Variant report

Variant	esv3333006
Chromosome Location	chr10:26908323-26985227
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:829)
CpG islands
(count:979)
Chromatin interactive
region (count:30)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:26973565-26973899	K562	blood:	n/a	n/a
2	ATF1	chr10:26964570-26964881	K562	blood:	n/a	n/a
3	ATF2	chr10:26917389-26917782	GM12878	blood:	n/a	n/a
4	ATF2	chr10:26917400-26917850	GM12878	blood:	n/a	n/a
5	ATF3	chr10:26954068-26954353	K562	blood:	n/a	n/a
6	ATF3	chr10:26926570-26926744	K562	blood:	n/a	chr10:26926582-26926591
7	BACH1	chr10:26910868-26911617	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:26973707-26973757	K562	blood:	n/a	n/a
9	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
10	BATF	chr10:26973677-26973926	GM12878	blood:	n/a	n/a
11	BATF	chr10:26917429-26917718	GM12878	blood:	n/a	n/a
12	BATF	chr10:26917280-26917726	GM12878	blood:	n/a	n/a
13	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
14	BCL11A	chr10:26917343-26917726	GM12878	blood:	n/a	n/a
15	BHLHE40	chr10:26917448-26917722	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:26973734-26973939	K562	blood:	n/a	n/a
17	BHLHE40	chr10:26980191-26980254	K562	blood:	n/a	n/a
18	BHLHE40	chr10:26963417-26963432	K562	blood:	n/a	n/a
19	BHLHE40	chr10:26962966-26962980	K562	blood:	n/a	n/a
20	BHLHE40	chr10:26926497-26926757	K562	blood:	n/a	n/a
21	BRCA1	chr10:26952423-26952612	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr10:26964318-26964954	K562	blood:	n/a	n/a
23	CEBPB	chr10:26954017-26954389	A549	lung:	n/a	chr10:26954199-26954210
24	CEBPB	chr10:26961963-26962220	IMR90	lung:	n/a	chr10:26962123-26962134
25	CEBPB	chr10:26954081-26954382	H1-hESC	embryonic stem cell:	n/a	chr10:26954199-26954210
26	CEBPB	chr10:26925024-26925342	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:26946966-26947172	K562	blood:	n/a	n/a
28	CEBPB	chr10:26954028-26954383	IMR90	lung:	n/a	chr10:26954199-26954210
29	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
30	CEBPB	chr10:26961963-26962323	K562	blood:	n/a	chr10:26962123-26962134
31	CEBPB	chr10:26954017-26954298	K562	blood:	n/a	chr10:26954199-26954210
32	CEBPB	chr10:26954005-26954489	K562	blood:	n/a	chr10:26954199-26954210
33	CEBPB	chr10:26925026-26925341	HepG2	liver:	n/a	n/a
34	CEBPB	chr10:26972547-26972840	HepG2	liver:	n/a	chr10:26972694-26972705
35	CEBPB	chr10:26967853-26968029	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr10:26967830-26968049	K562	blood:	n/a	n/a
37	CEBPB	chr10:26925020-26925337	A549	lung:	n/a	n/a
38	CEBPB	chr10:26954040-26954379	HepG2	liver:	n/a	chr10:26954199-26954210
39	CEBPB	chr10:26972520-26972834	IMR90	lung:	n/a	chr10:26972694-26972705
40	CEBPB	chr10:26972612-26972824	A549	lung:	n/a	chr10:26972694-26972705
41	CEBPB	chr10:26946921-26947139	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:26972539-26972809	K562	blood:	n/a	chr10:26972694-26972705
43	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
44	CEBPB	chr10:26962043-26962214	HepG2	liver:	n/a	chr10:26962123-26962134
45	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
46	CEBPB	chr10:26925018-26925342	K562	blood:	n/a	n/a
47	CEBPD	chr10:26954260-26954812	K562	blood:	n/a	n/a
48	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr10:26955538-26955614	K562	blood:	n/a	n/a
50	CTCF	chr10:26936655-26936852	GM19238	blood:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26942225-26942275	NHBE	bronchial:	n/a
2	chr10:26911186-26911236	HCT-116	colon:	n/a
3	chr10:26942225-26942275	Jurkat	blood:	n/a
4	chr10:26942225-26942275	NHBE	bronchial:	n/a
5	chr10:26911186-26911236	HCT-116	colon:	n/a
6	chr10:26942225-26942275	Jurkat	blood:	n/a
7	chr10:26911451-26911501	HepG2	liver:	n/a
8	chr10:26931969-26932019	AG04450	lung:	fetal
9	chr10:26942165-26942215	PrEC	prostate:	n/a
10	chr10:26911451-26911501	AG04450	lung:	fetal
11	chr10:26911186-26911236	HRCEpiC	kidney:	n/a
12	chr10:26932057-26932107	HPAEpiC	pulmonary alveolar:	n/a
13	chr10:26931731-26931781	HPAEpiC	pulmonary alveolar:	n/a
14	chr10:26931912-26931962	RPTEC	kidney:	n/a
15	chr10:26932036-26932086	HCPEpiC	choroid plexus:	n/a
16	chr10:26931912-26931962	HEK293	kidney:	embryo
17	chr10:26931978-26932028	HPAEpiC	pulmonary alveolar:	n/a
18	chr10:26911451-26911501	AG04449	skin:	fetal
19	chr10:26931978-26932028	H1-hESC	embryonic stem cell:	embryo
20	chr10:26911451-26911501	HCM	heart:	n/a
21	chr10:26931731-26931781	HL-60	blood:	n/a
22	chr10:26931912-26931962	PrEC	prostate:	n/a
