Variant report

Variant	nsv1046911
Chromosome Location	chr10:26894348-26969381
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:781)
CpG islands
(count:916)
Chromatin interactive
region (count:27)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	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	BATF	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
9	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
10	BATF	chr10:26917429-26917718	GM12878	blood:	n/a	n/a
11	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
12	BATF	chr10:26917280-26917726	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:26917343-26917726	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:26917448-26917722	GM12878	blood:	n/a	n/a
15	BHLHE40	chr10:26962966-26962980	K562	blood:	n/a	n/a
16	BHLHE40	chr10:26926497-26926757	K562	blood:	n/a	n/a
17	BHLHE40	chr10:26963417-26963432	K562	blood:	n/a	n/a
18	BRCA1	chr10:26952423-26952612	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr10:26964318-26964954	K562	blood:	n/a	n/a
20	CEBPB	chr10:26954005-26954489	K562	blood:	n/a	chr10:26954199-26954210
21	CEBPB	chr10:26946966-26947172	K562	blood:	n/a	n/a
22	CEBPB	chr10:26925026-26925341	HepG2	liver:	n/a	n/a
23	CEBPB	chr10:26925024-26925342	IMR90	lung:	n/a	n/a
24	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
25	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
26	CEBPB	chr10:26925018-26925342	K562	blood:	n/a	n/a
27	CEBPB	chr10:26925020-26925337	A549	lung:	n/a	n/a
28	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
29	CEBPB	chr10:26967830-26968049	K562	blood:	n/a	n/a
30	CEBPB	chr10:26961963-26962220	IMR90	lung:	n/a	chr10:26962123-26962134
31	CEBPB	chr10:26962043-26962214	HepG2	liver:	n/a	chr10:26962123-26962134
32	CEBPB	chr10:26954040-26954379	HepG2	liver:	n/a	chr10:26954199-26954210
33	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
34	CEBPB	chr10:26954081-26954382	H1-hESC	embryonic stem cell:	n/a	chr10:26954199-26954210
35	CEBPB	chr10:26954028-26954383	IMR90	lung:	n/a	chr10:26954199-26954210
36	CEBPB	chr10:26967853-26968029	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr10:26946921-26947139	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:26954017-26954389	A549	lung:	n/a	chr10:26954199-26954210
39	CEBPB	chr10:26954017-26954298	K562	blood:	n/a	chr10:26954199-26954210
40	CEBPB	chr10:26961963-26962323	K562	blood:	n/a	chr10:26962123-26962134
41	CEBPD	chr10:26954260-26954812	K562	blood:	n/a	n/a
42	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr10:26955538-26955614	K562	blood:	n/a	n/a
44	CTCF	chr10:26936620-26936770	GM12871	blood:	n/a	n/a
45	CTCF	chr10:26936740-26936890	WI-38	lung:	n/a	n/a
46	CTCF	chr10:26916460-26916610	NHEK	skin:	n/a	n/a
47	CTCF	chr10:26895380-26895530	SAEC	small airway:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
48	CTCF	chr10:26895440-26895590	GM12801	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
49	CTCF	chr10:26936656-26936835	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:26916360-26916510	AG04449	skin:	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	chr10:26931969-26932019	HEK293	kidney:	embryo
2	chr10:26931969-26932019	HEK293	kidney:	embryo
3	chr10:26932036-26932086	Jurkat	blood:	n/a
4	chr10:26931986-26932036	BE2_C	brain:	n/a
5	chr10:26931926-26931976	HCM	heart:	n/a
6	chr10:26931912-26931962	A549	lung:	n/a
7	chr10:26931991-26932041	IMR90	lung:	fetal
8	chr10:26931912-26931962	SK-N-SH_RA	brain:	n/a
9	chr10:26931986-26932036	GM19239	blood:	n/a
10	chr10:26931912-26931962	HPAEpiC	pulmonary alveolar:	n/a
11	chr10:26932057-26932107	MCF-7	breast:	n/a
12	chr10:26911186-26911236	H1-hESC	embryonic stem cell:	embryo
13	chr10:26930863-26930913	SKMC	muscle:	n/a
14	chr10:26911451-26911501	CMK	blood:	n/a
15	chr10:26930863-26930913	PANC-1	pancreas:	n/a
16	chr10:26931926-26931976	HEEpiC	esophagus:	n/a
17	chr10:26911186-26911236	NHDF-neo	bronchial:	n/a
18	chr10:26932036-26932086	NHBE	bronchial:	n/a
19	chr10:26931991-26932041	BE2_C	brain:	n/a
20	chr10:26931986-26932036	SK-N-SH_RA	brain:	n/a
21	chr10:26942165-26942215	HRPEpiC	eye:	n/a
22	chr10:26932036-26932086	HRCEpiC	kidney:	n/a
23	chr10:26931986-26932036	HEK293	kidney:	embryo
