Variant report

Variant	esv3444715
Chromosome Location	chr15:52820360-52822458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:488)
CpG islands
(count:917)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:488 , 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	BACH1	chr15:52820536-52820720	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr15:52820727-52821738	GM12878	blood:	n/a	chr15:52821698-52821707 chr15:52821465-52821478 chr15:52821464-52821473 chr15:52821087-52821100 chr15:52821458-52821471 chr15:52821341-52821354
3	BHLHE40	chr15:52821431-52821535	K562	blood:	n/a	n/a
4	BRCA1	chr15:52821370-52821426	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr15:52821276-52821432	GM12878	blood:	n/a	n/a
6	CCNT2	chr15:52820760-52821671	K562	blood:	n/a	n/a
7	CHD1	chr15:52820682-52820773	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr15:52821215-52821232	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr15:52820389-52820432	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr15:52821519-52821543	K562	blood:	n/a	n/a
11	CHD2	chr15:52821246-52821440	GM12878	blood:	n/a	n/a
12	CHD2	chr15:52820739-52820874	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr15:52820914-52821649	Hela-S3	cervix:	n/a	chr15:52821471-52821481
14	CREB1	chr15:52820806-52821673	A549	lung:	n/a	n/a
15	CTBP2	chr15:52820248-52822017	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr15:52821033-52821078	MCF-7	breast:	n/a	n/a
17	CTCF	chr15:52820940-52821090	GM12875	blood:	n/a	n/a
18	CTCF	chr15:52821340-52821490	GM12870	blood:	n/a	n/a
19	CTCF	chr15:52821300-52821450	GM12867	blood:	n/a	n/a
20	CTCF	chr15:52821280-52821430	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr15:52820980-52821130	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr15:52821340-52821499	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr15:52820972-52821126	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr15:52820886-52821617	GM12878	blood:	n/a	chr15:52821565-52821578 chr15:52821179-52821192
25	CTCF	chr15:52821309-52821514	MCF-7	breast:	n/a	n/a
26	CTCF	chr15:52821280-52821430	HPF	lung:	n/a	n/a
27	CTCF	chr15:52820963-52821150	GM10266	blood:	n/a	n/a
28	CTCF	chr15:52820961-52821159	LNCaP	prostate:	n/a	n/a
29	CTCF	chr15:52820920-52821070	GM12864	blood:	n/a	n/a
30	CTCF	chr15:52821283-52821554	GM12892	blood:	n/a	n/a
31	CTCF	chr15:52821280-52821430	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr15:52821060-52821210	HPAF	blood vessel:	n/a	chr15:52821179-52821192
33	CTCF	chr15:52820960-52821110	AG04449	skin:	n/a	n/a
34	CTCF	chr15:52820980-52821130	GM12873	blood:	n/a	n/a
35	CTCF	chr15:52821000-52821150	GM12866	blood:	n/a	n/a
36	CTCF	chr15:52821340-52821490	AG09309	skin:	n/a	n/a
37	CTCF	chr15:52820940-52821090	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr15:52821780-52821930	MCF-7	breast:	n/a	chr15:52821865-52821875
39	CTCF	chr15:52821278-52821552	GM19238	blood:	n/a	n/a
40	CTCF	chr15:52821317-52821508	GM10248	blood:	n/a	n/a
41	CTCF	chr15:52821300-52821450	AG10803	skin:	n/a	n/a
42	CTCF	chr15:52821021-52821133	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr15:52821001-52821144	GM13976	blood:	n/a	n/a
44	CTCF	chr15:52821340-52821490	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr15:52821300-52821545	GM19239	blood:	n/a	n/a
46	CTCF	chr15:52820981-52821110	A549	lung:	n/a	n/a
