Variant report

Variant	esv3428029
Chromosome Location	chr11:75377804-75381602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:156)
CpG islands
(count:978)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:156 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:75378170-75378417	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr11:75379974-75380101	K562	blood:	n/a	n/a
3	CHD2	chr11:75380047-75380122	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr11:75378089-75380205	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr11:75378524-75378569	GM19239	blood:	n/a	n/a
6	CTCF	chr11:75378440-75378590	Caco-2	colon:	n/a	n/a
7	CTCF	chr11:75378380-75378530	A549	lung:	n/a	n/a
8	CTCF	chr11:75380004-75380091	Medullo	brain:	n/a	n/a
9	CTCF	chr11:75378380-75378530	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr11:75378466-75378598	Fibrobl	skin:	n/a	n/a
11	CTCF	chr11:75379920-75380070	GM12874	blood:	n/a	n/a
12	CTCF	chr11:75378360-75378510	GM12865	blood:	n/a	n/a
13	CTCF	chr11:75379740-75379890	GM12871	blood:	n/a	n/a
14	CTCF	chr11:75378592-75378597	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr11:75378446-75378666	MCF-7	breast:	n/a	n/a
16	CTCF	chr11:75378860-75379010	Caco-2	colon:	n/a	n/a
17	CTCF	chr11:75379800-75379950	Caco-2	colon:	n/a	n/a
18	CTCF	chr11:75379940-75380090	NHEK	skin:	n/a	n/a
19	CTCF	chr11:75379900-75380050	AG04449	skin:	n/a	n/a
20	CTCF	chr11:75378460-75378610	Caco-2	colon:	n/a	n/a
21	CTCF	chr11:75378420-75378570	GM12867	blood:	n/a	n/a
22	CTCF	chr11:75378480-75378630	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr11:75379960-75380110	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr11:75379940-75380090	AG09319	gingival:	n/a	n/a
25	CTCF	chr11:75378540-75378690	GM12866	blood:	n/a	n/a
26	CTCF	chr11:75378496-75378606	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:75378440-75378590	SAEC	small airway:	n/a	n/a
28	CTCF	chr11:75378540-75378690	BE2_C	brain:	n/a	n/a
29	CTCF	chr11:75378340-75378490	GM06990	blood:	n/a	n/a
30	CTCF	chr11:75379660-75379810	WERI-Rb-1	eye:	n/a	chr11:75379715-75379728
31	CTCF	chr11:75380020-75380170	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr11:75378513-75378579	MCF-7	breast:	n/a	n/a
33	CTCF	chr11:75378460-75378610	HMEC	breast:	n/a	n/a
34	CTCF	chr11:75378420-75378570	HepG2	liver:	n/a	n/a
35	CTCF	chr11:75378500-75378650	GM12872	blood:	n/a	n/a
36	CTCF	chr11:75379920-75380070	Caco-2	colon:	n/a	n/a
37	CTCF	chr11:75378407-75378641	HepG2	liver:	n/a	n/a
38	CTCF	chr11:75378461-75378635	NHEK	skin:	n/a	n/a
39	CTCF	chr11:75378440-75378590	HepG2	liver:	n/a	n/a
40	CTCF	chr11:75379880-75380030	HFF	foreskin:	n/a	n/a
41	CTCF	chr11:75378440-75378590	AG09309	skin:	n/a	n/a
42	CTCF	chr11:75379940-75380090	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr11:75380080-75380230	SK-N-SH_RA	brain:	n/a	chr11:75380194-75380202
44	CTCF	chr11:75378505-75378562	Gliobla	brain:	n/a	n/a
45	CTCF	chr11:75378528-75378545	GM19240	blood:	n/a	n/a
46	CTCF	chr11:75379900-75380050	BJ	skin:	n/a	n/a
47	CTCF	chr11:75379960-75380110	HMEC	breast:	n/a	n/a
