Variant report

Variant	nsv897627
Chromosome Location	chr11:62984868-63119486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:581)
CpG islands
(count:671)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:63048505-63048725	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:63042279-63042618	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:63058059-63058071	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:63015225-63015718	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:63057050-63057851	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:63013702-63013786	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:62997354-62997741	HepG2	liver:	n/a	chr11:62997612-62997628
8	ARID3A	chr11:63017494-63019185	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:62994277-62994554	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:63006675-63007142	HepG2	liver:	n/a	chr11:63006781-63006797
11	ARID3A	chr11:63008154-63009152	HepG2	liver:	n/a	n/a
12	ATF1	chr11:63094842-63094868	K562	blood:	n/a	n/a
13	BHLHE40	chr11:63008262-63008801	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:63018778-63019222	HepG2	liver:	n/a	chr11:63019015-63019026
15	CEBPB	chr11:63008109-63008880	MCF-7	breast:	n/a	chr11:63008635-63008646
16	CEBPB	chr11:63008151-63008821	MCF-7	breast:	n/a	chr11:63008635-63008646
17	CEBPB	chr11:63070914-63071095	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:63017650-63017936	HepG2	liver:	n/a	chr11:63017813-63017824
19	CEBPB	chr11:63008162-63008869	HepG2	liver:	n/a	chr11:63008635-63008646
20	CEBPB	chr11:63008165-63008475	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:63008500-63008805	HepG2	liver:	n/a	chr11:63008635-63008646
22	CEBPB	chr11:63089047-63089257	A549	lung:	n/a	chr11:63089164-63089175
23	CEBPB	chr11:63008170-63008883	HepG2	liver:	n/a	chr11:63008635-63008646
24	CEBPB	chr11:63018573-63019219	HepG2	liver:	n/a	chr11:63019015-63019026
25	CEBPB	chr11:63008296-63008763	A549	lung:	n/a	chr11:63008635-63008646
26	CEBPB	chr11:63008163-63008912	HepG2	liver:	n/a	chr11:63008635-63008646
27	CEBPB	chr11:63089035-63089313	HepG2	liver:	n/a	chr11:63089164-63089175
28	CEBPB	chr11:63017574-63018211	HepG2	liver:	n/a	chr11:63017813-63017824
29	CEBPB	chr11:63008634-63008650	Hela-S3	cervix:	n/a	chr11:63008635-63008646
30	CEBPB	chr11:63018903-63019138	HepG2	liver:	n/a	chr11:63019015-63019026
31	CEBPB	chr11:63017662-63018061	HepG2	liver:	n/a	chr11:63017813-63017824
32	CEBPB	chr11:63017642-63018008	HepG2	liver:	n/a	chr11:63017813-63017824
33	CEBPB	chr11:63050144-63050310	HepG2	liver:	n/a	chr11:63050171-63050182
34	CEBPD	chr11:63017665-63017925	HepG2	liver:	n/a	n/a
35	CEBPD	chr11:63008160-63008441	HepG2	liver:	n/a	n/a
36	CEBPD	chr11:63008507-63008820	HepG2	liver:	n/a	n/a
37	CTCF	chr11:63044880-63045030	GM12866	blood:	n/a	n/a
38	CTCF	chr11:63030520-63030670	A549	lung:	n/a	n/a
39	CTCF	chr11:63044980-63045130	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr11:62995340-62995490	HepG2	liver:	n/a	n/a
41	CTCF	chr11:62995260-62995410	NHEK	skin:	n/a	n/a
42	CTCF	chr11:63042371-63042534	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr11:63044940-63045090	GM12874	blood:	n/a	n/a
44	CTCF	chr11:63044715-63045330	A549	lung:	n/a	n/a
45	CTCF	chr11:63042349-63042561	HepG2	liver:	n/a	n/a
46	CTCF	chr11:63044947-63045077	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr11:63044920-63045070	GM12871	blood:	n/a	n/a
48	CTCF	chr11:63003809-63003890	GM13976	blood:	n/a	n/a
49	CTCF	chr11:62995378-62995428	Gliobla	brain:	n/a	n/a
50	CTCF	chr11:63044820-63045183	T-47D	breast:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:63057478-63057528	AG04449	skin:	fetal
2	chr11:62997983-62998033	Caco-2	colon:	n/a
3	chr11:63035103-63035153	RPTEC	kidney:	n/a
4	chr11:63035103-63035153	HEEpiC	esophagus:	n/a
5	chr11:62997983-62998033	ovcar-3	ovarian:	n/a
6	chr11:63080472-63080522	HepG2	liver:	n/a
7	chr11:63033729-63033779	GM12891	blood:	n/a
8	chr11:62997004-62997054	GM06990	blood:	n/a
9	chr11:63033729-63033779	AG09309	skin:	n/a
10	chr11:63057478-63057528	HCF	heart:	n/a
11	chr11:62997983-62998033	PFSK-1	brain:	n/a
