Variant report

Variant	nsv977720
Chromosome Location	chr15:59157444-59165373
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:381)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:59158433-59158785	K562	blood:	n/a	n/a
2	ATF2	chr15:59158413-59158831	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr15:59158379-59158846	A549	lung:	n/a	n/a
4	BHLHE40	chr15:59156764-59157975	HepG2	liver:	n/a	n/a
5	BHLHE40	chr15:59158552-59158660	K562	blood:	n/a	n/a
6	BRCA1	chr15:59158404-59158783	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr15:59158338-59158849	HCT-116	colon:	n/a	n/a
8	CBX3	chr15:59158467-59158820	K562	blood:	n/a	n/a
9	CBX3	chr15:59158322-59158859	K562	blood:	n/a	n/a
10	CEBPB	chr15:59158421-59158779	A549	lung:	n/a	n/a
11	CEBPB	chr15:59158493-59158756	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr15:59162663-59163018	IMR90	lung:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
13	CEBPB	chr15:59162674-59162956	HepG2	liver:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
14	CEBPB	chr15:59158393-59158795	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr15:59162674-59162950	A549	lung:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
16	CEBPB	chr15:59158412-59158786	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:59157246-59157444	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr15:59158440-59158761	K562	blood:	n/a	n/a
19	CEBPB	chr15:59158510-59158639	HepG2	liver:	n/a	n/a
20	CEBPB	chr15:59158385-59158785	HepG2	liver:	n/a	n/a
21	CEBPB	chr15:59158532-59158702	IMR90	lung:	n/a	n/a
22	CEBPB	chr15:59162742-59162903	H1-hESC	embryonic stem cell:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
23	CEBPB	chr15:59158401-59158752	K562	blood:	n/a	n/a
24	CEBPB	chr15:59162691-59162955	K562	blood:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
25	CEBPB	chr15:59162707-59162916	Hela-S3	cervix:	n/a	chr15:59162827-59162840 chr15:59162828-59162839 chr15:59162829-59162838 chr15:59162827-59162838
26	CHD2	chr15:59157172-59157651	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr15:59156789-59158056	HepG2	liver:	n/a	n/a
28	CHD2	chr15:59158476-59158713	HepG2	liver:	n/a	n/a
29	CHD2	chr15:59158383-59158751	Hela-S3	cervix:	n/a	n/a
30	CREB1	chr15:59158467-59158744	A549	lung:	n/a	n/a
31	CREB1	chr15:59158421-59158849	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr15:59158337-59158917	HepG2	liver:	n/a	n/a
33	CREB1	chr15:59158348-59158829	A549	lung:	n/a	n/a
34	CREB1	chr15:59158380-59158850	HepG2	liver:	n/a	n/a
35	CREB1	chr15:59158393-59158840	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr15:59158389-59158809	ECC-1	luminal epithelium:	n/a	n/a
37	CREB1	chr15:59158325-59158790	K562	blood:	n/a	n/a
38	CTCF	chr15:59158580-59158730	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr15:59158560-59158710	HVMF	connective:	n/a	n/a
40	CTCF	chr15:59158491-59158818	K562	blood:	n/a	n/a
41	CTCF	chr15:59158546-59158718	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr15:59158540-59158690	HCT-116	colon:	n/a	n/a
43	CTCF	chr15:59158520-59158670	AG09319	gingival:	n/a	n/a
44	CTCF	chr15:59158594-59158727	MCF-7	breast:	n/a	n/a
45	CTCF	chr15:59158527-59158732	HepG2	liver:	n/a	n/a
46	CTCF	chr15:59158600-59158750	GM12871	blood:	n/a	n/a
47	CTCF	chr15:59158550-59158769	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr15:59158467-59158782	HepG2	liver:	n/a	n/a
49	CTCF	chr15:59158466-59158816	K562	blood:	n/a	n/a
50	CTCF	chr15:59158580-59158730	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59160318-59160368	HCPEpiC	choroid plexus:	n/a
2	chr15:59157857-59157907	SK-N-MC	brain:	n/a
3	chr15:59157857-59157907	NHDF-neo	bronchial:	n/a
4	chr15:59160318-59160368	HNPCEpiC	eye:	n/a
5	chr15:59157523-59157573	HEK293	kidney:	embryo
6	chr15:59157579-59157629	AoSMC	blood vessel:	n/a
7	chr15:59160318-59160368	SK-N-SH_RA	brain:	n/a
8	chr15:59157857-59157907	PrEC	prostate:	n/a
9	chr15:59157523-59157573	K562	blood:	n/a
10	chr15:59157523-59157573	ProgFib	skin:	n/a
11	chr15:59157857-59157907	SKMC	muscle:	n/a
12	chr15:59157579-59157629	PrEC	prostate:	n/a
13	chr15:59157857-59157907	HAEpiC	amniotic membrane:	n/a
14	chr15:59157523-59157573	Caco-2	colon:	n/a
15	chr15:59157523-59157573	NH-A	brain:	n/a
16	chr15:59157579-59157629	NHBE	bronchial:	n/a
17	chr15:59157523-59157573	AG04450	lung:	fetal
18	chr15:59157579-59157629	MCF10A-Er-Src	breast:	n/a
19	chr15:59157523-59157573	HRE	kidney:	n/a
20	chr15:59160318-59160368	HMEC	breast:	n/a
21	chr15:59157579-59157629	PFSK-1	brain:	n/a
22	chr15:59157857-59157907	U87	brain:	n/a
23	chr15:59157523-59157573	GM06990	blood:	n/a
24	chr15:59160318-59160368	GM12878	blood:	n/a
25	chr15:59157523-59157573	IMR90	lung:	fetal
26	chr15:59160318-59160368	NHBE	bronchial:	n/a
27	chr15:59157523-59157573	BE2_C	brain:	n/a
28	chr15:59157857-59157907	HRE	kidney:	n/a
29	chr15:59157857-59157907	PFSK-1	brain:	n/a
30	chr15:59157857-59157907	AG04449	skin:	fetal
31	chr15:59157857-59157907	Hepatocyte	liver:	n/a
32	chr15:59157579-59157629	BJ	skin:	n/a
33	chr15:59157857-59157907	HCF	heart:	n/a
