Variant report

Variant	nsv983035
Chromosome Location	chr11:65494712-65529501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:302)
CpG islands
(count:184)
Chromatin interactive
region (count:52)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:65511997-65512236	HepG2	liver:	n/a	n/a
2	BACH1	chr11:65522471-65522639	K562	blood:	n/a	n/a
3	BHLHE40	chr11:65512094-65512208	K562	blood:	n/a	n/a
4	BRCA1	chr11:65511981-65512200	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr11:65511980-65512400	K562	blood:	n/a	n/a
6	CBX3	chr11:65504339-65504736	HCT-116	colon:	n/a	n/a
7	CBX3	chr11:65504350-65504653	K562	blood:	n/a	n/a
8	CEBPB	chr11:65511491-65512172	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:65504776-65504970	IMR90	lung:	n/a	n/a
10	CEBPB	chr11:65523260-65523658	K562	blood:	n/a	n/a
11	CEBPB	chr11:65521144-65521406	HepG2	liver:	n/a	n/a
12	CHD2	chr11:65511980-65512160	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr11:65511446-65511777	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr11:65512073-65512086	HepG2	liver:	n/a	n/a
15	CTCF	chr11:65512040-65512190	GM12866	blood:	n/a	n/a
16	CTCF	chr11:65511851-65512444	MCF-7	breast:	n/a	n/a
17	CTCF	chr11:65512040-65512190	GM12869	blood:	n/a	n/a
18	CTCF	chr11:65511960-65512110	RPTEC	kidney:	n/a	n/a
19	CTCF	chr11:65512060-65512210	BJ	skin:	n/a	n/a
20	CTCF	chr11:65512060-65512210	AG04449	skin:	n/a	n/a
21	CTCF	chr11:65512022-65512215	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:65512060-65512210	HCFaa	heart:	n/a	n/a
23	CTCF	chr11:65512080-65512230	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr11:65512082-65512135	GM10266	blood:	n/a	n/a
25	CTCF	chr11:65512100-65512250	GM12871	blood:	n/a	n/a
26	CTCF	chr11:65511811-65511875	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:65512020-65512170	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:65511980-65512130	HAc	cerebellar:	n/a	n/a
29	CTCF	chr11:65512000-65512233	K562	blood:	n/a	n/a
30	CTCF	chr11:65512044-65512188	ProgFib	skin:	n/a	n/a
31	CTCF	chr11:65512020-65512170	HAc	cerebellar:	n/a	n/a
32	CTCF	chr11:65512040-65512190	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr11:65511980-65512292	A549	lung:	n/a	n/a
34	CTCF	chr11:65511877-65512487	HCT-116	colon:	n/a	n/a
35	CTCF	chr11:65512031-65512201	NHEK	skin:	n/a	n/a
36	CTCF	chr11:65512060-65512210	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr11:65512040-65512190	HPF	lung:	n/a	n/a
38	CTCF	chr11:65512260-65512410	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr11:65512060-65512210	MCF-7	breast:	n/a	n/a
40	CTCF	chr11:65512018-65512185	LNCaP	prostate:	n/a	n/a
41	CTCF	chr11:65512060-65512210	AG09319	gingival:	n/a	n/a
42	CTCF	chr11:65512060-65512210	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr11:65512020-65512170	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr11:65512040-65512190	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr11:65512040-65512190	HL-60	blood:	n/a	n/a
46	CTCF	chr11:65512035-65512175	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr11:65512060-65512210	GM12868	blood:	n/a	n/a
48	CTCF	chr11:65511945-65512331	K562	blood:	n/a	n/a
49	CTCF	chr11:65512000-65512150	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr11:65512007-65512225	A549	lung:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65495317-65495367	RPTEC	kidney:	n/a
2	chr11:65495317-65495367	RPTEC	kidney:	n/a
3	chr11:65495335-65495385	HEEpiC	esophagus:	n/a
4	chr11:65495335-65495385	GM12892	blood:	n/a
5	chr11:65495249-65495299	HCT-116	colon:	n/a
6	chr11:65495317-65495367	HEK293	kidney:	embryo
7	chr11:65495317-65495367	LNCaP	prostate:	n/a
8	chr11:65495249-65495299	SK-N-SH_RA	brain:	n/a
9	chr11:65495335-65495385	Hela-S3	cervix:	n/a
10	chr11:65495317-65495367	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:65495335-65495385	HNPCEpiC	eye:	n/a
12	chr11:65495249-65495299	AG09319	gingival:	n/a
13	chr11:65495249-65495299	AG04449	skin:	fetal
14	chr11:65495249-65495299	HRPEpiC	eye:	n/a
15	chr11:65495335-65495385	GM19239	blood:	n/a
16	chr11:65495335-65495385	NHBE	bronchial:	n/a
17	chr11:65495317-65495367	HRE	kidney:	n/a
18	chr11:65495249-65495299	T-47D	breast:	n/a
19	chr11:65495335-65495385	HL-60	blood:	n/a
20	chr11:65495335-65495385	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:65495249-65495299	AG09309	skin:	n/a
22	chr11:65495317-65495367	HRPEpiC	eye:	n/a
23	chr11:65495249-65495299	HRE	kidney:	n/a
24	chr11:65495335-65495385	Hepatocyte	liver:	n/a
