Variant report

Variant	nsv869452
Chromosome Location	chr9:140724997-141018984
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2613)
CpG islands
(count:3906)
Chromatin interactive
region (count:118)
LncRNA
region (count:25)
Mature miRNA
region (count: 1)
miRNA target
sites (count:3)

(count:2613 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

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	chr9:140773050-140773062	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:140778170-140778249	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	chr9:140747930-140748125	GM12878	blood:	n/a	n/a
10	BATF	chr9:140731105-140731321	GM12878	blood:	n/a	n/a
11	BATF	chr9:140768794-140769134	GM12878	blood:	n/a	n/a
12	BATF	chr9:140761031-140761428	GM12878	blood:	n/a	n/a
13	BATF	chr9:140768772-140769151	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:140768767-140769277	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:140761035-140761355	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:140768831-140769188	GM12878	blood:	n/a	n/a
17	BCL3	chr9:140760724-140761478	GM12878	blood:	n/a	n/a
18	BCL3	chr9:140910297-140910754	GM12878	blood:	n/a	n/a
19	BCL3	chr9:140993643-140993893	GM12878	blood:	n/a	n/a
20	BCL3	chr9:140904990-140905244	GM12878	blood:	n/a	n/a
21	BCL3	chr9:140910358-140910716	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:140772955-140773232	K562	blood:	n/a	chr9:140773100-140773109
23	BHLHE40	chr9:140851209-140851501	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
25	BHLHE40	chr9:140862896-140863013	K562	blood:	n/a	n/a
26	BHLHE40	chr9:140782765-140782847	K562	blood:	n/a	n/a
27	BHLHE40	chr9:140760778-140760955	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:140993839-140994191	K562	blood:	n/a	n/a
29	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
30	BHLHE40	chr9:140993888-140994157	HepG2	liver:	n/a	n/a
31	BHLHE40	chr9:140731130-140731329	K562	blood:	n/a	n/a
32	BHLHE40	chr9:140851159-140851515	K562	blood:	n/a	n/a
33	BHLHE40	chr9:140761159-140761359	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:140879411-140879615	HepG2	liver:	n/a	n/a
35	BHLHE40	chr9:140851240-140851513	HepG2	liver:	n/a	n/a
36	BRCA1	chr9:140910350-140910549	GM12878	blood:	n/a	n/a
37	BRCA1	chr9:140761625-140761775	GM12878	blood:	n/a	n/a
38	BRCA1	chr9:140841105-140841139	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr9:140980062-140980441	K562	blood:	n/a	n/a
40	CBX3	chr9:140851178-140851459	K562	blood:	n/a	n/a
41	CBX3	chr9:140839953-140840442	HCT-116	colon:	n/a	n/a
42	CBX3	chr9:140980110-140980451	HCT-116	colon:	n/a	n/a
43	CBX3	chr9:140980114-140980383	K562	blood:	n/a	n/a
44	CBX3	chr9:140778966-140779313	K562	blood:	n/a	n/a
45	CCNT2	chr9:140773119-140773339	K562	blood:	n/a	chr9:140773196-140773205
46	CCNT2	chr9:140918130-140918232	K562	blood:	n/a	n/a
47	CCNT2	chr9:140928501-140928648	K562	blood:	n/a	n/a
48	CCNT2	chr9:140729504-140729518	K562	blood:	n/a	n/a
49	CEBPB	chr9:140731077-140731484	Hela-S3	cervix:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
50	CEBPB	chr9:140896195-140896462	K562	blood:	n/a	chr9:140896330-140896341 chr9:140896305-140896316

