Variant report

Variant	esv1008867
Chromosome Location	chr1:220986965-220999703
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	CEBPB	chr1:220999260-220999543	MCF-7	breast:	n/a	chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999412-220999423 chr1:220999413-220999422
2	CEBPB	chr1:220999178-220999589	Hela-S3	cervix:	n/a	chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999412-220999423 chr1:220999413-220999422
3	CEBPB	chr1:220999153-220999587	HepG2	liver:	n/a	chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999412-220999423 chr1:220999413-220999422
4	CEBPB	chr1:220999414-220999472	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr1:220999142-220999631	A549	lung:	n/a	chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999412-220999423 chr1:220999413-220999422
6	CEBPB	chr1:220999104-220999567	IMR90	lung:	n/a	chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999412-220999423 chr1:220999413-220999422
7	CEBPB	chr1:220999266-220999531	MCF-7	breast:	n/a	chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999412-220999423 chr1:220999413-220999422
8	CEBPB	chr1:220999215-220999548	K562	blood:	n/a	chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999412-220999423 chr1:220999413-220999422
9	CEBPB	chr1:220999133-220999587	A549	lung:	n/a	chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999413-220999422 chr1:220999412-220999423 chr1:220999413-220999422
10	E2F4	chr1:220999136-220999457	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F6	chr1:220997590-220998076	H1-hESC	embryonic stem cell:	n/a	n/a
12	FOS	chr1:220999163-220999500	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr1:220999084-220999557	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr1:220999139-220999504	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr1:220999162-220999504	MCF10A-Er-Src	breast:	n/a	n/a
16	FOXP2	chr1:220992121-220992477	PFSK-1	brain:	n/a	n/a
17	GTF2F1	chr1:220992437-220992448	H1-hESC	embryonic stem cell:	n/a	n/a
18	JUN	chr1:220992191-220992533	HUVEC	blood vessel:	n/a	chr1:220992345-220992353 chr1:220992344-220992353 chr1:220992345-220992352
19	JUND	chr1:220992179-220992522	H1-hESC	embryonic stem cell:	n/a	chr1:220992345-220992353 chr1:220992344-220992353 chr1:220992345-220992352 chr1:220992343-220992354
20	JUND	chr1:220992237-220992387	H1-hESC	embryonic stem cell:	n/a	chr1:220992345-220992353 chr1:220992344-220992353 chr1:220992345-220992352 chr1:220992343-220992354
21	JUND	chr1:220992309-220992487	HepG2	liver:	n/a	chr1:220992345-220992353 chr1:220992344-220992353 chr1:220992345-220992352 chr1:220992343-220992354
22	MAFK	chr1:220993180-220993380	IMR90	lung:	n/a	n/a
23	MAFK	chr1:220992193-220992802	IMR90	lung:	n/a	n/a
24	MAFK	chr1:220993147-220993263	HepG2	liver:	n/a	n/a
25	MAFK	chr1:220990825-220990925	HepG2	liver:	n/a	n/a
26	MAX	chr1:220998754-220998966	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAX	chr1:220989283-220989397	HepG2	liver:	n/a	n/a
28	MAX	chr1:220998746-220998945	K562	blood:	n/a	n/a
29	MYC	chr1:220999148-220999591	MCF10A-Er-Src	breast:	n/a	n/a
30	MYC	chr1:220993058-220993067	MCF10A-Er-Src	breast:	n/a	n/a
31	MYC	chr1:220999169-220999474	MCF10A-Er-Src	breast:	n/a	n/a
32	NANOG	chr1:220992086-220992460	H1-hESC	embryonic stem cell:	n/a	n/a
33	NFYB	chr1:220990786-220990988	Hela-S3	cervix:	n/a	chr1:220990862-220990877 chr1:220990926-220990941 chr1:220990903-220990918
34	NFYB	chr1:220990718-220990981	K562	blood:	n/a	chr1:220990862-220990877 chr1:220990926-220990941 chr1:220990903-220990918
35	NFYB	chr1:220990793-220990940	GM12878	blood:	n/a	chr1:220990862-220990877 chr1:220990903-220990918
36	POLR2A	chr1:220991456-220992400	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr1:220989467-220989788	HepG2	liver:	n/a	n/a
38	POLR2A	chr1:220994012-220994473	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr1:220987108-220987208	GM12878	blood:	n/a	n/a
40	POLR2A	chr1:220996871-220996882	HepG2	liver:	n/a	n/a
41	POLR2A	chr1:220989349-220989385	HepG2	liver:	n/a	n/a
42	POLR2A	chr1:220987187-220987511	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr1:220987786-220987868	HepG2	liver:	n/a	n/a
44	POLR2A	chr1:220987881-220988007	HepG2	liver:	n/a	n/a
45	POLR2A	chr1:220991113-220991142	HepG2	liver:	n/a	n/a
46	POLR2A	chr1:220992326-220992376	HepG2	liver:	n/a	n/a
47	POLR2A	chr1:220988155-220990339	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr1:220992103-220992376	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr1:220992111-220992370	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr1:220997468-220998154	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:220992242-220992292	BJ	skin:	n/a
2	chr1:220998876-220998926	HepG2	liver:	n/a
3	chr1:220992242-220992292	CMK	blood:	n/a
4	chr1:220987469-220987519	LNCaP	prostate:	n/a
5	chr1:220998876-220998926	HAEpiC	amniotic membrane:	n/a
6	chr1:220992242-220992292	NH-A	brain:	n/a
7	chr1:220998876-220998926	HRPEpiC	eye:	n/a
8	chr1:220998876-220998926	ECC-1	luminal epithelium:	n/a
9	chr1:220987469-220987519	NH-A	brain:	n/a
10	chr1:220992242-220992292	HepG2	liver:	n/a
11	chr1:220987469-220987519	CMK	blood:	n/a
