Variant report

Variant	nsv1039217
Chromosome Location	chr11:33341724-33473614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1448)
CpG islands
(count:1037)
Chromatin interactive
region (count:99)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:1448 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33383925-33384254	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33342559-33342940	K562	blood:	n/a	n/a
3	ARID3A	chr11:33394101-33394301	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:33364523-33364723	K562	blood:	n/a	n/a
5	ARID3A	chr11:33351288-33351628	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:33467294-33467606	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:33351286-33351649	K562	blood:	n/a	n/a
8	ARID3A	chr11:33383912-33384198	K562	blood:	n/a	n/a
9	ATF1	chr11:33394198-33394335	K562	blood:	n/a	n/a
10	ATF1	chr11:33351332-33351614	K562	blood:	n/a	n/a
11	ATF1	chr11:33342458-33342912	K562	blood:	n/a	n/a
12	ATF1	chr11:33341606-33341888	K562	blood:	n/a	n/a
13	ATF2	chr11:33404441-33405009	GM12878	blood:	n/a	n/a
14	ATF2	chr11:33409042-33410013	GM12878	blood:	n/a	n/a
15	ATF2	chr11:33404542-33405049	GM12878	blood:	n/a	n/a
16	ATF2	chr11:33411036-33411671	GM12878	blood:	n/a	n/a
17	ATF2	chr11:33409013-33410089	GM12878	blood:	n/a	n/a
18	ATF3	chr11:33342449-33342699	K562	blood:	n/a	n/a
19	ATF3	chr11:33382233-33382453	K562	blood:	n/a	chr11:33382358-33382372
20	BACH1	chr11:33397385-33398563	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr11:33364471-33364818	K562	blood:	n/a	n/a
22	BATF	chr11:33409566-33409855	GM12878	blood:	n/a	n/a
23	BATF	chr11:33363592-33363812	GM12878	blood:	n/a	n/a
24	BATF	chr11:33363521-33363808	GM12878	blood:	n/a	n/a
25	BATF	chr11:33404575-33404911	GM12878	blood:	n/a	n/a
26	BATF	chr11:33408990-33409983	GM12878	blood:	n/a	n/a
27	BATF	chr11:33411172-33411511	GM12878	blood:	n/a	n/a
28	BATF	chr11:33404521-33404947	GM12878	blood:	n/a	n/a
29	BCL11A	chr11:33409572-33409836	GM12878	blood:	n/a	n/a
30	BCL11A	chr11:33404557-33404945	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:33409034-33409543	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:33409556-33409888	GM12878	blood:	n/a	n/a
33	BCL3	chr11:33404619-33404913	GM12878	blood:	n/a	n/a
34	BCL3	chr11:33409282-33409904	GM12878	blood:	n/a	n/a
35	BCLAF1	chr11:33409067-33410001	GM12878	blood:	n/a	n/a
36	BCLAF1	chr11:33404519-33404990	GM12878	blood:	n/a	n/a
37	BCLAF1	chr11:33409061-33410037	GM12878	blood:	n/a	n/a
38	BCLAF1	chr11:33341910-33342551	GM12878	blood:	n/a	n/a
39	BHLHE40	chr11:33401529-33401825	GM12878	blood:	n/a	n/a
40	BHLHE40	chr11:33427892-33427983	K562	blood:	n/a	n/a
41	BHLHE40	chr11:33369101-33369338	GM12878	blood:	n/a	n/a
42	BHLHE40	chr11:33342530-33342916	K562	blood:	n/a	n/a
43	BHLHE40	chr11:33345920-33346220	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:33404539-33405771	GM12878	blood:	n/a	n/a
45	CEBPB	chr11:33382242-33382528	A549	lung:	n/a	n/a
46	CEBPB	chr11:33342462-33342728	K562	blood:	n/a	n/a
47	CEBPB	chr11:33425244-33425411	IMR90	lung:	n/a	n/a
48	CEBPB	chr11:33382214-33382535	HepG2	liver:	n/a	n/a
49	CEBPB	chr11:33382210-33382548	K562	blood:	n/a	n/a
50	CEBPB	chr11:33417934-33418273	A549	lung:	n/a	chr11:33418096-33418109 chr11:33418098-33418107 chr11:33418096-33418107 chr11:33418098-33418107 chr11:33418098-33418107

