Variant report

Variant	nsv471255
Chromosome Location	chr15:78063585-78131097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1090)
CpG islands
(count:1099)
Chromatin interactive
region (count:65)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78077195-78077543	K562	blood:	n/a	n/a
2	BACH1	chr15:78111596-78111934	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:78112581-78112794	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr15:78088327-78088760	GM12878	blood:	n/a	n/a
5	BCL3	chr15:78088304-78088829	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:78101148-78101512	HepG2	liver:	n/a	chr15:78101316-78101325 chr15:78101317-78101326 chr15:78101317-78101326
7	BHLHE40	chr15:78096532-78096945	K562	blood:	n/a	n/a
8	BHLHE40	chr15:78089629-78089938	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:78113815-78114121	K562	blood:	n/a	chr15:78113828-78113844
10	BHLHE40	chr15:78113211-78113483	K562	blood:	n/a	chr15:78113370-78113391 chr15:78113374-78113387
11	BHLHE40	chr15:78077441-78077584	K562	blood:	n/a	n/a
12	BHLHE40	chr15:78095857-78096131	K562	blood:	n/a	n/a
13	BHLHE40	chr15:78104173-78104542	K562	blood:	n/a	chr15:78104303-78104324 chr15:78104308-78104317 chr15:78104309-78104318 chr15:78104310-78104319 chr15:78104309-78104318 chr15:78104307-78104320
14	BHLHE40	chr15:78102084-78102117	K562	blood:	n/a	n/a
15	BHLHE40	chr15:78112561-78112947	K562	blood:	n/a	n/a
16	BHLHE40	chr15:78101143-78101495	K562	blood:	n/a	chr15:78101316-78101325 chr15:78101317-78101326 chr15:78101317-78101326
17	BRCA1	chr15:78116340-78116364	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr15:78077171-78077598	K562	blood:	n/a	n/a
19	CCNT2	chr15:78112531-78112910	K562	blood:	n/a	n/a
20	CEBPB	chr15:78077418-78077509	K562	blood:	n/a	n/a
21	CEBPB	chr15:78097862-78098204	HepG2	liver:	n/a	chr15:78098032-78098043
22	CEBPB	chr15:78097908-78098155	H1-hESC	embryonic stem cell:	n/a	chr15:78098032-78098043
23	CEBPB	chr15:78097972-78098198	Hela-S3	cervix:	n/a	chr15:78098032-78098043
24	CEBPB	chr15:78097872-78098202	A549	lung:	n/a	chr15:78098032-78098043
25	CEBPB	chr15:78097866-78098207	IMR90	lung:	n/a	chr15:78098032-78098043
26	CEBPB	chr15:78097885-78098211	K562	blood:	n/a	chr15:78098032-78098043
27	CEBPB	chr15:78097916-78098237	MCF-7	breast:	n/a	chr15:78098032-78098043
28	CHD1	chr15:78111718-78111742	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr15:78112768-78112882	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr15:78128582-78129087	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr15:78122597-78122722	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr15:78114017-78114116	K562	blood:	n/a	n/a
33	CHD2	chr15:78093119-78093139	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr15:78095843-78096168	K562	blood:	n/a	n/a
35	CHD2	chr15:78089582-78089843	GM12878	blood:	n/a	n/a
36	CHD2	chr15:78112731-78112878	Hela-S3	cervix:	n/a	n/a
37	CREB1	chr15:78077295-78077568	A549	lung:	n/a	n/a
38	CREB1	chr15:78112210-78112963	A549	lung:	n/a	n/a
39	CTBP2	chr15:78111581-78112011	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr15:78115800-78115950	GM12871	blood:	n/a	n/a
41	CTCF	chr15:78113940-78114090	HMF	breast:	n/a	chr15:78113982-78114000
42	CTCF	chr15:78077360-78077510	HPF	lung:	n/a	n/a
43	CTCF	chr15:78115760-78115910	MCF-7	breast:	n/a	n/a
44	CTCF	chr15:78113920-78114070	AG04450	lung:	n/a	chr15:78113982-78114000
45	CTCF	chr15:78113940-78114090	NHDF-neo	bronchial:	n/a	chr15:78113982-78114000
46	CTCF	chr15:78113705-78114256	A549	lung:	n/a	chr15:78113982-78114000
47	CTCF	chr15:78077280-78077430	HCM	heart:	n/a	n/a
48	CTCF	chr15:78077360-78077510	GM06990	blood:	n/a	n/a
49	CTCF	chr15:78112640-78112790	HRPEpiC	eye:	n/a	chr15:78112771-78112781
50	CTCF	chr15:78113960-78114110	GM12868	blood:	n/a	chr15:78113982-78114000

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78112026-78112076	PFSK-1	brain:	n/a
2	chr15:78112026-78112076	PFSK-1	brain:	n/a
3	chr15:78110106-78110156	AG04450	lung:	fetal
4	chr15:78103228-78103278	U87	brain:	n/a
5	chr15:78111390-78111440	NH-A	brain:	n/a
6	chr15:78077656-78077706	HRPEpiC	eye:	n/a
7	chr15:78113237-78113287	HCT-116	colon:	n/a
8	chr15:78109450-78109500	U87	brain:	n/a
9	chr15:78112847-78112897	HRPEpiC	eye:	n/a
10	chr15:78114888-78114938	NHDF-neo	bronchial:	n/a
11	chr15:78113667-78113717	GM12891	blood:	n/a
12	chr15:78114278-78114328	HCPEpiC	choroid plexus:	n/a
13	chr15:78111390-78111440	SKMC	muscle:	n/a
14	chr15:78109450-78109500	HUVEC	blood vessel:	n/a
15	chr15:78110857-78110907	NHDF-neo	bronchial:	n/a
16	chr15:78110857-78110907	CMK	blood:	n/a
17	chr15:78112847-78112897	HCPEpiC	choroid plexus:	n/a
18	chr15:78110903-78110953	NHBE	bronchial:	n/a
