Variant report

Variant	esv3437612
Chromosome Location	chr1:151693528-151694776
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:71)
CpG islands
(count:427)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:71 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:151694680-151694917	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr1:151694644-151694973	HepG2	liver:	n/a	n/a
3	CEBPB	chr1:151694559-151695024	A549	lung:	n/a	n/a
4	CEBPB	chr1:151694575-151695070	MCF-7	breast:	n/a	n/a
5	CEBPB	chr1:151694628-151694985	IMR90	lung:	n/a	n/a
6	CEBPB	chr1:151694641-151694962	A549	lung:	n/a	n/a
7	CEBPB	chr1:151694690-151694949	K562	blood:	n/a	n/a
8	CEBPB	chr1:151694651-151694900	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr1:151694069-151694178	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr1:151694163-151694349	A549	lung:	n/a	n/a
11	CTCF	chr1:151694160-151694310	A549	lung:	n/a	n/a
12	CTCF	chr1:151694100-151694250	HCT-116	colon:	n/a	n/a
13	CTCF	chr1:151694149-151694334	GM12891	blood:	n/a	n/a
14	CTCF	chr1:151694160-151694310	HPAF	blood vessel:	n/a	n/a
15	CTCF	chr1:151694240-151694390	HFF-Myc	foreskin:	n/a	n/a
16	CTCF	chr1:151694180-151694330	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr1:151694138-151694330	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr1:151693880-151694030	AG04449	skin:	n/a	n/a
19	CTCF	chr1:151694120-151694270	GM12875	blood:	n/a	n/a
20	CTCF	chr1:151694200-151694350	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr1:151694200-151694350	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr1:151694200-151694350	HCT-116	colon:	n/a	n/a
23	CTCF	chr1:151694240-151694390	RPTEC	kidney:	n/a	n/a
24	CTCF	chr1:151694199-151694338	Fibrobl	skin:	n/a	n/a
25	CTCF	chr1:151694153-151694273	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr1:151694080-151694230	RPTEC	kidney:	n/a	n/a
27	CTCF	chr1:151693480-151693630	NHLF	lung:	n/a	n/a
28	CTCF	chr1:151694360-151694510	A549	lung:	n/a	n/a
29	CTCF	chr1:151694200-151694350	A549	lung:	n/a	n/a
30	CTCF	chr1:151694160-151694310	HFF	foreskin:	n/a	n/a
31	CTCF	chr1:151694220-151694370	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr1:151694068-151694303	A549	lung:	n/a	n/a
33	GATA2	chr1:151694055-151694362	SH-SY5Y	brain:	n/a	n/a
34	HDAC2	chr1:151693973-151694168	H1-hESC	embryonic stem cell:	n/a	n/a
35	MAX	chr1:151694038-151694110	GM12878	blood:	n/a	n/a
36	MXI1	chr1:151692896-151693897	IMR90	lung:	n/a	n/a
37	MXI1	chr1:151693910-151694173	H1-hESC	embryonic stem cell:	n/a	n/a
38	MXI1	chr1:151693945-151694194	GM12878	blood:	n/a	n/a
39	MXI1	chr1:151692377-151694954	SK-N-SH	brain:	n/a	n/a
40	NANOG	chr1:151693925-151694160	H1-hESC	embryonic stem cell:	n/a	n/a
41	NR3C1	chr1:151693390-151693768	A549	lung:	n/a	chr1:151693501-151693518
42	POLR2A	chr1:151693851-151694275	H1-neurons	neurons:	n/a	n/a
43	RAD21	chr1:151694085-151694332	SK-N-SH_RA	brain:	n/a	n/a
44	RAD21	chr1:151694047-151694336	A549	lung:	n/a	n/a
45	RAD21	chr1:151694122-151694294	A549	lung:	n/a	n/a
46	RAD21	chr1:151694039-151694373	A549	lung:	n/a	n/a
47	RAD21	chr1:151693966-151694383	SK-N-SH_RA	brain:	n/a	n/a
48	RCOR1	chr1:151693997-151694117	GM12878	blood:	n/a	n/a
49	RCOR1	chr1:151694012-151694035	HepG2	liver:	n/a	n/a
50	SIN3A	chr1:151693881-151694471	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151693838-151693888	HAEpiC	amniotic membrane:	n/a
2	chr1:151693838-151693888	HepG2	liver:	n/a
3	chr1:151694281-151694331	PANC-1	pancreas:	n/a
4	chr1:151694108-151694158	HIPEpiC	eye:	n/a
5	chr1:151694281-151694331	GM19239	blood:	n/a
6	chr1:151694123-151694173	HIPEpiC	eye:	n/a
7	chr1:151693503-151693553	HCM	heart:	n/a
8	chr1:151693503-151693553	HRPEpiC	eye:	n/a
9	chr1:151694320-151694370	HCPEpiC	choroid plexus:	n/a
10	chr1:151693960-151694010	HRCEpiC	kidney:	n/a
11	chr1:151694108-151694158	SAEC	small airway:	n/a
12	chr1:151693960-151694010	ovcar-3	ovarian:	n/a
13	chr1:151694320-151694370	SK-N-MC	brain:	n/a
14	chr1:151694123-151694173	HCPEpiC	choroid plexus:	n/a
15	chr1:151694320-151694370	ProgFib	skin:	n/a
16	chr1:151693960-151694010	AoSMC	blood vessel:	n/a
17	chr1:151694320-151694370	AG04450	lung:	fetal
18	chr1:151694281-151694331	PrEC	prostate:	n/a
19	chr1:151694320-151694370	ECC-1	luminal epithelium:	n/a
20	chr1:151694108-151694158	MCF-7	breast:	n/a
21	chr1:151693503-151693553	HCF	heart:	n/a
22	chr1:151693960-151694010	MCF10A-Er-Src	breast:	n/a
23	chr1:151693960-151694010	GM06990	blood:	n/a
24	chr1:151693838-151693888	HEEpiC	esophagus:	n/a
25	chr1:151693960-151694010	Hepatocyte	liver:	n/a
26	chr1:151693503-151693553	HEK293	kidney:	embryo
27	chr1:151693503-151693553	IMR90	lung:	fetal
28	chr1:151693838-151693888	MCF10A-Er-Src	breast:	n/a
29	chr1:151694108-151694158	BE2_C	brain:	n/a
