Variant report

Variant	nsv897908
Chromosome Location	chr11:71927468-71956890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1915)
CpG islands
(count:2628)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1915 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71935316-71935332	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:71934226-71934702	K562	blood:	n/a	chr11:71934635-71934651
3	ARID3A	chr11:71934520-71934741	HepG2	liver:	n/a	chr11:71934635-71934651
4	ATF2	chr11:71950345-71950869	GM12878	blood:	n/a	n/a
5	ATF2	chr11:71948937-71949664	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:71949146-71949549	GM12878	blood:	n/a	n/a
7	ATF2	chr11:71949019-71949601	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr11:71933938-71934596	GM12878	blood:	n/a	n/a
9	ATF2	chr11:71934385-71934745	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr11:71955520-71955834	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr11:71949208-71949529	K562	blood:	n/a	n/a
12	BACH1	chr11:71956291-71956293	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:71933856-71934677	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:71934546-71934672	K562	blood:	n/a	n/a
15	BACH1	chr11:71951991-71952347	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr11:71955407-71955757	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:71949157-71949418	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr11:71950550-71950854	GM12878	blood:	n/a	n/a
19	BCL3	chr11:71950862-71951168	GM12878	blood:	n/a	n/a
20	BCL3	chr11:71950436-71951227	GM12878	blood:	n/a	n/a
21	BCL3	chr11:71949148-71949594	A549	lung:	n/a	chr11:71949241-71949250 chr11:71949277-71949286
22	BCL3	chr11:71949402-71950016	A549	lung:	n/a	n/a
23	BCL3	chr11:71950198-71950904	A549	lung:	n/a	n/a
24	BCL3	chr11:71950226-71950969	A549	lung:	n/a	n/a
25	BCLAF1	chr11:71934932-71935319	GM12878	blood:	n/a	chr11:71934983-71934996
26	BCLAF1	chr11:71934051-71934574	GM12878	blood:	n/a	chr11:71934557-71934566 chr11:71934311-71934320 chr11:71934314-71934327 chr11:71934405-71934414
27	BHLHE40	chr11:71936260-71936264	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:71934179-71934761	K562	blood:	n/a	chr11:71934552-71934568 chr11:71934420-71934436
29	BHLHE40	chr11:71932250-71932705	K562	blood:	n/a	n/a
30	BHLHE40	chr11:71934071-71934744	GM12878	blood:	n/a	chr11:71934552-71934568 chr11:71934420-71934436
31	BHLHE40	chr11:71933540-71933802	HepG2	liver:	n/a	n/a
32	BHLHE40	chr11:71932187-71932424	HepG2	liver:	n/a	n/a
33	BHLHE40	chr11:71933635-71933803	K562	blood:	n/a	n/a
34	BHLHE40	chr11:71932157-71932448	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:71933338-71933388	K562	blood:	n/a	n/a
36	BHLHE40	chr11:71949252-71949460	K562	blood:	n/a	n/a
37	BHLHE40	chr11:71952174-71952190	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:71934999-71935134	K562	blood:	n/a	n/a
39	BRCA1	chr11:71935281-71935519	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr11:71934131-71934729	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr11:71949019-71949496	H1-hESC	embryonic stem cell:	n/a	n/a
42	CBX3	chr11:71934087-71934776	K562	blood:	n/a	n/a
43	CBX3	chr11:71949147-71949669	K562	blood:	n/a	n/a
44	CCNT2	chr11:71950517-71951216	K562	blood:	n/a	n/a
45	CCNT2	chr11:71933585-71935323	K562	blood:	n/a	chr11:71933680-71933700 chr11:71934318-71934327
46	CCNT2	chr11:71935571-71936374	K562	blood:	n/a	chr11:71935741-71935750 chr11:71935780-71935789
47	CCNT2	chr11:71949044-71949516	K562	blood:	n/a	chr11:71949222-71949231
48	CEBPB	chr11:71949231-71949488	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr11:71927353-71927660	K562	blood:	n/a	chr11:71927496-71927507
50	CEBPB	chr11:71927424-71927659	Hela-S3	cervix:	n/a	chr11:71927496-71927507

(count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71950660-71950710	ECC-1	luminal epithelium:	n/a
2	chr11:71951714-71951764	NH-A	brain:	n/a
3	chr11:71953387-71953437	GM12878	blood:	n/a
4	chr11:71951279-71951329	AG04449	skin:	fetal
5	chr11:71950053-71950103	SK-N-SH	brain:	n/a
6	chr11:71950660-71950710	ECC-1	luminal epithelium:	n/a
7	chr11:71951714-71951764	NH-A	brain:	n/a
8	chr11:71953387-71953437	GM12878	blood:	n/a
9	chr11:71951279-71951329	AG04449	skin:	fetal
10	chr11:71950053-71950103	SK-N-SH	brain:	n/a
11	chr11:71935881-71935931	HAEpiC	amniotic membrane:	n/a
12	chr11:71955332-71955382	Hepatocyte	liver:	n/a
13	chr11:71953387-71953437	A549	lung:	n/a
14	chr11:71955164-71955214	HCPEpiC	choroid plexus:	n/a
15	chr11:71955337-71955387	U87	brain:	n/a
16	chr11:71951714-71951764	SK-N-MC	brain:	n/a
17	chr11:71955113-71955163	Jurkat	blood:	n/a
18	chr11:71936303-71936353	MCF-7	breast:	n/a
19	chr11:71952131-71952181	HIPEpiC	eye:	n/a
20	chr11:71951714-71951764	HCF	heart:	n/a
