Variant report

Variant	esv2759632
Chromosome Location	chr8:100028848-100196681
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:983)
CpG islands
(count:122)
Chromatin interactive
region (count:86)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100103092-100103687	K562	blood:	n/a	n/a
2	ARID3A	chr8:100058615-100058867	K562	blood:	n/a	n/a
3	ARID3A	chr8:100149959-100150472	K562	blood:	n/a	n/a
4	ARID3A	chr8:100046312-100046577	K562	blood:	n/a	n/a
5	ARID3A	chr8:100124728-100124858	K562	blood:	n/a	n/a
6	ARID3A	chr8:100038356-100038875	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:100046132-100046815	HepG2	liver:	n/a	n/a
8	ATF1	chr8:100177666-100177787	K562	blood:	n/a	n/a
9	ATF1	chr8:100150113-100150549	K562	blood:	n/a	n/a
10	ATF1	chr8:100103355-100103611	K562	blood:	n/a	n/a
11	ATF1	chr8:100058613-100058861	K562	blood:	n/a	n/a
12	ATF1	chr8:100135547-100135703	K562	blood:	n/a	n/a
13	ATF2	chr8:100093166-100093626	GM12878	blood:	n/a	n/a
14	ATF2	chr8:100092901-100093701	GM12878	blood:	n/a	n/a
15	ATF3	chr8:100150017-100150481	K562	blood:	n/a	n/a
16	ATF3	chr8:100103253-100103550	K562	blood:	n/a	n/a
17	BACH1	chr8:100150185-100150441	K562	blood:	n/a	n/a
18	BACH1	chr8:100182411-100182437	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr8:100093275-100093603	GM12878	blood:	n/a	n/a
20	BATF	chr8:100093290-100093609	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:100093229-100093561	GM12878	blood:	n/a	chr8:100093423-100093432
22	BCLAF1	chr8:100092916-100093613	GM12878	blood:	n/a	chr8:100093423-100093432
23	BDP1	chr8:100031640-100031902	Hela-S3	cervix:	n/a	n/a
24	BHLHE40	chr8:100047020-100047214	K562	blood:	n/a	n/a
25	BHLHE40	chr8:100150155-100150410	K562	blood:	n/a	n/a
26	CBX3	chr8:100082907-100083212	K562	blood:	n/a	n/a
27	CBX3	chr8:100045439-100045866	K562	blood:	n/a	n/a
28	CBX3	chr8:100036731-100037054	K562	blood:	n/a	n/a
29	CBX3	chr8:100036599-100037193	HCT-116	colon:	n/a	n/a
30	CBX3	chr8:100150051-100150770	K562	blood:	n/a	n/a
31	CBX3	chr8:100150104-100150431	K562	blood:	n/a	n/a
32	CBX3	chr8:100045458-100045813	K562	blood:	n/a	n/a
33	CBX3	chr8:100046502-100047344	K562	blood:	n/a	n/a
34	CBX3	chr8:100036539-100037091	K562	blood:	n/a	n/a
35	CBX3	chr8:100036707-100037211	HCT-116	colon:	n/a	n/a
36	CCNT2	chr8:100103316-100103587	K562	blood:	n/a	n/a
37	CCNT2	chr8:100150101-100150431	K562	blood:	n/a	n/a
38	CCNT2	chr8:100058664-100058876	K562	blood:	n/a	n/a
39	CEBPB	chr8:100077718-100077940	K562	blood:	n/a	chr8:100077849-100077860
40	CEBPB	chr8:100031558-100032043	IMR90	lung:	n/a	chr8:100031780-100031791
41	CEBPB	chr8:100031547-100031974	A549	lung:	n/a	chr8:100031780-100031791
42	CEBPB	chr8:100075976-100076309	HepG2	liver:	n/a	chr8:100076127-100076138
43	CEBPB	chr8:100047214-100047221	K562	blood:	n/a	n/a
44	CEBPB	chr8:100032773-100033151	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:100031718-100031931	K562	blood:	n/a	chr8:100031780-100031791
46	CEBPB	chr8:100100423-100100719	IMR90	lung:	n/a	chr8:100100587-100100600
47	CEBPB	chr8:100046476-100046781	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:100048891-100049101	K562	blood:	n/a	n/a
49	CEBPB	chr8:100077714-100078025	A549	lung:	n/a	chr8:100077849-100077860
50	CEBPB	chr8:100150009-100150483	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100157208-100157258	AG09319	gingival:	n/a
2	chr8:100157208-100157258	RPTEC	kidney:	n/a
3	chr8:100157208-100157258	HAEpiC	amniotic membrane:	n/a
4	chr8:100157208-100157258	AG09309	skin:	n/a
5	chr8:100104103-100104153	HCT-116	colon:	n/a
6	chr8:100104103-100104153	U87	brain:	n/a
7	chr8:100157208-100157258	AG04450	lung:	fetal
8	chr8:100104103-100104153	HRCEpiC	kidney:	n/a
9	chr8:100157208-100157258	HEEpiC	esophagus:	n/a
10	chr8:100157208-100157258	H1-hESC	embryonic stem cell:	embryo
11	chr8:100157208-100157258	HRPEpiC	eye:	n/a
12	chr8:100104103-100104153	AG10803	skin:	n/a
13	chr8:100157208-100157258	GM06990	blood:	n/a
14	chr8:100104103-100104153	GM12891	blood:	n/a
15	chr8:100157208-100157258	CMK	blood:	n/a
16	chr8:100157208-100157258	SK-N-MC	brain:	n/a
17	chr8:100104103-100104153	NH-A	brain:	n/a
18	chr8:100104103-100104153	T-47D	breast:	n/a
19	chr8:100157208-100157258	MCF-7	breast:	n/a
20	chr8:100104103-100104153	HUVEC	blood vessel:	n/a
21	chr8:100157208-100157258	NT2-D1	testis:	n/a
22	chr8:100104103-100104153	NHBE	bronchial:	n/a
23	chr8:100157208-100157258	BE2_C	brain:	n/a
24	chr8:100104103-100104153	A549	lung:	n/a
25	chr8:100104103-100104153	PANC-1	pancreas:	n/a
26	chr8:100157208-100157258	GM19239	blood:	n/a
