Variant report

Variant	esv2754300
Chromosome Location	chr9:117048446-117088446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1035)
CpG islands
(count:305)
Chromatin interactive
region (count:37)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:117084358-117084903	HepG2	liver:	n/a	n/a
2	ATF1	chr9:117080165-117080332	K562	blood:	n/a	n/a
3	ATF2	chr9:117050503-117050900	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr9:117050431-117050865	A549	lung:	n/a	n/a
5	ATF3	chr9:117080162-117080453	K562	blood:	n/a	n/a
6	BACH1	chr9:117069753-117069785	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:117050529-117050848	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr9:117050379-117050786	A549	lung:	n/a	chr9:117050674-117050683
9	BCL3	chr9:117080178-117080438	GM12878	blood:	n/a	n/a
10	BCL3	chr9:117080117-117080458	GM12878	blood:	n/a	n/a
11	BCL3	chr9:117050371-117050932	A549	lung:	n/a	chr9:117050674-117050683
12	BHLHE40	chr9:117068113-117068430	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:117068161-117068341	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:117084718-117085030	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:117085114-117085542	HepG2	liver:	n/a	n/a
16	BHLHE40	chr9:117068003-117068369	K562	blood:	n/a	n/a
17	BHLHE40	chr9:117053342-117053611	K562	blood:	n/a	n/a
18	BRCA1	chr9:117068353-117068553	HepG2	liver:	n/a	n/a
19	BRCA1	chr9:117068164-117068380	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr9:117053310-117053516	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:117080076-117080472	K562	blood:	n/a	chr9:117080273-117080284
22	CEBPB	chr9:117080082-117080511	IMR90	lung:	n/a	chr9:117080273-117080284
23	CEBPB	chr9:117077405-117077763	HepG2	liver:	n/a	chr9:117077571-117077582 chr9:117077573-117077582 chr9:117077571-117077584
24	CEBPB	chr9:117050809-117050812	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:117080205-117080383	K562	blood:	n/a	chr9:117080273-117080284
26	CEBPB	chr9:117053422-117053529	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr9:117050569-117050707	A549	lung:	n/a	n/a
28	CEBPB	chr9:117080115-117080579	A549	lung:	n/a	chr9:117080273-117080284
29	CEBPB	chr9:117084690-117085081	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:117080094-117080487	K562	blood:	n/a	chr9:117080273-117080284
31	CEBPB	chr9:117084769-117085000	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:117080097-117080535	Hela-S3	cervix:	n/a	chr9:117080273-117080284
33	CEBPB	chr9:117080094-117080477	HepG2	liver:	n/a	chr9:117080273-117080284
34	CEBPB	chr9:117078053-117078318	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:117084795-117084978	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:117084691-117085065	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:117080214-117080319	HepG2	liver:	n/a	chr9:117080273-117080284
38	CEBPB	chr9:117070321-117070327	IMR90	lung:	n/a	n/a
39	CEBPB	chr9:117080119-117080474	A549	lung:	n/a	chr9:117080273-117080284
40	CEBPB	chr9:117077520-117077679	IMR90	lung:	n/a	chr9:117077571-117077582 chr9:117077573-117077582 chr9:117077571-117077584
41	CEBPD	chr9:117080879-117081604	K562	blood:	n/a	n/a
42	CHD2	chr9:117050592-117050922	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr9:117053387-117053605	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr9:117085014-117085045	HepG2	liver:	n/a	n/a
45	CHD2	chr9:117069224-117069313	HepG2	liver:	n/a	n/a
46	CHD2	chr9:117068092-117068359	HepG2	liver:	n/a	n/a
47	CREB1	chr9:117053301-117053663	A549	lung:	n/a	n/a
48	CTCF	chr9:117053380-117053530	HFF-Myc	foreskin:	n/a	chr9:117053448-117053469 chr9:117053454-117053470 chr9:117053455-117053468 chr9:117053455-117053468 chr9:117053453-117053471
49	CTCF	chr9:117067600-117067890	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr9:117068540-117068690	NHDF-neo	bronchial:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117068159-117068209	ProgFib	skin:	n/a
2	chr9:117085966-117086016	BE2_C	brain:	n/a
3	chr9:117085966-117086016	HEEpiC	esophagus:	n/a
4	chr9:117084602-117084652	MCF10A-Er-Src	breast:	n/a
5	chr9:117068532-117068582	HL-60	blood:	n/a
6	chr9:117085966-117086016	RPTEC	kidney:	n/a
7	chr9:117068159-117068209	A549	lung:	n/a
8	chr9:117068159-117068209	Hela-S3	cervix:	n/a
9	chr9:117068361-117068411	SK-N-MC	brain:	n/a
10	chr9:117085966-117086016	Hepatocyte	liver:	n/a
11	chr9:117084602-117084652	HCT-116	colon:	n/a
