Variant report

Variant	nsv1003490
Chromosome Location	chr4:103391483-103521772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2370)
CpG islands
(count:1100)
Chromatin interactive
region (count:158)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2370 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:103435697-103436116	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:103393741-103394341	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:103497012-103497331	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:103426031-103426436	HepG2	liver:	n/a	chr4:103426037-103426053 chr4:103426038-103426054
5	ARID3A	chr4:103422419-103422497	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:103423428-103423977	K562	blood:	n/a	n/a
7	ARID3A	chr4:103423127-103423903	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:103481283-103481344	K562	blood:	n/a	n/a
9	ARID3A	chr4:103425308-103425429	K562	blood:	n/a	n/a
10	ARID3A	chr4:103426914-103427114	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:103424393-103425266	HepG2	liver:	n/a	n/a
12	ATF1	chr4:103482780-103482850	K562	blood:	n/a	n/a
13	ATF1	chr4:103470052-103470119	K562	blood:	n/a	n/a
14	ATF1	chr4:103446350-103446507	K562	blood:	n/a	n/a
15	ATF2	chr4:103500846-103501584	GM12878	blood:	n/a	n/a
16	ATF2	chr4:103464118-103464690	GM12878	blood:	n/a	n/a
17	ATF2	chr4:103422951-103423653	GM12878	blood:	n/a	n/a
18	ATF2	chr4:103507105-103508223	GM12878	blood:	n/a	n/a
19	ATF2	chr4:103421662-103422167	GM12878	blood:	n/a	n/a
20	ATF2	chr4:103485318-103486080	GM12878	blood:	n/a	n/a
21	ATF2	chr4:103422841-103423891	GM12878	blood:	n/a	n/a
22	ATF2	chr4:103464116-103464637	GM12878	blood:	n/a	n/a
23	ATF2	chr4:103467707-103468230	GM12878	blood:	n/a	n/a
24	ATF2	chr4:103467584-103468353	GM12878	blood:	n/a	n/a
25	ATF2	chr4:103506439-103506910	GM12878	blood:	n/a	n/a
26	ATF2	chr4:103422176-103422703	GM12878	blood:	n/a	chr4:103422577-103422591
27	ATF2	chr4:103473953-103474364	GM12878	blood:	n/a	n/a
28	ATF2	chr4:103481194-103481741	GM12878	blood:	n/a	n/a
29	ATF2	chr4:103422336-103422605	GM12878	blood:	n/a	chr4:103422577-103422591
30	ATF2	chr4:103456394-103457222	GM12878	blood:	n/a	n/a
31	ATF2	chr4:103456290-103457324	GM12878	blood:	n/a	n/a
32	ATF2	chr4:103485364-103486250	GM12878	blood:	n/a	n/a
33	BACH1	chr4:103422814-103423269	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr4:103422903-103422972	K562	blood:	n/a	n/a
35	BATF	chr4:103506542-103506860	GM12878	blood:	n/a	chr4:103506716-103506727
36	BATF	chr4:103501706-103501943	GM12878	blood:	n/a	n/a
37	BATF	chr4:103485489-103485892	GM12878	blood:	n/a	n/a
38	BATF	chr4:103464134-103464421	GM12878	blood:	n/a	n/a
39	BATF	chr4:103456925-103457269	GM12878	blood:	n/a	chr4:103457135-103457145 chr4:103457131-103457141 chr4:103457130-103457141
40	BATF	chr4:103467775-103468215	GM12878	blood:	n/a	n/a
41	BATF	chr4:103507465-103507793	GM12878	blood:	n/a	n/a
42	BATF	chr4:103422394-103422574	GM12878	blood:	n/a	n/a
43	BATF	chr4:103456514-103456880	GM12878	blood:	n/a	chr4:103456746-103456757 chr4:103456718-103456729
44	BATF	chr4:103507066-103507811	GM12878	blood:	n/a	n/a
45	BATF	chr4:103423200-103423659	GM12878	blood:	n/a	n/a
46	BATF	chr4:103456579-103456914	GM12878	blood:	n/a	chr4:103456746-103456757 chr4:103456718-103456729
47	BATF	chr4:103506527-103506842	GM12878	blood:	n/a	chr4:103506716-103506727
48	BATF	chr4:103501677-103502000	GM12878	blood:	n/a	n/a
49	BATF	chr4:103467872-103468229	GM12878	blood:	n/a	n/a
50	BATF	chr4:103464139-103464581	GM12878	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:103458703-103458753	HAEpiC	amniotic membrane:	n/a
2	chr4:103422050-103422100	H1-hESC	embryonic stem cell:	embryo
3	chr4:103458703-103458753	HAEpiC	amniotic membrane:	n/a
4	chr4:103422050-103422100	H1-hESC	embryonic stem cell:	embryo
5	chr4:103423146-103423196	HCF	heart:	n/a
6	chr4:103422246-103422296	HUVEC	blood vessel:	n/a
7	chr4:103422429-103422479	Hepatocyte	liver:	n/a
8	chr4:103419193-103419243	GM12878	blood:	n/a
9	chr4:103426288-103426338	AG10803	skin:	n/a
10	chr4:103422974-103423024	NB4	blood:	n/a
11	chr4:103458703-103458753	HCM	heart:	n/a
12	chr4:103422246-103422296	HMEC	breast:	n/a
13	chr4:103499194-103499244	HMEC	breast:	n/a
14	chr4:103422196-103422246	AG10803	skin:	n/a
15	chr4:103499194-103499244	NT2-D1	testis:	n/a
16	chr4:103423146-103423196	SK-N-MC	brain:	n/a
17	chr4:103482058-103482108	HMEC	breast:	n/a
18	chr4:103422460-103422510	HRCEpiC	kidney:	n/a
19	chr4:103422429-103422479	K562	blood:	n/a
