Variant report

Variant	esv3435095
Chromosome Location	chr3:75411828-75648366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2611)
CpG islands
(count:2321)
Chromatin interactive
region (count:8)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2611 , 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	chr3:75484451-75484710	K562	blood:	n/a	n/a
4	ATF1	chr3:75442553-75442767	K562	blood:	n/a	n/a
5	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
6	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
7	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
8	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
9	BATF	chr3:75411604-75411874	GM12878	blood:	n/a	n/a
10	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
11	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
12	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
13	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
14	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
15	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
16	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
17	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
18	BATF	chr3:75596078-75596520	GM12878	blood:	n/a	n/a
19	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
20	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
21	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
22	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
23	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
24	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
25	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
26	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
27	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
28	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
29	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
30	BATF	chr3:75551976-75552365	GM12878	blood:	n/a	n/a
31	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:75566204-75566463	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:75483449-75483810	GM12878	blood:	n/a	chr3:75483516-75483525
34	BCL11A	chr3:75551437-75551623	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
36	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:75609659-75609871	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:75483447-75484322	GM12878	blood:	n/a	chr3:75483516-75483525
39	BCL11A	chr3:75471268-75471550	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:75615329-75615521	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:75467554-75467709	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a
43	BCL11A	chr3:75551326-75551720	GM12878	blood:	n/a	n/a
44	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
45	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
46	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
47	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
48	BCL11A	chr3:75596331-75596513	GM12878	blood:	n/a	n/a
49	BCL11A	chr3:75527598-75527864	GM12878	blood:	n/a	n/a
50	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817

(count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75445095-75445145	AG04450	lung:	fetal
2	chr3:75487529-75487579	HCF	heart:	n/a
3	chr3:75628932-75628982	CMK	blood:	n/a
4	chr3:75445095-75445145	AG04450	lung:	fetal
5	chr3:75487529-75487579	HCF	heart:	n/a
6	chr3:75628932-75628982	CMK	blood:	n/a
7	chr3:75629433-75629483	PANC-1	pancreas:	n/a
8	chr3:75414693-75414743	GM12891	blood:	n/a
9	chr3:75628932-75628982	PANC-1	pancreas:	n/a
10	chr3:75555994-75556044	SK-N-SH	brain:	n/a
11	chr3:75628819-75628869	MCF-7	breast:	n/a
12	chr3:75484440-75484490	Jurkat	blood:	n/a
13	chr3:75443047-75443097	SAEC	small airway:	n/a
14	chr3:75484209-75484259	HCF	heart:	n/a
15	chr3:75414486-75414536	Hela-S3	cervix:	n/a
16	chr3:75484209-75484259	SK-N-SH	brain:	n/a
17	chr3:75445610-75445660	GM12878	blood:	n/a
18	chr3:75414486-75414536	T-47D	breast:	n/a
19	chr3:75484209-75484259	AG09309	skin:	n/a
20	chr3:75555938-75555988	A549	lung:	n/a
21	chr3:75441804-75441854	GM12891	blood:	n/a
22	chr3:75555994-75556044	NHBE	bronchial:	n/a
23	chr3:75413083-75413133	H1-hESC	embryonic stem cell:	embryo
24	chr3:75415561-75415611	SK-N-MC	brain:	n/a
25	chr3:75483803-75483853	HUVEC	blood vessel:	n/a
26	chr3:75629433-75629483	BE2_C	brain:	n/a
27	chr3:75445095-75445145	U87	brain:	n/a
28	chr3:75553723-75553773	SKMC	muscle:	n/a
29	chr3:75553723-75553773	AG09309	skin:	n/a
30	chr3:75412866-75412916	LNCaP	prostate:	n/a
31	chr3:75445738-75445788	ProgFib	skin:	n/a
32	chr3:75628932-75628982	Hepatocyte	liver:	n/a
33	chr3:75414693-75414743	GM12878	blood:	n/a
34	chr3:75414693-75414743	ovcar-3	ovarian:	n/a
35	chr3:75415591-75415641	ProgFib	skin:	n/a
36	chr3:75484213-75484263	MCF-7	breast:	n/a
37	chr3:75482182-75482232	HRCEpiC	kidney:	n/a
38	chr3:75412866-75412916	NH-A	brain:	n/a
39	chr3:75481281-75481331	HRCEpiC	kidney:	n/a
40	chr3:75487529-75487579	SK-N-SH	brain:	n/a
41	chr3:75448983-75449033	GM12878	blood:	n/a
42	chr3:75628932-75628982	NH-A	brain:	n/a
43	chr3:75555938-75555988	GM12891	blood:	n/a
44	chr3:75445610-75445660	HAEpiC	amniotic membrane:	n/a
45	chr3:75443047-75443097	CMK	blood:	n/a
46	chr3:75445502-75445552	GM12878	blood:	n/a
47	chr3:75445502-75445552	HepG2	liver:	n/a
48	chr3:75632533-75632583	AG10803	skin:	n/a
49	chr3:75415526-75415576	PANC-1	pancreas:	n/a
50	chr3:75413083-75413133	HNPCEpiC	eye:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 9452 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:9452 , 50 per page) page: 1 2 3 4 5 6 7 ... 190

