Variant report

Variant	nsv530047
Chromosome Location	chr1:93273425-93308213
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1643)
CpG islands
(count:1040)
Chromatin interactive
region (count:59)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1643 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:93292462-93292463	K562	blood:	n/a	n/a
2	ARID3A	chr1:93283970-93284133	K562	blood:	n/a	n/a
3	ARID3A	chr1:93297361-93297842	K562	blood:	n/a	n/a
4	ARID3A	chr1:93297404-93297888	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:93288466-93288710	HepG2	liver:	n/a	n/a
6	ATF1	chr1:93297336-93298017	K562	blood:	n/a	n/a
7	ATF2	chr1:93297256-93298349	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:93297268-93298064	GM12878	blood:	n/a	n/a
9	ATF2	chr1:93297278-93298105	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:93297201-93298105	GM12878	blood:	n/a	n/a
11	ATF3	chr1:93297325-93297865	A549	lung:	n/a	n/a
12	ATF3	chr1:93297270-93298005	K562	blood:	n/a	n/a
13	ATF3	chr1:93297349-93297825	A549	lung:	n/a	n/a
14	ATF3	chr1:93292315-93292609	K562	blood:	n/a	n/a
15	BACH1	chr1:93296738-93296758	K562	blood:	n/a	n/a
16	BACH1	chr1:93297366-93298159	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr1:93297315-93297869	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:93297350-93298012	GM12878	blood:	n/a	chr1:93297974-93297987
19	BCL3	chr1:93308176-93309977	A549	lung:	n/a	n/a
20	BCL3	chr1:93297243-93298061	A549	lung:	n/a	chr1:93297974-93297987
21	BCL3	chr1:93297285-93298129	A549	lung:	n/a	chr1:93297974-93297987
22	BCLAF1	chr1:93297269-93298143	GM12878	blood:	n/a	chr1:93297974-93297987
23	BCLAF1	chr1:93297200-93298065	GM12878	blood:	n/a	chr1:93297974-93297987
24	BHLHE40	chr1:93297310-93298194	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:93297285-93298122	K562	blood:	n/a	n/a
26	BHLHE40	chr1:93297287-93298203	HepG2	liver:	n/a	n/a
27	BRCA1	chr1:93297345-93298063	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr1:93297422-93298072	HepG2	liver:	n/a	n/a
29	BRCA1	chr1:93297210-93297906	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr1:93300119-93300236	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr1:93283975-93284223	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr1:93288462-93288799	K562	blood:	n/a	n/a
33	CBX3	chr1:93297343-93297963	K562	blood:	n/a	n/a
34	CBX3	chr1:93297213-93298098	K562	blood:	n/a	n/a
35	CCNT2	chr1:93297370-93298216	K562	blood:	n/a	chr1:93297860-93297869
36	CEBPB	chr1:93297610-93298002	K562	blood:	n/a	n/a
37	CEBPB	chr1:93288448-93288779	HepG2	liver:	n/a	chr1:93288677-93288688
38	CEBPB	chr1:93293236-93293415	HepG2	liver:	n/a	chr1:93293280-93293291
39	CEBPB	chr1:93297254-93298148	GM12878	blood:	n/a	n/a
40	CEBPB	chr1:93288591-93288797	K562	blood:	n/a	chr1:93288677-93288688
41	CEBPB	chr1:93288228-93288856	HepG2	liver:	n/a	chr1:93288677-93288688
42	CEBPB	chr1:93288458-93288850	IMR90	lung:	n/a	chr1:93288677-93288688
43	CEBPB	chr1:93288556-93288811	Hela-S3	cervix:	n/a	chr1:93288677-93288688
44	CEBPB	chr1:93288589-93288728	HepG2	liver:	n/a	chr1:93288677-93288688
45	CEBPB	chr1:93297459-93297975	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:93288458-93288893	HepG2	liver:	n/a	chr1:93288677-93288688
47	CEBPB	chr1:93288525-93288835	MCF-7	breast:	n/a	chr1:93288677-93288688
48	CEBPB	chr1:93274021-93274393	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr1:93284061-93284169	K562	blood:	n/a	n/a
50	CEBPB	chr1:93297346-93297791	GM12878	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93307974-93308024	U87	brain:	n/a
2	chr1:93296860-93296910	HMEC	breast:	n/a
3	chr1:93297504-93297554	U87	brain:	n/a
4	chr1:93307974-93308024	U87	brain:	n/a
5	chr1:93296860-93296910	HMEC	breast:	n/a
6	chr1:93297504-93297554	U87	brain:	n/a
7	chr1:93297732-93297782	GM19239	blood:	n/a
8	chr1:93302925-93302975	HCPEpiC	choroid plexus:	n/a
9	chr1:93301669-93301719	AG09309	skin:	n/a
10	chr1:93297552-93297602	HCF	heart:	n/a
11	chr1:93296109-93296159	U87	brain:	n/a
12	chr1:93307974-93308024	HEEpiC	esophagus:	n/a
13	chr1:93297504-93297554	SAEC	small airway:	n/a
14	chr1:93296860-93296910	Caco-2	colon:	n/a
15	chr1:93296988-93297038	GM12892	blood:	n/a
16	chr1:93297822-93297872	BE2_C	brain:	n/a
17	chr1:93297732-93297782	AG09309	skin:	n/a
18	chr1:93302028-93302078	PANC-1	pancreas:	n/a
19	chr1:93302028-93302078	AG09309	skin:	n/a
20	chr1:93296988-93297038	HepG2	liver:	n/a
21	chr1:93296988-93297038	SK-N-MC	brain:	n/a
22	chr1:93298059-93298109	AG04450	lung:	fetal
23	chr1:93297552-93297602	GM12891	blood:	n/a
24	chr1:93302028-93302078	A549	lung:	n/a