30	chr1:151693960-151694010	Hela-S3	cervix:	n/a
31	chr1:151693960-151694010	NT2-D1	testis:	n/a
32	chr1:151693838-151693888	SK-N-MC	brain:	n/a
33	chr1:151693503-151693553	A549	lung:	n/a
34	chr1:151694123-151694173	HAEpiC	amniotic membrane:	n/a
35	chr1:151694108-151694158	CMK	blood:	n/a
36	chr1:151693838-151693888	GM12878	blood:	n/a
37	chr1:151694281-151694331	SKMC	muscle:	n/a
38	chr1:151694320-151694370	AoSMC	blood vessel:	n/a
39	chr1:151694108-151694158	HMEC	breast:	n/a
40	chr1:151694320-151694370	PrEC	prostate:	n/a
41	chr1:151693960-151694010	RPTEC	kidney:	n/a
42	chr1:151693838-151693888	AG04450	lung:	fetal
43	chr1:151693503-151693553	HRE	kidney:	n/a
44	chr1:151694108-151694158	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:151694108-151694158	AG04449	skin:	fetal
46	chr1:151693838-151693888	SK-N-SH_RA	brain:	n/a
47	chr1:151694108-151694158	K562	blood:	n/a
48	chr1:151693838-151693888	HIPEpiC	eye:	n/a
49	chr1:151694320-151694370	A549	lung:	n/a
50	chr1:151693503-151693553	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:151430404..151432335-chr1:151692913..151695013,2	MCF-7	breast:
2	chr1:151685651..151688876-chr1:151692359..151694505,3	MCF-7	breast:
3	chr1:151674905..151676971-chr1:151691184..151693969,2	MCF-7	breast:
4	chr1:151693523..151696845-chr1:151699758..151701957,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL589765.1-1	chr1:151694605-151694638	NONHSAT006412

No data

Variant related genes	Relation type
RIIAD1	TF binding region
CELF3	TF binding region
RIIAD1	CpG island
CELF3	CpG island
ENSG00000143442	chromatin interactions
ENSG00000178796	chromatin interactions
ENSG00000159409	chromatin interactions

Extended variants
information (count: 45 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:45 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532642112	chr1:151693544-151693545	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs552346821	chr1:151693547-151693548	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs183073908	chr1:151693576-151693577	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs532270682	chr1:151693593-151693594	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs558919618	chr1:151693638-151693639	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs577489972	chr1:151693646-151693647	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs78349558	chr1:151693661-151693662	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs367867166	chr1:151693704-151693705	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs187204418	chr1:151693711-151693712	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs568756341	chr1:151693747-151693748	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs376262543	chr1:151693793-151693794	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs373882766	chr1:151693856-151693857	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs190402093	chr1:151693869-151693870	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs562934705	chr1:151693874-151693875	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs551220375	chr1:151693916-151693917	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs575765954	chr1:151693929-151693930	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs570910997	chr1:151693931-151693932	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs539529956	chr1:151693949-151693950	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs552270982	chr1:151693950-151693951	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs566509099	chr1:151693953-151693954	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs148228259	chr1:151693968-151693969	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs535065668	chr1:151694011-151694012	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs554907050	chr1:151694051-151694052	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs575186247	chr1:151694061-151694062	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs544053641	chr1:151694069-151694070	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs557938513	chr1:151694118-151694119	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs577750258	chr1:151694153-151694154	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs182282746	chr1:151694203-151694204	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs186895692	chr1:151694240-151694241	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs1879533	chr1:151694241-151694242	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs370597857	chr1:151694289-151694290	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs41263704	chr1:151694298-151694299	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs562037622	