Variant report

Variant	esv3324692
Chromosome Location	chr11:64806676-64811174
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:486)
CpG islands
(count:918)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:64808420-64808475	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:64808320-64808487	K562	blood:	n/a	n/a
3	BACH1	chr11:64808270-64809299	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr11:64808154-64808711	A549	lung:	n/a	n/a
5	BCL3	chr11:64808063-64808988	A549	lung:	n/a	n/a
6	BCLAF1	chr11:64808137-64808632	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:64808186-64808984	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:64808446-64808904	HepG2	liver:	n/a	n/a
9	BHLHE40	chr11:64808439-64809082	K562	blood:	n/a	n/a
10	BRCA1	chr11:64808233-64808570	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr11:64808469-64808580	GM12878	blood:	n/a	n/a
12	BRCA1	chr11:64809201-64809204	HepG2	liver:	n/a	n/a
13	BRCA1	chr11:64809359-64809392	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr11:64808106-64808726	K562	blood:	n/a	n/a
15	CCNT2	chr11:64808170-64809287	K562	blood:	n/a	n/a
16	CEBPB	chr11:64808159-64808617	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:64808237-64808472	K562	blood:	n/a	n/a
18	CEBPB	chr11:64808897-64808976	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr11:64808461-64808527	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:64808300-64808516	HepG2	liver:	n/a	n/a
21	CEBPD	chr11:64808221-64808920	HepG2	liver:	n/a	n/a
22	CHD1	chr11:64808420-64808527	GM12878	blood:	n/a	n/a
23	CHD1	chr11:64808769-64809023	GM12878	blood:	n/a	n/a
24	CHD2	chr11:64808281-64808788	GM12878	blood:	n/a	chr11:64808357-64808367
25	CHD2	chr11:64808899-64808907	K562	blood:	n/a	n/a
26	CHD2	chr11:64808360-64808732	HepG2	liver:	n/a	n/a
27	CHD2	chr11:64808209-64809119	Hela-S3	cervix:	n/a	chr11:64808357-64808367
28	CHD2	chr11:64808119-64808609	H1-hESC	embryonic stem cell:	n/a	chr11:64808357-64808367
29	CHD2	chr11:64808419-64808574	K562	blood:	n/a	n/a
30	CREB1	chr11:64808008-64809445	HepG2	liver:	n/a	n/a
31	CREB1	chr11:64808217-64809100	A549	lung:	n/a	n/a
32	CREB1	chr11:64808252-64808876	GM12878	blood:	n/a	n/a
33	CREB1	chr11:64808241-64809261	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr11:64809083-64809228	GM12892	blood:	n/a	n/a
35	CTCF	chr11:64809050-64809174	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr11:64809103-64809155	MCF-7	breast:	n/a	n/a
37	CTCF	chr11:64808466-64808542	GM19239	blood:	n/a	n/a
38	CTCF	chr11:64808641-64808662	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr11:64808940-64809090	GM12864	blood:	n/a	n/a
40	CTCF	chr11:64809074-64809146	NHEK	skin:	n/a	n/a
41	CTCF	chr11:64809230-64809233	GM12892	blood:	n/a	n/a
42	CTCF	chr11:64808664-64808665	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr11:64808840-64808990	GM12868	blood:	n/a	n/a
44	CTCF	chr11:64808960-64809110	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr11:64809102-64809137	GM19238	blood:	n/a	n/a
46	CTCF	chr11:64809083-64809089	GM19238	blood:	n/a	n/a
47	CTCF	chr11:64808790-64808869	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr11:64809063-64809199	MCF-7	breast:	n/a	n/a
49	CTCF	chr11:64808320-64808470	HRE	kidney:	n/a	n/a
50	CTCF	chr11:64808760-64808910	AG04449	skin:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64808437-64808487	AG04450	lung:	fetal
2	chr11:64808083-64808133	SK-N-SH_RA	brain:	n/a
3	chr11:64808083-64808133	BJ	skin:	n/a
4	chr11:64808437-64808487	AG04450	lung:	fetal
5	chr11:64808083-64808133	SK-N-SH_RA	brain:	n/a
6	chr11:64808083-64808133	BJ	skin:	n/a
7	chr11:64808083-64808133	HMEC	breast:	n/a
8	chr11:64808285-64808335	GM12892	blood:	n/a
9	chr11:64807766-64807816	NHDF-neo	bronchial:	n/a
10	chr11:64809369-64809419	AG04449	skin:	fetal
11	chr11:64808428-64808478	HEK293	kidney:	embryo
12	chr11:64809102-64809152	SK-N-MC	brain:	n/a
13	chr11:64808331-64808381	U87	brain:	n/a
14	chr11:64808285-64808335	ovcar-3	ovarian:	n/a
15	chr11:64808437-64808487	GM19239	blood:	n/a
16	chr11:64808357-64808407	K562	blood:	n/a
17	chr11:64807235-64807285	HEEpiC	esophagus:	n/a
18	chr11:64808083-64808133	AG09309	skin:	n/a
19	chr11:64808343-64808393	AG09319	gingival:	n/a
20	chr11:64807235-64807285	ECC-1	luminal epithelium:	n/a
21	chr11:64808081-64808131	HCM	heart:	n/a
22	chr11:64808285-64808335	GM12878	blood:	n/a
23	chr11:64809369-64809419	HIPEpiC	eye:	n/a
24	chr11:64807766-64807816	ProgFib	skin:	n/a
25	chr11:64807766-64807816	IMR90	lung:	fetal
26	chr11:64808331-64808381	AG04449	skin:	fetal
27	chr11:64808357-64808407	BJ	skin:	n/a
