Variant report

Variant	nsv540371
Chromosome Location	chr9:140757062-141018985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2285)
CpG islands
(count:2686)
Chromatin interactive
region (count:112)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:140884817-140885010	K562	blood:	n/a	n/a
2	ATF2	chr9:140761215-140761514	GM12878	blood:	n/a	n/a
3	ATF3	chr9:140772113-140772351	H1-hESC	embryonic stem cell:	n/a	chr9:140772176-140772196
4	ATF3	chr9:140851195-140851422	K562	blood:	n/a	n/a
5	ATF3	chr9:140772100-140772314	K562	blood:	n/a	chr9:140772176-140772196
6	BACH1	chr9:140778170-140778249	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:140773050-140773062	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:140918133-140918313	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:140768794-140769134	GM12878	blood:	n/a	n/a
10	BATF	chr9:140768772-140769151	GM12878	blood:	n/a	n/a
11	BATF	chr9:140761031-140761428	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:140761035-140761355	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:140768767-140769277	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:140768831-140769188	GM12878	blood:	n/a	n/a
15	BCL3	chr9:140760724-140761478	GM12878	blood:	n/a	n/a
16	BCL3	chr9:140910358-140910716	GM12878	blood:	n/a	n/a
17	BCL3	chr9:140904990-140905244	GM12878	blood:	n/a	n/a
18	BCL3	chr9:140993643-140993893	GM12878	blood:	n/a	n/a
19	BCL3	chr9:140910297-140910754	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:140851159-140851515	K562	blood:	n/a	n/a
21	BHLHE40	chr9:140772955-140773232	K562	blood:	n/a	chr9:140773100-140773109
22	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
23	BHLHE40	chr9:140760778-140760955	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:140862896-140863013	K562	blood:	n/a	n/a
25	BHLHE40	chr9:140782765-140782847	K562	blood:	n/a	n/a
26	BHLHE40	chr9:140851209-140851501	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:140993839-140994191	K562	blood:	n/a	n/a
28	BHLHE40	chr9:140879411-140879615	HepG2	liver:	n/a	n/a
29	BHLHE40	chr9:140761159-140761359	GM12878	blood:	n/a	n/a
30	BHLHE40	chr9:140993888-140994157	HepG2	liver:	n/a	n/a
31	BHLHE40	chr9:140851240-140851513	HepG2	liver:	n/a	n/a
32	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
33	BRCA1	chr9:140910350-140910549	GM12878	blood:	n/a	n/a
34	BRCA1	chr9:140841105-140841139	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr9:140761625-140761775	GM12878	blood:	n/a	n/a
36	CBX3	chr9:140839953-140840442	HCT-116	colon:	n/a	n/a
37	CBX3	chr9:140980110-140980451	HCT-116	colon:	n/a	n/a
38	CBX3	chr9:140980062-140980441	K562	blood:	n/a	n/a
39	CBX3	chr9:140980114-140980383	K562	blood:	n/a	n/a
40	CBX3	chr9:140778966-140779313	K562	blood:	n/a	n/a
41	CBX3	chr9:140851178-140851459	K562	blood:	n/a	n/a
42	CCNT2	chr9:140918130-140918232	K562	blood:	n/a	n/a
43	CCNT2	chr9:140928501-140928648	K562	blood:	n/a	n/a
44	CCNT2	chr9:140773119-140773339	K562	blood:	n/a	chr9:140773196-140773205
45	CEBPB	chr9:140926106-140926306	K562	blood:	n/a	n/a
46	CEBPB	chr9:140986459-140986918	MCF-7	breast:	n/a	n/a
47	CEBPB	chr9:140942551-140942648	Hela-S3	cervix:	n/a	chr9:140942603-140942614
48	CEBPB	chr9:140968659-140968695	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr9:140990326-140990648	Hela-S3	cervix:	n/a	chr9:140990481-140990492
50	CEBPB	chr9:140990421-140990624	K562	blood:	n/a	chr9:140990481-140990492

