Variant report

Variant	nsv998179
Chromosome Location	chr4:56425126-56694339
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1932)
CpG islands
(count:2995)
Chromatin interactive
region (count:167)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1932 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56597276-56597725	K562	blood:	n/a	n/a
2	ARID3A	chr4:56519920-56520587	K562	blood:	n/a	n/a
3	ARID3A	chr4:56515038-56515098	K562	blood:	n/a	n/a
4	ARID3A	chr4:56599903-56600328	K562	blood:	n/a	n/a
5	ARID3A	chr4:56608965-56609070	K562	blood:	n/a	n/a
6	ARID3A	chr4:56536930-56537271	K562	blood:	n/a	n/a
7	ARID3A	chr4:56595714-56597053	K562	blood:	n/a	n/a
8	ARID3A	chr4:56602401-56602562	K562	blood:	n/a	n/a
9	ARID3A	chr4:56602821-56603153	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:56493426-56493494	K562	blood:	n/a	n/a
11	ARID3A	chr4:56474539-56474545	K562	blood:	n/a	n/a
12	ARID3A	chr4:56602788-56603227	K562	blood:	n/a	n/a
13	ARID3A	chr4:56503388-56504015	K562	blood:	n/a	n/a
14	ARID3A	chr4:56589584-56589800	K562	blood:	n/a	n/a
15	ARID3A	chr4:56518503-56518691	K562	blood:	n/a	n/a
16	ARID3A	chr4:56501495-56501827	K562	blood:	n/a	n/a
17	ARID3A	chr4:56535243-56535280	K562	blood:	n/a	n/a
18	ARID3A	chr4:56426252-56426628	K562	blood:	n/a	n/a
19	ATF1	chr4:56501416-56501837	K562	blood:	n/a	n/a
20	ATF1	chr4:56498147-56498454	K562	blood:	n/a	n/a
21	ATF1	chr4:56595957-56597096	K562	blood:	n/a	n/a
22	ATF1	chr4:56536954-56537234	K562	blood:	n/a	n/a
23	ATF2	chr4:56428063-56428473	GM12878	blood:	n/a	n/a
24	ATF2	chr4:56427972-56428514	GM12878	blood:	n/a	n/a
25	ATF2	chr4:56685758-56686253	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr4:56634460-56634806	K562	blood:	n/a	n/a
27	ATF3	chr4:56599950-56600410	K562	blood:	n/a	n/a
28	ATF3	chr4:56600082-56600281	K562	blood:	n/a	n/a
29	BACH1	chr4:56502806-56503160	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr4:56688683-56688702	K562	blood:	n/a	n/a
31	BACH1	chr4:56436319-56436321	K562	blood:	n/a	n/a
32	BACH1	chr4:56608951-56609115	K562	blood:	n/a	n/a
33	BACH1	chr4:56483945-56484132	K562	blood:	n/a	n/a
34	BACH1	chr4:56539608-56539938	K562	blood:	n/a	n/a
35	BACH1	chr4:56479913-56479931	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr4:56539736-56539823	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr4:56502324-56502563	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr4:56503675-56503978	K562	blood:	n/a	n/a
39	BACH1	chr4:56503593-56503801	H1-hESC	embryonic stem cell:	n/a	n/a
40	BATF	chr4:56428056-56428358	GM12878	blood:	n/a	n/a
41	BATF	chr4:56483976-56484328	GM12878	blood:	n/a	n/a
42	BATF	chr4:56483933-56484337	GM12878	blood:	n/a	n/a
43	BATF	chr4:56428063-56428387	GM12878	blood:	n/a	n/a
44	BCL11A	chr4:56428121-56428373	GM12878	blood:	n/a	n/a
45	BCL11A	chr4:56428067-56428467	GM12878	blood:	n/a	n/a
46	BCL3	chr4:56458572-56459349	K562	blood:	n/a	n/a
47	BCL3	chr4:56428095-56428445	GM12878	blood:	n/a	n/a
48	BCL3	chr4:56459850-56460592	K562	blood:	n/a	chr4:56460261-56460270
49	BCL3	chr4:56428071-56428362	GM12878	blood:	n/a	n/a
50	BCLAF1	chr4:56428031-56428380	GM12878	blood:	n/a	n/a

(count:2995 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56656788-56656838	HRE	kidney:	n/a
2	chr4:56458370-56458420	AG09309	skin:	n/a
3	chr4:56658357-56658407	BE2_C	brain:	n/a
4	chr4:56459255-56459305	HIPEpiC	eye:	n/a
5	chr4:56502788-56502838	K562	blood:	n/a
6	chr4:56504657-56504707	AG09319	gingival:	n/a
7	chr4:56656788-56656838	HRE	kidney:	n/a
8	chr4:56458370-56458420	AG09309	skin:	n/a
9	chr4:56658357-56658407	BE2_C	brain:	n/a
10	chr4:56459255-56459305	HIPEpiC	eye:	n/a
11	chr4:56502788-56502838	K562	blood:	n/a
12	chr4:56504657-56504707	AG09319	gingival:	n/a
13	chr4:56686117-56686167	BJ	skin:	n/a
14	chr4:56685845-56685895	AG04450	lung:	fetal
15	chr4:56663994-56664044	NHDF-neo	bronchial:	n/a
16	chr4:56659922-56659972	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:56501727-56501777	GM19239	blood:	n/a
18	chr4:56502392-56502442	BJ	skin:	n/a
19	chr4:56458513-56458563	PFSK-1	brain:	n/a
20	chr4:56660398-56660448	HUVEC	blood vessel:	n/a
21	chr4:56500362-56500412	SK-N-SH	brain:	n/a
22	chr4:56458370-56458420	HCT-116	colon:	n/a
23	chr4:56502392-56502442	PFSK-1	brain:	n/a
24	chr4:56686117-56686167	GM06990	blood:	n/a
25	chr4:56660460-56660510	U87	brain:	n/a
26	chr4:56458183-56458233	MCF10A-Er-Src	breast:	n/a
27	chr4:56502598-56502648	AG09319	gingival:	n/a
28	chr4:56502116-56502166	IMR90	lung:	fetal
29	chr4:56660460-56660510	HCF	heart:	n/a
30	chr4:56475905-56475955	BE2_C	brain:	n/a
31	chr4:56663994-56664044	HepG2	liver:	n/a
