Variant report

Variant	nsv832116
Chromosome Location	chr11:34539536-34673900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2748)
CpG islands
(count:671)
Chromatin interactive
region (count:170)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34655611-34656115	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:34607536-34608144	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:34621007-34621577	K562	blood:	n/a	n/a
4	ARID3A	chr11:34608910-34609101	K562	blood:	n/a	n/a
5	ARID3A	chr11:34630869-34631861	K562	blood:	n/a	n/a
6	ARID3A	chr11:34661875-34662144	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:34607346-34608170	K562	blood:	n/a	n/a
8	ARID3A	chr11:34627281-34627282	K562	blood:	n/a	n/a
9	ARID3A	chr11:34638435-34638685	K562	blood:	n/a	chr11:34638645-34638661 chr11:34638644-34638660
10	ARID3A	chr11:34664524-34664676	K562	blood:	n/a	n/a
11	ARID3A	chr11:34622158-34622628	HepG2	liver:	n/a	n/a
12	ARID3A	chr11:34667925-34667948	K562	blood:	n/a	n/a
13	ARID3A	chr11:34673150-34674076	K562	blood:	n/a	n/a
14	ARID3A	chr11:34624675-34625683	K562	blood:	n/a	chr11:34625467-34625483 chr11:34625466-34625482
15	ARID3A	chr11:34640475-34640903	K562	blood:	n/a	n/a
16	ARID3A	chr11:34621841-34622087	K562	blood:	n/a	n/a
17	ATF1	chr11:34640574-34640880	K562	blood:	n/a	n/a
18	ATF1	chr11:34621029-34621369	K562	blood:	n/a	n/a
19	ATF1	chr11:34673739-34674051	K562	blood:	n/a	n/a
20	ATF1	chr11:34631415-34631756	K562	blood:	n/a	n/a
21	ATF1	chr11:34624747-34625461	K562	blood:	n/a	n/a
22	ATF1	chr11:34607431-34608012	K562	blood:	n/a	n/a
23	ATF1	chr11:34592103-34592434	K562	blood:	n/a	chr11:34592276-34592290
24	ATF1	chr11:34636333-34636609	K562	blood:	n/a	n/a
25	ATF1	chr11:34621838-34622246	K562	blood:	n/a	n/a
26	ATF1	chr11:34589265-34589460	K562	blood:	n/a	n/a
27	ATF2	chr11:34673623-34674581	GM12878	blood:	n/a	n/a
28	ATF2	chr11:34636272-34636677	GM12878	blood:	n/a	n/a
29	ATF2	chr11:34607185-34608030	GM12878	blood:	n/a	n/a
30	ATF2	chr11:34607654-34608184	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr11:34634791-34635580	GM12878	blood:	n/a	n/a
32	ATF2	chr11:34644852-34645273	GM12878	blood:	n/a	n/a
33	ATF2	chr11:34634958-34635411	GM12878	blood:	n/a	n/a
34	ATF2	chr11:34655408-34656051	GM12878	blood:	n/a	n/a
35	ATF2	chr11:34671884-34672577	GM12878	blood:	n/a	n/a
36	ATF2	chr11:34671847-34672599	GM12878	blood:	n/a	n/a
37	ATF3	chr11:34661411-34662279	A549	lung:	n/a	n/a
38	ATF3	chr11:34673654-34674049	K562	blood:	n/a	n/a
39	ATF3	chr11:34661628-34662235	A549	lung:	n/a	n/a
40	ATF3	chr11:34621797-34622499	A549	lung:	n/a	n/a
41	ATF3	chr11:34592129-34592305	K562	blood:	n/a	n/a
42	ATF3	chr11:34621807-34622586	A549	lung:	n/a	n/a
43	BACH1	chr11:34631266-34631430	K562	blood:	n/a	n/a
44	BACH1	chr11:34621205-34621404	K562	blood:	n/a	n/a
45	BACH1	chr11:34607707-34608030	H1-hESC	embryonic stem cell:	n/a	n/a
46	BATF	chr11:34645527-34645908	GM12878	blood:	n/a	n/a
47	BATF	chr11:34635028-34635421	GM12878	blood:	n/a	n/a
48	BATF	chr11:34607208-34607570	GM12878	blood:	n/a	chr11:34607478-34607486 chr11:34607255-34607264
49	BATF	chr11:34655400-34656160	GM12878	blood:	n/a	n/a
50	BATF	chr11:34672024-34672548	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34642885-34642935	HCF	heart:	n/a
2	chr11:34608061-34608111	BJ	skin:	n/a
3	chr11:34622359-34622409	IMR90	lung:	fetal
4	chr11:34642463-34642513	HIPEpiC	eye:	n/a
5	chr11:34672025-34672075	NHDF-neo	bronchial:	n/a
6	chr11:34672025-34672075	AG09309	skin:	n/a
7	chr11:34642303-34642353	HAEpiC	amniotic membrane:	n/a
8	chr11:34666060-34666110	HCT-116	colon:	n/a
9	chr11:34608041-34608091	ECC-1	luminal epithelium:	n/a
10	chr11:34654233-34654283	IMR90	lung:	fetal
11	chr11:34608041-34608091	GM12891	blood:	n/a
12	chr11:34642885-34642935	BE2_C	brain:	n/a
13	chr11:34642463-34642513	PFSK-1	brain:	n/a
14	chr11:34654233-34654283	H1-hESC	embryonic stem cell:	embryo
15	chr11:34622359-34622409	PFSK-1	brain:	n/a
16	chr11:34622359-34622409	MCF-7	breast:	n/a
17	chr11:34641925-34641975	U87	brain:	n/a
18	chr11:34642463-34642513	SK-N-SH_RA	brain:	n/a
19	chr11:34641925-34641975	GM12892	blood:	n/a
20	chr11:34608041-34608091	NHBE	bronchial:	n/a
21	chr11:34608061-34608111	IMR90	lung:	fetal
22	chr11:34642463-34642513	U87	brain:	n/a
23	chr11:34672025-34672075	BJ	skin:	n/a
24	chr11:34622359-34622409	ProgFib	skin:	n/a
25	chr11:34642463-34642513	RPTEC	kidney:	n/a
26	chr11:34622359-34622409	BJ	skin:	n/a
27	chr11:34642303-34642353	HMEC	breast:	n/a