(count:2686 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140773483-140773533	ovcar-3	ovarian:	n/a
2	chr9:140818325-140818375	BE2_C	brain:	n/a
3	chr9:140773483-140773533	ovcar-3	ovarian:	n/a
4	chr9:140818325-140818375	BE2_C	brain:	n/a
5	chr9:141012312-141012362	H1-hESC	embryonic stem cell:	embryo
6	chr9:140773147-140773197	MCF-7	breast:	n/a
7	chr9:141017457-141017507	HRCEpiC	kidney:	n/a
8	chr9:141017001-141017051	GM12891	blood:	n/a
9	chr9:140770915-140770965	K562	blood:	n/a
10	chr9:140815937-140815987	IMR90	lung:	fetal
11	chr9:141012312-141012362	HUVEC	blood vessel:	n/a
12	chr9:141012312-141012362	HRCEpiC	kidney:	n/a
13	chr9:140957018-140957068	HL-60	blood:	n/a
14	chr9:140818325-140818375	HRCEpiC	kidney:	n/a
15	chr9:140939579-140939629	PANC-1	pancreas:	n/a
16	chr9:140773129-140773179	GM12892	blood:	n/a
17	chr9:141016367-141016417	IMR90	lung:	fetal
18	chr9:140772545-140772595	PFSK-1	brain:	n/a
19	chr9:140917413-140917463	AG09319	gingival:	n/a
20	chr9:140775967-140776017	AG09309	skin:	n/a
21	chr9:140775041-140775091	T-47D	breast:	n/a
22	chr9:141014674-141014724	Jurkat	blood:	n/a
23	chr9:141007633-141007683	ovcar-3	ovarian:	n/a
24	chr9:141016367-141016417	HUVEC	blood vessel:	n/a
25	chr9:140771661-140771711	GM19239	blood:	n/a
26	chr9:140970188-140970238	SK-N-SH	brain:	n/a
27	chr9:140771599-140771649	PANC-1	pancreas:	n/a
28	chr9:140813541-140813591	ECC-1	luminal epithelium:	n/a
29	chr9:140775967-140776017	NT2-D1	testis:	n/a
30	chr9:140917431-140917481	HEEpiC	esophagus:	n/a
31	chr9:140768247-140768297	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:141014674-141014724	HUVEC	blood vessel:	n/a
33	chr9:140970188-140970238	HEK293	kidney:	embryo
34	chr9:140816336-140816386	ovcar-3	ovarian:	n/a
35	chr9:140771661-140771711	NHDF-neo	bronchial:	n/a
36	chr9:140770915-140770965	PFSK-1	brain:	n/a
37	chr9:140771990-140772040	AG10803	skin:	n/a
38	chr9:141017001-141017051	GM12892	blood:	n/a
39	chr9:141014674-141014724	LNCaP	prostate:	n/a
40	chr9:140771599-140771649	HCF	heart:	n/a
41	chr9:140939374-140939424	NB4	blood:	n/a
42	chr9:140815937-140815987	HUVEC	blood vessel:	n/a
43	chr9:140775041-140775091	HepG2	liver:	n/a
44	chr9:140773147-140773197	GM12892	blood:	n/a
45	chr9:140937920-140937970	AG09309	skin:	n/a
46	chr9:140916980-140917030	GM06990	blood:	n/a
47	chr9:140775041-140775091	NHBE	bronchial:	n/a
48	chr9:140818325-140818375	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:140916078-140916128	ECC-1	luminal epithelium:	n/a
50	chr9:140814587-140814637	GM06990	blood:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
2	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
3	chr9:140955941..140956581-chr9:140995170..140996036,2	MCF-7	breast:
4	chr9:140777999..140780667-chr9:140783373..140786900,7	MCF-7	breast:
5	chr9:140958325..140960613-chr9:140962095..140963626,2	K562	blood:
6	chr9:140777999..140780667-chr9:140783373..140786900,7	MCF-7	breast:
7	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
8	chr9:140862016..140865668-chr9:140879753..140883106,4	MCF-7	breast:
9	chr14:100197709..100198229-chr9:140777193..140778054,2	MCF-7	breast:
10	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
11	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
12	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
13	chr9:140796431..140799040-chr9:140804864..140806682,2	K562	blood:
14	chr9:140797540..140799636-chr9:140804864..140807689,2	K562	blood:
15	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
16	chr9:140960893..140963806-chr9:140965235..140966903,2	K562	blood:
17	chr9:140778196..140781664-chr9:140782755..140784568,3	K562	blood:
18	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
19	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
20	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:
21	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
22	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
23	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
24	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
25	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
26	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
27	chr1:149223401..149224369-chr9:140873101..140874123,8	MCF-7	breast:
28	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
29	chr9:140909435..140911470-chr9:140917464..140919841,2	MCF-7	breast:
30	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
31	chr9:140884223..140886209-chr9:140893112..140896030,2	K562	blood:
32	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
33	chr9:140775069..140778564-chr9:140787877..140791721,3	MCF-7	breast:
34	chr9:140870732..140873052-chr9:140876120..140877929,2	K562	blood:
35	chr9:140962197..140963909-chr9:140964440..140967429,2	K562	blood:
36	chr9:137024514..137025058-chr9:141013083..141013583,2	HCT-116	colon:
37	chr9:140884223..140886209-chr9:140893112..140896030,2	K562	blood:
38	chr9:140864855..140867051-chr9:140878528..140880494,2	K562	blood:
39	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
40	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
41	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
42	chr9:140889129..140892271-chr9:140900387..140902590,3	K562	blood:
43	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
44	chr9:140878818..140881702-chr9:140884301..140887041,2	MCF-7	breast:
45	chr9:140869140..140872298-chr9:140874733..140877130,3	MCF-7	breast:
46	chr9:140772539..140775418-chr9:140775684..140778164,5	MCF-7	breast:
47	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
48	chr9:140771023..140775053-chr9:140775846..140778577,6	MCF-7	breast:
49	chr9:140865657..140867593-chr9:140877024..140879679,2	MCF-7	breast:
50	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL772363.1-1	chr9:140769915-140770132	XLOC_007904
2	lnc-AL772363.1-1	chr9:140767616-140767710	XLOC_007904
3	lnc-AL772363.1-1	chr9:140767517-140767710	XLOC_007904
4	lnc-AL772363.1-6	chr9:140937901-140938239	NONHSAT135763
5	lnc-AL772363.1-6	chr9:140934955-140937453	NONHSAT135763
6	lnc-AL772363.1-1	chr9:140777289-140777454	ENSG00000203987.2
7	lnc-AL772363.1-7	chr9:140954806-140956852	NONHSAT135764
8	lnc-AL772363.1-1	chr9:140784498-140787022	ENSG00000203987.2
9	lnc-AL772363.1-3	chr9:140843115-140843211	NONHSAT135761
10	lnc-AL772363.1-3	chr9:140843618-140844002	NONHSAT135761
11	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
12	lnc-AL772363.1-1	chr9:140769915-140770844	XLOC_007904
13	lnc-AL772363.1-1	chr9:140762377-140762689	ENSG00000203987.2
14	lnc-AL772363.1-6	chr9:140939331-140939523	NONHSAT135763
15	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
16	lnc-AL772363.1-1	chr9:140771009-140771749	XLOC_007904
17	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
18	lnc-AL772363.1-1	chr9:140768516-140768666	ENSG00000203987.2
19	lnc-AL772363.1-1	chr9:140762365-140762689	XLOC_007904
20	lnc-AL772363.1-1	chr9:140771009-140771749	XLOC_007904
21	lnc-AL772363.1-1	chr9:140769915-140770132	XLOC_007904
22	lnc-AL772363.1-1	chr9:140769915-140770132	ENSG00000203987.2
23	lnc-AL772363.1-1	chr9:140762379-140762689	ENSG00000203987.2
24	lnc-AL772363.1-7	chr9:140954809-140955130	NONHSAT135765
25	lnc-AL772363.1-7	chr9:140955477-140955599	NONHSAT135765