48	CTCF	chr11:75378420-75378570	AG04449	skin:	n/a	n/a
49	CTCF	chr11:75378420-75378570	BJ	skin:	n/a	n/a
50	CTCF	chr11:75378475-75378620	GM19238	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75379491-75379541	HL-60	blood:	n/a
2	chr11:75379166-75379216	HEEpiC	esophagus:	n/a
3	chr11:75379491-75379541	HL-60	blood:	n/a
4	chr11:75379166-75379216	HEEpiC	esophagus:	n/a
5	chr11:75378272-75378322	AoSMC	blood vessel:	n/a
6	chr11:75379568-75379618	AG04450	lung:	fetal
7	chr11:75379432-75379482	HCM	heart:	n/a
8	chr11:75379491-75379541	HCPEpiC	choroid plexus:	n/a
9	chr11:75379432-75379482	HCT-116	colon:	n/a
10	chr11:75379166-75379216	H1-hESC	embryonic stem cell:	embryo
11	chr11:75379613-75379663	IMR90	lung:	fetal
12	chr11:75379568-75379618	GM12891	blood:	n/a
13	chr11:75379491-75379541	H1-hESC	embryonic stem cell:	embryo
14	chr11:75379166-75379216	LNCaP	prostate:	n/a
15	chr11:75378502-75378552	AG09319	gingival:	n/a
16	chr11:75378502-75378552	BE2_C	brain:	n/a
17	chr11:75379867-75379917	SK-N-SH	brain:	n/a
18	chr11:75379568-75379618	ECC-1	luminal epithelium:	n/a
19	chr11:75379620-75379670	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:75379491-75379541	HUVEC	blood vessel:	n/a
21	chr11:75379613-75379663	HCT-116	colon:	n/a
22	chr11:75380895-75380945	HCM	heart:	n/a
23	chr11:75379166-75379216	GM12891	blood:	n/a
24	chr11:75379620-75379670	ProgFib	skin:	n/a
25	chr11:75379568-75379618	Hepatocyte	liver:	n/a
26	chr11:75378502-75378552	Caco-2	colon:	n/a
27	chr11:75379166-75379216	NHBE	bronchial:	n/a
28	chr11:75379432-75379482	GM12891	blood:	n/a
29	chr11:75379624-75379674	AG09309	skin:	n/a
30	chr11:75379173-75379223	Hela-S3	cervix:	n/a
31	chr11:75379624-75379674	GM06990	blood:	n/a
32	chr11:75380895-75380945	MCF-7	breast:	n/a
33	chr11:75379173-75379223	PFSK-1	brain:	n/a
34	chr11:75379624-75379674	HNPCEpiC	eye:	n/a
35	chr11:75379501-75379551	HCT-116	colon:	n/a
36	chr11:75379166-75379216	GM12878	blood:	n/a
37	chr11:75378500-75378550	Jurkat	blood:	n/a
38	chr11:75379432-75379482	AoSMC	blood vessel:	n/a
39	chr11:75379867-75379917	HRPEpiC	eye:	n/a
40	chr11:75379491-75379541	HNPCEpiC	eye:	n/a
41	chr11:75379867-75379917	SK-N-MC	brain:	n/a
42	chr11:75379166-75379216	HMEC	breast:	n/a
43	chr11:75378272-75378322	HRE	kidney:	n/a
44	chr11:75379166-75379216	SAEC	small airway:	n/a
45	chr11:75379568-75379618	HL-60	blood:	n/a
46	chr11:75379624-75379674	BJ	skin:	n/a
47	chr11:75378502-75378552	AoSMC	blood vessel:	n/a
48	chr11:75379501-75379551	GM19239	blood:	n/a
49	chr11:75379501-75379551	SK-N-MC	brain:	n/a
50	chr11:75378502-75378552	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:75369962..75371623-chr11:75376445..75378438,2	K562	blood:
2	chr11:75371977..75373733-chr11:75376017..75378232,2	K562	blood:
3	chr11:75362323..75365214-chr11:75375705..75377919,2	K562	blood:
4	chr11:75271851..75274774-chr11:75376979..75378673,2	K562	blood:
5	chr11:75368854..75370589-chr11:75380930..75383566,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MOGAT2-4	chr11:75379481-75382008	NONHSAT023118

