Variant report

Variant	esv1843215
Chromosome Location	chr15:34666802-34867469
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1815)
CpG islands
(count:1832)
Chromatin interactive
region (count:37)
LncRNA
region (count:12)
Mature miRNA
region (count: 4)
miRNA target
sites (count:2)

(count:1815 , 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	chr15:34781246-34781587	K562	blood:	n/a	n/a
2	ARID3A	chr15:34731584-34731600	K562	blood:	n/a	n/a
3	ATF1	chr15:34808283-34808324	K562	blood:	n/a	n/a
4	ATF1	chr15:34807442-34807640	K562	blood:	n/a	n/a
5	ATF1	chr15:34761374-34761389	K562	blood:	n/a	n/a
6	ATF3	chr15:34781262-34781502	K562	blood:	n/a	n/a
7	BACH1	chr15:34806578-34807213	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:34729369-34729390	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr15:34842337-34842744	GM12878	blood:	n/a	n/a
10	BATF	chr15:34696017-34696728	GM12878	blood:	n/a	n/a
11	BATF	chr15:34808073-34808311	GM12878	blood:	n/a	n/a
12	BATF	chr15:34696116-34696523	GM12878	blood:	n/a	n/a
13	BATF	chr15:34842238-34842949	GM12878	blood:	n/a	n/a
14	BATF	chr15:34815930-34816436	GM12878	blood:	n/a	n/a
15	BATF	chr15:34762243-34762455	GM12878	blood:	n/a	n/a
16	BATF	chr15:34695261-34695641	GM12878	blood:	n/a	n/a
17	BATF	chr15:34841482-34841862	GM12878	blood:	n/a	n/a
18	BATF	chr15:34841508-34841849	GM12878	blood:	n/a	n/a
19	BATF	chr15:34695287-34695628	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:34696015-34696513	GM12878	blood:	n/a	n/a
21	BCL11A	chr15:34816077-34816245	GM12878	blood:	n/a	chr15:34816149-34816162
22	BCL11A	chr15:34842236-34842734	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:34841554-34841859	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:34695333-34695638	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:34729008-34729495	GM12878	blood:	n/a	chr15:34729354-34729367 chr15:34729445-34729458
26	BCLAF1	chr15:34729841-34730371	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:34806518-34806718	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:34781166-34781584	K562	blood:	n/a	n/a
29	BHLHE40	chr15:34804947-34805071	K562	blood:	n/a	chr15:34805006-34805019 chr15:34805002-34805023
30	BHLHE40	chr15:34729075-34729345	K562	blood:	n/a	n/a
31	BHLHE40	chr15:34806536-34807767	K562	blood:	n/a	chr15:34807373-34807389 chr15:34806722-34806738
32	BHLHE40	chr15:34754120-34754185	K562	blood:	n/a	n/a
33	BHLHE40	chr15:34728512-34728697	K562	blood:	n/a	n/a
34	BHLHE40	chr15:34729879-34730508	K562	blood:	n/a	n/a
35	BHLHE40	chr15:34807389-34807610	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:34729903-34730377	HepG2	liver:	n/a	n/a
37	BHLHE40	chr15:34807981-34808415	GM12878	blood:	n/a	n/a
38	BHLHE40	chr15:34729886-34730498	GM12878	blood:	n/a	n/a
39	BHLHE40	chr15:34806954-34807627	HepG2	liver:	n/a	chr15:34807373-34807389
40	BHLHE40	chr15:34808048-34808404	K562	blood:	n/a	n/a
41	CBX3	chr15:34729841-34730369	K562	blood:	n/a	n/a
42	CBX3	chr15:34781179-34781807	K562	blood:	n/a	n/a
43	CBX3	chr15:34729907-34730280	HCT-116	colon:	n/a	n/a
44	CBX3	chr15:34729889-34730257	K562	blood:	n/a	n/a
45	CBX3	chr15:34732091-34732455	K562	blood:	n/a	n/a
46	CBX3	chr15:34807187-34807674	K562	blood:	n/a	n/a
47	CCNT2	chr15:34729140-34729519	K562	blood:	n/a	n/a
48	CCNT2	chr15:34729860-34730211	K562	blood:	n/a	n/a
49	CCNT2	chr15:34806457-34807498	K562	blood:	n/a	chr15:34806756-34806765
50	CEBPB	chr15:34735109-34735561	K562	blood:	n/a	n/a

