Variant report

Variant	nsv1035967
Chromosome Location	chr15:51949866-52008736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:797)
Chromatin interactive
region (count:84)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 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	chr15:51994768-51995431	K562	blood:	n/a	n/a
2	ARID3A	chr15:51965660-51965996	K562	blood:	n/a	n/a
3	ARID3A	chr15:51989365-51989783	K562	blood:	n/a	n/a
4	ARID3A	chr15:51998629-51998905	K562	blood:	n/a	n/a
5	ATF1	chr15:51973437-51973899	K562	blood:	n/a	chr15:51973584-51973598
6	ATF1	chr15:51964374-51964827	K562	blood:	n/a	n/a
7	ATF1	chr15:51989394-51989656	K562	blood:	n/a	n/a
8	ATF1	chr15:51994949-51995255	K562	blood:	n/a	n/a
9	ATF1	chr15:51984292-51984686	K562	blood:	n/a	n/a
10	ATF1	chr15:51998486-51998938	K562	blood:	n/a	n/a
11	ATF3	chr15:51973405-51973799	K562	blood:	n/a	chr15:51973587-51973607 chr15:51973759-51973768
12	ATF3	chr15:51989403-51989671	K562	blood:	n/a	n/a
13	BACH1	chr15:51964468-51964470	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:51995079-51995208	K562	blood:	n/a	n/a
15	BACH1	chr15:52003210-52003279	K562	blood:	n/a	n/a
16	BACH1	chr15:51973550-51974054	H1-hESC	embryonic stem cell:	n/a	n/a
17	BHLHE40	chr15:51998497-51998880	K562	blood:	n/a	n/a
18	BHLHE40	chr15:51999816-51999922	K562	blood:	n/a	n/a
19	BHLHE40	chr15:51964338-51964566	K562	blood:	n/a	n/a
20	BHLHE40	chr15:51965417-51965949	K562	blood:	n/a	n/a
21	BHLHE40	chr15:51994978-51995152	K562	blood:	n/a	n/a
22	BHLHE40	chr15:51973338-51974136	K562	blood:	n/a	n/a
23	BHLHE40	chr15:51988822-51988995	K562	blood:	n/a	n/a
24	BRCA1	chr15:51973445-51973506	HepG2	liver:	n/a	n/a
25	BRCA1	chr15:51973491-51974101	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr15:51979787-51979970	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr15:51973259-51973943	K562	blood:	n/a	chr15:51973517-51973528
28	CBX3	chr15:51964240-51964629	K562	blood:	n/a	n/a
29	CBX3	chr15:51973504-51973836	K562	blood:	n/a	chr15:51973517-51973528
30	CBX3	chr15:51965560-51966051	K562	blood:	n/a	n/a
31	CCNT2	chr15:51989456-51989777	K562	blood:	n/a	n/a
32	CCNT2	chr15:51973439-51973965	K562	blood:	n/a	chr15:51973766-51973775
33	CCNT2	chr15:51965762-51965962	K562	blood:	n/a	n/a
34	CCNT2	chr15:51994947-51995399	K562	blood:	n/a	n/a
35	CEBPB	chr15:51961447-51961606	K562	blood:	n/a	n/a
36	CEBPB	chr15:51989350-51989767	K562	blood:	n/a	n/a
37	CEBPB	chr15:51957065-51957402	K562	blood:	n/a	chr15:51957215-51957226
38	CEBPB	chr15:51970384-51970637	K562	blood:	n/a	chr15:51970448-51970461
39	CEBPB	chr15:51962657-51962984	A549	lung:	n/a	chr15:51962803-51962814
40	CEBPB	chr15:51962625-51962974	HepG2	liver:	n/a	chr15:51962803-51962814
41	CEBPB	chr15:51958041-51958260	A549	lung:	n/a	n/a
42	CEBPB	chr15:51962636-51962957	IMR90	lung:	n/a	chr15:51962803-51962814
43	CEBPB	chr15:51962693-51962940	Hela-S3	cervix:	n/a	chr15:51962803-51962814
44	CEBPB	chr15:51998612-51998819	K562	blood:	n/a	n/a
45	CEBPB	chr15:51950798-51951357	MCF-7	breast:	n/a	n/a
46	CEBPB	chr15:51950908-51951207	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr15:51989413-51989793	K562	blood:	n/a	n/a
48	CEBPB	chr15:51950829-51951339	MCF-7	breast:	n/a	n/a
49	CEBPB	chr15:51950991-51951195	K562	blood:	n/a	n/a
50	CEBPB	chr15:51970291-51970691	Hela-S3	cervix:	n/a	chr15:51970448-51970461

(count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:51973199-51973249	RPTEC	kidney:	n/a
2	chr15:51973661-51973711	T-47D	breast:	n/a
3	chr15:51997390-51997440	NH-A	brain:	n/a
4	chr15:51997390-51997440	Hela-S3	cervix:	n/a
5	chr15:51973199-51973249	RPTEC	kidney:	n/a
6	chr15:51973661-51973711	T-47D	breast:	n/a
7	chr15:51997390-51997440	NH-A	brain:	n/a
8	chr15:51997390-51997440	Hela-S3	cervix:	n/a
9	chr15:51977697-51977747	ECC-1	luminal epithelium:	n/a
10	chr15:51972699-51972749	ovcar-3	ovarian:	n/a
11	chr15:51973920-51973970	CMK	blood:	n/a
12	chr15:51973591-51973641	PFSK-1	brain:	n/a
13	chr15:51973591-51973641	GM06990	blood:	n/a
14	chr15:51973534-51973584	Caco-2	colon:	n/a
15	chr15:51977697-51977747	T-47D	breast:	n/a
16	chr15:51973764-51973814	HepG2	liver:	n/a
17	chr15:51972699-51972749	AoSMC	blood vessel:	n/a
18	chr15:51973460-51973510	HMEC	breast:	n/a
19	chr15:51970968-51971018	Hepatocyte	liver:	n/a
20	chr15:51972699-51972749	BJ	skin:	n/a
21	chr15:51972699-51972749	A549	lung:	n/a
22	chr15:51964706-51964756	PFSK-1	brain:	n/a
23	chr15:51973224-51973274	GM12878	blood:	n/a
24	chr15:51973460-51973510	HCPEpiC	choroid plexus:	n/a
25	chr15:51977697-51977747	NHBE	bronchial:	n/a
26	chr15:51972699-51972749	LNCaP	prostate:	n/a
