Variant report

Variant	nsv569312
Chromosome Location	chr15:45381998-45460422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2441)
CpG islands
(count:4887)
Chromatin interactive
region (count:105)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2441 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45418662-45419119	K562	blood:	n/a	n/a
2	ARID3A	chr15:45414357-45414389	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:45418745-45419155	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:45459757-45459773	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:45410346-45410617	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:45459297-45459300	K562	blood:	n/a	n/a
7	ARID3A	chr15:45423781-45424095	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:45459687-45459941	K562	blood:	n/a	n/a
9	ATF1	chr15:45383460-45383796	K562	blood:	n/a	n/a
10	ATF1	chr15:45449331-45449609	K562	blood:	n/a	n/a
11	ATF1	chr15:45450234-45450549	K562	blood:	n/a	n/a
12	ATF1	chr15:45455746-45455775	K562	blood:	n/a	n/a
13	ATF2	chr15:45450203-45450634	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr15:45455191-45455598	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr15:45459029-45459297	K562	blood:	n/a	chr15:45459163-45459172
16	ATF3	chr15:45455123-45455624	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr15:45410310-45410641	K562	blood:	n/a	n/a
18	BACH1	chr15:45408630-45409090	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:45424869-45424892	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:45390335-45390345	K562	blood:	n/a	n/a
21	BACH1	chr15:45406429-45406479	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr15:45421066-45421370	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr15:45459461-45459883	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr15:45455222-45455621	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr15:45410343-45410746	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr15:45404699-45405166	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr15:45413200-45413678	GM12878	blood:	n/a	n/a
28	BATF	chr15:45413226-45413597	GM12878	blood:	n/a	n/a
29	BCL11A	chr15:45413347-45413584	GM12878	blood:	n/a	n/a
30	BCL11A	chr15:45413229-45413657	GM12878	blood:	n/a	n/a
31	BCL3	chr15:45459523-45459793	GM12878	blood:	n/a	n/a
32	BCLAF1	chr15:45455247-45455602	GM12878	blood:	n/a	chr15:45455524-45455533 chr15:45455286-45455299 chr15:45455428-45455436
33	BCLAF1	chr15:45410225-45410681	GM12878	blood:	n/a	n/a
34	BCLAF1	chr15:45458947-45459967	GM12878	blood:	n/a	chr15:45459191-45459204 chr15:45459123-45459136
35	BHLHE40	chr15:45431833-45431914	K562	blood:	n/a	n/a
36	BHLHE40	chr15:45427134-45427453	GM12878	blood:	n/a	n/a
37	BHLHE40	chr15:45458677-45459264	K562	blood:	n/a	n/a
38	BHLHE40	chr15:45410307-45410689	K562	blood:	n/a	n/a
39	BHLHE40	chr15:45455035-45455664	HepG2	liver:	n/a	chr15:45455345-45455361
40	BHLHE40	chr15:45459057-45459957	GM12878	blood:	n/a	n/a
41	BHLHE40	chr15:45418905-45419058	K562	blood:	n/a	n/a
42	BHLHE40	chr15:45455280-45455636	K562	blood:	n/a	chr15:45455345-45455361
43	BHLHE40	chr15:45459621-45459920	K562	blood:	n/a	n/a
44	BRCA1	chr15:45410328-45410576	HepG2	liver:	n/a	n/a
45	BRCA1	chr15:45419959-45419986	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr15:45455411-45455611	GM12878	blood:	n/a	n/a
47	BRCA1	chr15:45410199-45410601	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr15:45455262-45455585	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr15:45459103-45459895	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr15:45455210-45455508	H1-hESC	embryonic stem cell:	n/a	n/a

(count:4887 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45407818-45407868	U87	brain:	n/a
2	chr15:45392065-45392115	ProgFib	skin:	n/a
3	chr15:45409942-45409992	SK-N-SH	brain:	n/a
4	chr15:45459300-45459350	HEK293	kidney:	embryo
5	chr15:45406939-45406989	RPTEC	kidney:	n/a
6	chr15:45408574-45408624	T-47D	breast:	n/a
7	chr15:45409170-45409220	HCM	heart:	n/a
8	chr15:45407818-45407868	U87	brain:	n/a
9	chr15:45392065-45392115	ProgFib	skin:	n/a
10	chr15:45409942-45409992	SK-N-SH	brain:	n/a
11	chr15:45459300-45459350	HEK293	kidney:	embryo
12	chr15:45406939-45406989	RPTEC	kidney:	n/a
13	chr15:45408574-45408624	T-47D	breast:	n/a
14	chr15:45409170-45409220	HCM	heart:	n/a
15	chr15:45440540-45440590	PANC-1	pancreas:	n/a
16	chr15:45421951-45422001	CMK	blood:	n/a
17	chr15:45400492-45400542	HL-60	blood:	n/a
18	chr15:45422004-45422054	Jurkat	blood:	n/a
19	chr15:45422553-45422603	SKMC	muscle:	n/a
20	chr15:45406534-45406584	IMR90	lung:	fetal
21	chr15:45401952-45402002	SK-N-SH	brain:	n/a
22	chr15:45408574-45408624	ECC-1	luminal epithelium:	n/a
