Variant report

Variant	nsv830020
Chromosome Location	chr4:103387343-103581284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3615)
CpG islands
(count:1342)
Chromatin interactive
region (count:214)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3615 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:103423428-103423977	K562	blood:	n/a	n/a
2	ARID3A	chr4:103548989-103549286	K562	blood:	n/a	n/a
3	ARID3A	chr4:103531285-103531467	K562	blood:	n/a	n/a
4	ARID3A	chr4:103546875-103547102	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:103425308-103425429	K562	blood:	n/a	n/a
6	ARID3A	chr4:103435697-103436116	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:103426914-103427114	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:103423127-103423903	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:103544866-103545055	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:103541793-103542848	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:103481283-103481344	K562	blood:	n/a	n/a
12	ARID3A	chr4:103426031-103426436	HepG2	liver:	n/a	chr4:103426037-103426053 chr4:103426038-103426054
13	ARID3A	chr4:103424393-103425266	HepG2	liver:	n/a	n/a
14	ARID3A	chr4:103422419-103422497	HepG2	liver:	n/a	n/a
15	ARID3A	chr4:103497012-103497331	HepG2	liver:	n/a	n/a
16	ARID3A	chr4:103541791-103542078	K562	blood:	n/a	n/a
17	ARID3A	chr4:103393741-103394341	HepG2	liver:	n/a	n/a
18	ATF1	chr4:103541812-103542229	K562	blood:	n/a	n/a
19	ATF1	chr4:103446350-103446507	K562	blood:	n/a	n/a
20	ATF1	chr4:103470052-103470119	K562	blood:	n/a	n/a
21	ATF1	chr4:103482780-103482850	K562	blood:	n/a	n/a
22	ATF2	chr4:103464116-103464637	GM12878	blood:	n/a	n/a
23	ATF2	chr4:103507105-103508223	GM12878	blood:	n/a	n/a
24	ATF2	chr4:103456290-103457324	GM12878	blood:	n/a	n/a
25	ATF2	chr4:103467707-103468230	GM12878	blood:	n/a	n/a
26	ATF2	chr4:103422176-103422703	GM12878	blood:	n/a	chr4:103422577-103422591
27	ATF2	chr4:103422336-103422605	GM12878	blood:	n/a	chr4:103422577-103422591
28	ATF2	chr4:103422841-103423891	GM12878	blood:	n/a	n/a
29	ATF2	chr4:103464118-103464690	GM12878	blood:	n/a	n/a
30	ATF2	chr4:103421662-103422167	GM12878	blood:	n/a	n/a
31	ATF2	chr4:103422951-103423653	GM12878	blood:	n/a	n/a
32	ATF2	chr4:103506439-103506910	GM12878	blood:	n/a	n/a
33	ATF2	chr4:103485318-103486080	GM12878	blood:	n/a	n/a
34	ATF2	chr4:103485364-103486250	GM12878	blood:	n/a	n/a
35	ATF2	chr4:103456394-103457222	GM12878	blood:	n/a	n/a
36	ATF2	chr4:103467584-103468353	GM12878	blood:	n/a	n/a
37	ATF2	chr4:103473953-103474364	GM12878	blood:	n/a	n/a
38	ATF2	chr4:103481194-103481741	GM12878	blood:	n/a	n/a
39	ATF2	chr4:103500846-103501584	GM12878	blood:	n/a	n/a
40	ATF3	chr4:103548927-103549261	K562	blood:	n/a	n/a
41	ATF3	chr4:103541746-103542326	A549	lung:	n/a	n/a
42	ATF3	chr4:103541846-103542431	A549	lung:	n/a	n/a
43	BACH1	chr4:103422814-103423269	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr4:103422903-103422972	K562	blood:	n/a	n/a
45	BATF	chr4:103456514-103456880	GM12878	blood:	n/a	chr4:103456746-103456757 chr4:103456718-103456729
46	BATF	chr4:103507465-103507793	GM12878	blood:	n/a	n/a
47	BATF	chr4:103485489-103485892	GM12878	blood:	n/a	n/a
48	BATF	chr4:103506527-103506842	GM12878	blood:	n/a	chr4:103506716-103506727
49	BATF	chr4:103481241-103481506	GM12878	blood:	n/a	n/a
50	BATF	chr4:103456579-103456914	GM12878	blood:	n/a	chr4:103456746-103456757 chr4:103456718-103456729