25	chr1:93293756-93293806	HCF	heart:	n/a
26	chr1:93297732-93297782	HRE	kidney:	n/a
27	chr1:93293756-93293806	AG09309	skin:	n/a
28	chr1:93297552-93297602	A549	lung:	n/a
29	chr1:93297552-93297602	HCM	heart:	n/a
30	chr1:93301669-93301719	CMK	blood:	n/a
31	chr1:93296860-93296910	SK-N-MC	brain:	n/a
32	chr1:93297071-93297121	LNCaP	prostate:	n/a
33	chr1:93301669-93301719	PrEC	prostate:	n/a
34	chr1:93298275-93298325	A549	lung:	n/a
35	chr1:93302028-93302078	Caco-2	colon:	n/a
36	chr1:93297504-93297554	CMK	blood:	n/a
37	chr1:93296988-93297038	GM12878	blood:	n/a
38	chr1:93293756-93293806	HCT-116	colon:	n/a
39	chr1:93298275-93298325	ECC-1	luminal epithelium:	n/a
40	chr1:93298093-93298143	GM12878	blood:	n/a
41	chr1:93298275-93298325	NHBE	bronchial:	n/a
42	chr1:93302167-93302217	GM12891	blood:	n/a
43	chr1:93297732-93297782	Hepatocyte	liver:	n/a
44	chr1:93296860-93296910	MCF-7	breast:	n/a
45	chr1:93298093-93298143	HAEpiC	amniotic membrane:	n/a
46	chr1:93298059-93298109	IMR90	lung:	fetal
47	chr1:93297552-93297602	CMK	blood:	n/a
48	chr1:93297071-93297121	PANC-1	pancreas:	n/a
49	chr1:93297071-93297121	T-47D	breast:	n/a
50	chr1:93302925-93302975	BE2_C	brain:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:93290582..93295028-chr1:93295962..93297870,4	MCF-7	breast:
2	chr1:93268938..93271046-chr1:93276676..93278269,2	K562	blood:
3	chr1:93214862..93218519-chr1:93302722..93305780,4	K562	blood:
4	chr1:93303345..93305385-chr1:93311213..93313203,2	MCF-7	breast:
5	chr1:93297303..93297935-chr3:57542001..57542627,2	Hela-S3	cervix:
6	chr1:93296314..93299115-chr1:93644282..93648010,4	K562	blood:
7	chr1:93214256..93215505-chr1:93283637..93284517,3	K562	blood:
8	chr1:93307980..93308638-chr17:79828861..79829826,2	Hela-S3	cervix:
9	chr1:93216027..93217718-chr1:93282953..93285543,2	MCF-7	breast:
10	chr1:93297145..93297697-chr21:34143917..34144494,2	Hela-S3	cervix:
11	chr1:93214410..93215230-chr1:93283967..93284512,2	MCF-7	breast:
12	chr1:92762794..92765730-chr1:93295925..93298205,3	K562	blood:
13	chr1:93297370..93297993-chr17:61920045..61920545,2	Hela-S3	cervix:
14	chr1:93287112..93289534-chr1:93296366..93298267,2	MCF-7	breast:
15	chr1:93282610..93284892-chr1:93288491..93290584,2	K562	blood:
16	chr1:93307013..93308611-chr1:93460458..93462751,2	K562	blood:
17	chr1:93248499..93251010-chr1:93306404..93307920,2	K562	blood:
18	chr1:93220670..93222907-chr1:93296640..93299176,3	MCF-7	breast:
19	chr1:93214232..93215219-chr1:93283675..93284503,5	MCF-7	breast:
20	chr1:93211573..93213718-chr1:93306717..93309071,2	K562	blood:
21	chr1:93277281..93280109-chr1:93281216..93283835,2	MCF-7	breast:
22	chr1:92764074..92765656-chr1:93296705..93299037,2	K562	blood:
23	chr1:93297215..93297885-chr10:70166541..70167415,2	Hela-S3	cervix:
24	chr1:93297134..93298053-chr1:213188509..213189760,3	NB4	blood:
25	chr1:93243993..93246087-chr1:93282223..93283796,2	K562	blood:
26	chr1:93282322..93284805-chr1:93286517..93288170,2	K562	blood:
27	chr1:93286088..93289627-chr1:93296091..93300055,5	K562	blood:
28	chr1:93297720..93299529-chr17:81006812..81009425,2	MCF-7	breast:
29	chr1:93249282..93251122-chr1:93279076..93281208,2	K562	blood:
30	chr1:93297145..93297889-chr5:177019241..177019876,2	HCT-116	colon:
31	chr1:93271712..93273787-chr1:93276299..93278239,2	K562	blood:
32	chr1:93293264..93295158-chr1:93296218..93298023,3	MCF-7	breast:
33	chr1:93282610..93284892-chr1:93288491..93290584,2	K562	blood:
34	chr1:93271712..93273787-chr1:93276299..93278239,2	K562	blood:
35	chr1:93290646..93292162-chr1:93296291..93299624,3	K562	blood:
36	chr1:93296297..93299381-chr1:93425183..93428047,4	K562	blood:
37	chr1:93256221..93258760-chr1:93295783..93299962,5	K562	blood:
38	chr1:93249434..93252765-chr1:93275686..93278447,3	K562	blood:
39	chr1:93297138..93298008-chr8:91657918..91658510,2	Hela-S3	cervix:
40	chr1:93296356..93298770-chr1:93426282..93429088,3	MCF-7	breast:
41	chr1:93249660..93252667-chr1:93296431..93299077,5	K562	blood:
42	chr1:93251020..93253744-chr1:93303793..93305482,2	K562	blood:
43	chr1:93302921..93305469-chr1:93643662..93645581,2	K562	blood:
44	chr1:93279082..93281535-chr1:93296111..93298029,2	K562	blood:
45	chr1:93296271..93298475-chr1:93543770..93546056,2	MCF-7	breast:
46	chr1:93249360..93255989-chr1:93295958..93302033,8	K562	blood:
47	chr1:93250918..93254010-chr1:93306747..93309482,3	K562	blood:
48	chr1:93296076..93299049-chr1:93541677..93546567,5	K562	blood:
49	chr1:93248724..93252766-chr1:93297083..93300077,5	MCF-7	breast:
50	chr1:93297206..93297853-chr15:41624641..41625546,2	HCT-116	colon:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RPL5	hsa-miR-328-3p	chr1:93303070-93303091
2	RPL5	hsa-miR-615-3p	chr1:93299107-93299128
3	RPL5	hsa-miR-16-5p	chr1:93306120-93306141
4	RPL5	hsa-miR-182-5p	chr1:93300377-93300400

Variant related genes	Relation type
ENSG00000251795	TF binding region
RPL5	TF binding region
SNORA66	TF binding region
SNORD21	TF binding region
ENSG00000207022	TF binding region
ENSG00000251795	CpG island
RPL5	CpG island
SNORA66	CpG island
SNORD21	CpG island
ENSG00000207022	CpG island
ENSG00000174840	chromatin interactions
ENSG00000180694	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000207022	chromatin interactions
ENSG00000141522	chromatin interactions
ENSG00000154511	chromatin interactions
ENSG00000108604	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000174606	chromatin interactions
ENSG00000067208	chromatin interactions
ENSG00000234202	chromatin interactions
ENSG00000204130	chromatin interactions
ENSG00000122483	chromatin interactions
ENSG00000143033	chromatin interactions
ENSG00000184840	chromatin interactions
ENSG00000175711	chromatin interactions
ENSG00000159086	chromatin interactions
ENSG00000223896	chromatin interactions
ENSG00000137804	chromatin interactions
ENSG00000104147	chromatin interactions
ENSG00000205930	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000117500	chromatin interactions

Extended variants
information (count: 1319 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1319 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72726460	chr1:93273459-93273460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184191202	chr1:93273473-93273474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535052320	chr1:93273566-93273567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546567974	chr1:93273658-93273659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74228381	chr1:93273731-93273732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145727267	chr1:93273771-93273772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148512166	chr1:93273791-93273792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535817896	chr1:93273792-93273793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376328299	chr1:93273800-93273801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575348962	chr1:93273862-93273863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539370414	chr1:93273877-93273878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557995422	chr1:93273878-93273879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573034979	chr1:93273889-93273890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540280703	chr1:93273897-93273898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561660985	chr1:93273934-93273935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs151064597	chr1:93274003-93274004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544278544	chr1:93274076-93274077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563753414	chr1:93274091-93274092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531100949	chr1:93274147-93274148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76258523	chr1:93274201-93274202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145133195	chr1:93274252-93274253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528778004	chr1:93274273-93274274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546629399	chr1:93274322-93274323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146839830	chr1:93274382-93274383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377522958	chr1:93274425-93274426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs36041647	chr1:93274437-93274438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370137450	chr1:93274446-93274447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12738964	chr1:93274450-93274451	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs550630634	chr1:93274544-93274545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140734614	chr1:93274607-93274608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539650377	chr1:93274678-93274679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181787270	chr1:93274702-93274703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34683096	chr1:93274738-93274739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562073100	chr1:93274754-93274755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566801991	chr1:93274833-93274834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12735511	