Variant report

Variant	nsv2200
Chromosome Location	chr18:8618182-8663130
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:844)
CpG islands
(count:733)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:844 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:8627542-8627984	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:8654472-8654917	K562	blood:	n/a	n/a
3	ARID3A	chr18:8654549-8654875	HepG2	liver:	n/a	n/a
4	ATF3	chr18:8658956-8659149	K562	blood:	n/a	n/a
5	BACH1	chr18:8662352-8662588	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr18:8623497-8623811	GM12878	blood:	n/a	n/a
7	BATF	chr18:8623434-8623893	GM12878	blood:	n/a	n/a
8	BCL3	chr18:8641827-8642050	GM12878	blood:	n/a	n/a
9	BCLAF1	chr18:8623369-8623862	GM12878	blood:	n/a	chr18:8623684-8623693 chr18:8623690-8623699
10	BHLHE40	chr18:8659917-8660271	K562	blood:	n/a	n/a
11	BHLHE40	chr18:8661857-8662100	K562	blood:	n/a	n/a
12	BHLHE40	chr18:8654966-8655360	K562	blood:	n/a	n/a
13	BHLHE40	chr18:8658928-8659127	K562	blood:	n/a	n/a
14	BHLHE40	chr18:8623506-8624140	GM12878	blood:	n/a	n/a
15	BHLHE40	chr18:8661858-8662019	GM12878	blood:	n/a	n/a
16	BHLHE40	chr18:8662507-8662855	GM12878	blood:	n/a	n/a
17	BRCA1	chr18:8661640-8661770	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr18:8659896-8660231	K562	blood:	n/a	n/a
19	CEBPB	chr18:8630632-8630939	HepG2	liver:	n/a	n/a
20	CEBPB	chr18:8654500-8654794	K562	blood:	n/a	n/a
21	CEBPB	chr18:8627306-8627863	HepG2	liver:	n/a	n/a
22	CEBPB	chr18:8654507-8654797	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr18:8658236-8658465	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr18:8624077-8624277	H1-hESC	embryonic stem cell:	n/a	chr18:8624195-8624206 chr18:8624214-8624225 chr18:8624213-8624226 chr18:8624197-8624206 chr18:8624196-8624207
25	CEBPB	chr18:8624071-8624369	K562	blood:	n/a	chr18:8624195-8624206 chr18:8624214-8624225 chr18:8624213-8624226 chr18:8624197-8624206 chr18:8624196-8624207
26	CEBPB	chr18:8624063-8624322	Hela-S3	cervix:	n/a	chr18:8624195-8624206 chr18:8624214-8624225 chr18:8624213-8624226 chr18:8624197-8624206 chr18:8624196-8624207
27	CEBPB	chr18:8624048-8624334	IMR90	lung:	n/a	chr18:8624195-8624206 chr18:8624214-8624225 chr18:8624213-8624226 chr18:8624197-8624206 chr18:8624196-8624207
28	CEBPB	chr18:8627588-8627789	HepG2	liver:	n/a	n/a
29	CEBPB	chr18:8624026-8624355	HepG2	liver:	n/a	chr18:8624195-8624206 chr18:8624214-8624225 chr18:8624213-8624226 chr18:8624197-8624206 chr18:8624196-8624207
30	CEBPB	chr18:8643519-8643673	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr18:8624045-8624347	A549	lung:	n/a	chr18:8624195-8624206 chr18:8624214-8624225 chr18:8624213-8624226 chr18:8624197-8624206 chr18:8624196-8624207
32	CHD1	chr18:8662059-8662164	GM12878	blood:	n/a	n/a
33	CHD2	chr18:8662479-8662832	GM12878	blood:	n/a	n/a
34	CHD2	chr18:8619800-8619867	GM12878	blood:	n/a	n/a
35	CTBP2	chr18:8661900-8662611	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr18:8654580-8654730	Hela-S3	cervix:	n/a	chr18:8654686-8654699 chr18:8654685-8654706 chr18:8654683-8654701
37	CTCF	chr18:8654462-8654901	GM12878	blood:	n/a	chr18:8654686-8654699 chr18:8654685-8654706 chr18:8654683-8654701
38	CTCF	chr18:8654545-8654821	ECC-1	luminal epithelium:	n/a	chr18:8654686-8654699 chr18:8654685-8654706 chr18:8654683-8654701
39	CTCF	chr18:8655160-8655310	HMEC	breast:	n/a	chr18:8655268-8655289
40	CTCF	chr18:8654640-8654790	HFF-Myc	foreskin:	n/a	chr18:8654686-8654699 chr18:8654685-8654706 chr18:8654683-8654701
41	CTCF	chr18:8654960-8655110	NHEK	skin:	n/a	n/a
42	CTCF	chr18:8654560-8654710	GM12866	blood:	n/a	chr18:8654686-8654699 chr18:8654685-8654706 chr18:8654683-8654701
43	CTCF	chr18:8654341-8654360	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr18:8655080-8655230	HFF	foreskin:	n/a	n/a
45	CTCF	chr18:8651814-8651916	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr18:8647460-8647610	GM06990	blood:	n/a	n/a
47	CTCF	chr18:8654980-8655130	HEK293	kidney:	n/a	n/a
48	CTCF	chr18:8655182-8655333	MCF-7	breast:	n/a	chr18:8655268-8655289
49	CTCF	chr18:8653880-8654030	AG09319	gingival:	n/a	n/a
50	CTCF	chr18:8654580-8654730	HVMF	connective:	n/a	chr18:8654686-8654699 chr18:8654685-8654706 chr18:8654683-8654701

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:8662015-8662065	K562	blood:	n/a
2	chr18:8662015-8662065	K562	blood:	n/a
3	chr18:8657945-8657995	RPTEC	kidney:	n/a
4	chr18:8659650-8659700	HEEpiC	esophagus:	n/a
5	chr18:8656138-8656188	GM12891	blood:	n/a
6	chr18:8660164-8660214	HEK293	kidney:	embryo
