Variant report

Variant	nsv904557
Chromosome Location	chr15:99956954-99991506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:620)
CpG islands
(count:1710)
Chromatin interactive
region (count:46)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:99961418-99962008	HepG2	liver:	n/a	n/a
2	ATF1	chr15:99991175-99991347	K562	blood:	n/a	n/a
3	ATF2	chr15:99965347-99965754	GM12878	blood:	n/a	n/a
4	BACH1	chr15:99987944-99987962	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr15:99965364-99965661	GM12878	blood:	n/a	chr15:99965442-99965451
6	BHLHE40	chr15:99973687-99973691	GM12878	blood:	n/a	n/a
7	BHLHE40	chr15:99965453-99965469	K562	blood:	n/a	n/a
8	BHLHE40	chr15:99961440-99962002	HepG2	liver:	n/a	n/a
9	BRCA1	chr15:99975665-99975680	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr15:99991255-99991532	HepG2	liver:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
11	CEBPB	chr15:99991138-99991628	ECC-1	luminal epithelium:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
12	CEBPB	chr15:99965381-99965715	IMR90	lung:	n/a	n/a
13	CEBPB	chr15:99961492-99961572	IMR90	lung:	n/a	n/a
14	CEBPB	chr15:99982704-99983088	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr15:99991224-99991516	K562	blood:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
16	CEBPB	chr15:99982646-99983055	IMR90	lung:	n/a	n/a
17	CEBPB	chr15:99961370-99961725	HepG2	liver:	n/a	n/a
18	CEBPB	chr15:99961467-99961647	HepG2	liver:	n/a	n/a
19	CEBPB	chr15:99961361-99961734	HepG2	liver:	n/a	n/a
20	CEBPB	chr15:99965407-99965607	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr15:99961470-99961726	MCF-7	breast:	n/a	n/a
22	CEBPB	chr15:99991175-99991573	ECC-1	luminal epithelium:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
23	CEBPB	chr15:99991393-99991413	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr15:99991151-99991660	MCF-7	breast:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
25	CEBPB	chr15:99991284-99991524	MCF-7	breast:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
26	CEBPD	chr15:99961442-99961604	HepG2	liver:	n/a	n/a
27	CHD2	chr15:99975690-99975908	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr15:99982693-99983140	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr15:99961572-99961672	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr15:99973825-99973857	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr15:99973694-99973933	GM12878	blood:	n/a	n/a
32	CHD2	chr15:99965573-99965713	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr15:99961599-99961785	HepG2	liver:	n/a	n/a
34	CTCF	chr15:99966240-99966390	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr15:99966240-99966390	NHEK	skin:	n/a	n/a
36	CTCF	chr15:99966280-99966430	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr15:99975620-99975770	HMEC	breast:	n/a	n/a
38	CTCF	chr15:99966160-99966310	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr15:99966193-99966442	MCF-7	breast:	n/a	n/a
40	CTCF	chr15:99975720-99975870	MCF-7	breast:	n/a	n/a
41	CTCF	chr15:99966180-99966330	HCFaa	heart:	n/a	n/a
42	CTCF	chr15:99973400-99973550	GM12875	blood:	n/a	n/a
43	CTCF	chr15:99966218-99966397	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr15:99966230-99966383	HepG2	liver:	n/a	n/a
45	CTCF	chr15:99978320-99978470	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr15:99966260-99966410	GM12872	blood:	n/a	n/a
47	CTCF	chr15:99972454-99972485	GM19240	blood:	n/a	n/a
48	CTCF	chr15:99975600-99975750	Caco-2	colon:	n/a	n/a
49	CTCF	chr15:99966054-99966614	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:99975728-99975731	LNCaP	prostate:	n/a	n/a

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99978986-99979036	Hepatocyte	liver:	n/a
2	chr15:99979584-99979634	ECC-1	luminal epithelium:	n/a
3	chr15:99978986-99979036	Hepatocyte	liver:	n/a
4	chr15:99979584-99979634	ECC-1	luminal epithelium:	n/a
5	chr15:99975010-99975060	NT2-D1	testis:	n/a
6	chr15:99975141-99975191	SK-N-SH	brain:	n/a
7	chr15:99975010-99975060	Hela-S3	cervix:	n/a
8	chr15:99966968-99967018	AG09309	skin:	n/a
9	chr15:99979584-99979634	T-47D	breast:	n/a
10	chr15:99975010-99975060	AG09309	skin:	n/a
11	chr15:99987288-99987338	Hepatocyte	liver:	n/a
12	chr15:99967055-99967105	T-47D	breast:	n/a
13	chr15:99979290-99979340	Caco-2	colon:	n/a
14	chr15:99982524-99982574	U87	brain:	n/a
15	chr15:99987955-99988005	SK-N-SH_RA	brain:	n/a
16	chr15:99974369-99974419	GM19239	blood:	n/a
17	chr15:99987894-99987944	K562	blood:	n/a