19	chr15:78111196-78111246	LNCaP	prostate:	n/a
20	chr15:78110106-78110156	AG04449	skin:	fetal
21	chr15:78112026-78112076	HMEC	breast:	n/a
22	chr15:78113667-78113717	PFSK-1	brain:	n/a
23	chr15:78118816-78118866	HCF	heart:	n/a
24	chr15:78114278-78114328	SKMC	muscle:	n/a
25	chr15:78113237-78113287	HEEpiC	esophagus:	n/a
26	chr15:78077656-78077706	HepG2	liver:	n/a
27	chr15:78110903-78110953	CMK	blood:	n/a
28	chr15:78113237-78113287	HUVEC	blood vessel:	n/a
29	chr15:78110857-78110907	T-47D	breast:	n/a
30	chr15:78103228-78103278	HRCEpiC	kidney:	n/a
31	chr15:78113237-78113287	AG04450	lung:	fetal
32	chr15:78112818-78112868	NT2-D1	testis:	n/a
33	chr15:78111390-78111440	HUVEC	blood vessel:	n/a
34	chr15:78112847-78112897	PANC-1	pancreas:	n/a
35	chr15:78112847-78112897	ECC-1	luminal epithelium:	n/a
36	chr15:78110903-78110953	GM19239	blood:	n/a
37	chr15:78110857-78110907	AoSMC	blood vessel:	n/a
38	chr15:78114278-78114328	HCT-116	colon:	n/a
39	chr15:78113667-78113717	SK-N-MC	brain:	n/a
40	chr15:78114888-78114938	HUVEC	blood vessel:	n/a
41	chr15:78110106-78110156	H1-hESC	embryonic stem cell:	embryo
42	chr15:78114888-78114938	SAEC	small airway:	n/a
43	chr15:78112026-78112076	IMR90	lung:	fetal
44	chr15:78111196-78111246	ovcar-3	ovarian:	n/a
45	chr15:78113667-78113717	ECC-1	luminal epithelium:	n/a
46	chr15:78112026-78112076	HAEpiC	amniotic membrane:	n/a
47	chr15:78108562-78108612	AG09319	gingival:	n/a
48	chr15:78112026-78112076	AG04450	lung:	fetal
49	chr15:78111196-78111246	HRE	kidney:	n/a
50	chr15:78110903-78110953	HCPEpiC	choroid plexus:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:78064180..78065710-chr15:78076746..78078989,2	K562	blood:
2	chr15:78115470..78116424-chr15:78167241..78167877,2	MCF-7	breast:
3	chr15:78099210..78100960-chr15:78102155..78104684,2	K562	blood:
4	chr15:78086471..78089118-chr20:52208956..52211312,2	MCF-7	breast:
5	chr15:78083797..78085667-chr15:78106019..78108853,2	K562	blood:
6	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
7	chr15:77951738..77952728-chr15:78113529..78114461,5	K562	blood:
8	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
9	chr15:77950482..77951067-chr15:78113646..78114389,2	K562	blood:
10	chr15:78092486..78095378-chr15:78106571..78109428,2	K562	blood:
11	chr15:78059582..78063718-chr15:78064964..78067132,3	K562	blood:
12	chr15:78097737..78099826-chr15:78103179..78105100,2	MCF-7	breast:
13	chr15:77951815..77952789-chr15:78075941..78076556,2	K562	blood:
14	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:
15	chr15:77925249..77927257-chr15:78113205..78115049,24	MCF-7	breast:
16	chr15:78107758..78109313-chr15:78111361..78113671,2	K562	blood:
17	chr15:78097737..78099826-chr15:78103179..78105100,2	MCF-7	breast:
18	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
19	chr15:77948459..77951097-chr15:78104975..78107913,2	MCF-7	breast:
20	chr15:78029999..78032267-chr15:78076792..78079270,2	MCF-7	breast:
21	chr15:78097066..78100710-chr15:78102142..78106147,5	K562	blood:
22	chr15:78059582..78063718-chr15:78064964..78067132,3	K562	blood:
23	chr15:78118529..78120395-chr15:78122461..78124625,2	K562	blood:
24	chr15:78103078..78104823-chr15:78106896..78108558,2	K562	blood:
25	chr15:78115466..78118484-chr15:78120011..78123409,3	MCF-7	breast:
26	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
27	chr15:78097465..78099114-chr15:78102921..78104806,2	K562	blood:
28	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
29	chr15:78125331..78127542-chr15:78130355..78132025,2	K562	blood:
30	chr15:78083797..78085667-chr15:78106019..78108853,2	K562	blood:
31	chr15:77925509..77926398-chr15:78076937..78077835,4	K562	blood:
32	chr15:78062199..78064857-chr15:78066773..78068430,2	K562	blood:
33	chr15:78097465..78099114-chr15:78102921..78104806,2	K562	blood:
34	chr15:77951783..77952314-chr15:78066187..78066759,2	MCF-7	breast:
35	chr15:77411244..77411752-chr15:78113897..78114465,2	K562	blood:
36	chr15:77835732..77836546-chr15:78113747..78114395,2	MCF-7	breast:
37	chr15:78116064..78118754-chr15:78122840..78125004,2	MCF-7	breast:
38	chr15:77925491..77927003-chr15:78065547..78066951,12	MCF-7	breast:
39	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
40	chr15:78092486..78095378-chr15:78106571..78109428,2	K562	blood:
41	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:
42	chr15:78116064..78118754-chr15:78122840..78125004,2	MCF-7	breast:
43	chr15:78129825..78131680-chr15:78135529..78137556,2	K562	blood:
44	chr15:78064180..78065710-chr15:78076746..78078989,2	K562	blood:
45	chr15:77951754..77952701-chr15:78076956..78077942,7	K562	blood:
46	chr15:78115466..78118484-chr15:78120011..78123409,3	MCF-7	breast:
47	chr15:78041656..78043427-chr15:78100097..78102130,2	MCF-7	breast:
