Variant report

Variant	nsv1041153
Chromosome Location	chr12:121171986-121208826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:518)
CpG islands
(count:1160)
Chromatin interactive
region (count:41)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121186082-121186538	HepG2	liver:	n/a	n/a
2	ATF2	chr12:121191421-121191624	GM12878	blood:	n/a	n/a
3	ATF2	chr12:121193022-121193539	GM12878	blood:	n/a	n/a
4	BACH1	chr12:121189207-121189634	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:121189221-121189560	K562	blood:	n/a	n/a
6	BATF	chr12:121193052-121193484	GM12878	blood:	n/a	n/a
7	BATF	chr12:121193103-121193394	GM12878	blood:	n/a	n/a
8	BCL11A	chr12:121193090-121193391	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:121191468-121191655	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:121183735-121183882	K562	blood:	n/a	n/a
11	BRCA1	chr12:121205355-121205477	GM12878	blood:	n/a	n/a
12	BRCA1	chr12:121179594-121179656	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:121181049-121181208	A549	lung:	n/a	n/a
14	CEBPB	chr12:121186267-121186388	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:121179708-121180272	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:121204842-121205251	ECC-1	luminal epithelium:	n/a	chr12:121205067-121205084
17	CEBPB	chr12:121204797-121205275	ECC-1	luminal epithelium:	n/a	chr12:121205067-121205084
18	CEBPB	chr12:121181086-121181226	K562	blood:	n/a	n/a
19	CEBPB	chr12:121195941-121196141	HepG2	liver:	n/a	chr12:121196046-121196057
20	CREB1	chr12:121205161-121205694	ECC-1	luminal epithelium:	n/a	chr12:121205418-121205431
21	CREB1	chr12:121205082-121205675	ECC-1	luminal epithelium:	n/a	chr12:121205418-121205431
22	CTCF	chr12:121188640-121188790	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr12:121175980-121176130	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr12:121198226-121198264	GM13976	blood:	n/a	n/a
25	CTCF	chr12:121188725-121188817	Gliobla	brain:	n/a	n/a
26	CTCF	chr12:121175920-121176070	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr12:121175880-121176030	AG04449	skin:	n/a	n/a
28	CTCF	chr12:121175840-121175990	AG10803	skin:	n/a	n/a
29	CTCF	chr12:121179260-121179410	HepG2	liver:	n/a	chr12:121179318-121179327 chr12:121179318-121179331
30	CTCF	chr12:121175880-121176030	HMEC	breast:	n/a	n/a
31	CTCF	chr12:121205480-121205630	GM12872	blood:	n/a	n/a
32	CTCF	chr12:121188740-121188890	HCT-116	colon:	n/a	n/a
33	CTCF	chr12:121175905-121176009	HepG2	liver:	n/a	n/a
34	CTCF	chr12:121198241-121198276	GM12891	blood:	n/a	n/a
35	CTCF	chr12:121175960-121176110	HAc	cerebellar:	n/a	n/a
36	CTCF	chr12:121187300-121187450	MCF-7	breast:	n/a	chr12:121187312-121187333 chr12:121187317-121187335 chr12:121187318-121187334
37	CTCF	chr12:121187248-121187389	MCF-7	breast:	n/a	chr12:121187312-121187333 chr12:121187317-121187335 chr12:121187318-121187334
38	CTCF	chr12:121175900-121176050	AG04449	skin:	n/a	n/a
39	CTCF	chr12:121188763-121188823	ProgFib	skin:	n/a	n/a
40	CTCF	chr12:121175761-121176111	K562	blood:	n/a	n/a
41	CTCF	chr12:121175900-121176050	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr12:121175723-121176254	A549	lung:	n/a	n/a
43	CTCF	chr12:121187258-121187396	Hela-S3	cervix:	n/a	chr12:121187312-121187333 chr12:121187317-121187335 chr12:121187318-121187334
44	CTCF	chr12:121188700-121188850	GM12870	blood:	n/a	n/a
45	CTCF	chr12:121188733-121188798	HepG2	liver:	n/a	n/a
46	CTCF	chr12:121175860-121176010	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:121188726-121188789	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:121188620-121188770	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:121188735-121188843	GM20000	blood:	n/a	n/a
50	CTCF	chr12:121175880-121176030	HPF	lung:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121198406-121198456	PrEC	prostate:	n/a
2	chr12:121198406-121198456	PrEC	prostate:	n/a
3	chr12:121175819-121175869	HepG2	liver:	n/a
4	chr12:121175674-121175724	GM12878	blood:	n/a
5	chr12:121177142-121177192	HUVEC	blood vessel:	n/a
6	chr12:121174878-121174928	HCPEpiC	choroid plexus:	n/a
7	chr12:121177288-121177338	NT2-D1	testis:	n/a
8	chr12:121202554-121202604	K562	blood:	n/a
9	chr12:121175674-121175724	HIPEpiC	eye:	n/a
10	chr12:121177340-121177390	IMR90	lung:	fetal
11	chr12:121202554-121202604	HRE	kidney:	n/a
12	chr12:121202554-121202604	ECC-1	luminal epithelium:	n/a
13	chr12:121197625-121197675	HNPCEpiC	eye:	n/a
14	chr12:121175417-121175467	NHBE	bronchial:	n/a
15	chr12:121177142-121177192	Caco-2	colon:	n/a
16	chr12:121177340-121177390	HRPEpiC	eye:	n/a
17	chr12:121175115-121175165	GM19239	blood:	n/a
