Variant report

Variant	esv1822592
Chromosome Location	chr15:77283956-77332539
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1437)
CpG islands
(count:1404)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1437 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77324454-77324600	HepG2	liver:	n/a	n/a
2	ATF2	chr15:77314306-77314560	GM12878	blood:	n/a	n/a
3	ATF2	chr15:77306056-77307216	GM12878	blood:	n/a	n/a
4	ATF2	chr15:77316619-77316962	GM12878	blood:	n/a	n/a
5	ATF2	chr15:77314226-77314800	GM12878	blood:	n/a	n/a
6	ATF2	chr15:77306145-77306892	GM12878	blood:	n/a	n/a
7	BACH1	chr15:77320425-77320611	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr15:77290041-77290431	GM12878	blood:	n/a	chr15:77290281-77290290
9	BATF	chr15:77312280-77312501	GM12878	blood:	n/a	n/a
10	BATF	chr15:77306056-77306497	GM12878	blood:	n/a	chr15:77306290-77306300 chr15:77306289-77306300 chr15:77306286-77306296
11	BATF	chr15:77306094-77306473	GM12878	blood:	n/a	chr15:77306290-77306300 chr15:77306289-77306300 chr15:77306286-77306296
12	BATF	chr15:77290050-77290368	GM12878	blood:	n/a	chr15:77290281-77290290
13	BCL11A	chr15:77306807-77307126	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:77306811-77307122	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:77290034-77290413	GM12878	blood:	n/a	chr15:77290214-77290223
16	BCL3	chr15:77327427-77328043	A549	lung:	n/a	n/a
17	BCL3	chr15:77326777-77327284	A549	lung:	n/a	n/a
18	BCL3	chr15:77319746-77319961	GM12878	blood:	n/a	n/a
19	BCL3	chr15:77326463-77328028	A549	lung:	n/a	n/a
20	BCL3	chr15:77325266-77325980	A549	lung:	n/a	n/a
21	BCL3	chr15:77319696-77320041	GM12878	blood:	n/a	n/a
22	BCL3	chr15:77325651-77326184	A549	lung:	n/a	n/a
23	BCLAF1	chr15:77306496-77307260	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:77319232-77319473	HepG2	liver:	n/a	n/a
25	BHLHE40	chr15:77327273-77327720	K562	blood:	n/a	chr15:77327366-77327387 chr15:77327372-77327381 chr15:77327370-77327383 chr15:77327371-77327380 chr15:77327372-77327381
26	BHLHE40	chr15:77320006-77320083	K562	blood:	n/a	n/a
27	BHLHE40	chr15:77323768-77323927	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:77284594-77284954	K562	blood:	n/a	n/a
29	BHLHE40	chr15:77319308-77319431	K562	blood:	n/a	n/a
30	BHLHE40	chr15:77320463-77320709	K562	blood:	n/a	chr15:77320651-77320667
31	BHLHE40	chr15:77312372-77312424	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:77316652-77316796	K562	blood:	n/a	n/a
33	BHLHE40	chr15:77315646-77315869	K562	blood:	n/a	n/a
34	BHLHE40	chr15:77290077-77290411	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:77306097-77307171	GM12878	blood:	n/a	chr15:77306365-77306381
36	BRCA1	chr15:77306336-77306522	GM12878	blood:	n/a	n/a
37	BRCA1	chr15:77316763-77316878	Hela-S3	cervix:	n/a	n/a
38	CCNT2	chr15:77320595-77320914	K562	blood:	n/a	n/a
39	CEBPB	chr15:77312536-77312661	K562	blood:	n/a	chr15:77312579-77312590
40	CEBPB	chr15:77289776-77290057	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:77312440-77312720	A549	lung:	n/a	chr15:77312579-77312590
42	CEBPB	chr15:77295317-77295425	A549	lung:	n/a	chr15:77295404-77295417 chr15:77295364-77295375 chr15:77295363-77295376
43	CEBPB	chr15:77324292-77324502	HepG2	liver:	n/a	n/a
44	CEBPB	chr15:77289866-77289963	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr15:77312427-77312735	HepG2	liver:	n/a	chr15:77312579-77312590
46	CEBPB	chr15:77316733-77316956	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr15:77295316-77295455	IMR90	lung:	n/a	chr15:77295404-77295417 chr15:77295364-77295375 chr15:77295363-77295376
48	CEBPB	chr15:77290539-77290692	A549	lung:	n/a	chr15:77290634-77290645
49	CEBPB	chr15:77306488-77306571	HepG2	liver:	n/a	n/a
50	CEBPB	chr15:77330718-77330925	Hela-S3	cervix:	n/a	chr15:77330791-77330804

