Variant report

Variant	nsv528349
Chromosome Location	chr3:138025396-138132393
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1968)
CpG islands
(count:2747)
Chromatin interactive
region (count:65)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1968 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138047265-138047489	K562	blood:	n/a	n/a
2	ARID3A	chr3:138051371-138051684	K562	blood:	n/a	n/a
3	ARID3A	chr3:138119682-138119990	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:138067151-138067346	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:138117981-138118405	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:138066913-138066915	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:138129663-138129710	K562	blood:	n/a	n/a
8	ARID3A	chr3:138048098-138048286	HepG2	liver:	n/a	n/a
9	ATF2	chr3:138089812-138090372	GM12878	blood:	n/a	n/a
10	ATF2	chr3:138089857-138090355	GM12878	blood:	n/a	n/a
11	ATF3	chr3:138109014-138109666	HCT-116	colon:	n/a	n/a
12	ATF3	chr3:138109096-138109544	A549	lung:	n/a	n/a
13	BACH1	chr3:138048065-138048758	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:138127504-138128011	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:138066908-138067906	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:138129506-138129569	K562	blood:	n/a	n/a
17	BACH1	chr3:138047485-138047488	K562	blood:	n/a	n/a
18	BATF	chr3:138107966-138108138	GM12878	blood:	n/a	n/a
19	BATF	chr3:138089911-138090297	GM12878	blood:	n/a	n/a
20	BATF	chr3:138089891-138090335	GM12878	blood:	n/a	n/a
21	BCLAF1	chr3:138089823-138090358	GM12878	blood:	n/a	chr3:138090065-138090074
22	BHLHE40	chr3:138066387-138066832	HepG2	liver:	n/a	n/a
23	BHLHE40	chr3:138118065-138118395	HepG2	liver:	n/a	n/a
24	BHLHE40	chr3:138131603-138131866	K562	blood:	n/a	n/a
25	BHLHE40	chr3:138041273-138041449	HepG2	liver:	n/a	n/a
26	BHLHE40	chr3:138067101-138067658	HepG2	liver:	n/a	chr3:138067348-138067364
27	BHLHE40	chr3:138078852-138079117	HepG2	liver:	n/a	chr3:138078992-138079001
28	BHLHE40	chr3:138078794-138079153	K562	blood:	n/a	chr3:138078992-138079001
29	BHLHE40	chr3:138066719-138066755	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:138129486-138129880	K562	blood:	n/a	n/a
31	BHLHE40	chr3:138102722-138102828	K562	blood:	n/a	n/a
32	BHLHE40	chr3:138048622-138048752	K562	blood:	n/a	n/a
33	BHLHE40	chr3:138078788-138079174	HepG2	liver:	n/a	chr3:138078992-138079001
34	BHLHE40	chr3:138117959-138119029	HepG2	liver:	n/a	n/a
35	BHLHE40	chr3:138089862-138090277	GM12878	blood:	n/a	n/a
36	BHLHE40	chr3:138041252-138041484	K562	blood:	n/a	n/a
37	BHLHE40	chr3:138118625-138118951	HepG2	liver:	n/a	n/a
38	BRCA1	chr3:138109188-138109450	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr3:138048783-138048785	HepG2	liver:	n/a	n/a
40	CBX3	chr3:138104995-138105351	HCT-116	colon:	n/a	n/a
41	CBX3	chr3:138129493-138129788	K562	blood:	n/a	n/a
42	CBX3	chr3:138108940-138109663	HCT-116	colon:	n/a	n/a
43	CCNT2	chr3:138067110-138067768	K562	blood:	n/a	chr3:138067204-138067213 chr3:138067288-138067297 chr3:138067632-138067641
44	CCNT2	chr3:138048543-138048894	K562	blood:	n/a	n/a
45	CEBPB	chr3:138070005-138070272	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:138026837-138027113	HepG2	liver:	n/a	chr3:138026977-138026988
47	CEBPB	chr3:138070077-138070277	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr3:138100817-138101176	H1-hESC	embryonic stem cell:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
49	CEBPB	chr3:138090011-138090255	GM12878	blood:	n/a	n/a
50	CEBPB	chr3:138100783-138101235	A549	lung:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998

(count:2747 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138067623-138067673	GM06990	blood:	n/a
2	chr3:138092089-138092139	ovcar-3	ovarian:	n/a
3	chr3:138067623-138067673	GM06990	blood:	n/a
4	chr3:138092089-138092139	ovcar-3	ovarian:	n/a
5	chr3:138067404-138067454	SAEC	small airway:	n/a
6	chr3:138048101-138048151	MCF10A-Er-Src	breast:	n/a
7	chr3:138043797-138043847	LNCaP	prostate:	n/a
8	chr3:138047362-138047412	Hela-S3	cervix:	n/a
9	chr3:138066216-138066266	PANC-1	pancreas:	n/a
10	chr3:138043797-138043847	SK-N-SH_RA	brain:	n/a
11	chr3:138067350-138067400	HAEpiC	amniotic membrane:	n/a
12	chr3:138066434-138066484	HRPEpiC	eye:	n/a
13	chr3:138048926-138048976	BE2_C	brain:	n/a
14	chr3:138067853-138067903	AG04449	skin:	fetal
15	chr3:138064802-138064852	LNCaP	prostate:	n/a
16	chr3:138062860-138062910	HAEpiC	amniotic membrane:	n/a
17	chr3:138045705-138045755	H1-hESC	embryonic stem cell:	embryo
18	chr3:138048728-138048778	GM12891	blood:	n/a
19	chr3:138121287-138121337	U87	brain:	n/a