20	chr4:103422050-103422100	GM19239	blood:	n/a
21	chr4:103422974-103423024	U87	brain:	n/a
22	chr4:103422050-103422100	HAEpiC	amniotic membrane:	n/a
23	chr4:103422460-103422510	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:103423492-103423542	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:103426288-103426338	AG04449	skin:	fetal
26	chr4:103423492-103423542	MCF-7	breast:	n/a
27	chr4:103426288-103426338	H1-hESC	embryonic stem cell:	embryo
28	chr4:103423368-103423418	AG10803	skin:	n/a
29	chr4:103499194-103499244	AG09309	skin:	n/a
30	chr4:103421224-103421274	BJ	skin:	n/a
31	chr4:103422974-103423024	NHBE	bronchial:	n/a
32	chr4:103423492-103423542	GM19239	blood:	n/a
33	chr4:103475833-103475883	Hela-S3	cervix:	n/a
34	chr4:103482058-103482108	PANC-1	pancreas:	n/a
35	chr4:103422460-103422510	PFSK-1	brain:	n/a
36	chr4:103422050-103422100	AoSMC	blood vessel:	n/a
37	chr4:103458703-103458753	IMR90	lung:	fetal
38	chr4:103426288-103426338	NH-A	brain:	n/a
39	chr4:103422974-103423024	H1-hESC	embryonic stem cell:	embryo
40	chr4:103475833-103475883	AG09319	gingival:	n/a
41	chr4:103475833-103475883	H1-hESC	embryonic stem cell:	embryo
42	chr4:103426288-103426338	HUVEC	blood vessel:	n/a
43	chr4:103423492-103423542	GM12892	blood:	n/a
44	chr4:103422460-103422510	IMR90	lung:	fetal
45	chr4:103422460-103422510	ovcar-3	ovarian:	n/a
46	chr4:103489295-103489345	HepG2	liver:	n/a
47	chr4:103422429-103422479	HAEpiC	amniotic membrane:	n/a
48	chr4:103422429-103422479	ProgFib	skin:	n/a
49	chr4:103422246-103422296	K562	blood:	n/a
50	chr4:103489295-103489345	HCT-116	colon:	n/a

(count:158 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:103421566..103424767-chr4:103746039..103749014,5	K562	blood:
2	chr4:103423042..103423659-chr7:72971558..72972250,3	Hela-S3	cervix:
3	chr4:103418457..103421752-chr4:103450464..103454174,4	MCF-7	breast:
4	chr4:103438442..103440658-chr4:103444124..103446101,2	MCF-7	breast:
5	chr4:103447755..103449902-chr4:103466038..103467792,2	K562	blood:
6	chr2:88927128..88927730-chr4:103423923..103424787,2	Hela-S3	cervix:
7	chr4:103507106..103510839-chr4:103511469..103515611,4	K562	blood:
8	chr4:103441543..103444001-chr4:103444588..103447284,2	K562	blood:
9	chr4:103420331..103423503-chr4:103475320..103478755,3	MCF-7	breast:
10	chr4:103481967..103484496-chr4:103488750..103491219,2	MCF-7	breast:
11	chr4:103395510..103397844-chr4:103422825..103425392,2	MCF-7	breast:
12	chr4:103422268..103425518-chr4:103448711..103450558,3	MCF-7	breast:
13	chr4:103422194..103424603-chr4:103745115..103749014,4	K562	blood:
14	chr4:103438526..103440026-chr4:103449881..103451773,2	K562	blood:
15	chr4:103425524..103427364-chr4:103430743..103433529,2	MCF-7	breast:
16	chr4:103482685..103484587-chr4:103487449..103489665,2	MCF-7	breast:
17	chr4:103439093..103441146-chr4:103445747..103447716,2	MCF-7	breast:
18	chr4:103424372..103425973-chr4:103466264..103468972,2	MCF-7	breast:
19	chr4:103421988..103424318-chr4:103485489..103487632,2	MCF-7	breast:
20	chr4:103474292..103476069-chr4:103481101..103483068,2	MCF-7	breast:
21	chr4:103442159..103444303-chr4:103446884..103449201,2	MCF-7	breast:
22	chr4:103264486..103268305-chr4:103421576..103425286,5	K562	blood:
23	chr4:103421988..103424318-chr4:103485489..103487632,2	MCF-7	breast:
24	chr4:103421940..103423639-chr4:103467327..103470380,3	MCF-7	breast:
25	chr4:103421129..103424060-chr4:103488906..103491146,3	MCF-7	breast:
26	chr4:103412443..103414141-chr4:103417200..103419328,2	K562	blood:
27	chr4:103442159..103444303-chr4:103446884..103449201,2	MCF-7	breast:
28	chr4:103369597..103371706-chr4:103422250..103424053,2	MCF-7	breast:
29	chr4:103418260..103419905-chr4:103421285..103422966,3	MCF-7	breast:
30	chr4:103428188..103431133-chr4:103431767..103434518,2	MCF-7	breast:
31	chr4:103419957..103425638-chr4:103495824..103504548,11	MCF-7	breast:
32	chr4:103424918..103426820-chr4:103440847..103443260,2	K562	blood:
33	chr4:103409701..103414030-chr4:103420750..103423743,3	K562	blood:
34	chr4:103424918..103426820-chr4:103440847..103443260,2	K562	blood:
35	chr19:48824602..48825469-chr4:103422328..103423053,2	Hela-S3	cervix:
36	chr4:103514947..103516619-chr4:103518321..103520402,2	K562	blood:
37	chr4:103482685..103484587-chr4:103487449..103489665,2	MCF-7	breast:
38	chr4:103420299..103423075-chr4:103789443..103791523,3	K562	blood:
39	chr11:62606453..62609348-chr4:103421636..103424436,2	MCF-7	breast:
40	chr4:103440956..103442582-chr4:103451787..103454591,2	MCF-7	breast:
41	chr4:103351901..103354156-chr4:103421461..103424407,3	MCF-7	breast:
42	chr4:103442194..103444788-chr4:103454206..103455780,2	MCF-7	breast:
43	chr4:103421751..103424038-chr4:103500019..103502227,2	MCF-7	breast:
44	chr4:103423143..103423688-chr5:10249942..10250633,2	Hela-S3	cervix:
45	chr4:103426144..103427805-chr4:103429263..103431794,2	MCF-7	breast:
46	chr4:103442194..103444788-chr4:103454206..103455780,2	MCF-7	breast:
47	chr4:103352302..103353294-chr4:103422214..103423235,3	K562	blood:
48	chr4:103422470..103425654-chr4:103747796..103750322,3	MCF-7	breast:
49	chr4:103420745..103423144-chr4:103433405..103436115,3	MCF-7	breast:
50	chr4:103474292..103476069-chr4:103481101..103483068,2	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

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

Extended variants
information (count: 4583 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:4583 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570951770	chr4:103391499-103391500	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs538570339	chr4:103391516-103391517	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs556588299	chr4:103391522-103391523	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs147284461	chr4:103391527-103391528	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs535477820	chr4:103391531-103391532	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs553735047	chr4:103391541-103391542	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs183212968	chr4:103391552-103391553	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs140805529	chr4:103391604-103391605	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141419336	chr4:103391605-103391606	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs74458418	chr4:103391786-103391787	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs35910516	chr4:103391843-103391844	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs72602441	chr4:103391850-103391851	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs556064721	chr4:103391891-103391892	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs75023760	chr4:103391899-103391900	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs111267380	chr4:103391907-103391908	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs34418499	chr4:103391944-103391945	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs529170336	chr4:103392002-103392003	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs145673763	chr4:103392019-103392020	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370196012	chr4:103392020-103392021	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs398107752	chr4:103392035-103392036	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547447642	chr4:103392047-103392048	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs569583902	chr4:103392056-103392057	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs559152644	chr4:103392064-103392065	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs535280822	chr4:103392075-103392076	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533092775	chr4:103392108-103392109	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs551176481	chr4:103392128-103392129	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs577481582	chr4:103392275-103392276	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112619481	chr4:103392293-103392294	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs569692230	chr4:103392304-103392305	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs541681747	chr4:103392320-103392321	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs371375634	chr4:103392328-103392329	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553365681	chr4:103392333-103392334	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549933687	chr4:103392343-103392344	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs150812000	chr4:103392393-103392394	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs35303101	chr4:103392397-103392398	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs78095733	chr4:103392428-103392429	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139211102	chr4:103392434-103392435	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565927370	chr4:103392509-103392510	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs186460353	chr4:103392536-103392537	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs570987238	chr4:103392592-103392593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149966373	