32	chr4:56458513-56458563	SK-N-MC	brain:	n/a
33	chr4:56458333-56458383	HMEC	breast:	n/a
34	chr4:56685845-56685895	SAEC	small airway:	n/a
35	chr4:56459255-56459305	HCT-116	colon:	n/a
36	chr4:56458513-56458563	SKMC	muscle:	n/a
37	chr4:56659770-56659820	LNCaP	prostate:	n/a
38	chr4:56458333-56458383	ovcar-3	ovarian:	n/a
39	chr4:56502849-56502899	NHDF-neo	bronchial:	n/a
40	chr4:56458449-56458499	SK-N-SH_RA	brain:	n/a
41	chr4:56660398-56660448	LNCaP	prostate:	n/a
42	chr4:56458333-56458383	MCF10A-Er-Src	breast:	n/a
43	chr4:56501978-56502028	PANC-1	pancreas:	n/a
44	chr4:56504657-56504707	HNPCEpiC	eye:	n/a
45	chr4:56502898-56502948	HepG2	liver:	n/a
46	chr4:56659924-56659974	HL-60	blood:	n/a
47	chr4:56458370-56458420	MCF-7	breast:	n/a
48	chr4:56660460-56660510	SKMC	muscle:	n/a
49	chr4:56660398-56660448	BJ	skin:	n/a
50	chr4:56659924-56659974	NHDF-neo	bronchial:	n/a

(count:167 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:56515936..56519934-chr4:56522100..56525314,4	K562	blood:
2	chr4:56685297..56688659-chr4:56689398..56693221,5	K562	blood:
3	chr4:56474369..56476951-chr4:56481028..56484786,4	K562	blood:
4	chr4:56407970..56411777-chr4:56498734..56501001,3	K562	blood:
5	chr4:56462852..56464632-chr4:56730445..56733358,2	K562	blood:
6	chr4:56468709..56470290-chr4:56471936..56473680,2	K562	blood:
7	chr4:56414679..56416401-chr4:56437993..56440947,2	K562	blood:
8	chr4:56596053..56598450-chr4:56609132..56610849,2	K562	blood:
9	chr4:56587276..56591232-chr4:56591490..56593918,4	K562	blood:
10	chr4:56517756..56519698-chr4:56525326..56526892,2	K562	blood:
11	chr4:56481534..56484408-chr4:56607415..56610057,2	K562	blood:
12	chr4:56498450..56502811-chr4:56593362..56599516,6	K562	blood:
13	chr4:56684715..56688659-chr4:56690017..56693221,5	K562	blood:
14	chr4:56472523..56475869-chr4:56480434..56484043,4	K562	blood:
15	chr4:56531998..56534382-chr4:56600029..56601817,2	K562	blood:
16	chr4:56581911..56585061-chr4:56585536..56588285,3	K562	blood:
17	chr4:56411609..56413805-chr4:56441922..56444264,3	K562	blood:
18	chr4:56522244..56525288-chr4:56525318..56527795,3	K562	blood:
19	chr4:56479641..56481239-chr4:56491828..56493480,2	K562	blood:
20	chr4:56481465..56483149-chr4:56595985..56597947,2	K562	blood:
21	chr4:56450779..56452312-chr4:56454254..56455945,2	MCF-7	breast:
22	chr4:56689856..56692803-chr4:56704303..56706924,2	K562	blood:
23	chr4:56471770..56474121-chr4:56475653..56477265,2	K562	blood:
24	chr4:56459983..56461740-chr4:56464229..56467052,3	K562	blood:
25	chr4:56517756..56519698-chr4:56525326..56526892,2	K562	blood:
26	chr4:56596053..56598450-chr4:56609132..56610849,2	K562	blood:
27	chr4:56459697..56462267-chr4:56481406..56483258,2	K562	blood:
28	chr4:56532999..56536054-chr4:56538312..56541698,3	K562	blood:
29	chr4:56588763..56591407-chr4:56594293..56596844,3	K562	blood:
30	chr4:56693482..56694037-chr4:56732799..56733387,2	K562	blood:
31	chr4:56262276..56264823-chr4:56597078..56599821,2	K562	blood:
32	chr4:56459697..56462267-chr4:56481406..56483258,2	K562	blood:
33	chr4:56609301..56611255-chr4:56614835..56616393,2	MCF-7	breast:
34	chr4:56631564..56634040-chr4:56635751..56638538,2	K562	blood:
35	chr4:56474369..56476951-chr4:56481028..56484786,4	K562	blood:
36	chr4:56529070..56532802-chr4:56534666..56538344,3	K562	blood:
37	chr4:56631566..56634040-chr4:56636504..56638538,3	K562	blood:
38	chr4:56479641..56482011-chr4:56491746..56493328,2	K562	blood:
39	chr4:56501809..56503830-chr4:56593462..56596328,2	K562	blood:
40	chr4:56517086..56520350-chr4:56522100..56524911,3	K562	blood:
41	chr4:56469594..56472542-chr4:56706462..56708819,2	K562	blood:
42	chr4:56459163..56461447-chr4:56461922..56464276,2	K562	blood:
43	chr4:56411908..56414251-chr4:56442457..56445363,2	K562	blood:
44	chr4:56411021..56413172-chr4:56427180..56429925,2	K562	blood:
45	chr4:56460832..56462856-chr4:56478236..56479860,2	MCF-7	breast:
46	chr4:56507649..56509909-chr4:56526051..56528840,3	K562	blood:
47	chr4:56303798..56306133-chr4:56600360..56603061,2	K562	blood:
48	chr4:56532999..56536054-chr4:56538312..56541698,3	K562	blood:
49	chr4:56523921..56526378-chr4:56528208..56530318,2	K562	blood:
50	chr4:56520164..56522203-chr4:56529132..56532078,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMU-1	chr4:56502711-56502865	NONHSAT096475
2	lnc-NMU-1	chr4:56471442-56471516	NONHSAT096475
3	lnc-NMU-1	chr4:56466689-56466742	NONHSAT096475
4	lnc-NMU-2	chr4:56501440-56501555	l_2648_chr4:56499345-56508927_adipose
5	lnc-NMU-1	chr4:56465309-56465348	NONHSAT096475
6	lnc-NMU-1	chr4:56475287-56475346	NONHSAT096475
7	lnc-NMU-1	chr4:56496569-56496629	NONHSAT096476