21	chr11:71952431-71952481	SK-N-MC	brain:	n/a
22	chr11:71955113-71955163	HRPEpiC	eye:	n/a
23	chr11:71955439-71955489	Hepatocyte	liver:	n/a
24	chr11:71951714-71951764	HL-60	blood:	n/a
25	chr11:71934276-71934326	BJ	skin:	n/a
26	chr11:71951714-71951764	GM12878	blood:	n/a
27	chr11:71935846-71935896	HNPCEpiC	eye:	n/a
28	chr11:71954982-71955032	NH-A	brain:	n/a
29	chr11:71935849-71935899	ProgFib	skin:	n/a
30	chr11:71953422-71953472	RPTEC	kidney:	n/a
31	chr11:71935849-71935899	RPTEC	kidney:	n/a
32	chr11:71955547-71955597	GM12892	blood:	n/a
33	chr11:71955113-71955163	HRE	kidney:	n/a
34	chr11:71927938-71927988	A549	lung:	n/a
35	chr11:71953387-71953437	HCM	heart:	n/a
36	chr11:71955547-71955597	SK-N-SH_RA	brain:	n/a
37	chr11:71935692-71935742	Jurkat	blood:	n/a
38	chr11:71956145-71956195	K562	blood:	n/a
39	chr11:71950053-71950103	HRE	kidney:	n/a
40	chr11:71955547-71955597	HL-60	blood:	n/a
41	chr11:71955164-71955214	U87	brain:	n/a
42	chr11:71934276-71934326	ECC-1	luminal epithelium:	n/a
43	chr11:71940261-71940311	AG09309	skin:	n/a
44	chr11:71927938-71927988	NB4	blood:	n/a
45	chr11:71950660-71950710	HEK293	kidney:	embryo
46	chr11:71956145-71956195	NT2-D1	testis:	n/a
47	chr11:71931577-71931627	PrEC	prostate:	n/a
48	chr11:71955401-71955451	PFSK-1	brain:	n/a
49	chr11:71935692-71935742	NB4	blood:	n/a
50	chr11:71955599-71955649	NT2-D1	testis:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:71951601..71953593-chr11:71954198..71956638,2	K562	blood:
2	chr11:71750373..71752525-chr11:71933775..71937280,4	MCF-7	breast:
3	chr11:71950675..71951425-chr12:120729547..120730055,2	Hela-S3	cervix:
4	chr11:71936774..71938727-chr11:71967262..71969274,2	MCF-7	breast:
5	chr11:71901671..71903414-chr11:71935255..71937663,2	K562	blood:
6	chr11:71901535..71906562-chr11:71933469..71937383,8	MCF-7	breast:
7	chr11:71927693..71930362-chr11:71935799..71938358,2	MCF-7	breast:
8	chr11:71899258..71901849-chr11:71937862..71940065,2	MCF-7	breast:
9	chr11:71736273..71736838-chr11:71948885..71950174,5	K562	blood:
10	chr11:71823487..71825907-chr11:71932451..71935590,3	K562	blood:
11	chr11:71933506..71936425-chr8:101962971..101964656,2	MCF-7	breast:
12	chr11:71822963..71824981-chr11:71949478..71951249,2	K562	blood:
13	chr11:71933976..71935544-chr6:30710899..30712644,2	MCF-7	breast:
14	chr11:71927693..71930362-chr11:71935799..71938358,2	MCF-7	breast:
15	chr11:71930243..71933219-chr11:72343934..72345638,2	K562	blood:
16	chr11:71933813..71936010-chr11:72394188..72397078,2	MCF-7	breast:
17	chr11:71723194..71726024-chr11:71949814..71951680,2	K562	blood:
18	chr11:71705470..71708103-chr11:71933163..71935736,2	K562	blood:
19	chr11:71928000..71929697-chr11:71932021..71933671,2	MCF-7	breast:
20	chr11:71812576..71816251-chr11:71934138..71937267,4	MCF-7	breast:
21	chr11:71935078..71937662-chr11:71961584..71963637,2	MCF-7	breast:
22	chr11:71929797..71931441-chr11:71932339..71934152,2	MCF-7	breast:
23	chr11:71928745..71931355-chr11:71933643..71936077,2	MCF-7	breast:
24	chr11:71821211..71823051-chr11:71942558..71945428,2	K562	blood:
25	chr11:71928745..71931355-chr11:71933643..71936077,2	MCF-7	breast:
26	chr11:71812032..71815862-chr11:71933743..71937376,6	MCF-7	breast:
27	chr11:71822594..71824677-chr11:71937330..71938993,2	MCF-7	breast:
28	chr11:71944736..71947658-chr11:71947860..71951396,7	K562	blood:
29	chr11:71790877..71793243-chr11:71934127..71937254,3	K562	blood:
30	chr11:71948375..71952014-chr11:71952052..71958381,8	MCF-7	breast:
31	chr11:71948375..71952014-chr11:71952052..71958381,8	MCF-7	breast:
32	chr11:71948874..71949407-chr11:72144827..72145714,3	K562	blood:
33	chr11:71926160..71927705-chr11:71931885..71934510,2	MCF-7	breast:
34	chr11:71899963..71900919-chr11:71934256..71934793,2	Hela-S3	cervix:
35	chr11:71810891..71813222-chr11:71944678..71946447,2	MCF-7	breast:
36	chr11:71933747..71936558-chr11:71962323..71967146,4	K562	blood:
37	chr11:71935409..71935957-chr11:72144881..72145767,2	MCF-7	breast:
38	chr11:71894266..71895107-chr11:71949011..71949837,3	MCF-7	breast:
39	chr11:71949479..71951633-chr11:72139393..72142208,2	K562	blood:
40	chr11:71748920..71751712-chr11:71934433..71936381,2	K562	blood:
41	chr11:71794597..71796676-chr11:71933862..71937757,3	K562	blood:
42	chr11:71935149..71936719-chr11:72144197..72145744,2	K562	blood:
43	chr11:71749038..71754852-chr11:71933473..71937860,9	MCF-7	breast:
44	chr11:71902919..71905831-chr11:71935320..71937132,2	MCF-7	breast:
45	chr11:71932379..71935171-chr11:72141438..72143643,2	K562	blood:
46	chr11:71903106..71905888-chr11:71932566..71934811,2	K562	blood:
47	chr11:71942537..71944052-chr11:72144068..72146926,2	K562	blood:
48	chr11:71822132..71825937-chr11:71933388..71938158,5	MCF-7	breast:
49	chr11:71933144..71936187-chr11:72142812..72145474,4	MCF-7	breast:
50	chr11:71820588..71822402-chr11:71934430..71936040,2	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	INPPL1	hsa-miR-184	chr11:71949831-71949837
2	INPPL1	hsa-miR-205-5p	chr11:71949830-71949849
3	INPPL1	hsa-miR-205-5p	chr11:71949842-71949849

Variant related genes	Relation type
INPPL1	TF binding region
FOLR2	TF binding region
PHOX2A	TF binding region
INPPL1	CpG island
FOLR2	CpG island
PHOX2A	CpG island
ENSG00000137522	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000238768	chromatin interactions
ENSG00000251143	chromatin interactions
ENSG00000165462	chromatin interactions
ENSG00000228286	chromatin interactions
ENSG00000110203	chromatin interactions
ENSG00000184154	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000110195	chromatin interactions
ENSG00000110200	chromatin interactions
ENSG00000137497	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000162129	chromatin interactions
ENSG00000256007	chromatin interactions
ENSG00000165457	chromatin interactions
ENSG00000165458	chromatin interactions

Extended variants
information (count: 1178 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1178 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11235469	chr11:71927468-71927469	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572020633	chr11:71927477-71927478	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs573042482	chr11:71927497-71927498	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs75608470	chr11:71927549-71927550	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs78302125	chr11:71927612-71927613	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559354827	chr11:71927638-71927639	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs74713277	chr11:71927644-71927645	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147103482	chr11:71927743-71927744	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs562879535	chr11:71927748-71927749	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373783462	chr11:71927769-71927770	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574784826	chr11:71927842-71927843	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188762134	chr11:71927862-71927863	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs199718953	chr11:71927876-71927877	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200232394	chr11:71927881-71927882	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs377616764	chr11:71927924-71927925	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs370957762	chr11:71927940-71927941	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375339393	chr11:71927959-71927960	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs138273410	chr11:71927960-71927961	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs371443707	chr11:71927973-71927974	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs374204064	chr11:71927980-71927981	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs368662044	chr11:71927981-71927982	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs372642282	chr11:71927989-71927990	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375389545	chr11:71928003-71928004	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs527641386	chr11:71928051-71928052	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374043791	chr11:71928056-71928057	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs71834554	chr11:71928057-71928058	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368957855	chr11:71928078-71928079	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200584719	chr11:71928082-71928083	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs541734217	chr11:71928143-71928144	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs373773450	chr11:71928172-71928173	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191661098	chr11:71928213-71928214	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564578643	chr11:71928225-71928226	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs184108606	chr11:71928227-71928228	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563543083	chr11:71928236-71928237	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs189183517	chr11:71928250-71928251	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs535749055	chr11:71928257-71928258	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547671458	chr11:71928265-71928266	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181717562	chr11:71928288-71928289	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113350612	chr11:71928318-71928319	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557594576	chr11:71928346-71928347	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs190234044	