34	chr15:59157579-59157629	SAEC	small airway:	n/a
35	chr15:59157579-59157629	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:59157579-59157629	HNPCEpiC	eye:	n/a
37	chr15:59160318-59160368	HEK293	kidney:	embryo
38	chr15:59157523-59157573	U87	brain:	n/a
39	chr15:59157523-59157573	Hela-S3	cervix:	n/a
40	chr15:59160318-59160368	NB4	blood:	n/a
41	chr15:59160318-59160368	Hela-S3	cervix:	n/a
42	chr15:59160318-59160368	NHDF-neo	bronchial:	n/a
43	chr15:59157857-59157907	SAEC	small airway:	n/a
44	chr15:59160318-59160368	H1-hESC	embryonic stem cell:	embryo
45	chr15:59157523-59157573	HPAEpiC	pulmonary alveolar:	n/a
46	chr15:59157579-59157629	HCPEpiC	choroid plexus:	n/a
47	chr15:59160318-59160368	PFSK-1	brain:	n/a
48	chr15:59160318-59160368	CMK	blood:	n/a
49	chr15:59157857-59157907	HepG2	liver:	n/a
50	chr15:59157579-59157629	ECC-1	luminal epithelium:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:59156007..59158196-chr15:59162780..59165304,2	K562	blood:
2	chr15:59150365..59151946-chr15:59158006..59159550,2	K562	blood:
3	chr15:59162668..59165557-chr15:59167625..59170277,3	K562	blood:
4	chr15:59165302..59167186-chr15:59171743..59174191,2	MCF-7	breast:
5	chr15:59158172..59158742-chr20:25371320..25372132,2	HCT-116	colon:
6	chr15:59141477..59144121-chr15:59157896..59159549,2	MCF-7	breast:
7	chr15:59158040..59159719-chr15:59224699..59227685,2	MCF-7	breast:
8	chr15:59158497..59160419-chr15:59185793..59188060,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM63B-3	chr15:59161858-59162333	NONHSAT044135

No data

Variant related genes	Relation type
ENSG00000259353	TF binding region
ENSG00000242747	TF binding region
ENSG00000259353	CpG island
ENSG00000242747	CpG island
ENSG00000259738	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000259353	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000157450	chromatin interactions

Extended variants
information (count: 286 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529004155	chr15:59157460-59157461	Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs547565779	chr15:59157539-59157540	Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
3	rs592407	chr15:59157540-59157541	Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs539662381	chr15:59157593-59157594	Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
5	rs557754446	chr15:59157601-59157602	Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
6	rs7183404	chr15:59157634-59157635	Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192489196	chr15:59157651-59157652	Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs115797917	chr15:59157685-59157686	Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs563771533	chr15:59157723-59157724	Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs147247569	chr15:59157749-59157750	Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs35999436	chr15:59157766-59157767	Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs573757469	chr15:59157800-59157801	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs558186471	chr15:59157952-59157953	Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs541130771	chr15:59157966-59157967	Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs183811196	chr15:59157982-59157983	Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs553480323	chr15:59158032-59158033	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs367826452	chr15:59158037-59158038	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs540942825	chr15:59158048-59158049	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs578097655	chr15:59158070-59158071	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs529284551	chr15:59158115-59158116	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs545610198	chr15:59158152-59158153	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs138677524	chr15:59158162-59158163	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs531252215	chr15:59158196-59158197	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs543399773	chr15:59158265-59158266	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs7162694	chr15:59158301-59158302	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs12440904	chr15:59158323-59158324	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547504246	chr15:59158336-59158337	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs549390929	chr15:59158379-59158380	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs565804461	chr15:59158390-59158391	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs367705481	chr15:59158413-59158414	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs368098756	chr15:59158447-59158448	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs565938256	chr15:59158523-59158524	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs532962809	chr15:59158532-59158533	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs551576613	chr15:59158542-59158543	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs541558782	chr15:59158585-59158586	