12	chr11:62997983-62998033	HRPEpiC	eye:	n/a
13	chr11:63057592-63057642	K562	blood:	n/a
14	chr11:63057592-63057642	GM12892	blood:	n/a
15	chr11:63066471-63066521	RPTEC	kidney:	n/a
16	chr11:63057478-63057528	HRE	kidney:	n/a
17	chr11:62997004-62997054	HL-60	blood:	n/a
18	chr11:63080490-63080540	U87	brain:	n/a
19	chr11:63057478-63057528	K562	blood:	n/a
20	chr11:63033729-63033779	PFSK-1	brain:	n/a
21	chr11:63080472-63080522	ProgFib	skin:	n/a
22	chr11:63057592-63057642	AG09319	gingival:	n/a
23	chr11:62997004-62997054	HCM	heart:	n/a
24	chr11:63080472-63080522	NHBE	bronchial:	n/a
25	chr11:62997004-62997054	HRPEpiC	eye:	n/a
26	chr11:62996801-62996851	BE2_C	brain:	n/a
27	chr11:63080472-63080522	SKMC	muscle:	n/a
28	chr11:63057478-63057528	HMEC	breast:	n/a
29	chr11:63035103-63035153	GM12878	blood:	n/a
30	chr11:63057478-63057528	HepG2	liver:	n/a
31	chr11:62997285-62997335	SK-N-SH	brain:	n/a
32	chr11:63080472-63080522	SK-N-SH	brain:	n/a
33	chr11:62996801-62996851	LNCaP	prostate:	n/a
34	chr11:63080472-63080522	HCF	heart:	n/a
35	chr11:62997983-62998033	HEEpiC	esophagus:	n/a
36	chr11:63057592-63057642	NHBE	bronchial:	n/a
37	chr11:63080472-63080522	HIPEpiC	eye:	n/a
38	chr11:63057478-63057528	GM19239	blood:	n/a
39	chr11:63033729-63033779	SK-N-SH_RA	brain:	n/a
40	chr11:63035103-63035153	SK-N-MC	brain:	n/a
41	chr11:62997004-62997054	U87	brain:	n/a
42	chr11:62997983-62998033	H1-hESC	embryonic stem cell:	embryo
43	chr11:62997004-62997054	AoSMC	blood vessel:	n/a
44	chr11:63035103-63035153	HRCEpiC	kidney:	n/a
45	chr11:63066471-63066521	HCT-116	colon:	n/a
46	chr11:63057478-63057528	PrEC	prostate:	n/a
47	chr11:62997004-62997054	HPAEpiC	pulmonary alveolar:	n/a
48	chr11:62997983-62998033	SKMC	muscle:	n/a
49	chr11:63080472-63080522	SK-N-MC	brain:	n/a
50	chr11:62997004-62997054	SK-N-SH	brain:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63036813..63039630-chr11:63043025..63045856,2	K562	blood:
2	chr11:63005254..63007411-chr11:63010336..63012960,2	K562	blood:
3	chr11:63044665..63045444-chr11:63402967..63403950,3	MCF-7	breast:
4	chr11:62997179..62998138-chr13:34015248..34015801,2	MCF-7	breast:
5	chr11:63103438..63104964-chr14:78144218..78145718,2	MCF-7	breast:
6	chr11:63072177..63073810-chr11:63074201..63076770,2	MCF-7	breast:
7	chr11:62990724..62992823-chr11:63013955..63016825,2	MCF-7	breast:
8	chr11:62980374..62982290-chr11:62983906..62985581,2	K562	blood:
9	chr11:63072177..63073810-chr11:63074201..63076770,2	MCF-7	breast:
10	chr11:63036813..63039630-chr11:63043025..63045856,2	K562	blood:
11	chr11:63044561..63045230-chr11:63246286..63246902,2	MCF-7	breast:
12	chr11:63065508..63067181-chr11:63068021..63070968,2	MCF-7	breast:
13	chr11:63042850..63045277-chr11:63045866..63048411,2	MCF-7	breast:
14	chr11:63057865..63060126-chr11:63074539..63077166,2	MCF-7	breast:
15	chr11:63042850..63045277-chr11:63045866..63048411,2	MCF-7	breast:
16	chr11:63057865..63060126-chr11:63074539..63077166,2	MCF-7	breast:
17	chr11:63042013..63042918-chr11:63403002..63403779,2	MCF-7	breast:
18	chr11:62992812..62995599-chr11:63006882..63009821,2	MCF-7	breast:
19	chr11:62992812..62995599-chr11:63006882..63009821,2	MCF-7	breast:
20	chr11:63065508..63067181-chr11:63068021..63070968,2	MCF-7	breast:
21	chr11:63044723..63045242-chr11:63275245..63276140,2	MCF-7	breast:
22	chr11:63044746..63045474-chr11:63275562..63276187,3	MCF-7	breast:
23	chr11:62990724..62992823-chr11:63013955..63016825,2	MCF-7	breast:
24	chr11:63005254..63007411-chr11:63010336..63012960,2	K562	blood:
25	chr11:62802803..62803858-chr11:63041979..63043067,8	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC22A9-2	chr11:63018729-63019657	l_487_chr11:63018728-63024659_testes
2	lnc-SLC22A9-1	chr11:63093324-63095856	l_488_chr11:63090922-63093361_brain
3	lnc-SLC22A9-2	chr11:63024450-63024659	l_487_chr11:63018728-63024659_testes
4	lnc-SLC22A9-1	chr11:63090923-63092662	l_488_chr11:63090922-63093361_brain

No data

Variant related genes	Relation type
ENSG00000256863	TF binding region
CCND2P1	TF binding region
SLC22A25	TF binding region
ENSG00000256181	TF binding region
SLC22A10	TF binding region
ENSG00000256863	CpG island
