Variant report

Variant	nsv160470
Chromosome Location	chr1:220919015-220922779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:272)
CpG islands
(count:856)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:220921377-220921582	HepG2	liver:	n/a	n/a
2	ATF2	chr1:220921237-220921801	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:220921181-220921772	A549	lung:	n/a	n/a
4	BCL3	chr1:220921201-220921672	A549	lung:	n/a	n/a
5	BHLHE40	chr1:220921288-220921678	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:220921271-220921720	HepG2	liver:	n/a	n/a
7	BRCA1	chr1:220921285-220921885	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr1:220921327-220921802	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:220921288-220921783	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:220921063-220921727	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:220921189-220921673	MCF-7	breast:	n/a	n/a
12	CEBPB	chr1:220921233-220921815	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:220921254-220921591	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:220921285-220921609	A549	lung:	n/a	n/a
15	CEBPB	chr1:220921254-220921647	HepG2	liver:	n/a	n/a
16	CEBPD	chr1:220921329-220921811	HepG2	liver:	n/a	n/a
17	CHD1	chr1:220921067-220922088	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr1:220921300-220921846	HepG2	liver:	n/a	n/a
19	CHD2	chr1:220921259-220922114	Hela-S3	cervix:	n/a	n/a
20	CREB1	chr1:220921387-220921711	A549	lung:	n/a	n/a
21	CREB1	chr1:220921184-220922070	HepG2	liver:	n/a	n/a
22	CREB1	chr1:220921386-220921784	A549	lung:	n/a	n/a
23	CTBP2	chr1:220921308-220922346	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:220922098-220922142	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr1:220921160-220921310	GM12873	blood:	n/a	n/a
26	CTCF	chr1:220921644-220921651	Lung_OC	lung:	n/a	n/a
27	CTCF	chr1:220921340-220921490	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr1:220921840-220921990	GM12864	blood:	n/a	n/a
29	CTCF	chr1:220921400-220921550	AG10803	skin:	n/a	n/a
30	CTCF	chr1:220921480-220921630	GM12865	blood:	n/a	n/a
31	CTCF	chr1:220921220-220921370	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr1:220921340-220921490	GM06990	blood:	n/a	n/a
33	CTCF	chr1:220921360-220921510	BJ	skin:	n/a	n/a
34	CTCF	chr1:220921200-220921350	HMEC	breast:	n/a	n/a
35	CTCF	chr1:220921260-220921410	HepG2	liver:	n/a	n/a
36	CTCF	chr1:220921320-220921470	GM12873	blood:	n/a	n/a
37	CTCF	chr1:220921260-220921410	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr1:220921200-220921350	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr1:220921280-220921430	RPTEC	kidney:	n/a	n/a
40	CTCF	chr1:220921320-220921470	AG10803	skin:	n/a	n/a
41	CTCF	chr1:220921480-220921630	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr1:220921180-220921330	HFF	foreskin:	n/a	n/a
43	CTCF	chr1:220922180-220922330	SAEC	small airway:	n/a	n/a
44	CTCF	chr1:220921280-220921430	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr1:220922094-220922168	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:220921300-220921450	HCFaa	heart:	n/a	n/a
47	CTCF	chr1:220921360-220921510	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:220921420-220921570	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr1:220921480-220921630	BJ	skin:	n/a	n/a
50	CTCF	chr1:220921340-220921490	GM12864	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:220921855-220921905	MCF-7	breast:	n/a
2	chr1:220922046-220922096	HL-60	blood:	n/a
3	chr1:220921855-220921905	MCF-7	breast:	n/a
4	chr1:220922046-220922096	HL-60	blood:	n/a
5	chr1:220922046-220922096	NHDF-neo	bronchial:	n/a
6	chr1:220921611-220921661	SK-N-MC	brain:	n/a
7	chr1:220921306-220921356	Hela-S3	cervix:	n/a
8	chr1:220921611-220921661	AoSMC	blood vessel:	n/a
9	chr1:220921216-220921266	AG09309	skin:	n/a
10	chr1:220921855-220921905	ECC-1	luminal epithelium:	n/a
11	chr1:220921670-220921720	NHBE	bronchial:	n/a
12	chr1:220921855-220921905	A549	lung:	n/a
13	chr1:220921432-220921482	SAEC	small airway:	n/a
14	chr1:220921859-220921909	T-47D	breast:	n/a
15	chr1:220921432-220921482	GM12892	blood:	n/a
16	chr1:220921611-220921661	GM12878	blood:	n/a
17	chr1:220921216-220921266	HNPCEpiC	eye:	n/a
18	chr1:220921670-220921720	BJ	skin:	n/a
19	chr1:220921611-220921661	GM12892	blood:	n/a
20	chr1:220922163-220922213	AG10803	skin:	n/a
21	chr1:220921306-220921356	HEEpiC	esophagus:	n/a
22	chr1:220921670-220921720	PFSK-1	brain:	n/a
23	chr1:220921614-220921664	BE2_C	brain:	n/a
24	chr1:220922123-220922173	ProgFib	skin:	n/a
25	chr1:220921611-220921661	NHBE	bronchial:	n/a
26	chr1:220921216-220921266	BE2_C	brain:	n/a
27	chr1:220922163-220922213	PrEC	prostate:	n/a
28	chr1:220921306-220921356	A549	lung:	n/a
29	chr1:220921412-220921462	HL-60	blood:	n/a
30	chr1:220922046-220922096	HIPEpiC	eye:	n/a
31	chr1:220921614-220921664	SKMC	muscle:	n/a
32	chr1:220921859-220921909	HRPEpiC	eye:	n/a
33	chr1:220921532-220921582	A549	lung:	n/a