18	chr15:99982524-99982574	BE2_C	brain:	n/a
19	chr15:99975010-99975060	ECC-1	luminal epithelium:	n/a
20	chr15:99979346-99979396	A549	lung:	n/a
21	chr15:99987871-99987921	ovcar-3	ovarian:	n/a
22	chr15:99987955-99988005	SK-N-MC	brain:	n/a
23	chr15:99975334-99975384	HEK293	kidney:	embryo
24	chr15:99979527-99979577	SAEC	small airway:	n/a
25	chr15:99987871-99987921	HL-60	blood:	n/a
26	chr15:99975470-99975520	AG10803	skin:	n/a
27	chr15:99974332-99974382	Jurkat	blood:	n/a
28	chr15:99971423-99971473	HepG2	liver:	n/a
29	chr15:99975310-99975360	HEEpiC	esophagus:	n/a
30	chr15:99979527-99979577	HUVEC	blood vessel:	n/a
31	chr15:99979527-99979577	A549	lung:	n/a
32	chr15:99975141-99975191	PrEC	prostate:	n/a
33	chr15:99979584-99979634	HRCEpiC	kidney:	n/a
34	chr15:99979059-99979109	HUVEC	blood vessel:	n/a
35	chr15:99987322-99987372	AG09319	gingival:	n/a
36	chr15:99975334-99975384	GM12878	blood:	n/a
37	chr15:99975334-99975384	HMEC	breast:	n/a
38	chr15:99987288-99987338	HIPEpiC	eye:	n/a
39	chr15:99975010-99975060	HIPEpiC	eye:	n/a
40	chr15:99966833-99966883	HMEC	breast:	n/a
41	chr15:99979013-99979063	ECC-1	luminal epithelium:	n/a
42	chr15:99966833-99966883	Jurkat	blood:	n/a
43	chr15:99979527-99979577	PANC-1	pancreas:	n/a
44	chr15:99975470-99975520	HRPEpiC	eye:	n/a
45	chr15:99987955-99988005	AG09309	skin:	n/a
46	chr15:99987322-99987372	HIPEpiC	eye:	n/a
47	chr15:99978986-99979036	PFSK-1	brain:	n/a
48	chr15:99987322-99987372	HRPEpiC	eye:	n/a
49	chr15:99971213-99971263	HCF	heart:	n/a
50	chr15:99987288-99987338	HAEpiC	amniotic membrane:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:99991338..99992840-chr15:100014340..100017006,2	MCF-7	breast:
2	chr15:99973224..99976448-chr15:99991050..99995157,5	MCF-7	breast:
3	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
4	chr15:99981264..99984715-chr15:99985641..99987973,4	MCF-7	breast:
5	chr15:99987398..99990235-chr15:100010575..100012559,2	MCF-7	breast:
6	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
7	chr15:99947710..99950479-chr15:99955909..99957738,2	MCF-7	breast:
8	chr15:99965843..99966811-chr15:100243795..100245106,3	MCF-7	breast:
9	chr15:99979583..99981872-chr15:99983556..99985309,2	MCF-7	breast:
10	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
11	chr15:99977572..99979807-chr15:99980072..99982815,2	K562	blood:
12	chr15:99962601..99965549-chr15:100104653..100107115,3	MCF-7	breast:
13	chr15:99979583..99981872-chr15:99983556..99985309,2	MCF-7	breast:
14	chr15:99984466..99986504-chr15:100104174..100107057,2	K562	blood:
15	chr15:99960211..99963086-chr15:99964919..99968237,3	MCF-7	breast:
16	chr15:99963793..99965594-chr15:99976352..99978718,2	K562	blood:
17	chr15:99966023..99966782-chr15:100243828..100244741,2	MCF-7	breast:
18	chr15:99976374..99976897-chr15:100105314..100105862,2	Hela-S3	cervix:
19	chr15:99965407..99967484-chr15:99969675..99971240,2	K562	blood:
20	chr15:99977572..99979807-chr15:99980072..99982815,2	K562	blood:
21	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
22	chr15:99966071..99969014-chr15:100104345..100107384,3	MCF-7	breast:
23	chr15:99960211..99963086-chr15:99964919..99968237,3	MCF-7	breast:
24	chr15:99966031..99966539-chr15:100044729..100045649,2	MCF-7	breast:
25	chr15:99966102..99966691-chr15:100044817..100045390,2	MCF-7	breast:
26	chr15:99976307..99978594-chr15:100018036..100019822,2	MCF-7	breast:
27	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
28	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
29	chr15:99979674..99981771-chr15:99994725..99997256,2	K562	blood:
30	chr15:99986076..99989977-chr15:99992374..99995201,3	K562	blood:
31	chr15:99985824..99988050-chr15:99992595..99995524,2	MCF-7	breast:
32	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
33	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
34	chr15:99960171..99963200-chr15:100104719..100108193,3	MCF-7	breast:
35	chr15:99981264..99984715-chr15:99985641..99987973,4	MCF-7	breast:
36	chr15:99973224..99976448-chr15:99991050..99995157,5	MCF-7	breast:
37	chr15:99981781..99983657-chr15:100018041..100019744,2	MCF-7	breast:
38	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
39	chr15:99964977..99967345-chr15:100103742..100106400,3	MCF-7	breast:
40	chr15:99971316..99975999-chr15:100104042..100107403,7	MCF-7	breast:
41	chr15:99963793..99965594-chr15:99976352..99978718,2	K562	blood:
42	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
43	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