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34727209-34727259	RPTEC	kidney:	n/a
2	chr15:34817982-34818032	HEEpiC	esophagus:	n/a
3	chr15:34727209-34727259	RPTEC	kidney:	n/a
4	chr15:34817982-34818032	HEEpiC	esophagus:	n/a
5	chr15:34729310-34729360	K562	blood:	n/a
6	chr15:34730071-34730121	AG09319	gingival:	n/a
7	chr15:34786594-34786644	MCF-7	breast:	n/a
8	chr15:34781705-34781755	GM12878	blood:	n/a
9	chr15:34729026-34729076	GM06990	blood:	n/a
10	chr15:34817982-34818032	AG10803	skin:	n/a
11	chr15:34785380-34785430	IMR90	lung:	fetal
12	chr15:34807050-34807100	HPAEpiC	pulmonary alveolar:	n/a
13	chr15:34671426-34671476	HRE	kidney:	n/a
14	chr15:34729310-34729360	NH-A	brain:	n/a
15	chr15:34807143-34807193	NH-A	brain:	n/a
16	chr15:34788017-34788067	Jurkat	blood:	n/a
17	chr15:34700272-34700322	GM19239	blood:	n/a
18	chr15:34807050-34807100	GM12892	blood:	n/a
19	chr15:34806592-34806642	H1-hESC	embryonic stem cell:	embryo
20	chr15:34791564-34791614	NHDF-neo	bronchial:	n/a
21	chr15:34806592-34806642	HRPEpiC	eye:	n/a
22	chr15:34781969-34782019	AG04449	skin:	fetal
23	chr15:34807679-34807729	HL-60	blood:	n/a
24	chr15:34781969-34782019	HEEpiC	esophagus:	n/a
25	chr15:34806349-34806399	NT2-D1	testis:	n/a
26	chr15:34807050-34807100	GM06990	blood:	n/a
27	chr15:34787420-34787470	HEK293	kidney:	embryo
28	chr15:34807679-34807729	NT2-D1	testis:	n/a
29	chr15:34807221-34807271	HMEC	breast:	n/a
30	chr15:34788847-34788897	Hela-S3	cervix:	n/a
31	chr15:34729026-34729076	Caco-2	colon:	n/a
32	chr15:34781705-34781755	HCPEpiC	choroid plexus:	n/a
33	chr15:34781891-34781941	HCT-116	colon:	n/a
34	chr15:34671426-34671476	AG09309	skin:	n/a
35	chr15:34787920-34787970	Caco-2	colon:	n/a
36	chr15:34782820-34782870	NHBE	bronchial:	n/a
37	chr15:34791564-34791614	SK-N-SH	brain:	n/a
38	chr15:34807679-34807729	HCPEpiC	choroid plexus:	n/a
39	chr15:34788847-34788897	SK-N-SH_RA	brain:	n/a
40	chr15:34785380-34785430	PFSK-1	brain:	n/a
41	chr15:34782167-34782217	H1-hESC	embryonic stem cell:	embryo
42	chr15:34785380-34785430	PrEC	prostate:	n/a
43	chr15:34700272-34700322	NT2-D1	testis:	n/a
44	chr15:34781705-34781755	HNPCEpiC	eye:	n/a
45	chr15:34782167-34782217	HCM	heart:	n/a
46	chr15:34807679-34807729	AG04450	lung:	fetal
47	chr15:34787920-34787970	HCPEpiC	choroid plexus:	n/a
48	chr15:34786594-34786644	NT2-D1	testis:	n/a
49	chr15:34787920-34787970	T-47D	breast:	n/a
50	chr15:34788017-34788067	AG10803	skin:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:34633931..34636680-chr15:34728775..34730381,2	K562	blood:
2	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
3	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
4	chr15:34728066..34730668-chr15:34791069..34792682,2	K562	blood:
5	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:
6	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
7	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
8	chr15:34727667..34729400-chr15:34875206..34876777,2	K562	blood:
9	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
10	chr15:34786054..34786721-chr7:5632299..5632821,2	HCT-116	colon:
11	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
12	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
13	chr15:34761476..34764376-chr15:34768521..34770931,2	K562	blood:
14	chr15:34658214..34660711-chr15:34806608..34809602,2	K562	blood:
15	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
16	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
17	chr15:34728131..34733225-chr15:34735717..34740218,7	K562	blood:
18	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
19	chr15:34655711..34662054-chr15:34662110..34667087,9	K562	blood:
20	chr15:34786049..34786720-chr7:5632277..5632906,2	NB4	blood:
21	chr15:34720616..34722466-chr15:34725764..34728714,2	K562	blood:
22	chr15:34727581..34729084-chr15:34874171..34876472,2	MCF-7	breast:
23	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
24	chr15:34762215..34765168-chr15:34878877..34880750,2	K562	blood:
25	chr15:34726561..34729987-chr15:34871215..34874723,3	K562	blood:
26	chr15:34729318..34730097-chr5:1799590..1800354,2	Hela-S3	cervix:
27	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
28	chr15:34728531..34731203-chr15:34733693..34737649,5	K562	blood:
29	chr15:34500776..34502841-chr15:34668848..34671428,2	K562	blood:
30	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
31	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
32	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
33	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
34	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
35	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
36	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
37	chr15:34761476..34764376-chr15:34768521..34770931,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJD2-4	chr15:34843392-34843477	NONHSAT140232
2	lnc-GJD2-4	chr15:34845096-34845292	NONHSAT140232
3	lnc-GOLGA8B-1	chr15:34752685-34752950	uc_384_-
4	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT140232
5	lnc-GJD2-4	chr15:34867026-34867115	NONHSAT041596
6	lnc-LPCAT4-1	chr15:34698878-34699071	NONHSAT041586
7	lnc-LPCAT4-1	chr15:34720816-34721126	NONHSAT041586
8	lnc-GJD2-4	chr15:34845174-34845292	NONHSAT041596
9	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT041596
10	lnc-GJD2-3	chr15:34858091-34858674	NONHSAT041597
11	lnc-LPCAT4-1	chr15:34699777-34699936	NONHSAT041586
12	lnc-C15orf55-4	chr15:34752685-34752950	uc_384_+

