Variant report

Variant	nsv1024785
Chromosome Location	chr8:8102513-8145999
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1544)
CpG islands
(count:122)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1544 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8111412-8112067	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8126032-8126609	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8127880-8128214	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:8130676-8131061	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:8145751-8146493	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:8105314-8105669	K562	blood:	n/a	n/a
7	ARID3A	chr8:8105348-8105599	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:8102923-8103018	K562	blood:	n/a	n/a
9	ARID3A	chr8:8127158-8127358	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:8114109-8114421	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:8136392-8136433	K562	blood:	n/a	n/a
12	ATF1	chr8:8118490-8118523	K562	blood:	n/a	n/a
13	ATF1	chr8:8144090-8144415	K562	blood:	n/a	n/a
14	ATF2	chr8:8126192-8126618	GM12878	blood:	n/a	n/a
15	ATF2	chr8:8126203-8126652	GM12878	blood:	n/a	n/a
16	ATF2	chr8:8141766-8142478	GM12878	blood:	n/a	n/a
17	ATF2	chr8:8141903-8142578	GM12878	blood:	n/a	n/a
18	ATF2	chr8:8143907-8144515	GM12878	blood:	n/a	n/a
19	ATF2	chr8:8136646-8137350	GM12878	blood:	n/a	n/a
20	ATF2	chr8:8143978-8144540	GM12878	blood:	n/a	n/a
21	ATF3	chr8:8145708-8146540	HCT-116	colon:	n/a	n/a
22	ATF3	chr8:8145665-8146549	A549	lung:	n/a	n/a
23	ATF3	chr8:8145720-8146548	HCT-116	colon:	n/a	n/a
24	ATF3	chr8:8127796-8128282	A549	lung:	n/a	n/a
25	ATF3	chr8:8145728-8146513	A549	lung:	n/a	n/a
26	BACH1	chr8:8130683-8130937	K562	blood:	n/a	n/a
27	BATF	chr8:8144007-8144450	GM12878	blood:	n/a	n/a
28	BATF	chr8:8144052-8144469	GM12878	blood:	n/a	n/a
29	BATF	chr8:8143398-8143620	GM12878	blood:	n/a	n/a
30	BATF	chr8:8126297-8126540	GM12878	blood:	n/a	chr8:8126405-8126416 chr8:8126421-8126431 chr8:8126417-8126427 chr8:8126420-8126431
31	BATF	chr8:8143371-8143632	GM12878	blood:	n/a	n/a
32	BATF	chr8:8136381-8136667	GM12878	blood:	n/a	n/a
33	BATF	chr8:8126185-8126638	GM12878	blood:	n/a	chr8:8126405-8126416 chr8:8126421-8126431 chr8:8126417-8126427 chr8:8126420-8126431
34	BATF	chr8:8130779-8131070	GM12878	blood:	n/a	n/a
35	BATF	chr8:8137532-8137784	GM12878	blood:	n/a	chr8:8137667-8137678 chr8:8137668-8137678
36	BATF	chr8:8141982-8142461	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:8144077-8144391	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:8136385-8136641	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:8142010-8142463	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:8144033-8144432	GM12878	blood:	n/a	n/a
41	BCL3	chr8:8127769-8128486	A549	lung:	n/a	n/a
42	BCL3	chr8:8127696-8128351	A549	lung:	n/a	n/a
43	BCL3	chr8:8145664-8146564	A549	lung:	n/a	n/a
44	BCL3	chr8:8145650-8146916	A549	lung:	n/a	n/a
45	BCLAF1	chr8:8141823-8142384	GM12878	blood:	n/a	n/a
46	BCLAF1	chr8:8136696-8137250	GM12878	blood:	n/a	n/a
47	BCLAF1	chr8:8140921-8141875	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:8130628-8131229	GM12878	blood:	n/a	n/a
49	BCLAF1	chr8:8143968-8144493	GM12878	blood:	n/a	n/a
50	BCLAF1	chr8:8141893-8142602	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8120624-8120674	A549	lung:	n/a
2	chr8:8120624-8120674	SAEC	small airway:	n/a
3	chr8:8131077-8131127	PANC-1	pancreas:	n/a
4	chr8:8120624-8120674	NHDF-neo	bronchial:	n/a
5	chr8:8120624-8120674	LNCaP	prostate:	n/a
6	chr8:8120624-8120674	AG09319	gingival:	n/a
7	chr8:8131077-8131127	AG10803	skin:	n/a
8	chr8:8120624-8120674	ovcar-3	ovarian:	n/a
9	chr8:8131077-8131127	Hepatocyte	liver:	n/a
10	chr8:8120624-8120674	NHBE	bronchial:	n/a
11	chr8:8131077-8131127	RPTEC	kidney:	n/a
12	chr8:8120624-8120674	Caco-2	colon:	n/a
13	chr8:8131077-8131127	PrEC	prostate:	n/a
14	chr8:8120624-8120674	Hela-S3	cervix:	n/a
15	chr8:8131077-8131127	CMK	blood:	n/a
16	chr8:8131077-8131127	AG09319	gingival:	n/a
17	chr8:8120624-8120674	AG04449	skin:	fetal
18	chr8:8120624-8120674	GM12878	blood:	n/a
19	chr8:8120624-8120674	PANC-1	pancreas:	n/a
