Variant report

Variant	nsv467719
Chromosome Location	chr11:18447611-18542227
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:312)
CpG islands
(count:976)
Chromatin interactive
region (count:38)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18479092-18479320	HepG2	liver:	n/a	n/a
2	ATF1	chr11:18512610-18512972	K562	blood:	n/a	n/a
3	ATF3	chr11:18517243-18517546	K562	blood:	n/a	n/a
4	BACH1	chr11:18542195-18542267	K562	blood:	n/a	n/a
5	BACH1	chr11:18477287-18477564	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:18533463-18533474	K562	blood:	n/a	n/a
7	BATF	chr11:18490527-18490838	GM12878	blood:	n/a	chr11:18490690-18490701 chr11:18490691-18490701
8	BATF	chr11:18490570-18490770	GM12878	blood:	n/a	chr11:18490690-18490701 chr11:18490691-18490701
9	BCL3	chr11:18507479-18507913	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:18474554-18474624	K562	blood:	n/a	n/a
11	BHLHE40	chr11:18479063-18479387	K562	blood:	n/a	n/a
12	BHLHE40	chr11:18479046-18479396	HepG2	liver:	n/a	n/a
13	BHLHE40	chr11:18479101-18479289	A549	lung:	n/a	n/a
14	BRCA1	chr11:18478869-18479367	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr11:18512616-18513161	K562	blood:	n/a	n/a
16	CEBPB	chr11:18534847-18534955	HepG2	liver:	n/a	chr11:18534898-18534909
17	CEBPB	chr11:18452469-18452615	HepG2	liver:	n/a	chr11:18452577-18452588
18	CEBPB	chr11:18517321-18517521	A549	lung:	n/a	chr11:18517421-18517432
19	CEBPB	chr11:18495203-18495432	HepG2	liver:	n/a	chr11:18495281-18495292
20	CEBPB	chr11:18488098-18488202	K562	blood:	n/a	n/a
21	CEBPB	chr11:18478449-18479397	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:18478565-18478628	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:18495235-18495455	K562	blood:	n/a	chr11:18495281-18495292
24	CEBPB	chr11:18495208-18495388	Hela-S3	cervix:	n/a	chr11:18495281-18495292
25	CEBPB	chr11:18534797-18534985	K562	blood:	n/a	chr11:18534898-18534909
26	CEBPB	chr11:18495103-18495392	IMR90	lung:	n/a	chr11:18495281-18495292
27	CEBPB	chr11:18460412-18460437	HepG2	liver:	n/a	n/a
28	CEBPB	chr11:18523073-18523354	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:18517327-18517551	H1-hESC	embryonic stem cell:	n/a	chr11:18517421-18517432
30	CEBPB	chr11:18517326-18517547	K562	blood:	n/a	chr11:18517421-18517432
31	CEBPB	chr11:18488096-18488199	A549	lung:	n/a	n/a
32	CEBPB	chr11:18534780-18534997	IMR90	lung:	n/a	chr11:18534898-18534909
33	CEBPB	chr11:18491531-18491555	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr11:18534770-18535019	A549	lung:	n/a	chr11:18534898-18534909
35	CEBPB	chr11:18491451-18491642	K562	blood:	n/a	n/a
36	CEBPB	chr11:18517355-18517545	HepG2	liver:	n/a	chr11:18517421-18517432
37	CEBPD	chr11:18512584-18513091	K562	blood:	n/a	n/a
38	CEBPD	chr11:18512566-18513121	K562	blood:	n/a	n/a
39	CHD2	chr11:18478989-18479353	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr11:18478499-18478521	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr11:18484740-18484890	A549	lung:	n/a	n/a
42	CTCF	chr11:18454740-18454890	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr11:18454783-18454868	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr11:18538102-18538149	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr11:18462999-18463059	GM10266	blood:	n/a	n/a
46	CTCF	chr11:18477426-18477601	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr11:18477620-18477770	BE2_C	brain:	n/a	n/a
48	CTCF	chr11:18477719-18477775	GM19239	blood:	n/a	n/a
49	CTCF	chr11:18478519-18478550	LNCaP	prostate:	n/a	n/a
50	CTCF	chr11:18477640-18477790	BE2_C	brain:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18478135-18478185	IMR90	lung:	fetal
2	chr11:18477153-18477203	Caco-2	colon:	n/a
3	chr11:18473775-18473825	PrEC	prostate:	n/a
4	chr11:18477153-18477203	HNPCEpiC	eye:	n/a
5	chr11:18473775-18473825	SK-N-MC	brain:	n/a
6	chr11:18478135-18478185	SK-N-SH	brain:	n/a
7	chr11:18483771-18483821	SK-N-MC	brain:	n/a
8	chr11:18477680-18477730	AG10803	skin:	n/a
9	chr11:18483771-18483821	NH-A	brain:	n/a
10	chr11:18477254-18477304	ovcar-3	ovarian:	n/a
11	chr11:18483771-18483821	AG10803	skin:	n/a
12	chr11:18477379-18477429	Caco-2	colon:	n/a
13	chr11:18477280-18477330	HUVEC	blood vessel:	n/a
14	chr11:18477303-18477353	BJ	skin:	n/a
15	chr11:18476081-18476131	AG09319	gingival:	n/a
16	chr11:18477254-18477304	HUVEC	blood vessel:	n/a
17	chr11:18500649-18500699	NH-A	brain:	n/a
18	chr11:18473775-18473825	HAEpiC	amniotic membrane:	n/a
19	chr11:18477379-18477429	SK-N-SH	brain:	n/a
