Variant report

Variant	nsv1053250
Chromosome Location	chr12:67067995-67381411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1748)
CpG islands
(count:1037)
Chromatin interactive
region (count:130)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:67254992-67255139	K562	blood:	n/a	n/a
2	ARID3A	chr12:67314051-67314273	K562	blood:	n/a	n/a
3	ARID3A	chr12:67254981-67255261	HepG2	liver:	n/a	n/a
4	ATF2	chr12:67170642-67171041	GM12878	blood:	n/a	n/a
5	BACH1	chr12:67263777-67263803	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:67076780-67076853	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr12:67170761-67171074	GM12878	blood:	n/a	n/a
8	BATF	chr12:67293386-67293615	GM12878	blood:	n/a	n/a
9	BATF	chr12:67170708-67171069	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:67170790-67171069	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:67170768-67171000	GM12878	blood:	n/a	n/a
12	BCLAF1	chr12:67082643-67082952	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:67314035-67314327	K562	blood:	n/a	n/a
14	BHLHE40	chr12:67279238-67279595	K562	blood:	n/a	n/a
15	BRCA1	chr12:67087970-67087977	GM12878	blood:	n/a	n/a
16	CCNT2	chr12:67302677-67302878	K562	blood:	n/a	n/a
17	CCNT2	chr12:67314049-67314384	K562	blood:	n/a	n/a
18	CEBPB	chr12:67178069-67178104	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:67370388-67370639	HepG2	liver:	n/a	chr12:67370540-67370551
20	CEBPB	chr12:67238386-67238695	HepG2	liver:	n/a	chr12:67238537-67238548
21	CEBPB	chr12:67271748-67271978	K562	blood:	n/a	n/a
22	CEBPB	chr12:67082643-67082935	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr12:67370407-67370706	IMR90	lung:	n/a	chr12:67370540-67370551
24	CEBPB	chr12:67113492-67113613	K562	blood:	n/a	n/a
25	CEBPB	chr12:67267949-67268209	K562	blood:	n/a	chr12:67268066-67268079 chr12:67268066-67268077 chr12:67268068-67268077
26	CEBPB	chr12:67138695-67138991	K562	blood:	n/a	n/a
27	CEBPB	chr12:67216756-67217273	Hela-S3	cervix:	n/a	chr12:67216932-67216943
28	CEBPB	chr12:67229596-67229628	A549	lung:	n/a	n/a
29	CEBPB	chr12:67238358-67238680	A549	lung:	n/a	chr12:67238537-67238548
30	CEBPB	chr12:67073534-67073750	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:67073474-67073755	K562	blood:	n/a	n/a
32	CEBPB	chr12:67073528-67073838	MCF-7	breast:	n/a	n/a
33	CEBPB	chr12:67138687-67139031	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr12:67131609-67131785	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr12:67217824-67218366	A549	lung:	n/a	n/a
36	CEBPB	chr12:67095950-67096156	HepG2	liver:	n/a	chr12:67096084-67096095
37	CEBPB	chr12:67170935-67171105	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr12:67073457-67073808	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:67252792-67252817	A549	lung:	n/a	chr12:67252801-67252812 chr12:67252799-67252812
40	CEBPB	chr12:67130864-67131019	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:67267895-67268214	HepG2	liver:	n/a	chr12:67268066-67268079 chr12:67267913-67267924 chr12:67267911-67267924 chr12:67268066-67268077 chr12:67268068-67268077
42	CEBPB	chr12:67267962-67268207	IMR90	lung:	n/a	chr12:67268066-67268079 chr12:67268066-67268077 chr12:67268068-67268077
43	CEBPB	chr12:67216684-67217075	MCF-7	breast:	n/a	chr12:67216932-67216943
44	CEBPB	chr12:67272501-67272773	H1-hESC	embryonic stem cell:	n/a	chr12:67272606-67272617
45	CEBPB	chr12:67131490-67131690	K562	blood:	n/a	n/a
46	CEBPB	chr12:67217673-67218383	MCF-7	breast:	n/a	n/a
47	CEBPB	chr12:67271680-67271954	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:67313908-67314351	K562	blood:	n/a	n/a
49	CEBPB	chr12:67267907-67268104	H1-hESC	embryonic stem cell:	n/a	chr12:67268066-67268079 chr12:67267913-67267924 chr12:67267911-67267924 chr12:67268066-67268077 chr12:67268068-67268077
50	CEBPB	chr12:67315198-67315283	K562	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:67072951-67073001	HEK293	kidney:	embryo
2	chr12:67192853-67192903	MCF10A-Er-Src	breast:	n/a
3	chr12:67160208-67160258	SK-N-SH_RA	brain:	n/a
4	chr12:67272574-67272624	Hela-S3	cervix:	n/a
5	chr12:67073062-67073112	GM12878	blood:	n/a
6	chr12:67073062-67073112	AG09309	skin:	n/a
7	chr12:67073760-67073810	SK-N-SH	brain:	n/a
8	chr12:67192853-67192903	HCF	heart:	n/a
9	chr12:67278182-67278232	BJ	skin:	n/a
10	chr12:67073760-67073810	HCF	heart:	n/a
11	chr12:67337583-67337633	AG10803	skin:	n/a
12	chr12:67072988-67073038	AG09319	gingival:	n/a
13	chr12:67337583-67337633	GM12878	blood:	n/a
14	chr12:67072951-67073001	CMK	blood:	n/a
15	chr12:67073022-67073072	HL-60	blood:	n/a
16	chr12:67354635-67354685	Caco-2	colon:	n/a
17	chr12:67073760-67073810	K562	blood:	n/a
18	chr12:67072951-67073001	HRCEpiC	kidney:	n/a
19	chr12:67337583-67337633	LNCaP	prostate:	n/a
20	chr12:67073062-67073112	CMK	blood:	n/a
21	chr12:67073266-67073316	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:67197936-67197986	HNPCEpiC	eye:	n/a
