Variant report

Variant	esv2755215
Chromosome Location	chr11:59515524-59529524
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:933)
CpG islands
(count:736)
Chromatin interactive
region (count:43)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:59523254-59523785	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:59523419-59523921	K562	blood:	n/a	n/a
3	ARID3A	chr11:59521549-59521749	K562	blood:	n/a	n/a
4	ARID3A	chr11:59524418-59524618	K562	blood:	n/a	n/a
5	ATF2	chr11:59521422-59521868	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:59521454-59521976	GM12878	blood:	n/a	n/a
7	ATF2	chr11:59521445-59521896	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr11:59523431-59523657	K562	blood:	n/a	n/a
9	ATF3	chr11:59523170-59523502	K562	blood:	n/a	n/a
10	ATF3	chr11:59521495-59521831	K562	blood:	n/a	n/a
11	ATF3	chr11:59523117-59523395	K562	blood:	n/a	n/a
12	BACH1	chr11:59522316-59522839	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:59524392-59524707	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:59524098-59524690	K562	blood:	n/a	n/a
15	BACH1	chr11:59521481-59521838	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr11:59524441-59524676	GM12878	blood:	n/a	chr11:59524540-59524551
17	BATF	chr11:59524405-59524623	GM12878	blood:	n/a	chr11:59524540-59524551
18	BHLHE40	chr11:59516559-59516677	K562	blood:	n/a	n/a
19	BHLHE40	chr11:59523092-59523651	HepG2	liver:	n/a	n/a
20	BHLHE40	chr11:59521493-59521818	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:59521511-59523765	K562	blood:	n/a	chr11:59522833-59522849
22	BHLHE40	chr11:59523246-59523639	A549	lung:	n/a	n/a
23	BHLHE40	chr11:59524324-59524737	K562	blood:	n/a	n/a
24	BRCA1	chr11:59521602-59521603	GM12878	blood:	n/a	n/a
25	BRCA1	chr11:59522313-59522619	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr11:59523192-59523757	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr11:59521296-59522730	K562	blood:	n/a	n/a
28	CBX3	chr11:59523076-59523821	K562	blood:	n/a	n/a
29	CBX3	chr11:59521461-59521771	K562	blood:	n/a	n/a
30	CCNT2	chr11:59522529-59523681	K562	blood:	n/a	chr11:59523266-59523275 chr11:59523261-59523270 chr11:59523641-59523650
31	CCNT2	chr11:59521553-59521847	K562	blood:	n/a	n/a
32	CEBPB	chr11:59521431-59521818	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:59521401-59521635	HepG2	liver:	n/a	n/a
34	CEBPB	chr11:59522250-59522570	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:59521371-59521843	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr11:59523142-59523842	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:59521436-59521605	K562	blood:	n/a	n/a
38	CEBPB	chr11:59521443-59521800	K562	blood:	n/a	n/a
39	CEBPB	chr11:59515550-59515822	K562	blood:	n/a	n/a
40	CEBPD	chr11:59523059-59523726	K562	blood:	n/a	n/a
41	CHD1	chr11:59521587-59521897	GM12878	blood:	n/a	n/a
42	CHD1	chr11:59521640-59521882	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr11:59522324-59522787	K562	blood:	n/a	n/a
44	CHD2	chr11:59521552-59521755	HepG2	liver:	n/a	n/a
45	CHD2	chr11:59521551-59521780	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr11:59523324-59523524	HepG2	liver:	n/a	n/a
47	CHD2	chr11:59522227-59523680	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr11:59522496-59522809	HepG2	liver:	n/a	n/a
49	CHD2	chr11:59523037-59523551	K562	blood:	n/a	n/a
50	CHD2	chr11:59521530-59521733	GM12878	blood:	n/a	n/a

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59522822-59522872	HRE	kidney:	n/a
2	chr11:59523399-59523449	NHBE	bronchial:	n/a
3	chr11:59521722-59521772	AG10803	skin:	n/a
4	chr11:59522917-59522967	MCF10A-Er-Src	breast:	n/a
5	chr11:59522822-59522872	HRE	kidney:	n/a
6	chr11:59523399-59523449	NHBE	bronchial:	n/a
7	chr11:59521722-59521772	AG10803	skin:	n/a
8	chr11:59522917-59522967	MCF10A-Er-Src	breast:	n/a
9	chr11:59523399-59523449	T-47D	breast:	n/a
10	chr11:59522822-59522872	T-47D	breast:	n/a
11	chr11:59521722-59521772	NHBE	bronchial:	n/a
12	chr11:59522087-59522137	U87	brain:	n/a
13	chr11:59521791-59521841	U87	brain:	n/a
14	chr11:59523120-59523170	NB4	blood:	n/a
15	chr11:59522917-59522967	PFSK-1	brain:	n/a
16	chr11:59518964-59519014	NHDF-neo	bronchial:	n/a
17	chr11:59518964-59519014	GM12892	blood:	n/a
18	chr11:59525433-59525483	MCF10A-Er-Src	breast:	n/a
19	chr11:59523120-59523170	HRPEpiC	eye:	n/a
20	chr11:59522087-59522137	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:59521722-59521772	HRE	kidney:	n/a