20	chr3:138047362-138047412	HPAEpiC	pulmonary alveolar:	n/a
21	chr3:138069423-138069473	NHBE	bronchial:	n/a
22	chr3:138067853-138067903	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:138101310-138101360	CMK	blood:	n/a
24	chr3:138069423-138069473	HCPEpiC	choroid plexus:	n/a
25	chr3:138069423-138069473	PrEC	prostate:	n/a
26	chr3:138071101-138071151	ovcar-3	ovarian:	n/a
27	chr3:138048926-138048976	Jurkat	blood:	n/a
28	chr3:138048670-138048720	HMEC	breast:	n/a
29	chr3:138067350-138067400	HUVEC	blood vessel:	n/a
30	chr3:138048728-138048778	HRE	kidney:	n/a
31	chr3:138067409-138067459	AG10803	skin:	n/a
32	chr3:138056475-138056525	BJ	skin:	n/a
33	chr3:138050155-138050205	HCF	heart:	n/a
34	chr3:138048335-138048385	HCT-116	colon:	n/a
35	chr3:138056475-138056525	SK-N-SH	brain:	n/a
36	chr3:138048728-138048778	PFSK-1	brain:	n/a
37	chr3:138048746-138048796	ovcar-3	ovarian:	n/a
38	chr3:138048728-138048778	K562	blood:	n/a
39	chr3:138128339-138128389	HEK293	kidney:	embryo
40	chr3:138085169-138085219	PFSK-1	brain:	n/a
41	chr3:138048838-138048888	GM19239	blood:	n/a
42	chr3:138078989-138079039	T-47D	breast:	n/a
43	chr3:138109298-138109348	HPAEpiC	pulmonary alveolar:	n/a
44	chr3:138048937-138048987	HIPEpiC	eye:	n/a
45	chr3:138066216-138066266	AG04449	skin:	fetal
46	chr3:138128339-138128389	GM12891	blood:	n/a
47	chr3:138067053-138067103	IMR90	lung:	fetal
48	chr3:138043797-138043847	A549	lung:	n/a
49	chr3:138045705-138045755	ovcar-3	ovarian:	n/a
50	chr3:138101310-138101360	SKMC	muscle:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:138043371..138046599-chr3:138047282..138051436,3	K562	blood:
2	chr3:138094416..138096515-chr3:138105748..138108016,2	MCF-7	breast:
3	chr3:138081144..138083981-chr3:138086003..138087797,3	MCF-7	breast:
4	chr3:138050301..138052204-chr3:138116487..138117341,9	MCF-7	breast:
5	chr3:138049031..138051913-chr3:138117150..138118923,2	MCF-7	breast:
6	chr3:137892553..137894321-chr3:138025304..138027665,2	K562	blood:
7	chr3:138108024..138110952-chr3:138113271..138115084,3	MCF-7	breast:
8	chr3:138069326..138072318-chr3:138105183..138106708,2	K562	blood:
9	chr3:138112036..138114862-chr3:138120590..138122113,2	K562	blood:
10	chr3:138051022..138051610-chr3:138144950..138145530,2	MCF-7	breast:
11	chr3:138042389..138044114-chr3:138065779..138068075,2	K562	blood:
12	chr3:138042389..138044114-chr3:138065779..138068075,2	K562	blood:
13	chr3:138061492..138063672-chr3:138066215..138068384,2	K562	blood:
14	chr3:138065940..138068792-chr3:138150528..138153476,2	K562	blood:
15	chr3:138043371..138046599-chr3:138047282..138051436,3	K562	blood:
16	chr3:138108137..138110673-chr3:138113889..138116211,2	K562	blood:
17	chr3:138066416..138068564-chr3:138071079..138073147,2	K562	blood:
18	chr3:138124875..138126534-chr3:138133315..138135134,2	MCF-7	breast:
19	chr3:138047736..138050493-chr3:138067682..138070270,2	MCF-7	breast:
20	chr3:138093996..138096598-chr4:123678799..123680914,2	MCF-7	breast:
21	chr1:109618765..109621666-chr3:138122913..138124560,2	MCF-7	breast:
22	chr3:138079655..138082250-chr3:138142327..138144870,2	K562	blood:
23	chr3:138130760..138133096-chr3:138134779..138137650,2	MCF-7	breast:
24	chr3:138047684..138048542-chr3:138066905..138067491,2	MCF-7	breast:
25	chr3:138071826..138074930-chr3:138082332..138084280,3	K562	blood:
26	chr3:138108137..138110673-chr3:138113889..138116211,2	K562	blood:
27	chr3:138069326..138072318-chr3:138105183..138106708,2	K562	blood:
28	chr3:138044559..138046647-chr3:138048473..138050103,2	MCF-7	breast:
29	chr3:138099681..138102999-chr3:138104936..138107535,3	MCF-7	breast:
30	chr3:138049031..138051913-chr3:138117150..138118923,2	MCF-7	breast:
31	chr3:138094416..138096515-chr3:138105748..138108016,2	MCF-7	breast:
32	chr3:138061037..138063195-chr3:138073891..138076466,2	MCF-7	breast:
33	chr3:138051070..138051808-chr3:138136099..138136657,2	MCF-7	breast:
34	chr3:138066201..138068907-chr3:138068935..138070591,2	MCF-7	breast:
35	chr3:138065032..138067985-chr3:138070541..138072955,3	MCF-7	breast:
36	chr3:138113362..138114985-chr3:138120209..138122090,2	K562	blood:
37	chr3:138113362..138114985-chr3:138120209..138122090,2	K562	blood:
38	chr3:138073894..138077050-chr3:138080713..138083758,3	MCF-7	breast:
39	chr3:138071826..138074930-chr3:138082332..138084280,3	K562	blood:
40	chr3:138108024..138110952-chr3:138113271..138115084,3	MCF-7	breast:
41	chr3:138020888..138022867-chr3:138025630..138028543,3	K562	blood:
42	chr3:138050301..138052204-chr3:138116487..138117341,9	MCF-7	breast:
43	chr3:138099681..138102999-chr3:138104936..138107535,3	MCF-7	breast:
44	chr3:138048191..138050080-chr3:138056957..138059318,2	MCF-7	breast:
45	chr3:138112677..138114319-chr3:138192057..138194447,2	MCF-7	breast:
46	chr3:138065895..138067916-chr3:138070047..138072579,2	K562	blood:
47	chr3:138073894..138077050-chr3:138080713..138083758,3	MCF-7	breast:
48	chr3:138067088..138069571-chr3:138075852..138077829,2	K562	blood:
49	chr3:138016564..138021250-chr3:138021841..138026048,7	K562	blood:
50	chr3:138084125..138087091-chr3:138095064..138097156,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARMC8-2	chr3:138068526-138069264	NONHSAT092326
2	lnc-ARMC8-2	chr3:138067749-138067874	NONHSAT092325
3	lnc-ARMC8-2	chr3:138067988-138068221	NONHSAT092326
4	lnc-ARMC8-2	chr3:138068526-138068793	NONHSAT092325

No data

Variant related genes	Relation type
MRAS	TF binding region
NME9	TF binding region
MRAS	CpG island
NME9	CpG island
ENSG00000078487	chromatin interactions
ENSG00000114098	chromatin interactions
ENSG00000158220	chromatin interactions
ENSG00000158186	chromatin interactions
ENSG00000138231	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000181322	chromatin interactions

Extended variants
information (count: 3774 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3774 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9846480	chr3:138025396-138025397	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs79975487	chr3:138025415-138025416	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs533568486	chr3:138025426-138025427	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540500378	chr3:138025428-138025429	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560752134	chr3:138025462-138025463	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185193744	chr3:138025506-138025507	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549368863	chr3:138025512-138025513	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371259297	chr3:138025534-138025535	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562211688	chr3:138025572-138025573	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531005618	chr3:138025609-138025610	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550829566	chr3:138025616-138025617	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs7638688	chr3:138025621-138025622	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs190006001	chr3:138025635-138025636	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551840282	chr3:138025677-138025678	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35670304	chr3:138025681-138025682	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533101253	chr3:138025683-138025684	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs533965829	chr3:138025701-138025702	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553716121	chr3:138025758-138025759	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567197623	chr3:138025760-138025761	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536146248	chr3:138025787-138025788	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs74373866	chr3:138025805-138025806	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs79286336	chr3:138025806-138025807	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372236800	chr3:138025824-138025825	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs73867059	chr3:138025837-138025838	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs566750022	chr3:138025895-138025896	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558598725	chr3:138025898-138025899	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs79607681	chr3:138025927-138025928	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114676339	chr3:138025967-138025968	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182548368	chr3:138025972-138025973	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149255320	chr3:138025988-138025989	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76751578	chr3:138026079-138026080	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543351553	chr3:138026109-138026110	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147324799	chr3:138026127-138026128	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs186537652	chr3:138026147-138026148	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551509224	chr3:138026162-138026163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112612691	chr3:138026173-138026174	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs191819927	chr3:138026204-138026205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs527806251	chr3:138026272-138026273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547145170	