8	lnc-NMU-1	chr4:56475287-56475346	NONHSAT096476
9	lnc-NMU-1	chr4:56482505-56482552	NONHSAT096475
10	lnc-NMU-1	chr4:56496569-56496627	NONHSAT096475
11	lnc-NMU-1	chr4:56465319-56465348	NONHSAT096476
12	lnc-NMU-2	chr4:56508763-56508927	l_2648_chr4:56499345-56508927_adipose
13	lnc-NMU-1	chr4:56466689-56466742	NONHSAT096476
14	lnc-NMU-1	chr4:56473604-56473633	NONHSAT096475
15	lnc-NMU-1	chr4:56482505-56482552	NONHSAT096476
16	lnc-NMU-2	chr4:56499346-56499878	l_2648_chr4:56499345-56508927_adipose
17	lnc-NMU-1	chr4:56473604-56473633	NONHSAT096476
18	lnc-NMU-1	chr4:56461484-56461578	NONHSAT096475

No data

Variant related genes	Relation type
NMU	TF binding region
RNU6-276P	TF binding region
ENSG00000250821	TF binding region
PDCL2	TF binding region
NMU	CpG island
RNU6-276P	CpG island
ENSG00000250821	CpG island
PDCL2	CpG island
ENSG00000109255	chromatin interactions
ENSG00000174799	chromatin interactions
ENSG00000128039	chromatin interactions
ENSG00000134851	chromatin interactions
ENSG00000090989	chromatin interactions
ENSG00000272969	chromatin interactions
ENSG00000134852	chromatin interactions
ENSG00000250821	chromatin interactions

Extended variants
information (count: 7422 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7422 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542548631	chr4:56425152-56425153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148900403	chr4:56425282-56425283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572353961	chr4:56425333-56425334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558924792	chr4:56425358-56425359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541386708	chr4:56425365-56425366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564586269	chr4:56425402-56425403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533450024	chr4:56425403-56425404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373708801	chr4:56425504-56425505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370844336	chr4:56425505-56425506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34941164	chr4:56425506-56425507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71194593	chr4:56425507-56425508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73819640	chr4:56425534-56425535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563866215	chr4:56425597-56425598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554032403	chr4:56425626-56425627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529651944	chr4:56425637-56425638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537975771	chr4:56425647-56425648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549419152	chr4:56425675-56425676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572298958	chr4:56425702-56425703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1552522	chr4:56425724-56425725	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs551342125	chr4:56425731-56425732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs56208011	chr4:56425761-56425762	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs536748713	chr4:56425786-56425787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145517241	chr4:56425821-56425822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188344361	chr4:56425845-56425846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374731802	chr4:56425892-56425893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34750660	chr4:56425903-56425904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193203615	chr4:56425910-56425911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184673376	chr4:56425943-56425944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188818238	chr4:56425957-56425958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1552523	chr4:56425989-56425990	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191297848	chr4:56426034-56426035	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs4865013	chr4:56426124-56426125	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs137886107	chr4:56426171-56426172	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs140772009	chr4:56426204-56426205	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs183778486	chr4:56426205-56426206	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs73155698	chr4:56426220-56426221	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs146895633	chr4:56426228-56426229	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs559832405	chr4:56426293-56426294	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs528763046	chr4:56426322-56426323	