Variant report

Variant	nsv560386
Chromosome Location	chr12:117822187-117991547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1055)
CpG islands
(count:122)
Chromatin interactive
region (count:50)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1055 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:117956587-117956998	HepG2	liver:	n/a	n/a
2	ATF3	chr12:117908677-117908831	K562	blood:	n/a	n/a
3	ATF3	chr12:117923605-117924406	A549	lung:	n/a	n/a
4	ATF3	chr12:117924657-117925694	A549	lung:	n/a	n/a
5	ATF3	chr12:117924630-117925637	A549	lung:	n/a	n/a
6	ATF3	chr12:117923612-117924233	A549	lung:	n/a	n/a
7	BCL3	chr12:117923665-117924357	A549	lung:	n/a	n/a
8	BCL3	chr12:117923638-117924508	A549	lung:	n/a	n/a
9	BCL3	chr12:117924618-117925660	A549	lung:	n/a	chr12:117925247-117925256
10	BCL3	chr12:117924619-117925716	A549	lung:	n/a	chr12:117925247-117925256
11	BHLHE40	chr12:117899679-117899828	K562	blood:	n/a	n/a
12	BHLHE40	chr12:117908782-117908789	K562	blood:	n/a	n/a
13	CBX3	chr12:117908623-117908894	K562	blood:	n/a	n/a
14	CBX3	chr12:117908662-117908963	K562	blood:	n/a	n/a
15	CBX3	chr12:117924767-117925597	HCT-116	colon:	n/a	n/a
16	CBX3	chr12:117924849-117925620	HCT-116	colon:	n/a	n/a
17	CEBPB	chr12:117891805-117892107	Hela-S3	cervix:	n/a	chr12:117891972-117891983
18	CEBPB	chr12:117891793-117892157	IMR90	lung:	n/a	chr12:117891972-117891983
19	CEBPB	chr12:117891753-117892233	MCF-7	breast:	n/a	chr12:117891972-117891983
20	CEBPB	chr12:117939348-117939727	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:117939419-117939678	A549	lung:	n/a	n/a
22	CEBPB	chr12:117941227-117941428	H1-hESC	embryonic stem cell:	n/a	chr12:117941262-117941273
23	CEBPB	chr12:117932577-117933197	A549	lung:	n/a	n/a
24	CEBPB	chr12:117941206-117941524	K562	blood:	n/a	chr12:117941262-117941273
25	CEBPB	chr12:117891797-117892160	K562	blood:	n/a	chr12:117891972-117891983
26	CEBPB	chr12:117923524-117925679	A549	lung:	n/a	n/a
27	CEBPB	chr12:117896249-117896604	MCF-7	breast:	n/a	chr12:117896398-117896409
28	CEBPB	chr12:117956753-117957069	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:117959205-117959489	HepG2	liver:	n/a	chr12:117959325-117959336 chr12:117959314-117959325
30	CEBPB	chr12:117939367-117939693	HepG2	liver:	n/a	n/a
31	CEBPB	chr12:117941131-117941461	HepG2	liver:	n/a	chr12:117941262-117941273
32	CEBPB	chr12:117891793-117892155	HepG2	liver:	n/a	chr12:117891972-117891983
33	CEBPB	chr12:117891793-117892169	A549	lung:	n/a	chr12:117891972-117891983
34	CEBPB	chr12:117939399-117939613	K562	blood:	n/a	n/a
35	CEBPB	chr12:117959183-117959414	A549	lung:	n/a	chr12:117959325-117959336 chr12:117959314-117959325
36	CEBPB	chr12:117959214-117959475	Hela-S3	cervix:	n/a	chr12:117959325-117959336 chr12:117959314-117959325
37	CEBPB	chr12:117923734-117924686	A549	lung:	n/a	n/a
38	CEBPB	chr12:117896317-117896460	HepG2	liver:	n/a	chr12:117896398-117896409
39	CEBPB	chr12:117891850-117892188	MCF-7	breast:	n/a	chr12:117891972-117891983
40	CEBPB	chr12:117939292-117939798	A549	lung:	n/a	n/a
41	CEBPB	chr12:117891788-117892249	A549	lung:	n/a	chr12:117891972-117891983
42	CEBPB	chr12:117925007-117925568	MCF-7	breast:	n/a	n/a
43	CEBPB	chr12:117891777-117892150	A549	lung:	n/a	chr12:117891972-117891983
44	CEBPB	chr12:117925096-117925560	A549	lung:	n/a	n/a
45	CEBPB	chr12:117939401-117939712	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr12:117941173-117941498	A549	lung:	n/a	chr12:117941262-117941273
47	CEBPB	chr12:117939523-117939619	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr12:117891801-117892166	H1-hESC	embryonic stem cell:	n/a	chr12:117891972-117891983
49	CEBPB	chr12:117896325-117896475	K562	blood:	n/a	chr12:117896398-117896409
50	CEBPB	chr12:117924854-117925513	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117845588-117845638	SAEC	small airway:	n/a
2	chr12:117845588-117845638	SK-N-MC	brain:	n/a
3	chr12:117901264-117901314	NHDF-neo	bronchial:	n/a
4	chr12:117901264-117901314	PrEC	prostate:	n/a
5	chr12:117901264-117901314	Jurkat	blood:	n/a
6	chr12:117845588-117845638	BJ	skin:	n/a
7	chr12:117845588-117845638	K562	blood:	n/a
8	chr12:117845588-117845638	HUVEC	blood vessel:	n/a
9	chr12:117845588-117845638	BE2_C	brain:	n/a
10	chr12:117845588-117845638	H1-hESC	embryonic stem cell:	embryo
11	chr12:117901264-117901314	AG04449	skin:	fetal
12	chr12:117901264-117901314	SKMC	muscle:	n/a
13	chr12:117845588-117845638	HRPEpiC	eye:	n/a
14	chr12:117845588-117845638	GM12878	blood:	n/a
15	chr12:117901264-117901314	PANC-1	pancreas:	n/a
16	chr12:117901264-117901314	HEK293	kidney:	embryo
17	chr12:117845588-117845638	AG09309	skin:	n/a
18	chr12:117845588-117845638	MCF10A-Er-Src	breast:	n/a
19	chr12:117845588-117845638	HRCEpiC	kidney:	n/a
20	chr12:117901264-117901314	HRE	kidney:	n/a
21	chr12:117845588-117845638	Jurkat	blood:	n/a
22	chr12:117901264-117901314	T-47D	breast:	n/a