chr3:138026324-138026325	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567136703	chr3:138026367-138026368	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139297343	chr3:138026383-138026384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556036557	chr3:138026422-138026423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569880435	chr3:138026437-138026438	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538614732	chr3:138026443-138026444	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs6795079	chr3:138026453-138026454	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs572077402	chr3:138026460-138026461	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs540772173	chr3:138026480-138026481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs557406166	chr3:138026524-138026525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375076718	chr3:138026532-138026533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374821950	chr3:138026533-138026534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:2705 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:137982000-138026600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr3:138005400-138027000	Weak transcription	Fetal Heart	heart
3	chr3:138017800-138025600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr3:138018200-138026200	Weak transcription	HSMMtube	muscle
5	chr3:138018200-138026400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr3:138018200-138026400	Weak transcription	Primary T cells from cord blood	blood
7	chr3:138018200-138042600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:138018600-138025600	Weak transcription	Thymus	Thymus
9	chr3:138019000-138025600	Weak transcription	Fetal Stomach	stomach
10	chr3:138019000-138025800	Weak transcription	Brain Germinal Matrix	brain
11	chr3:138019000-138026800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr3:138019200-138025400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr3:138019600-138025400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr3:138023200-138026800	Weak transcription	Brain Anterior Caudate	brain
15	chr3:138024000-138031400	Weak transcription	Pancreas	Pancrea
16	chr3:138024200-138026800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr3:138025000-138026200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr3:138025200-138026000	ZNF genes & repeats	Aorta	Aorta
19	chr3:138026200-138042600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr3:138026600-138027200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
21	chr3:138026800-138027000	ZNF genes & repeats	Brain Anterior Caudate	brain
22	chr3:138026800-138027000	Enhancers	K562	blood
23	chr3:138026800-138027200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr3:138027000-138027400	ZNF genes & repeats	Fetal Heart	heart
25	chr3:138028800-138046600	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr3:138033200-138034400	Enhancers	NH-A	brain
27	chr3:138033400-138034000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr3:138033400-138034200	Enhancers	HUVEC	blood vessel
29	chr3:138033400-138034200	Enhancers	Osteobl	bone
30	chr3:138033400-138034400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:138033400-138034400	Enhancers	NHEK	skin
32	chr3:138033600-138034200	Enhancers	HMEC	breast
33	chr3:138033600-138034400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr3:138033800-138034600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr3:138034000-138034600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr3:138034400-138042400	Weak transcription	NHEK	skin
37	chr3:138034600-138039200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:138035600-138046800	Weak transcription	Brain Anterior Caudate	brain
39	chr3:138035800-138037600	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr3:138036200-138036600	Enhancers	Psoas Muscle	Psoas
41	chr3:138036400-138036800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr3:138036600-138037000	Weak transcription	Psoas Muscle	Psoas
43	chr3:138037000-138037200	Enhancers	Psoas Muscle	Psoas
44	chr3:138037200-138042200	Weak transcription	Psoas Muscle	Psoas
45	chr3:138037600-138041600	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr3:138038400-138038600	Enhancers	Gastric	stomach
47	chr3:138038600-138048200	Weak transcription	Gastric	stomach
48	chr3:138038800-138039400	Enhancers	HepG2	liver
49	chr3:138039200-138039800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr3:138039800-138040000	Enhancers	Primary T cells from cord blood	blood

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