Variant report

Variant	nsv968485
Chromosome Location	chr8:39149416-39182473
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:63)
CpG islands
(count:550)
Chromatin interactive
region (count:4)
LncRNA
region (count:60)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:63 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:39169144-39169211	K562	blood:	n/a	n/a
2	BACH1	chr8:39180150-39180194	K562	blood:	n/a	n/a
3	CEBPB	chr8:39172365-39172592	A549	lung:	n/a	chr8:39172538-39172549
4	CEBPB	chr8:39172450-39172643	K562	blood:	n/a	chr8:39172538-39172549
5	CEBPB	chr8:39169394-39169417	A549	lung:	n/a	n/a
6	CTCF	chr8:39150997-39151043	GM13976	blood:	n/a	n/a
7	CTCF	chr8:39166617-39166716	GM13976	blood:	n/a	n/a
8	CTCF	chr8:39160540-39160690	HepG2	liver:	n/a	n/a
9	CTCF	chr8:39163600-39163750	GM12865	blood:	n/a	n/a
10	CTCF	chr8:39160639-39160734	H1-hESC	embryonic stem cell:	n/a	n/a
11	E2F4	chr8:39152575-39152969	MCF10A-Er-Src	breast:	n/a	n/a
12	EBF1	chr8:39163080-39163318	GM12878	blood:	n/a	chr8:39163227-39163238
13	EBF1	chr8:39163040-39163449	GM12878	blood:	n/a	chr8:39163227-39163238
14	FAM48A	chr8:39168075-39168140	GM12878	blood:	n/a	n/a
15	FOXA1	chr8:39165553-39165768	T-47D	breast:	n/a	chr8:39165686-39165701
16	FOXA1	chr8:39165528-39165802	T-47D	breast:	n/a	chr8:39165686-39165701
17	GATA3	chr8:39175786-39175969	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr8:39176687-39176905	SH-SY5Y	brain:	n/a	n/a
19	IRF1	chr8:39153827-39153867	K562	blood:	n/a	n/a
20	IRF1	chr8:39168091-39168172	K562	blood:	n/a	n/a
21	IRF3	chr8:39159398-39159440	GM12878	blood:	n/a	n/a
22	JUND	chr8:39150666-39150818	HepG2	liver:	n/a	n/a
23	MAFF	chr8:39181637-39181913	K562	blood:	n/a	chr8:39181770-39181788
24	MAFF	chr8:39181622-39181884	HepG2	liver:	n/a	chr8:39181770-39181788
25	MAFK	chr8:39161824-39161928	HepG2	liver:	n/a	n/a
26	MAFK	chr8:39181642-39181936	K562	blood:	n/a	chr8:39181772-39181787
27	MAFK	chr8:39181609-39181948	HepG2	liver:	n/a	chr8:39181772-39181787
28	MAFK	chr8:39172493-39172519	K562	blood:	n/a	n/a
29	MAFK	chr8:39181653-39181894	HepG2	liver:	n/a	chr8:39181772-39181787
30	MAFK	chr8:39181625-39181906	IMR90	lung:	n/a	chr8:39181772-39181787
31	MAX	chr8:39165476-39165625	K562	blood:	n/a	n/a
32	MAX	chr8:39165413-39165644	K562	blood:	n/a	n/a
33	MAZ	chr8:39182070-39182092	HepG2	liver:	n/a	n/a
34	MYC	chr8:39167497-39167511	H1-hESC	embryonic stem cell:	n/a	n/a
35	NR3C1	chr8:39149626-39149775	ECC-1	luminal epithelium:	n/a	n/a
36	NRF1	chr8:39164161-39164177	GM12878	blood:	n/a	n/a
37	POLR2A	chr8:39155463-39155525	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr8:39150783-39150830	GM12878	blood:	n/a	n/a
39	POLR2A	chr8:39159138-39159442	H1-neurons	neurons:	n/a	n/a
40	POLR2A	chr8:39158322-39158361	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr8:39159160-39159353	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr8:39160543-39160783	Gliobla	brain:	n/a	n/a
43	POLR2A	chr8:39176290-39176490	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr8:39152801-39153130	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr8:39170599-39170795	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr8:39160838-39160857	Gliobla	brain:	n/a	n/a
