Variant report

Variant	nsv520660
Chromosome Location	chr2:47590034-47601106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:509)
CpG islands
(count:734)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:47600972-47601258	HepG2	liver:	n/a	chr2:47601231-47601247 chr2:47601232-47601248
2	ARID3A	chr2:47601036-47601225	K562	blood:	n/a	n/a
3	ATF2	chr2:47595993-47596516	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:47595969-47596216	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr2:47596268-47596439	K562	blood:	n/a	n/a
6	ATF3	chr2:47596129-47596540	K562	blood:	n/a	n/a
7	ATF3	chr2:47596170-47596573	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr2:47596157-47596491	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr2:47596201-47596607	HepG2	liver:	n/a	n/a
10	BACH1	chr2:47596066-47596613	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr2:47601101-47601133	K562	blood:	n/a	n/a
12	BHLHE40	chr2:47596415-47596567	K562	blood:	n/a	n/a
13	BHLHE40	chr2:47600966-47601276	HepG2	liver:	n/a	n/a
14	CCNT2	chr2:47596102-47597274	K562	blood:	n/a	n/a
15	CEBPD	chr2:47597014-47597295	HepG2	liver:	n/a	n/a
16	CEBPD	chr2:47596183-47596513	HepG2	liver:	n/a	n/a
17	CHD1	chr2:47596738-47597225	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr2:47597003-47597204	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr2:47596164-47596757	K562	blood:	n/a	n/a
20	CHD2	chr2:47595961-47596630	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr2:47596218-47596619	HepG2	liver:	n/a	n/a
22	CHD2	chr2:47596191-47596365	Hela-S3	cervix:	n/a	n/a
23	CREB1	chr2:47596030-47597404	HepG2	liver:	n/a	n/a
24	CREB1	chr2:47596017-47596952	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr2:47596076-47596649	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTBP2	chr2:47596148-47597467	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr2:47601020-47601205	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:47596780-47596930	BJ	skin:	n/a	n/a
29	CTCF	chr2:47596646-47596673	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:47601060-47601210	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr2:47600868-47601303	K562	blood:	n/a	n/a
32	CTCF	chr2:47597060-47597210	HepG2	liver:	n/a	chr2:47597093-47597106 chr2:47597096-47597109
33	CTCF	chr2:47601018-47601210	Gliobla	brain:	n/a	n/a
34	CTCF	chr2:47596391-47596516	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:47601020-47601170	GM12869	blood:	n/a	n/a
36	CTCF	chr2:47601020-47601170	Caco-2	colon:	n/a	n/a
37	CTCF	chr2:47601080-47601230	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:47596520-47596670	GM12874	blood:	n/a	n/a
39	CTCF	chr2:47601040-47601190	HRE	kidney:	n/a	n/a
40	CTCF	chr2:47601080-47601230	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr2:47596624-47596709	A549	lung:	n/a	n/a
42	CTCF	chr2:47596620-47596770	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr2:47601040-47601190	HMEC	breast:	n/a	n/a
44	CTCF	chr2:47601018-47601192	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:47601060-47601210	RPTEC	kidney:	n/a	n/a
46	CTCF	chr2:47596566-47596737	NHEK	skin:	n/a	n/a
47	CTCF	chr2:47600932-47601240	GM12878	blood:	n/a	n/a
48	CTCF	chr2:47601060-47601210	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr2:47596887-47597000	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:47601060-47601210	GM12873	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:47597118-47597168	HL-60	blood:	n/a
2	chr2:47596787-47596837	SK-N-SH	brain:	n/a
3	chr2:47597118-47597168	HL-60	blood:	n/a
4	chr2:47596787-47596837	SK-N-SH	brain:	n/a
5	chr2:47597331-47597381	Caco-2	colon:	n/a
6	chr2:47597331-47597381	MCF10A-Er-Src	breast:	n/a
7	chr2:47596073-47596123	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:47600173-47600223	RPTEC	kidney:	n/a
