Variant report

Variant	nsv1052412
Chromosome Location	chr10:26890945-26961634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:738)
CpG islands
(count:916)
Chromatin interactive
region (count:21)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:26895385-26895597	K562	blood:	n/a	n/a
2	ATF2	chr10:26917400-26917850	GM12878	blood:	n/a	n/a
3	ATF2	chr10:26917389-26917782	GM12878	blood:	n/a	n/a
4	ATF3	chr10:26926570-26926744	K562	blood:	n/a	chr10:26926582-26926591
5	ATF3	chr10:26954068-26954353	K562	blood:	n/a	n/a
6	BACH1	chr10:26910868-26911617	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
8	BATF	chr10:26917280-26917726	GM12878	blood:	n/a	n/a
9	BATF	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
10	BATF	chr10:26917429-26917718	GM12878	blood:	n/a	n/a
11	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
12	BCL11A	chr10:26917343-26917726	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:26926497-26926757	K562	blood:	n/a	n/a
14	BHLHE40	chr10:26917448-26917722	GM12878	blood:	n/a	n/a
15	BRCA1	chr10:26952423-26952612	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr10:26954040-26954379	HepG2	liver:	n/a	chr10:26954199-26954210
17	CEBPB	chr10:26925020-26925337	A549	lung:	n/a	n/a
18	CEBPB	chr10:26925018-26925342	K562	blood:	n/a	n/a
19	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
20	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
21	CEBPB	chr10:26954017-26954389	A549	lung:	n/a	chr10:26954199-26954210
22	CEBPB	chr10:26954081-26954382	H1-hESC	embryonic stem cell:	n/a	chr10:26954199-26954210
23	CEBPB	chr10:26925026-26925341	HepG2	liver:	n/a	n/a
24	CEBPB	chr10:26954028-26954383	IMR90	lung:	n/a	chr10:26954199-26954210
25	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
26	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
27	CEBPB	chr10:26954017-26954298	K562	blood:	n/a	chr10:26954199-26954210
28	CEBPB	chr10:26954005-26954489	K562	blood:	n/a	chr10:26954199-26954210
29	CEBPB	chr10:26946921-26947139	HepG2	liver:	n/a	n/a
30	CEBPB	chr10:26925024-26925342	IMR90	lung:	n/a	n/a
31	CEBPB	chr10:26946966-26947172	K562	blood:	n/a	n/a
32	CEBPD	chr10:26954260-26954812	K562	blood:	n/a	n/a
33	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr10:26955538-26955614	K562	blood:	n/a	n/a
35	CTCF	chr10:26916340-26916490	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr10:26936620-26936770	GM12873	blood:	n/a	n/a
37	CTCF	chr10:26895540-26895690	RPTEC	kidney:	n/a	n/a
38	CTCF	chr10:26941268-26941339	GM13977	blood:	n/a	n/a
39	CTCF	chr10:26916340-26916490	GM12864	blood:	n/a	n/a
40	CTCF	chr10:26892329-26892425	GM19239	blood:	n/a	n/a
41	CTCF	chr10:26895400-26895550	HUVEC	blood vessel:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
42	CTCF	chr10:26916420-26916570	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr10:26895400-26895550	AG09309	skin:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
44	CTCF	chr10:26936635-26936849	Gliobla	brain:	n/a	n/a
45	CTCF	chr10:26936700-26936850	GM12867	blood:	n/a	n/a
46	CTCF	chr10:26895340-26895490	HVMF	connective:	n/a	n/a
47	CTCF	chr10:26895560-26895710	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr10:26895376-26895626	LNCaP	prostate:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
49	CTCF	chr10:26936662-26936814	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr10:26936660-26936810	GM12873	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26931986-26932036	HCPEpiC	choroid plexus:	n/a
2	chr10:26931986-26932036	HCPEpiC	choroid plexus:	n/a
3	chr10:26931731-26931781	AG09309	skin:	n/a
4	chr10:26931731-26931781	BJ	skin:	n/a
5	chr10:26931969-26932019	PANC-1	pancreas:	n/a
6	chr10:26931731-26931781	ECC-1	luminal epithelium:	n/a
7	chr10:26931978-26932028	NHBE	bronchial:	n/a
8	chr10:26931978-26932028	ECC-1	luminal epithelium:	n/a
9	chr10:26931969-26932019	HPAEpiC	pulmonary alveolar:	n/a
10	chr10:26932057-26932107	RPTEC	kidney:	n/a
11	chr10:26911186-26911236	NT2-D1	testis:	n/a
12	chr10:26942225-26942275	HAEpiC	amniotic membrane:	n/a
13	chr10:26931978-26932028	Caco-2	colon:	n/a
14	chr10:26911451-26911501	Caco-2	colon:	n/a
15	chr10:26932036-26932086	GM12892	blood:	n/a
