Variant report

Variant	nsv1012783
Chromosome Location	chr3:75415863-75649222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2579)
CpG islands
(count:1893)
Chromatin interactive
region (count:8)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2579 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

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	ATF1	chr3:75442553-75442767	K562	blood:	n/a	n/a
4	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
5	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
6	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
7	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
8	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
9	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
10	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
11	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
12	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
13	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
14	BATF	chr3:75551976-75552365	GM12878	blood:	n/a	n/a
15	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
16	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
17	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
18	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
19	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
20	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
21	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
22	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
23	BATF	chr3:75596078-75596520	GM12878	blood:	n/a	n/a
24	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
25	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
26	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
27	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
28	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
29	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
30	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:75551437-75551623	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
33	BCL11A	chr3:75483447-75484322	GM12878	blood:	n/a	chr3:75483516-75483525
34	BCL11A	chr3:75483449-75483810	GM12878	blood:	n/a	chr3:75483516-75483525
35	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
36	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:75471268-75471550	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:75483008-75483267	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:75596331-75596513	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:75609659-75609871	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:75615329-75615521	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:75551326-75551720	GM12878	blood:	n/a	n/a
43	BCL11A	chr3:75566204-75566463	GM12878	blood:	n/a	n/a
44	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
45	BCL11A	chr3:75527598-75527864	GM12878	blood:	n/a	n/a
46	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
47	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817
48	BCL11A	chr3:75467554-75467709	GM12878	blood:	n/a	n/a
49	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
50	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75481281-75481331	HUVEC	blood vessel:	n/a
2	chr3:75444752-75444802	GM19239	blood:	n/a
3	chr3:75481281-75481331	HUVEC	blood vessel:	n/a
4	chr3:75444752-75444802	GM19239	blood:	n/a
5	chr3:75416171-75416221	SK-N-MC	brain:	n/a
6	chr3:75487529-75487579	BJ	skin:	n/a
7	chr3:75631426-75631476	MCF10A-Er-Src	breast:	n/a
8	chr3:75631426-75631476	NHBE	bronchial:	n/a
9	chr3:75445502-75445552	SK-N-SH_RA	brain:	n/a
10	chr3:75448983-75449033	AoSMC	blood vessel:	n/a
11	chr3:75484209-75484259	HIPEpiC	eye:	n/a
12	chr3:75555938-75555988	HCM	heart:	n/a
13	chr3:75553723-75553773	SK-N-SH	brain:	n/a
14	chr3:75444752-75444802	RPTEC	kidney:	n/a
15	chr3:75628819-75628869	HPAEpiC	pulmonary alveolar:	n/a
16	chr3:75484440-75484490	GM12891	blood:	n/a
17	chr3:75443047-75443097	Caco-2	colon:	n/a
18	chr3:75482182-75482232	ovcar-3	ovarian:	n/a
19	chr3:75556027-75556077	BE2_C	brain:	n/a
20	chr3:75484213-75484263	Hela-S3	cervix:	n/a
21	chr3:75553294-75553344	HNPCEpiC	eye:	n/a
22	chr3:75555938-75555988	U87	brain:	n/a
23	chr3:75632533-75632583	AG04449	skin:	fetal
24	chr3:75445502-75445552	HCF	heart:	n/a
25	chr3:75444752-75444802	HRPEpiC	eye:	n/a
26	chr3:75555938-75555988	NH-A	brain:	n/a
27	chr3:75484213-75484263	NB4	blood:	n/a
28	chr3:75485448-75485498	GM06990	blood:	n/a
29	chr3:75553294-75553344	MCF10A-Er-Src	breast:	n/a
30	chr3:75487529-75487579	GM12892	blood:	n/a
31	chr3:75484516-75484566	AG09319	gingival:	n/a
32	chr3:75484440-75484490	HEK293	kidney:	embryo
33	chr3:75484440-75484490	HCPEpiC	choroid plexus:	n/a
34	chr3:75484209-75484259	HUVEC	blood vessel:	n/a
35	chr3:75628932-75628982	ProgFib	skin:	n/a
36	chr3:75556027-75556077	NT2-D1	testis:	n/a
37	chr3:75628932-75628982	SAEC	small airway:	n/a
38	chr3:75481281-75481331	Hepatocyte	liver:	n/a
39	chr3:75632533-75632583	HUVEC	blood vessel:	n/a
40	chr3:75445610-75445660	NT2-D1	testis:	n/a
41	chr3:75445610-75445660	GM12891	blood:	n/a
42	chr3:75484516-75484566	H1-hESC	embryonic stem cell:	embryo
43	chr3:75481281-75481331	HepG2	liver:	n/a
44	chr3:75443047-75443097	HEK293	kidney:	embryo
45	chr3:75487529-75487579	PFSK-1	brain:	n/a
46	chr3:75482182-75482232	HCF	heart:	n/a
47	chr3:75484440-75484490	H1-hESC	embryonic stem cell:	embryo
48	chr3:75445502-75445552	K562	blood:	n/a
49	chr3:75444752-75444802	AG04450	lung:	fetal
50	chr3:75553723-75553773	HepG2	liver:	n/a