No data

Variant related genes	Relation type
MAP6	TF binding region
MAP6	CpG island
ENSG00000149257	chromatin interactions

Extended variants
information (count: 88 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:88 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562245060	chr11:75377883-75377884	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs77562234	chr11:75377936-75377937	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs60768503	chr11:75378003-75378004	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186220994	chr11:75378086-75378087	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs556698686	chr11:75378106-75378107	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528016635	chr11:75378107-75378108	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548101071	chr11:75378121-75378122	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568607831	chr11:75378139-75378140	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs73488497	chr11:75378146-75378147	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs557888960	chr11:75378159-75378160	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116469513	chr11:75378179-75378180	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374398386	chr11:75378246-75378247	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149966120	chr11:75378323-75378324	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570148199	chr11:75378324-75378325	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535560524	chr11:75378353-75378354	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190691579	chr11:75378448-75378449	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs367646609	chr11:75378593-75378594	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540179939	chr11:75378658-75378659	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12225010	chr11:75378674-75378675	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs576681430	chr11:75378755-75378756	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545418011	chr11:75378857-75378858	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370290525	chr11:75378883-75378884	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531469715	chr11:75379019-75379020	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115871621	chr11:75379022-75379023	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562348164	chr11:75379097-75379098	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527889112	chr11:75379130-75379131	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547964028	chr11:75379192-75379193	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571182244	chr11:75379236-75379237	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533630603	chr11:75379247-75379248	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550230646	chr11:75379278-75379279	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569926806	chr11:75379355-75379356	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535988495	chr11:75379391-75379392	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200554061	chr11:75379394-75379395	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558683103	chr11:75379441-75379442	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375639735	chr11:75379460-75379461	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145697422	chr11:75379630-75379631	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs566127517	chr11:75379642-75379643	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs111311628	chr11:75379752-75379753	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs533743550	chr11:75379767-75379768	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs553523987	chr11:75379774-75379775	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs576742897	chr11:75379815-75379816	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs545678336	chr11:75379843-75379844	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs556152857	chr11:75379922-75379923	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs373724096	chr11:75379947-75379948	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs575943698	chr11:75379948-75379949	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs535536779	chr11:75379983-75379984	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs541767975	chr11:75380032-75380033	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs561630973	chr11:75380059-75380060	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs116924871	chr11:75380096-75380097	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs182564787	chr11:75380351-75380352	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD

Chromatin state (count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75364600-75378000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr11:75367600-75378200	Weak transcription	Aorta	Aorta
3	chr11:75375400-75378000	Weak transcription	Pancreas	Pancrea
4	chr11:75375600-75378000	Weak transcription	Spleen	Spleen
5	chr11:75376400-75378000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr11:75376400-75378000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr11:75376600-75378000	Active TSS	Brain Cingulate Gyrus	brain
8	chr11:75376600-75380200	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr11:75376600-75380600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:75377000-75378400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr11:75377200-75378400	Active TSS	Fetal Brain Male	brain
12	chr11:75377200-75378600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr11:75377400-75378400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr11:75377600-75378000	Active TSS	Brain Anterior Caudate	brain
15	chr11:75377600-75378000	Active TSS	Fetal Brain Female	brain
16	chr11:75377600-75379400	Bivalent/Poised TSS	Fetal Intestine Small	intestine
17	chr11:75377800-75378000	Flanking Active TSS	Brain Germinal Matrix	brain
18	chr11:75377800-75378000	Enhancers	Brain Hippocampus Middle	brain
19	chr11:75377800-75378000	Enhancers	Brain Substantia Nigra	brain
20	chr11:75377800-75378000	Enhancers	Stomach Smooth Muscle	stomach
21	chr11:75377800-75378200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:75377800-75378200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr11:75377800-75378400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:75377800-75378400	Enhancers	Fetal Heart	heart
25	chr11:75377800-75378600	Flanking Active TSS	Brain Angular Gyrus	brain
26	chr11:75377800-75378600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
27	chr11:75377800-75379400	Bivalent/Poised TSS	Fetal Stomach	stomach
28	chr11:75377800-75380400	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr11:75378000-75378200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
30	chr11:75378000-75378200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
31	chr11:75378000-75378200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:75378000-75378200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
33	chr11:75378000-75378200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
34	chr11:75378000-75378200	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr11:75378000-75378200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr11:75378000-75378200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr11:75378000-75378200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr11:75378000-75378200	Bivalent Enhancer	Adipose Nuclei	Adipose
39	chr11:75378000-75378200	Bivalent Enhancer	Liver	Liver
40	chr11:75378000-75378200	Enhancers	Colon Smooth Muscle	Colon
41	chr11:75378000-75378200	Bivalent Enhancer	Fetal Intestine Large	intestine
42	chr11:75378000-75378200	Bivalent Enhancer	Fetal Lung	lung
43	chr11:75378000-75378200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr11:75378000-75378200	Enhancers	Gastric	stomach
45	chr11:75378000-75378200	Enhancers	Left Ventricle	heart
46	chr11:75378000-75378200	Enhancers	Ovary	ovary
47	chr11:75378000-75378200	Enhancers	Pancreas	Pancrea
48	chr11:75378000-75378200	Bivalent Enhancer	Rectal Smooth Muscle	rectum
49	chr11:75378000-75378200	Enhancers	Right Ventricle	heart
50	chr11:75378000-75378200	Bivalent Enhancer	A549	lung

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