Variant report

Variant	nsv904190
Chromosome Location	chr15:45892672-45960897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1838)
CpG islands
(count:1162)
Chromatin interactive
region (count:78)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:1838 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45940982-45941313	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:45947081-45947129	K562	blood:	n/a	n/a
3	ARID3A	chr15:45906466-45906752	K562	blood:	n/a	n/a
4	ARID3A	chr15:45929838-45930064	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:45933053-45934166	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:45927581-45927944	HepG2	liver:	n/a	n/a
7	ATF1	chr15:45929927-45930186	K562	blood:	n/a	n/a
8	ATF2	chr15:45929595-45930236	GM12878	blood:	n/a	n/a
9	ATF2	chr15:45898535-45898968	GM12878	blood:	n/a	n/a
10	ATF3	chr15:45933529-45934026	A549	lung:	n/a	n/a
11	ATF3	chr15:45933511-45933985	A549	lung:	n/a	n/a
12	BACH1	chr15:45926652-45927051	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:45927520-45927822	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr15:45898623-45898950	GM12878	blood:	n/a	chr15:45898757-45898768
15	BATF	chr15:45929665-45930062	GM12878	blood:	n/a	chr15:45929752-45929761
16	BCL3	chr15:45937705-45938213	A549	lung:	n/a	n/a
17	BCL3	chr15:45933471-45934112	A549	lung:	n/a	n/a
18	BCL3	chr15:45926702-45927242	A549	lung:	n/a	chr15:45926874-45926882 chr15:45927118-45927131
19	BCL3	chr15:45926885-45927432	GM12878	blood:	n/a	chr15:45927118-45927131
20	BCL3	chr15:45933382-45934078	A549	lung:	n/a	n/a
21	BCLAF1	chr15:45926899-45927741	GM12878	blood:	n/a	chr15:45927118-45927131
22	BCLAF1	chr15:45929647-45930164	GM12878	blood:	n/a	chr15:45929889-45929898
23	BCLAF1	chr15:45929678-45930152	GM12878	blood:	n/a	chr15:45929889-45929898
24	BHLHE40	chr15:45906491-45906774	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:45926758-45927200	HepG2	liver:	n/a	n/a
26	BHLHE40	chr15:45929697-45930207	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:45926868-45927890	GM12878	blood:	n/a	chr15:45927409-45927425
28	BRCA1	chr15:45927157-45927272	HepG2	liver:	n/a	n/a
29	BRCA1	chr15:45926717-45927897	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr15:45926746-45926825	HepG2	liver:	n/a	n/a
31	BRCA1	chr15:45929853-45930011	GM12878	blood:	n/a	n/a
32	CBX3	chr15:45932687-45933203	HCT-116	colon:	n/a	n/a
33	CCNT2	chr15:45926887-45927087	K562	blood:	n/a	n/a
34	CEBPB	chr15:45898672-45898925	IMR90	lung:	n/a	n/a
35	CEBPB	chr15:45926688-45927169	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr15:45926726-45927093	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:45926741-45927094	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr15:45929767-45930296	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr15:45946343-45946474	HepG2	liver:	n/a	chr15:45946389-45946400 chr15:45946389-45946402 chr15:45946389-45946402
40	CEBPB	chr15:45933591-45934058	MCF-7	breast:	n/a	chr15:45933772-45933785 chr15:45933772-45933783
41	CEBPB	chr15:45933474-45934015	HepG2	liver:	n/a	chr15:45933772-45933785 chr15:45933772-45933783
42	CEBPB	chr15:45933540-45934027	Hela-S3	cervix:	n/a	chr15:45933772-45933785 chr15:45933772-45933783
43	CEBPB	chr15:45933352-45934239	A549	lung:	n/a	chr15:45933772-45933785 chr15:45933772-45933783
44	CEBPB	chr15:45937526-45937900	HepG2	liver:	n/a	n/a
45	CEBPB	chr15:45941177-45941419	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:45937591-45937846	K562	blood:	n/a	n/a
47	CEBPB	chr15:45932742-45933148	IMR90	lung:	n/a	n/a
48	CEBPB	chr15:45933456-45934070	A549	lung:	n/a	chr15:45933772-45933785 chr15:45933772-45933783
49	CEBPB	chr15:45937532-45937896	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr15:45929657-45930205	IMR90	lung:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45926878-45926928	PFSK-1	brain:	n/a
2	chr15:45927086-45927136	NHDF-neo	bronchial:	n/a
3	chr15:45927050-45927100	HPAEpiC	pulmonary alveolar:	n/a
4	chr15:45926878-45926928	PFSK-1	brain:	n/a
5	chr15:45927086-45927136	NHDF-neo	bronchial:	n/a
6	chr15:45927050-45927100	HPAEpiC	pulmonary alveolar:	n/a
7	chr15:45927012-45927062	HCM	heart:	n/a
8	chr15:45929860-45929910	HRE	kidney:	n/a
9	chr15:45927123-45927173	Hepatocyte	liver:	n/a
10	chr15:45927126-45927176	RPTEC	kidney:	n/a
11	chr15:45927554-45927604	SK-N-SH_RA	brain:	n/a
12	chr15:45929860-45929910	HCPEpiC	choroid plexus:	n/a
13	chr15:45943467-45943517	HepG2	liver:	n/a
14	chr15:45927554-45927604	NH-A	brain:	n/a
15	chr15:45932303-45932353	HEK293	kidney:	embryo
16	chr15:45927123-45927173	NH-A	brain:	n/a
17	chr15:45952725-45952775	AG10803	skin:	n/a
18	chr15:45937757-45937807	HIPEpiC	eye:	n/a
19	chr15:45937757-45937807	NHBE	bronchial:	n/a
20	chr15:45900639-45900689	GM12891	blood:	n/a
21	chr15:45927123-45927173	HRE	kidney:	n/a
