Variant report

Variant	nsv1038506
Chromosome Location	chr9:140575692-140622394
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1339)
CpG islands
(count:732)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1339 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:140584600-140584950	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:140579525-140580074	K562	blood:	n/a	n/a
3	ARID3A	chr9:140589695-140589979	HepG2	liver:	n/a	n/a
4	ATF1	chr9:140579568-140579816	K562	blood:	n/a	n/a
5	ATF2	chr9:140599708-140600308	GM12878	blood:	n/a	n/a
6	ATF2	chr9:140615932-140616395	GM12878	blood:	n/a	n/a
7	ATF2	chr9:140615735-140616429	GM12878	blood:	n/a	n/a
8	BACH1	chr9:140589663-140589942	K562	blood:	n/a	n/a
9	BACH1	chr9:140610803-140610830	K562	blood:	n/a	n/a
10	BACH1	chr9:140618399-140618691	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:140610468-140611052	GM12878	blood:	n/a	n/a
12	BATF	chr9:140610458-140611042	GM12878	blood:	n/a	n/a
13	BATF	chr9:140615504-140615792	GM12878	blood:	n/a	n/a
14	BATF	chr9:140620781-140621220	GM12878	blood:	n/a	n/a
15	BATF	chr9:140615522-140615833	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:140620838-140621162	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:140599949-140600304	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:140610385-140611128	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:140620769-140621207	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:140615461-140615880	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:140610384-140611091	GM12878	blood:	n/a	n/a
22	BCL3	chr9:140615753-140616334	GM12878	blood:	n/a	n/a
23	BCL3	chr9:140618456-140618788	GM12878	blood:	n/a	n/a
24	BCL3	chr9:140613611-140613872	GM12878	blood:	n/a	n/a
25	BCL3	chr9:140615844-140616336	GM12878	blood:	n/a	n/a
26	BCLAF1	chr9:140599725-140600419	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:140615531-140615811	HepG2	liver:	n/a	n/a
28	BHLHE40	chr9:140576952-140577527	GM12878	blood:	n/a	n/a
29	BHLHE40	chr9:140577270-140577418	K562	blood:	n/a	n/a
30	BHLHE40	chr9:140599853-140600268	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:140610467-140611054	HepG2	liver:	n/a	n/a
32	BHLHE40	chr9:140589719-140589890	K562	blood:	n/a	n/a
33	BRCA1	chr9:140615519-140615856	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr9:140610638-140610691	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr9:140585356-140585369	GM12878	blood:	n/a	n/a
36	BRCA1	chr9:140589839-140589992	HepG2	liver:	n/a	n/a
37	CBX3	chr9:140597074-140597422	K562	blood:	n/a	n/a
38	CBX3	chr9:140615543-140615836	K562	blood:	n/a	n/a
39	CBX3	chr9:140610397-140611092	K562	blood:	n/a	n/a
40	CBX3	chr9:140610334-140611181	K562	blood:	n/a	n/a
41	CBX3	chr9:140596958-140597792	K562	blood:	n/a	n/a
42	CBX3	chr9:140612298-140612850	K562	blood:	n/a	n/a
43	CBX3	chr9:140615473-140615838	K562	blood:	n/a	n/a
44	CEBPB	chr9:140579503-140579685	K562	blood:	n/a	chr9:140579613-140579624
45	CEBPB	chr9:140584652-140584959	A549	lung:	n/a	chr9:140584788-140584799
46	CEBPB	chr9:140584569-140584997	Hela-S3	cervix:	n/a	chr9:140584788-140584799
47	CEBPB	chr9:140620727-140621285	GM12878	blood:	n/a	n/a
48	CEBPB	chr9:140579508-140579769	HepG2	liver:	n/a	chr9:140579613-140579624
49	CEBPB	chr9:140584608-140584990	HepG2	liver:	n/a	chr9:140584788-140584799
50	CEBPB	chr9:140593921-140594244	A549	lung:	n/a	chr9:140594077-140594088