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1233-3p	chr15:34674270-34674289	MIMAT0005588
hsa-miR-1233-5p	chr15:34820548-34820569	MIMAT0022943_1
hsa-miR-1233-3p	chr15:34820491-34820510	MIMAT0005588_1
hsa-miR-1233-5p	chr15:34674327-34674348	MIMAT0022943

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGA8B	hsa-miR-15a-5p	chr15:34817527-34817548
2	GOLGA8B	hsa-miR-32-5p	chr15:34818291-34818311

Variant related genes	Relation type
MIR1233-1	TF binding region
ENSG00000261081	TF binding region
ENSG00000261559	TF binding region
MIR1233-2	TF binding region
ENSG00000259892	TF binding region
ENSG00000260639	TF binding region
ENSG00000259904	TF binding region
GOLGA8A	TF binding region
HNRNPLP2	TF binding region
GOLGA8B	TF binding region
ENSG00000266205	TF binding region
MIR1233-1	CpG island
ENSG00000261081	CpG island
ENSG00000261559	CpG island
MIR1233-2	CpG island
ENSG00000259892	CpG island
ENSG00000260639	CpG island
ENSG00000259904	CpG island
GOLGA8A	CpG island
HNRNPLP2	CpG island
GOLGA8B	CpG island
ENSG00000266205	CpG island
ENSG00000075618	chromatin interactions
ENSG00000184507	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000259917	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000171421	chromatin interactions
ENSG00000134152	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000176454	chromatin interactions

