Variant report

Variant	nsv879496
Chromosome Location	chr4:76493256-76620803
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1875)
CpG islands
(count:2199)
Chromatin interactive
region (count:122)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:1875 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:76498686-76499128	K562	blood:	n/a	n/a
2	ARID3A	chr4:76504917-76505191	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:76598270-76599204	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:76597168-76597286	K562	blood:	n/a	n/a
5	ARID3A	chr4:76561205-76561247	K562	blood:	n/a	n/a
6	ARID3A	chr4:76598564-76599049	K562	blood:	n/a	n/a
7	ATF1	chr4:76598515-76599544	K562	blood:	n/a	n/a
8	ATF2	chr4:76597638-76599141	GM12878	blood:	n/a	n/a
9	ATF2	chr4:76598611-76599072	GM12878	blood:	n/a	n/a
10	ATF2	chr4:76498541-76498935	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:76598714-76599219	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:76597634-76598059	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:76598256-76599323	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:76597374-76597526	K562	blood:	n/a	n/a
15	BACH1	chr4:76555535-76556403	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:76598580-76598918	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:76554379-76554459	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:76523480-76523909	K562	blood:	n/a	n/a
19	BACH1	chr4:76597734-76597919	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:76523703-76523984	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr4:76504820-76505113	GM12878	blood:	n/a	n/a
22	BCL3	chr4:76598019-76599112	A549	lung:	n/a	chr4:76598030-76598039
23	BCL3	chr4:76598068-76599018	A549	lung:	n/a	n/a
24	BCL3	chr4:76504872-76505183	GM12878	blood:	n/a	n/a
25	BCL3	chr4:76598090-76598962	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:76598155-76599036	GM12878	blood:	n/a	n/a
27	BCLAF1	chr4:76597484-76597988	GM12878	blood:	n/a	n/a
28	BCLAF1	chr4:76498583-76499078	GM12878	blood:	n/a	n/a
29	BCLAF1	chr4:76597013-76599220	GM12878	blood:	n/a	chr4:76598030-76598039
30	BHLHE40	chr4:76498625-76499066	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:76597588-76598137	K562	blood:	n/a	n/a
32	BHLHE40	chr4:76597709-76599309	HepG2	liver:	n/a	n/a
33	BHLHE40	chr4:76597630-76599115	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:76498745-76499186	K562	blood:	n/a	n/a
35	BHLHE40	chr4:76598350-76599448	K562	blood:	n/a	n/a
36	BHLHE40	chr4:76555744-76555914	GM12878	blood:	n/a	n/a
37	BRCA1	chr4:76531035-76531112	HepG2	liver:	n/a	n/a
38	BRCA1	chr4:76597862-76598027	GM12878	blood:	n/a	n/a
39	BRCA1	chr4:76598760-76599270	HepG2	liver:	n/a	n/a
40	BRCA1	chr4:76597753-76597953	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr4:76598383-76599083	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr4:76597181-76597686	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr4:76603736-76604075	K562	blood:	n/a	n/a
44	CBX3	chr4:76598370-76599291	K562	blood:	n/a	n/a
45	CBX3	chr4:76597637-76598364	K562	blood:	n/a	n/a
46	CBX3	chr4:76612270-76612718	K562	blood:	n/a	n/a
47	CCNT2	chr4:76597694-76599018	K562	blood:	n/a	chr4:76597896-76597905
48	CEBPB	chr4:76577347-76577625	MCF-7	breast:	n/a	chr4:76577503-76577516
49	CEBPB	chr4:76577316-76577627	MCF-7	breast:	n/a	chr4:76577503-76577516
50	CEBPB	chr4:76498835-76499173	K562	blood:	n/a	chr4:76499142-76499155

(count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:76598793-76598843	MCF10A-Er-Src	breast:	n/a
2	chr4:76559064-76559114	MCF10A-Er-Src	breast:	n/a
3	chr4:76555777-76555827	HNPCEpiC	eye:	n/a
4	chr4:76598793-76598843	MCF10A-Er-Src	breast:	n/a
5	chr4:76559064-76559114	MCF10A-Er-Src	breast:	n/a
6	chr4:76555777-76555827	HNPCEpiC	eye:	n/a
7	chr4:76598670-76598720	NH-A	brain:	n/a
8	chr4:76598524-76598574	IMR90	lung:	fetal
9	chr4:76598670-76598720	GM12891	blood:	n/a
10	chr4:76555832-76555882	HNPCEpiC	eye:	n/a
11	chr4:76598670-76598720	U87	brain:	n/a
12	chr4:76570750-76570800	SK-N-SH_RA	brain:	n/a
13	chr4:76555856-76555906	HAEpiC	amniotic membrane:	n/a
14	chr4:76598919-76598969	HIPEpiC	eye:	n/a
15	chr4:76598919-76598969	SK-N-MC	brain:	n/a
16	chr4:76556042-76556092	HCPEpiC	choroid plexus:	n/a
17	chr4:76594199-76594249	GM06990	blood:	n/a
18	chr4:76598524-76598574	Caco-2	colon:	n/a
19	chr4:76598474-76598524	GM12892	blood:	n/a
20	chr4:76598767-76598817	HCPEpiC	choroid plexus:	n/a
21	chr4:76554724-76554774	SKMC	muscle:	n/a
22	chr4:76598817-76598867	HL-60	blood:	n/a
23	chr4:76570750-76570800	IMR90	lung:	fetal
24	chr4:76555856-76555906	AG09319	gingival:	n/a
25	chr4:76556042-76556092	HCF	heart:	n/a
26	chr4:76598793-76598843	HCT-116	colon:	n/a
27	chr4:76598474-76598524	U87	brain:	n/a
28	chr4:76599597-76599647	NH-A	brain:	n/a
29	chr4:76503516-76503566	GM12892	blood:	n/a
