Variant report

Variant	esv1794722
Chromosome Location	chr10:89690827-89725294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:89691648-89691960	K562	blood:	n/a	n/a
2	ARID3A	chr10:89715977-89716066	HepG2	liver:	n/a	n/a
3	ATF1	chr10:89691662-89691909	K562	blood:	n/a	n/a
4	ATF2	chr10:89690977-89691901	GM12878	blood:	n/a	n/a
5	ATF2	chr10:89690821-89691719	GM12878	blood:	n/a	n/a
6	ATF3	chr10:89699280-89699454	K562	blood:	n/a	n/a
7	BACH1	chr10:89708379-89708697	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:89708352-89708593	K562	blood:	n/a	n/a
9	BATF	chr10:89691222-89691524	GM12878	blood:	n/a	n/a
10	BATF	chr10:89691207-89691590	GM12878	blood:	n/a	n/a
11	BCL3	chr10:89691208-89691611	GM12878	blood:	n/a	n/a
12	BCL3	chr10:89719899-89720474	A549	lung:	n/a	n/a
13	BCLAF1	chr10:89706486-89707437	GM12878	blood:	n/a	n/a
14	BCLAF1	chr10:89705531-89706248	GM12878	blood:	n/a	n/a
15	CBX3	chr10:89708370-89708575	K562	blood:	n/a	n/a
16	CBX3	chr10:89708342-89708646	K562	blood:	n/a	n/a
17	CEBPB	chr10:89712397-89712785	A549	lung:	n/a	chr10:89712582-89712593
18	CEBPB	chr10:89709444-89709628	IMR90	lung:	n/a	n/a
19	CEBPB	chr10:89692598-89692923	K562	blood:	n/a	chr10:89692767-89692778 chr10:89692620-89692633
20	CEBPB	chr10:89712426-89712793	A549	lung:	n/a	chr10:89712582-89712593
21	CEBPB	chr10:89719951-89720325	A549	lung:	n/a	n/a
22	CEBPB	chr10:89696721-89696941	K562	blood:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
23	CEBPB	chr10:89696650-89696923	A549	lung:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
24	CEBPB	chr10:89721117-89721455	A549	lung:	n/a	n/a
25	CEBPB	chr10:89692303-89692476	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:89713859-89714022	MCF-7	breast:	n/a	chr10:89713931-89713942
27	CEBPB	chr10:89720017-89720323	A549	lung:	n/a	n/a
28	CEBPB	chr10:89696622-89696957	IMR90	lung:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
29	CEBPB	chr10:89692215-89692929	IMR90	lung:	n/a	chr10:89692767-89692778 chr10:89692620-89692633
30	CEBPB	chr10:89709528-89709601	K562	blood:	n/a	n/a
31	CEBPB	chr10:89713783-89714100	IMR90	lung:	n/a	chr10:89713931-89713942
32	CEBPB	chr10:89709451-89709611	A549	lung:	n/a	n/a
33	CEBPB	chr10:89712479-89712676	K562	blood:	n/a	chr10:89712582-89712593
34	CEBPB	chr10:89712400-89712823	ECC-1	luminal epithelium:	n/a	chr10:89712582-89712593
35	CEBPB	chr10:89721096-89721476	A549	lung:	n/a	n/a
36	CEBPB	chr10:89713772-89714086	H1-hESC	embryonic stem cell:	n/a	chr10:89713931-89713942
37	CEBPB	chr10:89721108-89721483	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:89713788-89713996	HepG2	liver:	n/a	chr10:89713931-89713942
39	CEBPB	chr10:89712400-89712779	IMR90	lung:	n/a	chr10:89712582-89712593
40	CEBPB	chr10:89712400-89712763	H1-hESC	embryonic stem cell:	n/a	chr10:89712582-89712593
41	CEBPB	chr10:89713810-89714091	K562	blood:	n/a	chr10:89713931-89713942
42	CEBPB	chr10:89692736-89692937	A549	lung:	n/a	chr10:89692767-89692778
43	CEBPB	chr10:89696655-89696952	Hela-S3	cervix:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
44	CEBPB	chr10:89712465-89712696	HepG2	liver:	n/a	chr10:89712582-89712593
45	CEBPB	chr10:89692759-89692786	HepG2	liver:	n/a	chr10:89692767-89692778
46	CEBPB	chr10:89712357-89712802	ECC-1	luminal epithelium:	n/a	chr10:89712582-89712593
47	CEBPB	chr10:89712375-89712819	MCF-7	breast:	n/a	chr10:89712582-89712593
48	CEBPB	chr10:89712384-89712817	MCF-7	breast:	n/a	chr10:89712582-89712593
49	CEBPB	chr10:89712350-89712838	Hela-S3	cervix:	n/a	chr10:89712582-89712593
50	CEBPB	chr10:89695689-89695731	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:89696774-89696824	HRE	kidney:	n/a
2	chr10:89696774-89696824	PANC-1	pancreas:	n/a
3	chr10:89696774-89696824	ProgFib	skin:	n/a
4	chr10:89696774-89696824	GM12878	blood:	n/a
5	chr10:89696774-89696824	GM19239	blood:	n/a
6	chr10:89696774-89696824	Hepatocyte	liver:	n/a
7	chr10:89696774-89696824	GM12892	blood:	n/a
8	chr10:89696774-89696824	BE2_C	brain:	n/a
9	chr10:89696774-89696824	HCPEpiC	choroid plexus:	n/a
10	chr10:89696774-89696824	NHDF-neo	bronchial:	n/a
11	chr10:89696774-89696824	RPTEC	kidney:	n/a
12	chr10:89696774-89696824	HAEpiC	amniotic membrane:	n/a
13	chr10:89696774-89696824	MCF10A-Er-Src	breast:	n/a
14	chr10:89696774-89696824	H1-hESC	embryonic stem cell:	embryo
15	chr10:89696774-89696824	MCF-7	breast:	n/a
16	chr10:89696774-89696824	LNCaP	prostate:	n/a
17	chr10:89696774-89696824	IMR90	lung:	fetal
18	chr10:89696774-89696824	HL-60	blood:	n/a
19	chr10:89696774-89696824	HNPCEpiC	eye:	n/a