25	chr11:65495335-65495385	GM12878	blood:	n/a
26	chr11:65495249-65495299	HAEpiC	amniotic membrane:	n/a
27	chr11:65495249-65495299	NHDF-neo	bronchial:	n/a
28	chr11:65495335-65495385	GM12891	blood:	n/a
29	chr11:65495317-65495367	NH-A	brain:	n/a
30	chr11:65495249-65495299	IMR90	lung:	fetal
31	chr11:65495249-65495299	GM12892	blood:	n/a
32	chr11:65495249-65495299	Caco-2	colon:	n/a
33	chr11:65495335-65495385	AG04449	skin:	fetal
34	chr11:65495317-65495367	H1-hESC	embryonic stem cell:	embryo
35	chr11:65495249-65495299	ProgFib	skin:	n/a
36	chr11:65495335-65495385	HCPEpiC	choroid plexus:	n/a
37	chr11:65495249-65495299	SAEC	small airway:	n/a
38	chr11:65495249-65495299	H1-hESC	embryonic stem cell:	embryo
39	chr11:65495317-65495367	BJ	skin:	n/a
40	chr11:65495317-65495367	ECC-1	luminal epithelium:	n/a
41	chr11:65495249-65495299	AG04450	lung:	fetal
42	chr11:65495317-65495367	U87	brain:	n/a
43	chr11:65495249-65495299	HCPEpiC	choroid plexus:	n/a
44	chr11:65495335-65495385	HMEC	breast:	n/a
45	chr11:65495249-65495299	BJ	skin:	n/a
46	chr11:65495249-65495299	GM06990	blood:	n/a
47	chr11:65495317-65495367	AG10803	skin:	n/a
48	chr11:65495249-65495299	GM12891	blood:	n/a
49	chr11:65495249-65495299	HCF	heart:	n/a
50	chr11:65495249-65495299	Hela-S3	cervix:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:65515092..65517628-chr11:65521131..65522711,2	K562	blood:
2	chr11:65511597..65512884-chr11:65585147..65586477,30	MCF-7	breast:
3	chr11:65510264..65512208-chr11:65547345..65548979,2	K562	blood:
4	chr11:65510782..65513153-chr11:65513586..65515481,2	K562	blood:
5	chr11:65511343..65512591-chr11:65585351..65586294,10	MCF-7	breast:
6	chr11:65478433..65481069-chr11:65493417..65495213,3	K562	blood:
7	chr11:65485948..65488920-chr11:65514361..65516768,2	K562	blood:
8	chr11:65495038..65497128-chr11:65537591..65539830,2	MCF-7	breast:
9	chr11:65510782..65513153-chr11:65513586..65515481,2	K562	blood:
10	chr11:65487463..65490934-chr11:65492571..65495479,8	K562	blood:
11	chr11:65507614..65509746-chr11:65624233..65626717,2	K562	blood:
12	chr11:65526354..65531692-chr11:65541770..65544711,4	K562	blood:
13	chr11:65491919..65494858-chr11:65497496..65500285,2	K562	blood:
14	chr11:65511623..65512514-chr11:65547091..65548129,3	MCF-7	breast:
15	chr11:65509847..65512521-chr11:65541079..65543934,2	K562	blood:
16	chr11:65488838..65491538-chr11:65497490..65499869,2	K562	blood:
17	chr11:65503407..65506385-chr11:65511458..65515051,3	K562	blood:
18	chr11:65511963..65512619-chr11:65537012..65537973,4	MCF-7	breast:
19	chr11:65515092..65517628-chr11:65521131..65522711,2	K562	blood:
20	chr11:65511713..65512488-chr11:65756361..65757355,2	MCF-7	breast:
21	chr11:65481113..65483884-chr11:65507663..65510016,2	K562	blood:
22	chr11:65479447..65481796-chr11:65522666..65526491,3	MCF-7	breast:
23	chr11:65492420..65494936-chr11:65657867..65659851,2	K562	blood:
24	chr11:65478910..65479852-chr11:65511683..65512451,2	MCF-7	breast:
25	chr11:65508695..65511331-chr11:65535308..65536839,2	MCF-7	breast:
26	chr11:65494883..65497549-chr11:65540068..65542666,2	K562	blood:
27	chr11:65522724..65524712-chr11:65531852..65533570,2	K562	blood:
28	chr11:65503760..65506587-chr11:65625828..65628619,2	MCF-7	breast:
29	chr11:65478491..65482258-chr11:65493417..65497237,3	K562	blood:
30	chr11:65511937..65512528-chr11:65537362..65537959,2	MCF-7	breast:
31	chr11:65511419..65513078-chr11:65625541..65627932,2	MCF-7	breast:
32	chr11:65517753..65520612-chr11:65618673..65621120,3	K562	blood:
33	chr11:65528026..65529884-chr11:65535933..65538399,2	K562	blood:
34	chr11:65515890..65517805-chr11:65606397..65609087,2	K562	blood:
35	chr11:65487426..65489327-chr11:65528069..65530288,2	K562	blood:
36	chr11:65479344..65482613-chr11:65506130..65509163,3	K562	blood:
37	chr11:65515499..65518000-chr11:65552995..65554929,2	MCF-7	breast:
38	chr11:65497418..65500057-chr11:65626115..65627970,2	MCF-7	breast:
39	chr11:65528882..65532514-chr11:65547670..65550990,4	K562	blood:
40	chr11:65487520..65489937-chr11:65492095..65496093,4	MCF-7	breast:
41	chr11:65492815..65494934-chr11:65514199..65515786,2	K562	blood:
42	chr11:65493436..65495930-chr11:65657867..65659544,2	K562	blood:
43	chr11:65486247..65489385-chr11:65493532..65496912,4	MCF-7	breast:
44	chr11:65477043..65480917-chr11:65508672..65511381,3	MCF-7	breast:
45	chr11:65511399..65513092-chr11:65547173..65549839,3	MCF-7	breast:
46	chr11:65507408..65509885-chr11:65553475..65556094,2	MCF-7	breast:
47	chr11:65478144..65479765-chr11:65498532..65500836,2	MCF-7	breast:
48	chr11:65492790..65496267-chr11:65497978..65500285,3	K562	blood:
49	chr11:65508777..65511701-chr11:65625140..65626747,2	MCF-7	breast:
50	chr11:65478948..65481631-chr11:65497554..65500417,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT5-2	chr11:65517511-65518055	l_499_chr11:65517510-65519666_brain
2	lnc-KAT5-2	chr11:65518340-65519666	l_499_chr11:65517510-65519666_brain
3	lnc-OVOL1-1	chr11:65513200-65513269	ENSG00000255557

No data

Variant related genes	Relation type
ENSG00000255557	TF binding region
ENSG00000255557	CpG island
ENSG00000175602	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000214659	chromatin interactions
ENSG00000172922	chromatin interactions
ENSG00000172977	chromatin interactions
ENSG00000254470	chromatin interactions
ENSG00000172818	chromatin interactions
ENSG00000255557	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000175827	chromatin interactions

Extended variants
information (count: 1042 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567061702	chr11:65494746-65494747	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs536328554	chr11:65494753-65494754	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs372513547	chr11:65494795-65494796	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs569402273	chr11:65494848-65494849	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538168759	chr11:65494850-65494851	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs543640113	chr11:65494856-65494857	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs558453107	chr11:65494864-65494865	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs578074154	chr11:65494977-65494978	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs181563756	chr11:65494983-65494984	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs537786	chr11:65494987-65494988	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs150873975	chr11:65494998-65494999	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs543087613	chr11:65495005-65495006	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs562563532	chr11:65495027-65495028	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs370797680	chr11:65495065-65495066	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs373086801	chr11:65495096-65495097	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs370200403	chr11:65495119-65495120	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs11227279	chr11:65495211-65495212	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559759187	chr11:65495229-65495230	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs139379610	chr11:65495231-65495232	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs564882458	chr11:65495236-65495237	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs527570665	chr11:65495246-65495247	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs547023240	chr11:65495250-65495251	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs373424209	chr11:65495273-65495274	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs529771274	chr11:65495281-65495282	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs549810056	chr11:65495325-65495326	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs569358213	chr11:65495333-65495334	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs538391154	chr11:65495334-65495335	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs376672117	chr11:65495336-65495337	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs374652982	chr11:65495338-65495339	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs186982080	chr11:65495363-65495364	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs534481985	chr11:65495375-65495376	ZNF genes & repeats Strong transcription Enhancers Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs554236402	chr11:65495403-65495404	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs73492413	chr11:65495428-65495429	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs556580684	chr11:65495460-65495461	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs149294929	chr11:65495465-65495466	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs576455945	chr11:65495482-65495483	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs544843405	chr11:65495483-65495484	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs564721465	chr11:65495534-65495535	