34	chr1:220921412-220921462	CMK	blood:	n/a
35	chr1:220921432-220921482	HCF	heart:	n/a
36	chr1:220922123-220922173	HEK293	kidney:	embryo
37	chr1:220922123-220922173	ovcar-3	ovarian:	n/a
38	chr1:220922217-220922267	ovcar-3	ovarian:	n/a
39	chr1:220921216-220921266	GM12891	blood:	n/a
40	chr1:220922046-220922096	BE2_C	brain:	n/a
41	chr1:220921611-220921661	ProgFib	skin:	n/a
42	chr1:220921614-220921664	HepG2	liver:	n/a
43	chr1:220921859-220921909	HEEpiC	esophagus:	n/a
44	chr1:220921611-220921661	AG04450	lung:	fetal
45	chr1:220922123-220922173	SK-N-MC	brain:	n/a
46	chr1:220921611-220921661	HCPEpiC	choroid plexus:	n/a
47	chr1:220921532-220921582	CMK	blood:	n/a
48	chr1:220922046-220922096	K562	blood:	n/a
49	chr1:220922163-220922213	AG09319	gingival:	n/a
50	chr1:220921614-220921664	PFSK-1	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:220922191..220924696-chr1:220926273..220928216,2	MCF-7	breast:
2	chr1:220920532..220923272-chr1:220926936..220929369,4	MCF-7	breast:
3	chr1:220862132..220866220-chr1:220920879..220923309,4	MCF-7	breast:
4	chr1:220915318..220916858-chr1:220919802..220921393,2	MCF-7	breast:
5	chr1:220921708..220923550-chr1:220934385..220936474,2	MCF-7	breast:
6	chr1:202857727..202858610-chr1:220921308..220922105,2	Hela-S3	cervix:
7	chr1:220920087..220922800-chr1:220958239..220960991,2	MCF-7	breast:
8	chr1:220921252..220921799-chr7:128695148..128695707,2	NB4	blood:
9	chr1:220920704..220923005-chr1:220929506..220932087,2	MCF-7	breast:

No data

Variant related genes	Relation type
MARC2	TF binding region
MARC2	CpG island
ENSG00000117791	chromatin interactions
ENSG00000162817	chromatin interactions
ENSG00000183155	chromatin interactions
ENSG00000186205	chromatin interactions
ENSG00000064419	chromatin interactions

Extended variants
information (count: 152 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:152 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565844361	chr1:220919057-220919058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534714989	chr1:220919060-220919061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12058891	chr1:220919065-220919066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs577662178	chr1:220919066-220919067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189556775	chr1:220919082-220919083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6699853	chr1:220919164-220919165	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs576357700	chr1:220919186-220919187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181562491	chr1:220919190-220919191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561962100	chr1:220919217-220919218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs234223	chr1:220919232-220919233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs376086984	chr1:220919248-220919249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564471912	chr1:220919255-220919256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533459967	chr1:220919287-220919288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369671158	chr1:220919298-220919299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185801912	chr1:220919335-220919336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550873409	chr1:220919370-220919371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563669267	chr1:220919388-220919389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571059259	chr1:220919469-220919470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559965201	chr1:220919483-220919484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529216614	chr1:220919550-220919551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549256484	chr1:220919552-220919553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565883176	chr1:220919579-220919580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150564788	chr1:220919703-220919704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551544238	chr1:220919787-220919788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74139892	chr1:220919809-220919810	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs537128088	chr1:220919838-220919839	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190612026	chr1:220919886-220919887	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533376290	chr1:220919913-220919914	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573268011	chr1:220919994-220919995	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs546645289	chr1:220920047-220920048	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs566574635	chr1:220920082-220920083	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs12133663	chr1:220920083-220920084	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555441092	chr1:220920102-220920103	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs111748558	chr1:220920142-220920143	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs572404389	