Variant report

Variant	esv3399192
Chromosome Location	chr11:58938776-58941074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:842)
CpG islands
(count:735)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58938922-58939443	HepG2	liver:	n/a	n/a
2	ATF1	chr11:58938929-58939683	K562	blood:	n/a	n/a
3	ATF2	chr11:58938762-58939567	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58938888-58939552	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr11:58938833-58939529	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:58938763-58939791	GM12878	blood:	n/a	n/a
7	ATF2	chr11:58940105-58941017	GM12878	blood:	n/a	n/a
8	ATF2	chr11:58940179-58940917	GM12878	blood:	n/a	n/a
9	ATF3	chr11:58938993-58939219	K562	blood:	n/a	n/a
10	ATF3	chr11:58938935-58939289	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr11:58938927-58939322	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr11:58938945-58939328	K562	blood:	n/a	n/a
13	BACH1	chr11:58939034-58939633	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:58940293-58940411	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr11:58940245-58940575	GM12878	blood:	n/a	n/a
16	BCL3	chr11:58939361-58939874	GM12878	blood:	n/a	n/a
17	BCL3	chr11:58938792-58939549	A549	lung:	n/a	n/a
18	BCL3	chr11:58940143-58940968	GM12878	blood:	n/a	chr11:58940822-58940831
19	BCLAF1	chr11:58938681-58939885	GM12878	blood:	n/a	n/a
20	BCLAF1	chr11:58940035-58941189	GM12878	blood:	n/a	chr11:58940040-58940053 chr11:58940822-58940831 chr11:58940050-58940063
21	BCLAF1	chr11:58938831-58939880	GM12878	blood:	n/a	n/a
22	BCLAF1	chr11:58939947-58941041	GM12878	blood:	n/a	chr11:58940040-58940053 chr11:58940822-58940831 chr11:58940050-58940063
23	BHLHE40	chr11:58938875-58939776	GM12878	blood:	n/a	n/a
24	BHLHE40	chr11:58938907-58939760	K562	blood:	n/a	n/a
25	BHLHE40	chr11:58938960-58939774	HepG2	liver:	n/a	n/a
26	BHLHE40	chr11:58939245-58939564	A549	lung:	n/a	n/a
27	BHLHE40	chr11:58940184-58940952	GM12878	blood:	n/a	chr11:58940289-58940305
28	BRCA1	chr11:58938948-58939572	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr11:58938978-58939196	HepG2	liver:	n/a	n/a
30	BRCA1	chr11:58939581-58939583	GM12878	blood:	n/a	n/a
31	BRCA1	chr11:58939446-58939700	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr11:58939431-58939651	K562	blood:	n/a	n/a
33	CBX3	chr11:58939323-58939794	K562	blood:	n/a	n/a
34	CCNT2	chr11:58938942-58940172	K562	blood:	n/a	chr11:58939582-58939591 chr11:58939560-58939569
35	CEBPB	chr11:58938933-58939330	MCF-7	breast:	n/a	n/a
36	CEBPB	chr11:58938880-58939759	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:58940861-58942026	H1-hESC	embryonic stem cell:	n/a	chr11:58941815-58941824 chr11:58941813-58941824 chr11:58941813-58941826 chr11:58941815-58941824 chr11:58941815-58941824 chr11:58941815-58941824
38	CEBPB	chr11:58938952-58939241	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:58938910-58939708	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr11:58938913-58939315	K562	blood:	n/a	n/a
41	CEBPB	chr11:58938912-58939618	A549	lung:	n/a	n/a
42	CEBPB	chr11:58938895-58939633	K562	blood:	n/a	n/a
43	CEBPB	chr11:58938680-58939750	GM12878	blood:	n/a	n/a
44	CEBPB	chr11:58938920-58939351	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:58938976-58939705	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:58938836-58939430	A549	lung:	n/a	n/a
47	CEBPB	chr11:58939022-58939178	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:58940355-58942383	Hela-S3	cervix:	n/a	chr11:58941815-58941824 chr11:58941813-58941824 chr11:58941813-58941826 chr11:58941815-58941824 chr11:58941815-58941824 chr11:58941815-58941824
49	CEBPB	chr11:58940554-58940633	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr11:58940727-58941087	H1-hESC	embryonic stem cell:	n/a	n/a

