Variant report

Variant	nsv610265
Chromosome Location	chr8:10241411-10290566
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10254636-10254879	HepG2	liver:	n/a	n/a
2	ATF2	chr8:10275357-10275714	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:10282612-10283138	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:10268444-10268969	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:10282676-10283036	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:10276673-10277091	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:10268651-10268866	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:10275307-10276030	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr8:10275298-10275573	K562	blood:	n/a	n/a
10	BHLHE40	chr8:10275324-10275524	HepG2	liver:	n/a	n/a
11	BHLHE40	chr8:10282699-10283004	GM12878	blood:	n/a	n/a
12	BRCA1	chr8:10275385-10275455	HepG2	liver:	n/a	n/a
13	BRCA1	chr8:10282666-10283014	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr8:10275279-10275543	K562	blood:	n/a	n/a
15	CCNT2	chr8:10282666-10283107	K562	blood:	n/a	n/a
16	CEBPB	chr8:10249675-10249890	HepG2	liver:	n/a	chr8:10249794-10249805
17	CEBPB	chr8:10248126-10248250	HepG2	liver:	n/a	chr8:10248204-10248221
18	CEBPB	chr8:10261640-10261652	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:10252938-10253304	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:10249763-10249853	Hela-S3	cervix:	n/a	chr8:10249794-10249805
21	CEBPB	chr8:10254573-10254808	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:10259940-10260083	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr8:10286712-10286743	HepG2	liver:	n/a	chr8:10286717-10286728
24	CEBPB	chr8:10249620-10249982	IMR90	lung:	n/a	chr8:10249794-10249805
25	CEBPB	chr8:10285722-10286019	IMR90	lung:	n/a	n/a
26	CHD1	chr8:10275384-10275697	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr8:10282658-10282853	K562	blood:	n/a	n/a
28	CHD2	chr8:10282685-10282959	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr8:10282831-10282865	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr8:10282655-10282933	GM12878	blood:	n/a	n/a
31	CHD2	chr8:10283992-10284108	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr8:10275284-10275546	GM12878	blood:	n/a	n/a
33	CREB1	chr8:10268552-10268984	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr8:10275333-10275638	A549	lung:	n/a	n/a
35	CREB1	chr8:10276778-10277271	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr8:10268447-10269019	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr8:10275390-10276080	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr8:10275360-10275510	GM12866	blood:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
39	CTCF	chr8:10275360-10275510	HRPEpiC	eye:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
40	CTCF	chr8:10275360-10275510	GM12864	blood:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
41	CTCF	chr8:10282774-10282978	LNCaP	prostate:	n/a	chr8:10282850-10282866 chr8:10282932-10282940 chr8:10282844-10282865 chr8:10282932-10282945 chr8:10282929-10282947 chr8:10282849-10282867
42	CTCF	chr8:10273516-10273566	GM12891	blood:	n/a	n/a
43	CTCF	chr8:10275265-10275591	Spleen_OC	spleen:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
44	CTCF	chr8:10282780-10282930	HFF	foreskin:	n/a	chr8:10282850-10282866 chr8:10282844-10282865 chr8:10282849-10282867
45	CTCF	chr8:10282780-10282930	GM12873	blood:	n/a	chr8:10282850-10282866 chr8:10282844-10282865 chr8:10282849-10282867
46	CTCF	chr8:10275380-10275530	GM12878	blood:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
47	CTCF	chr8:10275257-10275595	GM12891	blood:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
48	CTCF	chr8:10282711-10283005	GM10248	blood:	n/a	chr8:10282850-10282866 chr8:10282932-10282940 chr8:10282844-10282865 chr8:10282932-10282945 chr8:10282929-10282947 chr8:10282849-10282867
49	CTCF	chr8:10282800-10282950	HEEpiC	esophagus:	n/a	chr8:10282850-10282866 chr8:10282932-10282940 chr8:10282844-10282865 chr8:10282932-10282945 chr8:10282929-10282947 chr8:10282849-10282867
50	CTCF	chr8:10282800-10282950	AG04449	skin:	n/a	chr8:10282850-10282866 chr8:10282932-10282940 chr8:10282844-10282865 chr8:10282932-10282945 chr8:10282929-10282947 chr8:10282849-10282867

