Variant report

Variant	nsv894495
Chromosome Location	chr9:139786465-139819625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:763)
CpG islands
(count:611)
Chromatin interactive
region (count:112)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:139795759-139796262	HepG2	liver:	n/a	n/a
2	ATF2	chr9:139796801-139797132	GM12878	blood:	n/a	n/a
3	ATF2	chr9:139793565-139794189	GM12878	blood:	n/a	n/a
4	ATF2	chr9:139796219-139797399	GM12878	blood:	n/a	n/a
5	ATF3	chr9:139797607-139798157	A549	lung:	n/a	n/a
6	ATF3	chr9:139796775-139797366	A549	lung:	n/a	n/a
7	ATF3	chr9:139796786-139797264	A549	lung:	n/a	n/a
8	BCL11A	chr9:139796813-139797131	GM12878	blood:	n/a	n/a
9	BCL3	chr9:139796862-139797143	GM12878	blood:	n/a	n/a
10	BCL3	chr9:139795421-139797476	A549	lung:	n/a	chr9:139797347-139797356
11	BCL3	chr9:139797597-139798176	A549	lung:	n/a	chr9:139797816-139797829
12	BCL3	chr9:139795624-139797410	A549	lung:	n/a	chr9:139797347-139797356
13	BCL3	chr9:139797618-139798144	A549	lung:	n/a	chr9:139797816-139797829
14	BCLAF1	chr9:139793519-139794276	GM12878	blood:	n/a	n/a
15	BCLAF1	chr9:139793643-139794077	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:139796283-139797305	GM12878	blood:	n/a	n/a
17	BCLAF1	chr9:139796179-139797280	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:139796177-139797269	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:139800923-139801103	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:139795536-139795546	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:139793691-139794097	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:139796129-139796748	A549	lung:	n/a	n/a
23	CEBPB	chr9:139806590-139806733	MCF-7	breast:	n/a	n/a
24	CEBPB	chr9:139796119-139797347	GM12878	blood:	n/a	n/a
25	CEBPB	chr9:139806673-139806682	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:139817946-139818046	A549	lung:	n/a	n/a
27	CEBPB	chr9:139795490-139795837	A549	lung:	n/a	n/a
28	CEBPB	chr9:139809028-139809108	K562	blood:	n/a	n/a
29	CEBPB	chr9:139817921-139818099	K562	blood:	n/a	n/a
30	CHD1	chr9:139795813-139797269	GM12878	blood:	n/a	n/a
31	CHD1	chr9:139793607-139793973	GM12878	blood:	n/a	n/a
32	CHD1	chr9:139801621-139801666	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr9:139793748-139793969	GM12878	blood:	n/a	n/a
34	CHD2	chr9:139795744-139795798	GM12878	blood:	n/a	n/a
35	CHD2	chr9:139796192-139797307	GM12878	blood:	n/a	n/a
36	CREB1	chr9:139796746-139797306	A549	lung:	n/a	n/a
37	CREB1	chr9:139797631-139798213	A549	lung:	n/a	n/a
38	CREB1	chr9:139797668-139798151	A549	lung:	n/a	n/a
39	CREB1	chr9:139795822-139796181	A549	lung:	n/a	n/a
40	CREB1	chr9:139795718-139796698	A549	lung:	n/a	n/a
41	CTCF	chr9:139793760-139793910	GM12875	blood:	n/a	n/a
42	CTCF	chr9:139805340-139805490	GM12864	blood:	n/a	chr9:139805457-139805475 chr9:139805463-139805472 chr9:139805452-139805473
43	CTCF	chr9:139805500-139805650	SAEC	small airway:	n/a	n/a
44	CTCF	chr9:139793620-139793770	GM12872	blood:	n/a	n/a
45	CTCF	chr9:139805380-139805530	GM12878	blood:	n/a	chr9:139805457-139805475 chr9:139805463-139805472 chr9:139805452-139805473
46	CTCF	chr9:139805394-139805522	GM19238	blood:	n/a	chr9:139805457-139805475 chr9:139805463-139805472 chr9:139805452-139805473
47	CTCF	chr9:139793580-139793730	A549	lung:	n/a	n/a
48	CTCF	chr9:139805360-139805510	GM06990	blood:	n/a	chr9:139805457-139805475 chr9:139805463-139805472 chr9:139805452-139805473
49	CTCF	chr9:139805380-139805530	GM12869	blood:	n/a	chr9:139805457-139805475 chr9:139805463-139805472 chr9:139805452-139805473
50	CTCF	chr9:139805398-139805569	H1-hESC	embryonic stem cell:	n/a	chr9:139805457-139805475 chr9:139805463-139805472 chr9:139805452-139805473