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs569819500	chr15:59158591-59158592	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs148568930	chr15:59158595-59158596	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs371823371	chr15:59158605-59158606	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs567320214	chr15:59158666-59158667	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs534737655	chr15:59158718-59158719	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs553168753	chr15:59158735-59158736	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs188632016	chr15:59158856-59158857	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs545237296	chr15:59158877-59158878	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs11636372	chr15:59158918-59158919	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs181412360	chr15:59158953-59158954	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs575959401	chr15:59158956-59158957	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs543337225	chr15:59158967-59158968	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs561607640	chr15:59158979-59158980	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs142938352	chr15:59159006-59159007	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs541057549	chr15:59159016-59159017	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	19238632	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	19318576	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59067000-59157800	Weak transcription	Hela-S3	cervix
2	chr15:59111800-59159600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:59120000-59169000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr15:59145000-59166600	Weak transcription	HSMMtube	muscle
5	chr15:59147200-59169000	Weak transcription	K562	blood
6	chr15:59147600-59174600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr15:59148000-59168600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr15:59148000-59169000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr15:59151200-59165400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr15:59154600-59170200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr15:59156400-59157600	Enhancers	Fetal Kidney	kidney
12	chr15:59156600-59157800	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr15:59156600-59158000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr15:59156600-59158200	Active TSS	Duodenum Mucosa	Duodenum
15	chr15:59156600-59158200	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr15:59156800-59157600	Active TSS	H9 Cell Line	embryonic stem cell
17	chr15:59156800-59157600	Active TSS	Primary hematopoietic stem cells	blood
18	chr15:59156800-59157600	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr15:59156800-59157800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
20	chr15:59156800-59157800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr15:59156800-59157800	Enhancers	Spleen	Spleen
22	chr15:59156800-59158000	Active TSS	Colon Smooth Muscle	Colon
23	chr15:59156800-59158000	Enhancers	Lung	lung
24	chr15:59156800-59158000	Flanking Active TSS	Pancreas	Pancrea
25	chr15:59156800-59158400	Active TSS	Fetal Intestine Large	intestine
26	chr15:59156800-59158600	Active TSS	HepG2	liver
27	chr15:59157000-59157600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr15:59157000-59157600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr15:59157000-59157600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
30	chr15:59157000-59157600	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr15:59157000-59157600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr15:59157000-59157600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr15:59157000-59157600	Active TSS	Brain Germinal Matrix	brain
34	chr15:59157000-59157600	Bivalent Enhancer	Fetal Brain Male	brain
35	chr15:59157000-59157600	Active TSS	Fetal Brain Female	brain
36	chr15:59157000-59157600	Flanking Active TSS	Psoas Muscle	Psoas
37	chr15:59157000-59157600	Flanking Active TSS	Right Atrium	heart
38	chr15:59157000-59157600	Active TSS	Stomach Mucosa	stomach
39	chr15:59157000-59157600	Enhancers	NH-A	brain
40	chr15:59157000-59157600	Enhancers	NHDF-Ad	bronchial
41	chr15:59157000-59157800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
42	chr15:59157000-59157800	Active TSS	Primary B cells from cord blood	blood
43	chr15:59157000-59157800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr15:59157000-59157800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr15:59157000-59157800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr15:59157000-59157800	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr15:59157000-59157800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr15:59157000-59157800	Active TSS	Brain Substantia Nigra	brain
49	chr15:59157000-59157800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
50	chr15:59157000-59158000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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