44	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
45	chr15:99981180..99982961-chr15:99993073..99995315,2	MCF-7	breast:
46	chr15:99949082..99949796-chr15:99965826..99966399,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC23-5	chr15:99971676-99972112	l_1247_chr15:99961345-99972053_liver
2	lnc-TTC23-5	chr15:99961346-99963761	l_1247_chr15:99961345-99972053_liver
3	lnc-TTC23-5	chr15:99971261-99971500	l_1247_chr15:99961345-99972053_liver
4	lnc-TTC23-3	chr15:99971033-99971233	ENSG00000259341.1
5	lnc-TTC23-5	chr15:99964546-99965708	l_1247_chr15:99961345-99972053_liver
6	lnc-TTC23-3	chr15:99967214-99967407	ENSG00000259341.1

No data

Variant related genes	Relation type
ENSG00000259341	TF binding region
ENSG00000259341	CpG island
ENSG00000259341	chromatin interactions
ENSG00000068305	chromatin interactions

Extended variants
information (count: 1561 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1561 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6598242	chr15:99956954-99956955	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114179326	chr15:99956956-99956957	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs537088476	chr15:99957013-99957014	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs76627858	chr15:99957041-99957042	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs115844809	chr15:99957060-99957061	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs187429473	chr15:99957068-99957069	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs369972414	chr15:99957072-99957073	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs553168373	chr15:99957104-99957105	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs574666622	chr15:99957111-99957112	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs535748956	chr15:99957112-99957113	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs371429102	chr15:99957121-99957122	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs557191541	chr15:99957123-99957124	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs111414749	chr15:99957144-99957145	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs546226457	chr15:99957168-99957169	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs529232488	chr15:99957193-99957194	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs557850381	chr15:99957208-99957209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573301664	chr15:99957227-99957228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1867090	chr15:99957262-99957263	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs115996443	chr15:99957271-99957272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529871797	chr15:99957273-99957274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191965016	chr15:99957311-99957312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184896015	chr15:99957335-99957336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530695131	chr15:99957348-99957349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544697557	chr15:99957367-99957368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150616224	chr15:99957368-99957369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570320489	chr15:99957405-99957406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187818359	chr15:99957447-99957448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546242974	chr15:99957465-99957466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140049288	chr15:99957568-99957569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35899227	chr15:99957584-99957585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535692216	chr15:99957621-99957622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557131784	chr15:99957669-99957670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569566388	chr15:99957680-99957681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12594256	chr15:99957704-99957705	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs558153541	chr15:99957722-99957723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573108374	chr15:99957735-99957736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192791659	chr15:99957745-99957746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555934928	chr15:99957748-99957749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574176354	chr15:99957776-99957777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542072724	chr15:99957804-99957805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548989291	