20	chr11:18477280-18477330	HCF	heart:	n/a
21	chr11:18477153-18477203	LNCaP	prostate:	n/a
22	chr11:18477379-18477429	RPTEC	kidney:	n/a
23	chr11:18477303-18477353	AG09319	gingival:	n/a
24	chr11:18477303-18477353	HCF	heart:	n/a
25	chr11:18473775-18473825	A549	lung:	n/a
26	chr11:18473775-18473825	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:18477299-18477349	ProgFib	skin:	n/a
28	chr11:18477299-18477349	HUVEC	blood vessel:	n/a
29	chr11:18477299-18477349	SK-N-SH_RA	brain:	n/a
30	chr11:18477299-18477349	ECC-1	luminal epithelium:	n/a
31	chr11:18477254-18477304	RPTEC	kidney:	n/a
32	chr11:18478135-18478185	PANC-1	pancreas:	n/a
33	chr11:18477303-18477353	T-47D	breast:	n/a
34	chr11:18477753-18477803	MCF-7	breast:	n/a
35	chr11:18477379-18477429	Jurkat	blood:	n/a
36	chr11:18478135-18478185	PFSK-1	brain:	n/a
37	chr11:18483771-18483821	HCF	heart:	n/a
38	chr11:18477534-18477584	AG10803	skin:	n/a
39	chr11:18477753-18477803	ovcar-3	ovarian:	n/a
40	chr11:18477153-18477203	NHBE	bronchial:	n/a
41	chr11:18476081-18476131	Jurkat	blood:	n/a
42	chr11:18477534-18477584	MCF-7	breast:	n/a
43	chr11:18476081-18476131	HL-60	blood:	n/a
44	chr11:18477280-18477330	SK-N-SH_RA	brain:	n/a
45	chr11:18477680-18477730	NHDF-neo	bronchial:	n/a
46	chr11:18500649-18500699	HepG2	liver:	n/a
47	chr11:18483771-18483821	Hela-S3	cervix:	n/a
48	chr11:18483771-18483821	Caco-2	colon:	n/a
49	chr11:18483771-18483821	GM12878	blood:	n/a
50	chr11:18477753-18477803	AG04449	skin:	fetal

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:18536192..18538162-chr11:18539914..18542011,2	K562	blood:
2	chr11:18456372..18458873-chr11:18461973..18463683,2	K562	blood:
3	chr11:18538795..18541461-chr11:18542619..18545172,2	K562	blood:
4	chr11:18464968..18467411-chr11:18470062..18474152,3	K562	blood:
5	chr11:18531181..18534158-chr11:18547173..18549352,2	MCF-7	breast:
6	chr11:18429496..18431588-chr11:18458511..18461417,2	K562	blood:
7	chr11:18528948..18532458-chr11:18541566..18545702,3	K562	blood:
8	chr11:18415520..18417740-chr11:18457174..18459027,2	K562	blood:
9	chr11:18530933..18533061-chr11:18534871..18536748,2	MCF-7	breast:
10	chr11:18467637..18469491-chr11:18477590..18480318,2	K562	blood:
11	chr11:18533507..18535312-chr11:18546583..18548769,2	K562	blood:
12	chr11:18474174..18475881-chr11:18477733..18480422,2	MCF-7	breast:
13	chr11:18464968..18467382-chr11:18471264..18474152,2	K562	blood:
14	chr11:18456372..18458873-chr11:18461973..18463683,2	K562	blood:
15	chr11:18470144..18471841-chr11:18477720..18480127,2	MCF-7	breast:
16	chr11:18489055..18490593-chr11:18496337..18497953,2	K562	blood:
17	chr11:18523134..18525555-chr11:18546904..18549561,3	K562	blood:
18	chr11:18416882..18418570-chr11:18504246..18506790,2	K562	blood:
19	chr11:18530933..18533061-chr11:18534871..18536748,2	MCF-7	breast:
20	chr11:18527234..18530120-chr11:18547134..18549808,2	MCF-7	breast:
21	chr11:18462496..18464309-chr11:18472211..18474246,2	MCF-7	breast:
22	chr11:18474174..18475881-chr11:18477733..18480422,2	MCF-7	breast:
23	chr11:18414619..18417567-chr11:18475840..18478644,2	K562	blood:
24	chr11:18430457..18432481-chr11:18456231..18458824,2	K562	blood:
25	chr11:18467637..18469491-chr11:18477590..18480318,2	K562	blood:
26	chr11:18533757..18535476-chr11:18537479..18539659,2	MCF-7	breast:
27	chr11:18502477..18505271-chr11:18547847..18549412,2	K562	blood:
28	chr11:18489055..18490593-chr11:18496337..18497953,2	K562	blood:
29	chr11:18538359..18545865-chr11:18546460..18550640,13	MCF-7	breast:
30	chr11:18535996..18538848-chr11:18539751..18543150,4	MCF-7	breast:
31	chr11:18415628..18417423-chr11:18491063..18493599,2	MCF-7	breast:
32	chr11:18540175..18542795-chr11:18547833..18549467,2	MCF-7	breast:
33	chr11:18470144..18471841-chr11:18477720..18480127,2	MCF-7	breast:
34	chr11:18539804..18546267-chr11:18546399..18550608,13	K562	blood:
35	chr11:18479966..18482806-chr11:18549124..18551467,2	K562	blood:
36	chr11:18442100..18443660-chr11:18447182..18449184,2	MCF-7	breast:
37	chr11:18533507..18535848-chr11:18546408..18548301,3	K562	blood:
38	chr11:18533757..18535476-chr11:18537479..18539659,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UEVLD-4	chr11:18532590-18533022	NONHSAT018293
2	lnc-TSG101-2	chr11:18471659-18472415	NONHSAT018286
3	lnc-UEVLD-5	chr11:18511790-18512502	NONHSAT018288
4	lnc-UEVLD-2	chr11:18530031-18530367	ENSG00000256588.1
5	lnc-UEVLD-2	chr11:18529155-18529447	ENSG00000256588.1