30	chr4:76503516-76503566	BJ	skin:	n/a
31	chr4:76555980-76556030	HepG2	liver:	n/a
32	chr4:76555547-76555597	NT2-D1	testis:	n/a
33	chr4:76570750-76570800	HRE	kidney:	n/a
34	chr4:76598524-76598574	GM06990	blood:	n/a
35	chr4:76598670-76598720	HUVEC	blood vessel:	n/a
36	chr4:76570006-76570056	NHDF-neo	bronchial:	n/a
37	chr4:76556042-76556092	HUVEC	blood vessel:	n/a
38	chr4:76554724-76554774	BJ	skin:	n/a
39	chr4:76602474-76602524	Jurkat	blood:	n/a
40	chr4:76554724-76554774	Hela-S3	cervix:	n/a
41	chr4:76598323-76598373	HL-60	blood:	n/a
42	chr4:76598477-76598527	NHDF-neo	bronchial:	n/a
43	chr4:76598477-76598527	NHBE	bronchial:	n/a
44	chr4:76555980-76556030	PANC-1	pancreas:	n/a
45	chr4:76556042-76556092	SK-N-SH	brain:	n/a
46	chr4:76556389-76556439	HMEC	breast:	n/a
47	chr4:76570006-76570056	HRPEpiC	eye:	n/a
48	chr4:76554724-76554774	HRPEpiC	eye:	n/a
49	chr4:76555547-76555597	IMR90	lung:	fetal
50	chr4:76555948-76555998	HMEC	breast:	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:76597218..76599428-chr4:76609865..76611973,3	MCF-7	breast:
2	chr4:76590473..76593101-chr4:76597101..76599656,3	MCF-7	breast:
3	chr4:75857686..75858496-chr4:76498606..76499305,2	K562	blood:
4	chr4:76615229..76618143-chr4:76619781..76621972,2	K562	blood:
5	chr4:76588077..76590101-chr4:76596082..76598712,2	MCF-7	breast:
6	chr4:76565197..76568229-chr4:76577343..76579851,3	K562	blood:
7	chr4:76600960..76603310-chr4:76607519..76610199,2	MCF-7	breast:
8	chr4:76498276..76499263-chr4:76633255..76634192,3	K562	blood:
9	chr4:76497545..76500510-chr4:76767738..76769614,2	MCF-7	breast:
10	chr4:76527827..76530761-chr4:76647722..76649257,2	K562	blood:
11	chr4:76497613..76499377-chr4:76649691..76652162,2	K562	blood:
12	chr4:76518218..76519826-chr4:76585370..76586995,2	K562	blood:
13	chr4:76598619..76599144-chr8:101733919..101734743,2	HCT-116	colon:
14	chr4:76580953..76583116-chr4:76591150..76593341,2	K562	blood:
15	chr4:76584903..76586465-chr4:76590671..76593356,2	K562	blood:
16	chr3:64008912..64009599-chr4:76498142..76499061,2	MCF-7	breast:
17	chr4:76498341..76499310-chr4:76579118..76579672,2	MCF-7	breast:
18	chr4:76575310..76582874-chr4:76594032..76598652,8	K562	blood:
19	chr4:76578830..76581490-chr4:76590294..76592891,2	MCF-7	breast:
20	chr4:76596470..76600480-chr4:76647707..76650691,10	MCF-7	breast:
21	chr4:76597717..76598408-chr4:76649173..76649798,2	MCF-7	breast:
22	chr4:76568880..76572103-chr4:76574675..76578166,4	K562	blood:
23	chr4:76437052..76441363-chr4:76597688..76599751,3	K562	blood:
24	chr4:76603137..76606116-chr4:76628851..76631613,2	K562	blood:
25	chr4:76518218..76519826-chr4:76585370..76586995,2	K562	blood:
26	chr4:76576940..76580449-chr4:76596844..76600362,4	MCF-7	breast:
27	chr4:76597281..76599503-chr4:76610907..76612825,2	K562	blood:
28	chr4:76560792..76563538-chr4:76565983..76568591,2	K562	blood:
29	chr4:76487529..76489758-chr4:76496405..76499306,2	MCF-7	breast:
30	chr1:149858225..149858943-chr4:76598538..76599313,2	Hela-S3	cervix:
31	chr4:76616814..76618583-chr4:76648133..76650358,2	K562	blood:
32	chr4:76620008..76622936-chr4:76627662..76629475,2	K562	blood:
33	chr4:76575878..76577705-chr4:76597266..76598785,2	MCF-7	breast:
34	chr4:76592494..76594914-chr4:76648376..76650712,2	K562	blood:
35	chr4:76588364..76594216-chr4:76595418..76601309,9	MCF-7	breast:
36	chr10:101190684..101191594-chr4:76598283..76598807,2	Hela-S3	cervix:
37	chr4:76594283..76597057-chr4:77067982..77070334,2	K562	blood:
38	chr4:76529277..76531401-chr4:76541879..76544287,2	K562	blood:
39	chr4:76498264..76499501-chr4:76769042..76769962,9	MCF-7	breast:
40	chr4:76594895..76597627-chr4:76694798..76696348,2	K562	blood:
41	chr4:76561971..76564906-chr4:76565312..76567173,3	MCF-7	breast:
42	chr4:76503538..76507372-chr4:76509349..76512097,4	K562	blood:
43	chr4:76595601..76600505-chr4:76645864..76652704,29	K562	blood:
44	chr4:76568880..76572103-chr4:76574675..76578166,4	K562	blood:
45	chr4:76561539..76563479-chr4:76597824..76600082,2	K562	blood:
46	chr4:76505499..76507050-chr4:76520964..76522729,2	K562	blood:
47	chr4:76566167..76568657-chr4:76571863..76573668,2	K562	blood:
48	chr4:76601357..76603766-chr4:76648167..76650136,2	MCF-7	breast:
49	chr4:76615229..76618143-chr4:76619781..76621972,2	K562	blood:
50	chr4:76498762..76499538-chr4:76704887..76705580,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf26-2	chr4:76498310-76498349	refGeneNc_4304_NR_033964
2	lnc-G3BP2-2	chr4:76522119-76522324	NONHSAT096931
3	lnc-G3BP2-2	chr4:76521264-76521524	NONHSAT096931
4	lnc-C4orf26-2	chr4:76505958-76506798	refGeneNc_4304_NR_033964
5	lnc-C4orf26-2	chr4:76502215-76502404	refGeneNc_4304_NR_033964
6	lnc-C4orf26-2	chr4:76499552-76499621	refGeneNc_4304_NR_033964

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	G3BP2	hsa-miR-124-3p	chr4:76569720-76569714