CCND2P1	CpG island
SLC22A25	CpG island
ENSG00000256181	CpG island
SLC22A10	CpG island
ENSG00000133317	chromatin interactions
ENSG00000256847	chromatin interactions
ENSG00000256863	chromatin interactions

Extended variants
information (count: 3907 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:3907 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11231409	chr11:62984868-62984869	Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554671567	chr11:62984882-62984883	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377461872	chr11:62984982-62984983	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371213572	chr11:62985033-62985034	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189470533	chr11:62985036-62985037	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371024672	chr11:62985037-62985038	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs36036316	chr11:62985052-62985053	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199866396	chr11:62985065-62985066	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199963255	chr11:62985083-62985084	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148704171	chr11:62985088-62985089	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142374110	chr11:62985098-62985099	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201958778	chr11:62985106-62985107	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34284198	chr11:62985122-62985123	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117914773	chr11:62985123-62985124	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145215297	chr11:62985144-62985145	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200325838	chr11:62985145-62985146	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181827369	chr11:62985148-62985149	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201370159	chr11:62985164-62985165	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147608080	chr11:62985165-62985166	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61746630	chr11:62985171-62985172	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563995072	chr11:62985173-62985174	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367780748	chr11:62985194-62985195	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199991723	chr11:62985198-62985199	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201877220	chr11:62985220-62985221	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369920257	chr11:62985230-62985231	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113162182	chr11:62985329-62985330	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566232515	chr11:62985363-62985364	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528677829	chr11:62985382-62985383	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548707182	chr11:62985424-62985425	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568443126	chr11:62985465-62985466	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537478089	chr11:62985483-62985484	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550530516	chr11:62985487-62985488	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144458834	chr11:62985525-62985526	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568694103	chr11:62985538-62985539	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12417255	chr11:62985544-62985545	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs368549190	chr11:62985556-62985557	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563490829	chr11:62985559-62985560	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534508197	chr11:62985599-62985600	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114995356	chr11:62985602-62985603	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574421335	chr11:62985605-62985606	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141040255	chr11:62985612-62985613	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185375068	chr11:62985665-62985666	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577617408	chr11:62985690-62985691	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546568705	