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2875202	chr3:75411845-75411846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4054272	chr3:75411859-75411860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564063788	chr3:75411862-75411863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4054273	chr3:75411881-75411882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528336824	chr3:75411917-75411918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs3966984	chr3:75411947-75411948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546510016	chr3:75411952-75411953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188490768	chr3:75411956-75411957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530180092	chr3:75411968-75411969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548651838	chr3:75411984-75411985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570124093	chr3:75411988-75411989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192188758	chr3:75412029-75412030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145957670	chr3:75412033-75412034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138699492	chr3:75412044-75412045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535306224	chr3:75412060-75412061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553338399	chr3:75412102-75412103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368660644	chr3:75412152-75412153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542017938	chr3:75412160-75412161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142771667	chr3:75412161-75412162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13082726	chr3:75412180-75412181	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs545411956	chr3:75412211-75412212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563724132	chr3:75412216-75412217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528401292	chr3:75412234-75412235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184391211	chr3:75412235-75412236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111769097	chr3:75412248-75412249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572539697	chr3:75412249-75412250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190714434	chr3:75412269-75412270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182222335	chr3:75412283-75412284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187295408	chr3:75412293-75412294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552637517	chr3:75412300-75412301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570856979	chr3:75412310-75412311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558083229	chr3:75412374-75412375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547281823	chr3:75412402-75412403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568617055	chr3:75412408-75412409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536070720	chr3:75412419-75412420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113351068	chr3:75412420-75412421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575031806	chr3:75412431-75412432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539123717	chr3:75412490-75412491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2103426	chr3:75412507-75412508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140488774	chr3:75412513-75412514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112283526	chr3:75412521-75412522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572784686	chr3:75412522-75412523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539800563	chr3:75412548-75412549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113876621	chr3:75412556-75412557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562017906	chr3:75412636-75412637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149086270	chr3:75412653-75412654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561372192	chr3:75412654-75412655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573825662	chr3:75412664-75412665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574956253	chr3:75412667-75412668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549006299	chr3:75412673-75412674	Enhancers Weak transcription	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
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:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75411000-75412000	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr3:75411000-75412200	Enhancers	Pancreas	Pancrea
3	chr3:75411000-75413400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:75411600-75412400	Enhancers	Placenta	Placenta
5	chr3:75411600-75412800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:75411800-75412200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr3:75412000-75413400	Enhancers	Stomach Mucosa	stomach
8	chr3:75413000-75413200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:75420200-75421800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:75421400-75423000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:75421800-75422600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:75422000-75422200	Flanking Active TSS	Osteobl	bone
13	chr3:75422000-75422400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr3:75422000-75422400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr3:75422000-75423000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr3:75422200-75422800	Enhancers	Osteobl	bone
17	chr3:75422600-75423000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:75423000-75423600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr3:75427600-75427800	Enhancers	Fetal Lung	lung
20	chr3:75427800-75428000	Enhancers	Fetal Heart	heart
21	chr3:75427800-75428200	Enhancers	Fetal Muscle Leg	muscle
22	chr3:75427800-75429000	Weak transcription	Fetal Lung	lung
23	chr3:75428000-75429000	Weak transcription	Fetal Heart	heart
24	chr3:75429000-75429200	Enhancers	Fetal Lung	lung
25	chr3:75429000-75429600	Enhancers	Fetal Heart	heart
26	chr3:75429000-75429600	Enhancers	Gastric	stomach
27	chr3:75429000-75429800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:75429000-75429800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:75429000-75429800	ZNF genes & repeats	Fetal Kidney	kidney
30	chr3:75429000-75429800	Enhancers	Pancreas	Pancrea
31	chr3:75429200-75429800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr3:75429200-75429800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr3:75429200-75429800	Active TSS	Fetal Lung	lung
34	chr3:75429200-75429800	ZNF genes & repeats	Dnd41	blood
35	chr3:75429400-75429800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr3:75429600-75429800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr3:75429800-75430200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr3:75429800-75445600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:75430000-75430200	Weak transcription	Fetal Kidney	kidney
40	chr3:75431600-75431800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:75431800-75432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:75432000-75432200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:75432200-75433000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr3:75432600-75432800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:75432600-75433000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:75432800-75433400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:75435800-75436000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr3:75435800-75436400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:75436400-75437400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:75437400-75437600	Enhancers	Muscle Satellite Cultured Cells	--

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