24	chr10:26930863-26930913	GM19239	blood:	n/a
25	chr10:26931926-26931976	GM19239	blood:	n/a
26	chr10:26931969-26932019	H1-hESC	embryonic stem cell:	embryo
27	chr10:26942225-26942275	AoSMC	blood vessel:	n/a
28	chr10:26932036-26932086	AG04450	lung:	fetal
29	chr10:26931978-26932028	ProgFib	skin:	n/a
30	chr10:26931912-26931962	Caco-2	colon:	n/a
31	chr10:26911451-26911501	SK-N-SH	brain:	n/a
32	chr10:26931731-26931781	NT2-D1	testis:	n/a
33	chr10:26931731-26931781	GM06990	blood:	n/a
34	chr10:26911186-26911236	HRCEpiC	kidney:	n/a
35	chr10:26911186-26911236	MCF-7	breast:	n/a
36	chr10:26942225-26942275	GM12878	blood:	n/a
37	chr10:26931978-26932028	AG09309	skin:	n/a
38	chr10:26932036-26932086	BJ	skin:	n/a
39	chr10:26932036-26932086	GM12892	blood:	n/a
40	chr10:26911186-26911236	SK-N-SH	brain:	n/a
41	chr10:26911186-26911236	IMR90	lung:	fetal
42	chr10:26931794-26931844	AG09309	skin:	n/a
43	chr10:26932057-26932107	Hela-S3	cervix:	n/a
44	chr10:26911186-26911236	HepG2	liver:	n/a
45	chr10:26931912-26931962	NB4	blood:	n/a
46	chr10:26931978-26932028	HepG2	liver:	n/a
47	chr10:26930863-26930913	CMK	blood:	n/a
48	chr10:26911451-26911501	HL-60	blood:	n/a
49	chr10:26942165-26942215	U87	brain:	n/a
50	chr10:26931978-26932028	NB4	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26955921..26958837-chr10:26961876..26965160,3	K562	blood:
2	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
3	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:
4	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:
5	chr10:26953025..26955897-chr10:26956336..26959208,3	K562	blood:
6	chr10:26895059..26895568-chr10:27171114..27171693,2	K562	blood:
7	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
8	chr10:26953025..26955897-chr10:26956336..26959208,3	K562	blood:
9	chr10:26968705..26971277-chr10:26973238..26975564,2	K562	blood:
10	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
11	chr10:26965108..26970102-chr10:26984839..26987979,6	K562	blood:
12	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
13	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
14	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
15	chr10:26954305..26956450-chr10:26987430..26988975,2	K562	blood:
16	chr10:26895319..26895931-chr10:26973740..26974253,2	K562	blood:
17	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:
18	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
19	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:
20	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
21	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:
22	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:
23	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:
24	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
25	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
26	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
27	chr10:26895094..26895872-chr10:26973347..26973911,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841
2	lnc-ABI1-1	chr10:26965045-26965088	ENSG00000227932.1
3	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841
4	lnc-PDSS1-1	chr10:26937880-26937946	NONHSAT011834
5	lnc-PDSS1-1	chr10:26939483-26939691	NONHSAT011840
6	lnc-APBB1IP-3	chr10:26922869-26923259	NONHSAT011843
7	lnc-APBB1IP-3	chr10:26920245-26920348	NONHSAT011843
8	lnc-PDSS1-1	chr10:26933843-26933945	XLOC_008421
9	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
10	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
11	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
12	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
13	lnc-PDSS1-1	chr10:26932157-26932525	XLOC_008421
14	lnc-PDSS1-1	chr10:26939483-26939586	ENSG00000231976
15	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes
16	lnc-APBB1IP-3	chr10:26918800-26919272	NONHSAT011843
17	lnc-PDSS1-1	chr10:26938261-26938522	ENSG00000231976
18	lnc-APBB1IP-3	chr10:26921785-26921901	NONHSAT011843
19	lnc-PDSS1-1	chr10:26937187-26937211	NONHSAT011834
20	lnc-ABI1-1	chr10:26953135-26953321	ENSG00000227932.1
21	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
22	lnc-PDSS1-1	chr10:26941994-26942040	ENSG00000231976
23	lnc-ABI1-1	chr10:26957336-26957423	ENSG00000227932.1