2	G3BP2	hsa-miR-92a-3p	chr4:76570224-76570218
3	G3BP2	hsa-miR-92a-3p	chr4:76570233-76570227
4	G3BP2	hsa-miR-26b-5p	chr4:76568629-76568622
5	G3BP2	hsa-miR-1	chr4:76569701-76569695
6	CDKL2	hsa-miR-26b-5p	chr4:76503110-76503131
7	G3BP2	hsa-miR-103a-3p	chr4:76570292-76570286
8	G3BP2	hsa-miR-26b-5p	chr4:76568623-76568645
9	G3BP2	hsa-miR-92a-3p	chr4:76570227-76570254
10	G3BP2	hsa-miR-361-5p	chr4:76568633-76568654
11	G3BP2	hsa-miR-103a-3p	chr4:76570287-76570309
12	G3BP2	hsa-miR-124-3p	chr4:76569714-76569733

Variant related genes	Relation type
ENSG00000201644	TF binding region
G3BP2	TF binding region
CDKL2	TF binding region
ENSG00000201644	CpG island
G3BP2	CpG island
CDKL2	CpG island
ENSG00000163743	chromatin interactions
ENSG00000224934	chromatin interactions
ENSG00000225793	chromatin interactions
ENSG00000138768	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000169116	chromatin interactions
ENSG00000203778	chromatin interactions
ENSG00000138750	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000160226	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000245322	chromatin interactions
ENSG00000074935	chromatin interactions
ENSG00000138744	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000232969	chromatin interactions
ENSG00000138769	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000174796	chromatin interactions
ENSG00000138757	chromatin interactions
ENSG00000263136	chromatin interactions

Extended variants
information (count: 4528 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4528 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6851864	chr4:76493256-76493257	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568763399	chr4:76493262-76493263	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs537739816	chr4:76493266-76493267	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs555687097	chr4:76493268-76493269	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs567500119	chr4:76493269-76493270	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs534923819	chr4:76493319-76493320	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs139732891	chr4:76493359-76493360	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs558431533	chr4:76493374-76493375	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs545178050	chr4:76493377-76493378	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs190234891	chr4:76493409-76493410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575588082	chr4:76493437-76493438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113606753	chr4:76493457-76493458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149931018	chr4:76493488-76493489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561193400	chr4:76493574-76493575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181408474	chr4:76493575-76493576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536605169	chr4:76493592-76493593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540394137	chr4:76493605-76493606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565097515	chr4:76493607-76493608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186418234	chr4:76493632-76493633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554948599	chr4:76493639-76493640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562501690	chr4:76493640-76493641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529683310	chr4:76493647-76493648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113415312	chr4:76493688-76493689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377413463	chr4:76493712-76493713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs367973784	chr4:76493727-76493728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567582726	chr4:76493755-76493756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535004919	chr4:76493756-76493757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546740301	chr4:76493778-76493779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11724280	chr4:76493824-76493825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146477705	chr4:76493903-76493904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561595827	chr4:76493923-76493924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34699757	chr4:76493924-76493925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397994035	chr4:76493934-76493935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7684865	chr4:76493999-76494000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539116262	chr4:76494003-76494004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191059757	chr4:76494004-76494005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7699620	chr4:76494014-76494015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11931211	chr4:76494034-76494035	