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs183456148	chr11:65495535-65495536	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs371018305	chr11:65495543-65495544	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs74638829	chr11:65495571-65495572	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs540897506	chr11:65495572-65495573	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs560734169	chr11:65495573-65495574	Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs529649337	chr11:65495678-65495679	Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs78412025	chr11:65495696-65495697	Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs563447460	chr11:65495708-65495709	Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs532101180	chr11:65495712-65495713	Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs186707806	chr11:65495720-65495721	Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs377724846	chr11:65495737-65495738	Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs571849255	chr11:65495742-65495743	Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65488400-65496200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr11:65492400-65494800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:65493000-65495400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr11:65494200-65495400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:65494800-65495400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:65495000-65495400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:65495400-65495600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:65495400-65495800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:65495400-65511400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr11:65495600-65495800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:65496000-65496200	Enhancers	K562	blood
12	chr11:65502400-65503000	Enhancers	Esophagus	oesophagus
13	chr11:65506800-65507800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr11:65507800-65511600	Weak transcription	Spleen	Spleen
15	chr11:65508200-65508400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:65508400-65509000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:65508600-65509000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:65509000-65511400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:65509400-65511200	Enhancers	Placenta	Placenta
20	chr11:65509800-65510600	Enhancers	Liver	Liver
21	chr11:65510000-65510400	Enhancers	Fetal Lung	lung
22	chr11:65510000-65510600	Enhancers	Hela-S3	cervix
23	chr11:65510200-65511400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:65510600-65510800	Flanking Active TSS	Hela-S3	cervix
25	chr11:65510800-65511200	Active TSS	Hela-S3	cervix
26	chr11:65511200-65511400	Enhancers	Colonic Mucosa	Colon
27	chr11:65511200-65511400	Bivalent Enhancer	HepG2	liver
28	chr11:65511200-65511600	Flanking Active TSS	Placenta	Placenta
29	chr11:65511200-65512400	Flanking Active TSS	Hela-S3	cervix
30	chr11:65511400-65511600	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr11:65511400-65511800	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr11:65511400-65512000	Flanking Active TSS	Colonic Mucosa	Colon
33	chr11:65511400-65512000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr11:65511400-65512000	Flanking Bivalent TSS/Enh	HepG2	liver
35	chr11:65511400-65512200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr11:65511400-65513000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr11:65511600-65511800	Bivalent Enhancer	Adipose Nuclei	Adipose
38	chr11:65511600-65511800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
39	chr11:65511600-65512000	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr11:65511600-65512000	Enhancers	Esophagus	oesophagus
41	chr11:65511600-65512000	Enhancers	Pancreas	Pancrea
42	chr11:65511600-65512200	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr11:65511600-65512800	Enhancers	Spleen	Spleen
44	chr11:65511600-65513000	Enhancers	Placenta	Placenta
45	chr11:65511800-65512000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
46	chr11:65511800-65512000	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr11:65511800-65512000	Bivalent Enhancer	NHEK	skin
48	chr11:65511800-65514200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr11:65512000-65512200	Enhancers	Colonic Mucosa	Colon
50	chr11:65512000-65512800	Bivalent/Poised TSS	HepG2	liver

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