Variant report

Variant	nsv1008402
Chromosome Location	chr3:232495-274182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:1224)
Chromatin interactive
region (count:0)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:247 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:254098-254530	GM12878	blood:	n/a	n/a
2	ATF2	chr3:254017-254518	GM12878	blood:	n/a	n/a
3	BACH1	chr3:238826-240389	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:271174-271333	K562	blood:	n/a	n/a
5	BACH1	chr3:238302-238499	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:254085-254416	GM12878	blood:	n/a	n/a
7	BATF	chr3:259675-259847	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:260263-260618	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:260829-261058	GM12878	blood:	n/a	n/a
10	CCNT2	chr3:238979-239034	K562	blood:	n/a	n/a
11	CEBPB	chr3:244050-244226	H1-hESC	embryonic stem cell:	n/a	chr3:244109-244120
12	CEBPB	chr3:242454-242771	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:243949-244303	HepG2	liver:	n/a	chr3:244109-244120
14	CEBPB	chr3:243974-244307	A549	lung:	n/a	chr3:244109-244120
15	CEBPB	chr3:242500-242742	K562	blood:	n/a	n/a
16	CEBPB	chr3:243976-244300	IMR90	lung:	n/a	chr3:244109-244120
17	CEBPB	chr3:271018-271333	H1-hESC	embryonic stem cell:	n/a	chr3:271305-271317
18	CEBPB	chr3:242440-242811	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:242447-242817	IMR90	lung:	n/a	n/a
20	CEBPB	chr3:242488-242808	A549	lung:	n/a	n/a
21	CHD1	chr3:239582-239589	GM12878	blood:	n/a	n/a
22	CHD1	chr3:238324-238476	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr3:239219-239240	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr3:238225-238590	GM12878	blood:	n/a	n/a
25	CREB1	chr3:254049-254528	GM12878	blood:	n/a	n/a
26	CTBP2	chr3:238125-240202	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr3:249720-249870	GM12872	blood:	n/a	n/a
28	CTCF	chr3:237400-237550	HPF	lung:	n/a	n/a
29	CTCF	chr3:237320-237470	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr3:239600-239750	GM12869	blood:	n/a	n/a
31	CTCF	chr3:249780-249930	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr3:239640-239790	GM12872	blood:	n/a	n/a
33	CTCF	chr3:249820-249970	GM12873	blood:	n/a	n/a
34	CTCF	chr3:249811-249893	HepG2	liver:	n/a	n/a
35	CTCF	chr3:239860-240010	GM12867	blood:	n/a	n/a
36	CTCF	chr3:249780-249930	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:249740-249890	GM12875	blood:	n/a	n/a
38	CTCF	chr3:249783-249898	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:249791-249910	GM20000	blood:	n/a	n/a
40	CTCF	chr3:249740-249890	GM12872	blood:	n/a	n/a
41	CTCF	chr3:249460-249610	HAc	cerebellar:	n/a	n/a
42	CTCF	chr3:249660-249810	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr3:239180-239330	GM12871	blood:	n/a	n/a
44	CTCF	chr3:249700-249850	GM12873	blood:	n/a	n/a
45	CTCF	chr3:237460-237610	HRE	kidney:	n/a	n/a
46	CTCF	chr3:249800-249950	GM12864	blood:	n/a	n/a
47	CTCF	chr3:249820-249970	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr3:249720-249870	HRE	kidney:	n/a	n/a
49	CTCF	chr3:249667-250017	GM12878	blood:	n/a	n/a
50	CTCF	chr3:249791-249929	GM12878	blood:	n/a	n/a

