Variant report

Variant	nsv1038299
Chromosome Location	chr11:75883568-75922608
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1087)
CpG islands
(count:2079)
Chromatin interactive
region (count:73)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1087 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:75919860-75920108	HepG2	liver:	n/a	n/a
2	ATF3	chr11:75919853-75920215	A549	lung:	n/a	n/a
3	ATF3	chr11:75919783-75920220	A549	lung:	n/a	n/a
4	BACH1	chr11:75918709-75918900	K562	blood:	n/a	n/a
5	BACH1	chr11:75916750-75916926	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:75918583-75919316	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:75921380-75922316	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:75919833-75920847	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr11:75919791-75920256	A549	lung:	n/a	chr11:75919827-75919836
10	BCL3	chr11:75918338-75918916	A549	lung:	n/a	chr11:75918813-75918822
11	BHLHE40	chr11:75918652-75918875	HepG2	liver:	n/a	n/a
12	BHLHE40	chr11:75917372-75917610	K562	blood:	n/a	chr11:75917535-75917551
13	BHLHE40	chr11:75917520-75917589	GM12878	blood:	n/a	chr11:75917535-75917551
14	BHLHE40	chr11:75895960-75896047	K562	blood:	n/a	n/a
15	BHLHE40	chr11:75921554-75922195	HepG2	liver:	n/a	chr11:75921944-75921960 chr11:75921941-75921957
16	BHLHE40	chr11:75919847-75920073	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:75918605-75918909	K562	blood:	n/a	n/a
18	BHLHE40	chr11:75918623-75918961	GM12878	blood:	n/a	n/a
19	BRCA1	chr11:75919889-75920503	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr11:75917362-75917369	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr11:75918536-75918947	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr11:75918218-75918990	K562	blood:	n/a	n/a
23	CBX3	chr11:75917274-75917681	K562	blood:	n/a	n/a
24	CCNT2	chr11:75895841-75896045	K562	blood:	n/a	n/a
25	CCNT2	chr11:75918618-75918977	K562	blood:	n/a	chr11:75918965-75918974
26	CCNT2	chr11:75917343-75917789	K562	blood:	n/a	n/a
27	CEBPB	chr11:75919827-75920136	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:75918279-75918452	K562	blood:	n/a	n/a
29	CEBPB	chr11:75918220-75919075	A549	lung:	n/a	n/a
30	CEBPB	chr11:75895861-75896066	K562	blood:	n/a	n/a
31	CEBPB	chr11:75917830-75918975	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:75918338-75918535	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:75917020-75917495	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr11:75918226-75919076	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr11:75901486-75901900	IMR90	lung:	n/a	n/a
36	CEBPB	chr11:75918206-75918835	K562	blood:	n/a	n/a
37	CEBPB	chr11:75918220-75918799	K562	blood:	n/a	n/a
38	CEBPD	chr11:75895671-75896175	K562	blood:	n/a	n/a
39	CHD1	chr11:75921665-75921675	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr11:75919753-75920608	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr11:75918661-75918743	K562	blood:	n/a	n/a
42	CHD2	chr11:75918664-75918877	HepG2	liver:	n/a	n/a
43	CHD2	chr11:75917460-75917518	K562	blood:	n/a	n/a
44	CHD2	chr11:75917373-75917427	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr11:75912766-75912860	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr11:75919710-75920049	HepG2	liver:	n/a	n/a
47	CHD2	chr11:75917274-75917679	Hela-S3	cervix:	n/a	chr11:75917589-75917599
48	CHD2	chr11:75918593-75918968	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr11:75919889-75920042	GM12878	blood:	n/a	n/a
50	CREB1	chr11:75917241-75917707	A549	lung:	n/a	n/a

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75922238-75922288	U87	brain:	n/a
2	chr11:75898203-75898253	HRCEpiC	kidney:	n/a
3	chr11:75918089-75918139	HUVEC	blood vessel:	n/a
4	chr11:75909015-75909065	HAEpiC	amniotic membrane:	n/a
5	chr11:75907205-75907255	RPTEC	kidney:	n/a
6	chr11:75922238-75922288	U87	brain:	n/a
7	chr11:75898203-75898253	HRCEpiC	kidney:	n/a
8	chr11:75918089-75918139	HUVEC	blood vessel:	n/a
9	chr11:75909015-75909065	HAEpiC	amniotic membrane:	n/a
10	chr11:75907205-75907255	RPTEC	kidney:	n/a
11	chr11:75905917-75905967	NT2-D1	testis:	n/a
12	chr11:75897427-75897477	HCPEpiC	choroid plexus:	n/a
13	chr11:75922172-75922222	A549	lung:	n/a
14	chr11:75917353-75917403	MCF10A-Er-Src	breast:	n/a
15	chr11:75919862-75919912	H1-hESC	embryonic stem cell:	embryo
16	chr11:75919130-75919180	BE2_C	brain:	n/a
17	chr11:75905718-75905768	MCF-7	breast:	n/a
18	chr11:75921940-75921990	HL-60	blood:	n/a
19	chr11:75921433-75921483	HIPEpiC	eye:	n/a
20	chr11:75919130-75919180	GM19239	blood:	n/a
21	chr11:75919862-75919912	PrEC	prostate:	n/a