28	chr11:34641925-34641975	SK-N-SH	brain:	n/a
29	chr11:34586278-34586328	GM12891	blood:	n/a
30	chr11:34622359-34622409	U87	brain:	n/a
31	chr11:34642885-34642935	AG04450	lung:	fetal
32	chr11:34586278-34586328	NHBE	bronchial:	n/a
33	chr11:34666060-34666110	HIPEpiC	eye:	n/a
34	chr11:34642885-34642935	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:34642303-34642353	HRCEpiC	kidney:	n/a
36	chr11:34608061-34608111	HL-60	blood:	n/a
37	chr11:34666060-34666110	ProgFib	skin:	n/a
38	chr11:34642303-34642353	PANC-1	pancreas:	n/a
39	chr11:34641925-34641975	SAEC	small airway:	n/a
40	chr11:34666060-34666110	HUVEC	blood vessel:	n/a
41	chr11:34642885-34642935	GM12891	blood:	n/a
42	chr11:34642303-34642353	Hepatocyte	liver:	n/a
43	chr11:34666060-34666110	NB4	blood:	n/a
44	chr11:34608061-34608111	K562	blood:	n/a
45	chr11:34608041-34608091	IMR90	lung:	fetal
46	chr11:34672025-34672075	HMEC	breast:	n/a
47	chr11:34642303-34642353	T-47D	breast:	n/a
48	chr11:34642885-34642935	SK-N-MC	brain:	n/a
49	chr11:34642303-34642353	HNPCEpiC	eye:	n/a
50	chr11:34641925-34641975	T-47D	breast:	n/a

(count:170 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:34642981..34644601-chr11:34653348..34655427,2	K562	blood:
2	chr11:34309640..34312411-chr11:34560642..34563280,2	K562	blood:
3	chr11:34621759..34624230-chr11:34829278..34830946,2	K562	blood:
4	chr11:34622016..34626475-chr11:34634436..34638216,4	K562	blood:
5	chr11:34658574..34661382-chr11:34673276..34674986,2	K562	blood:
6	chr11:34607478..34608063-chr11:34675671..34676201,2	K562	blood:
7	chr11:34621045..34623041-chr11:34631011..34633370,3	K562	blood:
8	chr11:34607496..34609587-chr11:34610286..34612192,2	K562	blood:
9	chr11:34616542..34620453-chr11:34622551..34624914,3	K562	blood:
10	chr11:34622395..34624050-chr11:34625059..34627992,2	K562	blood:
11	chr11:34604587..34607493-chr11:34890085..34892245,2	K562	blood:
12	chr11:34641388..34644237-chr11:34660618..34663413,3	MCF-7	breast:
13	chr11:34659576..34666077-chr11:34671950..34677960,8	MCF-7	breast:
14	chr11:34623436..34625468-chr11:34629882..34632091,2	MCF-7	breast:
15	chr11:34580789..34582824-chr11:34590788..34592588,2	MCF-7	breast:
16	chr11:34636228..34637747-chr11:34653006..34655349,2	K562	blood:
17	chr11:34569316..34570958-chr11:34584270..34586034,2	MCF-7	breast:
18	chr11:34626866..34628480-chr11:34633656..34636586,2	K562	blood:
19	chr11:34621491..34624249-chr11:34628284..34630730,3	K562	blood:
20	chr11:34561144..34563825-chr11:34565776..34568336,2	MCF-7	breast:
21	chr11:34576201..34578567-chr11:34586570..34588865,2	K562	blood:
22	chr11:34619511..34621145-chr11:34630606..34632621,2	K562	blood:
23	chr11:34618804..34621129-chr11:34885676..34887484,2	K562	blood:
24	chr11:34640457..34642067-chr11:34645201..34647926,2	K562	blood:
25	chr11:34600502..34602509-chr11:34619599..34621196,2	K562	blood:
26	chr11:34647092..34649318-chr11:34661381..34664170,2	MCF-7	breast:
27	chr11:34568732..34570985-chr11:34586878..34589056,2	MCF-7	breast:
28	chr11:34623810..34626247-chr11:34658951..34660726,2	K562	blood:
29	chr11:34621233..34623041-chr11:34631125..34633370,2	K562	blood:
30	chr11:34590206..34592254-chr11:34601369..34603799,2	K562	blood:
31	chr11:34669421..34671173-chr11:34672153..34673980,2	MCF-7	breast:
32	chr11:34646456..34649204-chr11:34658693..34661498,2	K562	blood:
33	chr11:34637828..34640376-chr11:34674188..34675830,2	K562	blood:
34	chr11:34598538..34599519-chr11:34911955..34912929,2	MCF-7	breast:
35	chr11:34608832..34611723-chr11:34620873..34624079,3	K562	blood:
36	chr11:34534199..34535559-chr11:34586614..34587431,4	MCF-7	breast:
37	chr11:34667026..34669860-chr11:34670729..34674074,4	MCF-7	breast:
38	chr11:34622395..34624050-chr11:34625059..34627992,2	K562	blood:
39	chr11:34641972..34644254-chr11:34644762..34647514,2	MCF-7	breast:
40	chr11:34586526..34588282-chr11:34590420..34591950,2	MCF-7	breast:
41	chr11:34660689..34662189-chr11:34672411..34674964,2	MCF-7	breast:
42	chr11:34569316..34570958-chr11:34584270..34586034,2	MCF-7	breast:
43	chr11:34669421..34671173-chr11:34672153..34673980,2	MCF-7	breast:
44	chr11:34568732..34570985-chr11:34586878..34589056,2	MCF-7	breast:
45	chr11:34568608..34571143-chr11:34742934..34745851,2	K562	blood:
46	chr11:34652119..34655863-chr11:34659054..34663383,5	MCF-7	breast:
47	chr11:34640806..34644782-chr11:34660554..34663507,4	MCF-7	breast:
48	chr11:34569575..34572188-chr11:34654026..34656831,2	MCF-7	breast:
49	chr11:34560082..34562731-chr11:34583590..34585196,2	MCF-7	breast:
50	chr11:34606565..34609157-chr11:34935586..34938708,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EHF-2	chr11:34592423-34592550	ENSG00000255427
2	lnc-EHF-2	chr11:34595094-34595529	ENSG00000255427
3	lnc-ELF5-2	chr11:34554561-34554713	ENSG00000255271
4	lnc-ELF5-2	chr11:34566308-34566415	ENSG00000255271
5	lnc-ELF5-2	chr11:34579344-34579471	ENSG00000255271

No data

Variant related genes	Relation type
ENSG00000255271	TF binding region
EHF	TF binding region
ELF5	TF binding region
ENSG00000255427	TF binding region
ENSG00000255271	CpG island
EHF	CpG island
ELF5	CpG island
ENSG00000255427	CpG island
ENSG00000164296	chromatin interactions
ENSG00000135373	chromatin interactions
ENSG00000149089	chromatin interactions
ENSG00000255271	chromatin interactions
ENSG00000113716	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000135374	chromatin interactions
ENSG00000255427	chromatin interactions

Extended variants
information (count: 4722 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:4722 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185779288	chr11:34539555-34539556	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs139517687	chr11:34539556-34539557	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565609429	chr11:34539571-34539572	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs562618061	chr11:34539625-34539626	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186446123	chr11:34540305-34540306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs556936558	chr11:34540375-34540376	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34147834	chr11:34540386-34540387	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75794165	chr11:34540412-34540413	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs4615999	chr11:34540414-34540415	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531449488	chr11:34540434-34540435	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs3847600	chr11:34540469-34540470	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs565341128	chr11:34540533-34540534	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542199581	chr11:34540539-34540540	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs183580153	chr11:34540575-34540576	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116207500	chr11:34540644-34540645	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs3847601	chr11:34540649-34540650	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs76398138	chr11:34540670-34540671	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549798839	chr11:34540694-34540695	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188719364	chr11:34540742-34540743	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs538772671	chr11:34540758-34540759	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564108051	chr11:34540829-34540830	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs10488738	chr11:34540909-34540910	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566028649	chr11:34540936-34540937	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs12794961	chr11:34540986-34540987	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114096914	chr11:34541044-34541045	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs79621248	chr11:34541047-34541048	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78147762	chr11:34541054-34541055	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192604393	chr11:34541107-34541108	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11032739	chr11:34541141-34541142	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs60942105	chr11:34541144-34541145	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs398075848	chr11:34541146-34541147	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs199564619	chr11:34541195-34541196	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576079113	chr11:34541246-34541247	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545140839	chr11:34541287-34541288	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554278072	chr11:34541291-34541292	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs527374288	chr11:34541314-34541315	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs151233487	chr11:34541364-34541365	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs836140	chr11:34541397-34541398	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186632684	chr11:34541403-34541404	