23	chr12:117845588-117845638	HIPEpiC	eye:	n/a
24	chr12:117845588-117845638	NB4	blood:	n/a
25	chr12:117845588-117845638	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:117845588-117845638	HMEC	breast:	n/a
27	chr12:117845588-117845638	SK-N-SH_RA	brain:	n/a
28	chr12:117845588-117845638	RPTEC	kidney:	n/a
29	chr12:117845588-117845638	HL-60	blood:	n/a
30	chr12:117845588-117845638	LNCaP	prostate:	n/a
31	chr12:117845588-117845638	NH-A	brain:	n/a
32	chr12:117901264-117901314	AG04450	lung:	fetal
33	chr12:117901264-117901314	SK-N-SH_RA	brain:	n/a
34	chr12:117901264-117901314	AG10803	skin:	n/a
35	chr12:117901264-117901314	SK-N-MC	brain:	n/a
36	chr12:117845588-117845638	NHDF-neo	bronchial:	n/a
37	chr12:117901264-117901314	BE2_C	brain:	n/a
38	chr12:117901264-117901314	LNCaP	prostate:	n/a
39	chr12:117845588-117845638	HCM	heart:	n/a
40	chr12:117901264-117901314	ECC-1	luminal epithelium:	n/a
41	chr12:117901264-117901314	Hela-S3	cervix:	n/a
42	chr12:117845588-117845638	HEK293	kidney:	embryo
43	chr12:117845588-117845638	AG04450	lung:	fetal
44	chr12:117845588-117845638	CMK	blood:	n/a
45	chr12:117901264-117901314	HCM	heart:	n/a
46	chr12:117845588-117845638	AG10803	skin:	n/a
47	chr12:117845588-117845638	PFSK-1	brain:	n/a
48	chr12:117901264-117901314	SK-N-SH	brain:	n/a
49	chr12:117901264-117901314	HepG2	liver:	n/a
50	chr12:117901264-117901314	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:117922408..117925128-chr12:117937120..117940013,2	MCF-7	breast:
2	chr12:117907351..117909804-chr12:117912936..117915339,2	K562	blood:
3	chr12:117881661..117883642-chr12:117884385..117886597,2	MCF-7	breast:
4	chr12:117887249..117891968-chr12:117894692..117899084,4	MCF-7	breast:
5	chr12:117650139..117651011-chr12:117839641..117840548,2	K562	blood:
6	chr12:117881661..117883642-chr12:117884385..117886597,2	MCF-7	breast:
7	chr12:117952997..117954824-chr12:117958093..117960432,2	K562	blood:
8	chr12:117808217..117808933-chr12:117910612..117911733,3	MCF-7	breast:
9	chr12:117934649..117936494-chr12:117937968..117939716,2	K562	blood:
10	chr12:117851047..117852638-chr12:117858181..117860156,2	MCF-7	breast:
11	chr12:117891223..117893076-chr12:117894478..117896317,2	MCF-7	breast:
12	chr12:117913625..117915169-chr12:117932222..117935019,2	MCF-7	breast:
13	chr12:117943124..117944687-chr12:117944971..117946627,2	K562	blood:
14	chr12:117955577..117957947-chr12:117959289..117962160,2	K562	blood:
15	chr12:117984255..117986499-chr12:117995179..117997923,2	K562	blood:
16	chr12:117913535..117916907-chr12:117919468..117922252,3	MCF-7	breast:
17	chr12:117933471..117935639-chr12:117944305..117946220,2	MCF-7	breast:
18	chr12:117967450..117970340-chr12:117970474..117972583,2	MCF-7	breast:
19	chr12:117900421..117902766-chr12:117918536..117920834,2	K562	blood:
20	chr12:117927918..117930716-chr12:117931239..117933024,2	MCF-7	breast:
21	chr12:117922408..117925128-chr12:117937120..117940013,2	MCF-7	breast:
22	chr12:117968610..117970355-chr12:117972527..117974840,2	K562	blood:
23	chr12:117851047..117852638-chr12:117858181..117860156,2	MCF-7	breast:
24	chr12:117801474..117803161-chr12:117984043..117986705,2	MCF-7	breast:
25	chr12:117933471..117935639-chr12:117944305..117946220,2	MCF-7	breast:
26	chr12:117952997..117954824-chr12:117958093..117960432,2	K562	blood:
27	chr12:117900421..117902766-chr12:117918536..117920834,2	K562	blood:
28	chr12:117813368..117815343-chr12:117831412..117833212,2	MCF-7	breast:
29	chr12:117913535..117916907-chr12:117919468..117922252,3	MCF-7	breast:
30	chr12:117907351..117909804-chr12:117912936..117915339,2	K562	blood:
31	chr12:117968610..117970355-chr12:117972527..117974840,2	K562	blood:
32	chr12:117888895..117891858-chr12:117912136..117914448,2	K562	blood:
33	chr12:117943124..117944687-chr12:117944971..117946627,2	K562	blood:
34	chr12:117650216..117651027-chr12:117908286..117909137,2	K562	blood:
35	chr1:54609374..54609957-chr12:117938978..117939810,2	MCF-7	breast:
36	chr12:117938022..117941768-chr12:117943153..117947077,5	K562	blood:
37	chr12:117937795..117939522-chr12:117945577..117947118,2	K562	blood:
38	chr12:117964525..117967248-chr12:117968335..117970597,2	MCF-7	breast:
39	chr12:117934649..117936494-chr12:117937968..117939716,2	K562	blood:
40	chr12:117955577..117957947-chr12:117959289..117962160,2	K562	blood:
41	chr12:117891223..117893076-chr12:117894478..117896317,2	MCF-7	breast:
42	chr12:117937795..117939522-chr12:117945577..117947118,2	K562	blood:
43	chr12:117818425..117820449-chr12:117830526..117832304,2	MCF-7	breast:
44	chr12:117938022..117941768-chr12:117943153..117947077,5	K562	blood:
45	chr12:117967450..117970340-chr12:117970474..117972583,2	MCF-7	breast:
46	chr12:117804326..117804994-chr12:117910584..117911095,2	MCF-7	breast:
47	chr12:117927918..117930716-chr12:117931239..117933024,2	MCF-7	breast:
48	chr12:117913625..117915169-chr12:117932222..117935019,2	MCF-7	breast:
49	chr12:117870858..117872885-chr12:118114785..118116553,2	MCF-7	breast:
50	chr12:117964525..117967248-chr12:117968335..117970597,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOS1-1	chr12:117889507-117890028	NONHSAT031006
2	lnc-KSR2-1	chr12:117876765-117877302	l_736_chr12:117875575-117878382_testes
3	lnc-KSR2-1	chr12:117877994-117878140	l_736_chr12:117875575-117878382_testes
4	lnc-FBXW8-2	chr12:117894714-117894791	ENSG00000255686.1
5	lnc-KSR2-1	chr12:117877771-117877976	l_736_chr12:117875575-117878382_testes
6	lnc-FBXW8-2	chr12:117890817-117891300	ENSG00000255686.1
7	lnc-FBXW8-5	chr12:117822308-117822424	l_735_chr12:117793644-117842406_testes
8	lnc-KSR2-1	chr12:117875576-117875615	l_736_chr12:117875575-117878382_testes
9	lnc-KSR2-1	chr12:117878150-117878382	l_736_chr12:117875575-117878382_testes
10	lnc-FBXW8-5	chr12:117842386-117842406	l_735_chr12:117793644-117842406_testes
11	lnc-NOS1-1	chr12:117889506-117889975	NONHSAT030989
12	lnc-FBXW8-2	chr12:117890856-117891246	NONHSAT031008
13	lnc-NOS1-2	chr12:117890859-117896866	NONHSAT031009

No data

Variant related genes	Relation type
ENSG00000255686	TF binding region
NOS1	TF binding region
ENSG00000255686	CpG island
NOS1	CpG island
ENSG00000089250	chromatin interactions
ENSG00000171435	chromatin interactions
ENSG00000255686	chromatin interactions

Extended variants
information (count: 6815 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6815 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1552229	chr12:117822187-117822188	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377611347	chr12:117822286-117822287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148787302	chr12:117822292-117822293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190304727	chr12:117822303-117822304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568231087	chr12:117822309-117822310	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs537144677	chr12:117822325-117822326	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs556979720	chr12:117822342-117822343	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs182700443	chr12:117822348-117822349	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs535683119	chr12:117822362-117822363	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs1552230	chr12:117822385-117822386	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs572230460	chr12:117822389-117822390	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs565077394	chr12:117822418-117822419	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs58264841	chr12:117822446-117822447	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs146832653	chr12:117822461-117822462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541155333	chr12:117822464-117822465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564124855	chr12:117822480-117822481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187526333	chr12:117822524-117822525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577655459	chr12:117822527-117822528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544468092	chr12:117822538-117822539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140660299	chr12:117822575-117822576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73395927	chr12:117822609-117822610	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs546075388	chr12:117822643-117822644	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs145834336	chr12:117822652-117822653	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs562642219	chr12:117822657-117822658	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs560481169	chr12:117822731-117822732	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs539454636	chr12:117822736-117822737	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs548456576	chr12:117822740-117822741	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs532158302	chr12:117822794-117822795	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs568273741	chr12:117822809-117822810	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs537293617	chr12:117822839-117822840	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs547214727	chr12:117822840-117822841	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs550502245	chr12:117822873-117822874	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs570558035	chr12:117822888-117822889	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs151058153	chr12:117822942-117822943	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs371681391	chr12:117822972-117822973	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs552564761	chr12:117822973-117822974	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs572478888	chr12:117822981-117822982	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs535750720	