Variant report

Variant	esv3423390
Chromosome Location	chr15:75742324-75744872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:761)
CpG islands
(count:915)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:75744012-75744700	K562	blood:	n/a	n/a
2	ARID3A	chr15:75744262-75745389	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:75742441-75743323	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:75742519-75742719	K562	blood:	n/a	n/a
5	ATF1	chr15:75744004-75744680	K562	blood:	n/a	n/a
6	ATF2	chr15:75744615-75745653	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:75744591-75746701	GM12878	blood:	n/a	n/a
8	ATF2	chr15:75744301-75745580	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:75742805-75743137	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:75744559-75745745	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr15:75742405-75743147	A549	lung:	n/a	chr15:75743070-75743078
12	BCL3	chr15:75743943-75745820	A549	lung:	n/a	chr15:75744036-75744045 chr15:75744010-75744019
13	BCL3	chr15:75743688-75746731	A549	lung:	n/a	chr15:75744036-75744045 chr15:75744010-75744019 chr15:75746383-75746392
14	BCL3	chr15:75742520-75743192	A549	lung:	n/a	chr15:75743162-75743171 chr15:75743070-75743078
15	BCLAF1	chr15:75744501-75745552	GM12878	blood:	n/a	n/a
16	BHLHE40	chr15:75742864-75743637	HepG2	liver:	n/a	n/a
17	BHLHE40	chr15:75742812-75743687	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:75742752-75743824	K562	blood:	n/a	n/a
19	BHLHE40	chr15:75744073-75745369	K562	blood:	n/a	n/a
20	BRCA1	chr15:75742956-75743075	HepG2	liver:	n/a	n/a
21	BRCA1	chr15:75743779-75743836	HepG2	liver:	n/a	n/a
22	BRCA1	chr15:75744638-75744893	HepG2	liver:	n/a	n/a
23	BRCA1	chr15:75742706-75743439	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr15:75744046-75744655	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr15:75744112-75744402	GM12878	blood:	n/a	n/a
26	CBX3	chr15:75744135-75745825	K562	blood:	n/a	n/a
27	CBX3	chr15:75742874-75743488	K562	blood:	n/a	n/a
28	CCNT2	chr15:75742874-75745292	K562	blood:	n/a	chr15:75743370-75743379 chr15:75743476-75743485 chr15:75743359-75743368 chr15:75743612-75743621 chr15:75744184-75744193 chr15:75743430-75743439 chr15:75743968-75743977 chr15:75744054-75744063
29	CEBPB	chr15:75743963-75744250	K562	blood:	n/a	n/a
30	CEBPB	chr15:75743965-75744445	IMR90	lung:	n/a	n/a
31	CEBPB	chr15:75744608-75745924	GM12878	blood:	n/a	n/a
32	CEBPB	chr15:75742649-75743540	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr15:75743880-75744551	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr15:75743747-75744566	HepG2	liver:	n/a	n/a
35	CEBPB	chr15:75743944-75744481	A549	lung:	n/a	n/a
36	CEBPD	chr15:75743910-75744210	HepG2	liver:	n/a	n/a
37	CEBPD	chr15:75742986-75744782	HepG2	liver:	n/a	n/a
38	CEBPZ	chr15:75743962-75744916	HepG2	liver:	n/a	n/a
39	CHD1	chr15:75742585-75742966	GM12878	blood:	n/a	n/a
40	CHD1	chr15:75743731-75743881	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr15:75744581-75746320	H1-hESC	embryonic stem cell:	n/a	chr15:75746254-75746264
42	CHD1	chr15:75743645-75743943	GM12878	blood:	n/a	n/a
43	CHD1	chr15:75742392-75742607	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr15:75742839-75743122	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr15:75742311-75749635	IMR90	lung:	n/a	chr15:75746254-75746264 chr15:75743636-75743646 chr15:75747775-75747785 chr15:75747345-75747355
46	CHD1	chr15:75744630-75746317	GM12878	blood:	n/a	chr15:75746254-75746264
47	CHD2	chr15:75743235-75743500	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr15:75743842-75745521	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr15:75742822-75743154	HepG2	liver:	n/a	n/a
50	CHD2	chr15:75743911-75744889	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75744262-75744312	PFSK-1	brain:	n/a
2	chr15:75743273-75743323	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:75744089-75744139	SK-N-SH	brain:	n/a
4	chr15:75743136-75743186	MCF10A-Er-Src	breast:	n/a
5	chr15:75743753-75743803	A549	lung:	n/a
6	chr15:75743999-75744049	CMK	blood:	n/a
7	chr15:75743273-75743323	AG09319	gingival:	n/a
8	chr15:75743136-75743186	K562	blood:	n/a
9	chr15:75743273-75743323	SK-N-SH	brain:	n/a
10	chr15:75744504-75744554	H1-hESC	embryonic stem cell:	embryo
11	chr15:75744117-75744167	NHBE	bronchial:	n/a
12	chr15:75744113-75744163	NT2-D1	testis:	n/a
13	chr15:75743753-75743803	SAEC	small airway:	n/a
14	chr15:75743273-75743323	SKMC	muscle:	n/a
15	chr15:75744002-75744052	HNPCEpiC	eye:	n/a
16	chr15:75744615-75744665	HRPEpiC	eye:	n/a
17	chr15:75743999-75744049	HCT-116	colon:	n/a
18	chr15:75744615-75744665	NB4	blood:	n/a
