Variant report

Variant	nsv902373
Chromosome Location	chr14:105012858-105078153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:836)
CpG islands
(count:3298)
Chromatin interactive
region (count:78)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105030612-105030699	HepG2	liver:	n/a	n/a
2	ATF1	chr14:105049108-105049359	K562	blood:	n/a	n/a
3	BACH1	chr14:105017437-105017581	H1-hESC	embryonic stem cell:	n/a	chr14:105017505-105017519
4	BACH1	chr14:105030294-105030472	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:105070922-105071333	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr14:105058585-105059125	GM12878	blood:	n/a	n/a
7	BCL3	chr14:105026558-105026874	GM12878	blood:	n/a	n/a
8	BCL3	chr14:105049920-105050553	GM12878	blood:	n/a	n/a
9	BCL3	chr14:105049928-105050457	GM12878	blood:	n/a	n/a
10	BCL3	chr14:105058332-105059108	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:105071194-105071232	HepG2	liver:	n/a	n/a
12	BHLHE40	chr14:105058691-105058948	K562	blood:	n/a	n/a
13	BHLHE40	chr14:105030483-105030583	K562	blood:	n/a	n/a
14	BHLHE40	chr14:105048982-105049405	K562	blood:	n/a	chr14:105049103-105049119 chr14:105049235-105049251
15	BHLHE40	chr14:105035074-105035221	GM12878	blood:	n/a	chr14:105035140-105035149 chr14:105035140-105035149 chr14:105035171-105035180 chr14:105035139-105035148
16	BHLHE40	chr14:105037493-105037708	HepG2	liver:	n/a	chr14:105037651-105037660
17	BHLHE40	chr14:105031559-105031911	K562	blood:	n/a	n/a
18	BHLHE40	chr14:105037468-105037828	K562	blood:	n/a	chr14:105037651-105037660
19	BHLHE40	chr14:105050136-105050429	K562	blood:	n/a	n/a
20	BHLHE40	chr14:105053435-105053692	K562	blood:	n/a	n/a
21	BHLHE40	chr14:105071080-105071347	K562	blood:	n/a	chr14:105071161-105071177
22	BHLHE40	chr14:105017210-105017578	K562	blood:	n/a	n/a
23	BHLHE40	chr14:105048407-105048698	K562	blood:	n/a	n/a
24	BHLHE40	chr14:105044257-105044558	K562	blood:	n/a	chr14:105044326-105044342
25	BHLHE40	chr14:105034976-105035325	K562	blood:	n/a	chr14:105035140-105035149 chr14:105035140-105035149 chr14:105035171-105035180 chr14:105035139-105035148
26	BHLHE40	chr14:105049819-105049820	K562	blood:	n/a	n/a
27	BHLHE40	chr14:105035066-105035269	HepG2	liver:	n/a	chr14:105035140-105035149 chr14:105035140-105035149 chr14:105035171-105035180 chr14:105035139-105035148
28	BRCA1	chr14:105039076-105039253	Hela-S3	cervix:	n/a	n/a
29	CCNT2	chr14:105044211-105044535	K562	blood:	n/a	n/a
30	CCNT2	chr14:105049056-105049405	K562	blood:	n/a	chr14:105049234-105049243
31	CCNT2	chr14:105071130-105071365	K562	blood:	n/a	n/a
32	CEBPB	chr14:105030314-105030615	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr14:105071172-105071282	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr14:105036587-105036787	K562	blood:	n/a	chr14:105036734-105036745 chr14:105036734-105036747 chr14:105036736-105036745 chr14:105036735-105036746
35	CEBPB	chr14:105036593-105036889	HepG2	liver:	n/a	chr14:105036734-105036745 chr14:105036734-105036747 chr14:105036736-105036745 chr14:105036735-105036746
36	CHD2	chr14:105070967-105071403	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr14:105030474-105030541	GM12878	blood:	n/a	n/a
38	CHD2	chr14:105030416-105030676	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr14:105043947-105043980	K562	blood:	n/a	n/a
40	CREB1	chr14:105071022-105071273	A549	lung:	n/a	n/a
41	CREB1	chr14:105030391-105030750	A549	lung:	n/a	n/a
42	CTCF	chr14:105030460-105030610	HCT-116	colon:	n/a	chr14:105030533-105030543 chr14:105030525-105030546 chr14:105030536-105030545 chr14:105030531-105030547 chr14:105030530-105030548
43	CTCF	chr14:105030380-105030530	HFF	foreskin:	n/a	n/a
44	CTCF	chr14:105043080-105043230	Caco-2	colon:	n/a	n/a
45	CTCF	chr14:105030460-105030610	HepG2	liver:	n/a	chr14:105030533-105030543 chr14:105030525-105030546 chr14:105030536-105030545 chr14:105030531-105030547 chr14:105030530-105030548
46	CTCF	chr14:105054806-105055071	LNCaP	prostate:	n/a	n/a