23	chr12:67072988-67073038	SKMC	muscle:	n/a
24	chr12:67073022-67073072	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:67278182-67278232	ProgFib	skin:	n/a
26	chr12:67192853-67192903	NHBE	bronchial:	n/a
27	chr12:67072769-67072819	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:67160208-67160258	AG09319	gingival:	n/a
29	chr12:67073062-67073112	ECC-1	luminal epithelium:	n/a
30	chr12:67197984-67198034	HEEpiC	esophagus:	n/a
31	chr12:67197851-67197901	NT2-D1	testis:	n/a
32	chr12:67072951-67073001	AG04449	skin:	fetal
33	chr12:67072951-67073001	NHBE	bronchial:	n/a
34	chr12:67127781-67127831	ProgFib	skin:	n/a
35	chr12:67073760-67073810	SK-N-MC	brain:	n/a
36	chr12:67354635-67354685	PrEC	prostate:	n/a
37	chr12:67197936-67197986	PrEC	prostate:	n/a
38	chr12:67278182-67278232	SKMC	muscle:	n/a
39	chr12:67278182-67278232	T-47D	breast:	n/a
40	chr12:67073022-67073072	PFSK-1	brain:	n/a
41	chr12:67073760-67073810	HAEpiC	amniotic membrane:	n/a
42	chr12:67073062-67073112	HEK293	kidney:	embryo
43	chr12:67073760-67073810	ovcar-3	ovarian:	n/a
44	chr12:67337583-67337633	AG09319	gingival:	n/a
45	chr12:67197984-67198034	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:67127781-67127831	HMEC	breast:	n/a
47	chr12:67073760-67073810	Caco-2	colon:	n/a
48	chr12:67354635-67354685	MCF10A-Er-Src	breast:	n/a
49	chr12:67354635-67354685	HMEC	breast:	n/a
50	chr12:67073266-67073316	A549	lung:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:67352176..67353838-chr12:67356274..67358051,2	MCF-7	breast:
2	chr12:67354444..67357348-chr12:67368007..67370761,2	MCF-7	breast:
3	chr12:67306214..67308962-chr12:67318247..67321230,2	MCF-7	breast:
4	chr12:67109144..67111332-chr12:67122763..67125755,2	K562	blood:
5	chr12:67197849..67199448-chr12:67204005..67205599,2	K562	blood:
6	chr12:67092025..67093817-chr12:67096340..67098697,2	MCF-7	breast:
7	chr12:67352176..67353838-chr12:67356274..67358051,2	MCF-7	breast:
8	chr12:67075881..67076642-chr12:67254630..67255196,2	MCF-7	breast:
9	chr12:67083332..67087175-chr12:67091989..67094050,4	K562	blood:
10	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
11	chr12:67133078..67135278-chr12:67140129..67142008,2	MCF-7	breast:
12	chr12:67102904..67104726-chr12:67105810..67107426,2	MCF-7	breast:
13	chr12:67082373..67083323-chr12:67255078..67255633,2	MCF-7	breast:
14	chr12:67092019..67092945-chr12:67254522..67255578,9	MCF-7	breast:
15	chr12:67300543..67302588-chr12:67306675..67309652,2	MCF-7	breast:
16	chr12:67208944..67211936-chr12:67215045..67216994,2	K562	blood:
17	chr12:67306567..67308676-chr12:67310361..67312988,2	K562	blood:
18	chr12:67155440..67157393-chr12:67158810..67161653,2	MCF-7	breast:
19	chr12:67331706..67334297-chr12:67337234..67339922,3	K562	blood:
20	chr12:67296511..67299023-chr12:67323435..67324974,2	MCF-7	breast:
21	chr12:67169597..67171791-chr2:190019336..190021927,2	MCF-7	breast:
22	chr12:67346635..67348185-chr12:67352722..67355002,2	MCF-7	breast:
23	chr12:67298346..67300741-chr12:67305071..67306583,2	MCF-7	breast:
24	chr12:67181348..67184002-chr12:67184358..67185894,2	K562	blood:
25	chr12:67092981..67095022-chr12:67095390..67096975,2	MCF-7	breast:
26	chr12:67105154..67107956-chr12:67110716..67113455,2	MCF-7	breast:
27	chr12:67255252..67257877-chr12:67460950..67463258,3	MCF-7	breast:
28	chr12:67197849..67200436-chr12:67204099..67206299,2	K562	blood:
29	chr12:67135712..67138658-chr12:67140137..67142202,2	K562	blood:
30	chr12:67092981..67095022-chr12:67095390..67096975,2	MCF-7	breast:
31	chr12:67331706..67333236-chr12:67337234..67339922,2	K562	blood:
32	chr12:67263616..67266720-chr12:67267325..67269969,3	MCF-7	breast:
33	chr12:67354444..67357348-chr12:67368007..67370761,2	MCF-7	breast:
34	chr12:67292063..67294236-chr12:67462037..67463720,2	MCF-7	breast:
35	chr12:67076449..67078895-chr12:67089539..67091893,2	MCF-7	breast:
36	chr12:67173926..67176766-chr12:67210508..67212832,2	MCF-7	breast:
37	chr12:67228648..67230716-chr12:67231553..67234052,2	K562	blood:
38	chr12:67308306..67310520-chr12:67311991..67314710,2	K562	blood:
39	chr12:67216740..67218475-chr12:67222220..67224061,2	MCF-7	breast:
40	chr12:67253380..67256928-chr12:67258329..67261239,3	K562	blood:
41	chr12:67174375..67176870-chr12:67178960..67180503,2	K562	blood:
42	chr12:67083332..67087175-chr12:67091989..67094050,4	K562	blood:
43	chr12:67073537..67076031-chr12:67078174..67080837,2	K562	blood:
44	chr12:67322533..67324494-chr12:67328156..67330477,2	K562	blood:
45	chr12:67253647..67256314-chr12:67565336..67566847,2	K562	blood:
46	chr12:67296029..67298947-chr12:67402634..67404774,2	K562	blood:
47	chr12:67109144..67111332-chr12:67122763..67125755,2	K562	blood:
48	chr12:67253715..67256707-chr12:67270307..67272731,2	K562	blood:
49	chr12:67075881..67076642-chr12:67254630..67255196,2	MCF-7	breast:
