binding region
RNU6-1177P	TF binding region
INADL	TF binding region
RNU6-414P	CpG island
RNU6-1177P	CpG island
INADL	CpG island
ENSG00000162599	chromatin interactions
ENSG00000132849	chromatin interactions
ENSG00000200575	chromatin interactions
ENSG00000162604	chromatin interactions
ENSG00000271200	chromatin interactions

Extended variants
information (count: 5089 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5089 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546104548	chr1:62242950-62242951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564412527	chr1:62242962-62242963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141118469	chr1:62243013-62243014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191290804	chr1:62243045-62243046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150348087	chr1:62243057-62243058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562083560	chr1:62243072-62243073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529386996	chr1:62243081-62243082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs525526	chr1:62243144-62243145	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs525523	chr1:62243149-62243150	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs183876471	chr1:62243150-62243151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150233721	chr1:62243183-62243184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190457784	chr1:62243226-62243227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193111416	chr1:62243231-62243232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546565382	chr1:62243260-62243261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371543522	chr1:62243272-62243273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374448966	chr1:62243307-62243308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557838384	chr1:62243341-62243342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369918743	chr1:62243345-62243346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145556827	chr1:62243372-62243373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7531375	chr1:62243375-62243376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60083553	chr1:62243378-62243379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373429187	chr1:62243379-62243380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs66470863	chr1:62243396-62243397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149368811	chr1:62243401-62243402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556749062	chr1:62243436-62243437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575455395	chr1:62243441-62243442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185856879	chr1:62243449-62243450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546258706	chr1:62243530-62243531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558042083	chr1:62243535-62243536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35755728	chr1:62243574-62243575	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs551628453	chr1:62243599-62243600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374739685	chr1:62243616-62243617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11207829	chr1:62243650-62243651	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs138419607	chr1:62243676-62243677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143819957	chr1:62243726-62243727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189984726	chr1:62243805-62243806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75696128	chr1:62243848-62243849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372807787	chr1:62243879-62243880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115489762	chr1:62243991-62243992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181624209	chr1:62244045-62244046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530728026	chr1:62244062-62244063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147256543	chr1:62244088-62244089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564411798	chr1:62244120-62244121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34708324	chr1:62244139-62244140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528390880	chr1:62244208-62244209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185398351	chr1:62244223-62244224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530850675	chr1:62244272-62244273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11207830	chr1:62244279-62244280	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs148689566	chr1:62244309-62244310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550654087	chr1:62244346-62244347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1921 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62210000-62253400	Weak transcription	Pancreas	Pancrea
2	chr1:62212200-62254400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:62212800-62255400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:62213600-62253000	Weak transcription	Fetal Kidney	kidney
5	chr1:62213600-62263200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:62217600-62254600	Weak transcription	Fetal Stomach	stomach
7	chr1:62219200-62246600	Weak transcription	Stomach Mucosa	stomach
8	chr1:62220200-62290200	Weak transcription	Lung	lung
9	chr1:62220200-62310800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:62221000-62246400	Weak transcription	Primary T cells from cord blood	blood
11	chr1:62221800-62263000	Weak transcription	Colonic Mucosa	Colon
12	chr1:62222000-62293000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr1:62222200-62260800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:62222800-62258400	Weak transcription	Esophagus	oesophagus
15	chr1:62224000-62247200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr1:62224000-62263000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr1:62224000-62267600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:62224000-62290800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:62224400-62253400	Weak transcription	Ovary	ovary
20	chr1:62224600-62247400	Weak transcription	Gastric	stomach
21	chr1:62224600-62263000	Weak transcription	Left Ventricle	heart
22	chr1:62225000-62284400	Weak transcription	Psoas Muscle	Psoas
23	chr1:62226200-62248000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:62227400-62245600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr1:62227800-62294600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr1:62228600-62245600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr1:62228600-62391800	Weak transcription	Small Intestine	intestine
28	chr1:62229000-62243800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr1:62230600-62246800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:62230600-62253600	Weak transcription	Adipose Nuclei	Adipose
31	chr1:62231800-62273400	Weak transcription	Colon Smooth Muscle	Colon
32	chr1:62232200-62262800	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr1:62232800-62267200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr1:62233000-62246000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:62233000-62263000	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr1:62233200-62263800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr1:62233400-62254800	Weak transcription	Fetal Lung	lung
38	chr1:62233400-62264200	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr1:62233400-62288800	Weak transcription	Brain Hippocampus Middle	brain
40	chr1:62233800-62246600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:62235000-62246400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr1:62235400-62245000	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr1:62235400-62246200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:62235400-62246400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr1:62235400-62253200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr1:62235400-62253400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:62235400-62263200	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr1:62235400-62288800	Weak transcription	A549	lung
49	chr1:62235600-62246400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr1:62235600-62246800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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