20	chr8:8131077-8131127	NB4	blood:	n/a
21	chr8:8131077-8131127	GM06990	blood:	n/a
22	chr8:8131077-8131127	HNPCEpiC	eye:	n/a
23	chr8:8120624-8120674	PFSK-1	brain:	n/a
24	chr8:8120624-8120674	HCT-116	colon:	n/a
25	chr8:8120624-8120674	AG04450	lung:	fetal
26	chr8:8120624-8120674	Hepatocyte	liver:	n/a
27	chr8:8120624-8120674	HNPCEpiC	eye:	n/a
28	chr8:8120624-8120674	HUVEC	blood vessel:	n/a
29	chr8:8120624-8120674	Jurkat	blood:	n/a
30	chr8:8131077-8131127	Hela-S3	cervix:	n/a
31	chr8:8120624-8120674	SK-N-MC	brain:	n/a
32	chr8:8120624-8120674	HRCEpiC	kidney:	n/a
33	chr8:8131077-8131127	SK-N-SH_RA	brain:	n/a
34	chr8:8131077-8131127	HCPEpiC	choroid plexus:	n/a
35	chr8:8120624-8120674	AG09309	skin:	n/a
36	chr8:8131077-8131127	HRPEpiC	eye:	n/a
37	chr8:8131077-8131127	ECC-1	luminal epithelium:	n/a
38	chr8:8120624-8120674	HEK293	kidney:	embryo
39	chr8:8131077-8131127	ProgFib	skin:	n/a
40	chr8:8120624-8120674	HL-60	blood:	n/a
41	chr8:8131077-8131127	ovcar-3	ovarian:	n/a
42	chr8:8131077-8131127	PFSK-1	brain:	n/a
43	chr8:8120624-8120674	HCM	heart:	n/a
44	chr8:8120624-8120674	AoSMC	blood vessel:	n/a
45	chr8:8120624-8120674	HIPEpiC	eye:	n/a
46	chr8:8120624-8120674	U87	brain:	n/a
47	chr8:8131077-8131127	HRE	kidney:	n/a
48	chr8:8120624-8120674	K562	blood:	n/a
49	chr8:8131077-8131127	GM19239	blood:	n/a
50	chr8:8131077-8131127	AG09309	skin:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8138288..8140321-chr8:8142532..8144155,2	MCF-7	breast:
2	chr8:8125550..8129443-chr8:8243752..8245349,3	MCF-7	breast:
3	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
4	chr8:8101610..8104279-chr8:8111391..8114092,2	K562	blood:
5	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
6	chr8:8130421..8131300-chr8:8175825..8176932,3	K562	blood:
7	chr8:8142616..8145069-chr8:8226333..8228141,2	MCF-7	breast:
8	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
9	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
10	chr8:8145925..8147772-chr8:8172599..8174671,2	MCF-7	breast:
11	chr8:8130322..8131342-chr8:8527334..8528198,3	MCF-7	breast:
12	chr8:8105365..8106008-chr8:8526894..8527465,2	K562	blood:
13	chr8:8108549..8111183-chr8:8240516..8242778,2	MCF-7	breast:
14	chr8:8101157..8102709-chr8:8124508..8126459,2	MCF-7	breast:
15	chr8:8126556..8131624-chr8:8143035..8148399,10	MCF-7	breast:
16	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
17	chr8:8128010..8130864-chr8:8317877..8319814,2	MCF-7	breast:
18	chr8:8105578..8107200-chr8:8525517..8527239,2	MCF-7	breast:
19	chr8:8129344..8132133-chr8:8525629..8527896,2	MCF-7	breast:
20	chr8:8144375..8149679-chr8:8240479..8246459,10	MCF-7	breast:
21	chr8:8130384..8131365-chr8:8526780..8528280,9	K562	blood:
22	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
23	chr8:8126193..8127836-chr8:8129384..8131743,2	MCF-7	breast:
24	chr8:8144670..8146200-chr8:8236707..8239376,2	MCF-7	breast:
25	chr8:8130411..8130935-chr8:8374466..8375028,2	K562	blood:
26	chr8:8131655..8133179-chr8:8135431..8137292,2	MCF-7	breast:
27	chr8:8142878..8144520-chr8:8146399..8149197,2	MCF-7	breast:
28	chr8:8105059..8106011-chr8:8526943..8527953,6	MCF-7	breast:
29	chr8:8131655..8133179-chr8:8135431..8137292,2	MCF-7	breast:
30	chr8:8140760..8143388-chr8:8146728..8148425,2	K562	blood:
31	chr8:8145815..8148362-chr8:8152420..8155525,4	MCF-7	breast:
32	chr8:8126193..8127836-chr8:8129384..8131743,2	MCF-7	breast:
33	chr8:8138288..8140321-chr8:8142532..8144155,2	MCF-7	breast:
34	chr8:8145045..8147805-chr8:8168275..8170393,2	MCF-7	breast:
35	chr8:8134161..8136694-chr8:8559309..8560894,2	MCF-7	breast:
36	chr8:8126556..8131624-chr8:8143035..8148399,10	MCF-7	breast:
37	chr8:8145200..8147453-chr8:8312155..8314860,2	MCF-7	breast:
38	chr8:8101610..8104492-chr8:8112542..8114092,2	K562	blood:
39	chr8:8141970..8144276-chr8:8242374..8245136,3	MCF-7	breast:
40	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
41	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
42	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
43	chr8:8098254..8100230-chr8:8106571..8108592,2	K562	blood:
44	chr8:8104258..8105835-chr8:8243426..8245376,2	MCF-7	breast:
45	chr8:8134812..8136654-chr8:8146118..8147961,3	K562	blood:

No data

Variant related genes	Relation type
ALG1L13P	TF binding region
ALG1L13P	CpG island
ENSG00000173295	chromatin interactions
ENSG00000253981	chromatin interactions
ENSG00000176305	chromatin interactions
ENSG00000182319	chromatin interactions
ENSG00000254153	chromatin interactions
ENSG00000253958	chromatin interactions

Extended variants
information (count: 2352 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:2352 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528109846	chr8:8102515-8102516	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs146752024	chr8:8102524-8102525	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs140350154	chr8:8102533-8102534	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs531143311	chr8:8102534-8102535	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs377740491	chr8:8102537-8102538	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs180983210	chr8:8102542-8102543	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs115007249	chr8:8102547-8102548	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs557203706	chr8:8102558-8102559	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs144950167	chr8:8102564-8102565	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs10092790	chr8:8102569-8102570	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs793755	chr8:8102615-8102616	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs370135617	chr8:8102740-8102741	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs114452480	chr8:8102747-8102748	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs143075832	chr8:8102756-8102757	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs577832513	chr8:8102771-8102772	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs575751988	chr8:8102821-8102822	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs184409106	chr8:8102831-8102832	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs541805055	chr8:8102857-8102858	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs188155325	chr8:8102939-8102940	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs181351250	chr8:8102987-8102988	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs148205461	chr8:8102994-8102995	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs185524773	chr8:8103019-8103020	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs140068197	chr8:8103061-8103062	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs564743964	chr8:8103094-8103095	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs190681288	chr8:8103121-8103122	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs551300198	chr8:8103147-8103148	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs118028992	chr8:8103178-8103179	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs73199797	chr8:8103193-8103194	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs547240648	chr8:8103197-8103198	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs566938806	chr8:8103234-8103235	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs538770281	chr8:8103286-8103287	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs181815676	chr8:8103309-8103310	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs146913111	chr8:8103311-8103312	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs376618987	chr8:8103329-8103330	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs571006396	chr8:8103343-8103344	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs369847935	chr8:8103345-8103346	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs569160722	chr8:8103359-8103360	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs536906991	chr8:8103361-8103362	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs80045563	chr8:8103372-8103373	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs139310405	chr8:8103383-8103384	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs536017165	chr8:8103406-8103407	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs552927640	chr8:8103414-8103415	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs143234768	chr8:8103415-8103416	