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TSG101	hsa-miR-20a-5p	chr11:18501924-18501918
2	TSG101	hsa-miR-33a-5p	chr11:18501922-18501943
3	TSG101	hsa-miR-20a-5p	chr11:18501918-18501939
4	TSG101	hsa-miR-93-5p	chr11:18501924-18501918
5	TSG101	hsa-miR-130b-3p	chr11:18501920-18501941
6	TSG101	hsa-miR-130b-3p	chr11:18502003-18502024
7	TSG101	hsa-miR-93-5p	chr11:18501918-18501939

Variant related genes	Relation type
ENSG00000256361	TF binding region
TSG101	TF binding region
LDHAL6A	TF binding region
ENSG00000256464	TF binding region
ENSG00000256588	TF binding region
ENSG00000256734	TF binding region
ENSG00000256361	CpG island
TSG101	CpG island
LDHAL6A	CpG island
ENSG00000256464	CpG island
ENSG00000256588	CpG island
ENSG00000256734	CpG island
ENSG00000134333	chromatin interactions
ENSG00000256588	chromatin interactions
ENSG00000256361	chromatin interactions
ENSG00000256734	chromatin interactions
ENSG00000074319	chromatin interactions

Extended variants
information (count: 3382 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3382 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111964255	chr11:18450893-18450894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576784645	chr11:18450900-18450901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535344207	chr11:18450927-18450928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376609405	chr11:18450937-18450938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531894354	chr11:18450950-18450951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561976722	chr11:18450979-18450980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529280916	chr11:18450981-18450982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190715347	chr11:18450982-18450983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377392479	chr11:18451064-18451065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182918180	chr11:18451086-18451087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs3740713	chr11:18451096-18451097	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
12	rs551127224	chr11:18451121-18451122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569635773	chr11:18451130-18451131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530742720	chr11:18451136-18451137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549243620	chr11:18451143-18451144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568736553	chr11:18451144-18451145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187263406	chr11:18451148-18451149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567189199	chr11:18451170-18451171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112136795	chr11:18451221-18451222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138672442	chr11:18451230-18451231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs33998563	chr11:18451249-18451250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370657331	chr11:18451262-18451263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374002407	chr11:18451290-18451291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11558333	chr11:18451328-18451329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139647819	chr11:18451339-18451340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200332423	chr11:18451356-18451357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144306480	chr11:18451372-18451373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372539242	chr11:18451385-18451386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146472745	chr11:18451386-18451387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183703514	chr11:18457324-18457325	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs35128109	chr11:18457349-18457350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs35313043	chr11:18457351-18457352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541112036	chr11:18457390-18457391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs35617285	chr11:18457406-18457407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188074527	chr11:18457536-18457537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376983923	chr11:18457549-18457550	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559162863	chr11:18457553-18457554	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541547303	chr11:18457566-18457567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs181997946	chr11:18457610-18457611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs149696484	