16	chr10:26942225-26942275	HRCEpiC	kidney:	n/a
17	chr10:26932036-26932086	T-47D	breast:	n/a
18	chr10:26911451-26911501	Hela-S3	cervix:	n/a
19	chr10:26942165-26942215	HPAEpiC	pulmonary alveolar:	n/a
20	chr10:26930863-26930913	HRPEpiC	eye:	n/a
21	chr10:26942225-26942275	LNCaP	prostate:	n/a
22	chr10:26931991-26932041	U87	brain:	n/a
23	chr10:26931969-26932019	PFSK-1	brain:	n/a
24	chr10:26911451-26911501	GM19239	blood:	n/a
25	chr10:26931969-26932019	MCF10A-Er-Src	breast:	n/a
26	chr10:26930863-26930913	SKMC	muscle:	n/a
27	chr10:26911186-26911236	HCPEpiC	choroid plexus:	n/a
28	chr10:26942225-26942275	H1-hESC	embryonic stem cell:	embryo
29	chr10:26930863-26930913	GM12878	blood:	n/a
30	chr10:26930863-26930913	RPTEC	kidney:	n/a
31	chr10:26931991-26932041	HepG2	liver:	n/a
32	chr10:26931731-26931781	NHDF-neo	bronchial:	n/a
33	chr10:26931969-26932019	HIPEpiC	eye:	n/a
34	chr10:26931978-26932028	IMR90	lung:	fetal
35	chr10:26931794-26931844	T-47D	breast:	n/a
36	chr10:26930863-26930913	HCF	heart:	n/a
37	chr10:26931969-26932019	GM12878	blood:	n/a
38	chr10:26931731-26931781	HRE	kidney:	n/a
39	chr10:26931731-26931781	PFSK-1	brain:	n/a
40	chr10:26911186-26911236	HEEpiC	esophagus:	n/a
41	chr10:26931912-26931962	HCM	heart:	n/a
42	chr10:26942225-26942275	HCM	heart:	n/a
43	chr10:26911186-26911236	HCT-116	colon:	n/a
44	chr10:26932036-26932086	NT2-D1	testis:	n/a
45	chr10:26930863-26930913	HNPCEpiC	eye:	n/a
46	chr10:26932057-26932107	HEK293	kidney:	embryo
47	chr10:26942225-26942275	SK-N-MC	brain:	n/a
48	chr10:26942165-26942215	H1-hESC	embryonic stem cell:	embryo
49	chr10:26932057-26932107	HUVEC	blood vessel:	n/a
50	chr10:26931926-26931976	GM12878	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26954305..26956450-chr10:26987430..26988975,2	K562	blood:
2	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
3	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
4	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
5	chr10:26895094..26895872-chr10:26973347..26973911,2	MCF-7	breast:
6	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
7	chr10:26953025..26955897-chr10:26956336..26959208,3	K562	blood:
8	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:
9	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:
10	chr10:26895059..26895568-chr10:27171114..27171693,2	K562	blood:
11	chr10:26955921..26958837-chr10:26961876..26965160,3	K562	blood:
12	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
13	chr10:26895319..26895931-chr10:26973740..26974253,2	K562	blood:
14	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
15	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
16	chr10:26953025..26955897-chr10:26956336..26959208,3	K562	blood:
17	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
18	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
19	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
20	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
21	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841
2	lnc-APBB1IP-3	chr10:26920245-26920348	NONHSAT011843
3	lnc-APBB1IP-3	chr10:26921785-26921901	NONHSAT011843
4	lnc-PDSS1-1	chr10:26937880-26937946	NONHSAT011834
5	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
6	lnc-APBB1IP-3	chr10:26918800-26919272	NONHSAT011843
7	lnc-PDSS1-1	chr10:26939483-26939586	ENSG00000231976
8	lnc-PDSS1-1	chr10:26937187-26937211	NONHSAT011834
9	lnc-PDSS1-1	chr10:26938261-26938522	ENSG00000231976
10	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
11	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841
12	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
13	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
14	lnc-PDSS1-1	chr10:26939483-26939691	NONHSAT011840
15	lnc-PDSS1-1	chr10:26932157-26932525	XLOC_008421
16	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
17	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes
18	lnc-PDSS1-1	chr10:26941994-26942040	ENSG00000231976
19	lnc-ABI1-1	chr10:26957336-26957423	ENSG00000227932.1
20	lnc-PDSS1-1	chr10:26933843-26933945	XLOC_008421
21	lnc-ABI1-1	chr10:26953135-26953321	ENSG00000227932.1
22	lnc-APBB1IP-3	chr10:26922869-26923259	NONHSAT011843