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs74947315	chr8:8103449-8103450	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs74630918	chr8:8103473-8103474	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs187418809	chr8:8103497-8103498	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs192209085	chr8:8103503-8103504	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs561540060	chr8:8103505-8103506	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs530448332	chr8:8103506-8103507	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs183691178	chr8:8103517-8103518	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:144)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	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
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	21138945	CNVD

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8086800-8108400	Weak transcription	NHEK	skin
2	chr8:8092200-8103600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:8092400-8103600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:8093600-8106000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:8094000-8105400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr8:8096200-8108400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr8:8097200-8105200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr8:8098200-8103400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:8100200-8108400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr8:8101400-8104400	Enhancers	Placenta	Placenta
11	chr8:8101400-8105200	Weak transcription	A549	lung
12	chr8:8101600-8103800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:8101800-8103000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr8:8101800-8103600	Weak transcription	Fetal Lung	lung
15	chr8:8102000-8102600	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr8:8102200-8108400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:8102400-8102600	Enhancers	K562	blood
18	chr8:8102400-8103000	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr8:8102400-8103600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:8102400-8103600	Weak transcription	HepG2	liver
21	chr8:8102400-8111400	Weak transcription	Fetal Intestine Small	intestine
22	chr8:8103000-8104400	Enhancers	H9 Cell Line	embryonic stem cell
23	chr8:8103600-8104400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:8103600-8104400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr8:8103600-8104600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr8:8103600-8104600	Enhancers	HepG2	liver
27	chr8:8103600-8105400	Enhancers	Fetal Lung	lung
28	chr8:8103800-8104000	Enhancers	Placenta Amnion	Placenta Amnion
29	chr8:8103800-8104200	Enhancers	Esophagus	oesophagus
30	chr8:8104000-8104200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr8:8104000-8104200	Weak transcription	Fetal Kidney	kidney
32	chr8:8104000-8105800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr8:8104200-8104400	Enhancers	Fetal Kidney	kidney
34	chr8:8104400-8108200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:8104400-8108400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr8:8104400-8108400	Weak transcription	Fetal Kidney	kidney
37	chr8:8104600-8108200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:8104600-8108400	Weak transcription	HepG2	liver
39	chr8:8105200-8105400	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr8:8105200-8106600	Enhancers	A549	lung
41	chr8:8105200-8106800	Enhancers	HMEC	breast
42	chr8:8105400-8108600	Weak transcription	Fetal Lung	lung
43	chr8:8105600-8105800	Enhancers	HUVEC	blood vessel
44	chr8:8105600-8106600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:8105800-8106000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr8:8105800-8106600	Enhancers	Placenta Amnion	Placenta Amnion
47	chr8:8106000-8106200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:8106200-8108200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr8:8106200-8113200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr8:8106600-8107800	Weak transcription	Placenta Amnion	Placenta Amnion

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