Variant report

Variant	esv1797986
Chromosome Location	chr3:75703610-75794588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3076)
CpG islands
(count:1469)
Chromatin interactive
region (count:5)
LncRNA
region (count:13)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:3076 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
3	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
5	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
8	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
9	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
10	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
11	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
12	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
13	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
14	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
15	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
16	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
17	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
18	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
19	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
20	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
21	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
22	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
23	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
24	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
25	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
26	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
27	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
28	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
29	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
30	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
31	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
32	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
33	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
34	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
35	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
36	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
37	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
38	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
39	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
40	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
41	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
42	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
43	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
44	ATF3	chr3:75717987-75718165	K562	blood:	n/a	n/a
45	ATF3	chr3:75718289-75718505	K562	blood:	n/a	n/a
46	ATF3	chr3:75788958-75789896	K562	blood:	n/a	n/a
47	BACH1	chr3:75744812-75745060	K562	blood:	n/a	n/a
48	BACH1	chr3:75787478-75787482	K562	blood:	n/a	n/a
49	BACH1	chr3:75734445-75734852	K562	blood:	n/a	n/a
50	BACH1	chr3:75739253-75739499	K562	blood:	n/a	n/a

(count:1469 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75708104-75708154	MCF-7	breast:	n/a
2	chr3:75704951-75705001	RPTEC	kidney:	n/a
3	chr3:75708197-75708247	SKMC	muscle:	n/a
4	chr3:75704498-75704548	HIPEpiC	eye:	n/a
5	chr3:75704498-75704548	Jurkat	blood:	n/a
6	chr3:75708104-75708154	MCF-7	breast:	n/a
7	chr3:75704951-75705001	RPTEC	kidney:	n/a
8	chr3:75708197-75708247	SKMC	muscle:	n/a
9	chr3:75704498-75704548	HIPEpiC	eye:	n/a
10	chr3:75704498-75704548	Jurkat	blood:	n/a
11	chr3:75720199-75720249	HIPEpiC	eye:	n/a
12	chr3:75717453-75717503	BJ	skin:	n/a
13	chr3:75704951-75705001	Jurkat	blood:	n/a
14	chr3:75707990-75708040	HEEpiC	esophagus:	n/a
15	chr3:75717453-75717503	GM12891	blood:	n/a
16	chr3:75707560-75707610	ProgFib	skin:	n/a
17	chr3:75717453-75717503	HAEpiC	amniotic membrane:	n/a
18	chr3:75720199-75720249	ECC-1	luminal epithelium:	n/a
19	chr3:75704573-75704623	HNPCEpiC	eye:	n/a
20	chr3:75707560-75707610	SK-N-SH_RA	brain:	n/a
21	chr3:75705922-75705972	AoSMC	blood vessel:	n/a
22	chr3:75720199-75720249	IMR90	lung:	fetal
23	chr3:75721888-75721938	AG10803	skin:	n/a
24	chr3:75717248-75717298	ProgFib	skin:	n/a
25	chr3:75705108-75705158	SK-N-SH_RA	brain:	n/a
26	chr3:75720876-75720926	GM19239	blood:	n/a
27	chr3:75704573-75704623	U87	brain:	n/a
28	chr3:75719149-75719199	CMK	blood:	n/a
29	chr3:75707990-75708040	PrEC	prostate:	n/a
30	chr3:75712695-75712745	H1-hESC	embryonic stem cell:	embryo
31	chr3:75704573-75704623	GM19239	blood:	n/a
32	chr3:75719149-75719199	HEK293	kidney:	embryo
33	chr3:75707560-75707610	AG09319	gingival:	n/a
34	chr3:75720199-75720249	NH-A	brain:	n/a
35	chr3:75712404-75712454	K562	blood:	n/a
36	chr3:75705922-75705972	Hepatocyte	liver:	n/a
37	chr3:75712404-75712454	SKMC	muscle:	n/a
38	chr3:75717453-75717503	RPTEC	kidney:	n/a
39	chr3:75721577-75721627	SK-N-SH	brain:	n/a
40	chr3:75704824-75704874	GM06990	blood:	n/a
41	chr3:75712695-75712745	MCF-7	breast:	n/a
42	chr3:75714447-75714497	SKMC	muscle:	n/a
43	chr3:75720199-75720249	HL-60	blood:	n/a
44	chr3:75704498-75704548	LNCaP	prostate:	n/a
45	chr3:75717248-75717298	ECC-1	luminal epithelium:	n/a
46	chr3:75719149-75719199	HMEC	breast:	n/a
47	chr3:75720876-75720926	AG09319	gingival:	n/a
48	chr3:75721577-75721627	AG04450	lung:	fetal
49	chr3:75719158-75719208	GM12878	blood:	n/a
50	chr3:75704951-75705001	NHDF-neo	bronchial:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
2	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
3	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
4	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:
5	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
2	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
3	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
4	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
5	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
6	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
7	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
8	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
9	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
10	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
11	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
12	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
13	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4273	chr3:75787441-75787458	MIMAT0016903