27	chr8:100157208-100157258	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:100104103-100104153	HL-60	blood:	n/a
29	chr8:100104103-100104153	HepG2	liver:	n/a
30	chr8:100157208-100157258	AoSMC	blood vessel:	n/a
31	chr8:100157208-100157258	SKMC	muscle:	n/a
32	chr8:100104103-100104153	HRPEpiC	eye:	n/a
33	chr8:100104103-100104153	HEEpiC	esophagus:	n/a
34	chr8:100157208-100157258	HNPCEpiC	eye:	n/a
35	chr8:100104103-100104153	MCF-7	breast:	n/a
36	chr8:100104103-100104153	SK-N-MC	brain:	n/a
37	chr8:100157208-100157258	HCT-116	colon:	n/a
38	chr8:100104103-100104153	AG09309	skin:	n/a
39	chr8:100157208-100157258	GM12891	blood:	n/a
40	chr8:100157208-100157258	SK-N-SH_RA	brain:	n/a
41	chr8:100157208-100157258	LNCaP	prostate:	n/a
42	chr8:100157208-100157258	HL-60	blood:	n/a
43	chr8:100157208-100157258	Caco-2	colon:	n/a
44	chr8:100157208-100157258	NH-A	brain:	n/a
45	chr8:100104103-100104153	SK-N-SH_RA	brain:	n/a
46	chr8:100104103-100104153	Hepatocyte	liver:	n/a
47	chr8:100104103-100104153	AoSMC	blood vessel:	n/a
48	chr8:100104103-100104153	RPTEC	kidney:	n/a
49	chr8:100157208-100157258	HEK293	kidney:	embryo
50	chr8:100104103-100104153	NHDF-neo	bronchial:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:100023854..100026580-chr8:100056839..100058625,2	MCF-7	breast:
2	chr8:100067262..100071049-chr8:100071737..100074698,3	MCF-7	breast:
3	chr8:100038785..100041042-chr8:100044049..100045799,2	K562	blood:
4	chr8:100087357..100089175-chr8:100091437..100093600,2	MCF-7	breast:
5	chr8:100103552..100105106-chr8:100109674..100111736,2	K562	blood:
6	chr8:100024034..100025700-chr8:100109623..100113452,3	MCF-7	breast:
7	chr8:100012703..100016134-chr8:100151109..100154697,3	MCF-7	breast:
8	chr8:100053284..100056633-chr8:100058644..100061245,3	MCF-7	breast:
9	chr8:100025833..100028756-chr8:100100624..100103335,2	MCF-7	breast:
10	chr8:100188351..100191240-chr8:100198710..100200651,2	K562	blood:
11	chr8:100115261..100117016-chr8:100117428..100119133,2	K562	blood:
12	chr8:100050345..100052932-chr8:100053932..100056597,2	K562	blood:
13	chr8:100038785..100041042-chr8:100044049..100045799,2	K562	blood:
14	chr8:100165081..100167634-chr8:100170824..100172995,2	K562	blood:
15	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:
16	chr8:100101168..100103542-chr8:100111717..100113562,2	K562	blood:
17	chr8:100125265..100128114-chr8:100129986..100133353,3	K562	blood:
18	chr8:100187208..100189859-chr8:100191478..100193795,2	MCF-7	breast:
19	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
20	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
21	chr8:100190689..100193029-chr8:100201859..100204401,2	K562	blood:
22	chr8:100037917..100039471-chr8:101961650..101964178,2	K562	blood:
23	chr12:75667737..75668646-chr8:100070765..100071465,2	MCF-7	breast:
24	chr8:100024345..100027040-chr8:100106649..100108605,2	MCF-7	breast:
25	chr8:100130524..100132088-chr8:100135733..100138707,2	K562	blood:
26	chr8:100189672..100191957-chr8:100789803..100791931,2	MCF-7	breast:
27	chr8:100136650..100138168-chr8:100240298..100242917,2	K562	blood:
28	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:
29	chr8:100024436..100026482-chr8:100177416..100178944,2	MCF-7	breast:
30	chr8:100043126..100045218-chr8:100045409..100048093,2	K562	blood:
31	chr8:100187208..100189859-chr8:100191478..100193795,2	MCF-7	breast:
32	chr8:100144557..100146496-chr8:100147591..100149372,3	MCF-7	breast:
33	chr8:100165081..100167634-chr8:100170824..100172995,2	K562	blood:
34	chr8:100023962..100027338-chr8:100028316..100036117,10	MCF-7	breast:
35	chr8:100023165..100025763-chr8:100036969..100038746,2	K562	blood:
36	chr8:100024284..100027084-chr8:100113982..100120280,5	MCF-7	breast:
37	chr8:100034595..100037008-chr8:100041968..100045380,3	MCF-7	breast:
38	chr8:100024118..100026755-chr8:100073445..100075343,2	MCF-7	breast:
39	chr8:100162823..100164704-chr8:100167097..100169098,2	K562	blood:
40	chr8:100181985..100183886-chr8:100189568..100191594,2	MCF-7	breast:
41	chr8:100023368..100025355-chr8:100122244..100124287,2	MCF-7	breast:
42	chr8:99955457..99958039-chr8:100115422..100117482,3	MCF-7	breast:
43	chr8:100181985..100183886-chr8:100189568..100191594,2	MCF-7	breast:
44	chr8:100023955..100026746-chr8:100146269..100148393,2	K562	blood:
45	chr8:100043379..100045451-chr8:100150795..100153462,2	MCF-7	breast:
46	chr8:99677331..99680175-chr8:100027131..100030033,2	K562	blood:
47	chr8:100101168..100103542-chr8:100111717..100113562,2	K562	blood:
48	chr8:99995141..99996042-chr8:100118104..100118628,2	MCF-7	breast:
49	chr8:100024437..100026977-chr8:100039956..100042496,2	MCF-7	breast:
50	chr8:100177691..100178432-chr8:111254768..111255288,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSR2-2	chr8:100132332-100132809	ENSG00000253532.1
2	lnc-OSR2-2	chr8:100131580-100131696	ENSG00000253532.1
3	lnc-STK3-3	chr8:100103966-100104326	ENSG00000253562.1
4	lnc-STK3-3	chr8:100106157-100106288	ENSG00000253562.1

No data

Variant related genes	Relation type
VPS13B	TF binding region
ENSG00000253948	TF binding region
ENSG00000253532	TF binding region
ENSG00000253562	TF binding region
VPS13B	CpG island
ENSG00000253948	CpG island
ENSG00000253532	CpG island
ENSG00000253562	CpG island
ENSG00000253532	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000253180	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000104375	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000104361	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000164920	chromatin interactions

Extended variants
information (count: 5706 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:5706 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530060335	chr8:100028850-100028851	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs4585717	chr8:100028851-100028852	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563233877	chr8:100028854-100028855	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs189277674	chr8:100028867-100028868	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs368063995	chr8:100028883-100028884	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs199899951	chr8:100028888-100028889	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs371530938	chr8:100028889-100028890	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs551956655	chr8:100028945-100028946	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs181072081	chr8:100028954-100028955	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs78294548	chr8:100028968-100028969	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs548011324	chr8:100028971-100028972	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs567617049	chr8:100029011-100029012	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs536502333	chr8:100029037-100029038	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs556450571	chr8:100029044-100029045	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs569683349	chr8:100029108-100029109	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs539046855	chr8:100029109-100029110	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs369683759	chr8:100029112-100029113	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs558764325	chr8:100029262-100029263	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs147261873	chr8:100029270-100029271	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs141927650	chr8:100029306-100029307	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs376358390	chr8:100029307-100029308	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs114204470	chr8:100029326-100029327	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs372905300	chr8:100029406-100029407	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs554699706	chr8:100029414-100029415	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs574693503	chr8:100029427-100029428	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs543706043	chr8:100029464-100029465	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs563595623	chr8:100029518-100029519	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs72668486	chr8:100029569-100029570	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs377227327	chr8:100029584-100029585	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs372319594	chr8:100029686-100029687	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs562201674	chr8:100029724-100029725	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs545818675	chr8:100029733-100029734	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs575789378	chr8:100029734-100029735	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs528236626	chr8:100029735-100029736	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs547984055	chr8:100029755-100029756	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs111825853	chr8:100029791-100029792	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs190242087	chr8:100029814-100029815	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs550035210	chr8:100029874-100029875	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs570044751	chr8:100029877-100029878	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs181464225	chr8:100029909-100029910	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs552586158	