9	chr2:47596410-47596460	GM12878	blood:	n/a
10	chr2:47596185-47596235	HRCEpiC	kidney:	n/a
11	chr2:47596185-47596235	HCM	heart:	n/a
12	chr2:47597331-47597381	MCF-7	breast:	n/a
13	chr2:47597331-47597381	ECC-1	luminal epithelium:	n/a
14	chr2:47595507-47595557	PrEC	prostate:	n/a
15	chr2:47597118-47597168	PrEC	prostate:	n/a
16	chr2:47596136-47596186	RPTEC	kidney:	n/a
17	chr2:47597118-47597168	AG04449	skin:	fetal
18	chr2:47596073-47596123	NB4	blood:	n/a
19	chr2:47596912-47596962	HAEpiC	amniotic membrane:	n/a
20	chr2:47596073-47596123	SK-N-MC	brain:	n/a
21	chr2:47596787-47596837	IMR90	lung:	fetal
22	chr2:47596073-47596123	HRE	kidney:	n/a
23	chr2:47596185-47596235	NH-A	brain:	n/a
24	chr2:47600173-47600223	HNPCEpiC	eye:	n/a
25	chr2:47597331-47597381	U87	brain:	n/a
26	chr2:47596430-47596480	NH-A	brain:	n/a
27	chr2:47600173-47600223	SAEC	small airway:	n/a
28	chr2:47597188-47597238	HRE	kidney:	n/a
29	chr2:47596136-47596186	U87	brain:	n/a
30	chr2:47595507-47595557	MCF10A-Er-Src	breast:	n/a
31	chr2:47597331-47597381	SK-N-SH	brain:	n/a
32	chr2:47596185-47596235	NT2-D1	testis:	n/a
33	chr2:47597118-47597168	IMR90	lung:	fetal
34	chr2:47596185-47596235	HCF	heart:	n/a
35	chr2:47595507-47595557	GM12878	blood:	n/a
36	chr2:47600173-47600223	PANC-1	pancreas:	n/a
37	chr2:47596430-47596480	GM12892	blood:	n/a
38	chr2:47596787-47596837	AoSMC	blood vessel:	n/a
39	chr2:47597188-47597238	HCPEpiC	choroid plexus:	n/a
40	chr2:47596136-47596186	HUVEC	blood vessel:	n/a
41	chr2:47596136-47596186	AG04449	skin:	fetal
42	chr2:47595507-47595557	ProgFib	skin:	n/a
43	chr2:47596136-47596186	AG09309	skin:	n/a
44	chr2:47596136-47596186	ECC-1	luminal epithelium:	n/a
45	chr2:47596410-47596460	GM12892	blood:	n/a
46	chr2:47597188-47597238	HRCEpiC	kidney:	n/a
47	chr2:47595507-47595557	NH-A	brain:	n/a
48	chr2:47596073-47596123	NH-A	brain:	n/a
49	chr2:47596136-47596186	HNPCEpiC	eye:	n/a
50	chr2:47596912-47596962	HRE	kidney:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:47570861..47572963-chr2:47596345..47598113,2	K562	blood:
2	chr2:47559485..47574826-chr2:47594341..47605593,65	MCF-7	breast:
3	chr2:47402779..47405652-chr2:47594724..47597829,3	K562	blood:
4	chr13:115000491..115001056-chr2:47597036..47597630,2	Hela-S3	cervix:
5	chr2:47572145..47573948-chr2:47589350..47592537,3	MCF-7	breast:
6	chr2:47595432..47597958-chr2:47630032..47632167,2	K562	blood:
7	chr2:47401421..47404385-chr2:47596204..47598281,3	MCF-7	breast:
8	chr2:47560518..47577182-chr2:47592669..47600258,43	MCF-7	breast:
9	chr2:47592763..47599978-chr2:47628456..47631890,7	K562	blood:
10	chr2:47588711..47590901-chr2:47594534..47597934,4	MCF-7	breast:
11	chr2:47595241..47598489-chr2:47628033..47632018,10	MCF-7	breast:
12	chr2:47596733..47599007-chr2:47599869..47602231,2	K562	blood:
13	chr17:62502573..62503177-chr2:47596612..47597409,2	Hela-S3	cervix:
14	chr2:47587435..47591464-chr2:47593988..47597001,4	K562	blood:
15	chr2:47598530..47600190-chr2:47604958..47607928,2	K562	blood:
16	chr2:47569761..47572467-chr2:47587479..47590349,2	MCF-7	breast:
17	chr2:47601008..47603575-chr2:47604857..47606633,2	K562	blood:
18	chr16:67280874..67281536-chr2:47596664..47597309,2	Hela-S3	cervix:
19	chr2:47586945..47591052-chr2:47593988..47597569,4	K562	blood:
20	chr2:47592495..47594332-chr2:47629734..47631747,2	K562	blood:
21	chr2:47401904..47404708-chr2:47598417..47601115,2	MCF-7	breast:
22	chr2:47591536..47594124-chr20:52549587..52551175,2	MCF-7	breast:
23	chr2:47580625..47583469-chr2:47590041..47591979,2	MCF-7	breast:
24	chr2:47597774..47599287-chr2:47627700..47629210,2	MCF-7	breast:
25	chr2:47596130..47596899-chr3:180319390..180320186,2	HCT-116	colon:
26	chr2:47587881..47592394-chr2:47594664..47598225,6	MCF-7	breast:

No data

Variant related genes	Relation type
MIR559	TF binding region
RN7SKP119	TF binding region
EPCAM	TF binding region
MIR559	CpG island
RN7SKP119	CpG island
EPCAM	CpG island
ENSG00000119888	chromatin interactions
ENSG00000135723	chromatin interactions
ENSG00000095002	chromatin interactions
ENSG00000143933	chromatin interactions
ENSG00000163728	chromatin interactions
ENSG00000234690	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000258890	chromatin interactions
ENSG00000130177	chromatin interactions
ENSG00000239774	chromatin interactions

Extended variants
information (count: 547 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4399763	chr2:47590034-47590035	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556133885	chr2:47590041-47590042	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186270327	chr2:47590047-47590048	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs117669405	chr2:47590049-47590050	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs75057043	chr2:47590055-47590056	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs4614976	chr2:47590070-47590071	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs561100428	chr2:47590078-47590079	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527851477	chr2:47590107-47590108	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs542867480	chr2:47590117-47590118	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs7608471	chr2:47590128-47590129	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528959350	chr2:47590129-47590130	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs550692444	chr2:47590203-47590204	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562429075	chr2:47590223-47590224	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs4550710	chr2:47590275-47590276	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs551674819	chr2:47590299-47590300	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373307606	chr2:47590343-47590344	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566791353	chr2:47590374-47590375	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs113804803	chr2:47590390-47590391	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
19	rs144678118	chr2:47590393-47590394	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs377233269	chr2:47590428-47590429	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs567503151	chr2:47590438-47590439	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs531798391	chr2:47590450-47590451	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs148492886	chr2:47590451-47590452	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs190783357	chr2:47590495-47590496	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs79566107	chr2:47590510-47590511	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs529877849	chr2:47590638-47590639	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs376214098	chr2:47590639-47590640	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs72882752	chr2:47590662-47590663	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs150576772	chr2:47590730-47590731	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs4952884	chr2:47590762-47590763	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs181649093	chr2:47590765-47590766	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs62139663	chr2:47590779-47590780	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs576588935	chr2:47590798-47590799	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs543925300	chr2:47590815-47590816	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs139581308	chr2:47590817-47590818	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs143339426	chr2:47590849-47590850	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs551383749	chr2:47590851-47590852	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs146705385	chr2:47590919-47590920	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7609348	chr2:47590930-47590931	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186654809	chr2:47590942-47590943	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs567306849	chr2:47590977-47590978	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs111987454	chr2:47590982-47590983	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs140276430	chr2:47590989-47590990	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs74794860	chr2:47591000-47591001	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
45	rs375552545	chr2:47591021-47591022	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs144013359	chr2:47591087-47591088	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs548723984	chr2:47591112-47591113	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs538780969	chr2:47591115-47591116	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs568689747	chr2:47591154-47591155	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540453792	chr2:47591155-47591156	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Myelofibrosis	22110671	CNVD
Hypotonia	17579669	CNVD
Hypotonia-Cystinuria syndrome	16385448	CNVD
Glioblastoma multiforme	17002787	CNVD
Cystinuria	17625506	CNVD
Breast cancer	16272173	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	22355333	CNVD
Colorectal cancer	17569143	CNVD
Hereditary non-polyposis colorectal cancer	16941473	CNVD
Lynch syndrome	16541406	CNVD
Non-syndromic sensorineural hearing loss	19173287	CNVD
Hereditary non-polyposis colorectal cancer	17228328	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Lynch syndrome	20937110	CNVD
Breast cancer	20616022	CNVD
Colorectal cancer	18708397	CNVD
Endometrial cancer	18708397	CNVD
Lynch syndrome	18708397	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD

Chromatin state (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47587000-47595600	Weak transcription	Colonic Mucosa	Colon
2	chr2:47588600-47595600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:47588600-47595800	Weak transcription	HMEC	breast
4	chr2:47589600-47595000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr2:47589600-47595200	Weak transcription	Fetal Intestine Small	intestine
6	chr2:47589600-47596200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr2:47592200-47592400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:47595000-47595800	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr2:47595000-47596200	Weak transcription	Right Atrium	heart
10	chr2:47595200-47596000	Enhancers	Fetal Intestine Small	intestine
11	chr2:47595600-47595800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr2:47595600-47595800	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr2:47595600-47595800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:47595600-47595800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:47595600-47595800	Enhancers	Colonic Mucosa	Colon
16	chr2:47595600-47595800	Enhancers	Fetal Intestine Large	intestine
17	chr2:47595600-47595800	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr2:47595600-47596000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr2:47595600-47596000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr2:47595600-47596000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:47595600-47596000	Enhancers	Pancreas	Pancrea
22	chr2:47595600-47596600	Bivalent/Poised TSS	Small Intestine	intestine
23	chr2:47595800-47596000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
24	chr2:47595800-47596000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
25	chr2:47595800-47596000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:47595800-47596000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr2:47595800-47596000	Bivalent Enhancer	Fetal Intestine Large	intestine
28	chr2:47595800-47596000	Enhancers	HMEC	breast
29	chr2:47595800-47596200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr2:47595800-47596200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr2:47595800-47596200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:47595800-47596200	Weak transcription	Colonic Mucosa	Colon
33	chr2:47595800-47596200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
34	chr2:47595800-47596400	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr2:47595800-47596600	Bivalent Enhancer	Primary B cells from cord blood	blood
36	chr2:47595800-47596800	Active TSS	Rectal Mucosa Donor 31	rectum
37	chr2:47595800-47597000	Active TSS	A549	lung
38	chr2:47595800-47598000	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr2:47595800-47598200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:47595800-47598400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
41	chr2:47595800-47599200	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr2:47596000-47596200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:47596000-47596200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:47596000-47596200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr2:47596000-47596200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
46	chr2:47596000-47596200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
47	chr2:47596000-47596200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:47596000-47596200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr2:47596000-47596200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr2:47596000-47596200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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