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs368022409	chr4:56426330-56426331	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs370486957	chr4:56426356-56426357	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs76470843	chr4:56426357-56426358	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs372079846	chr4:56426358-56426359	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs559979528	chr4:56426359-56426360	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs398092381	chr4:56426366-56426367	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs564530716	chr4:56426368-56426369	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs189299821	chr4:56426377-56426378	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs144692662	chr4:56426392-56426393	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs182047928	chr4:56426410-56426411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187657150	chr4:56426457-56426458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD
Breast cancer	21785460	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1244 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56416800-56425600	Weak transcription	K562	blood
2	chr4:56418800-56431800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:56425600-56426000	Enhancers	K562	blood
4	chr4:56426000-56426400	Flanking Active TSS	K562	blood
5	chr4:56426400-56426800	Enhancers	K562	blood
6	chr4:56426800-56427000	ZNF genes & repeats	K562	blood
7	chr4:56427000-56427200	Enhancers	K562	blood
8	chr4:56427200-56430800	Weak transcription	K562	blood
9	chr4:56427600-56429000	Enhancers	Primary B cells from peripheral blood	blood
10	chr4:56427600-56429200	Enhancers	GM12878-XiMat	blood
11	chr4:56427800-56428200	Enhancers	Primary B cells from cord blood	blood
12	chr4:56427800-56429000	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr4:56429000-56430000	Weak transcription	Primary B cells from peripheral blood	blood
14	chr4:56429400-56430200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:56429600-56430200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:56429800-56430200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:56429800-56430400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:56429800-56430600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr4:56429800-56430800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr4:56430000-56430200	Enhancers	Primary B cells from peripheral blood	blood
21	chr4:56430000-56430600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:56430000-56430600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:56430400-56433000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr4:56430800-56431200	Enhancers	K562	blood
25	chr4:56431200-56434800	Weak transcription	K562	blood
26	chr4:56431800-56432200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:56432000-56442000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:56432200-56434600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:56434600-56435600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:56434800-56435200	Genic enhancers	K562	blood
31	chr4:56435200-56435800	Enhancers	GM12878-XiMat	blood
32	chr4:56435200-56440600	Weak transcription	K562	blood
33	chr4:56435600-56441400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:56437400-56438600	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr4:56437800-56438200	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr4:56439000-56440800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:56440600-56441200	Strong transcription	K562	blood
38	chr4:56440800-56441600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:56441200-56464400	Weak transcription	K562	blood
40	chr4:56441600-56443400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:56444000-56444200	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr4:56444200-56444800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr4:56444200-56445600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr4:56444800-56445200	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr4:56445200-56445400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr4:56445400-56445600	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr4:56449800-56450000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:56450000-56450800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:56454200-56454600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr4:56454400-56454800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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