50	chr12:67067995..67069958-chr12:67071524..67073123,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRIP1-1	chr12:67301276-67301326	XLOC_010109
2	lnc-CAND1-4	chr12:67350633-67350919	l_673_chr12:67349535-67350919_adrenal
3	lnc-TMBIM4-4	chr12:67122111-67122188	l_672_chr12:67111893-67114021_adrenal
4	lnc-GRIP1-5	chr12:67364375-67366403	NONHSAT029235
5	lnc-TMBIM4-4	chr12:67111894-67112178	l_672_chr12:67111893-67114021_adrenal
6	lnc-TMBIM4-4	chr12:67113856-67114021	l_672_chr12:67111893-67114021_adrenal
7	lnc-TMBIM4-4	chr12:67112662-67112726	l_672_chr12:67111893-67114021_adrenal
8	lnc-GRIP1-1	chr12:67285593-67290880	XLOC_010109
9	lnc-GRIP1-1	chr12:67285656-67285734	ENSG00000256248
10	lnc-CAND1-4	chr12:67349536-67349564	l_673_chr12:67349535-67350919_adrenal
11	lnc-CAND1-4	chr12:67350272-67350614	l_673_chr12:67349535-67350919_adrenal
12	lnc-TMBIM4-4	chr12:67115010-67115062	l_672_chr12:67111893-67114021_adrenal
13	lnc-TMBIM4-4	chr12:67131414-67131624	l_672_chr12:67111893-67114021_adrenal
14	lnc-TMBIM4-4	chr12:67113331-67113418	l_672_chr12:67111893-67114021_adrenal

No data

Variant related genes	Relation type
GRIP1	TF binding region
GRIP1	CpG island
ENSG00000155974	chromatin interactions
ENSG00000111530	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000256248	chromatin interactions
DCBLD2	miRNA target sites

Extended variants
information (count: 11129 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:11129 , 50 per page) page: 1 2 3 4 5 6 7 ... 223

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535702088	chr12:67068073-67068074	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs555635215	chr12:67068122-67068123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541210882	chr12:67068199-67068200	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs569147049	chr12:67068211-67068212	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553167101	chr12:67068240-67068241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs577787540	chr12:67068329-67068330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs78426711	chr12:67068336-67068337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs143150339	chr12:67068358-67068359	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538038365	chr12:67068461-67068462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs192824061	chr12:67068462-67068463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542641777	chr12:67068464-67068465	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185070156	chr12:67068465-67068466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528534228	chr12:67068490-67068491	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188460455	chr12:67068583-67068584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113082055	chr12:67068605-67068606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs77440923	chr12:67068609-67068610	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs71436020	chr12:67068625-67068626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs1531647	chr12:67068626-67068627	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs536618676	chr12:67068643-67068644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536539641	chr12:67068659-67068660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs61926121	chr12:67068663-67068664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567286021	chr12:67068699-67068700	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7310363	chr12:67068708-67068709	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542185515	chr12:67068716-67068717	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs74329537	chr12:67068742-67068743	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372434966	chr12:67068827-67068828	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs9325184	chr12:67068880-67068881	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs139873142	chr12:67068938-67068939	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs556955713	chr12:67068980-67068981	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575532144	chr12:67068982-67068983	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs7310442	chr12:67069003-67069004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs560919054	chr12:67069006-67069007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528470137	chr12:67069018-67069019	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145616686	chr12:67069094-67069095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs565419398	chr12:67069098-67069099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544050830	chr12:67069125-67069126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372643143	chr12:67069185-67069186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs180965302	chr12:67069204-67069205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115774312	