22	chr11:59521791-59521841	SKMC	muscle:	n/a
23	chr11:59522917-59522967	PANC-1	pancreas:	n/a
24	chr11:59521791-59521841	AoSMC	blood vessel:	n/a
25	chr11:59521665-59521715	HIPEpiC	eye:	n/a
26	chr11:59523120-59523170	AG09319	gingival:	n/a
27	chr11:59518964-59519014	HCT-116	colon:	n/a
28	chr11:59521665-59521715	LNCaP	prostate:	n/a
29	chr11:59521722-59521772	MCF10A-Er-Src	breast:	n/a
30	chr11:59522827-59522877	NT2-D1	testis:	n/a
31	chr11:59521791-59521841	H1-hESC	embryonic stem cell:	embryo
32	chr11:59522917-59522967	NT2-D1	testis:	n/a
33	chr11:59522917-59522967	CMK	blood:	n/a
34	chr11:59522822-59522872	SAEC	small airway:	n/a
35	chr11:59522822-59522872	HNPCEpiC	eye:	n/a
36	chr11:59522917-59522967	H1-hESC	embryonic stem cell:	embryo
37	chr11:59518964-59519014	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:59522542-59522592	HEK293	kidney:	embryo
39	chr11:59522822-59522872	SK-N-SH	brain:	n/a
40	chr11:59522087-59522137	CMK	blood:	n/a
41	chr11:59521791-59521841	HRE	kidney:	n/a
42	chr11:59522087-59522137	HRPEpiC	eye:	n/a
43	chr11:59522542-59522592	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:59518964-59519014	MCF-7	breast:	n/a
45	chr11:59521722-59521772	PrEC	prostate:	n/a
46	chr11:59522542-59522592	AG09319	gingival:	n/a
47	chr11:59522827-59522877	GM19239	blood:	n/a
48	chr11:59522087-59522137	SKMC	muscle:	n/a
49	chr11:59521722-59521772	Jurkat	blood:	n/a
50	chr11:59521722-59521772	HCPEpiC	choroid plexus:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:59381725..59384642-chr11:59521273..59522941,2	K562	blood:
2	chr11:59520651..59522378-chr11:59577196..59579780,2	K562	blood:
3	chr11:59521037..59522134-chr11:59569735..59571070,7	MCF-7	breast:
4	chr11:59524470..59526644-chr11:59576559..59579477,2	K562	blood:
5	chr11:59435116..59437063-chr11:59524775..59526282,2	MCF-7	breast:
6	chr1:114301552..114304210-chr11:59521950..59524919,2	MCF-7	breast:
7	chr11:59480505..59482058-chr11:59521372..59523220,2	MCF-7	breast:
8	chr1:114300956..114303148-chr11:59521456..59522999,2	MCF-7	breast:
9	chr11:59521347..59522076-chr11:59577896..59578446,2	MCF-7	breast:
10	chr11:59517040..59519378-chr11:59520146..59522699,3	K562	blood:
11	chr11:59520935..59525781-chr11:59552803..59557885,8	MCF-7	breast:
12	chr11:59522643..59524451-chr16:67197812..67200302,2	MCF-7	breast:
13	chr11:59436132..59436823-chr11:59522370..59523215,2	Hela-S3	cervix:
14	chr11:59524561..59526544-chr11:59527654..59529309,2	K562	blood:
15	chr11:59514703..59516740-chr11:59522091..59524203,2	MCF-7	breast:
16	chr11:59434813..59437700-chr11:59527969..59532130,3	K562	blood:
17	chr11:59434314..59436454-chr11:59523129..59524749,2	MCF-7	breast:
18	chr11:59524561..59526544-chr11:59527654..59529309,2	K562	blood:
19	chr11:59528800..59530439-chr11:59536843..59538361,2	K562	blood:
20	chr11:59501872..59503940-chr11:59513222..59515810,2	K562	blood:
21	chr11:59513939..59516832-chr11:59518797..59521533,2	K562	blood:
22	chr11:59434813..59437700-chr11:59529153..59532130,2	K562	blood:
23	chr11:59527952..59530580-chr11:59535251..59538243,2	MCF-7	breast:
24	chr11:59528968..59531092-chr11:59531275..59534785,3	MCF-7	breast:
25	chr11:59521605..59525070-chr11:59543036..59549785,6	MCF-7	breast:
26	chr11:59521565..59522093-chr11:59577744..59578503,3	K562	blood:
27	chr11:59435275..59437958-chr11:59523274..59525120,2	K562	blood:
28	chr11:59521183..59522129-chr11:59897665..59898553,3	K562	blood:
29	chr11:59527108..59529447-chr11:59575542..59578069,2	K562	blood:
30	chr11:59514703..59516740-chr11:59522091..59524203,2	MCF-7	breast:
31	chr11:59525592..59530085-chr11:59541874..59544413,4	MCF-7	breast:
32	chr11:59523011..59526082-chr11:59538557..59541399,3	K562	blood:
33	chr11:59479954..59482315-chr11:59521677..59523287,2	K562	blood:
34	chr11:59524086..59527100-chr11:59562036..59566257,3	K562	blood:
35	chr11:59515464..59518097-chr11:59523433..59525658,2	K562	blood:
36	chr11:59520214..59524923-chr11:59576549..59579669,4	MCF-7	breast:
37	chr11:59524342..59526503-chr11:59895914..59898117,2	K562	blood:
38	chr11:59520634..59522259-chr11:59568757..59570737,15	MCF-7	breast:
39	chr11:59521192..59521888-chr11:59568592..59569530,2	MCF-7	breast:
40	chr11:59521189..59522029-chr11:59569757..59570741,3	K562	blood:
41	chr11:59338335..59341054-chr11:59523391..59525087,2	K562	blood:
42	chr11:59519722..59526041-chr11:59575307..59578961,7	MCF-7	breast:
43	chr11:59507824..59511507-chr11:59512548..59517699,5	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR10V1-1	chr11:59521753-59522448	ENSG00000254477.1