22	chr11:75916460-75916510	HRCEpiC	kidney:	n/a
23	chr11:75898132-75898182	SK-N-SH	brain:	n/a
24	chr11:75896332-75896382	NHDF-neo	bronchial:	n/a
25	chr11:75917404-75917454	NT2-D1	testis:	n/a
26	chr11:75917251-75917301	NB4	blood:	n/a
27	chr11:75902270-75902320	HL-60	blood:	n/a
28	chr11:75905917-75905967	HCT-116	colon:	n/a
29	chr11:75902270-75902320	K562	blood:	n/a
30	chr11:75921940-75921990	AG10803	skin:	n/a
31	chr11:75921433-75921483	HepG2	liver:	n/a
32	chr11:75919698-75919748	HCM	heart:	n/a
33	chr11:75921433-75921483	HNPCEpiC	eye:	n/a
34	chr11:75917724-75917774	HCT-116	colon:	n/a
35	chr11:75916460-75916510	SK-N-MC	brain:	n/a
36	chr11:75917353-75917403	AG04449	skin:	fetal
37	chr11:75905917-75905967	HRE	kidney:	n/a
38	chr11:75917724-75917774	GM06990	blood:	n/a
39	chr11:75916460-75916510	Hela-S3	cervix:	n/a
40	chr11:75898132-75898182	PFSK-1	brain:	n/a
41	chr11:75905917-75905967	AG04449	skin:	fetal
42	chr11:75919698-75919748	HRPEpiC	eye:	n/a
43	chr11:75922238-75922288	NB4	blood:	n/a
44	chr11:75916460-75916510	GM12878	blood:	n/a
45	chr11:75922323-75922373	AG09309	skin:	n/a
46	chr11:75917353-75917403	HIPEpiC	eye:	n/a
47	chr11:75922172-75922222	PANC-1	pancreas:	n/a
48	chr11:75898195-75898245	Caco-2	colon:	n/a
49	chr11:75921808-75921858	AG04450	lung:	fetal
50	chr11:75905718-75905768	HepG2	liver:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:75918587..75919130-chr11:76223991..76224816,2	MCF-7	breast:
2	chr11:75915411..75918045-chr11:75920337..75923182,4	MCF-7	breast:
3	chr11:75898285..75900069-chr11:75902238..75904019,2	K562	blood:
4	chr11:75917185..75919350-chr11:75920586..75922926,4	K562	blood:
5	chr11:75919537..75920594-chr11:76028825..76030444,6	MCF-7	breast:
6	chr11:75902153..75903768-chr11:75945033..75947723,2	K562	blood:
7	chr11:75878808..75880535-chr11:75885544..75887523,2	K562	blood:
8	chr11:75526830..75528448-chr11:75885826..75888721,2	K562	blood:
9	chr11:75917185..75919350-chr11:75920586..75922926,4	K562	blood:
10	chr11:75919323..75921624-chr11:75923992..75926827,3	MCF-7	breast:
11	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
12	chr11:75895025..75897686-chr11:75910991..75913944,2	K562	blood:
13	chr11:75918308..75919483-chr11:76029559..76030293,4	MCF-7	breast:
14	chr11:75913612..75915944-chr11:75916007..75917749,2	K562	blood:
15	chr11:75918736..75920705-chr11:76028307..76032444,3	MCF-7	breast:
16	chr11:75901629..75903680-chr11:75921082..75923446,2	K562	blood:
17	chr11:75895025..75897686-chr11:75910991..75913944,2	K562	blood:
18	chr11:75888382..75891358-chr11:75893738..75896231,2	MCF-7	breast:
19	chr11:75919338..75920436-chr11:76029517..76030609,7	MCF-7	breast:
20	chr1:156698046..156698801-chr11:75908969..75909469,2	Hela-S3	cervix:
21	chr11:75907802..75910235-chr11:75912499..75914692,2	K562	blood:
22	chr11:75904809..75906919-chr11:75917526..75920230,2	K562	blood:
23	chr11:75918395..75919729-chr11:75947370..75948224,3	K562	blood:
24	chr11:75877596..75879712-chr11:75888366..75889930,2	K562	blood:
25	chr11:75908327..75910235-chr11:75911530..75913999,2	K562	blood:
26	chr11:75892849..75895480-chr11:75897932..75899434,2	K562	blood:
27	chr11:75874099..75876373-chr11:75881253..75883763,2	MCF-7	breast:
28	chr11:75908679..75911274-chr11:75914998..75917762,2	K562	blood:
29	chr11:75901629..75903680-chr11:75921082..75923446,2	K562	blood:
30	chr11:75881616..75884148-chr11:75897760..75900480,2	MCF-7	breast:
31	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
32	chr11:75915411..75918045-chr11:75920337..75923182,4	MCF-7	breast:
33	chr11:75918322..75919263-chr11:76029385..76030419,7	MCF-7	breast:
34	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
35	chr11:75907463..75909415-chr11:75917684..75920104,2	MCF-7	breast:
36	chr11:75862934..75863810-chr11:75918354..75919268,2	K562	blood:
37	chr11:75918273..75920931-chr11:75945404..75947823,5	MCF-7	breast:
38	chr11:75913811..75916068-chr11:75920291..75921987,2	K562	blood:
39	chr11:75918366..75919493-chr11:76391585..76392458,3	K562	blood:
40	chr11:75886513..75888497-chr11:75907057..75909283,2	MCF-7	breast:
41	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
42	chr11:75901884..75904848-chr11:76015737..76018383,2	MCF-7	breast:
43	chr11:75919626..75920483-chr11:76029554..76030079,2	K562	blood:
44	chr11:75919700..75922037-chr11:76092044..76093720,2	MCF-7	breast:
45	chr11:75887769..75890550-chr11:75903812..75906303,2	K562	blood:
46	chr11:75918865..75921360-chr11:76155223..76156994,2	MCF-7	breast:
47	chr11:75918665..75919393-chr11:76002890..76003539,3	MCF-7	breast:
48	chr11:75886596..75888940-chr11:75889618..75892110,2	MCF-7	breast:
49	chr11:75881616..75884148-chr11:75897760..75900480,2	MCF-7	breast:
50	chr11:75907463..75909415-chr11:75917684..75920104,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKRIR-3	chr11:75921391-75921774	NONHSAT023149
2	lnc-UVRAG-2	chr11:75905685-75906115	ENSG00000254933.1
3	lnc-WNT11-1	chr11:75922000-75922293	ENSG00000255362
4	lnc-PRKRIR-3	chr11:75917466-75917542	NONHSAT023149
5	lnc-UVRAG-2	chr11:75901769-75901950	ENSG00000254933.1

No data

Variant related genes	Relation type
WNT11	TF binding region
ENSG00000254933	TF binding region
WNT11	CpG island
ENSG00000254933	CpG island
ENSG00000254933	chromatin interactions
ENSG00000137492	chromatin interactions
ENSG00000085741	chromatin interactions
ENSG00000158636	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000179240	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000143303	chromatin interactions

Extended variants
information (count: 1627 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1627 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546054396	chr11:75883570-75883571	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375383234	chr11:75883586-75883587	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556631431	chr11:75883587-75883588	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183079995	chr11:75883610-75883611	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs375689334	chr11:75883628-75883629	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs547580017	chr11:75883642-75883643	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs369936408	chr11:75883645-75883646	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs371706389	chr11:75883700-75883701	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs561685536	chr11:75883705-75883706	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs75817650	chr11:75883722-75883723	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs541686099	chr11:75883725-75883726	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs568296204	chr11:75883756-75883757	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs147134430	chr11:75883772-75883773	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs533337078	chr11:75883781-75883782	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs4944090	chr11:75883803-75883804	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs376639757	chr11:75883813-75883814	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs569916452	chr11:75883819-75883820	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs529305341	chr11:75883826-75883827	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs149443795	chr11:75883830-75883831	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs140334324	chr11:75883835-75883836	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs551011760	chr11:75883838-75883839	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs111727591	chr11:75883842-75883843	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs552959325	chr11:75883951-75883952	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs567147482	chr11:75883952-75883953	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs570802111	chr11:75884059-75884060	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs79688925	chr11:75884106-75884107	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs539641750	chr11:75884109-75884110	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs190368407	chr11:75884143-75884144	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs576313550	chr11:75884146-75884147	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs535501088	chr11:75884149-75884150	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs555194747	chr11:75884165-75884166	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs571988784	chr11:75884191-75884192	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs141199961	chr11:75884242-75884243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534262139	chr11:75884272-75884273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183578028	chr11:75884273-75884274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567204099	chr11:75884307-75884308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73003390	chr11:75884343-75884344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188176130	chr11:75884378-75884379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534416713	chr11:75884404-75884405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542250435	chr11:75884405-75884406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529484464	