47	CTCF	chr14:105030460-105030610	NHDF-neo	bronchial:	n/a	chr14:105030533-105030543 chr14:105030525-105030546 chr14:105030536-105030545 chr14:105030531-105030547 chr14:105030530-105030548
48	CTCF	chr14:105043060-105043210	Caco-2	colon:	n/a	n/a
49	CTCF	chr14:105059700-105059850	AG04449	skin:	n/a	n/a
50	CTCF	chr14:105030390-105030705	NHEK	skin:	n/a	chr14:105030533-105030543 chr14:105030525-105030546 chr14:105030536-105030545 chr14:105030531-105030547 chr14:105030530-105030548

(count:3298 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105041708-105041758	AG10803	skin:	n/a
2	chr14:105037265-105037315	HMEC	breast:	n/a
3	chr14:105071313-105071363	ECC-1	luminal epithelium:	n/a
4	chr14:105071695-105071745	HMEC	breast:	n/a
5	chr14:105041708-105041758	AG10803	skin:	n/a
6	chr14:105037265-105037315	HMEC	breast:	n/a
7	chr14:105071313-105071363	ECC-1	luminal epithelium:	n/a
8	chr14:105071695-105071745	HMEC	breast:	n/a
9	chr14:105045187-105045237	NH-A	brain:	n/a
10	chr14:105045030-105045080	GM12878	blood:	n/a
11	chr14:105071695-105071745	H1-hESC	embryonic stem cell:	embryo
12	chr14:105051261-105051311	PrEC	prostate:	n/a
13	chr14:105041159-105041209	ECC-1	luminal epithelium:	n/a
14	chr14:105045187-105045237	GM19239	blood:	n/a
15	chr14:105075280-105075330	HEK293	kidney:	embryo
16	chr14:105053550-105053600	GM12892	blood:	n/a
17	chr14:105046247-105046297	HCT-116	colon:	n/a
18	chr14:105041541-105041591	IMR90	lung:	fetal
19	chr14:105045938-105045988	ovcar-3	ovarian:	n/a
20	chr14:105054436-105054486	AG09309	skin:	n/a
21	chr14:105066731-105066781	AG09319	gingival:	n/a
22	chr14:105071714-105071764	GM12891	blood:	n/a
23	chr14:105071714-105071764	NT2-D1	testis:	n/a
24	chr14:105066731-105066781	GM12892	blood:	n/a
25	chr14:105045347-105045397	GM19239	blood:	n/a
26	chr14:105058234-105058284	NHBE	bronchial:	n/a
27	chr14:105034096-105034146	HRCEpiC	kidney:	n/a
28	chr14:105041159-105041209	BE2_C	brain:	n/a
29	chr14:105054940-105054990	HPAEpiC	pulmonary alveolar:	n/a
30	chr14:105036374-105036424	NHDF-neo	bronchial:	n/a
31	chr14:105031193-105031243	HUVEC	blood vessel:	n/a
32	chr14:105041541-105041591	LNCaP	prostate:	n/a
33	chr14:105053550-105053600	ECC-1	luminal epithelium:	n/a
34	chr14:105052804-105052854	HEEpiC	esophagus:	n/a
35	chr14:105036374-105036424	SK-N-SH_RA	brain:	n/a
36	chr14:105018912-105018962	HMEC	breast:	n/a
37	chr14:105045347-105045397	T-47D	breast:	n/a
38	chr14:105044984-105045034	HCPEpiC	choroid plexus:	n/a
39	chr14:105031193-105031243	AG04449	skin:	fetal
40	chr14:105045187-105045237	AG04449	skin:	fetal
41	chr14:105041382-105041432	HPAEpiC	pulmonary alveolar:	n/a
42	chr14:105054940-105054990	PrEC	prostate:	n/a
43	chr14:105041452-105041502	SK-N-SH	brain:	n/a
44	chr14:105033467-105033517	GM12878	blood:	n/a
45	chr14:105048531-105048581	HMEC	breast:	n/a
46	chr14:105041159-105041209	HCF	heart:	n/a
47	chr14:105041452-105041502	NH-A	brain:	n/a
48	chr14:105036374-105036424	Caco-2	colon:	n/a
49	chr14:105054436-105054486	ovcar-3	ovarian:	n/a
50	chr14:105031243-105031293	HNPCEpiC	eye:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:105032385..105034173-chr14:105061495..105063938,2	K562	blood:
2	chr14:104578163..104580512-chr14:105027254..105029393,2	MCF-7	breast:
3	chr14:105022528..105025531-chr14:105027060..105029977,3	K562	blood:
4	chr14:105035401..105038783-chr14:105042040..105045385,3	MCF-7	breast:
5	chr14:105062712..105065139-chr14:105069999..105072445,2	K562	blood:
6	chr14:104603560..104604807-chr14:105030044..105030981,6	MCF-7	breast:
7	chr14:104694080..104694805-chr14:105030047..105031033,2	MCF-7	breast:
8	chr14:105029275..105030973-chr14:105053381..105055372,2	MCF-7	breast:
9	chr14:105053139..105055951-chr14:105056833..105058762,2	MCF-7	breast:
10	chr14:105017921..105022172-chr14:105022189..105024897,5	MCF-7	breast:
11	chr14:105017735..105019335-chr6:28831183..28833671,2	MCF-7	breast:
12	chr14:105074893..105076947-chr14:105079863..105082631,2	MCF-7	breast:
13	chr14:104652967..104655075-chr14:105050050..105051684,2	MCF-7	breast:
14	chr14:105016071..105018557-chr14:105018817..105021096,3	K562	blood:
15	chr14:105042988..105044600-chr14:105047915..105049629,2	K562	blood:
16	chr14:105027918..105029787-chr14:105034276..105037133,2	MCF-7	breast:
17	chr14:105030217..105030977-chr14:105106374..105106938,2	K562	blood:
18	chr14:105051680..105054326-chr14:105056453..105058154,2	K562	blood:
19	chr14:105013872..105015383-chr14:105019169..105021029,2	K562	blood:
20	chr14:105034085..105038904-chr14:105041483..105045004,4	MCF-7	breast:
21	chr14:105071154..105074580-chr14:105074693..105076354,3	MCF-7	breast:
22	chr14:105046780..105049204-chr14:105060096..105062523,2	K562	blood:
23	chr14:105035401..105038783-chr14:105042040..105045385,3	MCF-7	breast:
24	chr14:105042911..105043577-chr14:105105904..105106844,3	MCF-7	breast:
25	chr14:104824690..104827500-chr14:105019187..105021176,2	MCF-7	breast:
26	chr14:104597425..104598274-chr14:105030009..105030913,3	MCF-7	breast:
27	chr14:104567251..104568942-chr14:105029276..105031338,2	MCF-7	breast:
28	chr14:105048877..105053029-chr14:105053228..105056172,3	MCF-7	breast:
29	chr14:104907597..104909438-chr14:105077013..105079589,2	K562	blood:
30	chr14:105016071..105018557-chr14:105018817..105021096,3	K562	blood:
31	chr14:105017888..105020132-chr14:105106949..105108571,2	MCF-7	breast:
32	chr14:105053139..105055951-chr14:105056833..105058762,2	MCF-7	breast:
33	chr14:105017921..105022172-chr14:105022189..105024897,5	MCF-7	breast:
34	chr14:105018505..105021042-chr14:105030444..105032502,2	MCF-7	breast:
35	chr14:105022528..105025531-chr14:105027060..105029977,3	K562	blood:
36	chr14:105040248..105042488-chr14:105045613..105048228,2	K562	blood:
37	chr14:104544095..104545346-chr14:105030053..105031029,7	K562	blood:
38	chr14:105032385..105034173-chr14:105061495..105063938,2	K562	blood:
39	chr14:105051460..105054318-chr14:105065676..105068171,2	MCF-7	breast:
40	chr14:105056244..105058754-chr14:105069412..105071602,2	MCF-7	breast:
41	chr14:105059280..105061677-chr14:105063252..105065833,2	K562	blood:
42	chr14:105053625..105056399-chr14:105056665..105059451,2	MCF-7	breast:
43	chr14:104599830..104602632-chr14:105024556..105026842,2	MCF-7	breast:
44	chr14:104603333..104605492-chr14:105030428..105032769,2	MCF-7	breast:
45	chr14:105056847..105059828-chr14:105062201..105064275,3	MCF-7	breast:
46	chr14:104603508..104604499-chr14:105029618..105031234,27	MCF-7	breast:
47	chr14:105025262..105028783-chr14:105030319..105032347,4	MCF-7	breast:
48	chr14:105027918..105029787-chr14:105034276..105037133,2	MCF-7	breast:
49	chr14:105051680..105054326-chr14:105056453..105058154,2	K562	blood:
50	chr14:105053087..105055483-chr14:105069492..105072343,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM179-1	chr14:105055962-105056184	ENSG00000259037.1
2	lnc-C14orf180-2	chr14:105069237-105069901	ucscGeneNc_uc001yrr_2
3	lnc-C14orf180-1	chr14:105058611-105058858	NONHSAT040262
4	lnc-TMEM179-1	chr14:105055358-105055677	ENSG00000259037.1
5	lnc-C14orf180-1	chr14:105058927-105058979	NONHSAT040262
6	lnc-C14orf180-1	chr14:105058773-105058979	NONHSAT040263
7	lnc-C14orf180-1	chr14:105058659-105058677	NONHSAT040263
8	lnc-C14orf180-2	chr14:105071099-105072888	NONHSAT040264
9	lnc-C14orf180-2	chr14:105070351-105071697	ucscGeneNc_uc001yrr_2

No data

Variant related genes	Relation type
C14orf180	TF binding region
TMEM179	TF binding region
ENSG00000259037	TF binding region
C14orf180	CpG island
TMEM179	CpG island
ENSG00000259037	CpG island
ENSG00000258748	chromatin interactions
ENSG00000066735	chromatin interactions
ENSG00000225595	chromatin interactions
ENSG00000184601	chromatin interactions
ENSG00000259037	chromatin interactions
ENSG00000258986	chromatin interactions

Extended variants