chr11:62985729-62985730	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560080718	chr11:62985735-62985736	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75008339	chr11:62985812-62985813	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548468734	chr11:62985833-62985834	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577156214	chr11:62985863-62985864	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562231098	chr11:62985881-62985882	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189782609	chr11:62985892-62985893	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Acute myeloid leukemia	20729466	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
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20409316	CNVD
Spinal muscular atrophy	17160897	CNVD
Retinitis pigmentosa	17160897	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	16417655	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:62981000-62988400	Strong transcription	Liver	Liver
2	chr11:62984800-62985000	Enhancers	HepG2	liver
3	chr11:62988400-62993000	Weak transcription	Liver	Liver
4	chr11:62993000-62994200	Enhancers	HepG2	liver
5	chr11:62993000-62996800	Strong transcription	Liver	Liver
6	chr11:62994200-62994600	Flanking Active TSS	HepG2	liver
7	chr11:62994600-62998200	Enhancers	HepG2	liver
8	chr11:62995000-62995200	Enhancers	Esophagus	oesophagus
9	chr11:62996800-62998000	Genic enhancers	Liver	Liver
10	chr11:62997200-62997800	Enhancers	Fetal Intestine Large	intestine
11	chr11:62998000-62998400	Enhancers	Liver	Liver
12	chr11:62998200-62999400	Weak transcription	HepG2	liver
13	chr11:62998400-63002800	Weak transcription	Liver	Liver
14	chr11:63002600-63004200	Weak transcription	HepG2	liver
15	chr11:63002800-63004400	Strong transcription	Liver	Liver
16	chr11:63003000-63004600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr11:63003400-63004200	Enhancers	Esophagus	oesophagus
18	chr11:63004200-63004600	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr11:63004200-63004600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr11:63004200-63007000	Enhancers	HepG2	liver
21	chr11:63004200-63008800	Weak transcription	Esophagus	oesophagus
22	chr11:63004400-63005200	ZNF genes & repeats	Liver	Liver
23	chr11:63004600-63008600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr11:63004600-63009000	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr11:63004600-63009000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr11:63005200-63005400	Transcr. at gene 5' and 3'	Liver	Liver
27	chr11:63005400-63006200	Genic enhancers	Liver	Liver
28	chr11:63006000-63006800	Enhancers	Fetal Intestine Small	intestine
29	chr11:63006200-63006400	Enhancers	Thymus	Thymus
30	chr11:63006200-63007200	Transcr. at gene 5' and 3'	Liver	Liver
31	chr11:63006400-63009000	Enhancers	Fetal Intestine Large	intestine
32	chr11:63006600-63008200	Weak transcription	Thymus	Thymus
33	chr11:63006800-63008400	Weak transcription	Fetal Intestine Small	intestine
34	chr11:63007000-63007400	Flanking Active TSS	HepG2	liver
35	chr11:63007200-63007600	Flanking Active TSS	Liver	Liver
36	chr11:63007200-63008800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:63007400-63007600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:63007400-63008400	Enhancers	HepG2	liver
39	chr11:63007600-63008000	Enhancers	Liver	Liver
40	chr11:63007600-63008200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:63008000-63008400	Flanking Active TSS	Liver	Liver
42	chr11:63008200-63009000	Enhancers	Adipose Nuclei	Adipose
43	chr11:63008200-63009000	Enhancers	Pancreas	Pancrea
44	chr11:63008200-63009400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr11:63008200-63012800	Enhancers	Thymus	Thymus
46	chr11:63008400-63008800	Enhancers	Liver	Liver
47	chr11:63008400-63008800	Flanking Active TSS	HepG2	liver
48	chr11:63008400-63009000	Enhancers	Fetal Intestine Small	intestine
49	chr11:63008600-63010600	Enhancers	Primary T cells from cord blood	blood
50	chr11:63008600-63011400	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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