22	chr15:45927554-45927604	HepG2	liver:	n/a
23	chr15:45927255-45927305	HNPCEpiC	eye:	n/a
24	chr15:45929860-45929910	SAEC	small airway:	n/a
25	chr15:45927050-45927100	SK-N-SH_RA	brain:	n/a
26	chr15:45952725-45952775	HepG2	liver:	n/a
27	chr15:45927921-45927971	HCPEpiC	choroid plexus:	n/a
28	chr15:45943467-45943517	NB4	blood:	n/a
29	chr15:45927012-45927062	AG09319	gingival:	n/a
30	chr15:45937757-45937807	LNCaP	prostate:	n/a
31	chr15:45932303-45932353	SK-N-SH	brain:	n/a
32	chr15:45927123-45927173	PANC-1	pancreas:	n/a
33	chr15:45900639-45900689	SK-N-SH_RA	brain:	n/a
34	chr15:45926780-45926830	GM06990	blood:	n/a
35	chr15:45927123-45927173	SAEC	small airway:	n/a
36	chr15:45932303-45932353	A549	lung:	n/a
37	chr15:45927255-45927305	AG09309	skin:	n/a
38	chr15:45943467-45943517	HEEpiC	esophagus:	n/a
39	chr15:45926780-45926830	PANC-1	pancreas:	n/a
40	chr15:45927921-45927971	PFSK-1	brain:	n/a
41	chr15:45924140-45924190	GM06990	blood:	n/a
42	chr15:45927126-45927176	GM06990	blood:	n/a
43	chr15:45927255-45927305	AoSMC	blood vessel:	n/a
44	chr15:45927086-45927136	PrEC	prostate:	n/a
45	chr15:45943467-45943517	GM12878	blood:	n/a
46	chr15:45943467-45943517	PFSK-1	brain:	n/a
47	chr15:45937757-45937807	HepG2	liver:	n/a
48	chr15:45926780-45926830	GM12878	blood:	n/a
49	chr15:45927218-45927268	HRE	kidney:	n/a
50	chr15:45932303-45932353	GM12878	blood:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:45927082..45927744-chr20:42085983..42086651,2	Hela-S3	cervix:
2	chr15:45923721..45925487-chr15:45925745..45928411,3	MCF-7	breast:
3	chr15:45877908..45881944-chr15:45926466..45928753,3	MCF-7	breast:
4	chr15:45722770..45723742-chr15:45906160..45907111,2	MCF-7	breast:
5	chr15:45926784..45929101-chr15:45955336..45958856,3	MCF-7	breast:
6	chr15:45457952..45460656-chr15:45900362..45903240,2	K562	blood:
7	chr1:144533680..144534341-chr15:45927018..45927807,2	Hela-S3	cervix:
8	chr15:45879090..45880889-chr15:45903152..45905270,2	K562	blood:
9	chr12:120729194..120729832-chr15:45926249..45927245,2	Hela-S3	cervix:
10	chr15:45911053..45913537-chr15:45922181..45923924,2	MCF-7	breast:
11	chr15:45692929..45695674-chr15:45926950..45929580,2	MCF-7	breast:
12	chr15:45940658..45942644-chr15:45946028..45948330,2	MCF-7	breast:
13	chr15:45815036..45815573-chr15:45903214..45904130,2	MCF-7	breast:
14	chr15:45931549..45933106-chr15:45935286..45937099,2	K562	blood:
15	chr15:45926716..45927538-chr3:169490885..169491684,2	Hela-S3	cervix:
16	chr15:45932766..45934482-chr15:45951327..45953164,2	MCF-7	breast:
17	chr15:45895546..45897491-chr15:45899127..45901340,2	K562	blood:
18	chr15:45940658..45942644-chr15:45946028..45948330,2	MCF-7	breast:
19	chr15:45927181..45929961-chr15:45939240..45941307,2	MCF-7	breast:
20	chr15:45926600..45927530-chr17:43393928..43394568,2	Hela-S3	cervix:
21	chr15:45934455..45936874-chr15:45938212..45940753,2	MCF-7	breast:
22	chr15:45927045..45928027-chr3:23958538..23959122,2	Hela-S3	cervix:
23	chr15:45880183..45881884-chr15:45892162..45895627,3	K562	blood:
24	chr15:45926667..45927553-chr5:149736913..149737832,2	Hela-S3	cervix:
25	chr15:45933052..45935436-chr15:45937380..45939217,2	K562	blood:
26	chr15:45899647..45900569-chr8:125884333..125885038,2	MCF-7	breast:
27	chr15:45945911..45948903-chr15:45960461..45962658,2	MCF-7	breast:
28	chr15:45895546..45897491-chr15:45899127..45901340,2	K562	blood:
29	chr15:45914454..45916102-chr15:45918794..45920610,2	K562	blood:
30	chr15:45750278..45751893-chr15:45902815..45904079,5	MCF-7	breast:
31	chr15:45749872..45750821-chr15:45905552..45906324,3	MCF-7	breast:
32	chr15:45879487..45881858-chr15:45891954..45893662,2	K562	blood:
33	chr15:45884544..45886810-chr15:45890101..45892721,2	K562	blood:
34	chr15:45749851..45751603-chr15:45905582..45907231,11	MCF-7	breast:
35	chr15:45951100..45953645-chr15:45956649..45958912,2	MCF-7	breast:
36	chr15:45927063..45929876-chr15:45998234..45999862,2	MCF-7	breast:
37	chr15:45749355..45751225-chr15:45902815..45904257,10	K562	blood:
38	chr15:45927252..45928181-chr2:70313986..70314551,2	Hela-S3	cervix:
39	chr15:45750222..45752081-chr15:45903810..45905357,2	MCF-7	breast:
40	chr15:45936300..45938060-chr15:45941234..45942847,2	MCF-7	breast:
41	chr15:45722138..45723083-chr15:45906168..45907021,2	MCF-7	breast:
42	chr15:45750024..45753283-chr15:45906121..45908328,3	K562	blood:
43	chr1:190088571..190089071-chr15:45927030..45927668,2	Hela-S3	cervix:
44	chr15:45926989..45927548-chrX:153625673..153626604,2	Hela-S3	cervix:
45	chr15:45750663..45751216-chr15:45906499..45907103,2	MCF-7	breast:
46	chr15:45908544..45910284-chr15:45911212..45913714,2	K562	blood:
47	chr15:45931689..45934379-chr15:45936432..45937938,2	MCF-7	breast:
48	chr15:45736069..45742318-chr15:45926037..45929619,6	MCF-7	breast:
49	chr15:45884792..45886658-chr15:45905385..45908007,2	MCF-7	breast:
50	chr15:45908544..45910284-chr15:45911212..45913714,2	K562	blood:

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PLDN	hsa-miR-101-3p	chr15:45901308-45901314
2	PLDN	hsa-miR-101-3p	chr15:45901295-45901315
3	PLDN	hsa-miR-124-3p	chr15:45898779-45898798
4	PLDN	hsa-miR-124-3p	chr15:45898791-45898798
5	PLDN	hsa-miR-30b-5p	chr15:45900177-45900196

Variant related genes	Relation type
SQRDL	TF binding region
SQRDL	CpG island
ENSG00000259354	chromatin interactions
ENSG00000174748	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000166920	chromatin interactions
ENSG00000265181	chromatin interactions
ENSG00000085274	chromatin interactions
ENSG00000070814	chromatin interactions
ENSG00000259539	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000148400	chromatin interactions
ENSG00000124193	chromatin interactions
ENSG00000197299	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000211519	chromatin interactions
ENSG00000172663	chromatin interactions
ENSG00000165119	chromatin interactions
ENSG00000252285	chromatin interactions
ENSG00000237886	chromatin interactions
ENSG00000179818	chromatin interactions
ENSG00000006062	chromatin interactions
ENSG00000171763	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000104164	chromatin interactions
ENSG00000137767	chromatin interactions
ENSG00000260170	chromatin interactions
ENSG00000178966	chromatin interactions
ENSG00000171766	chromatin interactions

Extended variants
information (count: 2605 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2605 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8025600	chr15:45892672-45892673	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186873359	chr15:45892735-45892736	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554208950	chr15:45892748-45892749	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs367765637	chr15:45892754-45892755	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs59593563	chr15:45892835-45892836	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs563442042	chr15:45892840-45892841	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs73420441	chr15:45892909-45892910	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs117544584	chr15:45892919-45892920	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575924883	chr15:45892928-45892929	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs541683235	chr15:45892952-45892953	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs375545947	chr15:45892957-45892958	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs191714308	chr15:45893015-45893016	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369266803	chr15:45893046-45893047	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs564193101	chr15:45893055-45893056	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs533089869	chr15:45893222-45893223	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145101567	chr15:45893248-45893249	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569706951	chr15:45893340-45893341	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528904382	chr15:45893352-45893353	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs138977922	chr15:45893375-45893376	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs568680734	chr15:45893429-45893430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs117862306	chr15:45893452-45893453	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs554102038	chr15:45893453-45893454	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs571734948	chr15:45893499-45893500	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs79988995	chr15:45893536-45893537	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532630623	chr15:45893550-45893551	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs78411719	chr15:45893575-45893576	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs556250591	chr15:45893585-45893586	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs575984199	chr15:45893648-45893649	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs541883191	chr15:45893673-45893674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141561249	chr15:45893683-45893684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547958143	chr15:45893817-45893818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572285233	chr15:45893835-45893836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs202125344	chr15:45893845-45893846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183061069	chr15:45893871-45893872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76297143	chr15:45893898-45893899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533049934	chr15:45893926-45893927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188096273	chr15:45893954-45893955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150909026	