23	chr10:26931991-26932041	AG09319	gingival:	n/a
24	chr10:26931794-26931844	HL-60	blood:	n/a
25	chr10:26932057-26932107	LNCaP	prostate:	n/a
26	chr10:26931986-26932036	HEK293	kidney:	embryo
27	chr10:26931926-26931976	HRCEpiC	kidney:	n/a
28	chr10:26931731-26931781	BJ	skin:	n/a
29	chr10:26931978-26932028	GM06990	blood:	n/a
30	chr10:26931978-26932028	HCT-116	colon:	n/a
31	chr10:26932036-26932086	ECC-1	luminal epithelium:	n/a
32	chr10:26931969-26932019	HCPEpiC	choroid plexus:	n/a
33	chr10:26911451-26911501	HAEpiC	amniotic membrane:	n/a
34	chr10:26931731-26931781	H1-hESC	embryonic stem cell:	embryo
35	chr10:26911451-26911501	Hepatocyte	liver:	n/a
36	chr10:26983600-26983650	GM19239	blood:	n/a
37	chr10:26931794-26931844	T-47D	breast:	n/a
38	chr10:26931969-26932019	ECC-1	luminal epithelium:	n/a
39	chr10:26931991-26932041	RPTEC	kidney:	n/a
40	chr10:26931926-26931976	Hepatocyte	liver:	n/a
41	chr10:26911186-26911236	HL-60	blood:	n/a
42	chr10:26930863-26930913	HCM	heart:	n/a
43	chr10:26942225-26942275	GM19239	blood:	n/a
44	chr10:26911451-26911501	T-47D	breast:	n/a
45	chr10:26931731-26931781	NH-A	brain:	n/a
46	chr10:26983600-26983650	NH-A	brain:	n/a
47	chr10:26931969-26932019	GM06990	blood:	n/a
48	chr10:26932036-26932086	MCF-7	breast:	n/a
49	chr10:26911451-26911501	BJ	skin:	n/a
50	chr10:26931926-26931976	HL-60	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26953025..26955897-chr10:26956336..26959208,3	K562	blood:
2	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
3	chr10:26968705..26971277-chr10:26973238..26975564,2	K562	blood:
4	chr10:26973781..26976716-chr10:26986143..26988490,2	K562	blood:
5	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
6	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:
7	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:
8	chr10:26985057..26986781-chr10:27006850..27009579,2	K562	blood:
9	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
10	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
11	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:
12	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
13	chr10:26968705..26971277-chr10:26973238..26975564,2	K562	blood:
14	chr10:26979944..26983109-chr10:26984592..26988021,5	MCF-7	breast:
15	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
16	chr10:26955921..26958837-chr10:26961876..26965160,3	K562	blood:
17	chr10:26895319..26895931-chr10:26973740..26974253,2	K562	blood:
18	chr10:26895094..26895872-chr10:26973347..26973911,2	MCF-7	breast:
19	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
20	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
21	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
22	chr10:26953025..26955897-chr10:26956336..26959208,3	K562	blood:
23	chr10:26954305..26956450-chr10:26987430..26988975,2	K562	blood:
24	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:
25	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
26	chr10:26972585..26978071-chr10:26984536..26988033,8	MCF-7	breast:
27	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:
28	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:
29	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:
30	chr10:26965108..26970102-chr10:26984839..26987979,6	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDSS1-3	chr10:26982000-26982046	NONHSAT011855
2	lnc-PDSS1-1	chr10:26938261-26938522	ENSG00000231976
3	lnc-PDSS1-3	chr10:26978267-26978528	NONHSAT011855
4	lnc-ABI1-1	chr10:26965045-26965088	ENSG00000227932.1
5	lnc-PDSS1-1	chr10:26941994-26942040	ENSG00000231976
6	lnc-APBB1IP-3	chr10:26918800-26919272	NONHSAT011843
7	lnc-PDSS1-1	chr10:26939483-26939586	ENSG00000231976
8	lnc-APBB1IP-3	chr10:26921785-26921901	NONHSAT011843
9	lnc-PDSS1-3	chr10:26978326-26978528	NONHSAT011853
10	lnc-PDSS1-3	chr10:26982000-26982389	NONHSAT011854
11	lnc-APBB1IP-3	chr10:26922869-26923259	NONHSAT011843
12	lnc-PDSS1-1	chr10:26939483-26939691	NONHSAT011840
13	lnc-PDSS1-3	chr10:26979489-26979592	NONHSAT011855
14	lnc-PDSS1-1	chr10:26937187-26937211	NONHSAT011834
15	lnc-APBB1IP-3	chr10:26920245-26920348	NONHSAT011843
16	lnc-PDSS1-5	chr10:26973849-26973951	NONHSAT011852
17	lnc-PDSS1-1	chr10:26937880-26937946	NONHSAT011834
18	lnc-PDSS1-1	chr10:26933843-26933945	XLOC_008421
19	lnc-ABI1-1	chr10:26957336-26957423	ENSG00000227932.1
20	lnc-PDSS1-3	chr10:26976921-26977217	NONHSAT011853
21	lnc-ABI1-1	chr10:26953135-26953321	ENSG00000227932.1
22	lnc-PDSS1-1	chr10:26932157-26932525	XLOC_008421
