Variant report

Variant	nsv831405
Chromosome Location	chr8:99095239-99260934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2640)
CpG islands
(count:2197)
Chromatin interactive
region (count:255)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2640 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:99129156-99129928	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:99132077-99132111	K562	blood:	n/a	n/a
3	ARID3A	chr8:99182441-99182445	K562	blood:	n/a	n/a
4	ATF1	chr8:99105435-99105836	K562	blood:	n/a	n/a
5	ATF1	chr8:99144765-99144965	K562	blood:	n/a	n/a
6	ATF1	chr8:99191345-99191703	K562	blood:	n/a	n/a
7	ATF1	chr8:99258083-99258400	K562	blood:	n/a	n/a
8	ATF2	chr8:99129084-99129589	GM12878	blood:	n/a	n/a
9	ATF2	chr8:99257113-99257518	GM12878	blood:	n/a	n/a
10	ATF3	chr8:99129278-99129674	H1-hESC	embryonic stem cell:	n/a	chr8:99129439-99129448
11	ATF3	chr8:99182201-99182632	A549	lung:	n/a	chr8:99182481-99182495
12	ATF3	chr8:99129367-99129553	GM12878	blood:	n/a	chr8:99129439-99129448
13	ATF3	chr8:99129217-99129742	GM12878	blood:	n/a	chr8:99129439-99129448
14	ATF3	chr8:99129159-99129767	HepG2	liver:	n/a	chr8:99129439-99129448
15	ATF3	chr8:99129286-99129659	HepG2	liver:	n/a	chr8:99129439-99129448
16	ATF3	chr8:99191475-99191677	K562	blood:	n/a	n/a
17	ATF3	chr8:99191327-99191693	K562	blood:	n/a	n/a
18	ATF3	chr8:99129209-99129736	H1-hESC	embryonic stem cell:	n/a	chr8:99129439-99129448
19	ATF3	chr8:99129281-99129619	K562	blood:	n/a	chr8:99129439-99129448
20	BACH1	chr8:99206325-99206460	K562	blood:	n/a	n/a
21	BACH1	chr8:99129108-99129639	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:99206261-99206534	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr8:99110340-99110543	GM12878	blood:	n/a	n/a
24	BATF	chr8:99198663-99198972	GM12878	blood:	n/a	n/a
25	BATF	chr8:99110333-99110625	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:99128952-99129645	GM12878	blood:	n/a	chr8:99129440-99129456
27	BHLHE40	chr8:99128997-99129612	K562	blood:	n/a	chr8:99129440-99129456
28	BHLHE40	chr8:99177573-99177675	K562	blood:	n/a	n/a
29	BHLHE40	chr8:99177011-99177136	K562	blood:	n/a	n/a
30	BHLHE40	chr8:99257202-99257637	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:99182323-99182510	K562	blood:	n/a	n/a
32	BHLHE40	chr8:99176974-99177750	HepG2	liver:	n/a	n/a
33	BHLHE40	chr8:99191439-99191623	K562	blood:	n/a	n/a
34	BHLHE40	chr8:99097929-99098118	K562	blood:	n/a	n/a
35	BHLHE40	chr8:99223787-99223904	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:99159410-99159708	K562	blood:	n/a	n/a
37	BRCA1	chr8:99129571-99129594	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr8:99129158-99129675	HepG2	liver:	n/a	n/a
39	BRCA1	chr8:99176932-99177132	HepG2	liver:	n/a	n/a
40	BRCA1	chr8:99182274-99182576	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr8:99129256-99129749	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr8:99129246-99129820	GM12878	blood:	n/a	n/a
43	BRCA1	chr8:99176137-99176155	GM12878	blood:	n/a	n/a
44	BRCA1	chr8:99097780-99098091	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr8:99105466-99105865	K562	blood:	n/a	n/a
46	CBX3	chr8:99238083-99238323	K562	blood:	n/a	n/a
47	CBX3	chr8:99129145-99129570	K562	blood:	n/a	n/a
48	CBX3	chr8:99181785-99182242	K562	blood:	n/a	n/a
49	CBX3	chr8:99238011-99238345	K562	blood:	n/a	n/a
50	CCNT2	chr8:99097917-99098202	K562	blood:	n/a	n/a