27	chr15:51973460-51973510	K562	blood:	n/a
28	chr15:51997390-51997440	Caco-2	colon:	n/a
29	chr15:51977697-51977747	AG10803	skin:	n/a
30	chr15:51973534-51973584	HRE	kidney:	n/a
31	chr15:51997390-51997440	NT2-D1	testis:	n/a
32	chr15:51973920-51973970	Hela-S3	cervix:	n/a
33	chr15:51970968-51971018	PrEC	prostate:	n/a
34	chr15:51997390-51997440	AG04449	skin:	fetal
35	chr15:51970968-51971018	GM12892	blood:	n/a
36	chr15:51973920-51973970	BE2_C	brain:	n/a
37	chr15:51973591-51973641	NB4	blood:	n/a
38	chr15:51973224-51973274	Caco-2	colon:	n/a
39	chr15:51972699-51972749	H1-hESC	embryonic stem cell:	embryo
40	chr15:51973460-51973510	LNCaP	prostate:	n/a
41	chr15:51970968-51971018	AG04450	lung:	fetal
42	chr15:51973224-51973274	GM12892	blood:	n/a
43	chr15:51973199-51973249	AG10803	skin:	n/a
44	chr15:51973764-51973814	A549	lung:	n/a
45	chr15:51972699-51972749	MCF10A-Er-Src	breast:	n/a
46	chr15:51973199-51973249	AG09309	skin:	n/a
47	chr15:51972699-51972749	Caco-2	colon:	n/a
48	chr15:51973764-51973814	AG04449	skin:	fetal
49	chr15:51964706-51964756	AG09309	skin:	n/a
50	chr15:51973661-51973711	HCF	heart:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:51997906..52000590-chr15:52024148..52026004,2	MCF-7	breast:
2	chr15:51950953..51953753-chr15:52026333..52028408,2	MCF-7	breast:
3	chr15:52005662..52007756-chr15:52028876..52031424,2	MCF-7	breast:
4	chr15:51965377..51967473-chr15:52008396..52010538,2	MCF-7	breast:
5	chr15:51985262..51987318-chr15:51998907..52000749,2	K562	blood:
6	chr15:51984106..51987260-chr15:51989301..51991929,3	MCF-7	breast:
7	chr15:51981798..51984182-chr15:51989191..51992186,3	K562	blood:
8	chr15:52002742..52004739-chr15:52023615..52025636,2	MCF-7	breast:
9	chr15:51990309..51992367-chr15:51994326..51996049,2	K562	blood:
10	chr15:51991390..51994698-chr15:51996190..51998071,3	K562	blood:
11	chr15:52000286..52003141-chr15:52008579..52010583,2	K562	blood:
12	chr15:51990868..51993765-chr15:52043379..52046034,2	K562	blood:
13	chr15:51965668..51968596-chr15:51971807..51974578,3	K562	blood:
14	chr15:51984640..51986605-chr15:51992060..51993889,2	K562	blood:
15	chr15:52000164..52002688-chr15:52006950..52009466,2	MCF-7	breast:
16	chr15:51990726..51993605-chr15:51996321..51998740,2	MCF-7	breast:
17	chr15:52001609..52004491-chr15:52007135..52009891,2	K562	blood:
18	chr15:51976806..51978342-chr15:51982300..51983965,2	MCF-7	breast:
19	chr15:51997530..52001140-chr15:52004851..52007449,4	K562	blood:
20	chr15:51984106..51987260-chr15:51989301..51991929,3	MCF-7	breast:
21	chr15:51974418..51976599-chr15:51979066..51980619,2	K562	blood:
22	chr15:51974117..51976857-chr15:51978812..51980643,2	MCF-7	breast:
23	chr15:51972403..51976508-chr15:51976780..51980487,4	K562	blood:
24	chr15:51983304..51986110-chr15:51988118..51990669,2	MCF-7	breast:
25	chr15:52008451..52011571-chr15:52027342..52031770,5	MCF-7	breast:
26	chr15:51960620..51962408-chr15:51966194..51968469,2	MCF-7	breast:
27	chr15:51964695..51967594-chr15:51978181..51980955,2	MCF-7	breast:
28	chr15:51991056..51992762-chr15:51996758..51999094,2	K562	blood:
29	chr15:51981798..51984182-chr15:51989191..51992186,3	K562	blood:
30	chr15:51983304..51986110-chr15:51988118..51990669,2	MCF-7	breast:
31	chr15:51984283..51986352-chr15:51990636..51992962,2	K562	blood:
32	chr15:51999340..52000856-chr15:52003112..52004684,2	K562	blood:
33	chr15:51970684..51971589-chr15:52068849..52069771,2	MCF-7	breast:
34	chr15:51965377..51967473-chr15:52008396..52010538,2	MCF-7	breast:
35	chr15:51985613..51987539-chr15:51999474..52001266,2	K562	blood:
36	chr15:51960620..51962408-chr15:51966194..51968469,2	MCF-7	breast:
37	chr15:51976555..51979151-chr15:51989814..51992249,2	MCF-7	breast:
38	chr15:51960322..51962005-chr15:52066189..52068560,2	MCF-7	breast:
39	chr15:51988416..51990476-chr15:51996919..51998873,2	MCF-7	breast:
40	chr15:51945649..51948145-chr15:51951610..51953731,2	K562	blood:
41	chr15:51974117..51976857-chr15:51978812..51980643,2	MCF-7	breast:
42	chr15:51984067..51985645-chr15:51997291..51999601,2	MCF-7	breast:
43	chr15:51974418..51976599-chr15:51979066..51980619,2	K562	blood:
44	chr15:51970627..51972181-chr15:52008855..52011853,2	MCF-7	breast:
45	chr15:51952049..51953706-chr15:52013977..52015547,2	K562	blood:
46	chr15:52000063..52002594-chr15:52042523..52044323,2	K562	blood:
47	chr15:51980744..51981706-chr15:52068316..52068940,3	MCF-7	breast:
48	chr15:51990726..51993605-chr15:51996321..51998740,2	MCF-7	breast:
49	chr15:51975005..51977651-chr15:51984880..51987418,3	K562	blood:
50	chr15:51976547..51978091-chr15:52028258..52031013,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYSMD2-2	chr15:51987830-51987962	ENSG00000259241.1
2	lnc-LYSMD2-2	chr15:51985413-51986134	ENSG00000259241.1
3	lnc-LYSMD2-1	chr15:52005297-52005353	ENSG00000259296.1
4	lnc-LYSMD2-1	chr15:52000192-52000471	ENSG00000259296.1
5	lnc-LYSMD2-1	chr15:52007368-52007417	ENSG00000259296.1
6	lnc-LYSMD2-1	chr15:52007355-52007591	NONHSAT043877

No data

Variant related genes	Relation type
ENSG00000259296	TF binding region
SCG3	TF binding region
ENSG00000259241	TF binding region
ENSG00000259296	CpG island
SCG3	CpG island
ENSG00000259241	CpG island
ENSG00000189050	chromatin interactions
ENSG00000128872	chromatin interactions
ENSG00000259241	chromatin interactions
ENSG00000259377	chromatin interactions
ENSG00000104112	chromatin interactions
ENSG00000140280	chromatin interactions
ENSG00000267302	chromatin interactions
ENSG00000069966	chromatin interactions
ENSG00000259296	chromatin interactions

Extended variants
information (count: 1946 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1946 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138035624	chr15:51950609-51950610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533030509	chr15:51950618-51950619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149482386	chr15:51950644-51950645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559703733	chr15:51950660-51950661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187690457	chr15:51950661-51950662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548804090	chr15:51950668-51950669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2607113	chr15:51950683-51950684	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs192748440	chr15:51950712-51950713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551109991	chr15:51950727-51950728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143972588	chr15:51950749-51950750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540118319	chr15:51950758-51950759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558525825	chr15:51950822-51950823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114892733	chr15:51950823-51950824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376800064	chr15:51950836-51950837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200990510	chr15:51950862-51950863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534246421	chr15:51950888-51950889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555482254	chr15:51950898-51950899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367748062	chr15:51950912-51950913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574039743	chr15:51950939-51950940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148606717	chr15:51950953-51950954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs77777772	chr15:51951073-51951074	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs561744422	chr15:51951080-51951081	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs74975660	chr15:51951102-51951103	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs77362376	chr15:51951112-51951113	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs560054547	chr15:51951134-51951135	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115086644	chr15:51951152-51951153	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs542560002	chr15:51951177-51951178	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs141503417	chr15:51951178-51951179	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs544113345	chr15:51951179-51951180	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs531411199	chr15:51951188-51951189	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs549641271	chr15:51951214-51951215	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs74666999	chr15:51951218-51951219	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs533609929	chr15:51951225-51951226	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs55982453	chr15:51951245-51951246	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs28576876	chr15:51951252-51951253	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs116720850	chr15:51951255-51951256	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs549325310	chr15:51951256-51951257	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs567574076	chr15:51951265-51951266	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs551079615	chr15:51951296-51951297	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs375324281	chr15:51951307-51951308	