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140612549-140612599	HRE	kidney:	n/a
2	chr9:140588475-140588525	ProgFib	skin:	n/a
3	chr9:140615230-140615280	GM12891	blood:	n/a
4	chr9:140605874-140605924	K562	blood:	n/a
5	chr9:140583757-140583807	Caco-2	colon:	n/a
6	chr9:140588811-140588861	HMEC	breast:	n/a
7	chr9:140613912-140613962	U87	brain:	n/a
8	chr9:140605874-140605924	H1-hESC	embryonic stem cell:	embryo
9	chr9:140612442-140612492	HNPCEpiC	eye:	n/a
10	chr9:140605874-140605924	HCF	heart:	n/a
11	chr9:140583757-140583807	SK-N-SH	brain:	n/a
12	chr9:140612442-140612492	SKMC	muscle:	n/a
13	chr9:140615230-140615280	PANC-1	pancreas:	n/a
14	chr9:140611316-140611366	NT2-D1	testis:	n/a
15	chr9:140586201-140586251	HCT-116	colon:	n/a
16	chr9:140588019-140588069	SK-N-MC	brain:	n/a
17	chr9:140586201-140586251	PrEC	prostate:	n/a
18	chr9:140588475-140588525	NT2-D1	testis:	n/a
19	chr9:140612549-140612599	Hepatocyte	liver:	n/a
20	chr9:140583757-140583807	HepG2	liver:	n/a
21	chr9:140605874-140605924	HCPEpiC	choroid plexus:	n/a
22	chr9:140615230-140615280	H1-hESC	embryonic stem cell:	embryo
23	chr9:140612442-140612492	HMEC	breast:	n/a
24	chr9:140588019-140588069	HMEC	breast:	n/a
25	chr9:140588475-140588525	Caco-2	colon:	n/a
26	chr9:140588811-140588861	NB4	blood:	n/a
27	chr9:140586201-140586251	ProgFib	skin:	n/a
28	chr9:140612549-140612599	HCPEpiC	choroid plexus:	n/a
29	chr9:140586201-140586251	K562	blood:	n/a
30	chr9:140612442-140612492	GM06990	blood:	n/a
31	chr9:140588811-140588861	AG09319	gingival:	n/a
32	chr9:140615230-140615280	AG10803	skin:	n/a
33	chr9:140611316-140611366	A549	lung:	n/a
34	chr9:140588475-140588525	HepG2	liver:	n/a
35	chr9:140613912-140613962	SAEC	small airway:	n/a
36	chr9:140612442-140612492	HCT-116	colon:	n/a
37	chr9:140611316-140611366	IMR90	lung:	fetal
38	chr9:140613912-140613962	Hepatocyte	liver:	n/a
39	chr9:140583757-140583807	SKMC	muscle:	n/a
40	chr9:140612442-140612492	HAEpiC	amniotic membrane:	n/a
41	chr9:140588019-140588069	U87	brain:	n/a
42	chr9:140605874-140605924	HCT-116	colon:	n/a
43	chr9:140586201-140586251	T-47D	breast:	n/a
44	chr9:140588019-140588069	K562	blood:	n/a
45	chr9:140611316-140611366	HL-60	blood:	n/a
46	chr9:140615230-140615280	HNPCEpiC	eye:	n/a
47	chr9:140613912-140613962	A549	lung:	n/a
48	chr9:140588475-140588525	HRPEpiC	eye:	n/a
49	chr9:140612549-140612599	Hela-S3	cervix:	n/a
50	chr9:140615546-140615596	Caco-2	colon:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:140569780..140572620-chr9:140576768..140579766,2	K562	blood:
2	chr9:140598819..140601234-chr9:140602896..140605674,2	K562	blood:
3	chr9:140510252..140513201-chr9:140591330..140593988,2	MCF-7	breast:
4	chr9:140576082..140579236-chr9:140582001..140584709,3	MCF-7	breast:
5	chr9:140591766..140593331-chr9:140667353..140669493,2	K562	blood:
6	chr9:140570597..140573721-chr9:140580223..140583053,3	MCF-7	breast:
7	chr9:140565648..140568027-chr9:140588903..140590884,2	MCF-7	breast:
8	chr9:140575772..140578110-chr9:140581931..140583477,2	MCF-7	breast:
9	chr9:140620032..140621601-chr9:140644743..140646680,2	K562	blood:
10	chr9:140621748..140624026-chr9:140624188..140625814,2	K562	blood:
11	chr9:140571698..140574262-chr9:140609421..140611418,2	K562	blood:
12	chr9:140588341..140590402-chr9:140592569..140594596,2	K562	blood:
13	chr9:140583140..140585041-chr9:140587706..140589780,2	MCF-7	breast:
14	chr9:140571660..140574434-chr9:140575012..140577308,2	MCF-7	breast:
15	chr9:140572176..140574298-chr9:140582921..140584758,3	MCF-7	breast:
16	chr9:140566819..140568166-chr9:140589329..140590605,6	MCF-7	breast:
17	chr9:140576034..140577675-chr9:140577860..140579633,2	K562	blood:
18	chr9:140582332..140584753-chr9:140585846..140587935,2	K562	blood:
19	chr9:140567353..140567947-chr9:140589446..140590314,3	K562	blood:
20	chr9:140500112..140502392-chr9:140581573..140583197,2	MCF-7	breast:
21	chr9:140589041..140590820-chr9:140640169..140641796,2	K562	blood:
22	chr9:140572665..140574180-chr9:140575707..140577465,2	MCF-7	breast:
23	chr9:140574379..140576037-chr9:140580035..140582050,2	K562	blood:
24	chr12:80990073..80992118-chr9:140601346..140604315,2	MCF-7	breast:
25	chr9:140603940..140605598-chr9:140612744..140614733,2	K562	blood:
26	chr9:140621172..140623675-chr9:140625261..140627208,2	MCF-7	breast:
27	chr9:140597489..140599006-chr9:140599356..140602224,2	MCF-7	breast:
28	chr9:140610530..140612311-chr9:140612330..140615282,2	K562	blood:
29	chr9:140597489..140599006-chr9:140599356..140602224,2	MCF-7	breast:
30	chr9:140558471..140560077-chr9:140589640..140592131,2	K562	blood:
31	chr9:140574379..140576037-chr9:140580035..140582050,2	K562	blood:
32	chr9:140567130..140567958-chr9:140589475..140590450,2	MCF-7	breast:
33	chr9:140620597..140623025-chr9:140630074..140631675,2	MCF-7	breast:
34	chr9:140511703..140514635-chr9:140580936..140583838,4	K562	blood:
35	chr9:140583140..140585041-chr9:140587706..140589780,2	MCF-7	breast:
36	chr9:140602697..140604949-chr9:140610948..140614150,3	MCF-7	breast:
37	chr9:140616597..140619590-chr9:140626319..140628863,2	K562	blood:
38	chr9:140611220..140612891-chr9:140615717..140617300,2	K562	blood:
39	chr9:140475324..140477749-chr9:140589448..140590973,2	K562	blood:
40	chr9:140603940..140605598-chr9:140612744..140614733,2	K562	blood:
41	chr9:140586032..140587999-chr9:140588162..140589795,2	MCF-7	breast:
42	chr9:140505378..140507784-chr9:140588869..140590581,2	MCF-7	breast:
43	chr9:140565997..140568359-chr9:140573708..140576027,2	MCF-7	breast:
44	chr9:140598819..140601234-chr9:140602896..140605674,2	K562	blood:
45	chr9:140588341..140590402-chr9:140592569..140594596,2	K562	blood:
46	chr9:140576082..140579236-chr9:140582001..140584709,3	MCF-7	breast:
47	chr9:140575772..140578110-chr9:140581931..140583477,2	MCF-7	breast:
48	chr9:140621427..140624098-chr9:140634265..140635909,2	K562	blood:
49	chr9:140582332..140584753-chr9:140585846..140587935,2	K562	blood:
50	chr9:140586032..140587999-chr9:140588162..140589795,2	MCF-7	breast:

No data

Variant related genes	Relation type
EHMT1	TF binding region
EHMT1	CpG island
ENSG00000197070	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000182154	chromatin interactions
ENSG00000130653	chromatin interactions
ENSG00000181090	chromatin interactions

Extended variants
information (count: 2164 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:2164 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527814117	chr9:140575723-140575724	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547474831	chr9:140575753-140575754	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375294625	chr9:140575840-140575841	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4979639	chr9:140575855-140575856	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs80139401	chr9:140575926-140575927	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560243355	chr9:140575947-140575948	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533319335	chr9:140575951-140575952	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577290735	chr9:140575969-140575970	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183402698	chr9:140575995-140575996	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186167238	chr9:140576102-140576103	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140777677	chr9:140576106-140576107	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373866261	chr9:140576107-140576108	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530414527	chr9:140576156-140576157	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529541996	chr9:140576212-140576213	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549635680	chr9:140576214-140576215	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551264248	chr9:140576239-140576240	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150106471	chr9:140576251-140576252	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533924257	chr9:140576314-140576315	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553854416	chr9:140576326-140576327	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570360012	chr9:140576333-140576334	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569655341	chr9:140576342-140576343	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539381863	chr9:140576348-140576349	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545943585	chr9:140576378-140576379	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113188954	chr9:140576395-140576396	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7871045	chr9:140576396-140576397	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs3860888	chr9:140576403-140576404	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs541705777	chr9:140576433-140576434	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371256685	chr9:140576439-140576440	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138388371	chr9:140576476-140576477	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199508241	chr9:140576487-140576488	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4979655	chr9:140576488-140576489	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs541136934	chr9:140576504-140576505	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146176330	chr9:140576517-140576518	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4567119	chr9:140576519-140576520	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs371767670	chr9:140576538-140576539	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543828417	chr9:140576545-140576546	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547009024	chr9:140576562-140576563	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529658022	chr9:140576590-140576591	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549697096	chr9:140576602-140576603	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566282809	chr9:140576607-140576608	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528654358	chr9:140576642-140576643	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376311671	chr9:140576643-140576644	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190580847	chr9:140576646-140576647	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570497055	chr9:140576647-140576648	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183512839	chr9:140576665-140576666	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187998055	chr9:140576669-140576670	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193007058	chr9:140576680-140576681	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111329809	chr9:140576689-140576690	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs3860889	chr9:140576690-140576691	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs569483560	chr9:140576695-140576696	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:20)

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
Breast cancer	21509527	CNVD

Chromatin state (count:2557 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140564000-140591200	Weak transcription	Aorta	Aorta
2	chr9:140564200-140599400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr9:140565600-140577000	Weak transcription	Esophagus	oesophagus
4	chr9:140565600-140577200	Weak transcription	HSMM	muscle
5	chr9:140567800-140582800	Weak transcription	A549	lung
6	chr9:140568000-140579600	Weak transcription	Osteobl	bone
7	chr9:140568200-140579600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr9:140568200-140579800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr9:140568200-140586000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr9:140568600-140577400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr9:140568600-140585200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr9:140568800-140579800	Weak transcription	NHLF	lung
13	chr9:140568800-140583200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr9:140568800-140583200	Weak transcription	HepG2	liver
15	chr9:140569200-140582600	Weak transcription	Hela-S3	cervix
16	chr9:140569200-140583200	Weak transcription	Adipose Nuclei	Adipose
17	chr9:140569200-140583200	Weak transcription	Liver	Liver
18	chr9:140569400-140577200	Weak transcription	Brain Hippocampus Middle	brain
19	chr9:140569400-140577200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr9:140569400-140577200	Weak transcription	Brain Substantia Nigra	brain
21	chr9:140569400-140582800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr9:140569400-140582800	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr9:140569400-140583200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr9:140569600-140589600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr9:140569600-140594600	Weak transcription	NHEK	skin
26	chr9:140571000-140577600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr9:140571800-140586000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr9:140572400-140576200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr9:140572600-140578600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr9:140572800-140577000	Weak transcription	Fetal Intestine Large	intestine
31	chr9:140572800-140577600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr9:140572800-140578000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:140573000-140578000	Enhancers	Primary B cells from peripheral blood	blood
34	chr9:140573000-140638400	Weak transcription	Small Intestine	intestine
35	chr9:140573200-140576400	Enhancers	Duodenum Mucosa	Duodenum
36	chr9:140573200-140578000	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr9:140573400-140579000	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr9:140573400-140580000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:140573600-140575800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr9:140573600-140578600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr9:140573800-140575800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:140573800-140575800	Genic enhancers	Primary T cells fromperipheralblood	blood
43	chr9:140573800-140576200	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr9:140573800-140576400	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr9:140573800-140577800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr9:140573800-140578200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr9:140574000-140577600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr9:140574000-140577800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr9:140574000-140579000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr9:140574000-140579400	Enhancers	H1 Cell Line	embryonic stem cell

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