23	lnc-PDSS1-3	chr10:26982000-26982381	NONHSAT011853
24	lnc-PDSS1-3	chr10:26977035-26977217	NONHSAT011854
25	lnc-ABI1-7	chr10:26984020-26986554	NONHSAT011856
26	lnc-PDSS1-3	chr10:26979489-26979726	NONHSAT011853
27	lnc-PDSS1-3	chr10:26977886-26977985	NONHSAT011853
28	lnc-PDSS1-5	chr10:26972163-26972531	NONHSAT011852
29	lnc-PDSS1-3	chr10:26978326-26978528	NONHSAT011854
30	lnc-PDSS1-3	chr10:26979489-26979592	NONHSAT011854

No data

Variant related genes	Relation type
ENSG00000234296	TF binding region
ENSG00000227932	TF binding region
LINC00202-2	TF binding region
PDSS1	TF binding region
ENSG00000234296	CpG island
ENSG00000227932	CpG island
LINC00202-2	CpG island
PDSS1	CpG island
ENSG00000148459	chromatin interactions
ENSG00000227932	chromatin interactions
PDGFRA	miRNA target sites
DNMT1	miRNA target sites

Extended variants
information (count: 3728 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:3728 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190349063	chr10:26908327-26908328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs202234980	chr10:26908333-26908334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549137781	chr10:26908337-26908338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530520787	chr10:26908347-26908348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559393697	chr10:26908348-26908349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7087647	chr10:26908355-26908356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs72481181	chr10:26908372-26908373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs114929685	chr10:26908386-26908387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570931362	chr10:26908420-26908421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35425910	chr10:26908431-26908432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181563767	chr10:26908457-26908458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186617381	chr10:26908465-26908466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200399462	chr10:26908467-26908468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7911815	chr10:26908475-26908476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535453997	chr10:26908476-26908477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7922616	chr10:26908487-26908488	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs369403099	chr10:26908523-26908524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534774251	chr10:26908542-26908543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566818107	chr10:26908568-26908569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146469898	chr10:26908570-26908571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377409864	chr10:26908575-26908576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542500051	chr10:26908582-26908583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561265942	chr10:26908592-26908593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200800456	chr10:26908602-26908603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191013475	chr10:26908611-26908612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368436134	chr10:26908614-26908615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546814109	chr10:26908616-26908617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180842474	chr10:26908619-26908620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374434932	chr10:26908642-26908643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542645207	chr10:26908679-26908680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559054809	chr10:26908686-26908687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372237207	chr10:26908689-26908690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528215315	chr10:26908691-26908692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185246798	chr10:26908723-26908724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375254363	chr10:26908724-26908725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189666598	chr10:26908741-26908742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183394094	chr10:26908742-26908743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72481182	chr10:26908798-26908799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs369761373	chr10:26908818-26908819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570018157	chr10:26908866-26908867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529503291	