2	lnc-OR10V1-1	chr11:59520488-59520670	ENSG00000254477.1

No data

Variant related genes	Relation type
OR10V2P	TF binding region
STX3	TF binding region
ENSG00000254477	TF binding region
OR10V2P	CpG island
STX3	CpG island
ENSG00000254477	CpG island
ENSG00000172289	chromatin interactions
ENSG00000255538	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000166900	chromatin interactions
ENSG00000110048	chromatin interactions
ENSG00000166902	chromatin interactions
ENSG00000254477	chromatin interactions
ENSG00000265690	chromatin interactions
ENSG00000102878	chromatin interactions
ENSG00000255139	chromatin interactions
ENSG00000116793	chromatin interactions
ENSG00000234964	chromatin interactions
ENSG00000254743	chromatin interactions
ENSG00000255355	chromatin interactions

Extended variants
information (count: 537 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536544	chr11:59515532-59515533	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527552768	chr11:59515535-59515536	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs184118707	chr11:59515545-59515546	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs548595147	chr11:59515591-59515592	Inactive region	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs76969527	chr11:59515620-59515621	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs537054379	chr11:59515678-59515679	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs549086	chr11:59515685-59515686	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs579373	chr11:59515704-59515705	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs563864809	chr11:59515721-59515722	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs145767725	chr11:59515779-59515780	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs187519619	chr11:59515794-59515795	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs138899207	chr11:59515829-59515830	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs535212346	chr11:59515841-59515842	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs377058680	chr11:59515895-59515896	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs575128374	chr11:59515925-59515926	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs376382785	chr11:59515972-59515973	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs555929339	chr11:59516017-59516018	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370245946	chr11:59516047-59516048	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs142908983	chr11:59516054-59516055	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs371727022	chr11:59516095-59516096	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs191347707	chr11:59516104-59516105	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs541644380	chr11:59516127-59516128	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs183926963	chr11:59516132-59516133	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs530329555	chr11:59516138-59516139	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs187136845	chr11:59516203-59516204	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs563654819	chr11:59516274-59516275	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs530901878	chr11:59516348-59516349	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs191785826	chr11:59516372-59516373	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs373645992	chr11:59516377-59516378	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs534646939	chr11:59516400-59516401	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs11230067	chr11:59516411-59516412	Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs567872342	chr11:59516445-59516446	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs184997537	chr11:59516454-59516455	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs507235	chr11:59516459-59516460	Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs497596	chr11:59516464-59516465	Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs539402209	chr11:59516482-59516483	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs554497566	chr11:59516521-59516522	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs190290947	chr11:59516541-59516542	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs181984697	chr11:59516545-59516546	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs541708816	chr11:59516611-59516612	