Variant report

Variant	esv2756185
Chromosome Location	chr3:75466085-75676582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2608)
CpG islands
(count:2749)
Chromatin interactive
region (count:9)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2608 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75482025-75482381	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
3	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
4	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
5	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
6	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
7	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
8	BATF	chr3:75596078-75596520	GM12878	blood:	n/a	n/a
9	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
10	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
11	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
12	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
13	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
14	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
15	BATF	chr3:75653770-75654057	GM12878	blood:	n/a	n/a
16	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
17	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
18	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
19	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
20	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
21	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
22	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
23	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
24	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
25	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
26	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
27	BATF	chr3:75653800-75653992	GM12878	blood:	n/a	n/a
28	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
29	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
30	BATF	chr3:75551976-75552365	GM12878	blood:	n/a	n/a
31	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:75483008-75483267	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:75527598-75527864	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:75566204-75566463	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
36	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
37	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817
38	BCL11A	chr3:75471268-75471550	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:75551437-75551623	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:75609659-75609871	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:75483447-75484322	GM12878	blood:	n/a	chr3:75483516-75483525
43	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
44	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
45	BCL11A	chr3:75467554-75467709	GM12878	blood:	n/a	n/a
46	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
47	BCL11A	chr3:75615329-75615521	GM12878	blood:	n/a	n/a
48	BCL11A	chr3:75551326-75551720	GM12878	blood:	n/a	n/a
49	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a
50	BCL11A	chr3:75471159-75471563	GM12878	blood:	n/a	n/a

(count:2749 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75484209-75484259	NT2-D1	testis:	n/a
2	chr3:75653319-75653369	BE2_C	brain:	n/a
3	chr3:75659629-75659679	Caco-2	colon:	n/a
4	chr3:75658490-75658540	Caco-2	colon:	n/a
5	chr3:75484209-75484259	NT2-D1	testis:	n/a
6	chr3:75653319-75653369	BE2_C	brain:	n/a
7	chr3:75659629-75659679	Caco-2	colon:	n/a
8	chr3:75658490-75658540	Caco-2	colon:	n/a
9	chr3:75668758-75668808	BJ	skin:	n/a
10	chr3:75659629-75659679	HepG2	liver:	n/a
11	chr3:75553723-75553773	HCT-116	colon:	n/a
12	chr3:75664059-75664109	LNCaP	prostate:	n/a
13	chr3:75553723-75553773	Hela-S3	cervix:	n/a
14	chr3:75661799-75661849	AoSMC	blood vessel:	n/a
15	chr3:75668035-75668085	PrEC	prostate:	n/a
16	chr3:75668035-75668085	SK-N-MC	brain:	n/a
17	chr3:75632533-75632583	HRE	kidney:	n/a
18	chr3:75658552-75658602	HNPCEpiC	eye:	n/a
19	chr3:75629039-75629089	AG04449	skin:	fetal
20	chr3:75555994-75556044	HRPEpiC	eye:	n/a
21	chr3:75484209-75484259	IMR90	lung:	fetal
22	chr3:75658552-75658602	AoSMC	blood vessel:	n/a
23	chr3:75658410-75658460	GM19239	blood:	n/a
24	chr3:75484209-75484259	NHBE	bronchial:	n/a
25	chr3:75667994-75668044	HUVEC	blood vessel:	n/a
26	chr3:75556027-75556077	HRCEpiC	kidney:	n/a
27	chr3:75661799-75661849	BE2_C	brain:	n/a
28	chr3:75671793-75671843	MCF10A-Er-Src	breast:	n/a
29	chr3:75664059-75664109	HAEpiC	amniotic membrane:	n/a
30	chr3:75657183-75657233	SKMC	muscle:	n/a
31	chr3:75484213-75484263	CMK	blood:	n/a
32	chr3:75484516-75484566	AG10803	skin:	n/a
33	chr3:75553762-75553812	CMK	blood:	n/a
34	chr3:75556027-75556077	BE2_C	brain:	n/a
35	chr3:75668627-75668677	A549	lung:	n/a
36	chr3:75668627-75668677	HCF	heart:	n/a
37	chr3:75628932-75628982	NT2-D1	testis:	n/a
38	chr3:75484213-75484263	AG09319	gingival:	n/a
39	chr3:75484213-75484263	HepG2	liver:	n/a
40	chr3:75661206-75661256	PFSK-1	brain:	n/a
41	chr3:75482182-75482232	ovcar-3	ovarian:	n/a
42	chr3:75668924-75668974	HepG2	liver:	n/a
43	chr3:75669109-75669159	NB4	blood:	n/a
44	chr3:75484209-75484259	AG10803	skin:	n/a
45	chr3:75484440-75484490	NHBE	bronchial:	n/a
46	chr3:75485110-75485160	HIPEpiC	eye:	n/a
47	chr3:75659629-75659679	PrEC	prostate:	n/a
48	chr3:75481281-75481331	HRPEpiC	eye:	n/a
49	chr3:75666381-75666431	HCF	heart:	n/a
50	chr3:75555994-75556044	SK-N-MC	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
2	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
3	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
4	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
5	chr3:75466672..75467412-chr3:129812592..129813394,2	NB4	blood:
6	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
7	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:
8	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
9	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:

(count:24 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 7502 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:7502 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386662446	chr3:75466085-75466086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs28561941	chr3:75466086-75466087	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs555715496	chr3:75466107-75466108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs367578954	chr3:75466128-75466129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117678297	chr3:75466138-75466139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140114006	chr3:75466140-75466141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7372577	chr3:75466151-75466152	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527496124	chr3:75466153-75466154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184754413	chr3:75466158-75466159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542802523	chr3:75466162-75466163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562181058	chr3:75466181-75466182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572018488	chr3:75466182-75466183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551023490	chr3:75466192-75466193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190259497	chr3:75466207-75466208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533725091	chr3:75466212-75466213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545854345	chr3:75466222-75466223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368448687	chr3:75466244-75466245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139645888	chr3:75466258-75466259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs151043835	chr3:75466282-75466283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534138055	chr3:75466298-75466299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181508595	chr3:75466355-75466356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529426545	chr3:75466368-75466369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59075206	chr3:75466369-75466370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397955286	chr3:75466377-75466378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576838569	chr3:75466385-75466386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186494695	chr3:75466386-75466387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574478657	chr3:75466398-75466399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542494267	chr3:75466403-75466404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149950283	chr3:75466432-75466433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199789733	chr3:75466442-75466443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189366759	chr3:75466449-75466450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538580326	chr3:75466463-75466464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs57239292	chr3:75466478-75466479	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs142129148	chr3:75466518-75466519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542866154	chr3:75466534-75466535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113708593	chr3:75466535-75466536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368709125	chr3:75466541-75466542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574220031	chr3:75466596-75466597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544711943	chr3:75466636-75466637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372193095	chr3:75466637-75466638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12494837	chr3:75466664-75466665	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs533178659	chr3:75466692-75466693	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564615636	chr3:75466748-75466749	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs147797633	chr3:75466755-75466756	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs560641570	chr3:75466768-75466769	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34857200	chr3:75466786-75466787	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549197552	chr3:75466797-75466798	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs111322470	chr3:75466802-75466803	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs537596330	chr3:75466809-75466810	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs373437662	chr3:75466831-75466832	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	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:1556 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75462800-75471600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr3:75463200-75471600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:75463200-75474600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:75463600-75471600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:75463800-75466800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:75463800-75470400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:75464000-75467800	Weak transcription	Fetal Muscle Leg	muscle
8	chr3:75464000-75476000	Weak transcription	Pancreas	Pancrea
9	chr3:75464200-75474800	Weak transcription	Brain Hippocampus Middle	brain
10	chr3:75464600-75467000	Weak transcription	Fetal Intestine Small	intestine
11	chr3:75464600-75468800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:75465400-75466800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:75465400-75471600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr3:75465400-75474000	Weak transcription	Fetal Intestine Large	intestine
15	chr3:75465400-75474800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr3:75465400-75476200	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr3:75465600-75467000	Weak transcription	Fetal Stomach	stomach
18	chr3:75465600-75474600	Weak transcription	Right Ventricle	heart
19	chr3:75465600-75474600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr3:75465600-75474800	Weak transcription	Aorta	Aorta
21	chr3:75465800-75467600	Enhancers	Stomach Mucosa	stomach
22	chr3:75465800-75468400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr3:75466200-75471400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:75466200-75471600	Weak transcription	Esophagus	oesophagus
25	chr3:75466800-75467000	ZNF genes & repeats	Lung	lung
26	chr3:75466800-75467200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:75466800-75467200	Enhancers	Spleen	Spleen
28	chr3:75466800-75467400	Enhancers	Fetal Muscle Trunk	muscle
29	chr3:75466800-75467600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr3:75466800-75467800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:75467000-75467200	Enhancers	Gastric	stomach
32	chr3:75467000-75467800	Strong transcription	Fetal Intestine Small	intestine
33	chr3:75467000-75467800	Strong transcription	Fetal Stomach	stomach
34	chr3:75467000-75472000	Weak transcription	Lung	lung
35	chr3:75467000-75477000	Weak transcription	NH-A	brain
36	chr3:75467200-75467600	Weak transcription	Spleen	Spleen
37	chr3:75467200-75472200	Weak transcription	Gastric	stomach
38	chr3:75467200-75474600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr3:75467400-75467600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr3:75467400-75470200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr3:75467600-75467800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr3:75467600-75467800	Enhancers	Primary hematopoietic stem cells	blood
43	chr3:75467600-75467800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr3:75467600-75467800	Enhancers	Spleen	Spleen
45	chr3:75467600-75474600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr3:75467600-75484400	Weak transcription	Stomach Mucosa	stomach
47	chr3:75467800-75468000	Enhancers	Fetal Muscle Leg	muscle
48	chr3:75467800-75470800	Weak transcription	Fetal Stomach	stomach
49	chr3:75467800-75471400	Weak transcription	Fetal Intestine Small	intestine
50	chr3:75467800-75471600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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