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10261798-10261848	NB4	blood:	n/a
2	chr8:10253076-10253126	U87	brain:	n/a
3	chr8:10273691-10273741	NT2-D1	testis:	n/a
4	chr8:10283275-10283325	LNCaP	prostate:	n/a
5	chr8:10283221-10283271	BE2_C	brain:	n/a
6	chr8:10283221-10283271	Caco-2	colon:	n/a
7	chr8:10268916-10268966	HCPEpiC	choroid plexus:	n/a
8	chr8:10283275-10283325	HEEpiC	esophagus:	n/a
9	chr8:10268916-10268966	SK-N-MC	brain:	n/a
10	chr8:10275927-10275977	HCT-116	colon:	n/a
11	chr8:10282809-10282859	HRE	kidney:	n/a
12	chr8:10262221-10262271	AG09309	skin:	n/a
13	chr8:10283152-10283202	ovcar-3	ovarian:	n/a
14	chr8:10282607-10282657	GM12892	blood:	n/a
15	chr8:10262628-10262678	HAEpiC	amniotic membrane:	n/a
16	chr8:10273726-10273776	PFSK-1	brain:	n/a
17	chr8:10264504-10264554	HEK293	kidney:	embryo
18	chr8:10261972-10262022	HEK293	kidney:	embryo
19	chr8:10262020-10262070	SAEC	small airway:	n/a
20	chr8:10262159-10262209	HUVEC	blood vessel:	n/a
21	chr8:10283152-10283202	CMK	blood:	n/a
22	chr8:10283795-10283845	NH-A	brain:	n/a
23	chr8:10273666-10273716	NHDF-neo	bronchial:	n/a
24	chr8:10253076-10253126	RPTEC	kidney:	n/a
25	chr8:10283275-10283325	AG10803	skin:	n/a
26	chr8:10283275-10283325	Hepatocyte	liver:	n/a
27	chr8:10282549-10282599	AG04449	skin:	fetal
28	chr8:10262020-10262070	HCT-116	colon:	n/a
29	chr8:10262020-10262070	HepG2	liver:	n/a
30	chr8:10253076-10253126	AG04450	lung:	fetal
31	chr8:10283275-10283325	GM12892	blood:	n/a
32	chr8:10273726-10273776	NHDF-neo	bronchial:	n/a
33	chr8:10286243-10286293	HEEpiC	esophagus:	n/a
34	chr8:10273666-10273716	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:10262020-10262070	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:10282607-10282657	T-47D	breast:	n/a
37	chr8:10262628-10262678	AoSMC	blood vessel:	n/a
38	chr8:10273726-10273776	LNCaP	prostate:	n/a
39	chr8:10261641-10261691	K562	blood:	n/a
40	chr8:10283858-10283908	ovcar-3	ovarian:	n/a
41	chr8:10261972-10262022	PFSK-1	brain:	n/a
42	chr8:10262020-10262070	NT2-D1	testis:	n/a
43	chr8:10262628-10262678	HIPEpiC	eye:	n/a
44	chr8:10283858-10283908	BE2_C	brain:	n/a
45	chr8:10261798-10261848	AG09319	gingival:	n/a
46	chr8:10273691-10273741	AG04450	lung:	fetal
47	chr8:10283275-10283325	GM06990	blood:	n/a
48	chr8:10262221-10262271	A549	lung:	n/a
49	chr8:10273890-10273940	ovcar-3	ovarian:	n/a
50	chr8:10262020-10262070	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr8:9898874..9899812-chr8:10282419..10282930,2	K562	blood:
2	chr8:10240370..10243141-chr8:10246115..10249322,3	K562	blood:
3	chr8:10230455..10233257-chr8:10241195..10243671,2	K562	blood:
4	chr8:10274936..10276062-chr8:10331610..10332507,4	MCF-7	breast:
5	chr8:10271744..10274704-chr8:10275996..10278041,2	MCF-7	breast:
6	chr8:10240370..10243141-chr8:10246978..10249322,2	K562	blood:
7	chr8:10281970..10284229-chr8:10318464..10320467,2	K562	blood:
8	chr8:10275131..10275838-chr8:10399365..10400272,2	MCF-7	breast:
9	chr8:10240370..10243141-chr8:10246978..10249322,2	K562	blood:
10	chr8:10271744..10274704-chr8:10275996..10278041,2	MCF-7	breast:
11	chr8:10240370..10243141-chr8:10246115..10249322,3	K562	blood:
12	chr8:10277398..10280414-chr8:10281254..10284079,3	K562	blood:
13	chr8:10277398..10280414-chr8:10281254..10284079,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP1L1-8	chr8:10281418-10284043	NONHSAT124985
2	lnc-PRSS55-4	chr8:10268611-10269075	NONHSAT124981

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MSRA	hsa-miR-124-3p	chr8:10286173-10286194
2	MSRA	hsa-miR-124-3p	chr8:10286187-10286194

Variant related genes	Relation type
ENSG00000261451	TF binding region
ENSG00000261451	CpG island
ENSG00000253641	chromatin interactions

