Variant report

Variant	nsv610172
Chromosome Location	chr8:8313010-8362710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:183)
Chromatin interactive
region (count:27)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8314706-8315018	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8324363-8325247	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8318936-8319027	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:8340777-8341233	HepG2	liver:	n/a	n/a
5	ATF2	chr8:8353476-8354189	GM12878	blood:	n/a	n/a
6	ATF2	chr8:8350336-8351041	GM12878	blood:	n/a	n/a
7	ATF2	chr8:8324529-8324992	GM12878	blood:	n/a	n/a
8	ATF2	chr8:8353515-8354183	GM12878	blood:	n/a	n/a
9	ATF2	chr8:8350224-8351026	GM12878	blood:	n/a	n/a
10	ATF2	chr8:8344838-8345446	GM12878	blood:	n/a	n/a
11	ATF2	chr8:8324550-8324879	GM12878	blood:	n/a	n/a
12	BACH1	chr8:8313375-8313563	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr8:8353652-8354011	GM12878	blood:	n/a	chr8:8353733-8353742
14	BATF	chr8:8353637-8354083	GM12878	blood:	n/a	chr8:8353733-8353742
15	BATF	chr8:8350565-8350887	GM12878	blood:	n/a	n/a
16	BATF	chr8:8341003-8341212	GM12878	blood:	n/a	n/a
17	BATF	chr8:8345103-8345453	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:8353657-8354012	GM12878	blood:	n/a	chr8:8353725-8353734
19	BCL11A	chr8:8353622-8354069	GM12878	blood:	n/a	chr8:8353725-8353734
20	BCL3	chr8:8353689-8353967	GM12878	blood:	n/a	chr8:8353725-8353734
21	BCL3	chr8:8353620-8353935	GM12878	blood:	n/a	chr8:8353725-8353734
22	BCL3	chr8:8340375-8341335	A549	lung:	n/a	chr8:8340757-8340766 chr8:8340756-8340765
23	BCLAF1	chr8:8353668-8354188	GM12878	blood:	n/a	chr8:8353725-8353734
24	BCLAF1	chr8:8350255-8351074	GM12878	blood:	n/a	n/a
25	BCLAF1	chr8:8353515-8354310	GM12878	blood:	n/a	chr8:8353725-8353734
26	BHLHE40	chr8:8313428-8313566	A549	lung:	n/a	n/a
27	BHLHE40	chr8:8313440-8313517	K562	blood:	n/a	n/a
28	BHLHE40	chr8:8350545-8350910	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:8324440-8325002	HepG2	liver:	n/a	n/a
30	BHLHE40	chr8:8353598-8354014	GM12878	blood:	n/a	n/a
31	BRCA1	chr8:8313642-8313649	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:8324596-8325001	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:8336696-8336860	HepG2	liver:	n/a	n/a
34	CEBPB	chr8:8340206-8340971	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr8:8340683-8341263	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:8313408-8313951	A549	lung:	n/a	chr8:8313825-8313836
37	CEBPB	chr8:8360168-8360478	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:8360304-8360309	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr8:8356588-8356980	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:8340230-8340969	A549	lung:	n/a	n/a
41	CEBPB	chr8:8313772-8313879	H1-hESC	embryonic stem cell:	n/a	chr8:8313825-8313836
42	CEBPB	chr8:8356667-8357000	A549	lung:	n/a	n/a
43	CEBPB	chr8:8356631-8356905	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr8:8313367-8313677	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:8360238-8360336	IMR90	lung:	n/a	n/a
46	CEBPB	chr8:8344231-8344352	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:8340499-8341024	A549	lung:	n/a	n/a
48	CEBPB	chr8:8340194-8341265	IMR90	lung:	n/a	n/a
49	CEBPB	chr8:8353492-8354133	GM12878	blood:	n/a	n/a
50	CEBPB	chr8:8344217-8344342	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8318774-8318824	Hepatocyte	liver:	n/a
2	chr8:8341955-8342005	HCF	heart:	n/a
3	chr8:8318774-8318824	U87	brain:	n/a
4	chr8:8313504-8313554	HAEpiC	amniotic membrane:	n/a
5	chr8:8313504-8313554	HEEpiC	esophagus:	n/a
6	chr8:8318774-8318824	AG09309	skin:	n/a
7	chr8:8318774-8318824	MCF10A-Er-Src	breast:	n/a
8	chr8:8341955-8342005	H1-hESC	embryonic stem cell:	embryo
9	chr8:8318774-8318824	HNPCEpiC	eye:	n/a
10	chr8:8318774-8318824	AG04449	skin:	fetal
11	chr8:8341955-8342005	BJ	skin:	n/a
12	chr8:8341955-8342005	HCPEpiC	choroid plexus:	n/a