chr11:71928349-71928350	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs149204136	chr11:71928363-71928364	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs552305575	chr11:71928450-71928451	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542698594	chr11:71928463-71928464	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs556336624	chr11:71928465-71928466	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs574646011	chr11:71928544-71928545	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs75156107	chr11:71928577-71928578	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs554012521	chr11:71928607-71928608	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562779086	chr11:71928645-71928646	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs180919749	chr11:71928659-71928660	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Lung cancer	18438408	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
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	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
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
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1987 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71927400-71927600	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr11:71927400-71929600	Enhancers	K562	blood
3	chr11:71927400-71930400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:71927600-71929800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr11:71927600-71930000	Enhancers	Primary B cells from peripheral blood	blood
6	chr11:71927800-71928000	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
7	chr11:71927800-71928000	Enhancers	Pancreas	Pancrea
8	chr11:71927800-71928000	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
9	chr11:71927800-71928000	Enhancers	Spleen	Spleen
10	chr11:71927800-71928600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:71927800-71928600	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr11:71927800-71929400	Active TSS	Adipose Nuclei	Adipose
13	chr11:71927800-71929600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
14	chr11:71927800-71929800	Enhancers	Primary B cells from cord blood	blood
15	chr11:71927800-71930000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr11:71927800-71930000	Active TSS	Placenta	Placenta
17	chr11:71927800-71930400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr11:71928000-71929000	Weak transcription	Spleen	Spleen
19	chr11:71928000-71933600	Weak transcription	Pancreas	Pancrea
20	chr11:71928400-71928600	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
21	chr11:71928400-71930000	Enhancers	Primary hematopoietic stem cells	blood
22	chr11:71928400-71930000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:71928600-71929400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr11:71928600-71929400	Enhancers	Fetal Thymus	thymus
25	chr11:71928800-71929400	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr11:71928800-71929600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr11:71929000-71929200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr11:71929000-71929200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr11:71929000-71929400	Enhancers	Primary T cells from cord blood	blood
30	chr11:71929000-71929400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr11:71929000-71929800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
32	chr11:71929000-71929800	Enhancers	Spleen	Spleen
33	chr11:71929200-71929400	Enhancers	GM12878-XiMat	blood
34	chr11:71929200-71929800	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr11:71929400-71929600	Enhancers	Colonic Mucosa	Colon
36	chr11:71929400-71929800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:71929400-71930000	Flanking Active TSS	Adipose Nuclei	Adipose
38	chr11:71929400-71930000	Active TSS	Fetal Muscle Trunk	muscle
39	chr11:71929400-71933000	Weak transcription	Fetal Thymus	thymus
40	chr11:71929400-71933200	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr11:71929400-71933400	Weak transcription	Primary T cells from cord blood	blood
42	chr11:71929600-71929800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:71929600-71929800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr11:71929600-71929800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
45	chr11:71929600-71929800	Enhancers	Lung	lung
46	chr11:71929600-71931800	Weak transcription	GM12878-XiMat	blood
47	chr11:71929600-71932600	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr11:71929600-71932600	Weak transcription	K562	blood
49	chr11:71929600-71933600	Weak transcription	Colonic Mucosa	Colon
50	chr11:71929800-71930400	Enhancers	Monocytes-CD14+_RO01746	blood

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