information (count: 3066 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:3066 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12435241	chr14:105012858-105012859	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78354537	chr14:105012865-105012866	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs575873197	chr14:105012877-105012878	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs113499138	chr14:105012957-105012958	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs192551360	chr14:105012981-105012982	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs561467447	chr14:105012990-105012991	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs112377800	chr14:105013000-105013001	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs575131342	chr14:105013001-105013002	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs555163514	chr14:105013004-105013005	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs113121907	chr14:105013006-105013007	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs112577507	chr14:105013007-105013008	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs36048730	chr14:105013031-105013032	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs559709851	chr14:105013032-105013033	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs183171377	chr14:105013039-105013040	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs187503581	chr14:105013042-105013043	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs35952476	chr14:105013056-105013057	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs74086912	chr14:105013104-105013105	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192603099	chr14:105013105-105013106	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs371789194	chr14:105013113-105013114	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs548320588	chr14:105013114-105013115	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs567911208	chr14:105013142-105013143	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs533777494	chr14:105013149-105013150	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs531424178	chr14:105013157-105013158	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs547077584	chr14:105013168-105013169	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs34785484	chr14:105013169-105013170	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs34677118	chr14:105013228-105013229	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs184851240	chr14:105013249-105013250	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs575845576	chr14:105013296-105013297	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs75645172	chr14:105013339-105013340	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs34220962	chr14:105013347-105013348	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs575068410	chr14:105013358-105013359	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs34967457	chr14:105013361-105013362	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs554279158	chr14:105013364-105013365	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs35374053	chr14:105013366-105013367	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs115204848	chr14:105013381-105013382	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs115903755	chr14:105013388-105013389	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs531779703	chr14:105013415-105013416	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs5027824	chr14:105013419-105013420	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs561682019	chr14:105013424-105013425	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs5811142	chr14:105013427-105013428	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs115083353	chr14:105013459-105013460	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs34925347	chr14:105013488-105013489	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs5027826	chr14:105013489-105013490	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs147457933	chr14:105013546-105013547	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs549893574	chr14:105013569-105013570	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs116983148	chr14:105013580-105013581	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs568456835	chr14:105013615-105013616	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs535465926	chr14:105013619-105013620	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs555277477	chr14:105013624-105013625	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs76385854	chr14:105013646-105013647	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20932292	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21980252	CNVD

