Variant report

Variant	nsv1601
Chromosome Location	chr15:72549885-72585176
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:975)
CpG islands
(count:978)
Chromatin interactive
region (count:76)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:975 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:72565098-72565342	K562	blood:	n/a	n/a
2	ATF1	chr15:72564876-72565276	K562	blood:	n/a	n/a
3	ATF3	chr15:72574154-72574368	K562	blood:	n/a	n/a
4	ATF3	chr15:72564796-72565317	GM12878	blood:	n/a	n/a
5	ATF3	chr15:72564747-72565442	A549	lung:	n/a	n/a
6	ATF3	chr15:72564937-72565698	A549	lung:	n/a	n/a
7	ATF3	chr15:72564897-72565121	GM12878	blood:	n/a	n/a
8	ATF3	chr15:72564782-72565351	K562	blood:	n/a	n/a
9	ATF3	chr15:72564879-72565196	K562	blood:	n/a	n/a
10	BACH1	chr15:72564364-72565436	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:72564966-72565159	K562	blood:	n/a	n/a
12	BATF	chr15:72574033-72574425	GM12878	blood:	n/a	chr15:72574265-72574276
13	BCL3	chr15:72564933-72565670	A549	lung:	n/a	n/a
14	BCL3	chr15:72564500-72565761	A549	lung:	n/a	chr15:72564782-72564795 chr15:72564658-72564671 chr15:72564659-72564672
15	BCLAF1	chr15:72564871-72565509	GM12878	blood:	n/a	n/a
16	BCLAF1	chr15:72564584-72565474	GM12878	blood:	n/a	chr15:72564782-72564795 chr15:72564658-72564671 chr15:72564659-72564672
17	BHLHE40	chr15:72568696-72568923	K562	blood:	n/a	n/a
18	BHLHE40	chr15:72578450-72578528	K562	blood:	n/a	n/a
19	BHLHE40	chr15:72577357-72577423	K562	blood:	n/a	n/a
20	BHLHE40	chr15:72564711-72565431	GM12878	blood:	n/a	chr15:72564787-72564803 chr15:72565064-72565080
21	BHLHE40	chr15:72578430-72578622	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:72574155-72574397	K562	blood:	n/a	n/a
23	BHLHE40	chr15:72564278-72565594	K562	blood:	n/a	chr15:72564787-72564803 chr15:72565064-72565080
24	BHLHE40	chr15:72564857-72565369	A549	lung:	n/a	chr15:72565064-72565080
25	BRCA1	chr15:72557791-72557795	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr15:72565040-72565622	GM12878	blood:	n/a	n/a
27	BRCA1	chr15:72564303-72564690	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr15:72564948-72565378	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr15:72564939-72565384	K562	blood:	n/a	n/a
30	CBX3	chr15:72564847-72565496	K562	blood:	n/a	chr15:72565419-72565430
31	CCNT2	chr15:72564398-72565444	K562	blood:	n/a	n/a
32	CEBPB	chr15:72573500-72573673	HepG2	liver:	n/a	chr15:72573574-72573585 chr15:72573574-72573585
33	CEBPB	chr15:72564691-72565436	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr15:72565175-72565390	K562	blood:	n/a	n/a
35	CEBPB	chr15:72565001-72565502	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr15:72565211-72565367	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr15:72564497-72565520	GM12878	blood:	n/a	n/a
38	CHD2	chr15:72564995-72565397	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr15:72564226-72565642	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr15:72564700-72565300	K562	blood:	n/a	n/a
41	CHD2	chr15:72564763-72565409	GM12878	blood:	n/a	n/a
42	CREB1	chr15:72564772-72565371	A549	lung:	n/a	n/a
43	CREB1	chr15:72564914-72565474	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr15:72564720-72565404	K562	blood:	n/a	n/a
45	CREB1	chr15:72564706-72565514	K562	blood:	n/a	n/a
46	CREB1	chr15:72564695-72565466	GM12878	blood:	n/a	n/a
47	CREB1	chr15:72564747-72565415	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr15:72564875-72565368	ECC-1	luminal epithelium:	n/a	n/a
49	CREB1	chr15:72564461-72565496	A549	lung:	n/a	n/a
50	CTBP2	chr15:72564528-72565545	H1-hESC	embryonic stem cell:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72565016-72565066	SAEC	small airway:	n/a
2	chr15:72582316-72582366	MCF10A-Er-Src	breast:	n/a
3	chr15:72565016-72565066	SAEC	small airway:	n/a
4	chr15:72582316-72582366	MCF10A-Er-Src	breast:	n/a
5	chr15:72561540-72561590	SK-N-SH_RA	brain:	n/a
6	chr15:72565016-72565066	A549	lung:	n/a
7	chr15:72565024-72565074	RPTEC	kidney:	n/a
8	chr15:72582316-72582366	NH-A	brain:	n/a
9	chr15:72565024-72565074	MCF-7	breast:	n/a
10	chr15:72564668-72564718	IMR90	lung:	fetal
11	chr15:72565024-72565074	AG09319	gingival:	n/a
12	chr15:72564668-72564718	SK-N-SH_RA	brain:	n/a
13	chr15:72565415-72565465	HepG2	liver:	n/a
14	chr15:72564179-72564229	ovcar-3	ovarian:	n/a
15	chr15:72564196-72564246	LNCaP	prostate:	n/a
16	chr15:72565024-72565074	NH-A	brain:	n/a
17	chr15:72582316-72582366	ECC-1	luminal epithelium:	n/a
18	chr15:72564179-72564229	SK-N-MC	brain:	n/a
19	chr15:72563412-72563462	PFSK-1	brain:	n/a
20	chr15:72581722-72581772	ProgFib	skin:	n/a
21	chr15:72565016-72565066	T-47D	breast:	n/a
22	chr15:72565415-72565465	PFSK-1	brain:	n/a
23	chr15:72563412-72563462	HepG2	liver:	n/a
24	chr15:72581722-72581772	GM12892	blood:	n/a