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33397821-33397871	HUVEC	blood vessel:	n/a
2	chr11:33396983-33397033	CMK	blood:	n/a
3	chr11:33442321-33442371	Hela-S3	cervix:	n/a
4	chr11:33399978-33400028	AG09309	skin:	n/a
5	chr11:33396983-33397033	ECC-1	luminal epithelium:	n/a
6	chr11:33453389-33453439	HRPEpiC	eye:	n/a
7	chr11:33397821-33397871	HCPEpiC	choroid plexus:	n/a
8	chr11:33397153-33397203	CMK	blood:	n/a
9	chr11:33396859-33396909	GM12891	blood:	n/a
10	chr11:33397821-33397871	AG04449	skin:	fetal
11	chr11:33397821-33397871	H1-hESC	embryonic stem cell:	embryo
12	chr11:33394273-33394323	HRCEpiC	kidney:	n/a
13	chr11:33398173-33398223	H1-hESC	embryonic stem cell:	embryo
14	chr11:33397821-33397871	GM12892	blood:	n/a
15	chr11:33394273-33394323	HNPCEpiC	eye:	n/a
16	chr11:33397387-33397437	HCF	heart:	n/a
17	chr11:33398245-33398295	AG10803	skin:	n/a
18	chr11:33394273-33394323	MCF-7	breast:	n/a
19	chr11:33397153-33397203	NH-A	brain:	n/a
20	chr11:33346306-33346356	NH-A	brain:	n/a
21	chr11:33397689-33397739	HRE	kidney:	n/a
22	chr11:33397679-33397729	HUVEC	blood vessel:	n/a
23	chr11:33398173-33398223	GM12891	blood:	n/a
24	chr11:33399978-33400028	ProgFib	skin:	n/a
25	chr11:33398366-33398416	HRPEpiC	eye:	n/a
26	chr11:33397387-33397437	MCF10A-Er-Src	breast:	n/a
27	chr11:33396983-33397033	HMEC	breast:	n/a
28	chr11:33396859-33396909	U87	brain:	n/a
29	chr11:33397821-33397871	SAEC	small airway:	n/a
30	chr11:33396859-33396909	ovcar-3	ovarian:	n/a
31	chr11:33397689-33397739	GM12892	blood:	n/a
32	chr11:33397153-33397203	HEEpiC	esophagus:	n/a
33	chr11:33453389-33453439	SK-N-SH	brain:	n/a
34	chr11:33397821-33397871	HNPCEpiC	eye:	n/a
35	chr11:33399978-33400028	ECC-1	luminal epithelium:	n/a
36	chr11:33396983-33397033	BE2_C	brain:	n/a
37	chr11:33396983-33397033	MCF10A-Er-Src	breast:	n/a
38	chr11:33442321-33442371	HNPCEpiC	eye:	n/a
39	chr11:33375412-33375462	AG09319	gingival:	n/a
40	chr11:33400574-33400624	BJ	skin:	n/a
41	chr11:33375412-33375462	AoSMC	blood vessel:	n/a
42	chr11:33397821-33397871	NT2-D1	testis:	n/a
43	chr11:33398366-33398416	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:33397689-33397739	NB4	blood:	n/a
45	chr11:33396859-33396909	GM12878	blood:	n/a
46	chr11:33397821-33397871	AG04450	lung:	fetal
47	chr11:33375412-33375462	CMK	blood:	n/a
48	chr11:33396859-33396909	HMEC	breast:	n/a
49	chr11:33397821-33397871	A549	lung:	n/a
50	chr11:33397821-33397871	HMEC	breast:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:33396319..33398155-chr11:33401081..33403706,2	MCF-7	breast:
2	chr11:33278606..33279290-chr11:33341646..33342645,2	MCF-7	breast:
3	chr11:33365715..33367217-chr11:33368914..33370934,2	K562	blood:
4	chr11:33391648..33394205-chr11:33396367..33400084,3	K562	blood:
5	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
6	chr11:33278431..33280994-chr11:33343148..33345280,2	MCF-7	breast:
7	chr11:33350757..33353405-chr11:33354429..33357042,2	K562	blood:
8	chr11:33276714..33280349-chr11:33350703..33354404,4	MCF-7	breast:
9	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
10	chr11:33350757..33353405-chr11:33354429..33357042,2	K562	blood:
11	chr11:33365715..33367217-chr11:33368914..33370934,2	K562	blood:
12	chr11:33404576..33406306-chr11:33408202..33410856,2	MCF-7	breast:
13	chr11:33384382..33386417-chr11:33393888..33396516,2	K562	blood:
14	chr11:33345699..33348337-chr11:33348377..33350579,2	K562	blood:
15	chr11:33416676..33419367-chr11:33423190..33425357,2	K562	blood:
16	chr11:33395838..33399105-chr11:33400150..33402846,3	MCF-7	breast:
17	chr11:33384382..33386417-chr11:33393888..33396516,2	K562	blood:
18	chr11:33377235..33380179-chr11:33384228..33387621,3	K562	blood:
19	chr11:33353025..33355412-chr11:33355874..33357955,2	MCF-7	breast:
20	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
21	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
22	chr11:32982327..32984023-chr11:33390393..33392493,2	K562	blood:
23	chr11:33277371..33280516-chr11:33349638..33353162,5	MCF-7	breast:
24	chr11:33345288..33347427-chr11:33347864..33349944,2	MCF-7	breast:
25	chr11:33347406..33349145-chr11:33350262..33352793,2	MCF-7	breast:
26	chr11:33278060..33280845-chr11:33344585..33346232,2	MCF-7	breast:
27	chr11:33422636..33425023-chr11:33427111..33429775,2	MCF-7	breast:
28	chr11:33182184..33185099-chr11:33348035..33349582,2	MCF-7	breast:
29	chr11:33377235..33380179-chr11:33384228..33387621,3	K562	blood:
30	chr11:33399022..33400859-chr11:33402110..33404984,2	K562	blood:
31	chr11:33278813..33281447-chr11:33356120..33358697,4	MCF-7	breast:
32	chr11:33421417..33423758-chr11:33435787..33437817,2	K562	blood:
33	chr11:33347406..33349145-chr11:33350262..33352793,2	MCF-7	breast:
34	chr11:33187513..33188468-chr11:33351019..33351906,6	K562	blood:
35	chr11:33372537..33375934-chr11:33378619..33381344,3	MCF-7	breast:
36	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
37	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
38	chr11:33278689..33280532-chr11:33344460..33346639,2	K562	blood:
39	chr11:33352566..33355131-chr11:33757100..33758985,2	MCF-7	breast:
40	chr11:33399022..33400859-chr11:33402110..33404984,2	K562	blood:
41	chr11:33187604..33188364-chr11:33351039..33351579,2	MCF-7	breast:
42	chr11:33432981..33435559-chr11:33436354..33439310,2	K562	blood:
43	chr11:33360349..33362095-chr11:33370787..33373728,2	MCF-7	breast:
44	chr11:33351340..33351943-chr11:33383658..33384527,2	K562	blood:
45	chr11:33403805..33405903-chr11:33414463..33417062,2	MCF-7	breast:
46	chr11:33372537..33375934-chr11:33378619..33381344,3	MCF-7	breast:
47	chr11:33370166..33372800-chr11:33374328..33376444,2	MCF-7	breast:
48	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
49	chr11:33345288..33347427-chr11:33347864..33349944,2	MCF-7	breast:
50	chr11:32982056..32982733-chr11:33350989..33351739,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701
2	lnc-HIPK3-2	chr11:33424762-33425151	NONHSAT018700