Extended variants
information (count: 2939 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:2939 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10283145	chr8:10241411-10241412	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574701773	chr8:10241416-10241417	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148787355	chr8:10241455-10241456	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188170256	chr8:10241466-10241467	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554463720	chr8:10241485-10241486	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568378102	chr8:10241498-10241499	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532423751	chr8:10241513-10241514	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551926131	chr8:10241520-10241521	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562501658	chr8:10241529-10241530	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536925145	chr8:10241536-10241537	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547891685	chr8:10241611-10241612	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557265532	chr8:10241623-10241624	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576522344	chr8:10241638-10241639	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567780636	chr8:10241662-10241663	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536469256	chr8:10241667-10241668	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546768032	chr8:10241669-10241670	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567085859	chr8:10241738-10241739	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374229540	chr8:10241761-10241762	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142467763	chr8:10241765-10241766	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117986188	chr8:10241788-10241789	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146886406	chr8:10241791-10241792	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140782126	chr8:10241792-10241793	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17151879	chr8:10241804-10241805	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs574967348	chr8:10241816-10241817	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs540470303	chr8:10241856-10241857	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs180970050	chr8:10241864-10241865	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs201010361	chr8:10241870-10241871	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs577111910	chr8:10241889-10241890	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs546081857	chr8:10241890-10241891	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs372609941	chr8:10241900-10241901	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs143216719	chr8:10241925-10241926	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs531353816	chr8:10241951-10241952	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs541396142	chr8:10241968-10241969	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs558814259	chr8:10241972-10241973	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs530123718	chr8:10241977-10241978	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs561473989	chr8:10241991-10241992	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs117886612	chr8:10242001-10242002	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146681826	chr8:10242003-10242004	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549583569	chr8:10242046-10242047	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377269646	chr8:10242050-10242051	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142410175	chr8:10242052-10242053	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532548322	chr8:10242069-10242070	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140209490	chr8:10242112-10242113	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186388847	chr8:10242153-10242154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150341610	chr8:10242155-10242156	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554989472	chr8:10242169-10242170	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138046342	chr8:10242176-10242177	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534285545	chr8:10242177-10242178	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191196792	chr8:10242193-10242194	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576977419	chr8:10242194-10242195	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
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
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
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
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
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Epilepsy	20502679	CNVD

Chromatin state (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10192600-10282400	Weak transcription	Gastric	stomach
2	chr8:10224000-10255800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr8:10228600-10247800	Weak transcription	Liver	Liver
4	chr8:10233800-10252400	Weak transcription	Fetal Brain Male	brain
5	chr8:10235200-10252400	Weak transcription	Brain Hippocampus Middle	brain
6	chr8:10235400-10256800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:10235600-10241600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr8:10235600-10244000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr8:10235600-10244400	Weak transcription	Duodenum Mucosa	Duodenum
10	chr8:10235800-10241600	Weak transcription	Right Atrium	heart
11	chr8:10236200-10247400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr8:10236200-10252600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr8:10236200-10255800	Weak transcription	Pancreas	Pancrea
14	chr8:10236200-10255800	Weak transcription	Right Ventricle	heart
15	chr8:10236800-10241800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr8:10237200-10247400	Weak transcription	Lung	lung
17	chr8:10239000-10241600	Enhancers	Psoas Muscle	Psoas
18	chr8:10239200-10241800	Enhancers	Primary T cells from cord blood	blood
19	chr8:10239200-10241800	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr8:10239600-10242000	Enhancers	Fetal Muscle Leg	muscle
21	chr8:10239800-10242000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:10239800-10242000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:10240000-10241600	Enhancers	Fetal Thymus	thymus
24	chr8:10240400-10256000	Weak transcription	Adipose Nuclei	Adipose
25	chr8:10240400-10256800	Weak transcription	Left Ventricle	heart
26	chr8:10240800-10243400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:10241200-10242200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:10241200-10242200	Enhancers	Fetal Brain Female	brain
29	chr8:10241200-10242400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:10241200-10247400	Weak transcription	Spleen	Spleen
31	chr8:10241400-10241600	Enhancers	HSMMtube	muscle
32	chr8:10241400-10243000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:10241400-10245000	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr8:10241600-10241800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr8:10241600-10241800	Enhancers	Placenta Amnion	Placenta Amnion
36	chr8:10241600-10242000	Enhancers	Right Atrium	heart
37	chr8:10241800-10242000	Enhancers	Brain Germinal Matrix	brain
38	chr8:10241800-10242000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr8:10241800-10242200	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr8:10241800-10242600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr8:10241800-10246800	Weak transcription	Primary T cells from cord blood	blood
42	chr8:10241800-10249600	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr8:10242000-10242200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr8:10242000-10243600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:10242000-10246200	Weak transcription	Fetal Muscle Leg	muscle
46	chr8:10242000-10255800	Weak transcription	Brain Germinal Matrix	brain
47	chr8:10242200-10242400	Enhancers	Placenta Amnion	Placenta Amnion
48	chr8:10242200-10248200	Weak transcription	Fetal Brain Female	brain
49	chr8:10242400-10244000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr8:10242600-10242800	Enhancers	H1 Cell Line	embryonic stem cell

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