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs536680446	chr4:76494047-76494048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374843010	chr4:76494099-76494100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62320962	chr4:76494133-76494134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs180919445	chr4:76494142-76494143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552881921	chr4:76494144-76494145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556968547	chr4:76494155-76494156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540537641	chr4:76494181-76494182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565050505	chr4:76494192-76494193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577010084	chr4:76494227-76494228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146673357	chr4:76494234-76494235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570262073	chr4:76494301-76494302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367869022	chr4:76494302-76494303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	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
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Oral squamous cell carcinoma	17134496	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Autism	18414403	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2643 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76487400-76498400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:76488800-76493600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr4:76490800-76493400	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr4:76491600-76493400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr4:76491800-76493400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr4:76491800-76498600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr4:76492800-76493400	Enhancers	Spleen	Spleen
8	chr4:76493000-76493400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:76493000-76493400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:76493400-76493800	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr4:76493400-76495400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:76493400-76498600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:76493400-76498800	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr4:76495000-76498600	Weak transcription	Right Atrium	heart
15	chr4:76498200-76498400	Enhancers	Hela-S3	cervix
16	chr4:76498400-76498800	Enhancers	Stomach Smooth Muscle	stomach
17	chr4:76498400-76498800	Flanking Active TSS	Hela-S3	cervix
18	chr4:76498400-76499000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:76498400-76499200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr4:76498600-76498800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:76498600-76498800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr4:76498600-76498800	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr4:76498600-76498800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:76498600-76498800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:76498600-76498800	Enhancers	Rectal Smooth Muscle	rectum
26	chr4:76498600-76498800	Enhancers	Right Atrium	heart
27	chr4:76498600-76498800	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr4:76498600-76498800	Enhancers	Dnd41	blood
29	chr4:76498600-76498800	Enhancers	GM12878-XiMat	blood
30	chr4:76498600-76499000	Active TSS	Primary T cells from cord blood	blood
31	chr4:76498600-76499000	Active TSS	Primary hematopoietic stem cells	blood
32	chr4:76498600-76499000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
33	chr4:76498600-76499000	Enhancers	Stomach Mucosa	stomach
34	chr4:76498600-76499000	Active TSS	A549	lung
35	chr4:76498600-76499000	Active TSS	HepG2	liver
36	chr4:76498600-76499000	Active TSS	HMEC	breast
37	chr4:76498600-76499000	Active TSS	Monocytes-CD14+_RO01746	blood
38	chr4:76498600-76499200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:76498600-76499200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:76498600-76499200	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr4:76498600-76499200	Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr4:76498600-76499200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr4:76498600-76499200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr4:76498600-76499200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr4:76498600-76499200	Active TSS	Brain Hippocampus Middle	brain
46	chr4:76498600-76499200	Enhancers	Lung	lung
47	chr4:76498600-76499200	Enhancers	Pancreas	Pancrea
48	chr4:76498600-76499200	Enhancers	Right Ventricle	heart
49	chr4:76498600-76499200	Active TSS	NHEK	skin
50	chr4:76498600-76499400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood

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