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs144642870	chr11:59516642-59516643	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs369634826	chr11:59516740-59516741	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs532804129	chr11:59516784-59516785	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542458492	chr11:59516785-59516786	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs148449480	chr11:59516802-59516803	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs504320	chr11:59516804-59516805	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs546175469	chr11:59516819-59516820	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564363439	chr11:59516877-59516878	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528476106	chr11:59516880-59516881	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546441595	chr11:59516898-59516899	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59515600-59515800	Enhancers	K562	blood
2	chr11:59515800-59516400	Weak transcription	K562	blood
3	chr11:59516400-59517000	Enhancers	K562	blood
4	chr11:59516600-59517000	Enhancers	Lung	lung
5	chr11:59517000-59521200	Weak transcription	K562	blood
6	chr11:59517800-59521200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr11:59518400-59518600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:59518600-59521000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:59519000-59519200	Enhancers	Duodenum Mucosa	Duodenum
10	chr11:59519000-59519200	Enhancers	Fetal Intestine Small	intestine
11	chr11:59519000-59521600	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr11:59519200-59520400	Weak transcription	Fetal Intestine Small	intestine
13	chr11:59519200-59521200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr11:59519400-59519600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:59519600-59521600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr11:59519800-59520000	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr11:59520000-59521600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:59520200-59521200	Enhancers	Fetal Intestine Large	intestine
19	chr11:59520400-59521200	Enhancers	Fetal Intestine Small	intestine
20	chr11:59521000-59521200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:59521000-59521200	Enhancers	Small Intestine	intestine
22	chr11:59521000-59521400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr11:59521000-59521400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr11:59521000-59521600	Enhancers	Colonic Mucosa	Colon
25	chr11:59521000-59521600	Bivalent Enhancer	Fetal Brain Male	brain
26	chr11:59521000-59521600	Enhancers	Placenta	Placenta
27	chr11:59521200-59521400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr11:59521200-59521400	Enhancers	Primary B cells from cord blood	blood
29	chr11:59521200-59521400	Flanking Active TSS	Fetal Intestine Large	intestine
30	chr11:59521200-59521400	Flanking Active TSS	Fetal Intestine Small	intestine
31	chr11:59521200-59521400	Enhancers	Stomach Smooth Muscle	stomach
32	chr11:59521200-59521600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr11:59521200-59521600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr11:59521200-59521600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr11:59521200-59521600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:59521200-59521600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr11:59521200-59521600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr11:59521200-59521600	Enhancers	Brain Cingulate Gyrus	brain
39	chr11:59521200-59521600	Enhancers	Brain Hippocampus Middle	brain
40	chr11:59521200-59521600	Flanking Active TSS	Duodenum Mucosa	Duodenum
41	chr11:59521200-59521600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr11:59521200-59521600	Enhancers	K562	blood
43	chr11:59521200-59522000	Active TSS	Rectal Smooth Muscle	rectum
44	chr11:59521200-59523600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:59521400-59521600	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr11:59521400-59521600	Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr11:59521400-59521600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr11:59521400-59521600	Active TSS	Primary hematopoietic stem cells	blood
49	chr11:59521400-59521600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr11:59521400-59521600	Enhancers	Primary T helper naive cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links