chr15:99957841-99957842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184324893	chr15:99957874-99957875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146404243	chr15:99957904-99957905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545753665	chr15:99957907-99957908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35120989	chr15:99957951-99957952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564115684	chr15:99957982-99957983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528038135	chr15:99957992-99957993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139748732	chr15:99957994-99957995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567862649	chr15:99957997-99957998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528935951	chr15:99958032-99958033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	20811773	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Emphysema	19352772	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99944800-99972400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:99950000-99964800	Weak transcription	Adipose Nuclei	Adipose
3	chr15:99950800-99965800	Weak transcription	Aorta	Aorta
4	chr15:99951000-99965200	Weak transcription	Spleen	Spleen
5	chr15:99953000-99965400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:99954800-99957200	Enhancers	Placenta	Placenta
7	chr15:99955200-99957200	Enhancers	Fetal Stomach	stomach
8	chr15:99955400-99964200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:99955600-99957000	Enhancers	Fetal Heart	heart
10	chr15:99955600-99963400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr15:99955600-99963600	Weak transcription	Left Ventricle	heart
12	chr15:99956200-99957400	Enhancers	Fetal Muscle Leg	muscle
13	chr15:99956400-99957200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr15:99956400-99963400	Weak transcription	Esophagus	oesophagus
15	chr15:99956600-99957000	Enhancers	Lung	lung
16	chr15:99956600-99957000	Enhancers	Placenta Amnion	Placenta Amnion
17	chr15:99956600-99957200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:99956800-99957000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr15:99956800-99957000	Enhancers	Right Atrium	heart
20	chr15:99956800-99957200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr15:99956800-99957200	Flanking Active TSS	HepG2	liver
22	chr15:99957000-99957200	Enhancers	Gastric	stomach
23	chr15:99957000-99961200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr15:99957000-99961200	Weak transcription	Right Atrium	heart
25	chr15:99957000-99964200	Weak transcription	Fetal Muscle Trunk	muscle
26	chr15:99957000-99964200	Weak transcription	Lung	lung
27	chr15:99957200-99961200	Weak transcription	HepG2	liver
28	chr15:99957200-99961400	Weak transcription	Placenta	Placenta
29	chr15:99957200-99961400	Weak transcription	Fetal Stomach	stomach
30	chr15:99957200-99961600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr15:99957200-99961600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr15:99957200-99965200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:99957200-99973200	Weak transcription	Gastric	stomach
34	chr15:99960800-99965000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr15:99961000-99961400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr15:99961000-99961600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr15:99961000-99962400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr15:99961000-99965000	Enhancers	Primary T cells from cord blood	blood
39	chr15:99961000-99966800	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr15:99961200-99961400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr15:99961200-99961600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr15:99961200-99961600	Active TSS	HepG2	liver
43	chr15:99961200-99961800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr15:99961200-99961800	Enhancers	Placenta Amnion	Placenta Amnion
45	chr15:99961400-99961800	Enhancers	Primary B cells from peripheral blood	blood
46	chr15:99961400-99961800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr15:99961400-99961800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr15:99961400-99961800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr15:99961400-99961800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr15:99961400-99961800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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