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:139801238-139801288	GM19239	blood:	n/a
2	chr9:139801238-139801288	GM19239	blood:	n/a
3	chr9:139801238-139801288	HAEpiC	amniotic membrane:	n/a
4	chr9:139818362-139818412	NH-A	brain:	n/a
5	chr9:139801358-139801408	AG09319	gingival:	n/a
6	chr9:139804179-139804229	PrEC	prostate:	n/a
7	chr9:139803690-139803740	SKMC	muscle:	n/a
8	chr9:139801358-139801408	HPAEpiC	pulmonary alveolar:	n/a
9	chr9:139801358-139801408	T-47D	breast:	n/a
10	chr9:139802044-139802094	HCT-116	colon:	n/a
11	chr9:139812357-139812407	Jurkat	blood:	n/a
12	chr9:139802603-139802653	SK-N-SH_RA	brain:	n/a
13	chr9:139804179-139804229	AG04450	lung:	fetal
14	chr9:139796499-139796549	SK-N-MC	brain:	n/a
15	chr9:139801238-139801288	AoSMC	blood vessel:	n/a
16	chr9:139804179-139804229	AoSMC	blood vessel:	n/a
17	chr9:139812357-139812407	PrEC	prostate:	n/a
18	chr9:139796499-139796549	HNPCEpiC	eye:	n/a
19	chr9:139812357-139812407	NB4	blood:	n/a
20	chr9:139802044-139802094	SAEC	small airway:	n/a
21	chr9:139796499-139796549	NHDF-neo	bronchial:	n/a
22	chr9:139803690-139803740	AG09309	skin:	n/a
23	chr9:139802044-139802094	H1-hESC	embryonic stem cell:	embryo
24	chr9:139802044-139802094	ovcar-3	ovarian:	n/a
25	chr9:139818475-139818525	AG09309	skin:	n/a
26	chr9:139812357-139812407	HL-60	blood:	n/a
27	chr9:139802044-139802094	HCM	heart:	n/a
28	chr9:139804179-139804229	SK-N-MC	brain:	n/a
29	chr9:139812357-139812407	GM12892	blood:	n/a
30	chr9:139804179-139804229	HUVEC	blood vessel:	n/a
31	chr9:139802603-139802653	AG10803	skin:	n/a
32	chr9:139801238-139801288	SK-N-MC	brain:	n/a
33	chr9:139812357-139812407	Caco-2	colon:	n/a
34	chr9:139803690-139803740	NT2-D1	testis:	n/a
35	chr9:139801238-139801288	GM12878	blood:	n/a
36	chr9:139796499-139796549	SKMC	muscle:	n/a
37	chr9:139804179-139804229	CMK	blood:	n/a
38	chr9:139818362-139818412	PFSK-1	brain:	n/a
39	chr9:139801238-139801288	PANC-1	pancreas:	n/a
40	chr9:139801238-139801288	MCF-7	breast:	n/a
41	chr9:139801358-139801408	NT2-D1	testis:	n/a
42	chr9:139818475-139818525	HIPEpiC	eye:	n/a
43	chr9:139803690-139803740	Jurkat	blood:	n/a
44	chr9:139796499-139796549	LNCaP	prostate:	n/a
45	chr9:139818475-139818525	MCF10A-Er-Src	breast:	n/a
46	chr9:139803690-139803740	AG09319	gingival:	n/a
47	chr9:139818362-139818412	GM06990	blood:	n/a
48	chr9:139801358-139801408	AG09309	skin:	n/a
49	chr9:139802044-139802094	SKMC	muscle:	n/a
50	chr9:139801238-139801288	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:139792856..139794821-chr9:139800116..139802562,2	MCF-7	breast:
2	chr9:139722005..139723538-chr9:139789677..139791201,2	K562	blood:
3	chr9:139795672..139799443-chr9:139799856..139804982,9	MCF-7	breast:
4	chr9:139798690..139801469-chr9:139809287..139811887,2	K562	blood:
5	chr9:139780016..139781830-chr9:139794857..139797433,2	K562	blood:
6	chr9:139806629..139808800-chr9:139814765..139817410,2	K562	blood:
7	chr9:139747109..139749937-chr9:139802751..139806100,4	MCF-7	breast:
8	chr9:139795556..139798405-chr9:139890172..139893015,2	MCF-7	breast:
9	chr9:139750451..139752807-chr9:139790265..139791919,2	K562	blood:
10	chr9:139808449..139810149-chr9:139812752..139815022,2	K562	blood:
11	chr9:139792507..139794136-chr9:139799233..139802028,2	K562	blood:
12	chr9:139800158..139801677-chr9:139804575..139806256,2	K562	blood:
13	chr9:139741851..139743877-chr9:139802198..139803831,2	MCF-7	breast:
14	chr9:139741649..139744546-chr9:139793332..139795839,3	MCF-7	breast:
15	chr9:139747315..139748990-chr9:139818865..139820541,2	MCF-7	breast:
16	chr9:139742261..139744866-chr9:139815519..139817769,2	MCF-7	breast:
17	chr9:139789464..139791827-chr9:139888606..139890570,2	MCF-7	breast:
18	chr9:139805973..139808132-chr9:139827611..139829478,2	K562	blood:
19	chr9:139794979..139797624-chr9:139802353..139803934,2	K562	blood:
20	chr9:139802317..139806633-chr9:139807461..139812727,6	K562	blood:
21	chr9:139816554..139819143-chr9:139870621..139872528,2	K562	blood:
22	chr1:179846415..179847120-chr9:139804027..139804720,2	NB4	blood:
23	chr9:139792836..139799400-chr9:139842261..139846047,7	MCF-7	breast:
24	chr9:139740288..139765167-chr9:139774067..139789146,84	MCF-7	breast:
25	chr9:139818284..139824330-chr9:139824492..139828191,6	K562	blood:
26	chr9:139760009..139761695-chr9:139817996..139820632,2	MCF-7	breast:
27	chr9:139780979..139783224-chr9:139810786..139814698,4	MCF-7	breast:
28	chr9:139795672..139799443-chr9:139799856..139804982,9	MCF-7	breast:
29	chr9:139760703..139762444-chr9:139806612..139809733,3	K562	blood:
30	chr9:139685391..139688312-chr9:139795592..139798395,3	MCF-7	breast:
31	chr9:139759393..139761898-chr9:139811485..139813607,2	MCF-7	breast:
32	chr9:139789889..139792030-chr9:139794319..139796971,2	MCF-7	breast:
33	chr9:139778819..139780705-chr9:139810347..139812332,2	MCF-7	breast:
34	chr9:139776995..139778781-chr9:139818911..139821367,2	MCF-7	breast:
35	chr9:139802369..139806544-chr9:139806670..139809687,5	MCF-7	breast:
36	chr9:139794659..139798542-chr9:139819213..139823469,5	MCF-7	breast:
37	chr9:139750688..139755458-chr9:139795433..139799837,5	MCF-7	breast:
38	chr9:139813120..139815752-chr9:139837094..139840081,2	MCF-7	breast:
39	chr9:139799800..139803528-chr9:139811115..139815321,4	MCF-7	breast:
40	chr9:139741638..139745300-chr9:139796064..139800031,7	MCF-7	breast:
41	chr9:139804187..139806513-chr9:139808686..139811169,3	MCF-7	breast:
42	chr9:139795947..139797778-chr9:139847021..139848590,2	MCF-7	breast:
43	chr9:139794025..139797630-chr9:139809923..139812397,4	MCF-7	breast:
44	chr9:139789514..139792273-chr9:139796475..139799525,3	K562	blood:
45	chr9:139778381..139782500-chr9:139800668..139805077,5	MCF-7	breast:
46	chr9:139811545..139813653-chr9:139815698..139818461,2	MCF-7	breast:
47	chr9:139784208..139786582-chr9:139790103..139791762,2	K562	blood:
48	chr9:139681911..139684166-chr9:139803845..139806276,2	MCF-7	breast:
49	chr9:139769964..139771564-chr9:139789375..139792259,2	K562	blood:
50	chr9:139810560..139812831-chr9:139819083..139821192,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAMDC4-3	chr9:139794255-139794736	expReg_chr9_9714_+

