Variant report

Variant	nsv822137
Chromosome Location	chr3:75626829-75762956
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4423)
CpG islands
(count:3482)
Chromatin interactive
region (count:7)
LncRNA
region (count:21)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:4423 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
2	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
3	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
6	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
7	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
8	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
9	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
10	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
11	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
12	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
13	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
14	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
15	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
16	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
17	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
18	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
19	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
20	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
21	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
22	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
23	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
24	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
25	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
26	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
27	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
28	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
29	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
30	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
31	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
32	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
33	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
34	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
35	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
36	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
37	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
38	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
39	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
40	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
41	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
42	ATF3	chr3:75717987-75718165	K562	blood:	n/a	n/a
43	ATF3	chr3:75718289-75718505	K562	blood:	n/a	n/a
44	BACH1	chr3:75739253-75739499	K562	blood:	n/a	n/a
45	BACH1	chr3:75744812-75745060	K562	blood:	n/a	n/a
46	BACH1	chr3:75704919-75705249	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr3:75740483-75740494	K562	blood:	n/a	n/a
48	BACH1	chr3:75734445-75734852	K562	blood:	n/a	n/a
49	BACH1	chr3:75710659-75710761	K562	blood:	n/a	n/a
50	BACH1	chr3:75693848-75694086	K562	blood:	n/a	n/a

(count:3482 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75668035-75668085	SKMC	muscle:	n/a
2	chr3:75679454-75679504	NHBE	bronchial:	n/a
3	chr3:75657758-75657808	IMR90	lung:	fetal
4	chr3:75668924-75668974	HRCEpiC	kidney:	n/a
5	chr3:75705108-75705158	Hepatocyte	liver:	n/a
6	chr3:75668035-75668085	SKMC	muscle:	n/a
7	chr3:75679454-75679504	NHBE	bronchial:	n/a
8	chr3:75657758-75657808	IMR90	lung:	fetal
9	chr3:75668924-75668974	HRCEpiC	kidney:	n/a
10	chr3:75705108-75705158	Hepatocyte	liver:	n/a
11	chr3:75658490-75658540	PANC-1	pancreas:	n/a
12	chr3:75632533-75632583	HL-60	blood:	n/a
13	chr3:75708104-75708154	NB4	blood:	n/a
14	chr3:75631426-75631476	HRCEpiC	kidney:	n/a
15	chr3:75712404-75712454	HUVEC	blood vessel:	n/a
16	chr3:75719149-75719199	IMR90	lung:	fetal
17	chr3:75628932-75628982	HCT-116	colon:	n/a
18	chr3:75632533-75632583	GM19239	blood:	n/a
19	chr3:75715783-75715833	MCF10A-Er-Src	breast:	n/a
20	chr3:75704573-75704623	SKMC	muscle:	n/a
21	chr3:75658552-75658602	HRCEpiC	kidney:	n/a
22	chr3:75668627-75668677	SK-N-MC	brain:	n/a
23	chr3:75668924-75668974	U87	brain:	n/a
24	chr3:75701993-75702043	AG04450	lung:	fetal
25	chr3:75669109-75669159	SK-N-SH_RA	brain:	n/a
26	chr3:75707805-75707855	HCM	heart:	n/a
27	chr3:75629433-75629483	RPTEC	kidney:	n/a
28	chr3:75659629-75659679	A549	lung:	n/a
29	chr3:75721888-75721938	HepG2	liver:	n/a
30	chr3:75628819-75628869	GM12878	blood:	n/a
31	chr3:75666381-75666431	HEK293	kidney:	embryo
32	chr3:75707990-75708040	ovcar-3	ovarian:	n/a
33	chr3:75704498-75704548	U87	brain:	n/a
34	chr3:75669109-75669159	AoSMC	blood vessel:	n/a
35	chr3:75717453-75717503	ovcar-3	ovarian:	n/a
36	chr3:75717453-75717503	AG09309	skin:	n/a
37	chr3:75666381-75666431	RPTEC	kidney:	n/a
38	chr3:75669109-75669159	HEEpiC	esophagus:	n/a
39	chr3:75629433-75629483	NHBE	bronchial:	n/a
40	chr3:75671115-75671165	AG04450	lung:	fetal
41	chr3:75715783-75715833	AoSMC	blood vessel:	n/a
42	chr3:75668758-75668808	K562	blood:	n/a
43	chr3:75679454-75679504	HCM	heart:	n/a
44	chr3:75653319-75653369	MCF-7	breast:	n/a
45	chr3:75629433-75629483	MCF10A-Er-Src	breast:	n/a
46	chr3:75705922-75705972	GM06990	blood:	n/a
47	chr3:75668035-75668085	HCPEpiC	choroid plexus:	n/a
48	chr3:75657758-75657808	NT2-D1	testis:	n/a
49	chr3:75658410-75658460	PrEC	prostate:	n/a
50	chr3:75708104-75708154	SKMC	muscle:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:
2	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
3	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
4	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
5	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
6	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
7	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
2	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
3	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
4	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
5	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
6	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
7	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
8	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
9	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
10	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
11	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
12	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
13	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
14	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
15	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
16	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
17	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
18	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
19	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
20	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
21	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1324	chr3:75679974-75679997	MIMAT0005956