48	chr15:78125331..78127542-chr15:78130355..78132025,2	K562	blood:
49	chr15:77925532..77926425-chr15:78076783..78078398,4	MCF-7	breast:
50	chr15:78044160..78046640-chr15:78075370..78077627,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D2B-7	chr15:78113121-78113196	NONHSAT047459
2	lnc-TBC1D2B-7	chr15:78112376-78112566	NONHSAT047460
3	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047459
4	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047460
5	lnc-SH2D7-5	chr15:78079529-78079589	XLOC_011317
6	lnc-SH2D7-5	chr15:78080231-78081011	XLOC_011317
7	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047458
8	lnc-TBC1D2B-7	chr15:78111613-78111870	NONHSAT047458
9	lnc-SH2D7-5	chr15:78080231-78080917	ENSG00000259213.1
10	lnc-SH2D7-5	chr15:78079535-78079589	ENSG00000259213.1
11	lnc-SH2D7-5	chr15:78080723-78081016	ENSG00000259213.1
12	lnc-SH2D7-5	chr15:78080414-78080487	ENSG00000259213.1

No data

Variant related genes	Relation type
ENSG00000259213	TF binding region
LINGO1	TF binding region
ENSG00000259213	CpG island
LINGO1	CpG island
ENSG00000259213	chromatin interactions
ENSG00000259281	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000169783	chromatin interactions

Extended variants
information (count: 2726 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2726 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11629474	chr15:78063585-78063586	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538557461	chr15:78063610-78063611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371704017	chr15:78063690-78063691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188271589	chr15:78063696-78063697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572302085	chr15:78063723-78063724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542288507	chr15:78063744-78063745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75645687	chr15:78063798-78063799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576073744	chr15:78063799-78063800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543517798	chr15:78063814-78063815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563081229	chr15:78063825-78063826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191210846	chr15:78063832-78063833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551998935	chr15:78063848-78063849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560794925	chr15:78063904-78063905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146723203	chr15:78063928-78063929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184757159	chr15:78063936-78063937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567622373	chr15:78063946-78063947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140455992	chr15:78063959-78063960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537956994	chr15:78063962-78063963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190511032	chr15:78063964-78063965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571398121	chr15:78064049-78064050	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs28495127	chr15:78064075-78064076	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs553531934	chr15:78064087-78064088	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572287355	chr15:78064173-78064174	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149945591	chr15:78064203-78064204	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532882795	chr15:78064207-78064208	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115219789	chr15:78064225-78064226	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554292010	chr15:78064231-78064232	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181723599	chr15:78064261-78064262	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543430693	chr15:78064286-78064287	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78733281	chr15:78064316-78064317	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576988817	chr15:78064344-78064345	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10851898	chr15:78064345-78064346	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs186811965	chr15:78064351-78064352	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527997230	chr15:78064452-78064453	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543258225	chr15:78064529-78064530	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189946724	chr15:78064547-78064548	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530797553	chr15:78064563-78064564	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531637147	chr15:78064586-78064587	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549761491	