(count:3906 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140917431-140917481	GM06990	blood:	n/a
2	chr9:140970188-140970238	ProgFib	skin:	n/a
3	chr9:140917431-140917481	GM06990	blood:	n/a
4	chr9:140970188-140970238	ProgFib	skin:	n/a
5	chr9:140920003-140920053	H1-hESC	embryonic stem cell:	embryo
6	chr9:140815010-140815060	SKMC	muscle:	n/a
7	chr9:140731022-140731072	K562	blood:	n/a
8	chr9:140813541-140813591	HIPEpiC	eye:	n/a
9	chr9:140729241-140729291	AG09309	skin:	n/a
10	chr9:140735359-140735409	GM06990	blood:	n/a
11	chr9:140775967-140776017	NHDF-neo	bronchial:	n/a
12	chr9:140815937-140815987	LNCaP	prostate:	n/a
13	chr9:140916078-140916128	K562	blood:	n/a
14	chr9:140939579-140939629	MCF-7	breast:	n/a
15	chr9:140944087-140944137	ECC-1	luminal epithelium:	n/a
16	chr9:140944087-140944137	HCT-116	colon:	n/a
17	chr9:140777406-140777456	Hela-S3	cervix:	n/a
18	chr9:140815010-140815060	AG04449	skin:	fetal
19	chr9:140939579-140939629	HCPEpiC	choroid plexus:	n/a
20	chr9:140773147-140773197	NHBE	bronchial:	n/a
21	chr9:140728301-140728351	AG04450	lung:	fetal
22	chr9:140733980-140734030	GM19239	blood:	n/a
23	chr9:140733980-140734030	GM12891	blood:	n/a
24	chr9:140727297-140727347	HRE	kidney:	n/a
25	chr9:140818325-140818375	HL-60	blood:	n/a
26	chr9:140814587-140814637	HCT-116	colon:	n/a
27	chr9:140944087-140944137	PANC-1	pancreas:	n/a
28	chr9:141017457-141017507	SK-N-MC	brain:	n/a
29	chr9:140731445-140731495	MCF-7	breast:	n/a
30	chr9:141013537-141013587	H1-hESC	embryonic stem cell:	embryo
31	chr9:140727297-140727347	AG09319	gingival:	n/a
32	chr9:140850133-140850183	K562	blood:	n/a
33	chr9:140970188-140970238	HAEpiC	amniotic membrane:	n/a
34	chr9:140778757-140778807	T-47D	breast:	n/a
35	chr9:141013112-141013162	HRPEpiC	eye:	n/a
36	chr9:140732731-140732781	IMR90	lung:	fetal
37	chr9:140731445-140731495	HRCEpiC	kidney:	n/a
38	chr9:141017001-141017051	SK-N-SH_RA	brain:	n/a
39	chr9:140726863-140726913	GM12878	blood:	n/a
40	chr9:140725587-140725637	SK-N-SH	brain:	n/a
41	chr9:140916078-140916128	HCF	heart:	n/a
42	chr9:140916078-140916128	T-47D	breast:	n/a
43	chr9:140771180-140771230	HCM	heart:	n/a
44	chr9:140733980-140734030	NHBE	bronchial:	n/a
45	chr9:140772545-140772595	NH-A	brain:	n/a
46	chr9:140728301-140728351	SK-N-MC	brain:	n/a
47	chr9:140729241-140729291	AG04450	lung:	fetal
48	chr9:140773483-140773533	GM12892	blood:	n/a
49	chr9:140725898-140725948	Hela-S3	cervix:	n/a
50	chr9:141012312-141012362	HMEC	breast:	n/a

(count:118 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:140955941..140956581-chr9:140995170..140996036,2	MCF-7	breast:
2	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
3	chr9:140870732..140873052-chr9:140876120..140877929,2	K562	blood:
4	chr9:140771023..140775053-chr9:140775846..140778577,6	MCF-7	breast:
5	chr9:140884223..140886209-chr9:140893112..140896030,2	K562	blood:
6	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
7	chr9:140884223..140886209-chr9:140893112..140896030,2	K562	blood:
8	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
9	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
10	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
11	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
12	chr9:140865657..140867593-chr9:140877024..140879679,2	MCF-7	breast:
13	chr9:140772539..140775418-chr9:140775684..140778164,5	MCF-7	breast:
14	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
15	chr9:140725074..140728358-chr9:140730980..140733506,3	K562	blood:
16	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
17	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
18	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
19	chr9:140860566..140865150-chr9:140867846..140870803,4	MCF-7	breast:
20	chr9:140772539..140775418-chr9:140775684..140778164,5	MCF-7	breast:
21	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
22	chr9:140720128..140722152-chr9:140723312..140725717,2	K562	blood:
23	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
24	chr9:140778196..140781664-chr9:140782755..140784568,3	K562	blood:
25	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
26	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
27	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
28	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
29	chr9:140841179..140843467-chr9:140845016..140846625,2	K562	blood:
30	chr9:140797540..140799636-chr9:140804864..140807689,2	K562	blood:
31	chr9:140722366..140725361-chr9:140730961..140733725,2	MCF-7	breast:
32	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
33	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
34	chr9:140763820..140766702-chr9:140806866..140808617,2	K562	blood:
35	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
36	chr9:140889129..140892271-chr9:140900387..140902590,3	K562	blood:
37	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
38	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
39	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
40	chr9:140844057..140846982-chr9:140852715..140855154,2	MCF-7	breast:
41	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
42	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
43	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
44	chr1:149223401..149224369-chr9:140873101..140874123,8	MCF-7	breast:
45	chr9:140864855..140867051-chr9:140878528..140880494,2	K562	blood:
46	chr9:140938244..140939922-chr9:140958739..140960627,2	K562	blood:
47	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
48	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
49	chr9:140960893..140963806-chr9:140965235..140966903,2	K562	blood:
50	chr9:140732797..140735433-chr9:140735710..140738705,2	MCF-7	breast:

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

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

miRNA name	Chromosome Location	mirBase accession
hsa-miR-602	chr9:140732886-140732908	MIMAT0003270

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	EHMT1	hsa-miR-615-3p	chr9:140729903-140729924
2	EHMT1	hsa-miR-30e-5p	chr9:140730456-140730473
3	EHMT1	hsa-miR-1	chr9:140730432-140730455

Variant related genes	Relation type
CACNA1B	TF binding region
ENSG00000203987	TF binding region
MIR602	TF binding region
EHMT1	TF binding region
CACNA1B	CpG island
ENSG00000203987	CpG island
MIR602	CpG island
EHMT1	CpG island
ENSG00000181090	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000207693	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000148408	chromatin interactions
PRRG1	miRNA target sites
GPM6A	miRNA target sites
AKAP11	miRNA target sites
ACIN1	miRNA target sites

