Variant report

Variant	esv2756429
Chromosome Location	chr3:75394265-75595318
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2167)
CpG islands
(count:2259)
Chromatin interactive
region (count:7)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2167 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

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	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
3	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
4	ATF1	chr3:75442553-75442767	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	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
8	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
9	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
10	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
11	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
12	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
13	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
14	BATF	chr3:75411604-75411874	GM12878	blood:	n/a	n/a
15	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
16	BATF	chr3:75551976-75552365	GM12878	blood:	n/a	n/a
17	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
18	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
19	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
20	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
21	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
22	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
23	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
24	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
25	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
26	BATF	chr3:75411520-75411813	GM12878	blood:	n/a	n/a
27	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
28	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
29	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
30	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
31	BCL11A	chr3:75467554-75467709	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:75551437-75551623	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:75483008-75483267	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817
35	BCL11A	chr3:75566204-75566463	GM12878	blood:	n/a	n/a
36	BCL11A	chr3:75527598-75527864	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:75471268-75471550	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
39	BCL11A	chr3:75551326-75551720	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
41	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:75471159-75471563	GM12878	blood:	n/a	n/a
43	BCL11A	chr3:75483447-75484322	GM12878	blood:	n/a	chr3:75483516-75483525
44	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
45	BCL11A	chr3:75483449-75483810	GM12878	blood:	n/a	chr3:75483516-75483525
46	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a
47	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
48	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
49	BCL3	chr3:75417298-75417641	GM12878	blood:	n/a	n/a
50	BCL3	chr3:75417319-75417660	GM12878	blood:	n/a	n/a

(count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75484516-75484566	HNPCEpiC	eye:	n/a
2	chr3:75555994-75556044	AG04449	skin:	fetal
3	chr3:75484516-75484566	HNPCEpiC	eye:	n/a
4	chr3:75555994-75556044	AG04449	skin:	fetal
5	chr3:75415526-75415576	HepG2	liver:	n/a
6	chr3:75484213-75484263	A549	lung:	n/a
7	chr3:75556027-75556077	NHBE	bronchial:	n/a
8	chr3:75411421-75411471	ovcar-3	ovarian:	n/a
9	chr3:75483803-75483853	Caco-2	colon:	n/a
10	chr3:75555994-75556044	GM12878	blood:	n/a
11	chr3:75484213-75484263	BJ	skin:	n/a
12	chr3:75483803-75483853	HCPEpiC	choroid plexus:	n/a
13	chr3:75483803-75483853	AG04450	lung:	fetal
14	chr3:75487529-75487579	HCM	heart:	n/a
15	chr3:75415526-75415576	U87	brain:	n/a
16	chr3:75414693-75414743	NH-A	brain:	n/a
17	chr3:75553723-75553773	GM06990	blood:	n/a
18	chr3:75553723-75553773	ECC-1	luminal epithelium:	n/a
19	chr3:75415526-75415576	NHBE	bronchial:	n/a
20	chr3:75410789-75410839	BE2_C	brain:	n/a
21	chr3:75445610-75445660	PANC-1	pancreas:	n/a
22	chr3:75412866-75412916	SK-N-SH	brain:	n/a
23	chr3:75555994-75556044	BJ	skin:	n/a
24	chr3:75487529-75487579	IMR90	lung:	fetal
25	chr3:75415526-75415576	MCF10A-Er-Src	breast:	n/a
26	chr3:75415526-75415576	HRE	kidney:	n/a
27	chr3:75484209-75484259	Jurkat	blood:	n/a
28	chr3:75487529-75487579	SAEC	small airway:	n/a
29	chr3:75553294-75553344	HEK293	kidney:	embryo
30	chr3:75485448-75485498	PFSK-1	brain:	n/a
31	chr3:75413083-75413133	AG10803	skin:	n/a
32	chr3:75441804-75441854	NT2-D1	testis:	n/a
33	chr3:75445738-75445788	RPTEC	kidney:	n/a
34	chr3:75487529-75487579	A549	lung:	n/a
35	chr3:75415591-75415641	T-47D	breast:	n/a
36	chr3:75481281-75481331	NHBE	bronchial:	n/a
37	chr3:75556027-75556077	GM19239	blood:	n/a
38	chr3:75482182-75482232	LNCaP	prostate:	n/a
39	chr3:75411038-75411088	HRPEpiC	eye:	n/a
40	chr3:75482182-75482232	AG09309	skin:	n/a
41	chr3:75415526-75415576	SK-N-SH	brain:	n/a
42	chr3:75444752-75444802	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:75415526-75415576	HEK293	kidney:	embryo
44	chr3:75484440-75484490	LNCaP	prostate:	n/a
45	chr3:75484209-75484259	HCF	heart:	n/a
46	chr3:75484209-75484259	HAEpiC	amniotic membrane:	n/a
47	chr3:75485448-75485498	GM12892	blood:	n/a
48	chr3:75411217-75411267	GM12878	blood:	n/a
49	chr3:75448983-75449033	AG10803	skin:	n/a
50	chr3:75553723-75553773	Caco-2	colon:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
2	chr3:75343035..75343810-chr3:75470999..75471871,7	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	chr3:75466672..75467412-chr3:129812592..129813394,2	NB4	blood:
6	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:
7	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
FAM86DP	TF binding region
ENSG00000266685	TF binding region
ENSG00000242953	TF binding region
OR7E55P	TF binding region
ENSG00000221602	TF binding region
OR7E66P	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E22P	TF binding region
LSP1P2	TF binding region
ENSG00000263782	TF binding region
ENPP7P2	TF binding region
ALG1L6P	TF binding region
ENSG00000272690	TF binding region
ENSG00000244699	TF binding region
FAM86DP	CpG island
ENSG00000266685	CpG island
ENSG00000242953	CpG island
OR7E55P	CpG island
ENSG00000221602	CpG island
OR7E66P	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E22P	CpG island
LSP1P2	CpG island
ENSG00000263782	CpG island
ENPP7P2	CpG island
ALG1L6P	CpG island
ENSG00000272690	CpG island
ENSG00000244699	CpG island
ENSG00000168298	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000251287	chromatin interactions
ENSG00000248243	chromatin interactions
ITGB1	miRNA target sites
SFRS5	miRNA target sites

