Variant report

Variant	esv3418566
Chromosome Location	chr11:17035326-17037224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:380)
CpG islands
(count:612)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17036440-17037210	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:17036145-17036156	HepG2	liver:	n/a	n/a
3	BACH1	chr11:17036133-17036192	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:17035550-17035605	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr11:17036715-17037219	A549	lung:	n/a	n/a
6	BCL3	chr11:17036311-17036869	A549	lung:	n/a	chr11:17036590-17036599
7	BHLHE40	chr11:17036486-17037136	HepG2	liver:	n/a	n/a
8	CEBPD	chr11:17036007-17036401	HepG2	liver:	n/a	n/a
9	CEBPD	chr11:17034926-17035668	HepG2	liver:	n/a	n/a
10	CHD1	chr11:17035596-17035599	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr11:17035272-17035452	HepG2	liver:	n/a	chr11:17035441-17035451
12	CHD2	chr11:17036526-17036750	HepG2	liver:	n/a	n/a
13	CHD2	chr11:17036167-17036308	HepG2	liver:	n/a	n/a
14	CREB1	chr11:17035875-17036268	A549	lung:	n/a	n/a
15	CREB1	chr11:17034354-17035789	A549	lung:	n/a	n/a
16	CREB1	chr11:17036550-17036832	A549	lung:	n/a	n/a
17	CTBP2	chr11:17034437-17035493	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr11:17035514-17035604	GM19240	blood:	n/a	n/a
19	CTCF	chr11:17036680-17036830	HCFaa	heart:	n/a	chr11:17036768-17036786
20	CTCF	chr11:17036720-17036870	AG04450	lung:	n/a	chr11:17036768-17036786
21	CTCF	chr11:17036761-17036804	GM12878	blood:	n/a	chr11:17036768-17036786
22	CTCF	chr11:17036720-17036870	GM12874	blood:	n/a	chr11:17036768-17036786
23	CTCF	chr11:17036680-17036830	WERI-Rb-1	eye:	n/a	chr11:17036768-17036786
24	CTCF	chr11:17036700-17036850	HCM	heart:	n/a	chr11:17036768-17036786
25	CTCF	chr11:17036660-17036810	GM12868	blood:	n/a	chr11:17036768-17036786
26	CTCF	chr11:17035560-17035710	GM12871	blood:	n/a	n/a
27	CTCF	chr11:17036683-17036845	K562	blood:	n/a	chr11:17036768-17036786
28	CTCF	chr11:17036760-17036910	K562	blood:	n/a	chr11:17036768-17036786
29	CTCF	chr11:17036680-17036830	K562	blood:	n/a	chr11:17036768-17036786
30	CTCF	chr11:17036660-17036810	MCF-7	breast:	n/a	chr11:17036768-17036786
31	CTCF	chr11:17036656-17036894	GM13977	blood:	n/a	chr11:17036768-17036786
32	CTCF	chr11:17036498-17037015	MCF-7	breast:	n/a	chr11:17036768-17036786
33	CTCF	chr11:17036660-17036810	NHDF-neo	bronchial:	n/a	chr11:17036768-17036786
34	CTCF	chr11:17036633-17036856	LNCaP	prostate:	n/a	chr11:17036768-17036786
35	CTCF	chr11:17036680-17036830	GM12870	blood:	n/a	chr11:17036768-17036786
36	CTCF	chr11:17036720-17036870	AG09319	gingival:	n/a	chr11:17036768-17036786
37	CTCF	chr11:17036684-17036855	Pancreas_OC	pancreas:	n/a	chr11:17036768-17036786
38	CTCF	chr11:17036656-17036826	K562	blood:	n/a	chr11:17036768-17036786
39	CTCF	chr11:17036568-17036890	H1-hESC	embryonic stem cell:	n/a	chr11:17036768-17036786
40	CTCF	chr11:17036720-17036870	GM12873	blood:	n/a	chr11:17036768-17036786
41	CTCF	chr11:17036636-17036882	H1-hESC	embryonic stem cell:	n/a	chr11:17036768-17036786
42	CTCF	chr11:17036600-17036750	HAc	cerebellar:	n/a	n/a
43	CTCF	chr11:17036670-17036837	GM10266	blood:	n/a	chr11:17036768-17036786
44	CTCF	chr11:17036632-17036872	Medullo	brain:	n/a	chr11:17036768-17036786
45	CTCF	chr11:17036440-17036590	GM12872	blood:	n/a	n/a
46	CTCF	chr11:17036706-17036830	Spleen_OC	spleen:	n/a	chr11:17036768-17036786
47	CTCF	chr11:17036700-17036850	GM12865	blood:	n/a	chr11:17036768-17036786
48	CTCF	chr11:17036596-17036910	K562	blood:	n/a	chr11:17036768-17036786
49	CTCF	chr11:17036680-17036830	HPF	lung:	n/a	chr11:17036768-17036786
50	CTCF	chr11:17036644-17036805	Lung_OC	lung:	n/a	chr11:17036768-17036786

