Variant report

Variant	nsv1034660
Chromosome Location	chr8:48265109-48411279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1163)
CpG islands
(count:671)
Chromatin interactive
region (count:72)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48352874-48353560	K562	blood:	n/a	chr8:48353449-48353465
2	ARID3A	chr8:48290032-48290503	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:48385021-48385529	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:48282003-48282308	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:48371417-48371596	K562	blood:	n/a	n/a
6	ARID3A	chr8:48265824-48266513	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:48281965-48282343	K562	blood:	n/a	n/a
8	ARID3A	chr8:48284765-48284924	K562	blood:	n/a	n/a
9	ARID3A	chr8:48371879-48372001	K562	blood:	n/a	n/a
10	ARID3A	chr8:48370977-48371215	K562	blood:	n/a	n/a
11	ATF1	chr8:48370999-48371277	K562	blood:	n/a	n/a
12	ATF1	chr8:48281968-48282356	K562	blood:	n/a	n/a
13	ATF1	chr8:48353062-48353371	K562	blood:	n/a	n/a
14	ATF1	chr8:48266083-48266495	K562	blood:	n/a	n/a
15	ATF2	chr8:48351620-48351896	GM12878	blood:	n/a	n/a
16	ATF2	chr8:48351488-48352019	GM12878	blood:	n/a	n/a
17	ATF3	chr8:48282010-48282221	HepG2	liver:	n/a	n/a
18	ATF3	chr8:48265721-48266444	A549	lung:	n/a	n/a
19	ATF3	chr8:48281943-48282320	HCT-116	colon:	n/a	n/a
20	ATF3	chr8:48281926-48282348	K562	blood:	n/a	n/a
21	ATF3	chr8:48265649-48266259	HCT-116	colon:	n/a	n/a
22	ATF3	chr8:48343852-48344341	K562	blood:	n/a	n/a
23	BACH1	chr8:48344301-48344555	K562	blood:	n/a	n/a
24	BATF	chr8:48351639-48351872	GM12878	blood:	n/a	n/a
25	BATF	chr8:48351608-48351855	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:48273287-48273483	GM12878	blood:	n/a	n/a
27	BCL3	chr8:48265724-48266572	A549	lung:	n/a	n/a
28	BHLHE40	chr8:48269887-48270043	K562	blood:	n/a	n/a
29	BHLHE40	chr8:48392120-48392554	K562	blood:	n/a	n/a
30	BHLHE40	chr8:48281981-48282334	K562	blood:	n/a	n/a
31	BHLHE40	chr8:48343922-48344285	K562	blood:	n/a	n/a
32	BHLHE40	chr8:48274468-48274746	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:48273214-48273476	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:48265752-48266090	HepG2	liver:	n/a	n/a
35	BHLHE40	chr8:48284752-48284905	K562	blood:	n/a	n/a
36	BRCA1	chr8:48265721-48266798	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr8:48333368-48333683	K562	blood:	n/a	n/a
38	CBX3	chr8:48366223-48366540	K562	blood:	n/a	n/a
39	CBX3	chr8:48352960-48353333	K562	blood:	n/a	n/a
40	CBX3	chr8:48265737-48266603	HCT-116	colon:	n/a	n/a
41	CBX3	chr8:48333378-48333582	K562	blood:	n/a	n/a
42	CBX3	chr8:48352862-48353396	K562	blood:	n/a	n/a
43	CBX3	chr8:48343909-48344313	K562	blood:	n/a	n/a
44	CBX3	chr8:48265593-48266657	HCT-116	colon:	n/a	n/a
45	CCNT2	chr8:48284749-48285033	K562	blood:	n/a	n/a
46	CCNT2	chr8:48282057-48282317	K562	blood:	n/a	n/a
47	CCNT2	chr8:48265875-48266439	K562	blood:	n/a	n/a
48	CEBPB	chr8:48281895-48282438	HCT-116	colon:	n/a	chr8:48282131-48282148
49	CEBPB	chr8:48265730-48266522	A549	lung:	n/a	chr8:48266294-48266311
50	CEBPB	chr8:48343966-48344317	K562	blood:	n/a	chr8:48344182-48344195

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48297271-48297321	GM12892	blood:	n/a
2	chr8:48397680-48397730	MCF10A-Er-Src	breast:	n/a
3	chr8:48343009-48343059	SK-N-MC	brain:	n/a
4	chr8:48325740-48325790	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:48297271-48297321	GM12878	blood:	n/a
6	chr8:48343009-48343059	HepG2	liver:	n/a
7	chr8:48344060-48344110	SK-N-SH_RA	brain:	n/a
8	chr8:48325740-48325790	SAEC	small airway:	n/a
9	chr8:48352024-48352074	HAEpiC	amniotic membrane:	n/a
10	chr8:48394027-48394077	NB4	blood:	n/a
11	chr8:48343009-48343059	GM12892	blood:	n/a
12	chr8:48397680-48397730	HPAEpiC	pulmonary alveolar:	n/a
13	chr8:48394027-48394077	BJ	skin:	n/a
14	chr8:48325740-48325790	HRE	kidney:	n/a
15	chr8:48394027-48394077	GM19239	blood:	n/a
16	chr8:48272891-48272941	HUVEC	blood vessel:	n/a
17	chr8:48343009-48343059	MCF-7	breast:	n/a
18	chr8:48394027-48394077	IMR90	lung:	fetal
19	chr8:48343009-48343059	HAEpiC	amniotic membrane:	n/a
20	chr8:48344060-48344110	NT2-D1	testis:	n/a
21	chr8:48352024-48352074	HRE	kidney:	n/a
22	chr8:48385636-48385686	GM12892	blood:	n/a
23	chr8:48265917-48265967	RPTEC	kidney:	n/a
24	chr8:48297271-48297321	HEEpiC	esophagus:	n/a