No data

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

Extended variants
information (count: 3296 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:3296 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541537982	chr10:26890958-26890959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548098791	chr10:26890964-26890965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530260689	chr10:26890985-26890986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547172369	chr10:26890991-26890992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560664711	chr10:26891000-26891001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149719289	chr10:26891001-26891002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77405343	chr10:26891006-26891007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569296979	chr10:26891015-26891016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538209566	chr10:26891018-26891019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548727098	chr10:26891104-26891105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568535733	chr10:26891130-26891131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148961440	chr10:26891131-26891132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143726341	chr10:26891148-26891149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146573233	chr10:26891155-26891156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7086998	chr10:26891185-26891186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539368629	chr10:26891205-26891206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556003695	chr10:26891213-26891214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144828707	chr10:26891233-26891234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575668533	chr10:26891238-26891239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78915562	chr10:26891256-26891257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561682347	chr10:26891272-26891273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185344551	chr10:26891273-26891274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76021530	chr10:26891284-26891285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560741161	chr10:26891306-26891307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76523161	chr10:26891308-26891309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532725372	chr10:26891334-26891335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149573042	chr10:26891343-26891344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368523488	chr10:26891351-26891352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188941070	chr10:26891352-26891353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72481176	chr10:26891354-26891355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545172359	chr10:26891384-26891385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531784876	chr10:26891467-26891468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371855713	chr10:26891484-26891485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144985541	chr10:26891519-26891520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544387391	chr10:26891526-26891527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376745981	chr10:26891536-26891537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562696031	chr10:26891548-26891549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112273847	chr10:26891560-26891561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181050787	chr10:26891567-26891568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561794031	chr10:26891593-26891594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185528559	chr10:26891601-26891602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74713256	chr10:26891632-26891633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74603099	chr10:26891649-26891650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117424426	chr10:26891674-26891675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189601172	chr10:26891678-26891679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535123212	chr10:26891739-26891740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555354611	chr10:26891747-26891748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547428844	chr10:26891769-26891770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571901240	chr10:26891771-26891772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180982827	chr10:26891781-26891782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26860800-26892600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr10:26864600-26894800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr10:26883200-26892800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr10:26883800-26894200	Weak transcription	Fetal Thymus	thymus
5	chr10:26890200-26891200	Enhancers	Thymus	Thymus
6	chr10:26891200-26892400	Weak transcription	Thymus	Thymus
7	chr10:26891800-26893200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr10:26892400-26893600	Enhancers	Thymus	Thymus
9	chr10:26892600-26892800	Flanking Active TSS	A549	lung
10	chr10:26892600-26893800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr10:26892600-26893800	Enhancers	Dnd41	blood
12	chr10:26892800-26893200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr10:26892800-26893400	Enhancers	Primary T cells from cord blood	blood
14	chr10:26892800-26893600	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr10:26892800-26893800	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr10:26893000-26893600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr10:26893600-26895600	Weak transcription	Thymus	Thymus
18	chr10:26893800-26894800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr10:26894200-26897600	Enhancers	Fetal Thymus	thymus
20	chr10:26894800-26895000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr10:26894800-26895400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr10:26895600-26897000	Enhancers	Thymus	Thymus
23	chr10:26900000-26900200	Enhancers	Stomach Mucosa	stomach
24	chr10:26900200-26900800	Weak transcription	Stomach Mucosa	stomach
25	chr10:26900800-26901200	Enhancers	Duodenum Mucosa	Duodenum
26	chr10:26900800-26901800	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr10:26900800-26902200	Enhancers	Liver	Liver
28	chr10:26900800-26902200	Enhancers	Fetal Intestine Small	intestine
29	chr10:26900800-26902200	Enhancers	Stomach Mucosa	stomach
30	chr10:26901200-26901800	Active TSS	Duodenum Mucosa	Duodenum
31	chr10:26901400-26902000	Enhancers	Fetal Intestine Large	intestine
32	chr10:26901800-26902000	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr10:26901800-26902200	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr10:26902200-26905600	Weak transcription	Liver	Liver
35	chr10:26902200-26909400	Weak transcription	Stomach Mucosa	stomach
36	chr10:26905600-26906000	Enhancers	Liver	Liver
37	chr10:26905800-26906000	Enhancers	Fetal Thymus	thymus
38	chr10:26906000-26907000	Weak transcription	Fetal Thymus	thymus
39	chr10:26906000-26910800	Weak transcription	Liver	Liver
40	chr10:26907000-26907400	Enhancers	Fetal Thymus	thymus
41	chr10:26907400-26910800	Weak transcription	Fetal Thymus	thymus
42	chr10:26908000-26911200	Weak transcription	Right Atrium	heart
43	chr10:26908400-26908600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr10:26909400-26909800	Enhancers	Stomach Mucosa	stomach
45	chr10:26909400-26910800	Enhancers	Fetal Intestine Small	intestine
46	chr10:26909800-26910000	Enhancers	Fetal Intestine Large	intestine
47	chr10:26909800-26910800	Weak transcription	Stomach Mucosa	stomach
48	chr10:26909800-26911000	Enhancers	Duodenum Mucosa	Duodenum
49	chr10:26910000-26910600	Weak transcription	Fetal Intestine Large	intestine
50	chr10:26910600-26910800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell

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