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77326735-77326785	CMK	blood:	n/a
2	chr15:77326735-77326785	CMK	blood:	n/a
3	chr15:77317370-77317420	HRCEpiC	kidney:	n/a
4	chr15:77320384-77320434	Hepatocyte	liver:	n/a
5	chr15:77324758-77324808	K562	blood:	n/a
6	chr15:77324526-77324576	HepG2	liver:	n/a
7	chr15:77317370-77317420	HEK293	kidney:	embryo
8	chr15:77286232-77286282	ovcar-3	ovarian:	n/a
9	chr15:77324758-77324808	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:77287345-77287395	Caco-2	colon:	n/a
11	chr15:77317370-77317420	PANC-1	pancreas:	n/a
12	chr15:77289047-77289097	CMK	blood:	n/a
13	chr15:77320384-77320434	AG04449	skin:	fetal
14	chr15:77287338-77287388	AoSMC	blood vessel:	n/a
15	chr15:77320787-77320837	AG10803	skin:	n/a
16	chr15:77287762-77287812	GM12878	blood:	n/a
17	chr15:77289047-77289097	SK-N-SH	brain:	n/a
18	chr15:77287338-77287388	H1-hESC	embryonic stem cell:	embryo
19	chr15:77323565-77323615	AG09309	skin:	n/a
20	chr15:77287338-77287388	AG10803	skin:	n/a
21	chr15:77286948-77286998	GM12892	blood:	n/a
22	chr15:77314406-77314456	NH-A	brain:	n/a
23	chr15:77324526-77324576	U87	brain:	n/a
24	chr15:77327887-77327937	CMK	blood:	n/a
25	chr15:77324758-77324808	SK-N-SH	brain:	n/a
26	chr15:77320384-77320434	AG09309	skin:	n/a
27	chr15:77323565-77323615	CMK	blood:	n/a
28	chr15:77320787-77320837	NHBE	bronchial:	n/a
29	chr15:77286948-77286998	SKMC	muscle:	n/a
30	chr15:77326735-77326785	ProgFib	skin:	n/a
31	chr15:77320672-77320722	T-47D	breast:	n/a
32	chr15:77320672-77320722	HRCEpiC	kidney:	n/a
33	chr15:77287243-77287293	AoSMC	blood vessel:	n/a
34	chr15:77287345-77287395	PFSK-1	brain:	n/a
35	chr15:77324607-77324657	Hela-S3	cervix:	n/a
36	chr15:77287345-77287395	CMK	blood:	n/a
37	chr15:77286948-77286998	LNCaP	prostate:	n/a
38	chr15:77327887-77327937	A549	lung:	n/a
39	chr15:77320384-77320434	HEEpiC	esophagus:	n/a
40	chr15:77287656-77287706	SK-N-SH	brain:	n/a
41	chr15:77286948-77286998	ProgFib	skin:	n/a
42	chr15:77289047-77289097	HIPEpiC	eye:	n/a
43	chr15:77320261-77320311	HNPCEpiC	eye:	n/a
44	chr15:77286232-77286282	SK-N-SH_RA	brain:	n/a
45	chr15:77317370-77317420	GM06990	blood:	n/a
46	chr15:77286232-77286282	CMK	blood:	n/a
47	chr15:77287762-77287812	HMEC	breast:	n/a
48	chr15:77287899-77287949	NT2-D1	testis:	n/a
49	chr15:77287243-77287293	ProgFib	skin:	n/a
50	chr15:77320672-77320722	NH-A	brain:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:77316409..77317242-chr15:77835418..77836097,2	MCF-7	breast:
2	chr15:77320466..77323005-chr15:77324460..77327682,3	MCF-7	breast:
3	chr15:77283555..77285967-chr15:77287143..77289785,2	K562	blood:
4	chr15:77316379..77317255-chr15:77925626..77926458,2	MCF-7	breast:
5	chr15:77280526..77282215-chr15:77292098..77294137,2	K562	blood:
6	chr15:77316407..77317258-chr15:77399611..77400626,4	MCF-7	breast:
7	chr15:77265408..77266372-chr15:77316053..77316927,2	MCF-7	breast:
8	chr15:77283310..77284980-chr15:77285061..77287100,2	MCF-7	breast:
9	chr15:77316351..77317289-chr15:77788854..77789825,3	K562	blood:
10	chr15:77283555..77285967-chr15:77287143..77289785,2	K562	blood:
11	chr15:77316331..77317283-chr15:77835334..77836400,5	K562	blood:
12	chr15:77320466..77323005-chr15:77324460..77327682,3	MCF-7	breast:
13	chr15:77305426..77307546-chr15:77319169..77320927,2	K562	blood:
14	chr15:77327656..77329511-chr15:77332033..77335172,3	K562	blood:
15	chr15:77327656..77330194-chr15:77332164..77335172,3	K562	blood:
16	chr15:77320639..77324428-chr15:77362244..77364696,3	K562	blood:
17	chr15:77282963..77284982-chr15:77290568..77292460,2	K562	blood:
18	chr15:77303183..77305636-chr15:77307103..77311098,3	K562	blood:
19	chr15:77325493..77328166-chr15:77329882..77331634,3	MCF-7	breast:
20	chr15:77265440..77266266-chr15:77305789..77306421,2	MCF-7	breast:
21	chr15:77282963..77284982-chr15:77290568..77292460,2	K562	blood:
22	chr15:77328280..77330879-chr15:77355103..77356921,2	K562	blood:
23	chr15:77316659..77317287-chr15:77410867..77411851,3	MCF-7	breast:
24	chr15:77315639..77319825-chr15:77322811..77328362,7	MCF-7	breast:
25	chr15:77311951..77316312-chr15:77325010..77329080,4	K562	blood:

No data

Variant related genes	Relation type
PSTPIP1	TF binding region
ENSG00000259652	TF binding region
PSTPIP1	CpG island
ENSG00000259652	CpG island
ENSG00000140368	chromatin interactions
ENSG00000140391	chromatin interactions

Extended variants
information (count: 2228 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2228 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559729961	chr15:77283967-77283968	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs11637631	chr15:77283977-77283978	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs548556519	chr15:77284004-77284005	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567595101	chr15:77284069-77284070	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531505524	chr15:77284092-77284093	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531620993	chr15:77284159-77284160	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2458245	chr15:77284160-77284161	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs568117402	chr15:77284199-77284200	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs539957109	chr15:77284227-77284228	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs78353619	chr15:77284284-77284285	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116334809	chr15:77284286-77284287	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534218511	chr15:77284324-77284325	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555468042	chr15:77284356-77284357	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574320954	chr15:77284394-77284395	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538108825	chr15:77284395-77284396	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs72742443	chr15:77284455-77284456	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2469228	chr15:77284493-77284494	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs544722826	chr15:77284514-77284515	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559841247	chr15:77284559-77284560	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571800911	chr15:77284575-77284576	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576845110	chr15:77284595-77284596	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538938879	chr15:77284644-77284645	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558953870	chr15:77284648-77284649	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs572337795	chr15:77284658-77284659	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188508303	chr15:77284661-77284662	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs561048444	chr15:77284678-77284679	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs531645482	chr15:77284716-77284717	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144834358	chr15:77284739-77284740	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs565112170	chr15:77284740-77284741	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs56307118	chr15:77284742-77284743	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs113446037	chr15:77284743-77284744	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs139502926	chr15:77284761-77284762	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs7359327	chr15:77284762-77284763	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534285478	chr15:77284773-77284774	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549360287	chr15:77284791-77284792	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs371002252	chr15:77284798-77284799	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538543964	chr15:77284804-77284805	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556549548	chr15:77284809-77284810	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs55747356	chr15:77284813-77284814	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs368197332	chr15:77284934-77284935	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs372263010	chr15:77284936-77284937	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538889584	chr15:77284992-77284993	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs118088681	chr15:77284993-77284994	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs571813069	chr15:77285037-77285038	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542319283	chr15:77285059-77285060	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs143394503	chr15:77285072-77285073	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs532319887	chr15:77285073-77285074	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs117398881	chr15:77285097-77285098	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs552179435	chr15:77285156-77285157	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs543384141	chr15:77285225-77285226	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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	17122850	CNVD
Acute myeloid leukemia	20962326	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1750 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77274000-77287200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr15:77281200-77286400	Weak transcription	Colonic Mucosa	Colon
3	chr15:77281200-77286400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:77281400-77285800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr15:77281400-77286000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr15:77281400-77286400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr15:77281600-77284600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr15:77281600-77285600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr15:77281600-77285600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr15:77281600-77285600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr15:77281600-77285600	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr15:77281600-77285600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr15:77281600-77285800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr15:77281600-77285800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr15:77281600-77286000	Weak transcription	Primary T cells from cord blood	blood
16	chr15:77281600-77286000	Weak transcription	Lung	lung
17	chr15:77281600-77286200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr15:77281600-77286400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr15:77281600-77287800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr15:77281600-77289000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr15:77281800-77284800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr15:77281800-77284800	Weak transcription	Brain Hippocampus Middle	brain
23	chr15:77281800-77285600	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr15:77281800-77285600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr15:77281800-77285800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr15:77281800-77286000	Weak transcription	Primary B cells from peripheral blood	blood
27	chr15:77281800-77286400	Weak transcription	Fetal Thymus	thymus
28	chr15:77281800-77287400	Weak transcription	Brain Anterior Caudate	brain
29	chr15:77281800-77287800	Weak transcription	Brain Angular Gyrus	brain
30	chr15:77281800-77288000	Weak transcription	Liver	Liver
31	chr15:77281800-77288600	Weak transcription	Left Ventricle	heart
32	chr15:77281800-77289000	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr15:77282000-77284200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr15:77282000-77284200	Weak transcription	Fetal Muscle Leg	muscle
35	chr15:77282000-77284600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr15:77282000-77284600	Weak transcription	Spleen	Spleen
37	chr15:77282000-77285400	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr15:77282000-77285600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr15:77282000-77287200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:77282000-77287200	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr15:77282000-77287400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr15:77282000-77287400	Weak transcription	Right Ventricle	heart
43	chr15:77282000-77287600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr15:77283000-77287200	Enhancers	Pancreas	Pancrea
45	chr15:77283000-77291000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr15:77283200-77286800	Enhancers	Primary B cells from cord blood	blood
47	chr15:77283400-77284000	Enhancers	Adipose Nuclei	Adipose
48	chr15:77283400-77284200	Enhancers	HSMMtube	muscle
49	chr15:77283400-77284400	Enhancers	HSMM	muscle
50	chr15:77283400-77285800	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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