Variant report

Variant	esv2757874
Chromosome Location	chr3:75346159-75617595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2620)
CpG islands
(count:2260)
Chromatin interactive
region (count:10)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2620 , 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	chr3:75442553-75442767	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	BACH1	chr3:75390901-75391145	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
10	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
11	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
12	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
13	BATF	chr3:75411520-75411813	GM12878	blood:	n/a	n/a
14	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
15	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
16	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
17	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
18	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
19	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
20	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
21	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
22	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
23	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
24	BATF	chr3:75411604-75411874	GM12878	blood:	n/a	n/a
25	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
26	BATF	chr3:75551976-75552365	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	chr3:75596078-75596520	GM12878	blood:	n/a	n/a
30	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
31	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
32	BATF	chr3:75386395-75386620	GM12878	blood:	n/a	n/a
33	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
34	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:75471159-75471563	GM12878	blood:	n/a	n/a
36	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
37	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:75483008-75483267	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:75551437-75551623	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:75527598-75527864	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:75609659-75609871	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
43	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817
44	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a
45	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a
46	BCL11A	chr3:75615329-75615521	GM12878	blood:	n/a	n/a
47	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
48	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
49	BCL11A	chr3:75483449-75483810	GM12878	blood:	n/a	chr3:75483516-75483525
50	BCL11A	chr3:75596331-75596513	GM12878	blood:	n/a	n/a

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75484440-75484490	HepG2	liver:	n/a
2	chr3:75411217-75411267	HCF	heart:	n/a
3	chr3:75484209-75484259	PFSK-1	brain:	n/a
4	chr3:75484440-75484490	HepG2	liver:	n/a
5	chr3:75411217-75411267	HCF	heart:	n/a
6	chr3:75484209-75484259	PFSK-1	brain:	n/a
7	chr3:75414693-75414743	A549	lung:	n/a
8	chr3:75555938-75555988	NB4	blood:	n/a
9	chr3:75487529-75487579	HL-60	blood:	n/a
10	chr3:75445502-75445552	AG09319	gingival:	n/a
11	chr3:75416171-75416221	NHBE	bronchial:	n/a
12	chr3:75487529-75487579	HCM	heart:	n/a
13	chr3:75484440-75484490	Hepatocyte	liver:	n/a
14	chr3:75555994-75556044	HCT-116	colon:	n/a
15	chr3:75410747-75410797	PrEC	prostate:	n/a
16	chr3:75414486-75414536	HCT-116	colon:	n/a
17	chr3:75410747-75410797	HNPCEpiC	eye:	n/a
18	chr3:75487529-75487579	Caco-2	colon:	n/a
19	chr3:75553762-75553812	HMEC	breast:	n/a
20	chr3:75445502-75445552	AoSMC	blood vessel:	n/a
21	chr3:75484213-75484263	HAEpiC	amniotic membrane:	n/a
22	chr3:75413083-75413133	GM12891	blood:	n/a
23	chr3:75484209-75484259	HRCEpiC	kidney:	n/a
24	chr3:75555994-75556044	PrEC	prostate:	n/a
25	chr3:75441804-75441854	HRE	kidney:	n/a
26	chr3:75553762-75553812	IMR90	lung:	fetal
27	chr3:75415561-75415611	U87	brain:	n/a
28	chr3:75448983-75449033	AG09309	skin:	n/a
29	chr3:75411038-75411088	AG04449	skin:	fetal
30	chr3:75553762-75553812	ProgFib	skin:	n/a
31	chr3:75445738-75445788	SK-N-SH_RA	brain:	n/a
32	chr3:75441804-75441854	BE2_C	brain:	n/a
33	chr3:75487529-75487579	HRE	kidney:	n/a
34	chr3:75441804-75441854	ProgFib	skin:	n/a
35	chr3:75415591-75415641	SK-N-MC	brain:	n/a
36	chr3:75553294-75553344	SK-N-MC	brain:	n/a
37	chr3:75445610-75445660	SK-N-SH_RA	brain:	n/a
38	chr3:75555938-75555988	H1-hESC	embryonic stem cell:	embryo
39	chr3:75415591-75415641	HIPEpiC	eye:	n/a
40	chr3:75553762-75553812	HAEpiC	amniotic membrane:	n/a
41	chr3:75416171-75416221	Caco-2	colon:	n/a
42	chr3:75411217-75411267	HCM	heart:	n/a
43	chr3:75485110-75485160	ovcar-3	ovarian:	n/a
44	chr3:75410789-75410839	HEEpiC	esophagus:	n/a
45	chr3:75410789-75410839	CMK	blood:	n/a
46	chr3:75411421-75411471	HAEpiC	amniotic membrane:	n/a
47	chr3:75444752-75444802	K562	blood:	n/a
48	chr3:75413083-75413133	AoSMC	blood vessel:	n/a
49	chr3:75445610-75445660	Hepatocyte	liver:	n/a
50	chr3:75485448-75485498	HPAEpiC	pulmonary alveolar:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75466672..75467412-chr3:129812592..129813394,2	NB4	blood:
2	chr3:75343455..75344253-chr3:75389889..75390567,2	MCF-7	breast:
3	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
4	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:
5	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
6	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
7	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
8	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
9	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
10	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:

(count:22 , 50 per page) page: 1

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

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
MYLKP1	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
MYLKP1	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
ENSG00000251287	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000248243	chromatin interactions
ENSG00000158483	chromatin interactions
SFRS5	miRNA target sites
ITGB1	miRNA target sites

Extended variants
information (count: 11499 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:11499 , 50 per page) page: 1 2 3 4 5 6 7 ... 230

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189539437	chr3:75346197-75346198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569797940	chr3:75349453-75349454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116628432	chr3:75349467-75349468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558920145	chr3:75349480-75349481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143214238	chr3:75349520-75349521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535206531	chr3:75349532-75349533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148127103	chr3:75349553-75349554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77769456	chr3:75349585-75349586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34487585	chr3:75349594-75349595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548172807	chr3:75349601-75349602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565587416	chr3:75349663-75349664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113101541	chr3:75349671-75349672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530631730	chr3:75349677-75349678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552307629	chr3:75349717-75349718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571771713	chr3:75349772-75349773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539131583	chr3:75349773-75349774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547850005	chr3:75349794-75349795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566060868	chr3:75349982-75349983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113968312	chr3:75349988-75349989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139432423	chr3:75350051-75350052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576643255	chr3:75350138-75350139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558524086	chr3:75350154-75350155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190377271	chr3:75350208-75350209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142598836	chr3:75350294-75350295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576577473	chr3:75350306-75350307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116925590	chr3:75350448-75350449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192799192	chr3:75350449-75350450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574073885	chr3:75350586-75350587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184147067	chr3:75350623-75350624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563443915	chr3:75350657-75350658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150986420	chr3:75350658-75350659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552134394	chr3:75350674-75350675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564261792	chr3:75350733-75350734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532684865	chr3:75350774-75350775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548803677	chr3:75350796-75350797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112232696	chr3:75350802-75350803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547887188	chr3:75350863-75350864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566148661	chr3:75350870-75350871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12490207	chr3:75350891-75350892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544102976	chr3:75350922-75350923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536267837	chr3:75350941-75350942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548525327	chr3:75350942-75350943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570259075	chr3:75350965-75350966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537749685	chr3:75351062-75351063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558766890	chr3:75351105-75351106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375243821	chr3:75351114-75351115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577008754	chr3:75351199-75351200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557290307	chr3:75351242-75351243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534441026	chr3:75351317-75351318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552673575	chr3:75351323-75351324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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

Chromatin state (count:1609 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75346000-75346200	Enhancers	Pancreas	Pancrea
2	chr3:75349400-75349600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr3:75349600-75351000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr3:75349800-75350000	Enhancers	Lung	lung
5	chr3:75349800-75351200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr3:75349800-75351600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:75350000-75350600	Weak transcription	Lung	lung
8	chr3:75350000-75351000	Enhancers	Fetal Lung	lung
9	chr3:75350600-75351400	Enhancers	Lung	lung
10	chr3:75351000-75352200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr3:75351000-75352600	Weak transcription	Fetal Lung	lung
12	chr3:75351200-75352000	Enhancers	Fetal Muscle Leg	muscle
13	chr3:75351400-75352400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr3:75352600-75353000	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr3:75352600-75353600	Enhancers	Fetal Lung	lung
16	chr3:75353200-75354200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:75353400-75353600	Enhancers	Aorta	Aorta
18	chr3:75358800-75359000	Enhancers	Pancreas	Pancrea
19	chr3:75359000-75374600	Weak transcription	Pancreas	Pancrea
20	chr3:75361600-75362200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:75361600-75362800	Enhancers	Primary hematopoietic stem cells	blood
22	chr3:75362800-75369800	Weak transcription	Primary hematopoietic stem cells	blood
23	chr3:75366000-75369800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr3:75368800-75370200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:75369000-75370400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr3:75369200-75370000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr3:75369800-75370000	Enhancers	Primary hematopoietic stem cells	blood
28	chr3:75369800-75370600	Enhancers	H1 Cell Line	embryonic stem cell
29	chr3:75369800-75370600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr3:75369800-75373400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr3:75370000-75370400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr3:75370000-75370600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr3:75370200-75370600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr3:75370200-75370800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr3:75370200-75371400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:75370400-75372000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr3:75370600-75377200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:75370800-75373200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr3:75371400-75371600	Enhancers	Right Atrium	heart
40	chr3:75371400-75372200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:75371400-75372200	Enhancers	Fetal Muscle Leg	muscle
42	chr3:75371600-75374600	Weak transcription	Right Atrium	heart
43	chr3:75372000-75372200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr3:75372200-75373600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr3:75373200-75373400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr3:75373400-75374400	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr3:75373600-75373800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:75374600-75375000	Enhancers	Pancreas	Pancrea
49	chr3:75374600-75375000	Enhancers	Right Atrium	heart
50	chr3:75374600-75377600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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