(count:2197 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99129609-99129659	SAEC	small airway:	n/a
2	chr8:99129609-99129659	SAEC	small airway:	n/a
3	chr8:99129593-99129643	NT2-D1	testis:	n/a
4	chr8:99129593-99129643	RPTEC	kidney:	n/a
5	chr8:99129593-99129643	HRPEpiC	eye:	n/a
6	chr8:99129222-99129272	PFSK-1	brain:	n/a
7	chr8:99178504-99178554	AG04449	skin:	fetal
8	chr8:99179021-99179071	U87	brain:	n/a
9	chr8:99126378-99126428	AG09319	gingival:	n/a
10	chr8:99180671-99180721	Hela-S3	cervix:	n/a
11	chr8:99224903-99224953	GM12891	blood:	n/a
12	chr8:99129593-99129643	HMEC	breast:	n/a
13	chr8:99129506-99129556	PrEC	prostate:	n/a
14	chr8:99129132-99129182	HCM	heart:	n/a
15	chr8:99180671-99180721	Jurkat	blood:	n/a
16	chr8:99129674-99129724	HL-60	blood:	n/a
17	chr8:99204880-99204930	HNPCEpiC	eye:	n/a
18	chr8:99129780-99129830	HRE	kidney:	n/a
19	chr8:99129593-99129643	HCM	heart:	n/a
20	chr8:99129780-99129830	NHBE	bronchial:	n/a
21	chr8:99129593-99129643	NB4	blood:	n/a
22	chr8:99130000-99130050	HL-60	blood:	n/a
23	chr8:99182490-99182540	U87	brain:	n/a
24	chr8:99224903-99224953	HCM	heart:	n/a
25	chr8:99129939-99129989	NT2-D1	testis:	n/a
26	chr8:99129132-99129182	Hepatocyte	liver:	n/a
27	chr8:99204880-99204930	HL-60	blood:	n/a
28	chr8:99178504-99178554	HRPEpiC	eye:	n/a
29	chr8:99129480-99129530	AG09319	gingival:	n/a
30	chr8:99129780-99129830	AG09309	skin:	n/a
31	chr8:99129925-99129975	GM12892	blood:	n/a
32	chr8:99129495-99129545	A549	lung:	n/a
33	chr8:99129291-99129341	SK-N-MC	brain:	n/a
34	chr8:99224903-99224953	HL-60	blood:	n/a
35	chr8:99129570-99129620	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:99130997-99131047	NB4	blood:	n/a
37	chr8:99130171-99130221	HL-60	blood:	n/a
38	chr8:99182441-99182491	HAEpiC	amniotic membrane:	n/a
39	chr8:99197040-99197090	H1-hESC	embryonic stem cell:	embryo
40	chr8:99129609-99129659	HEK293	kidney:	embryo
41	chr8:99129483-99129533	HUVEC	blood vessel:	n/a
42	chr8:99129132-99129182	NB4	blood:	n/a
43	chr8:99129518-99129568	HCM	heart:	n/a
44	chr8:99129222-99129272	HCPEpiC	choroid plexus:	n/a
45	chr8:99129593-99129643	PFSK-1	brain:	n/a
46	chr8:99224903-99224953	AG09319	gingival:	n/a
47	chr8:99258458-99258508	SAEC	small airway:	n/a
48	chr8:99180671-99180721	SK-N-SH	brain:	n/a
49	chr8:99129319-99129369	PrEC	prostate:	n/a
50	chr8:99224903-99224953	LNCaP	prostate:	n/a