Extended variants
information (count: 9531 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:9531 , 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	rs12496616	chr3:75394265-75394266	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527854415	chr3:75394319-75394320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183654402	chr3:75394337-75394338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112479934	chr3:75394346-75394347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187183403	chr3:75394347-75394348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190861858	chr3:75394413-75394414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559627492	chr3:75394439-75394440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182380467	chr3:75394451-75394452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549480959	chr3:75394462-75394463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567636135	chr3:75394487-75394488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186912380	chr3:75394507-75394508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149845685	chr3:75394516-75394517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571263059	chr3:75394572-75394573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191373146	chr3:75394577-75394578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554037108	chr3:75394581-75394582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371699361	chr3:75394617-75394618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375770850	chr3:75394623-75394624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536424192	chr3:75394636-75394637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367626713	chr3:75394642-75394643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183199649	chr3:75394648-75394649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188255939	chr3:75394654-75394655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372211851	chr3:75394675-75394676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528961921	chr3:75394697-75394698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543457499	chr3:75394708-75394709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377247096	chr3:75394733-75394734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58077312	chr3:75394747-75394748	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs576897606	chr3:75394748-75394749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146385405	chr3:75394766-75394767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549019363	chr3:75394769-75394770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6767960	chr3:75394787-75394788	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs529930714	chr3:75394797-75394798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554092874	chr3:75394826-75394827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76754395	chr3:75394846-75394847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551777344	chr3:75394876-75394877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192909582	chr3:75394879-75394880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531717736	chr3:75394918-75394919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549825134	chr3:75394920-75394921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372996629	chr3:75394925-75394926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75443152	chr3:75394930-75394931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185121754	chr3:75394961-75394962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547711933	chr3:75394963-75394964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566227348	chr3:75394980-75394981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375456001	chr3:75395036-75395037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6768177	chr3:75395043-75395044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs189382417	chr3:75395061-75395062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139767264	chr3:75395119-75395120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144359470	chr3:75395134-75395135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73840493	chr3:75395155-75395156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs146608266	chr3:75395163-75395164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116741338	chr3:75395192-75395193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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

Chromatin state (count:1431 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75391000-75400600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:75393200-75395000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:75394400-75394600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr3:75399400-75400800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr3:75400600-75400800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:75400800-75401800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:75403200-75403600	Enhancers	Stomach Mucosa	stomach
8	chr3:75411000-75411400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr3:75411000-75412000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr3:75411000-75412200	Enhancers	Pancreas	Pancrea
11	chr3:75411000-75413400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:75411200-75411600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr3:75411200-75411600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:75411600-75412400	Enhancers	Placenta	Placenta
15	chr3:75411600-75412800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:75411800-75412200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr3:75412000-75413400	Enhancers	Stomach Mucosa	stomach
18	chr3:75413000-75413200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:75420200-75421800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:75421400-75423000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:75421800-75422600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:75422000-75422200	Flanking Active TSS	Osteobl	bone
23	chr3:75422000-75422400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:75422000-75422400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:75422000-75423000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr3:75422200-75422800	Enhancers	Osteobl	bone
27	chr3:75422600-75423000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:75423000-75423600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:75427600-75427800	Enhancers	Fetal Lung	lung
30	chr3:75427800-75428000	Enhancers	Fetal Heart	heart
31	chr3:75427800-75428200	Enhancers	Fetal Muscle Leg	muscle
32	chr3:75427800-75429000	Weak transcription	Fetal Lung	lung
33	chr3:75428000-75429000	Weak transcription	Fetal Heart	heart
34	chr3:75429000-75429200	Enhancers	Fetal Lung	lung
35	chr3:75429000-75429600	Enhancers	Fetal Heart	heart
36	chr3:75429000-75429600	Enhancers	Gastric	stomach
37	chr3:75429000-75429800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr3:75429000-75429800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr3:75429000-75429800	ZNF genes & repeats	Fetal Kidney	kidney
40	chr3:75429000-75429800	Enhancers	Pancreas	Pancrea
41	chr3:75429200-75429800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr3:75429200-75429800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr3:75429200-75429800	Active TSS	Fetal Lung	lung
44	chr3:75429200-75429800	ZNF genes & repeats	Dnd41	blood
45	chr3:75429400-75429800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr3:75429600-75429800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr3:75429800-75430200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr3:75429800-75445600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr3:75430000-75430200	Weak transcription	Fetal Kidney	kidney
50	chr3:75431600-75431800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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