No data

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

Extended variants
information (count: 3502 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:3502 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10829032	chr10:26894348-26894349	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146591408	chr10:26894372-26894373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371247258	chr10:26894380-26894381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574677438	chr10:26894405-26894406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546411971	chr10:26894410-26894411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141274039	chr10:26894469-26894470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs787028	chr10:26894544-26894545	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs186493040	chr10:26894591-26894592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2985468	chr10:26894611-26894612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550553949	chr10:26894632-26894633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376095397	chr10:26894677-26894678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563469688	chr10:26894690-26894691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372392395	chr10:26894727-26894728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35025871	chr10:26894733-26894734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537368739	chr10:26894774-26894775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557597222	chr10:26894783-26894784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567587996	chr10:26894801-26894802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536624996	chr10:26894826-26894827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570452622	chr10:26894838-26894839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs57427513	chr10:26894860-26894861	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs61838890	chr10:26894877-26894878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573363738	chr10:26894882-26894883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539097071	chr10:26894891-26894892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190534458	chr10:26894894-26894895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575484287	chr10:26894902-26894903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183142895	chr10:26894917-26894918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185654235	chr10:26894949-26894950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566225961	chr10:26894967-26894968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528786444	chr10:26894969-26894970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191359252	chr10:26895005-26895006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540222271	chr10:26895014-26895015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560031154	chr10:26895017-26895018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532079369	chr10:26895047-26895048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146776263	chr10:26895197-26895198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376165110	chr10:26895214-26895215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530992508	chr10:26895221-26895222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551016292	chr10:26895241-26895242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567942405	chr10:26895287-26895288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183278612	chr10:26895314-26895315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373845691	chr10:26895432-26895433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149012708	chr10:26895441-26895442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143833719	chr10:26895444-26895445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558577693	chr10:26895459-26895460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375277018	chr10:26895460-26895461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141967176	chr10:26895487-26895488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187453742	chr10:26895496-26895497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556190077	chr10:26895516-26895517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146752844	chr10:26895537-26895538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569804840	chr10:26895554-26895555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2183041	chr10:26895560-26895561	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26864600-26894800	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr10:26893600-26895600	Weak transcription	Thymus	Thymus
3	chr10:26893800-26894800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr10:26894200-26897600	Enhancers	Fetal Thymus	thymus
5	chr10:26894800-26895000	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr10:26894800-26895400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr10:26895600-26897000	Enhancers	Thymus	Thymus
8	chr10:26900000-26900200	Enhancers	Stomach Mucosa	stomach
9	chr10:26900200-26900800	Weak transcription	Stomach Mucosa	stomach
10	chr10:26900800-26901200	Enhancers	Duodenum Mucosa	Duodenum
11	chr10:26900800-26901800	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr10:26900800-26902200	Enhancers	Liver	Liver
13	chr10:26900800-26902200	Enhancers	Fetal Intestine Small	intestine
14	chr10:26900800-26902200	Enhancers	Stomach Mucosa	stomach
15	chr10:26901200-26901800	Active TSS	Duodenum Mucosa	Duodenum
16	chr10:26901400-26902000	Enhancers	Fetal Intestine Large	intestine
17	chr10:26901800-26902000	Flanking Active TSS	Duodenum Mucosa	Duodenum
18	chr10:26901800-26902200	Active TSS	Rectal Mucosa Donor 29	rectum
19	chr10:26902200-26905600	Weak transcription	Liver	Liver
20	chr10:26902200-26909400	Weak transcription	Stomach Mucosa	stomach
21	chr10:26905600-26906000	Enhancers	Liver	Liver
22	chr10:26905800-26906000	Enhancers	Fetal Thymus	thymus
23	chr10:26906000-26907000	Weak transcription	Fetal Thymus	thymus
24	chr10:26906000-26910800	Weak transcription	Liver	Liver
25	chr10:26907000-26907400	Enhancers	Fetal Thymus	thymus
26	chr10:26907400-26910800	Weak transcription	Fetal Thymus	thymus
27	chr10:26908000-26911200	Weak transcription	Right Atrium	heart
28	chr10:26908400-26908600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr10:26909400-26909800	Enhancers	Stomach Mucosa	stomach
30	chr10:26909400-26910800	Enhancers	Fetal Intestine Small	intestine
31	chr10:26909800-26910000	Enhancers	Fetal Intestine Large	intestine
32	chr10:26909800-26910800	Weak transcription	Stomach Mucosa	stomach
33	chr10:26909800-26911000	Enhancers	Duodenum Mucosa	Duodenum
34	chr10:26910000-26910600	Weak transcription	Fetal Intestine Large	intestine
35	chr10:26910600-26910800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
36	chr10:26910600-26910800	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr10:26910600-26910800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr10:26910600-26910800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr10:26910600-26910800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr10:26910600-26910800	Enhancers	Fetal Intestine Large	intestine
41	chr10:26910600-26910800	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr10:26910600-26910800	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr10:26910600-26910800	Enhancers	NHEK	skin
44	chr10:26910600-26911000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr10:26910600-26911200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr10:26910600-26911800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr10:26910800-26911000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr10:26910800-26911000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr10:26910800-26911000	Enhancers	Primary hematopoietic stem cells	blood
50	chr10:26910800-26911000	Enhancers	Adipose Nuclei	Adipose

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