chr11:18457679-18457680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12293002	chr11:18457687-18457688	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs539173855	chr11:18457693-18457694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs16935431	chr11:18457704-18457705	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs567249116	chr11:18457705-18457706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs534740566	chr11:18457711-18457712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546705792	chr11:18457817-18457818	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566321783	chr11:18457864-18457865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539974554	chr11:18457949-18457950	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115364688	chr11:18458002-18458003	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374146119	chr11:18458029-18458030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1488 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18450800-18451200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:18451000-18451400	Enhancers	K562	blood
3	chr11:18457200-18479200	Weak transcription	Pancreas	Pancrea
4	chr11:18463200-18463800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:18463400-18463800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr11:18463400-18463800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr11:18463400-18463800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:18463400-18464000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr11:18471000-18471400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr11:18474200-18475000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:18474400-18474800	Enhancers	NHDF-Ad	bronchial
12	chr11:18474400-18475000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr11:18474400-18475000	Enhancers	Hela-S3	cervix
14	chr11:18475000-18476000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr11:18476000-18476200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr11:18476800-18477000	Active TSS	Spleen	Spleen
17	chr11:18477000-18477200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:18477000-18477600	Enhancers	Spleen	Spleen
19	chr11:18477200-18477400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:18477200-18477400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:18477200-18477600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr11:18477200-18477800	Active TSS	Brain Germinal Matrix	brain
23	chr11:18477200-18477800	Active TSS	Ovary	ovary
24	chr11:18477200-18478000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:18477400-18477600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
26	chr11:18477400-18477600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr11:18477400-18477600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:18477400-18477600	Bivalent Enhancer	Right Ventricle	heart
29	chr11:18477400-18477800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:18477400-18477800	Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr11:18477400-18477800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr11:18477400-18477800	Active TSS	Fetal Brain Female	brain
33	chr11:18477400-18478000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr11:18477400-18478000	Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr11:18477400-18478000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
36	chr11:18477600-18477800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr11:18477600-18477800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr11:18477600-18478200	Enhancers	Right Ventricle	heart
39	chr11:18477600-18498400	Weak transcription	Spleen	Spleen
40	chr11:18477800-18478000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr11:18477800-18478000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:18477800-18498000	Weak transcription	Fetal Brain Female	brain
43	chr11:18478200-18480200	Enhancers	Hela-S3	cervix
44	chr11:18478200-18497600	Weak transcription	Right Ventricle	heart
45	chr11:18478400-18479600	Enhancers	Stomach Mucosa	stomach
46	chr11:18479000-18479800	Enhancers	Fetal Intestine Large	intestine
47	chr11:18479000-18480000	Enhancers	HUVEC	blood vessel
48	chr11:18479200-18479400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr11:18479200-18479800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr11:18479200-18479800	Enhancers	Gastric	stomach

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