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58940866-58940916	AG09309	skin:	n/a
2	chr11:58939047-58939097	GM06990	blood:	n/a
3	chr11:58940964-58941014	SK-N-MC	brain:	n/a
4	chr11:58940866-58940916	AG09309	skin:	n/a
5	chr11:58939047-58939097	GM06990	blood:	n/a
6	chr11:58940964-58941014	SK-N-MC	brain:	n/a
7	chr11:58939272-58939322	NT2-D1	testis:	n/a
8	chr11:58939797-58939847	HRE	kidney:	n/a
9	chr11:58941051-58941101	HCPEpiC	choroid plexus:	n/a
10	chr11:58940866-58940916	NH-A	brain:	n/a
11	chr11:58939272-58939322	SK-N-MC	brain:	n/a
12	chr11:58939691-58939741	HCF	heart:	n/a
13	chr11:58939694-58939744	A549	lung:	n/a
14	chr11:58940964-58941014	GM19239	blood:	n/a
15	chr11:58941051-58941101	GM06990	blood:	n/a
16	chr11:58939818-58939868	GM06990	blood:	n/a
17	chr11:58941051-58941101	T-47D	breast:	n/a
18	chr11:58939953-58940003	H1-hESC	embryonic stem cell:	embryo
19	chr11:58939818-58939868	NHDF-neo	bronchial:	n/a
20	chr11:58939953-58940003	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:58939691-58939741	HCM	heart:	n/a
22	chr11:58939694-58939744	HRPEpiC	eye:	n/a
23	chr11:58939151-58939201	AG09309	skin:	n/a
24	chr11:58939272-58939322	GM19239	blood:	n/a
25	chr11:58939272-58939322	AG09319	gingival:	n/a
26	chr11:58939953-58940003	HIPEpiC	eye:	n/a
27	chr11:58939802-58939852	GM19239	blood:	n/a
28	chr11:58939797-58939847	HRPEpiC	eye:	n/a
29	chr11:58939797-58939847	NB4	blood:	n/a
30	chr11:58939818-58939868	IMR90	lung:	fetal
31	chr11:58939797-58939847	HCT-116	colon:	n/a
32	chr11:58941051-58941101	K562	blood:	n/a
33	chr11:58941051-58941101	Caco-2	colon:	n/a
34	chr11:58939047-58939097	AG04450	lung:	fetal
35	chr11:58939272-58939322	IMR90	lung:	fetal
36	chr11:58940866-58940916	HAEpiC	amniotic membrane:	n/a
37	chr11:58939953-58940003	AoSMC	blood vessel:	n/a
38	chr11:58940964-58941014	AG09309	skin:	n/a
39	chr11:58939047-58939097	AoSMC	blood vessel:	n/a
40	chr11:58939151-58939201	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:58939047-58939097	SK-N-SH	brain:	n/a
42	chr11:58941051-58941101	NH-A	brain:	n/a
43	chr11:58941051-58941101	SK-N-SH	brain:	n/a
44	chr11:58941051-58941101	SK-N-SH_RA	brain:	n/a
45	chr11:58939047-58939097	Caco-2	colon:	n/a
46	chr11:58940866-58940916	ECC-1	luminal epithelium:	n/a
47	chr11:58939272-58939322	AG10803	skin:	n/a
48	chr11:58939047-58939097	NB4	blood:	n/a
49	chr11:58939797-58939847	Jurkat	blood:	n/a
50	chr11:58939694-58939744	AG04449	skin:	fetal

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58938934..58939576-chr11:59051413..59052308,3	MCF-7	breast:
2	chr11:58939007..58939939-chr11:58975144..58976495,4	MCF-7	breast:
3	chr11:58938973..58939965-chr11:59447518..59448398,3	K562	blood:
4	chr11:58938664..58939165-chr11:59051489..59052229,2	K562	blood:
5	chr11:58939029..58939641-chr11:58968515..58969414,2	MCF-7	breast:
6	chr11:58343237..58345881-chr11:58936566..58939542,2	K562	blood:
7	chr11:58940155..58942428-chr11:58942468..58945192,2	MCF-7	breast:
8	chr11:58939119..58939626-chr11:58968685..58969428,2	K562	blood:
9	chr11:58937186..58939247-chr11:58980596..58982199,2	K562	blood:
10	chr11:58911158..58913877-chr11:58937423..58939058,2	K562	blood:

No data

Variant related genes	Relation type
DTX4	TF binding region
DTX4	CpG island
ENSG00000110031	chromatin interactions
ENSG00000214797	chromatin interactions
ENSG00000263999	chromatin interactions
ENSG00000166801	chromatin interactions