chr1:151694300-151694301	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs148732878	chr1:151694421-151694422	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs551256801	chr1:151694432-151694433	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs571067250	chr1:151694445-151694446	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs558596067	chr1:151694461-151694462	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs374413476	chr1:151694485-151694486	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs546704509	chr1:151694496-151694497	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs142274759	chr1:151694500-151694501	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs193236517	chr1:151694588-151694589	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs374103330	chr1:151694614-151694615	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs78151238	chr1:151694626-151694627	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs376788992	chr1:151694627-151694628	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs371327983	chr1:151694644-151694645	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151691000-151694200	Weak transcription	Spleen	Spleen
2	chr1:151692600-151693600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:151692600-151694000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:151692600-151694600	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr1:151692600-151694600	Enhancers	Small Intestine	intestine
6	chr1:151692800-151693600	Flanking Active TSS	Stomach Smooth Muscle	stomach
7	chr1:151692800-151693600	Bivalent Enhancer	K562	blood
8	chr1:151692800-151693800	Flanking Active TSS	GM12878-XiMat	blood
9	chr1:151692800-151693800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
10	chr1:151692800-151694000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr1:151692800-151694400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:151693000-151693600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:151693000-151693600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr1:151693000-151693600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr1:151693000-151693600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:151693000-151693600	Flanking Active TSS	Brain Cingulate Gyrus	brain
17	chr1:151693000-151693600	Bivalent Enhancer	Fetal Kidney	kidney
18	chr1:151693000-151693600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr1:151693000-151693800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:151693000-151693800	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
21	chr1:151693000-151693800	Flanking Active TSS	Primary B cells from peripheral blood	blood
22	chr1:151693000-151693800	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr1:151693000-151693800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
24	chr1:151693000-151693800	Flanking Active TSS	Liver	Liver
25	chr1:151693000-151693800	Flanking Active TSS	Brain Hippocampus Middle	brain
26	chr1:151693000-151693800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
27	chr1:151693000-151693800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr1:151693000-151693800	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr1:151693000-151693800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
30	chr1:151693000-151693800	Flanking Active TSS	Fetal Lung	lung
31	chr1:151693000-151693800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr1:151693000-151693800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr1:151693000-151693800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
34	chr1:151693000-151693800	Active TSS	Hela-S3	cervix
35	chr1:151693000-151693800	Flanking Active TSS	Osteobl	bone
36	chr1:151693000-151694000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:151693000-151694000	Enhancers	Brain Germinal Matrix	brain
38	chr1:151693000-151694000	Enhancers	Placenta	Placenta
39	chr1:151693000-151694000	Active TSS	Right Ventricle	heart
40	chr1:151693000-151694200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr1:151693000-151694200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr1:151693000-151694200	Active TSS	Colonic Mucosa	Colon
43	chr1:151693000-151694200	Active TSS	Colon Smooth Muscle	Colon
44	chr1:151693000-151694200	Active TSS	Lung	lung
45	chr1:151693000-151694200	Active TSS	Right Atrium	heart
46	chr1:151693000-151694200	Active TSS	NHLF	lung
47	chr1:151693000-151694400	Active TSS	Aorta	Aorta
48	chr1:151693000-151694400	Enhancers	Pancreas	Pancrea
49	chr1:151693000-151694600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:151693000-151694600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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