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17036142-17036192	HRE	kidney:	n/a
2	chr11:17036644-17036694	HAEpiC	amniotic membrane:	n/a
3	chr11:17036142-17036192	HRE	kidney:	n/a
4	chr11:17036644-17036694	HAEpiC	amniotic membrane:	n/a
5	chr11:17036644-17036694	ProgFib	skin:	n/a
6	chr11:17036644-17036694	PrEC	prostate:	n/a
7	chr11:17035876-17035926	Caco-2	colon:	n/a
8	chr11:17035876-17035926	SK-N-SH_RA	brain:	n/a
9	chr11:17035779-17035829	NH-A	brain:	n/a
10	chr11:17036137-17036187	HepG2	liver:	n/a
11	chr11:17036137-17036187	HUVEC	blood vessel:	n/a
12	chr11:17035411-17035461	HCPEpiC	choroid plexus:	n/a
13	chr11:17036337-17036387	PFSK-1	brain:	n/a
14	chr11:17035779-17035829	HUVEC	blood vessel:	n/a
15	chr11:17036581-17036631	T-47D	breast:	n/a
16	chr11:17036142-17036192	HCM	heart:	n/a
17	chr11:17036644-17036694	GM12878	blood:	n/a
18	chr11:17036644-17036694	Hepatocyte	liver:	n/a
19	chr11:17036644-17036694	HEK293	kidney:	embryo
20	chr11:17036403-17036453	LNCaP	prostate:	n/a
21	chr11:17036403-17036453	HMEC	breast:	n/a
22	chr11:17036337-17036387	HUVEC	blood vessel:	n/a
23	chr11:17036137-17036187	H1-hESC	embryonic stem cell:	embryo
24	chr11:17036337-17036387	Hepatocyte	liver:	n/a
25	chr11:17036042-17036092	HAEpiC	amniotic membrane:	n/a
26	chr11:17036337-17036387	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:17035876-17035926	RPTEC	kidney:	n/a
28	chr11:17035411-17035461	CMK	blood:	n/a
29	chr11:17036644-17036694	HepG2	liver:	n/a
30	chr11:17035876-17035926	HRCEpiC	kidney:	n/a
31	chr11:17036042-17036092	SK-N-SH	brain:	n/a
32	chr11:17035779-17035829	AG10803	skin:	n/a
33	chr11:17036403-17036453	PrEC	prostate:	n/a
34	chr11:17036042-17036092	HCF	heart:	n/a
35	chr11:17036137-17036187	NHDF-neo	bronchial:	n/a
36	chr11:17036644-17036694	HNPCEpiC	eye:	n/a
37	chr11:17036403-17036453	BJ	skin:	n/a
38	chr11:17036142-17036192	PrEC	prostate:	n/a
39	chr11:17036644-17036694	HUVEC	blood vessel:	n/a
40	chr11:17036581-17036631	HAEpiC	amniotic membrane:	n/a
41	chr11:17036042-17036092	ECC-1	luminal epithelium:	n/a
42	chr11:17036042-17036092	BJ	skin:	n/a
43	chr11:17035876-17035926	IMR90	lung:	fetal
44	chr11:17036581-17036631	HRE	kidney:	n/a
45	chr11:17036403-17036453	Hela-S3	cervix:	n/a
46	chr11:17036042-17036092	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:17036581-17036631	NH-A	brain:	n/a
48	chr11:17036042-17036092	SKMC	muscle:	n/a
49	chr11:17036337-17036387	ProgFib	skin:	n/a
50	chr11:17036403-17036453	HRE	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:16995340..16999228-chr11:17033547..17036418,3	MCF-7	breast:
2	chr11:16994632..16996478-chr11:17034698..17036230,2	MCF-7	breast:
3	chr11:16967271..16967926-chr11:17036420..17037064,2	MCF-7	breast:
4	chr11:17037168..17039319-chr11:17083342..17085313,2	MCF-7	breast:
5	chr11:17034631..17037564-chr11:17097951..17099758,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUCB2-7	chr11:17035545-17035914	NONHSAT018197

No data

Variant related genes	Relation type
PLEKHA7	TF binding region
OR7E14P	TF binding region
PLEKHA7	CpG island
OR7E14P	CpG island
ENSG00000251928	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000244398	chromatin interactions

Extended variants
information (count: 67 )
Associated
traits (count: 52 )