chr1:220920173-220920174	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs569166798	chr1:220920174-220920175	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538166351	chr1:220920179-220920180	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564690056	chr1:220920224-220920225	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs72472364	chr1:220920305-220920306	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs112560055	chr1:220920339-220920340	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543860935	chr1:220920361-220920362	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12738566	chr1:220920374-220920375	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs11800654	chr1:220920386-220920387	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs369908343	chr1:220920405-220920406	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs549394018	chr1:220920473-220920474	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182964758	chr1:220920492-220920493	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs369883800	chr1:220920509-220920510	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs371755147	chr1:220920517-220920518	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72472365	chr1:220920518-220920519	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571392952	chr1:220920520-220920521	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220906400-220921000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:220908400-220920800	Weak transcription	Pancreas	Pancrea
3	chr1:220915600-220919800	Weak transcription	Liver	Liver
4	chr1:220915800-220921400	Weak transcription	Gastric	stomach
5	chr1:220916200-220921200	Weak transcription	Lung	lung
6	chr1:220918600-220921200	Weak transcription	Esophagus	oesophagus
7	chr1:220919400-220920600	Enhancers	Fetal Heart	heart
8	chr1:220919400-220920800	Enhancers	Fetal Intestine Large	intestine
9	chr1:220919400-220920800	Enhancers	Fetal Intestine Small	intestine
10	chr1:220919600-220920800	Enhancers	Duodenum Mucosa	Duodenum
11	chr1:220919800-220920600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
12	chr1:220919800-220920600	Enhancers	Fetal Muscle Leg	muscle
13	chr1:220919800-220920800	Enhancers	Liver	Liver
14	chr1:220919800-220920800	Enhancers	Fetal Lung	lung
15	chr1:220919800-220920800	Bivalent Enhancer	HepG2	liver
16	chr1:220920000-220920200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
17	chr1:220920000-220920800	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr1:220920000-220920800	Enhancers	Fetal Muscle Trunk	muscle
19	chr1:220920000-220920800	Enhancers	A549	lung
20	chr1:220920000-220921000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:220920200-220920400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
22	chr1:220920200-220920400	Enhancers	Aorta	Aorta
23	chr1:220920200-220920600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
24	chr1:220920200-220920800	Enhancers	Fetal Stomach	stomach
25	chr1:220920200-220921000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
26	chr1:220920200-220921200	Enhancers	Placenta	Placenta
27	chr1:220920400-220920600	Enhancers	Stomach Smooth Muscle	stomach
28	chr1:220920400-220920800	Enhancers	Rectal Smooth Muscle	rectum
29	chr1:220920400-220921000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr1:220920400-220921000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr1:220920400-220921400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
32	chr1:220920600-220920800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:220920600-220920800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr1:220920600-220920800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr1:220920600-220920800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:220920600-220920800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:220920600-220920800	Enhancers	Adipose Nuclei	Adipose
38	chr1:220920600-220920800	Enhancers	Colon Smooth Muscle	Colon
39	chr1:220920600-220920800	Enhancers	Fetal Brain Female	brain
40	chr1:220920600-220920800	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr1:220920600-220920800	Enhancers	Hela-S3	cervix
42	chr1:220920600-220921000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:220920600-220921200	Flanking Active TSS	Fetal Heart	heart
44	chr1:220920600-220921400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
45	chr1:220920600-220921400	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr1:220920600-220921600	Flanking Active TSS	Fetal Muscle Leg	muscle
47	chr1:220920600-220922600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
48	chr1:220920600-220922800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
49	chr1:220920800-220921000	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:220920800-220921000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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