13	chr8:8313504-8313554	HRE	kidney:	n/a
14	chr8:8341955-8342005	HRPEpiC	eye:	n/a
15	chr8:8313504-8313554	NH-A	brain:	n/a
16	chr8:8341955-8342005	PANC-1	pancreas:	n/a
17	chr8:8341955-8342005	NH-A	brain:	n/a
18	chr8:8341955-8342005	AG04450	lung:	fetal
19	chr8:8341955-8342005	HRCEpiC	kidney:	n/a
20	chr8:8318774-8318824	SK-N-MC	brain:	n/a
21	chr8:8313504-8313554	NT2-D1	testis:	n/a
22	chr8:8318774-8318824	GM12878	blood:	n/a
23	chr8:8318774-8318824	HIPEpiC	eye:	n/a
24	chr8:8313504-8313554	CMK	blood:	n/a
25	chr8:8341955-8342005	LNCaP	prostate:	n/a
26	chr8:8313504-8313554	NB4	blood:	n/a
27	chr8:8341955-8342005	NB4	blood:	n/a
28	chr8:8341955-8342005	AG10803	skin:	n/a
29	chr8:8341955-8342005	A549	lung:	n/a
30	chr8:8318774-8318824	SAEC	small airway:	n/a
31	chr8:8313504-8313554	AG04449	skin:	fetal
32	chr8:8313504-8313554	HIPEpiC	eye:	n/a
33	chr8:8313504-8313554	SK-N-MC	brain:	n/a
34	chr8:8318774-8318824	Hela-S3	cervix:	n/a
35	chr8:8341955-8342005	PFSK-1	brain:	n/a
36	chr8:8313504-8313554	GM12891	blood:	n/a
37	chr8:8313504-8313554	GM19239	blood:	n/a
38	chr8:8313504-8313554	HL-60	blood:	n/a
39	chr8:8341955-8342005	HIPEpiC	eye:	n/a
40	chr8:8313504-8313554	HRCEpiC	kidney:	n/a
41	chr8:8318774-8318824	GM12891	blood:	n/a
42	chr8:8341955-8342005	GM06990	blood:	n/a
43	chr8:8341955-8342005	HAEpiC	amniotic membrane:	n/a
44	chr8:8341955-8342005	HEK293	kidney:	embryo
45	chr8:8313504-8313554	HCT-116	colon:	n/a
46	chr8:8341955-8342005	ECC-1	luminal epithelium:	n/a
47	chr8:8318774-8318824	BE2_C	brain:	n/a
48	chr8:8341955-8342005	Hepatocyte	liver:	n/a
49	chr8:8341955-8342005	SKMC	muscle:	n/a
50	chr8:8313504-8313554	IMR90	lung:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8237866..8240823-chr8:8310722..8313327,2	MCF-7	breast:
2	chr8:8241927..8245169-chr8:8316549..8319625,5	MCF-7	breast:
3	chr8:8241777..8245267-chr8:8311182..8314962,7	MCF-7	breast:
4	chr8:8307359..8308990-chr8:8310543..8313387,3	MCF-7	breast:
5	chr8:8241273..8244866-chr8:8311320..8315481,8	MCF-7	breast:
6	chr8:8242477..8244553-chr8:8320092..8324260,3	MCF-7	breast:
7	chr8:8361888..8365563-chr8:8365721..8369530,3	MCF-7	breast:
8	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
9	chr8:8317671..8320936-chr8:8323021..8325939,5	MCF-7	breast:
10	chr8:8145200..8147453-chr8:8312155..8314860,2	MCF-7	breast:
11	chr8:8234038..8235691-chr8:8350629..8352175,2	MCF-7	breast:
12	chr8:8317400..8319199-chr8:8344944..8347907,2	MCF-7	breast:
13	chr8:8298645..8300548-chr8:8312022..8313794,2	MCF-7	breast:
14	chr8:8174141..8174643-chr8:8351385..8352080,2	K562	blood:
15	chr8:8308652..8310168-chr8:8314593..8316228,2	MCF-7	breast:
16	chr8:8353865..8355858-chr8:8364054..8366551,2	MCF-7	breast:
17	chr8:8242160..8245521-chr8:8318713..8321604,3	MCF-7	breast:
18	chr8:8360593..8362443-chr8:8363816..8365760,2	K562	blood:
19	chr8:8310535..8312786-chr8:8315430..8317371,2	MCF-7	breast:
20	chr8:8147966..8148515-chr8:8336160..8336710,2	MCF-7	breast:
21	chr8:8346656..8348719-chr8:8355280..8357515,2	K562	blood:
22	chr8:8312145..8315725-chr8:8317532..8320911,6	MCF-7	breast:
23	chr8:8311665..8315626-chr8:8317447..8320934,9	MCF-7	breast:
24	chr8:8317141..8321564-chr8:8323708..8327409,4	MCF-7	breast:
25	chr8:8346656..8348719-chr8:8355280..8357515,2	K562	blood:
26	chr8:8336166..8336977-chr8:8365242..8366154,6	MCF-7	breast:
27	chr8:8336166..8336956-chr8:8365242..8366153,3	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-2	chr8:8314419-8314592	ENSG00000254153
2	lnc-PRAGMIN.1-2	chr8:8318630-8318847	ENSG00000254153
3	lnc-PRAGMIN.1-8	chr8:8327533-8327591	NONHSAT124876
4	lnc-PRAGMIN.1-8	chr8:8344925-8345359	NONHSAT124876
5	lnc-PRAGMIN.1-8	chr8:8340447-8340532	NONHSAT124876
6	lnc-AC068020.1-4	chr8:8322957-8323060	NONHSAT124875
7	lnc-AC068020.1-4	chr8:8328275-8328408	NONHSAT124875
8	lnc-PRAGMIN.1-2	chr8:8315919-8316036	ENSG00000254153

No data

Variant related genes	Relation type