chr15:45893982-45893983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536261624	chr15:45894023-45894024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190792480	chr15:45894047-45894048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138580678	chr15:45894065-45894066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368359654	chr15:45894066-45894067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570277316	chr15:45894080-45894081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550970604	chr15:45894088-45894089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182352953	chr15:45894121-45894122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528003322	chr15:45894183-45894184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547965209	chr15:45894230-45894231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548467728	chr15:45894250-45894251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539649380	chr15:45894252-45894253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186607098	chr15:45894266-45894267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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

Chromatin state (count:2543 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45880400-45900400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:45881000-45900200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr15:45881000-45908600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr15:45881000-45908800	Weak transcription	Esophagus	oesophagus
5	chr15:45881200-45895800	Weak transcription	Spleen	Spleen
6	chr15:45881200-45898000	Weak transcription	Pancreas	Pancrea
7	chr15:45881200-45899800	Weak transcription	Small Intestine	intestine
8	chr15:45881200-45900200	Weak transcription	Colonic Mucosa	Colon
9	chr15:45881200-45900200	Weak transcription	Gastric	stomach
10	chr15:45881200-45909000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr15:45881400-45898200	Weak transcription	HSMMtube	muscle
12	chr15:45881600-45901800	Weak transcription	Psoas Muscle	Psoas
13	chr15:45881800-45896400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:45881800-45896800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr15:45881800-45898000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr15:45881800-45898200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr15:45881800-45903400	Weak transcription	Brain Substantia Nigra	brain
18	chr15:45881800-45904800	Weak transcription	NHEK	skin
19	chr15:45882000-45908600	Weak transcription	NHLF	lung
20	chr15:45882200-45898200	Weak transcription	HSMM	muscle
21	chr15:45883000-45898600	Weak transcription	NHDF-Ad	bronchial
22	chr15:45883000-45899000	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr15:45883400-45898000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr15:45884000-45896400	Weak transcription	Brain Angular Gyrus	brain
25	chr15:45884000-45898600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr15:45884400-45901200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr15:45884600-45900800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr15:45884800-45902200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr15:45885000-45899000	Weak transcription	Rectal Smooth Muscle	rectum
30	chr15:45885000-45902400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr15:45885200-45896600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr15:45885200-45898600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr15:45886000-45897800	Weak transcription	Colon Smooth Muscle	Colon
34	chr15:45886200-45898200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr15:45886200-45898600	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr15:45886800-45898000	Weak transcription	HUVEC	blood vessel
37	chr15:45886800-45898200	Weak transcription	Osteobl	bone
38	chr15:45887400-45895600	Weak transcription	Left Ventricle	heart
39	chr15:45887400-45902200	Weak transcription	Fetal Brain Male	brain
40	chr15:45887600-45896200	Weak transcription	NH-A	brain
41	chr15:45887600-45898000	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr15:45887600-45898200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr15:45887600-45900600	Weak transcription	HMEC	breast
44	chr15:45888600-45893000	Weak transcription	Ovary	ovary
45	chr15:45888600-45898000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr15:45888600-45898200	Weak transcription	Lung	lung
47	chr15:45888600-45899400	Weak transcription	Right Ventricle	heart
48	chr15:45888800-45896800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr15:45888800-45904800	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr15:45889000-45894200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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