20	chr10:89696774-89696824	HCF	heart:	n/a
21	chr10:89696774-89696824	HPAEpiC	pulmonary alveolar:	n/a
22	chr10:89696774-89696824	AG04450	lung:	fetal
23	chr10:89696774-89696824	HepG2	liver:	n/a
24	chr10:89696774-89696824	SK-N-SH	brain:	n/a
25	chr10:89696774-89696824	AG09309	skin:	n/a
26	chr10:89696774-89696824	HMEC	breast:	n/a
27	chr10:89696774-89696824	Jurkat	blood:	n/a
28	chr10:89696774-89696824	GM06990	blood:	n/a
29	chr10:89696774-89696824	HRCEpiC	kidney:	n/a
30	chr10:89696774-89696824	ECC-1	luminal epithelium:	n/a
31	chr10:89696774-89696824	A549	lung:	n/a
32	chr10:89696774-89696824	NT2-D1	testis:	n/a
33	chr10:89696774-89696824	HCT-116	colon:	n/a
34	chr10:89696774-89696824	PFSK-1	brain:	n/a
35	chr10:89696774-89696824	NH-A	brain:	n/a
36	chr10:89696774-89696824	SK-N-SH_RA	brain:	n/a
37	chr10:89696774-89696824	SAEC	small airway:	n/a
38	chr10:89696774-89696824	SK-N-MC	brain:	n/a
39	chr10:89696774-89696824	HEK293	kidney:	embryo
40	chr10:89696774-89696824	SKMC	muscle:	n/a
41	chr10:89696774-89696824	CMK	blood:	n/a
42	chr10:89696774-89696824	AG04449	skin:	fetal
43	chr10:89696774-89696824	AoSMC	blood vessel:	n/a
44	chr10:89696774-89696824	AG09319	gingival:	n/a
45	chr10:89696774-89696824	U87	brain:	n/a
46	chr10:89696774-89696824	GM12891	blood:	n/a
47	chr10:89696774-89696824	HIPEpiC	eye:	n/a
48	chr10:89696774-89696824	NHBE	bronchial:	n/a
49	chr10:89696774-89696824	HCM	heart:	n/a
50	chr10:89696774-89696824	PrEC	prostate:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:89620282..89622359-chr10:89713432..89715194,2	MCF-7	breast:
2	chr10:89623108..89624927-chr10:89720086..89724191,3	MCF-7	breast:
3	chr10:89683604..89685198-chr10:89700673..89703491,2	K562	blood:
4	chr10:89696435..89697962-chr10:89699594..89701674,2	MCF-7	breast:
5	chr10:89688499..89690095-chr10:89694777..89697091,2	MCF-7	breast:
6	chr10:89578473..89580973-chr10:89716614..89719298,2	K562	blood:
7	chr10:89685840..89688439-chr10:89700788..89703474,2	MCF-7	breast:
8	chr10:89724975..89728613-chr10:89729224..89733070,3	K562	blood:
9	chr10:89621748..89623902-chr10:89723296..89725562,2	MCF-7	breast:
10	chr10:89622549..89624064-chr10:89699463..89701923,2	MCF-7	breast:
11	chr10:89696435..89697962-chr10:89699594..89701674,2	MCF-7	breast:
12	chr10:89622117..89624180-chr10:89706154..89707950,2	MCF-7	breast:
13	chr10:89705366..89707879-chr20:50382836..50384376,2	MCF-7	breast:
14	chr10:89620590..89623557-chr10:89689802..89694135,6	MCF-7	breast:
15	chr10:89708994..89710668-chr10:89716753..89718565,2	K562	blood:
16	chr10:89692563..89694138-chr10:89862900..89864985,2	MCF-7	breast:
17	chr10:89708994..89710668-chr10:89716753..89718565,2	K562	blood:
18	chr10:89685265..89687757-chr10:89688407..89691640,3	MCF-7	breast:
19	chr10:89703009..89705949-chr10:89706838..89708569,3	K562	blood:
20	chr10:89686969..89688514-chr10:89688807..89691753,2	K562	blood:
21	chr10:89721575..89723341-chr10:89728907..89731665,2	MCF-7	breast:
22	chr10:89622018..89624165-chr10:89707247..89709029,2	K562	blood:
23	chr10:89724830..89727506-chr10:89728128..89730724,2	K562	blood:
24	chr10:89704548..89706247-chr10:89707891..89709573,2	MCF-7	breast:
25	chr10:89639384..89642070-chr10:89695863..89697662,2	K562	blood:
26	chr10:89721293..89722807-chr20:55841031..55842902,2	MCF-7	breast:
27	chr10:89623373..89624894-chr10:89719879..89721616,2	MCF-7	breast:
28	chr10:89620372..89623295-chr10:89720146..89723263,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPSS2-10	chr10:89706925-89708694	NONHSAT015462
2	lnc-KLLN-1	chr10:89698640-89699108	ENSG00000245981
3	lnc-KLLN-1	chr10:89707608-89708694	ENSG00000245981
4	lnc-PAPSS2-9	chr10:89696356-89696835	expReg_chr10_5676_+

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PTEN	hsa-miR-20a-5p	chr10:89707212-89707241
2	PTEN	hsa-miR-221-3p	chr10:89706946-89706968
3	PTEN	hsa-miR-216a-5p	chr10:89707820-89707843
4	PTEN	hsa-miR-107	chr10:89707878-89707901
5	PTEN	hsa-miR-103a-3p	chr10:89707878-89707901
6	PTEN	hsa-miR-141-3p	chr10:89707760-89707781
7	PTEN	hsa-miR-26a-5p	chr10:89725270-89725276
8	PTEN	hsa-miR-222-3p	chr10:89706949-89706968
9	PTEN	hsa-miR-26a-5p	chr10:89725255-89725276

Variant related genes	Relation type
ENSG00000213613	TF binding region
PTEN	TF binding region
ENSG00000213613	CpG island
PTEN	CpG island
ENSG00000213613	chromatin interactions
ENSG00000227268	chromatin interactions
ENSG00000171862	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000101144	chromatin interactions
ZEB2	miRNA target sites
NR2C2AP	miRNA target sites

Extended variants