12	chr1:220992242-220992292	PFSK-1	brain:	n/a
13	chr1:220998876-220998926	ProgFib	skin:	n/a
14	chr1:220998876-220998926	Hela-S3	cervix:	n/a
15	chr1:220992242-220992292	Caco-2	colon:	n/a
16	chr1:220987469-220987519	PrEC	prostate:	n/a
17	chr1:220987469-220987519	SKMC	muscle:	n/a
18	chr1:220987469-220987519	HAEpiC	amniotic membrane:	n/a
19	chr1:220987469-220987519	Hepatocyte	liver:	n/a
20	chr1:220998876-220998926	CMK	blood:	n/a
21	chr1:220998876-220998926	AG04450	lung:	fetal
22	chr1:220998876-220998926	HRCEpiC	kidney:	n/a
23	chr1:220987469-220987519	GM12892	blood:	n/a
24	chr1:220992242-220992292	AG09319	gingival:	n/a
25	chr1:220998876-220998926	AG04449	skin:	fetal
26	chr1:220992242-220992292	NT2-D1	testis:	n/a
27	chr1:220992242-220992292	RPTEC	kidney:	n/a
28	chr1:220998876-220998926	A549	lung:	n/a
29	chr1:220992242-220992292	SK-N-MC	brain:	n/a
30	chr1:220987469-220987519	HCT-116	colon:	n/a
31	chr1:220998876-220998926	NHBE	bronchial:	n/a
32	chr1:220987469-220987519	ovcar-3	ovarian:	n/a
33	chr1:220987469-220987519	HUVEC	blood vessel:	n/a
34	chr1:220998876-220998926	HMEC	breast:	n/a
35	chr1:220987469-220987519	AG04449	skin:	fetal
36	chr1:220987469-220987519	ProgFib	skin:	n/a
37	chr1:220987469-220987519	MCF10A-Er-Src	breast:	n/a
38	chr1:220987469-220987519	AG09309	skin:	n/a
39	chr1:220998876-220998926	Hepatocyte	liver:	n/a
40	chr1:220987469-220987519	K562	blood:	n/a
41	chr1:220987469-220987519	HRCEpiC	kidney:	n/a
42	chr1:220998876-220998926	HUVEC	blood vessel:	n/a
43	chr1:220998876-220998926	SAEC	small airway:	n/a
44	chr1:220998876-220998926	MCF-7	breast:	n/a
45	chr1:220992242-220992292	HNPCEpiC	eye:	n/a
46	chr1:220987469-220987519	SAEC	small airway:	n/a
47	chr1:220987469-220987519	Caco-2	colon:	n/a
48	chr1:220987469-220987519	HMEC	breast:	n/a
49	chr1:220987469-220987519	GM12878	blood:	n/a
50	chr1:220992242-220992292	HCM	heart:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARC1-3	chr1:220998962-220999389	ENSG00000221571.2

Variant related genes	Relation type
RNU6ATAC35P	TF binding region
ENSG00000238078	TF binding region
RNU6ATAC35P	CpG island
ENSG00000238078	CpG island

Extended variants
information (count: 486 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568964112	chr1:220986967-220986968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115745620	chr1:220987058-220987059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs41314252	chr1:220987104-220987105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558279647	chr1:220987133-220987134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2807840	chr1:220987155-220987156	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs183847944	chr1:220987187-220987188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553601232	chr1:220987191-220987192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72472359	chr1:220987192-220987193	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs549417029	chr1:220987221-220987222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556779078	chr1:220987227-220987228	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545616120	chr1:220987239-220987240	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558860903	chr1:220987256-220987257	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575734105	chr1:220987257-220987258	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188567473	chr1:220987258-220987259	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111398786	chr1:220987272-220987273	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544677635	chr1:220987289-220987290	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192828229	chr1:220987290-220987291	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113630478	chr1:220987313-220987314	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185455922	chr1:220987385-220987386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554352519	chr1:220987398-220987399	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112021741	chr1:220987448-220987449	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540551962	chr1:220987452-220987453	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11118608	chr1:220987469-220987470	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs552397552	chr1:220987470-220987471	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372065558	chr1:220987512-220987513	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190379528	chr1:220987535-220987536	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139486432	chr1:220987606-220987607	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567737302	chr1:220987608-220987609	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149663631	chr1:220987614-220987615	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34935190	chr1:220987672-220987673	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547061532	chr1:220987695-220987696	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551968858	chr1:220987815-220987816	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570441789	chr1:220987828-220987829	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567182155	