18	chr12:121202554-121202604	Caco-2	colon:	n/a
19	chr12:121175674-121175724	HEK293	kidney:	embryo
20	chr12:121175481-121175531	AG09319	gingival:	n/a
21	chr12:121177413-121177463	Jurkat	blood:	n/a
22	chr12:121197625-121197675	NH-A	brain:	n/a
23	chr12:121177340-121177390	ovcar-3	ovarian:	n/a
24	chr12:121175115-121175165	A549	lung:	n/a
25	chr12:121177221-121177271	BE2_C	brain:	n/a
26	chr12:121174878-121174928	K562	blood:	n/a
27	chr12:121177340-121177390	AG09309	skin:	n/a
28	chr12:121177142-121177192	HL-60	blood:	n/a
29	chr12:121177413-121177463	HCF	heart:	n/a
30	chr12:121175481-121175531	GM06990	blood:	n/a
31	chr12:121198447-121198497	ECC-1	luminal epithelium:	n/a
32	chr12:121197729-121197779	CMK	blood:	n/a
33	chr12:121197625-121197675	K562	blood:	n/a
34	chr12:121175417-121175467	HCT-116	colon:	n/a
35	chr12:121202554-121202604	HepG2	liver:	n/a
36	chr12:121174878-121174928	Caco-2	colon:	n/a
37	chr12:121177340-121177390	NHBE	bronchial:	n/a
38	chr12:121177413-121177463	AG04450	lung:	fetal
39	chr12:121175010-121175060	HCPEpiC	choroid plexus:	n/a
40	chr12:121177413-121177463	AG10803	skin:	n/a
41	chr12:121175417-121175467	T-47D	breast:	n/a
42	chr12:121179966-121180016	A549	lung:	n/a
43	chr12:121175819-121175869	AG04450	lung:	fetal
44	chr12:121203948-121203998	AG04450	lung:	fetal
45	chr12:121177288-121177338	U87	brain:	n/a
46	chr12:121177413-121177463	SK-N-SH_RA	brain:	n/a
47	chr12:121179966-121180016	HCM	heart:	n/a
48	chr12:121177221-121177271	AG09309	skin:	n/a
49	chr12:121198406-121198456	HEEpiC	esophagus:	n/a
50	chr12:121177142-121177192	BE2_C	brain:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:121197842..121198350-chr12:121409283..121409799,2	MCF-7	breast:
2	chr12:121158850..121162908-chr12:121176341..121179016,3	K562	blood:
3	chr12:121180108..121181747-chr12:121181944..121183466,2	K562	blood:
4	chr12:121203090..121205836-chr12:121209356..121211928,2	MCF-7	breast:
5	chr11:67141023..67142718-chr12:121176121..121177621,2	MCF-7	breast:
6	chr12:120965517..120967163-chr12:121175492..121177700,2	K562	blood:
7	chr12:121197854..121198510-chr12:121441406..121442179,2	MCF-7	breast:
8	chr12:121180108..121181747-chr12:121181944..121183466,2	K562	blood:
9	chr12:121171766..121173339-chr12:121175246..121177538,2	K562	blood:
10	chr12:121166233..121168963-chr12:121173743..121176239,2	K562	blood:
11	chr12:121161764..121164291-chr12:121170206..121171996,2	K562	blood:
12	chr12:121205065..121207154-chr12:121208257..121210269,2	K562	blood:
13	chr12:121164614..121167510-chr12:121171430..121173002,2	K562	blood:
14	chr12:121166188..121170592-chr12:121174629..121177744,4	K562	blood:
15	chr12:121173832..121176734-chr12:121177102..121180443,4	K562	blood:
16	chr12:121174261..121175937-chr12:121403993..121406712,2	MCF-7	breast:
17	chr12:121175837..121176393-chr12:121409274..121410074,2	MCF-7	breast:
18	chr12:121175546..121176448-chr12:121409310..121410146,4	MCF-7	breast:
19	chr12:121171766..121173339-chr12:121175246..121177538,2	K562	blood:
20	chr12:121161408..121164023-chr12:121176552..121178436,2	K562	blood:
21	chr12:121170705..121172790-chr12:121179544..121181594,2	MCF-7	breast:
22	chr12:121161679..121164638-chr12:121193767..121195391,2	K562	blood:
23	chr12:121199470..121201795-chr12:121202855..121205373,2	MCF-7	breast:
24	chr12:121170705..121172790-chr12:121179544..121181594,2	MCF-7	breast:
25	chr12:121166701..121168249-chr12:121176996..121179213,2	MCF-7	breast:
26	chr12:121123033..121125000-chr12:121205934..121208435,2	K562	blood:
27	chr1:45186381..45189343-chr12:121198720..121200674,2	K562	blood:
28	chr12:121186636..121188144-chr12:121188175..121190452,2	MCF-7	breast:
29	chr12:121186636..121188144-chr12:121188175..121190452,2	MCF-7	breast:
30	chr12:121208540..121211022-chr12:121211135..121213895,3	K562	blood:
31	chr12:121162627..121165577-chr12:121173142..121175211,3	MCF-7	breast:
32	chr12:121173832..121176734-chr12:121177102..121180443,4	K562	blood:
33	chr12:121199470..121201795-chr12:121202855..121205373,2	MCF-7	breast:
34	chr12:121179321..121181352-chr12:121340474..121342443,2	MCF-7	breast:
35	chr12:121202024..121204515-chr12:121206771..121210558,3	K562	blood:
36	chr12:121161643..121163742-chr12:121186483..121188547,2	MCF-7	breast:
37	chr12:121191123..121193615-chr12:121194473..121197241,2	K562	blood:
38	chr12:121146426..121149148-chr12:121171776..121173750,2	MCF-7	breast:
39	chr12:121169092..121171751-chr12:121174629..121176427,2	K562	blood:
40	chr12:121167755..121169709-chr12:121199569..121201088,2	K562	blood:
41	chr12:121191123..121193615-chr12:121194473..121197241,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACADS-1	chr12:121197146-121197844	expReg_chr12_11530_+
2	lnc-SPPL3.1-1	chr12:121178273-121178346	ENSG00000255946.1
3	lnc-SPPL3.1-1	chr12:121179015-121179321	ENSG00000255946.1
4	lnc-SPPL3.1-1	chr12:121199194-121199395	ENSG00000255946.1

No data

Variant related genes	Relation type
SPPL3	TF binding region
ENSG00000255946	TF binding region
SPPL3	CpG island
ENSG00000255946	CpG island
ENSG00000256569	chromatin interactions
ENSG00000256514	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000157837	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000175970	chromatin interactions
ENSG00000110917	chromatin interactions
ENSG00000272214	chromatin interactions
ENSG00000122971	chromatin interactions
ENSG00000265455	chromatin interactions

Extended variants
information (count: 1728 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1728 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535204724	chr12:121171994-121171995	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs541916258	chr12:121172009-121172010	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555132510	chr12:121172028-121172029	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147040592	chr12:121172089-121172090	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187427413	chr12:121172139-121172140	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563489437	chr12:121172159-121172160	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577077866	chr12:121172222-121172223	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7957395	chr12:121172223-121172224	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559220282	chr12:121172232-121172233	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528304086	chr12:121172233-121172234	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs376861742	chr12:121172245-121172246	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191840307	chr12:121172257-121172258	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11065235	chr12:121172266-121172267	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs530475278	chr12:121172267-121172268	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34683471	chr12:121172320-121172321	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550558376	chr12:121172339-121172340	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570390987	chr12:121172343-121172344	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35084008	chr12:121172392-121172393	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539412306	chr12:121172408-121172409	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs78571707	chr12:121172409-121172410	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184730234	chr12:121172434-121172435	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187613046	chr12:121172462-121172463	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs555175307	chr12:121172468-121172469	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549428930	chr12:121172493-121172494	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145167701	chr12:121172506-121172507	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs574835093	chr12:121172556-121172557	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs34601782	chr12:121172557-121172558	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs77935865	chr12:121172572-121172573	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567687655	chr12:121172585-121172586	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149133021	chr12:121172594-121172595	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557419494	chr12:121172615-121172616	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577216106	chr12:121172616-121172617	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545776667	chr12:121172621-121172622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs192678814	chr12:121172623-121172624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572773000	chr12:121172624-121172625	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541627085	chr12:121172663-121172664	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370521728	chr12:121172716-121172717	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs11065236	chr12:121172739-121172740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530720406	chr12:121172744-121172745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs185678301	chr12:121172757-121172758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564183037	chr12:121172835-121172836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373956060	