19	chr15:75743999-75744049	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:75744225-75744275	CMK	blood:	n/a
21	chr15:75744460-75744510	Jurkat	blood:	n/a
22	chr15:75744035-75744085	BE2_C	brain:	n/a
23	chr15:75743273-75743323	MCF-7	breast:	n/a
24	chr15:75744117-75744167	NT2-D1	testis:	n/a
25	chr15:75744117-75744167	Hepatocyte	liver:	n/a
26	chr15:75744460-75744510	HUVEC	blood vessel:	n/a
27	chr15:75744089-75744139	ProgFib	skin:	n/a
28	chr15:75744615-75744665	Hepatocyte	liver:	n/a
29	chr15:75743999-75744049	IMR90	lung:	fetal
30	chr15:75744035-75744085	GM12892	blood:	n/a
31	chr15:75743273-75743323	ovcar-3	ovarian:	n/a
32	chr15:75744035-75744085	Hepatocyte	liver:	n/a
33	chr15:75744045-75744095	HIPEpiC	eye:	n/a
34	chr15:75744615-75744665	GM12891	blood:	n/a
35	chr15:75744504-75744554	GM12878	blood:	n/a
36	chr15:75744089-75744139	HCT-116	colon:	n/a
37	chr15:75744035-75744085	MCF-7	breast:	n/a
38	chr15:75743273-75743323	HNPCEpiC	eye:	n/a
39	chr15:75744113-75744163	NH-A	brain:	n/a
40	chr15:75744045-75744095	HCT-116	colon:	n/a
41	chr15:75743136-75743186	AG10803	skin:	n/a
42	chr15:75744262-75744312	AG09319	gingival:	n/a
43	chr15:75744615-75744665	HCM	heart:	n/a
44	chr15:75744089-75744139	Caco-2	colon:	n/a
45	chr15:75744460-75744510	SK-N-MC	brain:	n/a
46	chr15:75744615-75744665	NHDF-neo	bronchial:	n/a
47	chr15:75744117-75744167	U87	brain:	n/a
48	chr15:75744117-75744167	SAEC	small airway:	n/a
49	chr15:75743753-75743803	HL-60	blood:	n/a
50	chr15:75744002-75744052	GM19239	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:75744354..75750304-chr15:75868474..75873810,11	K562	blood:
2	chr15:75729900..75734080-chr15:75744771..75746662,3	MCF-7	breast:
3	chr15:75744661..75745311-chr2:200324243..200325040,2	Hela-S3	cervix:
4	chr15:75639534..75641718-chr15:75744816..75747084,2	MCF-7	breast:
5	chr15:75744060..75744813-chr6:33678935..33679655,2	Hela-S3	cervix:
6	chr15:75741578..75748579-chr15:75928515..75935579,16	K562	blood:
7	chr15:75726359..75728321-chr15:75740878..75743039,2	K562	blood:
8	chr15:75743703..75744660-chr19:34855798..34856573,2	NB4	blood:
9	chr15:75744318..75747084-chr15:75809053..75812043,2	MCF-7	breast:
10	chr15:75743610..75746369-chr15:75937608..75941096,3	K562	blood:
11	chr10:127407240..127408007-chr15:75744395..75745221,2	Hela-S3	cervix:
12	chr10:105726556..105727455-chr15:75743634..75744480,2	Hela-S3	cervix:
13	chr15:75656095..75662590-chr15:75739456..75750037,27	MCF-7	breast:
14	chr15:75744190..75746911-chr15:75963679..75965801,2	MCF-7	breast:
15	chr15:75744555..75745490-chr5:43484073..43484661,2	Hela-S3	cervix:
16	chr15:75627797..75629612-chr15:75743113..75745396,2	K562	blood:
17	chr15:75744565..75747167-chr15:75943528..75946295,2	MCF-7	breast:
18	chr15:75741664..75745730-chr15:75869940..75872786,3	MCF-7	breast:
19	chr15:75134544..75136731-chr15:75744372..75746938,2	MCF-7	breast:
20	chr15:75673195..75675877-chr15:75743620..75745869,3	MCF-7	breast:
21	chr10:88280192..88281055-chr15:75744822..75745795,2	Hela-S3	cervix:
22	chr15:75660401..75660959-chr15:75744394..75745370,2	Hela-S3	cervix:
23	chr15:75721974..75724275-chr15:75744152..75746354,2	K562	blood:
24	chr15:75741711..75746813-chr15:75868980..75872679,7	MCF-7	breast:
25	chr15:75743363..75745017-chr15:75917841..75919520,2	K562	blood:
26	chr1:42800990..42801643-chr15:75744547..75745460,2	Hela-S3	cervix:
27	chr15:75744486..75745315-chr6:30034956..30035626,2	Hela-S3	cervix:
28	chr15:75639207..75640858-chr15:75743116..75744779,2	MCF-7	breast:
29	chr15:75743800..75745854-chr15:75871441..75873983,2	K562	blood:
30	chr15:75744276..75746320-chr20:45987544..45989803,2	MCF-7	breast:
31	chr14:45722471..45723281-chr15:75743983..75744975,2	Hela-S3	cervix:
32	chr15:75743471..75745101-chr15:75938448..75940487,2	MCF-7	breast:
33	chr10:13203295..13204064-chr15:75743431..75743952,2	Hela-S3	cervix:
34	chr15:75742140..75749687-chr15:75929409..75934974,27	MCF-7	breast:
35	chr15:75741052..75746522-chr15:75930202..75934500,7	MCF-7	breast:
36	chr15:75743021..75745154-chr15:78857416..78860250,2	MCF-7	breast:
37	chr15:75657601..75665504-chr15:75739437..75749700,27	K562	blood:
38	chr15:75741578..75748624-chr15:75927989..75935113,20	K562	blood:
39	chr15:41166323..41166984-chr15:75743572..75744484,2	Hela-S3	cervix:
40	chr15:75743503..75749103-chr15:75916446..75919686,11	K562	blood:
41	chr15:75744615..75746777-chr4:41938834..41941720,2	MCF-7	breast:
42	chr1:28831835..28832602-chr15:75743874..75744556,2	Hela-S3	cervix:
43	chr15:75657484..75665083-chr15:75741604..75749517,41	MCF-7	breast:
44	chr15:75640869..75642530-chr15:75742504..75744688,2	K562	blood:
45	chr15:75658070..75664945-chr15:75741625..75749756,25	K562	blood:

No data

Variant related genes	Relation type