chr10:26908875-26908876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113353195	chr10:26908896-26908897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375945986	chr10:26908936-26908937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373354892	chr10:26908938-26908939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538358548	chr10:26908955-26908956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191947772	chr10:26908965-26908966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535147049	chr10:26908992-26908993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111523328	chr10:26909037-26909038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571506392	chr10:26909053-26909054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537238030	chr10:26909080-26909081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:42)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26902200-26909400	Weak transcription	Stomach Mucosa	stomach
2	chr10:26906000-26910800	Weak transcription	Liver	Liver
3	chr10:26907400-26910800	Weak transcription	Fetal Thymus	thymus
4	chr10:26908000-26911200	Weak transcription	Right Atrium	heart
5	chr10:26908400-26908600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr10:26909400-26909800	Enhancers	Stomach Mucosa	stomach
7	chr10:26909400-26910800	Enhancers	Fetal Intestine Small	intestine
8	chr10:26909800-26910000	Enhancers	Fetal Intestine Large	intestine
9	chr10:26909800-26910800	Weak transcription	Stomach Mucosa	stomach
10	chr10:26909800-26911000	Enhancers	Duodenum Mucosa	Duodenum
11	chr10:26910000-26910600	Weak transcription	Fetal Intestine Large	intestine
12	chr10:26910600-26910800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr10:26910600-26910800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr10:26910600-26910800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr10:26910600-26910800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:26910600-26910800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr10:26910600-26910800	Enhancers	Fetal Intestine Large	intestine
18	chr10:26910600-26910800	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr10:26910600-26910800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr10:26910600-26910800	Enhancers	NHEK	skin
21	chr10:26910600-26911000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr10:26910600-26911200	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr10:26910600-26911800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr10:26910800-26911000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr10:26910800-26911000	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr10:26910800-26911000	Enhancers	Primary hematopoietic stem cells	blood
27	chr10:26910800-26911000	Enhancers	Adipose Nuclei	Adipose
28	chr10:26910800-26911000	Flanking Active TSS	Fetal Intestine Large	intestine
29	chr10:26910800-26911000	Flanking Active TSS	Fetal Intestine Small	intestine
30	chr10:26910800-26911000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
31	chr10:26910800-26911000	Flanking Active TSS	Stomach Mucosa	stomach
32	chr10:26910800-26911000	Enhancers	HMEC	breast
33	chr10:26910800-26911200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
34	chr10:26910800-26911200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
35	chr10:26910800-26911200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr10:26910800-26911200	Bivalent/Poised TSS	Fetal Stomach	stomach
37	chr10:26910800-26911200	Enhancers	Fetal Thymus	thymus
38	chr10:26910800-26911200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr10:26910800-26911400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
40	chr10:26910800-26911400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
41	chr10:26910800-26911400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
42	chr10:26910800-26911600	Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr10:26910800-26911600	Active TSS	Pancreas	Pancrea
44	chr10:26910800-26911600	Flanking Active TSS	NHEK	skin
45	chr10:26910800-26911800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
46	chr10:26910800-26911800	Flanking Active TSS	Liver	Liver
47	chr10:26910800-26911800	Active TSS	Rectal Smooth Muscle	rectum
48	chr10:26910800-26912000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr10:26910800-26912000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
50	chr10:26910800-26912000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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