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:103475833-103475883	BJ	skin:	n/a
2	chr4:103499194-103499244	HCT-116	colon:	n/a
3	chr4:103537858-103537908	RPTEC	kidney:	n/a
4	chr4:103419193-103419243	K562	blood:	n/a
5	chr4:103423146-103423196	HCM	heart:	n/a
6	chr4:103489295-103489345	GM12891	blood:	n/a
7	chr4:103422196-103422246	SAEC	small airway:	n/a
8	chr4:103499194-103499244	HCPEpiC	choroid plexus:	n/a
9	chr4:103553119-103553169	SK-N-SH_RA	brain:	n/a
10	chr4:103553119-103553169	RPTEC	kidney:	n/a
11	chr4:103422196-103422246	HUVEC	blood vessel:	n/a
12	chr4:103482058-103482108	ovcar-3	ovarian:	n/a
13	chr4:103423368-103423418	PrEC	prostate:	n/a
14	chr4:103422460-103422510	H1-hESC	embryonic stem cell:	embryo
15	chr4:103422246-103422296	MCF10A-Er-Src	breast:	n/a
16	chr4:103422050-103422100	BE2_C	brain:	n/a
17	chr4:103528099-103528149	HEK293	kidney:	embryo
18	chr4:103422196-103422246	MCF-7	breast:	n/a
19	chr4:103423368-103423418	MCF-7	breast:	n/a
20	chr4:103422974-103423024	HepG2	liver:	n/a
21	chr4:103419193-103419243	HCF	heart:	n/a
22	chr4:103422974-103423024	AG10803	skin:	n/a
23	chr4:103422246-103422296	U87	brain:	n/a
24	chr4:103419193-103419243	HEK293	kidney:	embryo
25	chr4:103542236-103542286	AG04450	lung:	fetal
26	chr4:103520637-103520687	HNPCEpiC	eye:	n/a
27	chr4:103423368-103423418	AG09309	skin:	n/a
28	chr4:103489295-103489345	HEEpiC	esophagus:	n/a
29	chr4:103422196-103422246	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:103542236-103542286	HIPEpiC	eye:	n/a
31	chr4:103475833-103475883	PANC-1	pancreas:	n/a
32	chr4:103419193-103419243	T-47D	breast:	n/a
33	chr4:103482058-103482108	MCF10A-Er-Src	breast:	n/a
34	chr4:103422050-103422100	HRE	kidney:	n/a
35	chr4:103482058-103482108	NHDF-neo	bronchial:	n/a
36	chr4:103489295-103489345	IMR90	lung:	fetal
37	chr4:103422974-103423024	HCM	heart:	n/a
38	chr4:103537858-103537908	HEEpiC	esophagus:	n/a
39	chr4:103537858-103537908	LNCaP	prostate:	n/a
40	chr4:103520637-103520687	HEEpiC	esophagus:	n/a
41	chr4:103458703-103458753	Caco-2	colon:	n/a
42	chr4:103482058-103482108	GM06990	blood:	n/a
43	chr4:103421224-103421274	SK-N-SH_RA	brain:	n/a
44	chr4:103419193-103419243	HIPEpiC	eye:	n/a
45	chr4:103499194-103499244	K562	blood:	n/a
46	chr4:103421224-103421274	NT2-D1	testis:	n/a
47	chr4:103528099-103528149	SK-N-SH_RA	brain:	n/a
48	chr4:103475833-103475883	PFSK-1	brain:	n/a
49	chr4:103528099-103528149	HIPEpiC	eye:	n/a
50	chr4:103421224-103421274	HCM	heart:	n/a