23	chr15:45422371-45422421	MCF-7	breast:	n/a
24	chr15:45422553-45422603	SK-N-SH_RA	brain:	n/a
25	chr15:45402305-45402355	NHBE	bronchial:	n/a
26	chr15:45409698-45409748	HepG2	liver:	n/a
27	chr15:45423543-45423593	AoSMC	blood vessel:	n/a
28	chr15:45421749-45421799	HEK293	kidney:	embryo
29	chr15:45410047-45410097	HIPEpiC	eye:	n/a
30	chr15:45458818-45458868	AoSMC	blood vessel:	n/a
31	chr15:45444323-45444373	BJ	skin:	n/a
32	chr15:45405103-45405153	K562	blood:	n/a
33	chr15:45434285-45434335	H1-hESC	embryonic stem cell:	embryo
34	chr15:45406486-45406536	CMK	blood:	n/a
35	chr15:45422062-45422112	HAEpiC	amniotic membrane:	n/a
36	chr15:45421951-45422001	NT2-D1	testis:	n/a
37	chr15:45422083-45422133	NHDF-neo	bronchial:	n/a
38	chr15:45402305-45402355	SAEC	small airway:	n/a
39	chr15:45422054-45422104	AG10803	skin:	n/a
40	chr15:45421068-45421118	PFSK-1	brain:	n/a
41	chr15:45427577-45427627	ProgFib	skin:	n/a
42	chr15:45427734-45427784	IMR90	lung:	fetal
43	chr15:45444918-45444968	HMEC	breast:	n/a
44	chr15:45406534-45406584	HCM	heart:	n/a
45	chr15:45417414-45417464	SKMC	muscle:	n/a
46	chr15:45459406-45459456	AG04450	lung:	fetal
47	chr15:45422095-45422145	GM12891	blood:	n/a
48	chr15:45422083-45422133	A549	lung:	n/a
49	chr15:45444704-45444754	IMR90	lung:	fetal
50	chr15:45421068-45421118	GM19239	blood:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:45449920..45453086-chr15:45456416..45459415,4	K562	blood:
2	chr15:45458064..45460777-chr15:45570184..45573179,2	MCF-7	breast:
3	chr15:45439215..45441093-chr15:45448771..45450612,2	MCF-7	breast:
4	chr15:45459427..45462384-chr15:45693635..45696116,3	K562	blood:
5	chr15:45411733..45414237-chr15:45457948..45460622,2	MCF-7	breast:
6	chr15:45454944..45455772-chr15:45568916..45570015,4	MCF-7	breast:
7	chr15:45424906..45427712-chr15:45434989..45436687,2	MCF-7	breast:
8	chr11:62608445..62609565-chr15:45458977..45459729,4	Hela-S3	cervix:
9	chr15:45435866..45441707-chr15:45442117..45446619,7	K562	blood:
10	chr15:45412250..45414388-chr15:45434468..45436699,2	K562	blood:
11	chr15:45402965..45405384-chr15:45407818..45410560,2	K562	blood:
12	chr15:45457813..45459796-chr15:45472458..45474302,2	MCF-7	breast:
13	chr15:45449609..45453236-chr15:45457803..45460650,4	K562	blood:
14	chr15:45458745..45459668-chr6:33393132..33393783,2	NB4	blood:
15	chr15:45434203..45436552-chr15:45443104..45444699,2	K562	blood:
16	chr15:45418967..45421770-chr15:45423953..45425588,2	K562	blood:
17	chr15:45459070..45459878-chr15:65588119..65588621,2	Hela-S3	cervix:
18	chr15:45458639..45462602-chr15:45463163..45466877,10	K562	blood:
19	chr15:45447883..45450231-chr15:45460797..45462764,2	K562	blood:
20	chr15:45394002..45396843-chr15:45411789..45413686,2	K562	blood:
21	chr15:45402172..45404057-chr15:45407808..45410481,2	MCF-7	breast:
22	chr15:45455320..45455877-chr15:45560433..45560990,3	MCF-7	breast:
23	chr15:45456567..45458793-chr15:45475778..45478216,2	MCF-7	breast:
24	chr15:45417539..45419456-chr15:45453596..45456552,2	K562	blood:
25	chr15:45457346..45461990-chr15:45488766..45494297,11	MCF-7	breast:
26	chr15:45443245..45445612-chr15:45693741..45696247,2	K562	blood:
27	chr15:45455358..45455932-chr15:45497094..45497614,2	K562	blood:
28	chr15:45444506..45446626-chr15:45455721..45457375,2	K562	blood:
29	chr15:45459071..45462844-chr15:45693635..45696532,4	K562	blood:
30	chr15:45410032..45410581-chr15:45418687..45419353,3	MCF-7	breast:
31	chr15:45457588..45459238-chr15:45747257..45749159,2	K562	blood:
32	chr15:45377878..45380609-chr15:45390291..45392505,2	MCF-7	breast:
33	chr15:45458782..45460452-chr15:45469150..45471146,2	MCF-7	breast:
34	chr15:45454280..45456253-chr15:45491439..45493847,2	K562	blood:
35	chr15:45409132..45413033-chr15:45458233..45460669,3	MCF-7	breast:
36	chr15:45380073..45381960-chr15:45400521..45403354,2	K562	blood:
37	chr15:45410636..45412600-chr15:45463074..45466007,2	K562	blood:
38	chr15:45410580..45412317-chr15:45415759..45418660,2	K562	blood:
39	chr15:45453899..45457914-chr15:45495194..45498173,3	K562	blood:
40	chr15:45451606..45453511-chr17:56707808..56709453,2	MCF-7	breast:
41	chr15:45456315..45459130-chr15:45878271..45881206,2	K562	blood:
42	chr15:45454753..45457923-chr15:45490933..45493735,3	K562	blood:
43	chr15:45419682..45422492-chr15:45439633..45442095,2	K562	blood:
44	chr15:45453204..45457090-chr15:45457382..45460922,8	K562	blood:
45	chr15:45458639..45463256-chr15:45489443..45493548,9	K562	blood:
46	chr1:151254368..151255147-chr15:45459225..45460088,2	Hela-S3	cervix:
47	chr15:45457736..45460170-chr15:45478587..45480947,2	MCF-7	breast:
48	chr15:45458882..45460694-chr15:45692968..45695992,3	MCF-7	breast:
49	chr15:45443966..45446125-chr15:45449579..45451751,2	K562	blood:
50	chr15:45393110..45394732-chr15:45395329..45397612,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHF-2	chr15:45459684-45459724	ENSG00000259539.1
2	lnc-DUOX2-3	chr15:45422021-45422078	NONHSAT042217
3	lnc-DUOX2-3	chr15:45422050-45422075	NONHSAT042218
4	lnc-DUOX2-3	chr15:45421371-45421813	NONHSAT042218
5	lnc-DUOX2-3	chr15:45421353-45421813	NONHSAT042217
6	lnc-SHF-2	chr15:45444862-45445415	ENSG00000259539.1

No data

Variant related genes	Relation type
ENSG00000259539	TF binding region
DUOX1	TF binding region
ENSG00000259519	TF binding region
DUOXA1	TF binding region
DUOX2	TF binding region
DUOXA2	TF binding region
ENSG00000259539	CpG island
DUOX1	CpG island
ENSG00000259519	CpG island
DUOXA1	CpG island
DUOX2	CpG island
DUOXA2	CpG island
ENSG00000140254	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000104164	chromatin interactions
ENSG00000138606	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000140279	chromatin interactions
ENSG00000259354	chromatin interactions
ENSG00000137857	chromatin interactions
ENSG00000259539	chromatin interactions
ENSG00000171763	chromatin interactions
ENSG00000259520	chromatin interactions
ENSG00000259932	chromatin interactions
ENSG00000132570	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000260035	chromatin interactions
ENSG00000260170	chromatin interactions
ENSG00000140474	chromatin interactions
ENSG00000259519	chromatin interactions
ENSG00000174243	chromatin interactions
ENSG00000171766	chromatin interactions
ENSG00000270103	chromatin interactions

Extended variants
information (count: 3511 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3511 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs166575	chr15:45381998-45381999	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183680539	chr15:45382044-45382045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111278043	chr15:45382104-45382105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535102036	chr15:45382112-45382113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201410897	chr15:45382171-45382172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142541249	chr15:45382175-45382176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375441213	chr15:45382189-45382190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572095944	chr15:45382193-45382194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558419320	chr15:45382321-45382322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188394908	chr15:45382332-45382333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564264553	chr15:45382372-45382373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373313856	chr15:45382387-45382388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182031396	chr15:45382520-45382521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs563486201	chr15:45382561-45382562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529217217	chr15:45382616-45382617	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs549237477	chr15:45382625-45382626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs8029279	chr15:45382637-45382638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577099465	chr15:45382666-45382667	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs116676456	chr15:45382677-45382678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs141243193	chr15:45382692-45382693	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35531227	chr15:45382800-45382801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs117360263	chr15:45382808-45382809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs535997474	chr15:45382821-45382822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150648544	chr15:45382829-45382830	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185838255	chr15:45382855-45382856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552859170	chr15:45382891-45382892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537142144	chr15:45382899-45382900	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs8028462	chr15:45382902-45382903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs189967835	chr15:45382909-45382910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181605931	chr15:45382960-45382961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186837085	chr15:45382982-45382983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555659662	chr15:45382986-45382987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35495563	chr15:45383015-45383016	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs77298391	chr15:45383082-45383083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs543149301	chr15:45383104-45383105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74786139	