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs184026857	chr15:51951338-51951339	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs556272884	chr15:51951361-51951362	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs577404800	chr15:51951365-51951366	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs114572276	chr15:51951417-51951418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553552230	chr15:51951445-51951446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140162252	chr15:51951492-51951493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542570871	chr15:51951563-51951564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560920484	chr15:51951603-51951604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575991082	chr15:51951652-51951653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543497819	chr15:51951668-51951669	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51950600-51951400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr15:51950800-51951000	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr15:51950800-51951800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr15:51951000-51951400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr15:51951400-51951600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr15:51960600-51964200	Enhancers	K562	blood
7	chr15:51963200-51963800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr15:51963200-51964200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr15:51963400-51965000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr15:51963400-51965200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr15:51963800-51965400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr15:51964000-51965000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr15:51964200-51964400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr15:51964200-51964600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr15:51964200-51964800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr15:51964200-51964800	Flanking Active TSS	K562	blood
17	chr15:51964200-51965000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr15:51964200-51965000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr15:51964200-51965000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr15:51964200-51965000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr15:51964200-51965400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:51964200-51965600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr15:51964400-51964600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr15:51964400-51964600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr15:51964400-51964800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr15:51964400-51965400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr15:51964600-51964800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr15:51964600-51964800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr15:51964800-51965200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr15:51964800-51965400	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr15:51964800-51965600	Enhancers	K562	blood
32	chr15:51964800-51965800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:51964800-51967400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr15:51965000-51965200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr15:51965000-51967200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr15:51965200-51965800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
37	chr15:51965400-51965600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr15:51965400-51965600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr15:51965400-51969600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr15:51965600-51966400	Flanking Active TSS	K562	blood
41	chr15:51965600-51972200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr15:51965800-51966000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr15:51966000-51967400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr15:51966400-51967400	Enhancers	K562	blood
45	chr15:51966600-51973400	Weak transcription	Right Atrium	heart
46	chr15:51967200-51967400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr15:51967200-51968200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr15:51967400-51967600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr15:51967400-51967600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr15:51967400-51967800	Enhancers	H1 Cell Line	embryonic stem cell

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