chr4:103392630-103392631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28844321	chr4:103392632-103392633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368782800	chr4:103392641-103392642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370674128	chr4:103392699-103392700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572052718	chr4:103392725-103392726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543270280	chr4:103392730-103392731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555587835	chr4:103392749-103392750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146024443	chr4:103392767-103392768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541328265	chr4:103392778-103392779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113901493	chr4:103392840-103392841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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

Chromatin state (count:3907 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103390600-103391600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr4:103390600-103391800	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr4:103390600-103391800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr4:103390600-103391800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr4:103390600-103391800	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr4:103390600-103391800	Enhancers	HUVEC	blood vessel
7	chr4:103390800-103391800	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr4:103391200-103391600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr4:103391200-103391800	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr4:103391200-103392000	Enhancers	Primary T cells from cord blood	blood
11	chr4:103391200-103392600	Enhancers	Dnd41	blood
12	chr4:103391200-103393600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr4:103392000-103395000	Weak transcription	Primary T cells from cord blood	blood
14	chr4:103392800-103393800	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr4:103393400-103396400	Enhancers	HepG2	liver
16	chr4:103393600-103393800	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr4:103393600-103394600	Enhancers	Fetal Intestine Small	intestine
18	chr4:103393600-103395000	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr4:103393800-103394400	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr4:103393800-103396400	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr4:103394400-103395400	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr4:103394800-103399200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:103395000-103395600	Enhancers	Primary T cells from cord blood	blood
24	chr4:103395600-103396400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:103395800-103396200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:103396000-103396600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:103396200-103396600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr4:103396200-103397400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr4:103396400-103396600	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr4:103396400-103398800	Weak transcription	HepG2	liver
31	chr4:103398000-103399200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:103398600-103399200	Enhancers	NH-A	brain
33	chr4:103398600-103399200	Enhancers	NHDF-Ad	bronchial
34	chr4:103398600-103399400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:103398800-103399200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:103398800-103399200	Enhancers	HepG2	liver
37	chr4:103399000-103399200	ZNF genes & repeats	K562	blood
38	chr4:103399000-103399400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:103399200-103399400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr4:103399200-103399400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:103399200-103399400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:103399200-103399400	Flanking Active TSS	HepG2	liver
43	chr4:103399200-103399600	Active TSS	K562	blood
44	chr4:103399200-103399800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr4:103399400-103399600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr4:103399400-103399600	Active TSS	HepG2	liver
47	chr4:103399600-103399800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:103399600-103399800	Flanking Active TSS	HepG2	liver
49	chr4:103399600-103416000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:103399800-103400000	Active TSS	HepG2	liver

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