No data

Variant related genes	Relation type
TRAF2	TF binding region
TRAF2	CpG island
ENSG00000107331	chromatin interactions
ENSG00000107281	chromatin interactions
ENSG00000186193	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000266507	chromatin interactions
ENSG00000198569	chromatin interactions
ENSG00000169583	chromatin interactions
ENSG00000184925	chromatin interactions
ENSG00000107317	chromatin interactions
ENSG00000180539	chromatin interactions
ENSG00000244187	chromatin interactions
ENSG00000169905	chromatin interactions
ENSG00000213213	chromatin interactions
ENSG00000272679	chromatin interactions
ENSG00000148362	chromatin interactions
ENSG00000176919	chromatin interactions
ENSG00000272896	chromatin interactions
ENSG00000159069	chromatin interactions
ENSG00000107223	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000127191	chromatin interactions
ENSG00000177943	chromatin interactions
ENSG00000196642	chromatin interactions
ENSG00000054148	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000273066	chromatin interactions

Extended variants
information (count: 1807 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1807 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17250078	chr9:139786465-139786466	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531635092	chr9:139786498-139786499	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs542036802	chr9:139786584-139786585	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs548160253	chr9:139786641-139786642	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs568566013	chr9:139786642-139786643	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs200912694	chr9:139786653-139786654	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs180907622	chr9:139786690-139786691	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs17250771	chr9:139786752-139786753	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs570919050	chr9:139786771-139786772	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs17243697	chr9:139786832-139786833	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs556946850	chr9:139786844-139786845	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs576800412	chr9:139786845-139786846	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs537875807	chr9:139786870-139786871	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs368598552	chr9:139786895-139786896	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs574497952	chr9:139786910-139786911	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs375372259	chr9:139786920-139786921	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs539907183	chr9:139786923-139786924	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs553934599	chr9:139787007-139787008	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs112153480	chr9:139787029-139787030	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs541321006	chr9:139787069-139787070	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs545584294	chr9:139787076-139787077	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs562344199	chr9:139787089-139787090	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs562474576	chr9:139787163-139787164	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs530902702	chr9:139787196-139787197	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs17243704	chr9:139787204-139787205	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs554881031	chr9:139787215-139787216	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs541841068	chr9:139787224-139787225	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs372517828	chr9:139787247-139787248	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113864783	chr9:139787299-139787300	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs141287063	chr9:139787307-139787308	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs150198781	chr9:139787330-139787331	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs377169201	chr9:139787343-139787344	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs145691266	chr9:139787382-139787383	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs574724011	chr9:139787436-139787437	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs17243711	chr9:139787440-139787441	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs2811761	chr9:139787453-139787454	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs530705324	chr9:139787465-139787466	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs2811760	chr9:139787537-139787538	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs554566655	chr9:139787545-139787546	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs113048579	chr9:139787548-139787549	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs567916932	chr9:139787566-139787567	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs149114084	chr9:139787621-139787622	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs567546619	chr9:139787648-139787649	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs2784033	chr9:139787655-139787656	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs576856020	chr9:139787674-139787675	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs545619152	chr9:139787700-139787701	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs555909574	chr9:139787739-139787740	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs552891731	chr9:139787772-139787773	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs2784032	chr9:139787778-139787779	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs541679763	chr9:139787823-139787824	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Urothelial carcinoma	21177765	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	20435627	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
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Hepatocellular carcinoma	22174799	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Mantle cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
Epilepsy	22083797	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Developmental delay	20877625	CNVD
Hypoplastic	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
Palpebral fissures	20877625	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	22495309	CNVD

Chromatin state (count:1438 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139782000-139790400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:139782000-139792600	Weak transcription	Small Intestine	intestine
3	chr9:139782000-139793800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr9:139782000-139794800	Weak transcription	Aorta	Aorta
5	chr9:139782200-139787200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr9:139782200-139787400	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr9:139782200-139787400	Weak transcription	Placenta	Placenta
8	chr9:139782200-139787400	Weak transcription	Left Ventricle	heart
9	chr9:139782200-139787400	Weak transcription	HSMM	muscle
10	chr9:139782200-139787400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr9:139782200-139787400	Weak transcription	NHLF	lung
12	chr9:139782200-139788800	Weak transcription	Fetal Muscle Leg	muscle
13	chr9:139782200-139790600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:139782200-139790600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr9:139782200-139792800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr9:139782200-139793000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr9:139782200-139793200	Weak transcription	Brain Hippocampus Middle	brain
18	chr9:139782200-139793200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr9:139782200-139793600	Weak transcription	Brain Angular Gyrus	brain
20	chr9:139782200-139793800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:139782200-139793800	Weak transcription	Brain Anterior Caudate	brain
22	chr9:139782200-139794400	Weak transcription	Fetal Kidney	kidney
23	chr9:139782200-139794600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr9:139782200-139794800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr9:139782200-139794800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr9:139782200-139794800	Weak transcription	Primary hematopoietic stem cells	blood
27	chr9:139782200-139794800	Weak transcription	Fetal Heart	heart
28	chr9:139782200-139794800	Weak transcription	HSMMtube	muscle
29	chr9:139782200-139795000	Weak transcription	Brain Substantia Nigra	brain
30	chr9:139782200-139795600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr9:139782200-139795600	Weak transcription	Colon Smooth Muscle	Colon
32	chr9:139782200-139795600	Weak transcription	NHDF-Ad	bronchial
33	chr9:139782200-139796200	Weak transcription	Psoas Muscle	Psoas
34	chr9:139782200-139835800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr9:139782200-139837000	Weak transcription	Fetal Brain Male	brain
36	chr9:139782400-139789000	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr9:139782400-139793000	Weak transcription	Primary B cells from cord blood	blood
38	chr9:139782400-139793200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:139782400-139793200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr9:139782400-139795400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:139782400-139795600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr9:139782800-139795000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr9:139783000-139789200	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr9:139783000-139790600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:139783000-139791000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr9:139783000-139793000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr9:139783000-139793200	Strong transcription	Fetal Intestine Small	intestine
48	chr9:139783000-139823600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr9:139783200-139788800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr9:139783200-139788800	Weak transcription	Right Ventricle	heart

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