12	chr9:117085966-117086016	SK-N-SH	brain:	n/a
13	chr9:117068159-117068209	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:117068159-117068209	LNCaP	prostate:	n/a
15	chr9:117068159-117068209	PrEC	prostate:	n/a
16	chr9:117068532-117068582	Hepatocyte	liver:	n/a
17	chr9:117068361-117068411	HepG2	liver:	n/a
18	chr9:117084602-117084652	RPTEC	kidney:	n/a
19	chr9:117068361-117068411	HUVEC	blood vessel:	n/a
20	chr9:117068532-117068582	HMEC	breast:	n/a
21	chr9:117085966-117086016	HIPEpiC	eye:	n/a
22	chr9:117068532-117068582	HUVEC	blood vessel:	n/a
23	chr9:117068361-117068411	A549	lung:	n/a
24	chr9:117084602-117084652	K562	blood:	n/a
25	chr9:117068159-117068209	GM06990	blood:	n/a
26	chr9:117085966-117086016	HRPEpiC	eye:	n/a
27	chr9:117068532-117068582	A549	lung:	n/a
28	chr9:117068361-117068411	K562	blood:	n/a
29	chr9:117084602-117084652	HL-60	blood:	n/a
30	chr9:117084602-117084652	NHBE	bronchial:	n/a
31	chr9:117068159-117068209	HNPCEpiC	eye:	n/a
32	chr9:117084602-117084652	Hela-S3	cervix:	n/a
33	chr9:117085966-117086016	PANC-1	pancreas:	n/a
34	chr9:117068532-117068582	AG04449	skin:	fetal
35	chr9:117068159-117068209	Hepatocyte	liver:	n/a
36	chr9:117068159-117068209	HUVEC	blood vessel:	n/a
37	chr9:117084602-117084652	NH-A	brain:	n/a
38	chr9:117068159-117068209	HEEpiC	esophagus:	n/a
39	chr9:117084602-117084652	HNPCEpiC	eye:	n/a
40	chr9:117068361-117068411	HCM	heart:	n/a
41	chr9:117068361-117068411	HRCEpiC	kidney:	n/a
42	chr9:117084602-117084652	HEK293	kidney:	embryo
43	chr9:117085966-117086016	PrEC	prostate:	n/a
44	chr9:117085966-117086016	ProgFib	skin:	n/a
45	chr9:117068532-117068582	GM12878	blood:	n/a
46	chr9:117068159-117068209	AG09319	gingival:	n/a
47	chr9:117068361-117068411	NHDF-neo	bronchial:	n/a
48	chr9:117068532-117068582	PFSK-1	brain:	n/a
49	chr9:117068532-117068582	BJ	skin:	n/a
50	chr9:117068361-117068411	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:116916702..116920015-chr9:117048012..117051881,4	K562	blood:
2	chr9:117053392..117053933-chr9:117067853..117068400,2	K562	blood:
3	chr9:117052909..117055629-chr9:117066648..117068962,2	MCF-7	breast:
4	chr9:116569447..116570300-chr9:117052628..117053509,2	MCF-7	breast:
5	chr9:116917252..116918213-chr9:117052941..117053917,4	K562	blood:
6	chr9:117062219..117064212-chr9:117064334..117066027,2	MCF-7	breast:
7	chr9:116916957..116918241-chr9:117052265..117054078,11	MCF-7	breast:
8	chr9:116844851..116845417-chr9:117067843..117068379,2	MCF-7	breast:
9	chr9:116843600..116846294-chr9:117069884..117072218,2	MCF-7	breast:
10	chr9:116869935..116870873-chr9:117052125..117052932,3	K562	blood:
11	chr9:117086796..117090916-chr9:117093612..117097049,4	K562	blood:
12	chr9:116499791..116500371-chr9:117053010..117053583,4	K562	blood:
13	chr9:117048708..117051555-chr9:117052234..117055024,3	MCF-7	breast:
14	chr9:116917474..116919144-chr9:117052623..117055969,3	MCF-7	breast:
15	chr9:116870303..116871233-chr9:117051501..117052146,3	MCF-7	breast:
16	chr9:117060520..117062937-chr9:117065825..117069499,4	MCF-7	breast:
17	chr9:116869916..116870857-chr9:117067860..117068426,2	K562	blood:
18	chr9:117060520..117062937-chr9:117065825..117069499,4	MCF-7	breast:
19	chr9:116917422..116918284-chr9:117067805..117069207,4	K562	blood:
20	chr9:117052946..117055732-chr9:117060999..117063186,2	K562	blood:
21	chr9:117053392..117053933-chr9:117067853..117068400,2	K562	blood:
22	chr9:116869923..116871115-chr9:117053002..117053726,3	K562	blood:
23	chr9:117001198..117001897-chr9:117053004..117053908,2	MCF-7	breast:
24	chr9:116844247..116845566-chr9:117052560..117054100,7	MCF-7	breast:
25	chr9:116844678..116846349-chr9:117050619..117053590,2	MCF-7	breast:
26	chr9:117073544..117075822-chr9:117160051..117162438,2	K562	blood:
27	chr9:117045835..117047585-chr9:117049040..117050988,2	MCF-7	breast:
28	chr9:116844450..116845667-chr9:117052850..117054752,10	K562	blood:
29	chr9:117043393..117045568-chr9:117050834..117052747,2	K562	blood:
30	chr9:116869934..116871127-chr9:117052704..117054035,13	MCF-7	breast:
31	chr9:116917096..116918203-chr9:117052981..117053630,5	MCF-7	breast:
32	chr9:117048708..117051555-chr9:117052234..117055024,3	MCF-7	breast:
33	chr9:117066557..117068874-chr9:117077753..117079545,2	MCF-7	breast:
34	chr9:116845927..116847866-chr9:117052148..117055626,3	MCF-7	breast:
35	chr9:117033926..117037136-chr9:117049130..117052892,3	MCF-7	breast:
36	chr9:117065267..117067834-chr9:117158317..117161019,2	MCF-7	breast:
37	chr9:116869895..116870973-chr9:117052879..117053661,10	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ORM1-1	chr9:117063725-117063822	NONHSAT134374
2	lnc-ORM1-1	chr9:117063564-117063599	NONHSAT134374
3	lnc-ORM1-1	chr9:117063352-117063405	NONHSAT134374
4	lnc-ORM1-1	chr9:117062642-117062967	NONHSAT134374

No data

Variant related genes	Relation type
ORM1	TF binding region
ORM2	TF binding region
COL27A1	TF binding region
ORM1	CpG island
ORM2	CpG island
COL27A1	CpG island
ENSG00000235119	chromatin interactions
ENSG00000196739	chromatin interactions

Extended variants
information (count: 1958 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190307011	chr9:117048446-117048447	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs564488200	chr9:117048455-117048456	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs554891300	chr9:117048459-117048460	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs16927834	chr9:117048473-117048474	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs202187737	chr9:117048480-117048481	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs386737840	chr9:117048481-117048482	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs374129492	chr9:117048482-117048483	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560537814	chr9:117048532-117048533	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577342274	chr9:117048561-117048562	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546011236	chr9:117048606-117048607	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4978577	chr9:117048609-117048610	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs568260295	chr9:117048669-117048670	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531776818	chr9:117048711-117048712	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs548597372	chr9:117048717-117048718	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529238246	chr9:117048765-117048766	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs562013222	chr9:117048782-117048783	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs75451914	chr9:117048791-117048792	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536393678	chr9:117048832-117048833	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs367841564	chr9:117048838-117048839	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs77943773	chr9:117048842-117048843	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181214604	chr9:117048862-117048863	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs75515923	chr9:117048903-117048904	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs552027937	chr9:117048917-117048918	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568608777	chr9:117048927-117048928	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537501172	chr9:117048930-117048931	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554153650	chr9:117048952-117048953	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574061627	chr9:117048961-117048962	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184988806	chr9:117048987-117048988	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs57153447	chr9:117049034-117049035	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188264911	chr9:117049049-117049050	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs79598593	chr9:117049086-117049087	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546365415	chr9:117049115-117049116	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs55880714	chr9:117049144-117049145	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs78591197	chr9:117049155-117049156	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs73548918	chr9:117049207-117049208	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs562079039	chr9:117049238-117049239	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181007418	chr9:117049247-117049248	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540185546	chr9:117049279-117049280	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs62555445	chr9:117049283-117049284	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs555500218	chr9:117049326-117049327	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373339810	chr9:117049337-117049338	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2418270	chr9:117049345-117049346	