Variant report

Variant	nsv1035367
Chromosome Location	chr15:74554972-74586538
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:471)
CpG islands
(count:244)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74583932-74584147	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:74583522-74584166	K562	blood:	n/a	n/a
3	ATF1	chr15:74583416-74584119	K562	blood:	n/a	n/a
4	BACH1	chr15:74583821-74584186	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr15:74577486-74577648	K562	blood:	n/a	n/a
6	BHLHE40	chr15:74583820-74584094	K562	blood:	n/a	n/a
7	BRCA1	chr15:74583859-74584101	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr15:74583830-74584118	K562	blood:	n/a	n/a
9	CBX3	chr15:74583452-74584214	K562	blood:	n/a	n/a
10	CEBPB	chr15:74583553-74584124	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr15:74577197-74577397	HepG2	liver:	n/a	chr15:74577286-74577299 chr15:74577286-74577297 chr15:74577286-74577299
12	CEBPB	chr15:74583519-74584064	K562	blood:	n/a	n/a
13	CEBPB	chr15:74568461-74568581	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr15:74583555-74584132	IMR90	lung:	n/a	n/a
15	CEBPB	chr15:74583535-74583988	K562	blood:	n/a	n/a
16	CEBPB	chr15:74583557-74584105	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr15:74556506-74556634	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPD	chr15:74583386-74583910	K562	blood:	n/a	n/a
19	CEBPD	chr15:74583444-74583982	K562	blood:	n/a	n/a
20	CHD2	chr15:74556409-74556696	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr15:74583800-74584198	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr15:74568304-74568562	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr15:74583871-74584205	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr15:74568371-74568451	K562	blood:	n/a	n/a
25	CHD2	chr15:74584062-74584121	HepG2	liver:	n/a	n/a
26	CTCF	chr15:74568535-74568540	GM12891	blood:	n/a	n/a
27	CTCF	chr15:74583960-74584110	AG04449	skin:	n/a	n/a
28	CTCF	chr15:74555840-74555990	NB4	blood:	n/a	n/a
29	CTCF	chr15:74555860-74556010	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr15:74581967-74582004	GM13976	blood:	n/a	n/a
31	CTCF	chr15:74584002-74584036	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr15:74555888-74555984	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr15:74555840-74555990	HEK293	kidney:	n/a	n/a
34	CTCF	chr15:74555880-74556030	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr15:74555960-74556110	BE2_C	brain:	n/a	n/a
36	CTCF	chr15:74584043-74584053	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr15:74563397-74563487	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr15:74555867-74555980	K562	blood:	n/a	n/a
39	CTCF	chr15:74563300-74563450	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr15:74555920-74556070	MCF-7	breast:	n/a	n/a
41	CTCF	chr15:74555804-74555993	K562	blood:	n/a	n/a
42	CTCF	chr15:74555780-74555930	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr15:74581568-74581601	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr15:74556040-74556190	HAc	cerebellar:	n/a	n/a
45	CTCF	chr15:74555856-74556037	MCF-7	breast:	n/a	n/a
46	CTCF	chr15:74563417-74563486	MCF-7	breast:	n/a	n/a
47	CTCF	chr15:74563180-74563330	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr15:74568360-74568510	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr15:74583951-74584053	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr15:74563200-74563350	GM06990	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	chr15:74557537-74557587	U87	brain:	n/a
2	chr15:74557527-74557577	ovcar-3	ovarian:	n/a
3	chr15:74556873-74556923	HAEpiC	amniotic membrane:	n/a
4	chr15:74557537-74557587	HPAEpiC	pulmonary alveolar:	n/a
5	chr15:74556873-74556923	AG09309	skin:	n/a
6	chr15:74557537-74557587	ProgFib	skin:	n/a
7	chr15:74557537-74557587	MCF10A-Er-Src	breast:	n/a
8	chr15:74557537-74557587	T-47D	breast:	n/a
9	chr15:74557527-74557577	NT2-D1	testis:	n/a
10	chr15:74557527-74557577	AG04450	lung:	fetal
11	chr15:74556873-74556923	AoSMC	blood vessel:	n/a