chr12:117823022-117823023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556570226	chr12:117823101-117823102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555680120	chr12:117823130-117823131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575527211	chr12:117823248-117823249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544819222	chr12:117823252-117823253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78969063	chr12:117823307-117823308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144529843	chr12:117823342-117823343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs578058715	chr12:117823384-117823385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12372265	chr12:117823466-117823467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576441440	chr12:117823496-117823497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376257891	chr12:117823525-117823526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559215474	chr12:117823712-117823713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540337508	chr12:117823722-117823723	Weak transcription	n/a	n/a	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	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117815600-117822400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:117822400-117822800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:117822600-117823000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr12:117822600-117823000	Bivalent Enhancer	Fetal Muscle Leg	muscle
5	chr12:117822800-117828600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr12:117825400-117825600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:117825400-117826400	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr12:117825400-117826600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr12:117825400-117828800	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr12:117825600-117825800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:117825800-117826600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:117826400-117827000	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr12:117826600-117827200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:117827000-117827200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr12:117828600-117829000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:117828800-117838000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr12:117829000-117834200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr12:117829600-117830800	Enhancers	Liver	Liver
19	chr12:117831600-117831800	Enhancers	Esophagus	oesophagus
20	chr12:117831800-117845800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr12:117832400-117832600	Enhancers	Esophagus	oesophagus
22	chr12:117834200-117834400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:117834400-117835200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr12:117836600-117836800	Enhancers	Psoas Muscle	Psoas
25	chr12:117836800-117838400	Weak transcription	Psoas Muscle	Psoas
26	chr12:117838000-117839600	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr12:117838200-117839600	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr12:117838400-117839200	Enhancers	Liver	Liver
29	chr12:117838400-117839200	Enhancers	Psoas Muscle	Psoas
30	chr12:117839200-117846200	Weak transcription	Psoas Muscle	Psoas
31	chr12:117839600-117841600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr12:117839600-117842000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr12:117840400-117840600	Enhancers	Pancreas	Pancrea
34	chr12:117841000-117841600	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr12:117841400-117842200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
36	chr12:117841600-117843200	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr12:117842000-117843200	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr12:117842200-117842400	Bivalent Enhancer	Fetal Muscle Leg	muscle
39	chr12:117842200-117842800	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr12:117842200-117842800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr12:117842600-117843000	Enhancers	Placenta	Placenta
42	chr12:117842800-117843200	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr12:117843200-117845400	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr12:117843200-117845800	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr12:117843200-117846000	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr12:117843600-117843800	Weak transcription	Pancreas	Pancrea
47	chr12:117843800-117844000	Enhancers	Pancreas	Pancrea
48	chr12:117844000-117844200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr12:117844000-117844800	Weak transcription	Pancreas	Pancrea
50	chr12:117844600-117845000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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