No data

Variant related genes	Relation type
FRG2C	TF binding region
MIR4273	TF binding region
LINC00960	TF binding region
RARRES2P1	TF binding region
AGGF1P3	TF binding region
RN7SL92P	TF binding region
ENSG00000236138	TF binding region
FRG2C	CpG island
MIR4273	CpG island
LINC00960	CpG island
RARRES2P1	CpG island
AGGF1P3	CpG island
RN7SL92P	CpG island
ENSG00000236138	CpG island
ENSG00000232815	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 9542 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:9542 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73843816	chr3:75703640-75703641	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs201591372	chr3:75703661-75703662	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs149970423	chr3:75703673-75703674	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs137947724	chr3:75703682-75703683	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs142408172	chr3:75703693-75703694	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs200174636	chr3:75703701-75703702	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs146687292	chr3:75703712-75703713	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs73843817	chr3:75703730-75703731	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs77466941	chr3:75703753-75703754	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs200968353	chr3:75703769-75703770	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs201923633	chr3:75703770-75703771	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs556492098	chr3:75703789-75703790	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs116142734	chr3:75703815-75703816	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs115288760	chr3:75703821-75703822	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs202217348	chr3:75703822-75703823	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs200535392	chr3:75703823-75703824	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs371279757	chr3:75703833-75703834	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs75984456	chr3:75703846-75703847	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs370266092	chr3:75703868-75703869	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs62247083	chr3:75703873-75703874	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs578190705	chr3:75703874-75703875	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs139914189	chr3:75703921-75703922	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs142544265	chr3:75703931-75703932	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs201930210	chr3:75703932-75703933	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs114106640	chr3:75703939-75703940	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs200729802	chr3:75703952-75703953	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs545426733	chr3:75703963-75703964	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs62247084	chr3:75703975-75703976	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs368000913	chr3:75703977-75703978	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs75866088	chr3:75703983-75703984	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs200222804	chr3:75704028-75704029	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs200828416	chr3:75704029-75704030	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs115119442	chr3:75704039-75704040	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs116663732	chr3:75704047-75704048	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs77824157	chr3:75704066-75704067	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs77514066	chr3:75704078-75704079	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs201549626	chr3:75704083-75704084	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs73843818	chr3:75704094-75704095	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs560485520	chr3:75704103-75704104	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs369013457	chr3:75704112-75704113	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs201090825	chr3:75704115-75704116	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs202009299	chr3:75704146-75704147	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs62247085	chr3:75704191-75704192	Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs142634300	chr3:75704208-75704209	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs79213942	chr3:75704219-75704220	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs372982374	chr3:75704220-75704221	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs148104710	chr3:75704223-75704224	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs144104372	chr3:75704240-75704241	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs74724616	chr3:75704273-75704274	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs142315588	chr3:75704276-75704277	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	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:1510 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75699400-75704600	Weak transcription	Pancreas	Pancrea
2	chr3:75699600-75704600	Weak transcription	Gastric	stomach
3	chr3:75700200-75704600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:75703400-75704600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:75704200-75704400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
6	chr3:75704200-75704400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
7	chr3:75704200-75704600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr3:75704200-75705200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr3:75704400-75704600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:75704400-75705200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
11	chr3:75704400-75705200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
12	chr3:75704400-75705200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
13	chr3:75704400-75705200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
14	chr3:75704400-75705200	Bivalent Enhancer	Brain Germinal Matrix	brain
15	chr3:75704400-75705200	Bivalent Enhancer	Fetal Brain Female	brain
16	chr3:75704400-75705200	ZNF genes & repeats	Right Atrium	heart
17	chr3:75704400-75705400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
18	chr3:75704400-75705400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
19	chr3:75704400-75705400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
20	chr3:75704600-75704800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr3:75704600-75704800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:75704600-75704800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
23	chr3:75704600-75704800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr3:75704600-75705000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr3:75704600-75705000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr3:75704600-75705000	ZNF genes & repeats	Gastric	stomach
27	chr3:75704600-75705000	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
28	chr3:75704600-75705000	Flanking Bivalent TSS/Enh	Right Ventricle	heart
29	chr3:75704600-75705200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:75704600-75705200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr3:75704600-75705200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:75704600-75705200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr3:75704600-75705200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:75704600-75705200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr3:75704600-75705200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr3:75704600-75705200	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr3:75704600-75705200	Bivalent Enhancer	Left Ventricle	heart
38	chr3:75704600-75705400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr3:75704600-75705400	ZNF genes & repeats	Pancreas	Pancrea
40	chr3:75704800-75705000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
41	chr3:75704800-75705000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
42	chr3:75704800-75705000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr3:75704800-75705000	Bivalent Enhancer	Fetal Brain Male	brain
44	chr3:75704800-75705000	Bivalent Enhancer	Spleen	Spleen
45	chr3:75704800-75705200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr3:75704800-75705200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:75704800-75705200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr3:75704800-75705200	Bivalent Enhancer	Fetal Stomach	stomach
49	chr3:75704800-75705200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
50	chr3:75705000-75705200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell

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