SIN3A	TF binding region
SIN3A	CpG island
ENSG00000140400	chromatin interactions
ENSG00000140474	chromatin interactions
ENSG00000198815	chromatin interactions
ENSG00000129534	chromatin interactions
ENSG00000065328	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000260235	chromatin interactions
ENSG00000137288	chromatin interactions
ENSG00000105220	chromatin interactions
ENSG00000065613	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000204619	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000173548	chromatin interactions
ENSG00000169410	chromatin interactions
ENSG00000104140	chromatin interactions
ENSG00000140398	chromatin interactions
ENSG00000140365	chromatin interactions
ENSG00000260274	chromatin interactions
ENSG00000234134	chromatin interactions
ENSG00000260206	chromatin interactions
ENSG00000169371	chromatin interactions
ENSG00000169684	chromatin interactions
ENSG00000109133	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000249492	chromatin interactions

Extended variants
information (count: 85 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188549600	chr15:75742327-75742328	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs534239230	chr15:75742334-75742335	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs559084751	chr15:75742357-75742358	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs573561634	chr15:75742362-75742363	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs537896851	chr15:75742461-75742462	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs180695296	chr15:75742493-75742494	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs370307879	chr15:75742519-75742520	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs573540516	chr15:75742521-75742522	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs7179862	chr15:75742530-75742531	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs556462060	chr15:75742531-75742532	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs374894508	chr15:75742533-75742534	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs186135654	chr15:75742560-75742561	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs116616506	chr15:75742573-75742574	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs572334386	chr15:75742645-75742646	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs190902979	chr15:75742657-75742658	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs572721453	chr15:75742660-75742661	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs542565181	chr15:75742667-75742668	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs182329777	chr15:75742686-75742687	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs113091118	chr15:75742693-75742694	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs529269093	chr15:75742730-75742731	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs550991194	chr15:75742761-75742762	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs562623431	chr15:75742789-75742790	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs533276647	chr15:75742860-75742861	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs7162587	chr15:75742894-75742895	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs566735189	chr15:75742895-75742896	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs371582233	chr15:75742913-75742914	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs534460995	chr15:75742963-75742964	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs549412602	chr15:75742981-75742982	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs567989475	chr15:75742983-75742984	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs9944231	chr15:75742992-75742993	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs11637068	chr15:75743002-75743003	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs556152962	chr15:75743036-75743037	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs187390873	chr15:75743050-75743051	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs538753239	chr15:75743086-75743087	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs553968741	chr15:75743121-75743122	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs572272477	chr15:75743137-75743138	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs190631696	chr15:75743160-75743161	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs554555519	chr15:75743197-75743198	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs553417700	chr15:75743224-75743225	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs576318367	chr15:75743225-75743226	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs377079379	