28	chr11:64808083-64808133	HCPEpiC	choroid plexus:	n/a
29	chr11:64808285-64808335	HCT-116	colon:	n/a
30	chr11:64808343-64808393	AG04449	skin:	fetal
31	chr11:64808357-64808407	HCM	heart:	n/a
32	chr11:64809369-64809419	HNPCEpiC	eye:	n/a
33	chr11:64809369-64809419	NT2-D1	testis:	n/a
34	chr11:64807235-64807285	A549	lung:	n/a
35	chr11:64808437-64808487	NHDF-neo	bronchial:	n/a
36	chr11:64808437-64808487	U87	brain:	n/a
37	chr11:64808367-64808417	NHDF-neo	bronchial:	n/a
38	chr11:64808343-64808393	AG10803	skin:	n/a
39	chr11:64808331-64808381	H1-hESC	embryonic stem cell:	embryo
40	chr11:64807766-64807816	HCT-116	colon:	n/a
41	chr11:64808357-64808407	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:64807235-64807285	GM12892	blood:	n/a
43	chr11:64809102-64809152	HCF	heart:	n/a
44	chr11:64808081-64808131	Hela-S3	cervix:	n/a
45	chr11:64808437-64808487	Hela-S3	cervix:	n/a
46	chr11:64808083-64808133	SK-N-MC	brain:	n/a
47	chr11:64807766-64807816	HEK293	kidney:	embryo
48	chr11:64807235-64807285	NHDF-neo	bronchial:	n/a
49	chr11:64808331-64808381	MCF10A-Er-Src	breast:	n/a
50	chr11:64808083-64808133	MCF-7	breast:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64793282..64795774-chr11:64807101..64811680,5	K562	blood:
2	chr11:64787088..64789367-chr11:64807052..64810027,2	MCF-7	breast:
3	chr11:64806463..64808805-chr11:64815100..64817067,2	K562	blood:
4	chr11:64808483..64810483-chr11:64810664..64814353,4	K562	blood:
5	chr11:64793389..64797015-chr11:64806765..64809007,6	K562	blood:
6	chr11:64780338..64782626-chr11:64806994..64809935,3	K562	blood:
7	chr11:64807534..64810713-chr11:64846257..64849828,3	MCF-7	breast:
8	chr11:64808732..64812218-chr11:64877838..64879922,3	MCF-7	breast:
9	chr11:64806835..64808889-chr11:64875130..64876967,2	K562	blood:
10	chr11:64803567..64805727-chr11:64810246..64813138,2	K562	blood:
11	chr11:64788946..64793194-chr11:64803720..64806785,4	K562	blood:
12	chr11:64804612..64806945-chr11:64807096..64809851,2	MCF-7	breast:
13	chr11:64692132..64694352-chr11:64806387..64808974,2	K562	blood:
14	chr11:64806669..64810557-chr11:64862016..64868359,8	K562	blood:
15	chr11:64545248..64547245-chr11:64807000..64808581,2	MCF-7	breast:
16	chr11:64806644..64812839-chr11:64862132..64865938,9	MCF-7	breast:
17	chr11:64806772..64810496-chr11:64862454..64866792,5	K562	blood:
18	chr11:64794773..64796855-chr11:64809238..64812332,3	K562	blood:
19	chr11:64645854..64647856-chr11:64806233..64808621,2	K562	blood:
20	chr11:64806922..64809393-chr11:64883452..64886674,3	MCF-7	breast:
21	chr11:64807549..64809979-chr11:64878035..64880006,2	K562	blood:
22	chr11:64807959..64809979-chr11:64878035..64880846,2	K562	blood:
23	chr11:64807050..64811411-chr11:64876533..64881108,6	MCF-7	breast:
24	chr11:64793793..64795353-chr11:64806843..64809654,4	MCF-7	breast:
25	chr11:64798286..64800870-chr11:64805869..64808336,2	K562	blood:
26	chr11:64808483..64810483-chr11:64810664..64814353,4	K562	blood:
27	chr11:64809180..64811372-chr11:64815514..64817240,2	K562	blood:
28	chr11:64808477..64810468-chr11:64816977..64818703,3	MCF-7	breast:
29	chr11:64810091..64812972-chr11:64883728..64886202,2	MCF-7	breast:
30	chr11:64806998..64808499-chr11:64948414..64950755,2	MCF-7	breast:
31	chr11:64682450..64685608-chr11:64808232..64811277,3	MCF-7	breast:
32	chr11:64810755..64812822-chr11:64850168..64852033,2	MCF-7	breast:
33	chr11:64804480..64810811-chr11:64850224..64856247,12	K562	blood:
34	chr11:64808323..64810154-chr11:64871056..64873673,2	MCF-7	breast:
35	chr11:64808945..64810714-chr11:64850630..64853153,2	K562	blood:
36	chr11:64806537..64808623-chr11:64852176..64854982,2	K562	blood:
37	chr11:64806821..64808860-chr11:64936413..64939146,2	K562	blood:
38	chr11:64807684..64812709-chr11:64850593..64853492,4	MCF-7	breast:
39	chr11:64780179..64786029-chr11:64807067..64810211,7	MCF-7	breast:
40	chr11:64807090..64809871-chr11:64850334..64853304,4	MCF-7	breast:
41	chr11:64805658..64811611-chr11:64862545..64865451,9	MCF-7	breast:
42	chr11:64793697..64796700-chr11:64806482..64812345,9	MCF-7	breast:
43	chr11:64807810..64812277-chr11:64813364..64817609,8	MCF-7	breast:
44	chr11:64807098..64808802-chr11:64850233..64851800,2	K562	blood:
45	chr11:64644663..64647408-chr11:64807363..64809566,4	MCF-7	breast:

No data

Variant related genes	Relation type
SAC3D1	TF binding region
SAC3D1	CpG island
ENSG00000149809	chromatin interactions
ENSG00000110025	chromatin interactions
ENSG00000110047	chromatin interactions
ENSG00000014216	chromatin interactions
ENSG00000266123	chromatin interactions
ENSG00000254614	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000213465	chromatin interactions