12	chr15:74556873-74556923	HCPEpiC	choroid plexus:	n/a
13	chr15:74557537-74557587	GM12878	blood:	n/a
14	chr15:74557527-74557577	NHDF-neo	bronchial:	n/a
15	chr15:74557527-74557577	T-47D	breast:	n/a
16	chr15:74556873-74556923	NB4	blood:	n/a
17	chr15:74557527-74557577	HMEC	breast:	n/a
18	chr15:74557527-74557577	AG09309	skin:	n/a
19	chr15:74557527-74557577	SAEC	small airway:	n/a
20	chr15:74556873-74556923	GM12891	blood:	n/a
21	chr15:74557537-74557587	AG09319	gingival:	n/a
22	chr15:74557537-74557587	SKMC	muscle:	n/a
23	chr15:74557537-74557587	NH-A	brain:	n/a
24	chr15:74583589-74583639	HCM	heart:	n/a
25	chr15:74583589-74583639	SKMC	muscle:	n/a
26	chr15:74556873-74556923	HMEC	breast:	n/a
27	chr15:74557537-74557587	AG10803	skin:	n/a
28	chr15:74556873-74556923	PFSK-1	brain:	n/a
29	chr15:74556873-74556923	HRE	kidney:	n/a
30	chr15:74583589-74583639	NB4	blood:	n/a
31	chr15:74583589-74583639	GM19239	blood:	n/a
32	chr15:74557527-74557577	Jurkat	blood:	n/a
33	chr15:74557537-74557587	RPTEC	kidney:	n/a
34	chr15:74583589-74583639	T-47D	breast:	n/a
35	chr15:74556873-74556923	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:74557537-74557587	HNPCEpiC	eye:	n/a
37	chr15:74557537-74557587	NB4	blood:	n/a
38	chr15:74557527-74557577	BJ	skin:	n/a
39	chr15:74557527-74557577	NB4	blood:	n/a
40	chr15:74556873-74556923	AG04449	skin:	fetal
41	chr15:74557537-74557587	SK-N-MC	brain:	n/a
42	chr15:74583589-74583639	MCF-7	breast:	n/a
43	chr15:74557527-74557577	ProgFib	skin:	n/a
44	chr15:74556873-74556923	HCM	heart:	n/a
45	chr15:74556873-74556923	SK-N-SH_RA	brain:	n/a
46	chr15:74556873-74556923	HEK293	kidney:	embryo
47	chr15:74557527-74557577	SKMC	muscle:	n/a
48	chr15:74583589-74583639	HMEC	breast:	n/a
49	chr15:74557537-74557587	ECC-1	luminal epithelium:	n/a
50	chr15:74557527-74557577	LNCaP	prostate:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74572770..74575577-chr15:74577511..74579830,2	K562	blood:
2	chr15:74585453..74587041-chr15:74587963..74590487,2	MCF-7	breast:
3	chr15:74557713..74559217-chr15:74572834..74574361,2	MCF-7	breast:
4	chr15:74550593..74553035-chr15:74555004..74556677,2	K562	blood:
5	chr15:74555453..74556406-chr15:74595045..74595674,2	MCF-7	breast:
6	chr15:74470292..74472068-chr15:74583811..74585513,2	MCF-7	breast:
7	chr15:74575150..74576809-chr15:74579303..74580864,2	MCF-7	breast:
8	chr15:74562822..74565405-chr15:74577566..74579863,2	MCF-7	breast:
9	chr15:74516266..74518836-chr15:74583231..74585495,2	MCF-7	breast:
10	chr15:74575150..74576809-chr15:74579303..74580864,2	MCF-7	breast:
11	chr15:74572285..74574506-chr15:74581544..74583553,2	K562	blood:
12	chr15:74585072..74587120-chr15:74590756..74593665,2	MCF-7	breast:
13	chr15:74562172..74563880-chr15:74570036..74571861,2	MCF-7	breast:
14	chr15:74560856..74563474-chr15:74582428..74584503,2	K562	blood:
15	chr15:74572285..74574506-chr15:74581544..74583553,2	K562	blood:
16	chr15:74573224..74575195-chr15:74587485..74589058,2	MCF-7	breast:
17	chr15:74553348..74555931-chr15:74563585..74566018,2	K562	blood:
18	chr15:74562822..74565405-chr15:74577566..74579863,2	MCF-7	breast:
19	chr15:74585941..74588102-chr15:74592216..74594032,2	MCF-7	breast:
20	chr15:74583146..74585264-chr15:74587760..74589552,2	K562	blood:
21	chr15:74570759..74572430-chr15:74582400..74584892,2	MCF-7	breast:
22	chr15:74560856..74563474-chr15:74582428..74584503,2	K562	blood:
23	chr15:74561608..74563533-chr15:74565338..74568191,2	K562	blood:
24	chr15:74556821..74558420-chr15:74583588..74586004,2	MCF-7	breast:
25	chr15:74562172..74563880-chr15:74570036..74571861,2	MCF-7	breast:
26	chr15:74572770..74575577-chr15:74577511..74579830,2	K562	blood:
27	chr15:74583306..74585518-chr15:74588891..74592358,3	MCF-7	breast:
28	chr15:74556821..74558420-chr15:74583588..74586004,2	MCF-7	breast:
29	chr15:74553348..74555931-chr15:74563585..74566018,2	K562	blood:
30	chr15:74561608..74563533-chr15:74565338..74568191,2	K562	blood:
31	chr15:74570759..74572430-chr15:74582400..74584892,2	MCF-7	breast:
32	chr15:74555720..74556384-chr15:74594990..74595654,2	MCF-7	breast:

No data

Variant related genes	Relation type
CCDC33	TF binding region
CCDC33	CpG island
ENSG00000261543	chromatin interactions
ENSG00000261384	chromatin interactions
ENSG00000140481	chromatin interactions

Extended variants
information (count: 1198 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1198 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369803674	chr15:74554982-74554983	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs367632082	chr15:74554988-74554989	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs558890522	chr15:74555015-74555016	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563885999	chr15:74555097-74555098	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200310609	chr15:74555162-74555163	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs439668	chr15:74555189-74555190	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541506952	chr15:74555191-74555192	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs395887	chr15:74555193-74555194	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs112899283	chr15:74555207-74555208	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs116335086	chr15:74555221-74555222	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs542957866	chr15:74555250-74555251	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs561138109	chr15:74555276-74555277	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs531611842	chr15:74555278-74555279	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs146421903	chr15:74555287-74555288	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs566255130	chr15:74555289-74555290	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs542275372	chr15:74555306-74555307	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs571209678	chr15:74555348-74555349	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532152012	chr15:74555383-74555384	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs547424597	chr15:74555394-74555395	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs566153576	chr15:74555416-74555417	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536417357	chr15:74555480-74555481	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182925055	chr15:74555490-74555491	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148320374	chr15:74555512-74555513	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs568533351	chr15:74555513-74555514	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537333645	chr15:74555526-74555527	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558723316	chr15:74555584-74555585	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs36046311	chr15:74555615-74555616	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs351158	chr15:74555636-74555637	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs557219051	chr15:74555674-74555675	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs140505423	chr15:74555679-74555680	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs553398406	chr15:74555713-74555714	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs572291067	chr15:74555729-74555730	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs542869757	chr15:74555770-74555771	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs188380244	chr15:74555806-74555807	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs560591607	chr15:74555824-74555825	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs190673942	chr15:74555855-74555856	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs570616043	chr15:74555998-74555999	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs575631636	chr15:74556009-74556010	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs111761074	chr15:74556010-74556011	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111227544	chr15:74556013-74556014	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs573073721	chr15:74556042-74556043	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529720384	chr15:74556044-74556045	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548409152	chr15:74556084-74556085	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541388109	chr15:74556120-74556121	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs115677533	chr15:74556133-74556134	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs574919595	chr15:74556137-74556138	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372166108	chr15:74556148-74556149	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs114066793	chr15:74556157-74556158	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs150447758	chr15:74556163-74556164	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs138272392	chr15:74556221-74556222	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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	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
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74548600-74558000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr15:74549200-74556200	Enhancers	Brain Germinal Matrix	brain
3	chr15:74549400-74557800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr15:74550000-74557800	Enhancers	Fetal Brain Male	brain
5	chr15:74551600-74555600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr15:74551600-74555600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr15:74552200-74555800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:74552200-74556000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:74552400-74555600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr15:74552400-74555800	Weak transcription	Fetal Heart	heart
11	chr15:74553200-74556600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr15:74553400-74556000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:74553800-74556400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr15:74553800-74557400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:74554000-74555200	Enhancers	Fetal Thymus	thymus
16	chr15:74554200-74555200	Weak transcription	Fetal Brain Female	brain
17	chr15:74554400-74555000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr15:74554400-74557600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr15:74554600-74555000	Enhancers	Adipose Nuclei	Adipose
20	chr15:74554600-74555000	Enhancers	Spleen	Spleen
21	chr15:74555000-74555400	Enhancers	HUVEC	blood vessel
22	chr15:74555000-74556000	Weak transcription	Spleen	Spleen
23	chr15:74555200-74557600	Enhancers	Fetal Brain Female	brain
24	chr15:74555400-74555600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
25	chr15:74555600-74555800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
26	chr15:74555600-74555800	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr15:74555600-74555800	Bivalent Enhancer	Fetal Stomach	stomach
28	chr15:74555600-74556200	Bivalent Enhancer	Fetal Lung	lung
29	chr15:74555600-74556400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr15:74555600-74556400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr15:74555600-74557000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:74555600-74557000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:74555600-74557400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr15:74555600-74557600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr15:74555600-74557600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr15:74555800-74556200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr15:74555800-74556400	Enhancers	Brain Hippocampus Middle	brain
38	chr15:74555800-74557000	Enhancers	Fetal Stomach	stomach
39	chr15:74555800-74557200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr15:74555800-74557600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr15:74556000-74556200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr15:74556000-74556200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:74556000-74556200	Bivalent Enhancer	Brain Angular Gyrus	brain
44	chr15:74556000-74556200	Enhancers	Fetal Heart	heart
45	chr15:74556000-74556200	Enhancers	Fetal Kidney	kidney
46	chr15:74556000-74556400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr15:74556000-74556400	Enhancers	Brain Substantia Nigra	brain
48	chr15:74556000-74556600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr15:74556000-74556800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr15:74556000-74557000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell

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