Variant report

Variant	esv2756300
Chromosome Location	chr3:75452819-75697169
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4293)
CpG islands
(count:2932)
Chromatin interactive
region (count:12)
LncRNA
region (count:30)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:4293 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
2	ARID3A	chr3:75482025-75482381	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
4	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
5	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
6	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
7	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
8	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
9	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
10	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
11	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
12	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
13	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
14	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
15	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
16	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
17	BACH1	chr3:75682306-75682660	K562	blood:	n/a	n/a
18	BACH1	chr3:75691900-75692752	K562	blood:	n/a	n/a
19	BACH1	chr3:75693848-75694086	K562	blood:	n/a	n/a
20	BACH1	chr3:75689184-75689642	K562	blood:	n/a	n/a
21	BATF	chr3:75684552-75684932	GM12878	blood:	n/a	chr3:75684801-75684810 chr3:75684754-75684765
22	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
23	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
24	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
25	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
26	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
27	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
28	BATF	chr3:75690250-75690725	GM12878	blood:	n/a	n/a
29	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
30	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
31	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
32	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
33	BATF	chr3:75653800-75653992	GM12878	blood:	n/a	n/a
34	BATF	chr3:75689635-75689852	GM12878	blood:	n/a	n/a
35	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
36	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
37	BATF	chr3:75691089-75692739	GM12878	blood:	n/a	n/a
38	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
39	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
40	BATF	chr3:75690125-75690707	GM12878	blood:	n/a	n/a
41	BATF	chr3:75596078-75596520	GM12878	blood:	n/a	n/a
42	BATF	chr3:75691364-75692601	GM12878	blood:	n/a	n/a
43	BATF	chr3:75680489-75680800	GM12878	blood:	n/a	n/a
44	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
45	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
46	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
47	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
48	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
49	BATF	chr3:75653770-75654057	GM12878	blood:	n/a	n/a
50	BATF	chr3:75684542-75684961	GM12878	blood:	n/a	chr3:75684801-75684810 chr3:75684754-75684765