chr12:121172849-121172850	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189234492	chr12:121172873-121172874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546587237	chr12:121172907-121172908	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143203994	chr12:121172908-121172909	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs148270270	chr12:121172922-121172923	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548811333	chr12:121172930-121172931	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs568603212	chr12:121173007-121173008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs7312316	chr12:121173031-121173032	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs557202530	chr12:121173058-121173059	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:986 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121164000-121177000	Weak transcription	Aorta	Aorta
2	chr12:121164200-121172600	Weak transcription	HSMMtube	muscle
3	chr12:121164200-121176400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr12:121164400-121174800	Weak transcription	Esophagus	oesophagus
5	chr12:121164400-121176000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr12:121164400-121176600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:121164400-121177600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:121164400-121179600	Weak transcription	Primary B cells from peripheral blood	blood
9	chr12:121164600-121172600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:121164600-121177000	Weak transcription	Small Intestine	intestine
11	chr12:121164600-121177200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr12:121164600-121178000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr12:121164800-121173600	Weak transcription	GM12878-XiMat	blood
14	chr12:121164800-121178800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr12:121165000-121175200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr12:121165000-121176000	Weak transcription	Fetal Heart	heart
17	chr12:121165000-121177800	Weak transcription	A549	lung
18	chr12:121165200-121179600	Weak transcription	Psoas Muscle	Psoas
19	chr12:121165600-121178000	Weak transcription	Stomach Mucosa	stomach
20	chr12:121166000-121174200	Weak transcription	Colonic Mucosa	Colon
21	chr12:121166000-121176200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:121166000-121179800	Strong transcription	Fetal Intestine Small	intestine
23	chr12:121167000-121178400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr12:121168400-121179200	Weak transcription	HepG2	liver
25	chr12:121168600-121174800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr12:121168600-121175800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr12:121168600-121176200	Weak transcription	Brain Hippocampus Middle	brain
28	chr12:121168600-121177000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr12:121168600-121196400	Weak transcription	Fetal Brain Female	brain
30	chr12:121168800-121174200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr12:121168800-121176400	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr12:121168800-121177800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr12:121168800-121178800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:121168800-121178800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr12:121169000-121173600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr12:121169000-121174200	Weak transcription	Gastric	stomach
37	chr12:121169000-121174200	Weak transcription	Lung	lung
38	chr12:121169000-121174200	Weak transcription	Right Ventricle	heart
39	chr12:121169000-121174600	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr12:121169000-121174800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:121169000-121174800	Weak transcription	Colon Smooth Muscle	Colon
42	chr12:121169000-121175200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr12:121169000-121175200	Weak transcription	Ovary	ovary
44	chr12:121169000-121175400	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr12:121169000-121175600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr12:121169000-121176000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:121169000-121176000	Weak transcription	Dnd41	blood
48	chr12:121169000-121176000	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr12:121169000-121176200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr12:121169000-121176200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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