ENSG00000149823	chromatin interactions
ENSG00000204710	chromatin interactions
ENSG00000254501	chromatin interactions
ENSG00000068971	chromatin interactions
ENSG00000162300	chromatin interactions
ENSG00000146670	chromatin interactions
ENSG00000110046	chromatin interactions
ENSG00000255173	chromatin interactions
ENSG00000269038	chromatin interactions
ENSG00000270775	chromatin interactions
ENSG00000168061	chromatin interactions
ENSG00000168060	chromatin interactions
ENSG00000273003	chromatin interactions
ENSG00000174276	chromatin interactions

Extended variants
information (count: 194 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:194 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112087782	chr11:64806679-64806680	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs201093162	chr11:64806697-64806698	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs372090770	chr11:64806701-64806702	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs539668424	chr11:64806702-64806703	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs552882594	chr11:64806714-64806715	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs572536816	chr11:64806772-64806773	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs12280476	chr11:64806916-64806917	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs377553726	chr11:64806930-64806931	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs192751146	chr11:64806934-64806935	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs10160463	chr11:64806957-64806958	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs574506937	chr11:64806985-64806986	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs543370730	chr11:64806995-64806996	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs34589041	chr11:64807005-64807006	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	18 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs184799793	chr11:64807023-64807024	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
15	rs546414470	chr11:64807027-64807028	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
16	rs189386912	chr11:64807029-64807030	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
17	rs182032141	chr11:64807031-64807032	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
18	rs367812140	chr11:64807119-64807120	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
19	rs199757412	chr11:64807122-64807123	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
20	rs2670910	chr11:64807136-64807137	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs530524917	chr11:64807148-64807149	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
22	rs201908657	chr11:64807164-64807165	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
23	rs368435072	chr11:64807175-64807176	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
24	rs370952013	chr11:64807185-64807186	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
25	rs146335404	chr11:64807213-64807214	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
26	rs138307140	chr11:64807220-64807221	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
27	rs374302516	chr11:64807232-64807233	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
28	rs495820	chr11:64807235-64807236	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs114564619	chr11:64807236-64807237	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
30	rs495935	chr11:64807278-64807279	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs546801450	chr11:64807293-64807294	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
32	rs653111	chr11:64807294-64807295	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	19 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs535237562	chr11:64807305-64807306	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
34	rs76150557	chr11:64807311-64807312	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
35	rs369495691	chr11:64807314-64807315	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
36	rs144558475	chr11:64807318-64807319	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
37	rs533711786	chr11:64807361-64807362	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
38	rs557065746	chr11:64807422-64807423	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
39	rs664118	chr11:64807447-64807448	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186061141	chr11:64807456-64807457	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
41	rs528338865	chr11:64807476-64807477	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