(count:2932 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75669109-75669159	HUVEC	blood vessel:	n/a
2	chr3:75668035-75668085	RPTEC	kidney:	n/a
3	chr3:75679024-75679074	RPTEC	kidney:	n/a
4	chr3:75658410-75658460	GM12891	blood:	n/a
5	chr3:75669109-75669159	HUVEC	blood vessel:	n/a
6	chr3:75668035-75668085	RPTEC	kidney:	n/a
7	chr3:75679024-75679074	RPTEC	kidney:	n/a
8	chr3:75658410-75658460	GM12891	blood:	n/a
9	chr3:75632533-75632583	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:75671793-75671843	H1-hESC	embryonic stem cell:	embryo
11	chr3:75484213-75484263	RPTEC	kidney:	n/a
12	chr3:75485448-75485498	HRCEpiC	kidney:	n/a
13	chr3:75628819-75628869	NB4	blood:	n/a
14	chr3:75679454-75679504	NHDF-neo	bronchial:	n/a
15	chr3:75484440-75484490	AG04449	skin:	fetal
16	chr3:75485110-75485160	NHBE	bronchial:	n/a
17	chr3:75667994-75668044	AG09319	gingival:	n/a
18	chr3:75657183-75657233	HepG2	liver:	n/a
19	chr3:75679024-75679074	HRCEpiC	kidney:	n/a
20	chr3:75658735-75658785	HCPEpiC	choroid plexus:	n/a
21	chr3:75666392-75666442	LNCaP	prostate:	n/a
22	chr3:75690456-75690506	SK-N-MC	brain:	n/a
23	chr3:75679024-75679074	HCPEpiC	choroid plexus:	n/a
24	chr3:75556027-75556077	U87	brain:	n/a
25	chr3:75658735-75658785	HCT-116	colon:	n/a
26	chr3:75667994-75668044	HCM	heart:	n/a
27	chr3:75679024-75679074	Caco-2	colon:	n/a
28	chr3:75632533-75632583	T-47D	breast:	n/a
29	chr3:75657183-75657233	GM12878	blood:	n/a
30	chr3:75671115-75671165	HNPCEpiC	eye:	n/a
31	chr3:75484440-75484490	MCF-7	breast:	n/a
32	chr3:75667994-75668044	HCT-116	colon:	n/a
33	chr3:75658552-75658602	GM12878	blood:	n/a
34	chr3:75679024-75679074	HL-60	blood:	n/a
35	chr3:75632533-75632583	ECC-1	luminal epithelium:	n/a
36	chr3:75661799-75661849	HMEC	breast:	n/a
37	chr3:75661320-75661370	SAEC	small airway:	n/a
38	chr3:75629433-75629483	U87	brain:	n/a
39	chr3:75668924-75668974	HIPEpiC	eye:	n/a
40	chr3:75658490-75658540	AoSMC	blood vessel:	n/a
41	chr3:75481281-75481331	HAEpiC	amniotic membrane:	n/a
42	chr3:75664059-75664109	SK-N-SH	brain:	n/a
43	chr3:75484213-75484263	LNCaP	prostate:	n/a
44	chr3:75668035-75668085	BJ	skin:	n/a
45	chr3:75485110-75485160	PFSK-1	brain:	n/a
46	chr3:75690456-75690506	MCF-7	breast:	n/a
47	chr3:75661799-75661849	HepG2	liver:	n/a
48	chr3:75668758-75668808	SAEC	small airway:	n/a
49	chr3:75487529-75487579	NHBE	bronchial:	n/a
50	chr3:75555994-75556044	HRPEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
2	chr3:75466672..75467412-chr3:129812592..129813394,2	NB4	blood:
3	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
4	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
5	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:
6	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
7	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
8	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:
9	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
10	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
11	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
12	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-3	chr3:75497520-75500553	NONHSAT090533
2	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
3	lnc-FRG2C-3	chr3:75501683-75501802	ENSG00000272690.1
4	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
5	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
6	lnc-FRG2C-3	chr3:75488905-75488988	XLOC_002710
7	lnc-FRG2C-3	chr3:75486207-75486426	XLOC_002710
8	lnc-FRG2C-3	chr3:75501348-75501809	ENSG00000272690.1
9	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
10	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
11	lnc-FRG2C-3	chr3:75488905-75488997	XLOC_002710
12	lnc-FRG2C-3	chr3:75485367-75485503	XLOC_002710
13	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
14	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
15	lnc-FRG2C-3	chr3:75485928-75486426	XLOC_002710
16	lnc-FRG2C-3	chr3:75492659-75492797	ENSG00000272690.1
17	lnc-FRG2C-3	chr3:75492659-75492775	XLOC_002710
18	lnc-FRG2C-3	chr3:75484499-75484564	ENSG00000272690.1
19	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
20	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
21	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
22	lnc-FRG2C-3	chr3:75501683-75501794	NONHSAT090533
23	lnc-FRG2C-3	chr3:75496316-75496447	ENSG00000272690.1
24	lnc-FRG2C-3	chr3:75505768-75506637	ENSG00000272690.1
25	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
26	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
27	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
28	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
29	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
30	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534

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

No data

Variant related genes	Relation type
UNC93B3	TF binding region
ENSG00000243422	TF binding region
ENSG00000239383	TF binding region
FAM86DP	TF binding region
ENSG00000221602	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E121P	TF binding region
ENPP7P2	TF binding region
ALG1L6P	TF binding region
ENSG00000272690	TF binding region
ENSG00000272710	TF binding region
MIR1324	TF binding region
UNC93B3	CpG island
ENSG00000243422	CpG island
ENSG00000239383	CpG island
FAM86DP	CpG island
ENSG00000221602	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
ENPP7P2	CpG island
ALG1L6P	CpG island
ENSG00000272690	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000251287	chromatin interactions
ENSG00000129925	chromatin interactions
ENSG00000248243	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000236829	chromatin interactions
ITGB1	miRNA target sites
SFRS5	miRNA target sites

Extended variants
information (count: 10168 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:10168 , 50 per page) page: 1 2 3 4 5 6 7 ... 204