25	chr15:72565016-72565066	MCF-7	breast:	n/a
26	chr15:72563412-72563462	PrEC	prostate:	n/a
27	chr15:72582206-72582256	GM12891	blood:	n/a
28	chr15:72565415-72565465	HEK293	kidney:	embryo
29	chr15:72563412-72563462	GM12891	blood:	n/a
30	chr15:72582316-72582366	ProgFib	skin:	n/a
31	chr15:72565024-72565074	MCF10A-Er-Src	breast:	n/a
32	chr15:72565016-72565066	AoSMC	blood vessel:	n/a
33	chr15:72582316-72582366	A549	lung:	n/a
34	chr15:72564668-72564718	RPTEC	kidney:	n/a
35	chr15:72567956-72568006	HEK293	kidney:	embryo
36	chr15:72563412-72563462	NHDF-neo	bronchial:	n/a
37	chr15:72563412-72563462	T-47D	breast:	n/a
38	chr15:72581722-72581772	CMK	blood:	n/a
39	chr15:72564196-72564246	AG09309	skin:	n/a
40	chr15:72581569-72581619	HCF	heart:	n/a
41	chr15:72581722-72581772	HNPCEpiC	eye:	n/a
42	chr15:72582206-72582256	HIPEpiC	eye:	n/a
43	chr15:72565024-72565074	SK-N-MC	brain:	n/a
44	chr15:72564179-72564229	PANC-1	pancreas:	n/a
45	chr15:72581722-72581772	NH-A	brain:	n/a
46	chr15:72563412-72563462	MCF-7	breast:	n/a
47	chr15:72565024-72565074	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:72565016-72565066	HPAEpiC	pulmonary alveolar:	n/a
49	chr15:72567956-72568006	HPAEpiC	pulmonary alveolar:	n/a
50	chr15:72582316-72582366	H1-hESC	embryonic stem cell:	embryo

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:72548498..72554612-chr15:72558312..72566000,13	MCF-7	breast:
2	chr15:72521313..72523545-chr15:72578405..72580075,2	MCF-7	breast:
3	chr15:72491830..72492669-chr15:72578199..72578950,2	MCF-7	breast:
4	chr15:72522016..72524904-chr15:72553366..72557370,3	K562	blood:
5	chr15:72564694..72565205-chr5:137878737..137879359,2	Hela-S3	cervix:
6	chr15:72549309..72551782-chr15:72559287..72560861,2	MCF-7	breast:
7	chr15:72542420..72544885-chr15:72551615..72554106,2	K562	blood:
8	chr15:72544452..72547416-chr15:72550112..72551734,3	MCF-7	breast:
9	chr15:72565313..72567062-chr15:72569631..72571154,2	K562	blood:
10	chr15:72555118..72559591-chr15:72562362..72567008,6	MCF-7	breast:
11	chr15:72577424..72579912-chr15:72581637..72583573,2	K562	blood:
12	chr15:72492162..72492716-chr15:72577997..72578627,3	K562	blood:
13	chr15:72522943..72525408-chr15:72560443..72562421,3	MCF-7	breast:
14	chr15:72523217..72525097-chr15:72577058..72579494,2	K562	blood:
15	chr15:72562851..72564645-chr15:72977653..72979663,2	K562	blood:
16	chr15:72522016..72523553-chr15:72554809..72557370,2	K562	blood:
17	chr15:72492101..72492689-chr15:72578026..72578875,3	MCF-7	breast:
18	chr15:72549098..72550957-chr15:72552862..72555615,2	K562	blood:
19	chr15:72564706..72566745-chr15:72598121..72601390,3	K562	blood:
20	chr15:72565043..72567062-chr15:72568655..72571579,4	K562	blood:
21	chr15:72473291..72475888-chr15:72577722..72579583,2	K562	blood:
22	chr15:72563468..72565339-chr15:73075771..73077281,2	MCF-7	breast:
23	chr15:72409322..72412006-chr15:72563414..72566011,3	MCF-7	breast:
24	chr15:72549098..72550957-chr15:72552862..72555615,2	K562	blood:
25	chr15:72537383..72539855-chr15:72564362..72566037,2	MCF-7	breast:
26	chr15:72410053..72410729-chr15:72564212..72565118,2	Hela-S3	cervix:
27	chr15:72553577..72557068-chr15:72560331..72566356,10	K562	blood:
28	chr15:72558362..72561235-chr15:72766233..72767996,2	MCF-7	breast:
29	chr15:72577424..72579912-chr15:72581637..72583573,2	K562	blood:
30	chr15:72513653..72518363-chr15:72563063..72568184,5	MCF-7	breast:
31	chr15:72555189..72557005-chr15:72563474..72566331,2	K562	blood:
32	chr15:72521272..72525431-chr15:72575824..72579485,5	MCF-7	breast:
33	chr15:72518884..72522571-chr15:72567985..72570130,3	K562	blood:
34	chr15:72520024..72526293-chr15:72562525..72566333,14	K562	blood:
35	chr15:72564731..72565486-chr15:72578008..72578878,2	MCF-7	breast:
36	chr15:72575298..72576860-chr15:72578215..72580118,2	K562	blood:
37	chr15:72572263..72574208-chr15:72582105..72583633,2	K562	blood:
38	chr15:72555118..72559591-chr15:72562362..72567008,6	MCF-7	breast:
39	chr15:72523926..72525574-chr15:72553644..72556454,2	MCF-7	breast:
40	chr15:72518424..72531344-chr15:72562525..72571046,23	K562	blood:
41	chr15:72563307..72566923-chr15:72766066..72767771,5	K562	blood:
42	chr15:72541554..72543753-chr15:72562332..72564348,2	K562	blood:
43	chr11:62572553..62573077-chr15:72564582..72565306,2	Hela-S3	cervix:
44	chr15:72561194..72564093-chr15:72666798..72669351,2	MCF-7	breast:
45	chr15:72514333..72526693-chr15:72558323..72568559,52	MCF-7	breast:
46	chr15:72564850..72566745-chr15:72598121..72600222,2	K562	blood:
47	chr15:72511264..72514966-chr15:72550675..72553290,3	MCF-7	breast:
48	chr15:72545613..72547175-chr15:72558549..72561473,2	MCF-7	breast:
49	chr15:72548319..72550602-chr15:72554767..72558019,3	K562	blood:
50	chr15:72523582..72526035-chr15:72559818..72561426,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PKM2-3	chr15:72564734-72564839	NONHSAT047076
2	lnc-PKM2-3	chr15:72563364-72563622	NONHSAT047076
3	lnc-HEXA-1	chr15:72583909-72583948	ENSG00000247056
4	lnc-PKM2-3	chr15:72559973-72560012	NONHSAT047076

No data

Variant related genes	Relation type
PARP6	TF binding region
ENSG00000261460	TF binding region
CELF6	TF binding region
PARP6	CpG island
ENSG00000261460	CpG island
CELF6	CpG island
ENSG00000140488	chromatin interactions
ENSG00000175318	chromatin interactions
ENSG00000260339	chromatin interactions
ENSG00000066933	chromatin interactions
ENSG00000140463	chromatin interactions
ENSG00000213614	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000120705	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000261460	chromatin interactions
ENSG00000166192	chromatin interactions
ENSG00000159322	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000260729	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000175202	chromatin interactions
ENSG00000137817	chromatin interactions
ENSG00000162231	chromatin interactions
C2orf42	miRNA target sites

Extended variants
information (count: 1203 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1203 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74025246	chr15:72549892-72549893	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142706619	chr15:72550025-72550026	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs184930870	chr15:72550033-72550034	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533402203	chr15:72550068-72550069	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551928388	chr15:72550102-72550103	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs552528895	chr15:72550116-72550117	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189394249	chr15:72550140-72550141	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375050075	chr15:72550180-72550181	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs182075252	chr15:72550193-72550194	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546625684	chr15:72550346-72550347	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs376983182	chr15:72550347-72550348	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs368315901	chr15:72550367-72550368	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs267604308	chr15:72550399-72550400	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs372692377	chr15:72550420-72550421	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs112878382	chr15:72550432-72550433	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs550443003	chr15:72550504-72550505	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs369096757	chr15:72550507-72550508	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs568917647	chr15:72550526-72550527	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs36027670	chr15:72550542-72550543	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs55973446	chr15:72550551-72550552	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs56043768	chr15:72550553-72550554	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs146526121	chr15:72550569-72550570	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs557907622	chr15:72550586-72550587	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534829968	chr15:72550736-72550737	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111744599	chr15:72550749-72550750	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs374547939	chr15:72551024-72551025	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs185036538	chr15:72551025-72551026	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs35324675	chr15:72551028-72551029	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs189012379	chr15:72551062-72551063	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs545772601	chr15:72551063-72551064	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs34407333	chr15:72551064-72551065	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs397690727	chr15:72551071-72551072	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs114583485	chr15:72551072-72551073	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs545286330	chr15:72551112-72551113	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs533710365	chr15:72551115-72551116	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs186404058	chr15:72551123-72551124	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs527994619	chr15:72551194-72551195	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs549743650	chr15:72551257-72551258	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561554385	chr15:72551274-72551275	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs139964433	chr15:72551342-72551343	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs550530008	