chr1:93274857-93274858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534041832	chr1:93274875-93274876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs66649041	chr1:93274885-93274886	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573652265	chr1:93274906-93274907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145902138	chr1:93274995-93274996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556259541	chr1:93275004-93275005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114934928	chr1:93275116-93275117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183731073	chr1:93275122-93275123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564512799	chr1:93275142-93275143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528768470	chr1:93275248-93275249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540476986	chr1:93275298-93275299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138312456	chr1:93275399-93275400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557458988	chr1:93275418-93275419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189119324	chr1:93275427-93275428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569383649	chr1:93275438-93275439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93270800-93273800	Weak transcription	HSMM	muscle
2	chr1:93271000-93273600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:93271000-93273600	Weak transcription	NHLF	lung
4	chr1:93271000-93276000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr1:93271200-93273600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:93271200-93273600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:93271200-93273600	Weak transcription	HUVEC	blood vessel
8	chr1:93271800-93273600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:93271800-93273600	Weak transcription	Hela-S3	cervix
10	chr1:93271800-93273600	Weak transcription	NHDF-Ad	bronchial
11	chr1:93271800-93273800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr1:93271800-93276800	Weak transcription	K562	blood
13	chr1:93272200-93273600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:93272200-93273600	Weak transcription	Placenta	Placenta
15	chr1:93272200-93273600	Weak transcription	Osteobl	bone
16	chr1:93272400-93273800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:93272600-93276000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:93273000-93275000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:93273000-93275200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:93273400-93275000	Enhancers	HMEC	breast
21	chr1:93273400-93275000	Enhancers	NHEK	skin
22	chr1:93273600-93274000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:93273600-93274000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:93273600-93274000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:93273600-93274000	Enhancers	NHLF	lung
26	chr1:93273600-93274200	Enhancers	HUVEC	blood vessel
27	chr1:93273600-93274200	Enhancers	NHDF-Ad	bronchial
28	chr1:93273600-93274400	Enhancers	Osteobl	bone
29	chr1:93273600-93274600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:93273600-93275000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:93273600-93275000	Enhancers	Placenta	Placenta
32	chr1:93273600-93275000	Enhancers	Hela-S3	cervix
33	chr1:93273800-93274000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:93273800-93274000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr1:93273800-93274000	Enhancers	HSMM	muscle
36	chr1:93274000-93274400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:93274000-93275800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:93274200-93274600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:93274400-93274600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:93274600-93274800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr1:93274600-93277200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:93274800-93283600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:93275000-93275800	Weak transcription	Placenta	Placenta
44	chr1:93275000-93276000	Weak transcription	HMEC	breast
45	chr1:93275200-93278000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:93275800-93276200	Enhancers	Placenta	Placenta
47	chr1:93276000-93276200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:93276000-93276200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:93276000-93276200	Enhancers	Placenta Amnion	Placenta Amnion
50	chr1:93276000-93276200	Enhancers	HMEC	breast

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