47	CTCF	chr15:52820980-52821130	HMEC	breast:	n/a	n/a
48	CTCF	chr15:52820780-52820930	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr15:52821340-52821490	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr15:52821300-52821520	LNCaP	prostate:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:52821161-52821211	NB4	blood:	n/a
2	chr15:52820584-52820634	HRCEpiC	kidney:	n/a
3	chr15:52821161-52821211	NB4	blood:	n/a
4	chr15:52820584-52820634	HRCEpiC	kidney:	n/a
5	chr15:52821917-52821967	NH-A	brain:	n/a
6	chr15:52821290-52821340	NH-A	brain:	n/a
7	chr15:52821290-52821340	AG09309	skin:	n/a
8	chr15:52820560-52820610	HRE	kidney:	n/a
9	chr15:52821541-52821591	IMR90	lung:	fetal
10	chr15:52821405-52821455	BE2_C	brain:	n/a
11	chr15:52821424-52821474	NHBE	bronchial:	n/a
12	chr15:52821541-52821591	HEEpiC	esophagus:	n/a
13	chr15:52821290-52821340	LNCaP	prostate:	n/a
14	chr15:52821405-52821455	HRE	kidney:	n/a
15	chr15:52821541-52821591	HNPCEpiC	eye:	n/a
16	chr15:52821541-52821591	NB4	blood:	n/a
17	chr15:52821541-52821591	HRPEpiC	eye:	n/a
18	chr15:52821424-52821474	SAEC	small airway:	n/a
19	chr15:52821378-52821428	MCF10A-Er-Src	breast:	n/a
20	chr15:52821378-52821428	AoSMC	blood vessel:	n/a
21	chr15:52821161-52821211	RPTEC	kidney:	n/a
22	chr15:52821378-52821428	HIPEpiC	eye:	n/a
23	chr15:52820560-52820610	NB4	blood:	n/a
24	chr15:52821161-52821211	SAEC	small airway:	n/a
25	chr15:52821013-52821063	A549	lung:	n/a
26	chr15:52820560-52820610	U87	brain:	n/a
27	chr15:52821917-52821967	SK-N-MC	brain:	n/a
28	chr15:52820584-52820634	SAEC	small airway:	n/a
29	chr15:52821378-52821428	Caco-2	colon:	n/a
30	chr15:52821854-52821904	HRE	kidney:	n/a
31	chr15:52821013-52821063	MCF-7	breast:	n/a
32	chr15:52821917-52821967	GM19239	blood:	n/a
33	chr15:52821378-52821428	HCM	heart:	n/a
34	chr15:52821854-52821904	HRPEpiC	eye:	n/a
35	chr15:52821161-52821211	GM19239	blood:	n/a
36	chr15:52821917-52821967	Caco-2	colon:	n/a
37	chr15:52821161-52821211	ovcar-3	ovarian:	n/a
38	chr15:52822439-52822489	BE2_C	brain:	n/a
39	chr15:52822439-52822489	HCM	heart:	n/a
40	chr15:52821541-52821591	AG04450	lung:	fetal
41	chr15:52821789-52821839	MCF-7	breast:	n/a
42	chr15:52821541-52821591	MCF10A-Er-Src	breast:	n/a
43	chr15:52820584-52820634	HMEC	breast:	n/a
44	chr15:52821290-52821340	HCT-116	colon:	n/a
45	chr15:52820560-52820610	ProgFib	skin:	n/a
46	chr15:52821541-52821591	HCT-116	colon:	n/a
47	chr15:52820584-52820634	MCF-7	breast:	n/a
48	chr15:52821161-52821211	ECC-1	luminal epithelium:	n/a
49	chr15:52821854-52821904	MCF10A-Er-Src	breast:	n/a
50	chr15:52822439-52822489	HepG2	liver:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:52820917..52821847-chr17:56736116..56736779,3	MCF-7	breast:
2	chr15:52819294..52821098-chr15:52860363..52863142,2	MCF-7	breast:
3	chr15:52821243..52824156-chr15:52859754..52862350,2	MCF-7	breast:
4	chr15:52820217..52824623-chr15:52859000..52863588,7	MCF-7	breast:
5	chr15:52785155..52787650-chr15:52822285..52825077,2	MCF-7	breast:
6	chr15:52718660..52721440-chr15:52817990..52820866,2	MCF-7	breast:
7	chr15:52816804..52818865-chr15:52821369..52824453,4	K562	blood:
8	chr15:52584393..52589074-chr15:52819513..52822265,5	MCF-7	breast:
9	chr15:52820950..52823000-chr15:52846878..52849661,2	MCF-7	breast:
10	chr15:52819283..52821980-chr16:88877332..88878840,2	MCF-7	breast:
11	chr15:52819791..52821534-chr15:52970285..52973265,2	MCF-7	breast:

No data

Variant related genes	Relation type
MYO5A	TF binding region
MYO5A	CpG island
ENSG00000128989	chromatin interactions
ENSG00000047346	chromatin interactions
ENSG00000128833	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000198931	chromatin interactions

Extended variants
information (count: 70 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:70 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538786992	chr15:52820385-52820386	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs547383056	chr15:52820414-52820415	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs376873990	chr15:52820445-52820446	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs370460859	chr15:52820479-52820480	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs536254843	chr15:52820508-52820509	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs563102056	chr15:52820532-52820533	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs542632649	chr15:52820575-52820576	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs60973956	chr15:52820588-52820589	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs537229116	chr15:52820604-52820605	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs371367222	chr15:52820655-52820656	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs558506164	chr15:52820734-52820735	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs577005131	chr15:52820775-52820776	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs1693512	chr15:52820786-52820787	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs28556791	chr15:52820812-52820813	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs574448673	chr15:52820861-52820862	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs551299923	chr15:52820881-52820882	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs1693513	chr15:52820904-52820905	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs368285169	chr15:52820919-52820920	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs370674763	chr15:52820949-52820950	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs531943467	chr15:52821030-52821031	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs550339097	chr15:52821064-52821065	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs565184696	chr15:52821079-52821080	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs375573111	chr15:52821097-52821098	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs532569377	chr15:52821100-52821101	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs28716632	chr15:52821125-52821126	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs550600899	chr15:52821140-52821141	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs113928619	chr15:52821146-52821147	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs1693514	chr15:52821162-52821163	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs546905930	chr15:52821256-52821257	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs565851456	chr15:52821260-52821261	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs12441299	chr15:52821303-52821304	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs536218711	chr15:52821336-52821337	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs548321339	chr15:52821360-52821361	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs569917965	chr15:52821398-52821399	Bivalent/Poised TSS Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs533378250	chr15:52821424-52821425	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs1693515	chr15:52821514-52821515	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs558716466	chr15:52821523-52821524	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs570615849	chr15:52821543-52821544	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs534822953	chr15:52821594-52821595	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs553073018	chr15:52821608-52821609	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs188348279	chr15:52821623-52821624	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs1693516	chr15:52821633-52821634	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs556720655	chr15:52821655-52821656	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs180763889	chr15:52821685-52821686	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs530484403	chr15:52821716-52821717	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs565245698	chr15:52821751-52821752	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs532533475	chr15:52821789-52821790	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs541249073	chr15:52821807-52821808	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs62023326	chr15:52821860-52821861	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs367666907	chr15:52821960-52821961	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52818200-52820400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr15:52818400-52822000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr15:52819400-52820400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr15:52819400-52822000	Active TSS	Brain Anterior Caudate	brain
5	chr15:52819600-52820400	Flanking Active TSS	HUVEC	blood vessel
6	chr15:52819600-52820600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr15:52819600-52821000	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr15:52819600-52821600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr15:52819600-52822000	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr15:52819600-52822000	Active TSS	Duodenum Smooth Muscle	Duodenum
11	chr15:52819800-52820400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:52819800-52820400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr15:52819800-52820400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr15:52819800-52820400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
15	chr15:52819800-52820400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr15:52819800-52820400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
17	chr15:52819800-52820400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr15:52819800-52820400	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr15:52819800-52820400	Flanking Active TSS	Brain Germinal Matrix	brain
20	chr15:52819800-52820400	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr15:52819800-52820400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
22	chr15:52819800-52820400	Enhancers	Spleen	Spleen
23	chr15:52819800-52820400	Flanking Active TSS	GM12878-XiMat	blood
24	chr15:52819800-52820400	Flanking Active TSS	HMEC	breast
25	chr15:52819800-52820400	Flanking Active TSS	NH-A	brain
26	chr15:52819800-52820400	Flanking Active TSS	NHEK	skin
27	chr15:52819800-52820400	Flanking Active TSS	NHLF	lung
28	chr15:52819800-52820600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr15:52819800-52820600	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr15:52819800-52820600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr15:52819800-52820600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:52819800-52820600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr15:52819800-52820600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
34	chr15:52819800-52820600	Flanking Active TSS	Dnd41	blood
35	chr15:52819800-52820800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr15:52819800-52820800	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr15:52819800-52820800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
38	chr15:52819800-52820800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr15:52819800-52820800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
40	chr15:52819800-52820800	Bivalent/Poised TSS	Stomach Mucosa	stomach
41	chr15:52819800-52821400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr15:52819800-52822000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
43	chr15:52819800-52822000	Active TSS	Brain Angular Gyrus	brain
44	chr15:52819800-52822200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr15:52819800-52822200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
46	chr15:52819800-52822600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
47	chr15:52820000-52820400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
48	chr15:52820000-52820400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr15:52820000-52820400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr15:52820000-52820400	Flanking Active TSS	Primary T cells from cord blood	blood

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