Extended variants
information (count: 67 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:67 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187499575	chr11:58938779-58938780	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs149906964	chr11:58938817-58938818	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs563967253	chr11:58938819-58938820	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs11229864	chr11:58938892-58938893	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs192716603	chr11:58938896-58938897	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs144968931	chr11:58938914-58938915	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs535160816	chr11:58938921-58938922	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs112814401	chr11:58938942-58938943	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs572434386	chr11:58938971-58938972	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs568300471	chr11:58939003-58939004	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs535593066	chr11:58939008-58939009	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs556976180	chr11:58939017-58939018	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs575467257	chr11:58939020-58939021	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs375812763	chr11:58939047-58939048	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs184577506	chr11:58939112-58939113	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs557364898	chr11:58939145-58939146	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs572482471	chr11:58939158-58939159	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs539986537	chr11:58939261-58939262	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs561440182	chr11:58939305-58939306	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs574943544	chr11:58939346-58939347	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs542363561	chr11:58939388-58939389	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs111476450	chr11:58939422-58939423	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs563852478	chr11:58939475-58939476	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs531204349	chr11:58939534-58939535	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs552891086	chr11:58939599-58939600	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564503084	chr11:58939600-58939601	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs148241194	chr11:58939613-58939614	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs199931969	chr11:58939685-58939686	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs73476933	chr11:58939686-58939687	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs144618446	chr11:58939709-58939710	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs3110104	chr11:58939811-58939812	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs550715067	chr11:58939850-58939851	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs376117316	chr11:58939899-58939900	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs112960759	chr11:58939941-58939942	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568942809	chr11:58939964-58939965	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs369992726	chr11:58940027-58940028	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557628578	chr11:58940029-58940030	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12796044	chr11:58940049-58940050	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372299507	chr11:58940083-58940084	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376626663	chr11:58940146-58940147	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533506336	chr11:58940179-58940180	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200185979	chr11:58940192-58940193	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368999650	chr11:58940227-58940228	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs573653897	chr11:58940233-58940234	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs373058754	chr11:58940263-58940264	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs542075372	chr11:58940277-58940278	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs12796683	chr11:58940278-58940279	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs74725520	chr11:58940282-58940283	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs374221571	chr11:58940292-58940293	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs377664524	chr11:58940296-58940297	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD

Chromatin state (count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58931200-58938800	Weak transcription	Primary B cells from cord blood	blood
2	chr11:58934800-58939000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr11:58937600-58939000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr11:58937600-58939000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:58937800-58938800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:58937800-58938800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:58937800-58938800	Weak transcription	HMEC	breast
8	chr11:58937800-58938800	Weak transcription	NHEK	skin
9	chr11:58937800-58939000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:58938200-58938800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr11:58938200-58939000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:58938200-58939000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr11:58938200-58939000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr11:58938600-58938800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr11:58938600-58938800	Enhancers	GM12878-XiMat	blood
16	chr11:58938600-58939200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:58938600-58942000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr11:58938800-58939000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr11:58938800-58939000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:58938800-58939000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr11:58938800-58939000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr11:58938800-58939000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr11:58938800-58939000	Enhancers	Primary B cells from cord blood	blood
24	chr11:58938800-58939000	Enhancers	Primary B cells from peripheral blood	blood
25	chr11:58938800-58939000	Enhancers	Primary T cells fromperipheralblood	blood
26	chr11:58938800-58939000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr11:58938800-58939000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:58938800-58939000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr11:58938800-58939000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
30	chr11:58938800-58939000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr11:58938800-58939000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
32	chr11:58938800-58939000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr11:58938800-58939000	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr11:58938800-58939000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:58938800-58939000	Enhancers	Liver	Liver
36	chr11:58938800-58939000	Enhancers	Duodenum Mucosa	Duodenum
37	chr11:58938800-58939000	Enhancers	Fetal Kidney	kidney
38	chr11:58938800-58939000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr11:58938800-58939000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
40	chr11:58938800-58939000	Bivalent Enhancer	A549	lung
41	chr11:58938800-58939000	Flanking Bivalent TSS/Enh	Dnd41	blood
42	chr11:58938800-58939000	Flanking Active TSS	GM12878-XiMat	blood
43	chr11:58938800-58939000	Enhancers	Hela-S3	cervix
44	chr11:58938800-58939000	Enhancers	HMEC	breast
45	chr11:58938800-58939000	Enhancers	NHEK	skin
46	chr11:58938800-58939200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
47	chr11:58938800-58939200	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr11:58938800-58939400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
49	chr11:58938800-58939400	Enhancers	Fetal Brain Male	brain
50	chr11:58938800-58939800	Flanking Active TSS	Primary hematopoietic stem cells	blood

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