Chromatin state (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105008000-105016600	Enhancers	Fetal Brain Male	brain
2	chr14:105009800-105014600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:105011600-105013000	Bivalent Enhancer	Fetal Muscle Leg	muscle
4	chr14:105011600-105013800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr14:105011800-105013000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
6	chr14:105011800-105013400	Bivalent Enhancer	Fetal Stomach	stomach
7	chr14:105012200-105013000	Flanking Active TSS	Brain Germinal Matrix	brain
8	chr14:105012400-105013000	Enhancers	Brain Angular Gyrus	brain
9	chr14:105012400-105013000	Enhancers	Brain Anterior Caudate	brain
10	chr14:105012400-105013000	Bivalent Enhancer	Brain Hippocampus Middle	brain
11	chr14:105012600-105013600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr14:105012600-105014800	Weak transcription	Spleen	Spleen
13	chr14:105012600-105015400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr14:105012600-105016000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:105012800-105013400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:105012800-105014400	Enhancers	Fetal Brain Female	brain
17	chr14:105013000-105016400	Enhancers	Brain Germinal Matrix	brain
18	chr14:105014000-105014200	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr14:105014400-105015400	Weak transcription	Fetal Brain Female	brain
20	chr14:105014600-105014800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr14:105014800-105015000	Enhancers	Spleen	Spleen
22	chr14:105014800-105015200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr14:105015000-105015600	Weak transcription	Spleen	Spleen
24	chr14:105015200-105015600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:105015200-105016000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr14:105015400-105015800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
27	chr14:105015400-105015800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr14:105015400-105015800	Enhancers	Fetal Brain Female	brain
29	chr14:105015400-105016000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:105015400-105016000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr14:105015400-105016200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr14:105015400-105016200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr14:105015600-105015800	Enhancers	Spleen	Spleen
34	chr14:105015600-105016400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr14:105015800-105016200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr14:105015800-105020600	Weak transcription	Fetal Brain Female	brain
37	chr14:105016000-105018200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:105016400-105019600	Weak transcription	Brain Germinal Matrix	brain
39	chr14:105016600-105017000	Weak transcription	Fetal Brain Male	brain
40	chr14:105017000-105018000	Enhancers	Fetal Brain Male	brain
41	chr14:105018000-105019200	Weak transcription	Fetal Brain Male	brain
42	chr14:105018200-105019600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr14:105018800-105019000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:105019200-105026600	Enhancers	Fetal Brain Male	brain
45	chr14:105019400-105021000	Bivalent Enhancer	Fetal Muscle Leg	muscle
46	chr14:105019600-105020400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:105019600-105023000	Enhancers	Brain Germinal Matrix	brain
48	chr14:105019600-105023400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr14:105019800-105020000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr14:105019800-105022200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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