No data

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HIPK3	hsa-miR-19b-3p	chr11:33375275-33375282
2	HIPK3	hsa-miR-106a-5p	chr11:33375245-33375267
3	HIPK3	hsa-miR-20b-5p	chr11:33375245-33375267
4	HIPK3	hsa-miR-106a-5p	chr11:33375709-33375730
5	HIPK3	hsa-miR-19b-3p	chr11:33358682-33358704
6	HIPK3	hsa-miR-124-3p	chr11:33375651-33375670
7	HIPK3	hsa-miR-335-5p	chr11:33375589-33375614
8	HIPK3	hsa-miR-20b-5p	chr11:33375709-33375730
9	HIPK3	hsa-miR-92a-3p	chr11:33375228-33375234
10	HIPK3	hsa-miR-92a-3p	chr11:33375388-33375409
11	HIPK3	hsa-miR-92a-3p	chr11:33375214-33375235
12	HIPK3	hsa-miR-124-3p	chr11:33375376-33375395
13	HIPK3	hsa-miR-124-3p	chr11:33375663-33375670
14	HIPK3	hsa-miR-19b-3p	chr11:33375260-33375282

Variant related genes	Relation type
ENSG00000255207	TF binding region
HIPK3	TF binding region
ENSG00000254537	TF binding region
ENSG00000223134	TF binding region
ENSG00000255207	CpG island
HIPK3	CpG island
ENSG00000254537	CpG island
ENSG00000223134	CpG island
ENSG00000223134	chromatin interactions
ENSG00000254537	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000255207	chromatin interactions