information (count: 1257 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:1257 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35917308	chr10:89690827-89690828	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs202004587	chr10:89690828-89690829	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555860513	chr10:89690864-89690865	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs577344597	chr10:89690890-89690891	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs377719086	chr10:89690912-89690913	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545969669	chr10:89690915-89690916	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138283451	chr10:89690919-89690920	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs528779015	chr10:89690926-89690927	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540571746	chr10:89690949-89690950	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs1799734	chr10:89690952-89690953	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368741886	chr10:89690953-89690954	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs3830675	chr10:89690954-89690955	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs34051577	chr10:89690955-89690956	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs2735364	chr10:89690956-89690957	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs2735365	chr10:89690991-89690992	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs149050419	chr10:89691029-89691030	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs2616600	chr10:89691044-89691045	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529329346	chr10:89691087-89691088	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs551023611	chr10:89691219-89691220	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564867773	chr10:89691244-89691245	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs35465320	chr10:89691246-89691247	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs2735366	chr10:89691273-89691274	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2616601	chr10:89691297-89691298	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs36092774	chr10:89691312-89691313	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs551552525	chr10:89691331-89691332	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs566554328	chr10:89691345-89691346	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534053841	chr10:89691353-89691354	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555388392	chr10:89691360-89691361	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs567223263	chr10:89691364-89691365	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs537424240	chr10:89691414-89691415	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143071863	chr10:89691474-89691475	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs35578993	chr10:89691520-89691521	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs181003042	chr10:89691534-89691535	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs138753463	chr10:89691553-89691554	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs576743554	chr10:89691629-89691630	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs559614101	chr10:89691695-89691696	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540894493	chr10:89691752-89691753	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs187123127	chr10:89691762-89691763	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs192457790	chr10:89691857-89691858	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs73354943	chr10:89691925-89691926	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs562920527	chr10:89691937-89691938	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2735367	chr10:89691942-89691943	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533421477	chr10:89691967-89691968	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551595881	chr10:89691969-89691970	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs181713121	chr10:89692012-89692013	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34546731	chr10:89692054-89692055	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs186106381	chr10:89692064-89692065	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs528190828	chr10:89692075-89692076	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs549186467	chr10:89692152-89692153	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551512012	chr10:89692168-89692169	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21569311	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Prostate cancer	21147910	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	20020426	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22065749	CNVD