chr1:220987849-220987850	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538959483	chr1:220987901-220987902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12042342	chr1:220987905-220987906	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182503316	chr1:220988007-220988008	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571037538	chr1:220988008-220988009	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2055117	chr1:220988032-220988033	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs555067111	chr1:220988066-220988067	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574972973	chr1:220988104-220988105	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368040889	chr1:220988106-220988107	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144512388	chr1:220988122-220988123	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185257574	chr1:220988146-220988147	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534292653	chr1:220988169-220988170	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139534836	chr1:220988172-220988173	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2807841	chr1:220988185-220988186	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs376493012	chr1:220988197-220988198	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4143773	chr1:220988242-220988243	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs7549963	chr1:220988260-220988261	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220966400-220996000	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr1:220971200-220991400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr1:220972800-220987600	Weak transcription	Fetal Brain Male	brain
4	chr1:220973200-220991800	Weak transcription	Brain Anterior Caudate	brain
5	chr1:220973400-221000200	Weak transcription	Placenta	Placenta
6	chr1:220974000-220992800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:220974200-220991200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:220975200-220992000	Weak transcription	Brain Germinal Matrix	brain
9	chr1:220975600-220988000	Weak transcription	Brain Angular Gyrus	brain
10	chr1:220975600-220991400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr1:220976400-220988000	Weak transcription	Spleen	Spleen
12	chr1:220978400-220991200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr1:220979400-220989400	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr1:220980400-221001400	Weak transcription	Gastric	stomach
15	chr1:220981000-220987600	Strong transcription	Hela-S3	cervix
16	chr1:220981400-220991600	Strong transcription	Fetal Intestine Small	intestine
17	chr1:220982400-220987200	Weak transcription	Brain Substantia Nigra	brain
18	chr1:220984000-220989400	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr1:220984000-220991600	Weak transcription	Small Intestine	intestine
20	chr1:220984000-220992200	Weak transcription	Esophagus	oesophagus
21	chr1:220984000-220997400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:220984000-220999800	Weak transcription	Colonic Mucosa	Colon
23	chr1:220984200-220987600	Strong transcription	HepG2	liver
24	chr1:220984200-220988400	Weak transcription	Fetal Lung	lung
25	chr1:220984200-220989400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr1:220984200-220990400	Strong transcription	Adipose Nuclei	Adipose
27	chr1:220984200-220991400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr1:220984200-220991400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr1:220984200-220991400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr1:220984200-220991600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:220984200-220991600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:220984200-220991800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr1:220984200-220992000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr1:220984200-220992200	Weak transcription	Lung	lung
35	chr1:220984200-220992400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr1:220984200-220993400	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr1:220984200-221001400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr1:220984400-220987400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
39	chr1:220984600-220989600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:220984600-220999600	Weak transcription	Left Ventricle	heart
41	chr1:220984600-221006600	Weak transcription	Psoas Muscle	Psoas
42	chr1:220984800-220988800	Weak transcription	Fetal Heart	heart
43	chr1:220984800-220991600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:220984800-220993000	Weak transcription	Right Ventricle	heart
45	chr1:220985000-220988600	Strong transcription	Fetal Intestine Large	intestine
46	chr1:220985000-220991800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:220985200-220987000	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr1:220985200-220987200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:220985200-220987200	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr1:220985400-220988000	Strong transcription	Liver	Liver

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