25	chr8:48344060-48344110	GM12891	blood:	n/a
26	chr8:48272891-48272941	AG09319	gingival:	n/a
27	chr8:48385636-48385686	SAEC	small airway:	n/a
28	chr8:48344060-48344110	MCF10A-Er-Src	breast:	n/a
29	chr8:48385636-48385686	HL-60	blood:	n/a
30	chr8:48397680-48397730	IMR90	lung:	fetal
31	chr8:48389903-48389953	HCPEpiC	choroid plexus:	n/a
32	chr8:48325740-48325790	AG10803	skin:	n/a
33	chr8:48394027-48394077	HRPEpiC	eye:	n/a
34	chr8:48397680-48397730	Jurkat	blood:	n/a
35	chr8:48344060-48344110	HRPEpiC	eye:	n/a
36	chr8:48297271-48297321	T-47D	breast:	n/a
37	chr8:48352024-48352074	HNPCEpiC	eye:	n/a
38	chr8:48394027-48394077	Jurkat	blood:	n/a
39	chr8:48389903-48389953	HNPCEpiC	eye:	n/a
40	chr8:48389903-48389953	HCF	heart:	n/a
41	chr8:48352024-48352074	SK-N-SH_RA	brain:	n/a
42	chr8:48385636-48385686	AG04450	lung:	fetal
43	chr8:48352024-48352074	HEEpiC	esophagus:	n/a
44	chr8:48325740-48325790	HIPEpiC	eye:	n/a
45	chr8:48397680-48397730	HMEC	breast:	n/a
46	chr8:48397680-48397730	HIPEpiC	eye:	n/a
47	chr8:48297271-48297321	PANC-1	pancreas:	n/a
48	chr8:48343009-48343059	PFSK-1	brain:	n/a
49	chr8:48325740-48325790	AG09309	skin:	n/a
50	chr8:48265917-48265967	HCF	heart:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:48367371..48370360-chr8:48387599..48389529,2	MCF-7	breast:
2	chr8:48391175..48393987-chr8:48395475..48396988,2	K562	blood:
3	chr8:48356855..48359120-chr8:48360293..48362250,2	K562	blood:
4	chr8:48316678..48319260-chr8:48343262..48344870,2	MCF-7	breast:
5	chr8:48337815..48339899-chr8:48341496..48344035,2	MCF-7	breast:
6	chr8:48403369..48405723-chr8:48406802..48408473,2	K562	blood:
7	chr8:48284342..48286022-chr8:48648925..48651105,2	MCF-7	breast:
8	chr8:48345796..48347342-chr8:48349198..48352084,2	MCF-7	breast:
9	chr8:48305764..48309024-chr8:53624660..53627223,3	K562	blood:
10	chr8:48296590..48299380-chr8:48299721..48303188,4	MCF-7	breast:
11	chr8:48356855..48359120-chr8:48360293..48362250,2	K562	blood:
12	chr8:48409859..48412795-chr8:48648152..48651126,2	MCF-7	breast:
13	chr8:48286201..48287772-chr8:48290885..48293117,2	MCF-7	breast:
14	chr8:48333919..48335509-chr8:48339722..48341416,2	K562	blood:
15	chr8:48276921..48279533-chr8:48290586..48293171,2	MCF-7	breast:
16	chr8:48345864..48348499-chr8:48349086..48353866,5	K562	blood:
17	chr8:48291685..48296788-chr8:48648654..48651770,5	MCF-7	breast:
18	chr8:48326655..48329493-chr8:48335487..48337638,2	K562	blood:
19	chr8:48301817..48303766-chr8:48305289..48307593,2	MCF-7	breast:
20	chr8:48289062..48291222-chr8:48292317..48294318,2	K562	blood:
21	chr8:48296378..48299348-chr8:48301045..48303894,3	K562	blood:
22	chr8:48320531..48322399-chr8:48323544..48325394,2	MCF-7	breast:
23	chr8:48287238..48289798-chr8:48645955..48647701,2	MCF-7	breast:
24	chr8:48300186..48303081-chr8:48648494..48650857,2	MCF-7	breast:
25	chr8:48296378..48299348-chr8:48301045..48303894,3	K562	blood:
26	chr8:48285193..48287244-chr8:48293396..48296107,2	K562	blood:
27	chr8:48404469..48406419-chr8:48408750..48411124,2	K562	blood:
28	chr8:48264421..48266947-chr8:48288790..48290307,2	MCF-7	breast:
29	chr6:58777113..58777667-chr8:48324823..48325324,2	MCF-7	breast:
30	chr8:48297848..48299871-chr8:48301045..48303414,2	K562	blood:
31	chr8:48342648..48346409-chr8:48649323..48652579,3	MCF-7	breast:
32	chr8:48337815..48339899-chr8:48341496..48344035,2	MCF-7	breast:
33	chr8:48297848..48299871-chr8:48301045..48303414,2	K562	blood:
34	chr8:48338641..48341078-chr8:48342654..48345157,3	K562	blood:
35	chr8:48355119..48356977-chr8:48650135..48651747,2	MCF-7	breast:
36	chr8:48274508..48277546-chr8:48285715..48288679,3	K562	blood:
37	chr8:48286201..48287772-chr8:48290885..48293117,2	MCF-7	breast:
38	chr8:48333919..48335509-chr8:48339722..48341416,2	K562	blood:
39	chr8:48270281..48272745-chr8:48274698..48276363,2	K562	blood:
40	chr8:48264373..48267024-chr8:48650520..48652799,3	MCF-7	breast:
41	chr8:48296590..48299380-chr8:48299721..48303188,4	MCF-7	breast:
42	chr8:48403369..48405723-chr8:48406802..48408473,2	K562	blood:
43	chr8:48385290..48387573-chr8:48390610..48393491,2	K562	blood:
44	chr8:48274508..48277546-chr8:48285715..48288679,3	K562	blood:
45	chr8:48352837..48354610-chr8:48358749..48360682,2	K562	blood:
46	chr8:48301817..48303766-chr8:48305289..48307593,2	MCF-7	breast:
47	chr8:48367371..48370360-chr8:48387599..48389529,2	MCF-7	breast:
48	chr8:48288492..48291157-chr8:48291634..48296219,4	MCF-7	breast:
49	chr8:48342172..48345072-chr8:48346372..48349504,3	K562	blood:
50	chr8:48282165..48284345-chr8:48648892..48650703,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-5	chr8:48300905-48301048	NONHSAT126443

No data

Variant related genes	Relation type
SPIDR	TF binding region
SPIDR	CpG island
ENSG00000023287	chromatin interactions
ENSG00000164808	chromatin interactions
ENSG00000221869	chromatin interactions

Extended variants
information (count: 5411 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:5411 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538907309	chr8:48265129-48265130	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs77095917	chr8:48265154-48265155	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs569431182	chr8:48265163-48265164	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs377162768	chr8:48265164-48265165	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs192342580	chr8:48265198-48265199	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536946354	chr8:48265246-48265247	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs16925237	chr8:48265279-48265280	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs573570090	chr8:48265290-48265291	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs13280591	chr8:48265307-48265308	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs13254303	chr8:48265308-48265309	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs117829528	chr8:48265310-48265311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552819332	chr8:48265355-48265356	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577659787	chr8:48265362-48265363	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs544041330	chr8:48265382-48265383	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs374024878	chr8:48265401-48265402	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs377672233	chr8:48265411-48265412	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs575068898	chr8:48265419-48265420	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs561133518	chr8:48265485-48265486	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542530930	chr8:48265543-48265544	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs184680739	chr8:48265603-48265604	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs142884241	chr8:48265605-48265606	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs57853552	chr8:48265620-48265621	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs397747696	chr8:48265642-48265643	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs140383570	chr8:48265664-48265665	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs143628143	chr8:48265677-48265678	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs557266480	chr8:48265705-48265706	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs565275609	chr8:48265721-48265722	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs187538376	chr8:48265773-48265774	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551045877	chr8:48265844-48265845	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs548687813	chr8:48265852-48265853	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148084455	chr8:48265869-48265870	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs536807107	chr8:48265898-48265899	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532519593	chr8:48266007-48266008	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs141845334	chr8:48266102-48266103	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs567131225	chr8:48266126-48266127	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534363215	chr8:48266170-48266171	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs565506336	chr8:48266226-48266227	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs150207609	chr8:48266230-48266231	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs138829669	chr8:48266243-48266244	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs538369501	chr8:48266267-48266268	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs10712418	chr8:48266276-48266277	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553437753	chr8:48266277-48266278	