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17028592	chr3:75452819-75452820	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs564462791	chr3:75452878-75452879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573592577	chr3:75452893-75452894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148501098	chr3:75452941-75452942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575369130	chr3:75452942-75452943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562296034	chr3:75452953-75452954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113646014	chr3:75452962-75452963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529495386	chr3:75452967-75452968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145353049	chr3:75452973-75452974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562446962	chr3:75452977-75452978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533005577	chr3:75452978-75452979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551106496	chr3:75452991-75452992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117379489	chr3:75452997-75452998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115590157	chr3:75453039-75453040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186880242	chr3:75453059-75453060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567161051	chr3:75453060-75453061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191770551	chr3:75453084-75453085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182300950	chr3:75453099-75453100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6793001	chr3:75453100-75453101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147838973	chr3:75453175-75453176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557887437	chr3:75453188-75453189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186427940	chr3:75453225-75453226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6782849	chr3:75453229-75453230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533595200	chr3:75453236-75453237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145229044	chr3:75453243-75453244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6806359	chr3:75453294-75453295	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs150990521	chr3:75453297-75453298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189887183	chr3:75453298-75453299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112899763	chr3:75453299-75453300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532908610	chr3:75453313-75453314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6782965	chr3:75453341-75453342	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs559753754	chr3:75453342-75453343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527284524	chr3:75453365-75453366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548909659	chr3:75453415-75453416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12107790	chr3:75453439-75453440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574474433	chr3:75453454-75453455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61559716	chr3:75453455-75453456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531590956	chr3:75453463-75453464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs397990186	chr3:75453469-75453470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs62259098	chr3:75453471-75453472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549723108	chr3:75453479-75453480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377405616	chr3:75453481-75453482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571390922	chr3:75453497-75453498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539576566	chr3:75453499-75453500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558268232	chr3:75453561-75453562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566912195	chr3:75453562-75453563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529334984	chr3:75453568-75453569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534188447	chr3:75453580-75453581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150105198	chr3:75453583-75453584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565713186	chr3:75453636-75453637	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	20877625	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:2316 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75452600-75454000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr3:75454000-75465000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr3:75456600-75456800	Enhancers	HSMMtube	muscle
4	chr3:75462400-75464600	Weak transcription	Fetal Stomach	stomach
5	chr3:75462800-75465000	Weak transcription	Fetal Intestine Large	intestine
6	chr3:75462800-75471600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:75463200-75471600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr3:75463200-75474600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr3:75463400-75465200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr3:75463600-75471600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:75463800-75466800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:75463800-75470400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr3:75464000-75467800	Weak transcription	Fetal Muscle Leg	muscle
14	chr3:75464000-75476000	Weak transcription	Pancreas	Pancrea
15	chr3:75464200-75474800	Weak transcription	Brain Hippocampus Middle	brain
16	chr3:75464600-75465000	Strong transcription	Fetal Stomach	stomach
17	chr3:75464600-75467000	Weak transcription	Fetal Intestine Small	intestine
18	chr3:75464600-75468800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:75465000-75465200	ZNF genes & repeats	Fetal Stomach	stomach
20	chr3:75465000-75465400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr3:75465000-75465400	ZNF genes & repeats	Fetal Intestine Large	intestine
22	chr3:75465000-75465800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr3:75465200-75465400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:75465200-75465400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr3:75465200-75465600	Strong transcription	Fetal Stomach	stomach
26	chr3:75465400-75466800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:75465400-75471600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr3:75465400-75474000	Weak transcription	Fetal Intestine Large	intestine
29	chr3:75465400-75474800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr3:75465400-75476200	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr3:75465600-75467000	Weak transcription	Fetal Stomach	stomach
32	chr3:75465600-75474600	Weak transcription	Right Ventricle	heart
33	chr3:75465600-75474600	Weak transcription	Stomach Smooth Muscle	stomach
34	chr3:75465600-75474800	Weak transcription	Aorta	Aorta
35	chr3:75465800-75467600	Enhancers	Stomach Mucosa	stomach
36	chr3:75465800-75468400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr3:75466200-75471400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:75466200-75471600	Weak transcription	Esophagus	oesophagus
39	chr3:75466800-75467000	ZNF genes & repeats	Lung	lung
40	chr3:75466800-75467200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr3:75466800-75467200	Enhancers	Spleen	Spleen
42	chr3:75466800-75467400	Enhancers	Fetal Muscle Trunk	muscle
43	chr3:75466800-75467600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:75466800-75467800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:75467000-75467200	Enhancers	Gastric	stomach
46	chr3:75467000-75467800	Strong transcription	Fetal Intestine Small	intestine
47	chr3:75467000-75467800	Strong transcription	Fetal Stomach	stomach
48	chr3:75467000-75472000	Weak transcription	Lung	lung
49	chr3:75467000-75477000	Weak transcription	NH-A	brain
50	chr3:75467200-75467600	Weak transcription	Spleen	Spleen

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