(count:8 , 50 per page) page: 1

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

(count:23 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000239383	TF binding region
FAM86DP	TF binding region
ENSG00000266685	TF binding region
ENSG00000242953	TF binding region
OR7E55P	TF binding region
ENSG00000221602	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
LSP1P2	TF binding region
OR7E121P	TF binding region
ENPP7P2	TF binding region
ALG1L6P	TF binding region
ENSG00000272690	TF binding region
ENSG00000244699	TF binding region
ENSG00000272710	TF binding region
ENSG00000239383	CpG island
FAM86DP	CpG island
ENSG00000266685	CpG island
ENSG00000242953	CpG island
OR7E55P	CpG island
ENSG00000221602	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
LSP1P2	CpG island
OR7E121P	CpG island
ENPP7P2	CpG island
ALG1L6P	CpG island
ENSG00000272690	CpG island
ENSG00000244699	CpG island
ENSG00000272710	CpG island
ENSG00000248243	chromatin interactions
ENSG00000251287	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000158483	chromatin interactions
ITGB1	miRNA target sites
SFRS5	miRNA target sites

Extended variants
information (count: 9346 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:9346 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184304596	chr3:75418514-75418515	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs562299563	chr3:75418524-75418525	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs149650558	chr3:75418525-75418526	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200543234	chr3:75418543-75418544	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs144335548	chr3:75418598-75418599	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs189667210	chr3:75418599-75418600	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs199872287	chr3:75418605-75418606	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs554528481	chr3:75418620-75418621	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs148357411	chr3:75418626-75418627	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs543279928	chr3:75418652-75418653	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs555181598	chr3:75418654-75418655	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs576253836	chr3:75418690-75418691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs367636053	chr3:75418693-75418694	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs548009596	chr3:75418772-75418773	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs184675109	chr3:75418776-75418777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs111761487	chr3:75418785-75418786	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs147476767	chr3:75418793-75418794	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs571623456	chr3:75418810-75418811	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs116125712	chr3:75418820-75418821	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs114551064	chr3:75418829-75418830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs371790212	chr3:75418849-75418850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs117728757	chr3:75418871-75418872	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs536944692	chr3:75418888-75418889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs555245128	chr3:75418975-75418976	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189222092	chr3:75419014-75419015	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs576585392	chr3:75419017-75419018	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs537204863	chr3:75419025-75419026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577940023	chr3:75419031-75419032	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs369792182	chr3:75419035-75419036	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs576831515	chr3:75419045-75419046	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs541056204	chr3:75419055-75419056	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs181584527	chr3:75419080-75419081	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs371869114	chr3:75419089-75419090	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs139985412	chr3:75419091-75419092	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs541730597	chr3:75419099-75419100	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563195184	chr3:75419103-75419104	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs145329440	chr3:75419114-75419115	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs539336990	chr3:75419136-75419137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs554144773	chr3:75419138-75419139	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs552050661	chr3:75419223-75419224	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs565411113	chr3:75419233-75419234	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs186472047	chr3:75419236-75419237	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs547856263	chr3:75419240-75419241	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs566067009	chr3:75419254-75419255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs190904259	chr3:75419263-75419264	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs547382449	chr3:75419289-75419290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs548904971	chr3:75419290-75419291	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs149965125	chr3:75419355-75419356	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs537669409	chr3:75419359-75419360	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs558870775	chr3:75419362-75419363	Inactive region	TF binding region	1 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
Non-syndromic sensorineural hearing loss	21293372	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	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:1612 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75420200-75421800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr3:75421400-75423000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:75421800-75422600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:75422000-75422200	Flanking Active TSS	Osteobl	bone
5	chr3:75422000-75422400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr3:75422000-75422400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:75422000-75423000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr3:75422200-75422800	Enhancers	Osteobl	bone
9	chr3:75422600-75423000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:75423000-75423600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr3:75427600-75427800	Enhancers	Fetal Lung	lung
12	chr3:75427800-75428000	Enhancers	Fetal Heart	heart
13	chr3:75427800-75428200	Enhancers	Fetal Muscle Leg	muscle
14	chr3:75427800-75429000	Weak transcription	Fetal Lung	lung
15	chr3:75428000-75429000	Weak transcription	Fetal Heart	heart
16	chr3:75429000-75429200	Enhancers	Fetal Lung	lung
17	chr3:75429000-75429600	Enhancers	Fetal Heart	heart
18	chr3:75429000-75429600	Enhancers	Gastric	stomach
19	chr3:75429000-75429800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:75429000-75429800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:75429000-75429800	ZNF genes & repeats	Fetal Kidney	kidney
22	chr3:75429000-75429800	Enhancers	Pancreas	Pancrea
23	chr3:75429200-75429800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr3:75429200-75429800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr3:75429200-75429800	Active TSS	Fetal Lung	lung
26	chr3:75429200-75429800	ZNF genes & repeats	Dnd41	blood
27	chr3:75429400-75429800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr3:75429600-75429800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr3:75429800-75430200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr3:75429800-75445600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr3:75430000-75430200	Weak transcription	Fetal Kidney	kidney
32	chr3:75431600-75431800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:75431800-75432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:75432000-75432200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:75432200-75433000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:75432600-75432800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:75432600-75433000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr3:75432800-75433400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:75435800-75436000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr3:75435800-75436400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:75436400-75437400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr3:75437400-75437600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr3:75437400-75437600	Enhancers	Osteobl	bone
44	chr3:75437400-75437800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:75437400-75438200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr3:75437400-75438200	Enhancers	Ovary	ovary
47	chr3:75437400-75438200	Enhancers	Right Atrium	heart
48	chr3:75437400-75438400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr3:75437400-75438400	Enhancers	Rectal Smooth Muscle	rectum
50	chr3:75437400-75438800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links