Extended variants
information (count: 5286 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:5286 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143472194	chr15:34666805-34666806	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs181507009	chr15:34666858-34666859	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs527429229	chr15:34666865-34666866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7164447	chr15:34666869-34666870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs4299124	chr15:34666870-34666871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs11401952	chr15:34666894-34666895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs398099717	chr15:34666895-34666896	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs4357912	chr15:34667016-34667017	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs4502190	chr15:34667028-34667029	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs184110750	chr15:34667039-34667040	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs76969626	chr15:34667070-34667071	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs4265776	chr15:34667075-34667076	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs188458557	chr15:34667161-34667162	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs539878184	chr15:34667164-34667165	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs75277966	chr15:34667181-34667182	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs78018012	chr15:34667331-34667332	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
17	rs12161976	chr15:34667347-34667348	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs57196965	chr15:34667377-34667378	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs538266087	chr15:34667382-34667383	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs144506423	chr15:34667384-34667385	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs201070957	chr15:34667385-34667386	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs77501756	chr15:34667398-34667399	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
23	rs565858348	chr15:34667437-34667438	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs201405825	chr15:34667451-34667452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9635383	chr15:34667452-34667453	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs77918030	chr15:34667494-34667495	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
27	rs369162171	chr15:34667497-34667498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545836963	chr15:34667525-34667526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564042052	chr15:34667532-34667533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531918589	chr15:34667540-34667541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549988769	chr15:34667594-34667595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568409737	chr15:34667603-34667604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180989140	chr15:34667628-34667629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185805709	chr15:34667735-34667736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78104802	chr15:34667754-34667755	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs199512002	chr15:34667763-34667764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12161941	chr15:34667766-34667767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376630066	chr15:34667767-34667768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539474264	chr15:34667768-34667769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372172421	chr15:34667779-34667780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371234693	chr15:34667780-34667781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376489604	chr15:34667781-34667782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373637932	chr15:34667782-34667783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368991596	chr15:34667784-34667785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs59214229	chr15:34667787-34667788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375699008	chr15:34667790-34667791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs202224040	chr15:34667794-34667795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371010874	chr15:34667796-34667797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375648195	chr15:34667810-34667811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375377688	chr15:34667811-34667812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1389 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34660400-34668600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:34660600-34668000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr15:34660800-34674200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr15:34660800-34674400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:34660800-34674400	Weak transcription	Fetal Lung	lung
6	chr15:34660800-34674800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr15:34661000-34671800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr15:34661000-34673800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr15:34661000-34678000	Weak transcription	Primary T cells from cord blood	blood
10	chr15:34661200-34679600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:34661200-34680800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr15:34661400-34672800	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr15:34661600-34674600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr15:34662600-34675400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr15:34662800-34667400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr15:34662800-34723600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr15:34663000-34674800	Weak transcription	GM12878-XiMat	blood
18	chr15:34663400-34674600	Weak transcription	HSMM	muscle
19	chr15:34665400-34675200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr15:34666000-34667000	Enhancers	Esophagus	oesophagus
21	chr15:34666000-34674600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr15:34666600-34667200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr15:34666800-34667600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr15:34666800-34674200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:34667000-34672800	Weak transcription	Esophagus	oesophagus
26	chr15:34667200-34691600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr15:34667400-34674600	Weak transcription	Adipose Nuclei	Adipose
28	chr15:34668400-34668600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr15:34668600-34668800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr15:34668600-34668800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr15:34668600-34669000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr15:34668600-34669000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr15:34668800-34669000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
34	chr15:34668800-34669000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr15:34668800-34669000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr15:34669400-34673800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr15:34669600-34674800	Weak transcription	Brain Hippocampus Middle	brain
38	chr15:34670000-34672600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:34670600-34674800	Weak transcription	Ovary	ovary
40	chr15:34670800-34674600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr15:34671200-34673600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr15:34671800-34672200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr15:34671800-34672200	Enhancers	Fetal Heart	heart
44	chr15:34672000-34680400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr15:34672200-34675600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr15:34672600-34673400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr15:34672800-34673000	Enhancers	Esophagus	oesophagus
48	chr15:34672800-34673000	Enhancers	Left Ventricle	heart
49	chr15:34672800-34673200	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr15:34673000-34675200	Weak transcription	Left Ventricle	heart

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