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:238611-238661	HRE	kidney:	n/a
2	chr3:240139-240189	HepG2	liver:	n/a
3	chr3:239229-239279	Hela-S3	cervix:	n/a
4	chr3:238496-238546	AoSMC	blood vessel:	n/a
5	chr3:238611-238661	HRE	kidney:	n/a
6	chr3:240139-240189	HepG2	liver:	n/a
7	chr3:239229-239279	Hela-S3	cervix:	n/a
8	chr3:238496-238546	AoSMC	blood vessel:	n/a
9	chr3:271185-271235	SK-N-SH_RA	brain:	n/a
10	chr3:239229-239279	NT2-D1	testis:	n/a
11	chr3:238618-238668	NH-A	brain:	n/a
12	chr3:238611-238661	LNCaP	prostate:	n/a
13	chr3:236078-236128	HAEpiC	amniotic membrane:	n/a
14	chr3:239207-239257	Hepatocyte	liver:	n/a
15	chr3:239665-239715	ProgFib	skin:	n/a
16	chr3:239229-239279	NH-A	brain:	n/a
17	chr3:243996-244046	RPTEC	kidney:	n/a
18	chr3:239188-239238	NT2-D1	testis:	n/a
19	chr3:238161-238211	HEK293	kidney:	embryo
20	chr3:238048-238098	GM12891	blood:	n/a
21	chr3:239229-239279	GM12878	blood:	n/a
22	chr3:238048-238098	A549	lung:	n/a
23	chr3:240139-240189	MCF-7	breast:	n/a
24	chr3:239229-239279	Hepatocyte	liver:	n/a
25	chr3:239229-239279	AG04450	lung:	fetal
26	chr3:239506-239556	K562	blood:	n/a
27	chr3:240139-240189	Hepatocyte	liver:	n/a
28	chr3:240139-240189	HCPEpiC	choroid plexus:	n/a
29	chr3:241182-241232	MCF-7	breast:	n/a
30	chr3:241182-241232	AG10803	skin:	n/a
31	chr3:238618-238668	AG09319	gingival:	n/a
32	chr3:240139-240189	AG09319	gingival:	n/a
33	chr3:239229-239279	NHDF-neo	bronchial:	n/a
34	chr3:239506-239556	Caco-2	colon:	n/a
35	chr3:238931-238981	Caco-2	colon:	n/a
36	chr3:238392-238442	H1-hESC	embryonic stem cell:	embryo
37	chr3:271185-271235	HMEC	breast:	n/a
38	chr3:239665-239715	SAEC	small airway:	n/a
39	chr3:238318-238368	MCF-7	breast:	n/a
40	chr3:239665-239715	HL-60	blood:	n/a
41	chr3:239665-239715	HMEC	breast:	n/a
42	chr3:240139-240189	ECC-1	luminal epithelium:	n/a
43	chr3:238931-238981	PANC-1	pancreas:	n/a
44	chr3:238618-238668	H1-hESC	embryonic stem cell:	embryo
45	chr3:243996-244046	LNCaP	prostate:	n/a
46	chr3:238931-238981	HEEpiC	esophagus:	n/a
47	chr3:243996-244046	HEEpiC	esophagus:	n/a
48	chr3:238931-238981	Hela-S3	cervix:	n/a
49	chr3:238392-238442	HRPEpiC	eye:	n/a
50	chr3:239229-239279	HEEpiC	esophagus:	n/a

No data

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
2	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
3	lnc-IL5RA-6	chr3:237540-237597	NONHSAT087559
4	lnc-CNTN6-7	chr3:239697-239775	NONHSAT087562
5	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
6	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
7	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
8	lnc-IL5RA-6	chr3:238139-238386	NONHSAT087559
9	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
10	lnc-CNTN6-7	chr3:238454-238746	NONHSAT087560
11	lnc-CNTN6-7	chr3:254887-255362	NONHSAT087562
12	lnc-IL5RA-6	chr3:238650-239024	ENSG00000224318.1
13	lnc-CNTN6-7	chr3:239326-239775	NONHSAT087561
14	lnc-IL5RA-6	chr3:238290-238385	ENSG00000224318.1
15	lnc-IL5RA-6	chr3:238290-238542	ENSG00000224318.1
16	lnc-IL5RA-6	chr3:237679-237723	NONHSAT087559
17	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
18	lnc-IL5RA-6	chr3:238650-238882	ENSG00000224318.1
19	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
20	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1

No data

Variant related genes	Relation type
CHL1-AS2	TF binding region
CHL1	TF binding region
CHL1-AS2	CpG island
CHL1	CpG island