chr15:78064588-78064589	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571436278	chr15:78064596-78064597	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs8035460	chr15:78064664-78064665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs181589959	chr15:78064726-78064727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568332102	chr15:78064727-78064728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145715812	chr15:78064736-78064737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554887495	chr15:78064783-78064784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148920727	chr15:78064799-78064800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569845809	chr15:78064804-78064805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143720332	chr15:78064805-78064806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537069646	chr15:78064823-78064824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185615665	chr15:78064846-78064847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:782 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78061800-78074800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:78062200-78068000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:78063000-78064600	Enhancers	Spleen	Spleen
4	chr15:78064000-78064600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
5	chr15:78064600-78068600	Weak transcription	Spleen	Spleen
6	chr15:78065200-78066600	Strong transcription	Fetal Intestine Small	intestine
7	chr15:78065800-78066200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr15:78066400-78068200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr15:78066600-78072600	Weak transcription	Fetal Intestine Small	intestine
10	chr15:78067200-78068000	Enhancers	Fetal Brain Female	brain
11	chr15:78067200-78068200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr15:78067400-78067600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr15:78067600-78068000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr15:78067600-78068600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr15:78068000-78068800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr15:78068000-78073000	Weak transcription	Fetal Brain Female	brain
17	chr15:78068000-78076400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr15:78068200-78068600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr15:78068200-78078200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr15:78068600-78068800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr15:78068600-78068800	Enhancers	Fetal Muscle Trunk	muscle
22	chr15:78068600-78069000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr15:78068600-78069200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr15:78068600-78069200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr15:78068600-78069200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr15:78068600-78069600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr15:78068600-78069600	Enhancers	Spleen	Spleen
28	chr15:78068600-78069800	Enhancers	Fetal Brain Male	brain
29	chr15:78068800-78069400	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr15:78069000-78069200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr15:78069000-78069400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr15:78069200-78069600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr15:78069200-78069600	Enhancers	Fetal Muscle Trunk	muscle
34	chr15:78069200-78072200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:78069400-78069600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr15:78069600-78070400	Weak transcription	Spleen	Spleen
37	chr15:78069800-78072000	Weak transcription	Fetal Brain Male	brain
38	chr15:78070400-78070600	Enhancers	Spleen	Spleen
39	chr15:78070400-78071600	Weak transcription	Fetal Stomach	stomach
40	chr15:78070600-78072000	Weak transcription	Spleen	Spleen
41	chr15:78072000-78072800	ZNF genes & repeats	Spleen	Spleen
42	chr15:78072000-78077600	Enhancers	Fetal Brain Male	brain
43	chr15:78072200-78072400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:78072400-78072600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr15:78072400-78072800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:78072400-78078400	Weak transcription	Brain Angular Gyrus	brain
47	chr15:78072600-78073400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr15:78072600-78073400	ZNF genes & repeats	Fetal Intestine Small	intestine
49	chr15:78072800-78073000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr15:78072800-78073600	ZNF genes & repeats	Brain Germinal Matrix	brain

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