(count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr8:99256959..99259667-chr8:99271247..99273915,3	MCF-7	breast:
2	chr8:99158558..99161122-chr8:99163037..99164574,2	MCF-7	breast:
3	chr8:99056253..99058055-chr8:99098038..99100996,2	K562	blood:
4	chr8:99174475..99186560-chr8:99297606..99308680,30	MCF-7	breast:
5	chr8:99146057..99148712-chr8:99151665..99153311,2	K562	blood:
6	chr8:99100601..99102222-chr8:99121756..99123505,2	MCF-7	breast:
7	chr8:99101375..99102935-chr8:99104912..99106463,2	K562	blood:
8	chr8:99171342..99172879-chr8:99955302..99957653,2	MCF-7	breast:
9	chr8:99223225..99225357-chr8:99305724..99307688,2	MCF-7	breast:
10	chr8:99172109..99174508-chr8:99178089..99181057,2	MCF-7	breast:
11	chr8:99255307..99258219-chr8:99258829..99262487,4	MCF-7	breast:
12	chr8:98879754..98881586-chr8:99098019..99100766,2	MCF-7	breast:
13	chr8:99171418..99173232-chr8:99174336..99176879,3	MCF-7	breast:
14	chr15:45315200..45316078-chr8:99129092..99129835,2	Hela-S3	cervix:
15	chr8:99252888..99255324-chr8:99266845..99268571,2	MCF-7	breast:
16	chr8:99128111..99130508-chr8:99140081..99143109,3	MCF-7	breast:
17	chr8:99189856..99193042-chr8:99195160..99197940,6	MCF-7	breast:
18	chr8:99191065..99193219-chr8:99216511..99219425,2	MCF-7	breast:
19	chr8:99182957..99185406-chr8:99368806..99370726,2	MCF-7	breast:
20	chr8:99177794..99180485-chr8:99476278..99478549,2	MCF-7	breast:
21	chr8:99253906..99256435-chr8:99304423..99307392,3	MCF-7	breast:
22	chr8:99260188..99262511-chr8:99265064..99267419,2	MCF-7	breast:
23	chr8:99114180..99116016-chr8:99124047..99126036,2	MCF-7	breast:
24	chr8:99231424..99232978-chr8:99255966..99257992,2	MCF-7	breast:
25	chr8:99057013..99059186-chr8:99120640..99122350,2	K562	blood:
26	chr8:99114206..99122182-chr8:99125725..99131082,14	MCF-7	breast:
27	chr8:99182015..99182842-chr8:99306372..99307100,3	MCF-7	breast:
28	chr8:99091170..99093628-chr8:99095565..99098052,2	K562	blood:
29	chr8:99157530..99160123-chr8:99161271..99164401,3	K562	blood:
30	chr8:99182184..99183318-chr8:99389877..99390743,4	MCF-7	breast:
31	chr8:99219727..99222711-chr8:99229918..99232191,2	MCF-7	breast:
32	chr8:99105894..99107758-chr8:99108714..99111067,2	MCF-7	breast:
33	chr8:99051546..99054747-chr8:99096963..99099980,5	MCF-7	breast:
34	chr8:99219935..99221824-chr8:99271736..99273785,2	MCF-7	breast:
35	chr8:99133667..99135899-chr8:99139871..99141539,2	K562	blood:
36	chr8:99104954..99107804-chr8:99110176..99112228,2	K562	blood:
37	chr8:99105894..99107758-chr8:99108714..99111067,2	MCF-7	breast:
38	chr8:99114868..99117757-chr8:99127759..99130747,2	MCF-7	breast:
39	chr8:99175652..99177046-chr8:99483003..99483808,7	K562	blood:
40	chr8:99177532..99181661-chr8:99182236..99184964,3	K562	blood:
41	chr8:99146057..99148712-chr8:99151665..99153311,2	K562	blood:
42	chr8:99247388..99250168-chr8:99250912..99253413,3	MCF-7	breast:
43	chr8:99181532..99184005-chr8:99338656..99341570,2	MCF-7	breast:
44	chr8:99177811..99179869-chr8:99182008..99183680,2	MCF-7	breast:
45	chr8:99212561..99215208-chr8:99218672..99220234,2	MCF-7	breast:
46	chr8:99230131..99233342-chr8:99304674..99307407,4	MCF-7	breast:
47	chr8:99181961..99182936-chr8:99483152..99483998,5	MCF-7	breast:
48	chr8:99164069..99166497-chr8:99168645..99171044,2	K562	blood:
49	chr8:99184801..99187794-chr8:99204671..99207468,2	MCF-7	breast:
50	chr8:99132071..99133669-chr8:99144692..99146393,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf47-1	chr8:99111578-99112805	NONHSAT127909
2	lnc-POP1-2	chr8:99173307-99173985	NONHSAT127912
3	lnc-POP1-1	chr8:99192050-99192272	XLOC_006879
4	lnc-POP1-1	chr8:99188751-99189136	XLOC_006879
5	lnc-POP1-1	chr8:99192061-99192272	NONHSAT127914
6	lnc-POP1-1	chr8:99192822-99192898	NONHSAT127914

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HRSP12	hsa-miR-375	chr8:99114622-99114643

Variant related genes	Relation type
POP1	TF binding region
RNU6-914P	TF binding region
NIPAL2	TF binding region
HRSP12	TF binding region
POP1	CpG island
RNU6-914P	CpG island
NIPAL2	CpG island
HRSP12	CpG island
ENSG00000185278	chromatin interactions
ENSG00000048544	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000252558	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000132541	chromatin interactions
ENSG00000104356	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000196290	chromatin interactions
ENSG00000140577	chromatin interactions
ENSG00000156482	chromatin interactions
ENSG00000140263	chromatin interactions
ENSG00000207067	chromatin interactions
ENSG00000132561	chromatin interactions
ENSG00000245970	chromatin interactions
ENSG00000240344	chromatin interactions
ENSG00000147649	chromatin interactions
ENSG00000104361	chromatin interactions
ENSG00000104341	chromatin interactions
ENSG00000268707	chromatin interactions
ENSG00000177954	chromatin interactions
ENSG00000152102	chromatin interactions
COMMD2	miRNA target sites
COPS2	miRNA target sites