No data

Variant related genes	Relation type
CACNA1B	TF binding region
ENSG00000203987	TF binding region
CACNA1B	CpG island
ENSG00000203987	CpG island
ENSG00000206737	chromatin interactions
ENSG00000148408	chromatin interactions
ENSG00000148399	chromatin interactions
PRRG1	miRNA target sites
GPM6A	miRNA target sites
AKAP11	miRNA target sites
ACIN1	miRNA target sites

Extended variants
information (count: 11468 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:11468 , 50 per page) page: 1 2 3 4 5 6 7 ... 230

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11795093	chr9:140757087-140757088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72766991	chr9:140757138-140757139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs577704990	chr9:140757139-140757140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185951184	chr9:140757166-140757167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567487753	chr9:140757206-140757207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149429357	chr9:140757207-140757208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377559568	chr9:140757208-140757209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544988351	chr9:140757225-140757226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113318786	chr9:140757246-140757247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546872519	chr9:140757265-140757266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566684614	chr9:140757269-140757270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538804853	chr9:140757270-140757271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9410153	chr9:140757308-140757309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs9410154	chr9:140757313-140757314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs9410155	chr9:140757322-140757323	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs113169570	chr9:140757334-140757335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11397816	chr9:140757338-140757339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565128093	chr9:140757353-140757354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540374119	chr9:140757373-140757374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4388522	chr9:140757385-140757386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112653555	chr9:140757412-140757413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370248777	chr9:140757429-140757430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577043960	chr9:140757435-140757436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560171625	chr9:140757436-140757437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113940042	chr9:140757462-140757463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182570067	chr9:140757499-140757500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575286803	chr9:140757532-140757533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185293225	chr9:140757548-140757549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77323679	chr9:140757556-140757557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532173274	chr9:140757577-140757578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76853132	chr9:140757584-140757585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552197186	chr9:140757603-140757604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145015529	chr9:140757624-140757625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575673296	chr9:140757630-140757631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546934007	chr9:140757633-140757634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12005546	chr9:140757635-140757636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs386739696	chr9:140757637-140757638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72766996	chr9:140757638-140757639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191415277	chr9:140757674-140757675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538333980	chr9:140757751-140757752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548270490	chr9:140757770-140757771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149081256	chr9:140757826-140757827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72766998	chr9:140757829-140757830	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs182737480	chr9:140757861-140757862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536426078	chr9:140757881-140757882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554069779	chr9:140757916-140757917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577104741	chr9:140757934-140757935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545647578	chr9:140757936-140757937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559144553	chr9:140757963-140757964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187772168	chr9:140758002-140758003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:19)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD

Chromatin state (count:1545 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140751400-140761600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:140759800-140762400	Enhancers	GM12878-XiMat	blood
3	chr9:140760200-140760400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:140760600-140760800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:140760600-140760800	Bivalent Enhancer	Fetal Muscle Leg	muscle
6	chr9:140761600-140761800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:140761800-140767800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:140766800-140767000	Bivalent Enhancer	K562	blood
9	chr9:140767800-140768400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:140768400-140768800	Bivalent Enhancer	K562	blood
11	chr9:140768600-140768800	Bivalent Enhancer	Hela-S3	cervix
12	chr9:140770000-140770600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:140770400-140770600	Bivalent Enhancer	Brain Germinal Matrix	brain
14	chr9:140770800-140771200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:140771200-140771400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:140771400-140771600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
17	chr9:140771400-140771600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:140771400-140771600	Bivalent Enhancer	Brain Germinal Matrix	brain
19	chr9:140771400-140773000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
20	chr9:140771600-140771800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:140771600-140772000	Bivalent Enhancer	Ovary	ovary
22	chr9:140771600-140772200	Enhancers	Fetal Brain Male	brain
23	chr9:140771600-140772200	Active TSS	Fetal Brain Female	brain
24	chr9:140771600-140772800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr9:140771600-140772800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:140771600-140773000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
27	chr9:140771600-140773000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
28	chr9:140771600-140773000	Bivalent Enhancer	Lung	lung
29	chr9:140771600-140773800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
30	chr9:140771600-140773800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
31	chr9:140771600-140773800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
32	chr9:140771800-140772000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
33	chr9:140771800-140772000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
34	chr9:140771800-140772000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr9:140771800-140772000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr9:140771800-140772000	Bivalent Enhancer	Right Ventricle	heart
37	chr9:140771800-140772200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr9:140771800-140772200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr9:140771800-140772200	Bivalent/Poised TSS	Thymus	Thymus
40	chr9:140771800-140772400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:140771800-140772600	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr9:140771800-140772800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr9:140771800-140772800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
44	chr9:140771800-140772800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr9:140771800-140773200	Active TSS	H9 Cell Line	embryonic stem cell
46	chr9:140771800-140773400	Active TSS	Brain Angular Gyrus	brain
47	chr9:140771800-140773400	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr9:140771800-140773800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr9:140771800-140773800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr9:140772000-140772200	Bivalent/Poised TSS	Right Ventricle	heart

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