Extended variants
information (count: 13119 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:13119 , 50 per page) page: 1 2 3 4 5 6 7 ... 263

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570870679	chr9:140725031-140725032	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs564666111	chr9:140725053-140725054	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528941425	chr9:140725060-140725061	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533162967	chr9:140725079-140725080	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7865298	chr9:140725091-140725092	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs11376299	chr9:140725105-140725106	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs11397094	chr9:140725107-140725108	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs7865308	chr9:140725113-140725114	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535718031	chr9:140725151-140725152	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555553602	chr9:140725187-140725188	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs142048615	chr9:140725193-140725194	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs575242119	chr9:140725199-140725200	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs73581172	chr9:140725249-140725250	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542208548	chr9:140725276-140725277	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188978118	chr9:140725284-140725285	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553450149	chr9:140725298-140725299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs576813925	chr9:140725313-140725314	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529451553	chr9:140725332-140725333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549717276	chr9:140725334-140725335	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs59026755	chr9:140725481-140725482	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs368886522	chr9:140725486-140725487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576281158	chr9:140725587-140725588	Weak transcription Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs147923026	chr9:140725588-140725589	Weak transcription Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs80049959	chr9:140725658-140725659	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560062165	chr9:140725692-140725693	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112535194	chr9:140725706-140725707	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs111444147	chr9:140725774-140725775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564431192	chr9:140725780-140725781	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs147071386	chr9:140725788-140725789	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs191848294	chr9:140725805-140725806	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs377574024	chr9:140725839-140725840	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571752053	chr9:140725841-140725842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs11999765	chr9:140725884-140725885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138387777	chr9:140725911-140725912	Weak transcription Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs143887326	chr9:140725922-140725923	Weak transcription Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs537143589	chr9:140725957-140725958	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs549242594	chr9:140725969-140725970	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565977550	chr9:140725993-140725994	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534880246	chr9:140726031-140726032	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184618764	chr9:140726035-140726036	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs75766126	chr9:140726049-140726050	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189503430	chr9:140726116-140726117	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150181350	chr9:140726123-140726124	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375642805	chr9:140726128-140726129	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs112109349	chr9:140726187-140726188	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs575976840	chr9:140726231-140726232	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535777929	chr9:140726241-140726242	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs73581177	chr9:140726243-140726244	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs113829182	chr9:140726269-140726270	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs7042686	chr9:140726306-140726307	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	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:1910 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140711000-140725400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:140712800-140731000	Weak transcription	Psoas Muscle	Psoas
3	chr9:140713000-140728800	Weak transcription	Small Intestine	intestine
4	chr9:140713000-140732200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr9:140713000-140747200	Weak transcription	Stomach Mucosa	stomach
6	chr9:140713600-140733400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:140713800-140733200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr9:140715200-140733800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr9:140716600-140732000	Weak transcription	Fetal Kidney	kidney
10	chr9:140716800-140732800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr9:140718000-140728400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:140718000-140732800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr9:140718000-140733200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr9:140718200-140731000	Strong transcription	Fetal Muscle Trunk	muscle
15	chr9:140718200-140732000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr9:140718400-140731800	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr9:140718400-140732000	Strong transcription	Adipose Nuclei	Adipose
18	chr9:140718400-140732200	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr9:140718400-140732600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr9:140718600-140731400	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr9:140718600-140732000	Strong transcription	Liver	Liver
22	chr9:140718600-140732400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr9:140718600-140732600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr9:140718600-140733400	Strong transcription	Stomach Smooth Muscle	stomach
25	chr9:140719200-140727000	Weak transcription	Fetal Heart	heart
26	chr9:140719200-140727400	Strong transcription	Esophagus	oesophagus
27	chr9:140719200-140730000	Weak transcription	NH-A	brain
28	chr9:140719200-140732000	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr9:140719200-140732800	Weak transcription	Fetal Brain Male	brain
30	chr9:140719400-140731800	Weak transcription	K562	blood
31	chr9:140719600-140728200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr9:140719800-140732600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:140720000-140727400	Weak transcription	NHDF-Ad	bronchial
34	chr9:140720000-140728600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr9:140720000-140730600	Weak transcription	NHEK	skin
36	chr9:140720000-140732600	Weak transcription	HUVEC	blood vessel
37	chr9:140720200-140732000	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr9:140720200-140732200	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr9:140720400-140731800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr9:140720400-140731800	Strong transcription	Thymus	Thymus
41	chr9:140720400-140732200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:140720400-140732200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr9:140720400-140732200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr9:140721000-140725000	Strong transcription	Brain Germinal Matrix	brain
45	chr9:140721000-140732400	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr9:140721200-140731400	Strong transcription	Fetal Muscle Leg	muscle
47	chr9:140721200-140731600	Strong transcription	Placenta	Placenta
48	chr9:140721200-140732000	Strong transcription	Primary B cells from peripheral blood	blood
49	chr9:140721200-140732000	Weak transcription	HSMM	muscle
50	chr9:140721200-140733000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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