47	POLR2A	chr8:39166908-39166996	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr8:39166116-39166195	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr8:39163247-39163378	Gliobla	brain:	n/a	n/a
50	POLR2A	chr8:39163317-39163439	A549	lung:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39171648-39171698	PANC-1	pancreas:	n/a
2	chr8:39171648-39171698	PANC-1	pancreas:	n/a
3	chr8:39172099-39172149	HNPCEpiC	eye:	n/a
4	chr8:39172111-39172161	AoSMC	blood vessel:	n/a
5	chr8:39172111-39172161	GM12892	blood:	n/a
6	chr8:39172099-39172149	HUVEC	blood vessel:	n/a
7	chr8:39172099-39172149	AG04449	skin:	fetal
8	chr8:39172120-39172170	K562	blood:	n/a
9	chr8:39171620-39171670	SAEC	small airway:	n/a
10	chr8:39172022-39172072	HCT-116	colon:	n/a
11	chr8:39171620-39171670	GM12891	blood:	n/a
12	chr8:39172020-39172070	PANC-1	pancreas:	n/a
13	chr8:39172099-39172149	ECC-1	luminal epithelium:	n/a
14	chr8:39171648-39171698	HCF	heart:	n/a
15	chr8:39172020-39172070	LNCaP	prostate:	n/a
16	chr8:39171620-39171670	HEEpiC	esophagus:	n/a
17	chr8:39171866-39171916	NHDF-neo	bronchial:	n/a
18	chr8:39172111-39172161	HRCEpiC	kidney:	n/a
19	chr8:39172099-39172149	SK-N-SH	brain:	n/a
20	chr8:39172020-39172070	IMR90	lung:	fetal
21	chr8:39172111-39172161	SK-N-SH	brain:	n/a
22	chr8:39172022-39172072	HEEpiC	esophagus:	n/a
23	chr8:39172097-39172147	LNCaP	prostate:	n/a
24	chr8:39172097-39172147	PFSK-1	brain:	n/a
25	chr8:39172020-39172070	HAEpiC	amniotic membrane:	n/a
26	chr8:39172022-39172072	ProgFib	skin:	n/a
27	chr8:39171648-39171698	HAEpiC	amniotic membrane:	n/a
28	chr8:39171620-39171670	SK-N-MC	brain:	n/a
29	chr8:39172020-39172070	HRCEpiC	kidney:	n/a
30	chr8:39171866-39171916	Jurkat	blood:	n/a
31	chr8:39172097-39172147	T-47D	breast:	n/a
32	chr8:39172020-39172070	AG04449	skin:	fetal
33	chr8:39172099-39172149	HRE	kidney:	n/a
34	chr8:39171866-39171916	IMR90	lung:	fetal
35	chr8:39172120-39172170	PANC-1	pancreas:	n/a
36	chr8:39172099-39172149	PFSK-1	brain:	n/a
37	chr8:39172022-39172072	PANC-1	pancreas:	n/a
38	chr8:39172097-39172147	SAEC	small airway:	n/a
39	chr8:39172022-39172072	HUVEC	blood vessel:	n/a
40	chr8:39172099-39172149	HCM	heart:	n/a
41	chr8:39171866-39171916	H1-hESC	embryonic stem cell:	embryo
42	chr8:39172022-39172072	AG04450	lung:	fetal
43	chr8:39171866-39171916	PFSK-1	brain:	n/a
44	chr8:39171648-39171698	HL-60	blood:	n/a
45	chr8:39172120-39172170	HEEpiC	esophagus:	n/a
46	chr8:39172099-39172149	HEK293	kidney:	embryo
47	chr8:39172099-39172149	HAEpiC	amniotic membrane:	n/a
48	chr8:39172097-39172147	AG09309	skin:	n/a
49	chr8:39171620-39171670	HCM	heart:	n/a
50	chr8:39171866-39171916	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:50661566..50662138-chr8:39161334..39161854,2	MCF-7	breast:
2	chr6:156717380..156718086-chr8:39158912..39159795,2	MCF-7	breast:
3	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
4	chr8:39170463..39172530-chr8:39174983..39176968,2	MCF-7	breast:

(count:60 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126156
2	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126153
3	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126155
4	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT147628
5	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126155
6	lnc-ADAM32-1	chr8:39172110-39172236	NONHSAT126148
7	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT147628
8	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126154
9	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126155
10	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126150
11	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126150
12	lnc-ADAM32-1	chr8:39181838-39181858	NONHSAT147629
13	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126150
14	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126152
15	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126155
16	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126151
17	lnc-ADAM32-1	chr8:39180489-39181258	NONHSAT126149
18	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126155
19	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126152
20	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126152
21	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126153
22	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126157
23	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126149
24	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126157
25	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126151
26	lnc-ADAM32-1	chr8:39173006-39173053	NONHSAT126156
27	lnc-ADAM32-1	chr8:39172151-39172236	NONHSAT126150
28	lnc-ADAM32-1	chr8:39172151-39172236	NONHSAT126149
29	lnc-TM2D2-6	chr8:39167428-39167962	NONHSAT126147
30	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126151
31	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126152
32	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126151
33	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126157
34	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126155
35	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT147628
36	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126149
37	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126148
38	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126152
39	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126150
40	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126153
41	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126153
42	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126153
43	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126149
44	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126152
45	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126151
46	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126154
47	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126156
48	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126156
49	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126154
50	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126156

No data

Variant related genes	Relation type
ADAM5	TF binding region
ENSG00000253160	TF binding region
ADAM5	CpG island
ENSG00000253160	CpG island
ENSG00000196115	chromatin interactions

Extended variants
information (count: 206 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:206 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147782269	chr8:39163218-39163219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575672764	chr8:39163222-39163223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555613114	chr8:39163265-39163266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193027231	chr8:39163276-39163277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565017960	chr8:39163288-39163289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527477869	chr8:39163325-39163326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139454176	chr8:39163361-39163362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145137856	chr8:39163370-39163371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535791711	chr8:39163421-39163422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147578616	chr8:39163455-39163456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550105914	chr8:39163485-39163486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570053839	chr8:39163552-39163553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532595045	chr8:39163604-39163605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140559962	chr8:39163632-39163633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150448051	chr8:39163639-39163640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs77777185	chr8:39163687-39163688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12681970	chr8:39163716-39163717	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs150390934	chr8:39163727-39163728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568326330	chr8:39163796-39163797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368657882	chr8:39167431-39167432	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs555264138	chr8:39167433-39167434	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs578001830	chr8:39167449-39167450	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs529260155	chr8:39167531-39167532	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs545175879	chr8:39167532-39167533	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs559695766	chr8:39167557-39167558	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs149175896	chr8:39167565-39167566	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs574272381	chr8:39167608-39167609	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs551617988	chr8:39167612-39167613	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs13266761	chr8:39167669-39167670	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs530675656	chr8:39167695-39167696	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs556820228	chr8:39167707-39167708	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs10958545	chr8:39167739-39167740	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs34443788	chr8:39167761-39167762	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs545691712	chr8:39167777-39167778	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs567408041	chr8:39167797-39167798	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs7831944	chr8:39167828-39167829	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs112245407	chr8:39167857-39167858	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs4587294	chr8:39167860-39167861	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564719910	chr8:39167923-39167924	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs117654399	chr8:39167927-39167928	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs571529788	chr8:39168115-39168116	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs148248244	chr8:39168116-39168117	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs553897357	chr8:39168151-39168152	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs201133194	chr8:39169178-39169179	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs567675824	chr8:39169183-39169184	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs117806406	chr8:39169202-39169203	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs556740372	chr8:39169219-39169220	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs139456629	chr8:39169228-39169229	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs539254846	chr8:39169238-39169239	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs190436101	chr8:39169252-39169253	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Melanoma	18172304	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Lung cancer	21569311	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20932292	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39163200-39163600	Enhancers	Gastric	stomach
2	chr8:39163200-39163800	Enhancers	Fetal Intestine Small	intestine
3	chr8:39171400-39171600	Bivalent Enhancer	Fetal Lung	lung
4	chr8:39171600-39171800	Enhancers	Fetal Brain Female	brain
5	chr8:39171600-39172000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr8:39171600-39172000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
7	chr8:39171600-39172400	Bivalent/Poised TSS	Fetal Lung	lung
8	chr8:39171800-39172000	Bivalent/Poised TSS	NH-A	brain
9	chr8:39171800-39172200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:39171800-39172200	Active TSS	Brain Anterior Caudate	brain
11	chr8:39171800-39172400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr8:39171800-39172400	Active TSS	Brain Angular Gyrus	brain
13	chr8:39171800-39172400	Active TSS	Brain Germinal Matrix	brain
14	chr8:39171800-39172400	Bivalent/Poised TSS	Fetal Brain Male	brain
15	chr8:39171800-39172400	Active TSS	Fetal Brain Female	brain
16	chr8:39172000-39172200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
17	chr8:39172000-39172200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:39172000-39172200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
19	chr8:39172000-39172200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:39172000-39172200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:39172000-39172200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:39172000-39172200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr8:39172000-39172200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
24	chr8:39172000-39172200	Enhancers	Fetal Heart	heart
25	chr8:39172000-39172200	Bivalent Enhancer	Psoas Muscle	Psoas
26	chr8:39172000-39172200	Active TSS	Rectal Smooth Muscle	rectum
27	chr8:39172000-39172200	Bivalent Enhancer	NHDF-Ad	bronchial
28	chr8:39172000-39172400	ZNF genes & repeats	Aorta	Aorta
29	chr8:39172000-39172400	Enhancers	Placenta	Placenta
30	chr8:39172000-39172600	Active TSS	Stomach Smooth Muscle	stomach
31	chr8:39172200-39172400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:39172200-39172400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
33	chr8:39172200-39172400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
34	chr8:39172200-39172400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
35	chr8:39172200-39172400	Bivalent/Poised TSS	Fetal Stomach	stomach
36	chr8:39172200-39172400	Flanking Active TSS	Rectal Smooth Muscle	rectum
37	chr8:39172400-39172800	Bivalent Enhancer	Fetal Lung	lung

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