42	rs373625640	chr11:64807513-64807514	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
43	rs553598973	chr11:64807519-64807520	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
44	rs573488433	chr11:64807532-64807533	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
45	rs542397345	chr11:64807540-64807541	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
46	rs498636	chr11:64807541-64807542	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs190250992	chr11:64807636-64807637	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
48	rs529452580	chr11:64807649-64807650	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
49	rs549474647	chr11:64807667-64807668	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
50	rs181128660	chr11:64807683-64807684	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Hodgkin''s lymphoma	18641027	CNVD

Chromatin state (count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64795200-64808000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:64795400-64808000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:64795600-64808000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr11:64795800-64807800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr11:64795800-64807800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr11:64795800-64808000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:64795800-64808000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr11:64796000-64807400	Weak transcription	Stomach Mucosa	stomach
9	chr11:64796000-64807600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr11:64796000-64807800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr11:64796000-64807800	Weak transcription	Fetal Kidney	kidney
12	chr11:64796000-64808000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr11:64796200-64807200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:64796200-64807200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr11:64796200-64807200	Weak transcription	K562	blood
16	chr11:64796200-64807800	Weak transcription	Small Intestine	intestine
17	chr11:64796200-64807800	Weak transcription	A549	lung
18	chr11:64796200-64807800	Weak transcription	HMEC	breast
19	chr11:64796200-64807800	Weak transcription	HUVEC	blood vessel
20	chr11:64796200-64807800	Weak transcription	NHEK	skin
21	chr11:64796200-64808000	Weak transcription	Osteobl	bone
22	chr11:64796400-64807400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr11:64796400-64807400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr11:64796400-64807600	Weak transcription	Fetal Brain Male	brain
25	chr11:64796400-64807800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr11:64796600-64807600	Strong transcription	Fetal Intestine Small	intestine
27	chr11:64796800-64807400	Strong transcription	Fetal Muscle Leg	muscle
28	chr11:64796800-64808000	Strong transcription	Fetal Stomach	stomach
29	chr11:64798400-64807400	Strong transcription	Skeletal Muscle Male	skeletal muscle
30	chr11:64798400-64807800	Strong transcription	Fetal Intestine Large	intestine
31	chr11:64798400-64807800	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr11:64798600-64807200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr11:64798600-64807600	Strong transcription	Brain Germinal Matrix	brain
34	chr11:64798600-64807600	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr11:64798600-64807800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr11:64798800-64807000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr11:64798800-64807400	Strong transcription	Adipose Nuclei	Adipose
38	chr11:64798800-64807600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr11:64798800-64807600	Strong transcription	Rectal Smooth Muscle	rectum
40	chr11:64799000-64807600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr11:64799000-64807600	Strong transcription	Right Ventricle	heart
42	chr11:64799400-64807400	Strong transcription	Colon Smooth Muscle	Colon
43	chr11:64799400-64807400	Strong transcription	Lung	lung
44	chr11:64799600-64807600	Strong transcription	Brain Angular Gyrus	brain
45	chr11:64799800-64807200	Weak transcription	Hela-S3	cervix
46	chr11:64800400-64808000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:64801200-64806800	Strong transcription	Dnd41	blood
48	chr11:64801200-64807600	Strong transcription	Fetal Brain Female	brain
49	chr11:64803600-64807800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr11:64804600-64806800	Strong transcription	Skeletal Muscle Female	skeletal muscle

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