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552352843	chr9:117049372-117049373	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs730989	chr9:117049418-117049419	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs375700944	chr9:117049474-117049475	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547854994	chr9:117049512-117049513	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs369431210	chr9:117049518-117049519	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533770398	chr9:117049533-117049534	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs62555446	chr9:117049546-117049547	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571119418	chr9:117049585-117049586	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Retinoblastoma	19183342	CNVD

Chromatin state (count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117005000-117050200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr9:117012400-117054400	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr9:117013400-117067800	Weak transcription	Right Ventricle	heart
4	chr9:117026600-117057000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr9:117026800-117050000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr9:117027800-117056800	Weak transcription	Colon Smooth Muscle	Colon
7	chr9:117028200-117077000	Weak transcription	Gastric	stomach
8	chr9:117038200-117052800	Weak transcription	Stomach Mucosa	stomach
9	chr9:117039400-117049400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr9:117039800-117076600	Weak transcription	Lung	lung
11	chr9:117040200-117053000	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr9:117041800-117061800	Weak transcription	Aorta	Aorta
13	chr9:117042000-117050000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr9:117043000-117051000	Strong transcription	HepG2	liver
15	chr9:117043200-117051800	Strong transcription	Liver	Liver
16	chr9:117043400-117051800	Genic enhancers	Fetal Muscle Leg	muscle
17	chr9:117043400-117053800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:117043800-117053800	Genic enhancers	Fetal Muscle Trunk	muscle
19	chr9:117043800-117074800	Strong transcription	Fetal Intestine Large	intestine
20	chr9:117043800-117075200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr9:117044200-117057600	Weak transcription	Right Atrium	heart
22	chr9:117044400-117057000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr9:117044800-117055000	Strong transcription	Fetal Intestine Small	intestine
24	chr9:117045600-117049200	Weak transcription	Fetal Thymus	thymus
25	chr9:117045600-117050000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr9:117045800-117050200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:117046000-117050400	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr9:117046000-117051000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr9:117046200-117050200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr9:117046200-117057000	Weak transcription	Brain Substantia Nigra	brain
31	chr9:117046400-117050600	Weak transcription	Spleen	Spleen
32	chr9:117046600-117050200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr9:117046600-117051200	Genic enhancers	Fetal Stomach	stomach
34	chr9:117046800-117048800	Enhancers	NHDF-Ad	bronchial
35	chr9:117046800-117049800	Weak transcription	HMEC	breast
36	chr9:117047000-117050600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr9:117047200-117048800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:117047200-117048800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:117047200-117048800	Enhancers	NH-A	brain
40	chr9:117047400-117048600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr9:117047400-117048600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr9:117047400-117048600	Enhancers	HSMM	muscle
43	chr9:117047400-117048800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr9:117047400-117048800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:117047400-117048800	Enhancers	Osteobl	bone
46	chr9:117047400-117049000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr9:117047400-117051800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:117047400-117054200	Weak transcription	Pancreas	Pancrea
49	chr9:117047600-117048600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr9:117047600-117048600	Enhancers	Fetal Lung	lung

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