Extended variants
information (count: 4942 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4942 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138309287	chr11:33341822-33341823	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552563515	chr11:33342073-33342074	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs11032225	chr11:33342108-33342109	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs11032226	chr11:33342109-33342110	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs183344345	chr11:33342196-33342197	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535310775	chr11:33342209-33342210	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111782087	chr11:33342302-33342303	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548630914	chr11:33342306-33342307	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568668875	chr11:33342315-33342316	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs149646041	chr11:33342319-33342320	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144409626	chr11:33342358-33342359	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138524003	chr11:33342425-33342426	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538231586	chr11:33342451-33342452	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558540898	chr11:33342452-33342453	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs560619522	chr11:33342490-33342491	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10836051	chr11:33342503-33342504	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs140711716	chr11:33342541-33342542	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11602207	chr11:33342568-33342569	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs561066826	chr11:33342572-33342573	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574249173	chr11:33342619-33342620	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs141581457	chr11:33342652-33342653	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs563413566	chr11:33342722-33342723	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs532483971	chr11:33342762-33342763	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs552424465	chr11:33342820-33342821	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs559677978	chr11:33342872-33342873	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs528525546	chr11:33342879-33342880	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs200759012	chr11:33342905-33342906	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs568780632	chr11:33343030-33343031	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs188067037	chr11:33343060-33343061	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs146199544	chr11:33343063-33343064	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs139211513	chr11:33343064-33343065	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs538714356	chr11:33343103-33343104	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs558413543	chr11:33343106-33343107	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs565658778	chr11:33343110-33343111	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534328268	chr11:33343298-33343299	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11032227	chr11:33343337-33343338	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs574412723	chr11:33343394-33343395	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543179163	chr11:33343424-33343425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556721080	chr11:33343463-33343464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576991441	chr11:33343516-33343517	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546277170	chr11:33343520-33343521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs71455502	chr11:33343588-33343589	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs71457303	chr11:33343590-33343591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs35935625	chr11:33343592-33343593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549876415	chr11:33343606-33343607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567876103	chr11:33343608-33343609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11825445	chr11:33343614-33343615	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs533776279	chr11:33343631-33343632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368581858	chr11:33343638-33343639	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs559255730	chr11:33343670-33343671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
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
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2088 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33317400-33345800	Weak transcription	Gastric	stomach
2	chr11:33318000-33360200	Weak transcription	Primary T cells from cord blood	blood
3	chr11:33319200-33348800	Weak transcription	Hela-S3	cervix
4	chr11:33319800-33342800	Weak transcription	Fetal Intestine Large	intestine
5	chr11:33319800-33352600	Weak transcription	Dnd41	blood
6	chr11:33320400-33341800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr11:33320600-33369400	Weak transcription	Fetal Brain Male	brain
8	chr11:33330200-33342600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr11:33332200-33360800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr11:33332600-33344200	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr11:33333000-33358200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:33333200-33343000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr11:33333200-33345200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr11:33333400-33346000	Weak transcription	Pancreas	Pancrea
15	chr11:33333400-33360200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr11:33333800-33342600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:33334600-33347000	Weak transcription	A549	lung
18	chr11:33335200-33342600	Weak transcription	Fetal Lung	lung
19	chr11:33336000-33342000	Weak transcription	HSMMtube	muscle
20	chr11:33337200-33346000	Weak transcription	Lung	lung
21	chr11:33337400-33341800	Weak transcription	NHLF	lung
22	chr11:33338000-33342000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr11:33338000-33343000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr11:33338000-33346000	Weak transcription	Rectal Smooth Muscle	rectum
25	chr11:33338400-33341800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:33338400-33352000	Weak transcription	Fetal Stomach	stomach
27	chr11:33339000-33342200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:33339000-33343000	Enhancers	Brain Angular Gyrus	brain
29	chr11:33339000-33343000	Enhancers	Brain Substantia Nigra	brain
30	chr11:33339000-33346000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:33339000-33346000	Weak transcription	Fetal Muscle Leg	muscle
32	chr11:33339000-33352600	Weak transcription	Fetal Muscle Trunk	muscle
33	chr11:33339200-33343000	Enhancers	Brain Hippocampus Middle	brain
34	chr11:33339200-33345400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:33339400-33345600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr11:33339400-33345800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr11:33339400-33346000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:33339600-33344400	Weak transcription	NHDF-Ad	bronchial
39	chr11:33339600-33345200	Weak transcription	Osteobl	bone
40	chr11:33339600-33347200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:33339600-33351000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:33339600-33353400	Weak transcription	NHEK	skin
43	chr11:33339600-33361200	Weak transcription	HUVEC	blood vessel
44	chr11:33339600-33362000	Weak transcription	HMEC	breast
45	chr11:33339800-33342600	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr11:33340000-33345200	Weak transcription	HSMM	muscle
47	chr11:33340200-33341800	Weak transcription	Brain Anterior Caudate	brain
48	chr11:33340200-33343200	Enhancers	Brain Cingulate Gyrus	brain
49	chr11:33340400-33341800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr11:33340400-33342200	Enhancers	Primary T helper cells fromperipheralblood	blood

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