7	chr18:8659563-8659613	ECC-1	luminal epithelium:	n/a
8	chr18:8657945-8657995	HRCEpiC	kidney:	n/a
9	chr18:8659964-8660014	AG09319	gingival:	n/a
10	chr18:8659509-8659559	SK-N-SH_RA	brain:	n/a
11	chr18:8662015-8662065	NB4	blood:	n/a
12	chr18:8660164-8660214	SK-N-MC	brain:	n/a
13	chr18:8657945-8657995	NHBE	bronchial:	n/a
14	chr18:8638786-8638836	NT2-D1	testis:	n/a
15	chr18:8638786-8638836	NH-A	brain:	n/a
16	chr18:8662015-8662065	SK-N-SH_RA	brain:	n/a
17	chr18:8659650-8659700	Caco-2	colon:	n/a
18	chr18:8662653-8662703	A549	lung:	n/a
19	chr18:8656138-8656188	IMR90	lung:	fetal
20	chr18:8659964-8660014	T-47D	breast:	n/a
21	chr18:8659509-8659559	LNCaP	prostate:	n/a
22	chr18:8657945-8657995	SAEC	small airway:	n/a
23	chr18:8659844-8659894	SK-N-SH	brain:	n/a
24	chr18:8658686-8658736	RPTEC	kidney:	n/a
25	chr18:8662653-8662703	SAEC	small airway:	n/a
26	chr18:8657945-8657995	GM12892	blood:	n/a
27	chr18:8656138-8656188	AG04450	lung:	fetal
28	chr18:8659509-8659559	GM12878	blood:	n/a
29	chr18:8656138-8656188	GM12892	blood:	n/a
30	chr18:8658686-8658736	Caco-2	colon:	n/a
31	chr18:8658686-8658736	IMR90	lung:	fetal
32	chr18:8662653-8662703	HCPEpiC	choroid plexus:	n/a
33	chr18:8659563-8659613	NH-A	brain:	n/a
34	chr18:8638786-8638836	NHDF-neo	bronchial:	n/a
35	chr18:8638786-8638836	LNCaP	prostate:	n/a
36	chr18:8656138-8656188	HEK293	kidney:	embryo
37	chr18:8659563-8659613	HRCEpiC	kidney:	n/a
38	chr18:8658686-8658736	T-47D	breast:	n/a
39	chr18:8658686-8658736	PFSK-1	brain:	n/a
40	chr18:8658686-8658736	A549	lung:	n/a
41	chr18:8659650-8659700	HRE	kidney:	n/a
42	chr18:8660164-8660214	Hepatocyte	liver:	n/a
43	chr18:8659650-8659700	HAEpiC	amniotic membrane:	n/a
44	chr18:8660164-8660214	MCF-7	breast:	n/a
45	chr18:8659844-8659894	AG04449	skin:	fetal
46	chr18:8662015-8662065	SK-N-SH	brain:	n/a
47	chr18:8659563-8659613	GM12891	blood:	n/a
48	chr18:8659563-8659613	AG09319	gingival:	n/a
49	chr18:8638786-8638836	ProgFib	skin:	n/a
50	chr18:8659964-8660014	Hepatocyte	liver:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:8608973..8610976-chr18:8624181..8625797,2	MCF-7	breast:
2	chr18:8654266..8655510-chr18:8982017..8983163,6	MCF-7	breast:
3	chr18:8643214..8643842-chr3:64008967..64009508,2	MCF-7	breast:
4	chr18:8626888..8629769-chr18:8634935..8637660,2	K562	blood:
5	chr18:8631252..8633110-chr18:8634888..8637488,2	MCF-7	breast:
6	chr18:8608936..8610499-chr18:8616344..8619062,2	MCF-7	breast:
7	chr18:8634368..8636828-chr18:8638233..8641594,3	MCF-7	breast:
8	chr18:8611515..8614387-chr18:8625715..8627247,2	MCF-7	breast:
9	chr18:8654145..8655107-chr18:8987974..8988486,3	K562	blood:
10	chr18:8658209..8662068-chr18:8705439..8707440,3	MCF-7	breast:
11	chr18:8615811..8618362-chr18:8979666..8982599,2	K562	blood:
12	chr12:92054336..92057097-chr18:8636709..8639419,2	MCF-7	breast:
13	chr18:8608406..8612122-chr18:8618832..8621107,4	K562	blood:
14	chr18:8625509..8627110-chr18:8627947..8629473,2	MCF-7	breast:
15	chr18:8659422..8661406-chr18:8668712..8671092,2	K562	blood:
16	chr18:8612004..8614198-chr18:8622613..8624128,2	MCF-7	breast:
17	chr18:8608610..8610450-chr18:8634759..8636817,2	MCF-7	breast:
18	chr18:8656592..8659415-chr18:8661915..8663898,2	K562	blood:
19	chr18:8656592..8659415-chr18:8661915..8663898,2	K562	blood:
20	chr18:8617866..8620402-chr18:8622519..8624289,2	MCF-7	breast:
21	chr18:8656651..8657422-chr18:8987942..8988820,2	MCF-7	breast:
22	chr18:8619952..8621664-chr18:8632642..8634722,2	K562	blood:
23	chr18:8661421..8663171-chr18:8666380..8669348,2	MCF-7	breast:
24	chr18:8643695..8645722-chr18:8755829..8757681,2	K562	blood:
25	chr18:8631252..8633110-chr18:8634888..8637488,2	MCF-7	breast:
26	chr18:8614780..8616926-chr18:8639443..8642312,2	MCF-7	breast:
27	chr18:8513167..8514688-chr18:8617025..8619164,2	K562	blood:
28	chr18:8624127..8626871-chr18:8632605..8635098,2	MCF-7	breast:
29	chr18:8654347..8655209-chr18:8696425..8697043,2	MCF-7	breast:
30	chr18:8653968..8654862-chr18:8988163..8988970,3	MCF-7	breast:
31	chr18:8618906..8620726-chr18:8622876..8625052,2	K562	blood:
32	chr18:8625509..8627110-chr18:8627947..8629473,2	MCF-7	breast:
33	chr18:8657777..8659380-chr18:8662029..8663549,2	MCF-7	breast:
34	chr18:8618906..8620726-chr18:8622876..8625052,2	K562	blood:
35	chr18:8633656..8636438-chr18:8640902..8643392,3	MCF-7	breast:
36	chr18:8609439..8612393-chr18:8636257..8639146,2	MCF-7	breast:
37	chr18:8614072..8616072-chr18:8617527..8620570,3	MCF-7	breast:
38	chr18:8654390..8655746-chr18:8988013..8989122,6	MCF-7	breast:
39	chr18:8627643..8629642-chr18:8643038..8645267,2	MCF-7	breast:
40	chr18:8616144..8618233-chr18:8705323..8707397,3	MCF-7	breast:
41	chr18:8611811..8615415-chr18:8621524..8625470,5	MCF-7	breast:
42	chr18:8627643..8629642-chr18:8643038..8645267,2	MCF-7	breast:
43	chr18:8617866..8620402-chr18:8622519..8624289,2	MCF-7	breast:
44	chr18:8657777..8659380-chr18:8662029..8663549,2	MCF-7	breast:
45	chr18:8625177..8627727-chr18:8631333..8633538,2	K562	blood:

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RAB12	hsa-miR-148a-3p	chr18:8639242-8639248
2	RAB12	hsa-miR-16-5p	chr18:8638963-8638988
3	RAB12	hsa-miR-186-5p	chr18:8639129-8639149
4	RAB12	hsa-miR-148a-3p	chr18:8639228-8639249
5	RAB12	hsa-miR-186-5p	chr18:8638686-8638707
6	RAB12	hsa-miR-130b-3p	chr18:8639225-8639248
7	RAB12	hsa-miR-130b-3p	chr18:8638306-8638327

Variant related genes	Relation type
ENSG00000266708	TF binding region
RAB12	TF binding region
ENSG00000266708	CpG island
RAB12	CpG island
ENSG00000163636	chromatin interactions
ENSG00000266708	chromatin interactions
ENSG00000168502	chromatin interactions
ENSG00000206418	chromatin interactions

Extended variants
information (count: 1938 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1938 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565008601	chr18:8618185-8618186	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs73942008	chr18:8618202-8618203	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs540915558	chr18:8618224-8618225	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559493639	chr18:8618325-8618326	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529957321	chr18:8618330-8618331	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183277711	chr18:8618387-8618388	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569728221	chr18:8618483-8618484	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112341782	chr18:8618521-8618522	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552128686	chr18:8618531-8618532	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369208911	chr18:8618547-8618548	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570655699	chr18:8618594-8618595	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs186441140	chr18:8618646-8618647	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147172784	chr18:8618653-8618654	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190849798	chr18:8618712-8618713	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138704625	chr18:8618722-8618723	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557654644	chr18:8618725-8618726	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575993742	chr18:8618742-8618743	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543471235	chr18:8618746-8618747	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs367774823	chr18:8618757-8618758	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183801573	chr18:8618766-8618767	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541084341	chr18:8618798-8618799	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527941039	chr18:8618834-8618835	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529873145	chr18:8618835-8618836	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541606808	chr18:8618859-8618860	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs55906430	chr18:8618905-8618906	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs377634510	chr18:8618922-8618923	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561498945	chr18:8618928-8618929	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556641944	chr18:8618959-8618960	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373356698	chr18:8618962-8618963	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562685322	chr18:8618996-8618997	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530209200	chr18:8619007-8619008	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552191973	chr18:8619035-8619036	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371698301	chr18:8619057-8619058	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs114008856	chr18:8619058-8619059	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188287719	chr18:8619068-8619069	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547041902	chr18:8619075-8619076	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142809060	chr18:8619140-8619141	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147391834	chr18:8619181-8619182	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148493412	chr18:8619195-8619196	