chr11:75884406-75884407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549433828	chr11:75884409-75884410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184918879	chr11:75884441-75884442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528476672	chr11:75884487-75884488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150758164	chr11:75884495-75884496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571671948	chr11:75884515-75884516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186606003	chr11:75884533-75884534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369506799	chr11:75884546-75884547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550115970	chr11:75884587-75884588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569841554	chr11:75884609-75884610	Weak transcription Enhancers	n/a	n/a	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
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	21858162	CNVD
Ovarian cancer	21240255	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1334 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75876600-75884400	Weak transcription	Esophagus	oesophagus
2	chr11:75877600-75887200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr11:75879800-75886600	Weak transcription	Fetal Muscle Leg	muscle
4	chr11:75881000-75887200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:75882600-75883800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:75883000-75883800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:75883400-75883600	Enhancers	Fetal Intestine Small	intestine
8	chr11:75883400-75884000	Bivalent Enhancer	Fetal Stomach	stomach
9	chr11:75883600-75884200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr11:75883600-75897000	Weak transcription	Fetal Intestine Small	intestine
11	chr11:75884400-75884800	Enhancers	Esophagus	oesophagus
12	chr11:75884600-75885200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr11:75886000-75887000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr11:75886000-75887400	Bivalent Enhancer	Fetal Stomach	stomach
15	chr11:75886200-75887800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:75886400-75888000	Enhancers	HepG2	liver
17	chr11:75886600-75887000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
18	chr11:75886600-75888200	Enhancers	Fetal Muscle Leg	muscle
19	chr11:75886600-75888800	Enhancers	Fetal Lung	lung
20	chr11:75886800-75887200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:75886800-75887600	Enhancers	Placenta	Placenta
22	chr11:75887000-75887600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr11:75887000-75887800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:75887000-75888000	Enhancers	GM12878-XiMat	blood
25	chr11:75887000-75888200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr11:75887000-75888800	Enhancers	Fetal Muscle Trunk	muscle
27	chr11:75887200-75887400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr11:75887200-75888000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr11:75887200-75888000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:75887200-75888200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr11:75887400-75888600	Enhancers	Fetal Stomach	stomach
32	chr11:75887600-75888200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:75887600-75892000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr11:75887800-75896400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr11:75888000-75888800	Flanking Active TSS	HepG2	liver
36	chr11:75888200-75888400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr11:75888200-75889400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:75888200-75895200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr11:75888400-75889600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:75888600-75889000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr11:75888800-75889000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:75888800-75889600	Enhancers	HepG2	liver
43	chr11:75888800-75894800	Weak transcription	Fetal Lung	lung
44	chr11:75889400-75889600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr11:75889400-75889600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:75889600-75889800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:75889600-75889800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr11:75889600-75889800	Bivalent Enhancer	Fetal Stomach	stomach
49	chr11:75889600-75890600	Weak transcription	HepG2	liver
50	chr11:75889600-75891000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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