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140929380	chr11:34541405-34541406	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569734187	chr11:34541435-34541436	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs79769374	chr11:34541476-34541477	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373343883	chr11:34541526-34541527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs115905386	chr11:34541527-34541528	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11032740	chr11:34541536-34541537	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377522105	chr11:34541542-34541543	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150181997	chr11:34541591-34541592	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs7115273	chr11:34541625-34541626	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567422692	chr11:34541680-34541681	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536573740	chr11:34541767-34541768	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	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
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1873 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34543800-34544000	Enhancers	Adipose Nuclei	Adipose
2	chr11:34543800-34544800	Enhancers	Lung	lung
3	chr11:34544600-34545200	Enhancers	Fetal Lung	lung
4	chr11:34544800-34545200	Enhancers	Fetal Heart	heart
5	chr11:34544800-34546800	Enhancers	Placenta	Placenta
6	chr11:34544800-34547600	Weak transcription	Lung	lung
7	chr11:34545800-34546200	Bivalent Enhancer	HepG2	liver
8	chr11:34546000-34546200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
9	chr11:34546200-34546800	Flanking Bivalent TSS/Enh	HepG2	liver
10	chr11:34546400-34546600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:34546400-34546600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:34546400-34546600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr11:34546600-34547000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr11:34546800-34547200	Weak transcription	Placenta	Placenta
15	chr11:34547200-34548200	Enhancers	Placenta	Placenta
16	chr11:34547800-34548000	Enhancers	Lung	lung
17	chr11:34547800-34548200	Active TSS	Duodenum Mucosa	Duodenum
18	chr11:34547800-34548200	Enhancers	Gastric	stomach
19	chr11:34547800-34551600	Enhancers	Liver	Liver
20	chr11:34547800-34552000	Enhancers	HepG2	liver
21	chr11:34548000-34548200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:34548000-34548400	Active TSS	GM12878-XiMat	blood
23	chr11:34550800-34551600	Enhancers	A549	lung
24	chr11:34555600-34556400	ZNF genes & repeats	Aorta	Aorta
25	chr11:34562600-34563200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr11:34562600-34563400	Enhancers	Adipose Nuclei	Adipose
27	chr11:34564200-34564600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr11:34564600-34566600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr11:34566600-34567200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:34566600-34569200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr11:34567200-34567600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:34567600-34567800	Enhancers	HepG2	liver
33	chr11:34567600-34568000	Enhancers	Brain Anterior Caudate	brain
34	chr11:34567600-34568000	Enhancers	Brain Hippocampus Middle	brain
35	chr11:34567600-34568600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:34567600-34568800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr11:34567600-34569200	Enhancers	Brain Angular Gyrus	brain
38	chr11:34567600-34569200	Enhancers	Brain Cingulate Gyrus	brain
39	chr11:34567600-34569400	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr11:34567600-34569400	Enhancers	Brain Substantia Nigra	brain
41	chr11:34567800-34568200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr11:34567800-34568200	Flanking Active TSS	HepG2	liver
43	chr11:34567800-34568600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:34567800-34568600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:34567800-34569000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr11:34567800-34569200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr11:34568000-34568200	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr11:34568000-34568200	Flanking Active TSS	Brain Hippocampus Middle	brain
49	chr11:34568000-34568200	Enhancers	Lung	lung
50	chr11:34568000-34568600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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