Extended variants
information (count: 6352 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:6352 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555495164	chr8:99095287-99095288	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs575524657	chr8:99095347-99095348	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs183626890	chr8:99095369-99095370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563799572	chr8:99095374-99095375	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375188973	chr8:99095427-99095428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs118173241	chr8:99095468-99095469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs559793679	chr8:99095502-99095503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528736419	chr8:99095510-99095511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561773511	chr8:99095548-99095549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548610688	chr8:99095580-99095581	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568282703	chr8:99095581-99095582	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs367771904	chr8:99095597-99095598	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531033402	chr8:99095653-99095654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371307211	chr8:99095656-99095657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570251476	chr8:99095668-99095669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539057522	chr8:99095678-99095679	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371489093	chr8:99095689-99095690	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188552706	chr8:99095794-99095795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146257564	chr8:99095807-99095808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535707113	chr8:99095832-99095833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs374945438	chr8:99095835-99095836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555720262	chr8:99095845-99095846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575944732	chr8:99095938-99095939	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192398275	chr8:99095960-99095961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139309238	chr8:99095972-99095973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184816373	chr8:99095983-99095984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188007267	chr8:99096009-99096010	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559659371	chr8:99096022-99096023	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs117227181	chr8:99096025-99096026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs80216536	chr8:99096037-99096038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs55648132	chr8:99096102-99096103	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs546844801	chr8:99096110-99096111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs376944668	chr8:99096132-99096133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs191376790	chr8:99096149-99096150	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs55724151	chr8:99096210-99096211	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs144295164	chr8:99096243-99096244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529044959	chr8:99096257-99096258	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112225338	chr8:99096281-99096282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373081634	chr8:99096282-99096283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs11298792	chr8:99096297-99096298	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs2444863	chr8:99096303-99096304	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs546391144	chr8:99096313-99096314	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566434834	chr8:99096326-99096327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs535132053	chr8:99096366-99096367	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs183817588	chr8:99096368-99096369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569212793	chr8:99096384-99096385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs80042806	chr8:99096459-99096460	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77827946	chr8:99096484-99096485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs189894681	chr8:99096588-99096589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79176049	chr8:99096593-99096594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Malignant melanoma	17260012	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	19455253	CNVD
Gastric cancer	22014070	CNVD
Sezary syndrome	18413736	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:3533 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99091200-99098200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:99092600-99098000	Weak transcription	Pancreas	Pancrea
3	chr8:99092600-99124400	Weak transcription	Gastric	stomach
4	chr8:99093000-99097600	Weak transcription	Stomach Mucosa	stomach
5	chr8:99093400-99100800	Weak transcription	Right Atrium	heart
6	chr8:99097400-99097600	Enhancers	A549	lung
7	chr8:99097600-99098000	Active TSS	Rectal Mucosa Donor 31	rectum
8	chr8:99097600-99098000	Enhancers	Stomach Mucosa	stomach
9	chr8:99097600-99098000	Active TSS	HepG2	liver
10	chr8:99097600-99098200	Enhancers	Colonic Mucosa	Colon
11	chr8:99097600-99098200	Enhancers	Hela-S3	cervix
12	chr8:99097600-99098400	Flanking Active TSS	A549	lung
13	chr8:99097800-99098200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
14	chr8:99097800-99098200	Enhancers	Brain Hippocampus Middle	brain
15	chr8:99098000-99098200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:99098000-99098200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:99098000-99098200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
18	chr8:99098000-99098200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr8:99098000-99098200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:99098000-99098200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:99098000-99098200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:99098000-99098200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr8:99098000-99098200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
24	chr8:99098000-99098200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr8:99098000-99098200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
26	chr8:99098000-99098200	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr8:99098000-99098200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:99098000-99098200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:99098000-99098200	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
30	chr8:99098000-99098200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr8:99098000-99098200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:99098000-99098200	Enhancers	Adipose Nuclei	Adipose
33	chr8:99098000-99098200	Enhancers	Liver	Liver
34	chr8:99098000-99098200	Enhancers	Brain Angular Gyrus	brain
35	chr8:99098000-99098200	Enhancers	Brain Substantia Nigra	brain
36	chr8:99098000-99098200	Enhancers	Fetal Kidney	kidney
37	chr8:99098000-99098200	Enhancers	Left Ventricle	heart
38	chr8:99098000-99098200	Enhancers	Pancreas	Pancrea
39	chr8:99098000-99098200	Enhancers	Psoas Muscle	Psoas
40	chr8:99098000-99098200	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
41	chr8:99098000-99098200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
42	chr8:99098000-99098200	Flanking Active TSS	Stomach Mucosa	stomach
43	chr8:99098000-99098200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
44	chr8:99098000-99098200	Flanking Active TSS	HepG2	liver
45	chr8:99098000-99098200	Flanking Bivalent TSS/Enh	HSMM	muscle
46	chr8:99098000-99098200	Enhancers	K562	blood
47	chr8:99098000-99098200	Flanking Active TSS	NH-A	brain
48	chr8:99098000-99098200	Flanking Active TSS	NHDF-Ad	bronchial
49	chr8:99098000-99098200	Enhancers	NHEK	skin
50	chr8:99098000-99098200	Enhancers	Osteobl	bone

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