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr4:103513440..103517294-chr4:103519105..103521250,3	MCF-7	breast:
2	chr4:103425524..103427364-chr4:103430743..103433529,2	MCF-7	breast:
3	chr4:103421329..103424416-chr4:103463200..103466057,3	K562	blood:
4	chr4:103422799..103424551-chr4:103548474..103550630,2	MCF-7	breast:
5	chr4:103441543..103444001-chr4:103444588..103447284,2	K562	blood:
6	chr4:103423143..103423688-chr5:10249942..10250633,2	Hela-S3	cervix:
7	chr4:103422194..103424603-chr4:103745115..103749014,4	K562	blood:
8	chr4:103480320..103483101-chr4:103483579..103486269,2	MCF-7	breast:
9	chr4:103393460..103395184-chr4:103421429..103423039,2	MCF-7	breast:
10	chr2:88927128..88927730-chr4:103423923..103424787,2	Hela-S3	cervix:
11	chr4:103541561..103542496-chr4:103929971..103930975,6	K562	blood:
12	chr4:103369853..103371586-chr4:103423446..103426290,2	K562	blood:
13	chr4:103542281..103545235-chr4:103546204..103549504,3	K562	blood:
14	chr4:103456268..103457811-chr4:103471948..103474293,2	MCF-7	breast:
15	chr4:103480320..103483101-chr4:103483579..103486269,2	MCF-7	breast:
16	chr4:103534750..103537170-chr4:103544463..103546367,2	K562	blood:
17	chr4:103434755..103437108-chr4:103437162..103439778,2	MCF-7	breast:
18	chr4:103385691..103388177-chr4:103389078..103391439,2	MCF-7	breast:
19	chr4:103424918..103426820-chr4:103440847..103443260,2	K562	blood:
20	chr3:32022654..32023494-chr4:103422493..103423209,2	Hela-S3	cervix:
21	chr4:103420331..103423503-chr4:103475320..103478755,3	MCF-7	breast:
22	chr11:62606453..62609348-chr4:103421636..103424436,2	MCF-7	breast:
23	chr4:103481967..103484496-chr4:103488750..103491219,2	MCF-7	breast:
24	chr4:103459557..103462461-chr4:103466718..103470732,3	K562	blood:
25	chr4:103421659..103423327-chr4:103467979..103470381,2	MCF-7	breast:
26	chr4:103439093..103441146-chr4:103445747..103447716,2	MCF-7	breast:
27	chr4:103421965..103423633-chr4:103471887..103473482,2	MCF-7	breast:
28	chr4:103541811..103542577-chr4:103929931..103930910,7	MCF-7	breast:
29	chr4:103421882..103423442-chr4:103462587..103465084,2	MCF-7	breast:
30	chr4:103577856..103580844-chr4:103747616..103749306,2	MCF-7	breast:
31	chr4:103421566..103424767-chr4:103746039..103749014,5	K562	blood:
32	chr4:103541547..103542382-chr4:103953390..103954339,3	K562	blood:
33	chr4:103421285..103424744-chr4:103439488..103445746,9	MCF-7	breast:
34	chr4:103558334..103560805-chr4:103747066..103749138,2	K562	blood:
35	chr4:103427425..103429169-chr4:103437672..103439992,2	K562	blood:
36	chr4:103558551..103561241-chr4:103562975..103564838,2	K562	blood:
37	chr4:103441543..103444001-chr4:103444588..103447284,2	K562	blood:
38	chr4:103421758..103423723-chr4:103430580..103432552,3	MCF-7	breast:
39	chr4:103438442..103440658-chr4:103444124..103446101,2	MCF-7	breast:
40	chr4:103438526..103440026-chr4:103449881..103451773,2	K562	blood:
41	chr4:103533614..103535745-chr4:103746792..103748941,2	K562	blood:
42	chr4:103419957..103425638-chr4:103495824..103504548,11	MCF-7	breast:
43	chr4:103442159..103444303-chr4:103446884..103449201,2	MCF-7	breast:
44	chr4:103421697..103423490-chr4:103540373..103542890,2	MCF-7	breast:
45	chr4:103447010..103448533-chr4:103454015..103456334,2	K562	blood:
46	chr4:103521932..103523756-chr4:104022119..104025012,2	K562	blood:
47	chr4:103262389..103264816-chr4:103397945..103400570,2	K562	blood:
48	chr4:103558551..103561241-chr4:103562975..103564838,2	K562	blood:
49	chr4:103541542..103542179-chr4:103953624..103954304,2	MCF-7	breast:
50	chr4:103421047..103423943-chr4:103521842..103524468,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC39A8-1	chr4:103421975-103422476	NONHSAT097590
2	lnc-SLC39A8-1	chr4:103421998-103422476	ENSG00000260651.1

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MANBA	hsa-miR-335-5p	chr4:103553072-103553095
2	NFKB1	hsa-miR-15a-5p	chr4:103538007-103538030
3	NFKB1	hsa-miR-26b-5p	chr4:103538263-103538283
4	NFKB1	hsa-miR-9-5p	chr4:103537765-103537787
5	NFKB1	hsa-miR-16-5p	chr4:103538006-103538030

Variant related genes	Relation type
MANBA	TF binding region
ENSG00000241981	TF binding region
ENSG00000260651	TF binding region
ENSG00000238553	TF binding region
NFKB1	TF binding region
MANBA	CpG island
ENSG00000241981	CpG island
ENSG00000260651	CpG island
ENSG00000238553	CpG island
NFKB1	CpG island
ENSG00000145354	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000248161	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000256294	chromatin interactions
ENSG00000109332	chromatin interactions
ENSG00000234028	chromatin interactions
ENSG00000241981	chromatin interactions
ENSG00000246560	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000144645	chromatin interactions
ENSG00000088766	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000106635	chromatin interactions
ENSG00000105479	chromatin interactions
ENSG00000238553	chromatin interactions
ENSG00000138821	chromatin interactions
ENSG00000197385	chromatin interactions
ENSG00000142227	chromatin interactions
ENSG00000273162	chromatin interactions
ENSG00000164038	chromatin interactions
ENSG00000164037	chromatin interactions
ENSG00000109320	chromatin interactions
ENSG00000065243	chromatin interactions
ENSG00000164039	chromatin interactions
ENSG00000260651	chromatin interactions
ENSG00000251572	chromatin interactions