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569618228	chr18:8619201-8619202	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs540128128	chr18:8619233-8619234	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs79296761	chr18:8619236-8619237	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142678961	chr18:8619256-8619257	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs550008513	chr18:8619264-8619265	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs534442846	chr18:8619279-8619280	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553065232	chr18:8619280-8619281	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574425382	chr18:8619309-8619310	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555431374	chr18:8619320-8619321	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72936887	chr18:8619334-8619335	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs11876907	chr18:8619336-8619337	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8610600-8634400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:8611600-8620400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr18:8612200-8621600	Weak transcription	Thymus	Thymus
4	chr18:8612600-8620400	Weak transcription	Esophagus	oesophagus
5	chr18:8612600-8623600	Weak transcription	Gastric	stomach
6	chr18:8612600-8625400	Weak transcription	Aorta	Aorta
7	chr18:8612600-8625600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr18:8612800-8620600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr18:8613000-8619200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr18:8613000-8620400	Weak transcription	Pancreas	Pancrea
11	chr18:8613000-8623400	Weak transcription	Placenta	Placenta
12	chr18:8613000-8623800	Weak transcription	Fetal Thymus	thymus
13	chr18:8613400-8623400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr18:8613600-8621600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr18:8613800-8621200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:8614000-8619400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr18:8614000-8623400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr18:8614200-8620400	Weak transcription	Spleen	Spleen
19	chr18:8615000-8618200	Strong transcription	Primary T cells from cord blood	blood
20	chr18:8615200-8619800	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr18:8615400-8623000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr18:8615400-8623800	Weak transcription	Fetal Muscle Trunk	muscle
23	chr18:8615600-8619400	Weak transcription	Lung	lung
24	chr18:8615600-8622200	Weak transcription	Fetal Intestine Small	intestine
25	chr18:8615600-8623400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr18:8615600-8625600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr18:8615800-8618200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr18:8615800-8618800	Weak transcription	Liver	Liver
29	chr18:8615800-8621400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr18:8615800-8623600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr18:8615800-8623800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr18:8616000-8618200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr18:8616000-8618200	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr18:8616000-8618800	Weak transcription	Primary B cells from peripheral blood	blood
35	chr18:8616000-8619000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr18:8616000-8619000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr18:8616000-8619200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr18:8616000-8619200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr18:8616000-8619400	Weak transcription	Brain Angular Gyrus	brain
40	chr18:8616000-8620200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr18:8616000-8620400	Weak transcription	Primary hematopoietic stem cells	blood
42	chr18:8616000-8620400	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr18:8616000-8620800	Weak transcription	HUVEC	blood vessel
44	chr18:8616000-8621000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr18:8616000-8623400	Weak transcription	Hela-S3	cervix
46	chr18:8616200-8618200	Enhancers	Colon Smooth Muscle	Colon
47	chr18:8616200-8619000	Weak transcription	Brain Substantia Nigra	brain
48	chr18:8616200-8619000	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr18:8616200-8620600	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr18:8616200-8620800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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