chr15:72551371-72551372	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189880962	chr15:72551448-72551449	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs7161909	chr15:72551480-72551481	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs551296393	chr15:72551508-72551509	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566286684	chr15:72551517-72551518	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs180680280	chr15:72551530-72551531	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556614756	chr15:72551590-72551591	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11637611	chr15:72551712-72551713	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs567209909	chr15:72551731-72551732	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs537873240	chr15:72551752-72551753	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Autism	20678247	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	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
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72524800-72551400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:72530400-72563400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:72530800-72561200	Strong transcription	Adipose Nuclei	Adipose
4	chr15:72531000-72562400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr15:72531000-72563000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr15:72531000-72563000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr15:72531000-72563400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr15:72531200-72562800	Strong transcription	Fetal Muscle Leg	muscle
9	chr15:72531800-72561400	Strong transcription	Stomach Smooth Muscle	stomach
10	chr15:72532000-72562600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr15:72532200-72561000	Strong transcription	Liver	Liver
12	chr15:72532200-72561000	Strong transcription	Fetal Intestine Large	intestine
13	chr15:72532200-72561600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr15:72532200-72562200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:72532200-72563000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr15:72532400-72562600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr15:72532600-72562200	Strong transcription	Brain Anterior Caudate	brain
18	chr15:72532600-72562800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr15:72532800-72563000	Strong transcription	HSMM	muscle
20	chr15:72533000-72562000	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr15:72533200-72562400	Strong transcription	Hela-S3	cervix
22	chr15:72533200-72562600	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr15:72536600-72564000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr15:72537200-72564200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr15:72537600-72563400	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr15:72538600-72561200	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr15:72538800-72562000	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr15:72539000-72562200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr15:72539200-72550200	Strong transcription	Fetal Stomach	stomach
30	chr15:72539200-72556600	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr15:72539200-72562200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr15:72539400-72553400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr15:72539400-72561200	Strong transcription	Left Ventricle	heart
34	chr15:72539400-72561600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr15:72539400-72562600	Strong transcription	Osteobl	bone
36	chr15:72539600-72561200	Strong transcription	Brain Germinal Matrix	brain
37	chr15:72539600-72562800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr15:72539800-72562800	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr15:72540200-72560000	Strong transcription	Rectal Mucosa Donor 31	rectum
40	chr15:72540200-72561400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
41	chr15:72540200-72561600	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr15:72540200-72561600	Strong transcription	HSMMtube	muscle
43	chr15:72540200-72562800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr15:72540200-72563200	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr15:72540400-72556600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr15:72540400-72560600	Strong transcription	Ovary	ovary
47	chr15:72540400-72561000	Strong transcription	Fetal Lung	lung
48	chr15:72540400-72561600	Strong transcription	Placenta Amnion	Placenta Amnion
49	chr15:72540400-72562800	Strong transcription	A549	lung
50	chr15:72540400-72563400	Strong transcription	Fetal Muscle Trunk	muscle

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