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs200184496	chr8:48266293-48266294	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143175400	chr8:48266338-48266339	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575133205	chr8:48266361-48266362	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs542393676	chr8:48266386-48266387	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs561077024	chr8:48266526-48266527	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573081296	chr8:48266532-48266533	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs552581507	chr8:48266562-48266563	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs192001814	chr8:48266580-48266581	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:2900 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48209400-48266000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr8:48228600-48265800	Weak transcription	K562	blood
3	chr8:48230400-48267400	Weak transcription	Spleen	Spleen
4	chr8:48238800-48274600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:48239000-48265800	Weak transcription	Aorta	Aorta
6	chr8:48247800-48276400	Weak transcription	Colonic Mucosa	Colon
7	chr8:48248800-48309600	Weak transcription	Thymus	Thymus
8	chr8:48249200-48265600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr8:48249200-48282000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:48249800-48266000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr8:48249800-48267200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr8:48249800-48277400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr8:48249800-48277800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr8:48253400-48267200	Weak transcription	Lung	lung
15	chr8:48253400-48274400	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr8:48253600-48273800	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr8:48254600-48268400	Weak transcription	Gastric	stomach
18	chr8:48255000-48265800	Weak transcription	Ovary	ovary
19	chr8:48256200-48274200	Weak transcription	Esophagus	oesophagus
20	chr8:48256400-48272200	Weak transcription	GM12878-XiMat	blood
21	chr8:48256400-48274200	Weak transcription	Primary T cells from cord blood	blood
22	chr8:48256400-48276200	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr8:48256400-48276800	Weak transcription	Dnd41	blood
24	chr8:48256400-48281000	Weak transcription	Primary hematopoietic stem cells	blood
25	chr8:48256600-48267400	Weak transcription	Fetal Muscle Trunk	muscle
26	chr8:48256600-48273000	Weak transcription	Primary B cells from peripheral blood	blood
27	chr8:48256800-48265800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr8:48256800-48265800	Weak transcription	Fetal Muscle Leg	muscle
29	chr8:48257000-48265800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr8:48260400-48265800	Weak transcription	HepG2	liver
31	chr8:48262400-48265200	Weak transcription	Fetal Intestine Large	intestine
32	chr8:48262400-48265400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:48262400-48265800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:48262400-48309600	Weak transcription	Fetal Stomach	stomach
35	chr8:48263200-48265800	Weak transcription	Fetal Intestine Small	intestine
36	chr8:48263200-48297200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr8:48264200-48265600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr8:48264400-48265600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:48264400-48265800	Enhancers	Osteobl	bone
40	chr8:48264400-48267000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:48264400-48276000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr8:48264600-48266200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:48264600-48266200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr8:48264600-48266200	Enhancers	Pancreas	Pancrea
45	chr8:48264800-48265200	Strong transcription	Primary B cells from cord blood	blood
46	chr8:48264800-48265400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr8:48264800-48265800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:48264800-48265800	Enhancers	Hela-S3	cervix
49	chr8:48264800-48266400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr8:48264800-48266400	Enhancers	HMEC	breast

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