chr15:45383157-45383158	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs76225422	chr15:45383165-45383166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557687978	chr15:45383166-45383167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373579060	chr15:45383173-45383174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs79571833	chr15:45383209-45383210	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190003741	chr15:45383227-45383228	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557759307	chr15:45383245-45383246	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573763996	chr15:45383277-45383278	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181297417	chr15:45383297-45383298	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553640042	chr15:45383347-45383348	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs568689367	chr15:45383427-45383428	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2554452	chr15:45383446-45383447	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564872961	chr15:45383448-45383449	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs116487477	chr15:45383470-45383471	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531731508	chr15:45383482-45383483	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2487 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45363800-45398400	Weak transcription	Gastric	stomach
2	chr15:45373600-45389400	Weak transcription	Pancreas	Pancrea
3	chr15:45379400-45384600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr15:45379800-45384200	Enhancers	K562	blood
5	chr15:45380800-45382000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:45380800-45382000	Enhancers	Osteobl	bone
7	chr15:45381000-45382000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr15:45381200-45382000	Flanking Active TSS	HepG2	liver
9	chr15:45381200-45382200	Enhancers	Fetal Heart	heart
10	chr15:45381400-45383400	Weak transcription	Left Ventricle	heart
11	chr15:45381400-45404600	Weak transcription	Right Atrium	heart
12	chr15:45381800-45383200	Weak transcription	Right Ventricle	heart
13	chr15:45382000-45383000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr15:45382000-45383200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:45382000-45384200	Enhancers	HepG2	liver
16	chr15:45382200-45383400	Weak transcription	Fetal Heart	heart
17	chr15:45383000-45383800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:45383000-45384200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr15:45383000-45384200	Enhancers	Osteobl	bone
20	chr15:45383200-45383400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr15:45383200-45383400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:45383200-45383400	Enhancers	Colonic Mucosa	Colon
23	chr15:45383200-45383600	Enhancers	Right Ventricle	heart
24	chr15:45383200-45383800	Enhancers	A549	lung
25	chr15:45383200-45384200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr15:45383200-45384200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:45383200-45384200	Bivalent Enhancer	HSMMtube	muscle
28	chr15:45383200-45384400	Enhancers	NHDF-Ad	bronchial
29	chr15:45383200-45384600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr15:45383400-45383800	Bivalent Enhancer	HSMM	muscle
31	chr15:45383400-45384200	Enhancers	Fetal Heart	heart
32	chr15:45383400-45395200	Weak transcription	Colonic Mucosa	Colon
33	chr15:45383600-45383800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
34	chr15:45383600-45383800	Enhancers	Left Ventricle	heart
35	chr15:45383600-45383800	Enhancers	Stomach Mucosa	stomach
36	chr15:45383600-45384000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
37	chr15:45383600-45384400	Enhancers	Esophagus	oesophagus
38	chr15:45383600-45386400	Weak transcription	Right Ventricle	heart
39	chr15:45383800-45384200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr15:45384200-45386200	Weak transcription	K562	blood
41	chr15:45384400-45386400	Weak transcription	Esophagus	oesophagus
42	chr15:45384600-45385600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr15:45385600-45385800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr15:45385600-45387400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr15:45386000-45386200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr15:45386200-45387000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:45386400-45386600	Enhancers	K562	blood
48	chr15:45386400-45386800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr15:45386400-45387200	Strong transcription	Esophagus	oesophagus
50	chr15:45386400-45387400	Enhancers	Right Ventricle	heart

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