chr15:75743249-75743250	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs544256750	chr15:75743332-75743333	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs562562458	chr15:75743361-75743362	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs533215444	chr15:75743386-75743387	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs545103694	chr15:75743437-75743438	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs560262531	chr15:75743532-75743533	Active TSS Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs8039632	chr15:75743605-75743606	Active TSS Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs368867905	chr15:75743670-75743671	Active TSS Weak transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs200044330	chr15:75743678-75743679	Active TSS Weak transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs8039672	chr15:75743689-75743690	Active TSS Weak transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
Congenital diaphragmatic hernia	21085971	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
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75717000-75742600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:75721200-75742600	Weak transcription	Aorta	Aorta
3	chr15:75723000-75742600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr15:75728800-75742600	Weak transcription	Esophagus	oesophagus
5	chr15:75735600-75742600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr15:75735800-75742400	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr15:75736000-75742800	Weak transcription	Lung	lung
8	chr15:75736200-75742600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:75740000-75742400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr15:75740000-75742600	Weak transcription	Brain Angular Gyrus	brain
11	chr15:75740200-75742400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr15:75740200-75742400	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr15:75740600-75742400	Enhancers	Primary B cells from cord blood	blood
14	chr15:75741000-75742400	Enhancers	Brain Germinal Matrix	brain
15	chr15:75741400-75742400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr15:75741600-75742400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr15:75741600-75742400	Enhancers	Brain Hippocampus Middle	brain
18	chr15:75741600-75742400	Enhancers	Fetal Heart	heart
19	chr15:75741600-75742400	Enhancers	K562	blood
20	chr15:75741600-75742600	Enhancers	Stomach Mucosa	stomach
21	chr15:75741600-75743000	Flanking Active TSS	Hela-S3	cervix
22	chr15:75741600-75743200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr15:75741600-75748800	Active TSS	Ovary	ovary
24	chr15:75741800-75742400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr15:75741800-75742400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:75741800-75742400	Enhancers	Primary T cells fromperipheralblood	blood
27	chr15:75741800-75742400	Enhancers	Primary hematopoietic stem cells	blood
28	chr15:75741800-75742400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr15:75741800-75742400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:75741800-75742400	Enhancers	Fetal Stomach	stomach
31	chr15:75741800-75742400	Enhancers	Fetal Thymus	thymus
32	chr15:75741800-75742400	Flanking Active TSS	HMEC	breast
33	chr15:75741800-75742400	Flanking Active TSS	NHEK	skin
34	chr15:75741800-75742600	Enhancers	Primary B cells from peripheral blood	blood
35	chr15:75741800-75742600	Flanking Active TSS	Stomach Smooth Muscle	stomach
36	chr15:75741800-75743000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr15:75741800-75743200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr15:75741800-75749000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr15:75742000-75742400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr15:75742000-75742400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr15:75742000-75742400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:75742000-75742400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr15:75742000-75742400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr15:75742000-75742400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr15:75742000-75742400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr15:75742000-75742400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
47	chr15:75742000-75742400	Flanking Active TSS	Fetal Intestine Large	intestine
48	chr15:75742000-75742400	Flanking Active TSS	Fetal Intestine Small	intestine
49	chr15:75742000-75742400	Enhancers	Fetal Muscle Leg	muscle
50	chr15:75742000-75742400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle

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