No data

Variant related genes	Relation type
UNC93B3	TF binding region
FRG2C	TF binding region
ENSG00000243422	TF binding region
ENSG00000239383	TF binding region
LINC00960	TF binding region
OR7E121P	TF binding region
RARRES2P1	TF binding region
AGGF1P3	TF binding region
RN7SL92P	TF binding region
ENSG00000236138	TF binding region
ENSG00000272710	TF binding region
MIR1324	TF binding region
UNC93B3	CpG island
FRG2C	CpG island
ENSG00000243422	CpG island
ENSG00000239383	CpG island
LINC00960	CpG island
OR7E121P	CpG island
RARRES2P1	CpG island
AGGF1P3	CpG island
RN7SL92P	CpG island
ENSG00000236138	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000236829	chromatin interactions
ENSG00000232815	chromatin interactions
ENSG00000129925	chromatin interactions

Extended variants
information (count: 9094 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:9094 , 50 per page) page: 1 2 3 4 5 6 7 ... 182

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72501827	chr3:75626857-75626858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs201415006	chr3:75626881-75626882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369027347	chr3:75626892-75626893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs199543079	chr3:75626920-75626921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs200820957	chr3:75626941-75626942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs58061534	chr3:75626958-75626959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201838266	chr3:75626961-75626962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs377012734	chr3:75627079-75627080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199669785	chr3:75627080-75627081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200571502	chr3:75627144-75627145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113090904	chr3:75627148-75627149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200144761	chr3:75627189-75627190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6769396	chr3:75627233-75627234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376314787	chr3:75627243-75627244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201267517	chr3:75627249-75627250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140003112	chr3:75627270-75627271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538927977	chr3:75627312-75627313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553486006	chr3:75627316-75627317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563565654	chr3:75627345-75627346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369505257	chr3:75627346-75627347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6809521	chr3:75627356-75627357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6794874	chr3:75627382-75627383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6807053	chr3:75627383-75627384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370356704	chr3:75627387-75627388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373279321	chr3:75627421-75627422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201708172	chr3:75627479-75627480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199923514	chr3:75627508-75627509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113306843	chr3:75627699-75627700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs6795222	chr3:75627704-75627705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375507169	chr3:75627811-75627812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114986729	chr3:75627819-75627820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200285090	chr3:75627851-75627852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200841086	chr3:75627872-75627873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112809625	chr3:75627888-75627889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200549718	chr3:75627889-75627890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111642559	chr3:75627903-75627904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368060104	chr3:75627908-75627909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199636160	chr3:75627926-75627927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113187720	chr3:75627986-75627987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201237176	chr3:75628021-75628022	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs113779102	chr3:75628023-75628024	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs62258810	chr3:75628284-75628285	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs369552788	chr3:75628314-75628315	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs112662217	chr3:75628346-75628347	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs7647430	chr3:75628512-75628513	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs376676745	chr3:75628612-75628613	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs112371132	chr3:75628617-75628618	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs199554202	chr3:75628716-75628717	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs13059625	chr3:75628868-75628869	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs7647771	chr3:75628914-75628915	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Oral squamous cell carcinoma	17134496	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2317 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75625600-75628000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:75626000-75627400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:75626800-75628200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr3:75627400-75628200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:75628000-75629000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:75628200-75628400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr3:75628200-75628400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:75628200-75628400	Bivalent Enhancer	Fetal Kidney	kidney
9	chr3:75628200-75629400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
11	chr3:75628400-75628600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
12	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:75628400-75628600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
15	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:75628400-75629400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
17	chr3:75628400-75629400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
18	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
19	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
20	chr3:75628400-75629600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
21	chr3:75628400-75629600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
22	chr3:75628400-75629600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
23	chr3:75628400-75629600	Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr3:75628400-75629600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr3:75628400-75629800	Active TSS	Brain Cingulate Gyrus	brain
26	chr3:75628600-75628800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr3:75628600-75628800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr3:75628600-75628800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:75628600-75628800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr3:75628600-75628800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr3:75628600-75628800	Enhancers	Brain Hippocampus Middle	brain
32	chr3:75628600-75628800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr3:75628600-75629000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:75628600-75629000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr3:75628600-75629000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr3:75628600-75629000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr3:75628600-75629200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr3:75628600-75629200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr3:75628600-75629200	Bivalent/Poised TSS	Fetal Intestine Large	intestine
40	chr3:75628600-75629400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr3:75628600-75629600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
42	chr3:75628600-75629600	Active TSS	H9 Cell Line	embryonic stem cell
43	chr3:75628600-75629600	Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr3:75628600-75629600	Active TSS	Fetal Brain Female	brain
45	chr3:75628600-75629800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr3:75628600-75629800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr3:75628600-75629800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr3:75628600-75630000	Enhancers	Primary B cells from peripheral blood	blood
49	chr3:75628800-75629000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr3:75628800-75629000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood

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