Extended variants
information (count: 7008 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:7008 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34226284	chr4:103387365-103387366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs567491985	chr4:103387406-103387407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2205438	chr4:103387413-103387414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs230490	chr4:103387419-103387420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs534777452	chr4:103387422-103387423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369934022	chr4:103387441-103387442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs116069451	chr4:103387542-103387543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs1585216	chr4:103387556-103387557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs77559485	chr4:103387573-103387574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539938596	chr4:103387581-103387582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559563261	chr4:103387597-103387598	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs577640870	chr4:103387600-103387601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs72694182	chr4:103387641-103387642	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551902043	chr4:103387650-103387651	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375080550	chr4:103387671-103387672	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554015667	chr4:103387672-103387673	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs73837224	chr4:103387689-103387690	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs142617931	chr4:103387692-103387693	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549143155	chr4:103387699-103387700	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs35205672	chr4:103387738-103387739	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542857251	chr4:103387760-103387761	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567641961	chr4:103387830-103387831	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs184214266	chr4:103387870-103387871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs55937925	chr4:103387944-103387945	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs571723594	chr4:103388023-103388024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200482759	chr4:103388070-103388071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574061239	chr4:103388081-103388082	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538480337	chr4:103388095-103388096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs114355521	chr4:103388108-103388109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575483691	chr4:103388112-103388113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542887594	chr4:103388156-103388157	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs79278981	chr4:103388168-103388169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146478367	chr4:103388289-103388290	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs77855727	chr4:103388303-103388304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564639121	chr4:103388307-103388308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189634631	chr4:103388366-103388367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545284629	chr4:103388395-103388396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563890185	chr4:103388402-103388403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531137399	chr4:103388403-103388404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140992421	chr4:103388408-103388409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192447979	chr4:103388411-103388412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184727976	chr4:103388424-103388425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528499515	chr4:103388436-103388437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546989190	chr4:103388439-103388440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs230489	chr4:103388441-103388442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
46	rs560044329	chr4:103388463-103388464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144702748	chr4:103388480-103388481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550532916	chr4:103388528-103388529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188786472	chr4:103388547-103388548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs230488	chr4:103388565-103388566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cancer	20164919	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:5747 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103381400-103387600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:103385400-103387600	Enhancers	Dnd41	blood
3	chr4:103385600-103387800	Enhancers	Primary T cells from cord blood	blood
4	chr4:103386000-103388200	Enhancers	HUVEC	blood vessel
5	chr4:103386600-103390600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr4:103386600-103390600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr4:103386600-103390600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr4:103386600-103390600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr4:103386600-103390600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr4:103386600-103390800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr4:103386600-103390800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr4:103386800-103390200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr4:103386800-103390800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr4:103387000-103387400	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr4:103387200-103387600	Enhancers	NHEK	skin
16	chr4:103387400-103387600	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr4:103387400-103387800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:103387600-103387800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:103387600-103390200	Weak transcription	Dnd41	blood
20	chr4:103387600-103390600	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr4:103387800-103390000	Weak transcription	Primary T cells from cord blood	blood
22	chr4:103388000-103388600	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr4:103388200-103390600	Weak transcription	HUVEC	blood vessel
24	chr4:103390000-103390800	Enhancers	Primary T cells from cord blood	blood
25	chr4:103390200-103390800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr4:103390200-103390800	Enhancers	Dnd41	blood
27	chr4:103390600-103390800	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr4:103390600-103391600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr4:103390600-103391800	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr4:103390600-103391800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr4:103390600-103391800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr4:103390600-103391800	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr4:103390600-103391800	Enhancers	HUVEC	blood vessel
34	chr4:103390800-103391000	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr4:103390800-103391200	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr4:103390800-103391200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr4:103390800-103391200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr4:103390800-103391200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr4:103390800-103391200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr4:103390800-103391200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr4:103390800-103391200	Flanking Active TSS	Dnd41	blood
42	chr4:103390800-103391800	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr4:103391200-103391600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr4:103391200-103391800	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr4:103391200-103392000	Enhancers	Primary T cells from cord blood	blood
46	chr4:103391200-103392600	Enhancers	Dnd41	blood
47	chr4:103391200-103393600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr4:103392000-103395000	Weak transcription	Primary T cells from cord blood	blood
49	chr4:103392800-103393800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr4:103393400-103396400	Enhancers	HepG2	liver

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