chr12:67069210-67069211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530382690	chr12:67069224-67069225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564224403	chr12:67069249-67069250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185136738	chr12:67069250-67069251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150696164	chr12:67069303-67069304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534608753	chr12:67069324-67069325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs59412681	chr12:67069396-67069397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs139849582	chr12:67069429-67069430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149819885	chr12:67069430-67069431	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139040884	chr12:67069457-67069458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557086667	chr12:67069459-67069460	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs145833701	chr12:67069463-67069464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioblastoma multiforme	21569311	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	19115005	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1662 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67062200-67071200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr12:67062400-67068600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr12:67062600-67068400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr12:67062800-67072600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:67063000-67071400	Weak transcription	Brain Germinal Matrix	brain
6	chr12:67065600-67072200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr12:67066000-67068800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr12:67066200-67068400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:67067600-67068400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:67067600-67069400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:67068000-67069000	Enhancers	GM12878-XiMat	blood
12	chr12:67068200-67068400	Enhancers	Primary B cells from cord blood	blood
13	chr12:67068400-67068600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:67068400-67068800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:67068400-67068800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr12:67068400-67068800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr12:67068400-67069000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:67068400-67069200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr12:67068600-67068800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:67068600-67069200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:67068600-67069200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr12:67068600-67072200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:67068800-67069000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:67068800-67072000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:67068800-67072200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr12:67068800-67072200	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr12:67068800-67072400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr12:67069000-67069200	Enhancers	Fetal Brain Female	brain
29	chr12:67069000-67071000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:67069000-67072200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr12:67069000-67072600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:67069200-67071200	Weak transcription	Fetal Brain Female	brain
33	chr12:67069200-67072400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr12:67069200-67072600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr12:67069400-67072200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr12:67069800-67070000	Enhancers	Primary B cells from cord blood	blood
37	chr12:67071000-67071400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:67071200-67071400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr12:67071200-67072600	Active TSS	Fetal Brain Male	brain
40	chr12:67071200-67072600	Active TSS	Fetal Brain Female	brain
41	chr12:67071200-67074200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr12:67071400-67071600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr12:67071400-67071600	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr12:67071400-67071600	Enhancers	Stomach Smooth Muscle	stomach
45	chr12:67071400-67072200	Enhancers	Brain Germinal Matrix	brain
46	chr12:67071400-67072400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr12:67071600-67071800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:67071600-67072400	Enhancers	Rectal Smooth Muscle	rectum
49	chr12:67071800-67072000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:67071800-67072200	Enhancers	Brain Inferior Temporal Lobe	brain

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