Cancer	22000013	CNVD
Colon cancer	22065749	CNVD
Endometrial cancer	22065749	CNVD
Lung cancer	20668451	CNVD
Breast cancer	17634833	CNVD
Cancer	20215515	CNVD
Glioblastoma multiforme	21727940	CNVD
Prostate cancer	19363497	CNVD
Prostate cancer	17700571	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Ovarian cancer	21781307	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20964600	CNVD
Endometrial cancer	19261849	CNVD
Central neurocytomas	17123091	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung adenocarcinoma	17982442	CNVD
Bannayan-Riley-Ruvalcaba syndrome	20848651	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:1367 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89647000-89711200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:89663800-89725400	Weak transcription	Colonic Mucosa	Colon
3	chr10:89666000-89712400	Weak transcription	Fetal Brain Male	brain
4	chr10:89673600-89726000	Weak transcription	Brain Substantia Nigra	brain
5	chr10:89674200-89695200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr10:89674200-89711000	Weak transcription	HepG2	liver
7	chr10:89674600-89695600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr10:89674800-89724400	Weak transcription	Fetal Brain Female	brain
9	chr10:89675400-89726000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr10:89675600-89705000	Weak transcription	Fetal Stomach	stomach
11	chr10:89675600-89705200	Weak transcription	Esophagus	oesophagus
12	chr10:89676600-89695400	Weak transcription	Brain Anterior Caudate	brain
13	chr10:89676800-89691000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr10:89678000-89694200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr10:89679800-89691600	Weak transcription	Brain Hippocampus Middle	brain
16	chr10:89681800-89691200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr10:89682000-89705200	Weak transcription	Fetal Intestine Small	intestine
18	chr10:89682000-89705200	Weak transcription	Left Ventricle	heart
19	chr10:89682000-89705600	Weak transcription	Lung	lung
20	chr10:89682400-89705200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr10:89683200-89695600	Weak transcription	Fetal Muscle Leg	muscle
22	chr10:89683200-89705000	Weak transcription	Thymus	Thymus
23	chr10:89683200-89715200	Weak transcription	Pancreas	Pancrea
24	chr10:89683200-89720800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr10:89683200-89723800	Weak transcription	Psoas Muscle	Psoas
26	chr10:89684000-89707400	Strong transcription	Dnd41	blood
27	chr10:89684000-89725600	Weak transcription	Gastric	stomach
28	chr10:89684000-89726200	Weak transcription	Spleen	Spleen
29	chr10:89684800-89702200	Weak transcription	Fetal Kidney	kidney
30	chr10:89685400-89692200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr10:89685800-89712400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr10:89686400-89691800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr10:89686400-89692800	Weak transcription	Placenta	Placenta
34	chr10:89686400-89693200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:89686600-89691200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr10:89686600-89692400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr10:89686600-89692800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr10:89686600-89695600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr10:89686600-89698800	Weak transcription	K562	blood
40	chr10:89686600-89711200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr10:89686800-89708400	Weak transcription	Aorta	Aorta
42	chr10:89686800-89710400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr10:89687000-89691200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr10:89687000-89691200	Enhancers	Liver	Liver
45	chr10:89687000-89712200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr10:89687200-89691200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr10:89687200-89692600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr10:89687200-89694000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr10:89687200-89705800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr10:89687200-89705800	Weak transcription	Small Intestine	intestine

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