chr8:100029910-100029911	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs201598674	chr8:100029911-100029912	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs565940205	chr8:100029914-100029915	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs185727840	chr8:100029940-100029941	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs562351662	chr8:100029967-100029968	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs555116138	chr8:100029968-100029969	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs191615538	chr8:100030047-100030048	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs574656851	chr8:100030048-100030049	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs183864337	chr8:100030116-100030117	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs577604403	chr8:100030212-100030213	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:2627 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100026200-100035400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:100026200-100036800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr8:100026200-100044000	Weak transcription	Esophagus	oesophagus
4	chr8:100026200-100047000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:100026200-100047000	Weak transcription	Gastric	stomach
6	chr8:100026200-100047200	Weak transcription	Small Intestine	intestine
7	chr8:100026200-100047600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:100026400-100029200	Weak transcription	Placenta	Placenta
9	chr8:100026400-100029400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:100026400-100030000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr8:100026400-100030800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr8:100026400-100031600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:100026400-100033800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr8:100026400-100036000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr8:100026400-100036200	Weak transcription	Psoas Muscle	Psoas
16	chr8:100026400-100036400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:100026400-100036400	Weak transcription	Brain Hippocampus Middle	brain
18	chr8:100026400-100036400	Weak transcription	Thymus	Thymus
19	chr8:100026400-100036800	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr8:100026400-100037400	Weak transcription	Stomach Mucosa	stomach
21	chr8:100026400-100039200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr8:100026400-100040600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr8:100026400-100044000	Weak transcription	Aorta	Aorta
24	chr8:100026400-100046200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr8:100026600-100030400	Weak transcription	Pancreas	Pancrea
26	chr8:100026600-100031800	Weak transcription	Brain Anterior Caudate	brain
27	chr8:100026600-100038600	Weak transcription	Left Ventricle	heart
28	chr8:100026600-100043800	Weak transcription	Spleen	Spleen
29	chr8:100026600-100047000	Weak transcription	Lung	lung
30	chr8:100026600-100083800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:100026800-100031400	Weak transcription	Fetal Muscle Trunk	muscle
32	chr8:100026800-100031600	Weak transcription	Duodenum Mucosa	Duodenum
33	chr8:100026800-100031800	Weak transcription	Fetal Heart	heart
34	chr8:100026800-100035600	Weak transcription	Brain Germinal Matrix	brain
35	chr8:100027000-100029000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr8:100027000-100029000	Weak transcription	Primary B cells from peripheral blood	blood
37	chr8:100027000-100030000	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr8:100027000-100030200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr8:100027000-100031000	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr8:100027000-100031600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr8:100027000-100031600	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr8:100027000-100031600	Weak transcription	Fetal Muscle Leg	muscle
43	chr8:100027000-100031800	Weak transcription	Liver	Liver
44	chr8:100027000-100031800	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr8:100027000-100031800	Weak transcription	Stomach Smooth Muscle	stomach
46	chr8:100027000-100031800	Weak transcription	A549	lung
47	chr8:100027000-100032200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:100027000-100032200	Weak transcription	HMEC	breast
49	chr8:100027000-100035200	Weak transcription	Brain Angular Gyrus	brain
50	chr8:100027000-100036000	Weak transcription	NHEK	skin

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