Extended variants
information (count: 1931 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1931 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565828779	chr3:233612-233613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527394707	chr3:233653-233654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536499007	chr3:233676-233677	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs554808861	chr3:233678-233679	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs569827349	chr3:233687-233688	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs191197208	chr3:233713-233714	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147742006	chr3:233736-233737	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs368812162	chr3:233744-233745	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs73814162	chr3:233747-233748	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs577995689	chr3:233758-233759	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs545063805	chr3:233818-233819	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs549525539	chr3:233839-233840	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs68172753	chr3:233889-233890	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs551915513	chr3:233905-233906	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs542870415	chr3:233910-233911	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs561159661	chr3:233915-233916	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs375947152	chr3:233965-233966	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs183745454	chr3:233975-233976	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs142659942	chr3:233990-233991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532175464	chr3:233993-233994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189714918	chr3:234051-234052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559256309	chr3:234062-234063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75329730	chr3:234095-234096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181354987	chr3:234122-234123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186788367	chr3:234137-234138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537227826	chr3:234183-234184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550288385	chr3:234215-234216	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs565691475	chr3:234217-234218	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs539073458	chr3:234234-234235	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs553887114	chr3:234239-234240	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs572071992	chr3:234247-234248	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs190032429	chr3:234265-234266	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs554823671	chr3:234285-234286	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs576266404	chr3:234293-234294	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs111482717	chr3:234317-234318	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs550196022	chr3:234329-234330	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs571954120	chr3:234359-234360	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs538601466	chr3:234366-234367	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs546241958	chr3:234368-234369	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs553759183	chr3:234370-234371	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs370779805	chr3:234399-234400	Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs370878789	chr3:234429-234430	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs138911566	chr3:234436-234437	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs576869345	chr3:234440-234441	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs541082367	chr3:234449-234450	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs116810567	chr3:234457-234458	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529686739	chr3:234463-234464	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs368786980	chr3:234481-234482	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs548538286	chr3:234487-234488	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs13086137	chr3:234489-234490	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:233600-233800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:233600-234400	Enhancers	Primary B cells from peripheral blood	blood
3	chr3:233800-235000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:234200-234800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr3:234600-234800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr3:235000-235200	Enhancers	Fetal Brain Female	brain
7	chr3:235000-236000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr3:235200-236000	Weak transcription	Fetal Brain Female	brain
9	chr3:235400-236600	Enhancers	Fetal Brain Male	brain
10	chr3:235800-236000	Enhancers	Adipose Nuclei	Adipose
11	chr3:235800-236400	Enhancers	Spleen	Spleen
12	chr3:235800-237000	Enhancers	Ovary	ovary
13	chr3:236000-236200	Flanking Active TSS	Adipose Nuclei	Adipose
14	chr3:236000-236400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr3:236000-236600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr3:236000-236800	Enhancers	Fetal Brain Female	brain
17	chr3:236200-236400	Enhancers	Brain Cingulate Gyrus	brain
18	chr3:236200-236400	Enhancers	Brain Substantia Nigra	brain
19	chr3:236200-237800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr3:236400-237000	Enhancers	Brain Germinal Matrix	brain
21	chr3:236400-237400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr3:236400-238200	Weak transcription	Spleen	Spleen
23	chr3:236600-237200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr3:236600-237200	Flanking Active TSS	Fetal Brain Male	brain
25	chr3:236800-238000	Active TSS	Fetal Brain Female	brain
26	chr3:237000-237200	Active TSS	Brain Germinal Matrix	brain
27	chr3:237000-237800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr3:237000-237800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:237000-240400	Active TSS	Ovary	ovary
30	chr3:237200-237400	Flanking Active TSS	Brain Germinal Matrix	brain
31	chr3:237200-237600	Active TSS	Brain Cingulate Gyrus	brain
32	chr3:237200-237800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr3:237200-240000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr3:237200-240200	Active TSS	Brain Anterior Caudate	brain
35	chr3:237200-241000	Active TSS	Brain Angular Gyrus	brain
36	chr3:237200-241000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:237200-241000	Active TSS	Fetal Brain Male	brain
38	chr3:237400-237600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr3:237400-241200	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr3:237600-237800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
41	chr3:237600-237800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
42	chr3:237600-240000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
43	chr3:237600-240200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
44	chr3:237600-241200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
45	chr3:237800-238000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
46	chr3:237800-238000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:237800-238000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr3:237800-238000	Active TSS	Brain Substantia Nigra	brain
49	chr3:237800-238200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
50	chr3:237800-238200	Bivalent Enhancer	Primary B cells from cord blood	blood

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