ENSG00000254153	TF binding region
ENSG00000254153	CpG island
ENSG00000254153	chromatin interactions
ENSG00000182319	chromatin interactions

Extended variants
information (count: 2555 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:2555 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2976871	chr8:8313010-8313011	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375136922	chr8:8313012-8313013	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs193159730	chr8:8313057-8313058	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs145791570	chr8:8313058-8313059	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs538398333	chr8:8313071-8313072	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs558342327	chr8:8313097-8313098	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2979177	chr8:8313112-8313113	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs184433042	chr8:8313121-8313122	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141648404	chr8:8313122-8313123	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs189536410	chr8:8313132-8313133	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs373060666	chr8:8313179-8313180	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs74318068	chr8:8313206-8313207	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560814881	chr8:8313225-8313226	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs563631553	chr8:8313229-8313230	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532862276	chr8:8313235-8313236	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs370800446	chr8:8313236-8313237	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs181842565	chr8:8313243-8313244	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs75397268	chr8:8313256-8313257	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs377381138	chr8:8313263-8313264	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs73186407	chr8:8313266-8313267	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs527726279	chr8:8313271-8313272	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs61323486	chr8:8313286-8313287	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs566390304	chr8:8313306-8313307	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs372689642	chr8:8313317-8313318	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs2921069	chr8:8313320-8313321	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs116307497	chr8:8313330-8313331	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561132206	chr8:8313341-8313342	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568985268	chr8:8313348-8313349	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs367634246	chr8:8313358-8313359	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs554410533	chr8:8313449-8313450	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs138379672	chr8:8313453-8313454	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs143862156	chr8:8313455-8313456	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs553815871	chr8:8313458-8313459	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577583702	chr8:8313492-8313493	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs546544290	chr8:8313504-8313505	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs143236467	chr8:8313545-8313546	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs148284188	chr8:8313568-8313569	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542306204	chr8:8313572-8313573	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561993420	chr8:8313591-8313592	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375827430	chr8:8313592-8313593	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183954144	chr8:8313637-8313638	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs547354288	chr8:8313654-8313655	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568642784	