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	rs147752044	chr11:17035406-17035407	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs565389079	chr11:17035419-17035420	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs560609345	chr11:17035449-17035450	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs545393853	chr11:17035487-17035488	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs532618168	chr11:17035488-17035489	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs200763602	chr11:17035493-17035494	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs529463905	chr11:17035520-17035521	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs551218404	chr11:17035521-17035522	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs201638220	chr11:17035522-17035523	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs536981348	chr11:17035585-17035586	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs375321429	chr11:17035617-17035618	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs370165972	chr11:17035622-17035623	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs548892513	chr11:17035626-17035627	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs566394768	chr11:17035650-17035651	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs111657537	chr11:17035655-17035656	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs558230599	chr11:17035658-17035659	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs113412249	chr11:17035664-17035665	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs201642255	chr11:17035678-17035679	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs192507839	chr11:17035706-17035707	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs202005932	chr11:17035713-17035714	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs61881311	chr11:17035718-17035719	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs200126779	chr11:17035740-17035741	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs541767414	chr11:17035773-17035774	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs560398043	chr11:17035778-17035779	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs572205724	chr11:17035808-17035809	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs565106794	chr11:17035834-17035835	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs368375112	chr11:17035848-17035849	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs544703997	chr11:17035935-17035936	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs372142254	chr11:17035955-17035956	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs534863160	chr11:17035968-17035969	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs530315891	chr11:17035987-17035988	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs113662255	chr11:17036012-17036013	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs75533032	chr11:17036091-17036092	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs527947871	chr11:17036123-17036124	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs552176307	chr11:17036143-17036144	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs35115039	chr11:17036157-17036158	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs34986803	chr11:17036180-17036181	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs555836182	chr11:17036203-17036204	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs567768572	chr11:17036293-17036294	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs535277246	chr11:17036315-17036316	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs553652396	chr11:17036368-17036369	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs572326810	chr11:17036408-17036409	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs192941419	chr11:17036413-17036414	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs545700444	chr11:17036447-17036448	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs7929923	chr11:17036466-17036467	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs577422875	chr11:17036469-17036470	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs553533381	chr11:17036512-17036513	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544568959	chr11:17036515-17036516	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562865696	chr11:17036552-17036553	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530155175	chr11:17036615-17036616	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17034200-17035400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:17034200-17035400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr11:17034200-17035400	Flanking Active TSS	Adipose Nuclei	Adipose
4	chr11:17034200-17035600	Active TSS	Stomach Mucosa	stomach
5	chr11:17034200-17035800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
6	chr11:17034200-17036400	Active TSS	Brain Substantia Nigra	brain
7	chr11:17034200-17036800	Active TSS	Brain Anterior Caudate	brain
8	chr11:17034400-17035600	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:17034400-17036400	Active TSS	Osteobl	bone
10	chr11:17034400-17036600	Active TSS	Pancreas	Pancrea
11	chr11:17034400-17036800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:17034400-17037000	Active TSS	Esophagus	oesophagus
13	chr11:17034400-17037000	Active TSS	Fetal Brain Female	brain
14	chr11:17034600-17035400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr11:17034600-17035400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
16	chr11:17034600-17035400	Flanking Active TSS	Placenta	Placenta
17	chr11:17034600-17035400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
18	chr11:17034600-17035400	Flanking Active TSS	HSMM	muscle
19	chr11:17034600-17035400	Flanking Active TSS	HUVEC	blood vessel
20	chr11:17034600-17035600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:17034600-17035600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
22	chr11:17034600-17035600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:17034600-17035600	Bivalent/Poised TSS	Fetal Intestine Small	intestine
24	chr11:17034600-17035600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
25	chr11:17034600-17035600	Flanking Active TSS	NH-A	brain
26	chr11:17034600-17035800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr11:17034600-17035800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr11:17034600-17036400	Active TSS	Liver	Liver
29	chr11:17034600-17036400	Active TSS	Colon Smooth Muscle	Colon
30	chr11:17034600-17036400	Active TSS	Gastric	stomach
31	chr11:17034600-17036400	Active TSS	Psoas Muscle	Psoas
32	chr11:17034600-17036600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr11:17034600-17036600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr11:17034600-17036600	Active TSS	Aorta	Aorta
35	chr11:17034600-17036600	Active TSS	Brain Cingulate Gyrus	brain
36	chr11:17034600-17036600	Active TSS	HSMMtube	muscle
37	chr11:17034600-17037000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
38	chr11:17034600-17037000	Active TSS	Brain Hippocampus Middle	brain
39	chr11:17034600-17037000	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr11:17034600-17037000	Active TSS	Right Atrium	heart
41	chr11:17034600-17037200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr11:17034600-17037200	Active TSS	Right Ventricle	heart
43	chr11:17034600-17037400	Active TSS	A549	lung
44	chr11:17034800-17035400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
45	chr11:17034800-17035400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
46	chr11:17034800-17035400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
47	chr11:17034800-17035400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
48	chr11:17034800-17035400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr11:17034800-17035400	Active TSS	Fetal Heart	heart
50	chr11:17034800-17035400	Active TSS	Fetal Kidney	kidney

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