chr8:8313658-8313659	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs564162049	chr8:8313659-8313660	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2976872	chr8:8313662-8313663	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs552224167	chr8:8313669-8313670	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs569027330	chr8:8313687-8313688	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs112561108	chr8:8313702-8313703	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs115538284	chr8:8313703-8313704	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375254306	chr8:8313740-8313741	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8309000-8313200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr8:8310800-8313400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr8:8311000-8313400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr8:8311000-8313400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr8:8311000-8313400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr8:8311000-8313400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:8311000-8313600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:8311000-8318600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr8:8312200-8314000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:8312200-8314000	Enhancers	Esophagus	oesophagus
11	chr8:8312200-8314000	Enhancers	Placenta	Placenta
12	chr8:8312200-8321000	Enhancers	Placenta Amnion	Placenta Amnion
13	chr8:8312400-8313400	Enhancers	Pancreas	Pancrea
14	chr8:8312400-8313800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:8312400-8316000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:8312800-8313200	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr8:8312800-8313400	Enhancers	Fetal Intestine Small	intestine
18	chr8:8312800-8313400	Enhancers	A549	lung
19	chr8:8312800-8313400	Enhancers	Hela-S3	cervix
20	chr8:8313000-8313400	Enhancers	Stomach Mucosa	stomach
21	chr8:8313000-8313400	Enhancers	HSMMtube	muscle
22	chr8:8313000-8313600	Enhancers	Fetal Intestine Large	intestine
23	chr8:8313000-8314200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr8:8313000-8314400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:8313000-8315600	Enhancers	HepG2	liver
26	chr8:8313200-8313400	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:8313200-8313400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:8313200-8313400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr8:8313200-8313400	Enhancers	Lung	lung
30	chr8:8313200-8313400	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr8:8313200-8313400	Enhancers	HSMM	muscle
32	chr8:8313200-8313800	Active TSS	Colonic Mucosa	Colon
33	chr8:8313200-8313800	Enhancers	NH-A	brain
34	chr8:8313200-8314000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:8313200-8314000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr8:8313200-8314000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:8313200-8314000	Enhancers	Duodenum Mucosa	Duodenum
38	chr8:8313200-8314000	Enhancers	Fetal Muscle Trunk	muscle
39	chr8:8313200-8314000	Enhancers	Fetal Muscle Leg	muscle
40	chr8:8313200-8314000	Enhancers	Gastric	stomach
41	chr8:8313200-8314000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
42	chr8:8313200-8314000	Enhancers	Osteobl	bone
43	chr8:8313200-8314200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr8:8313200-8314200	Enhancers	HMEC	breast
45	chr8:8313200-8314400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:8313200-8315200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:8313200-8316200	Enhancers	NHEK	skin
48	chr8:8313400-8313600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr8:8313400-8313600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr8:8313400-8313800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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