Variant report

Variant	nsv610266
Chromosome Location	chr8:10250758-10294330
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	chr8:10268444-10268969	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:10275357-10275714	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:10282612-10283138	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:10268651-10268866	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	chr8:10275307-10276030	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:10282676-10283036	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	chr8:10282666-10283014	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr8:10275385-10275455	HepG2	liver:	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	chr8:10285722-10286019	IMR90	lung:	n/a	n/a
17	CEBPB	chr8:10286712-10286743	HepG2	liver:	n/a	chr8:10286717-10286728
18	CEBPB	chr8:10252938-10253304	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:10254573-10254808	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:10259940-10260083	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:10261640-10261652	HepG2	liver:	n/a	n/a
22	CHD1	chr8:10275384-10275697	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr8:10282685-10282959	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr8:10282655-10282933	GM12878	blood:	n/a	n/a
25	CHD2	chr8:10275284-10275546	GM12878	blood:	n/a	n/a
26	CHD2	chr8:10282658-10282853	K562	blood:	n/a	n/a
27	CHD2	chr8:10283992-10284108	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr8:10282831-10282865	Hela-S3	cervix:	n/a	n/a
29	CREB1	chr8:10268552-10268984	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr8:10268447-10269019	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr8:10276778-10277271	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr8:10275333-10275638	A549	lung:	n/a	n/a
33	CTBP2	chr8:10275390-10276080	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr8:10275320-10275470	AG09309	skin:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
35	CTCF	chr8:10282780-10282930	HRPEpiC	eye:	n/a	chr8:10282850-10282866 chr8:10282844-10282865 chr8:10282849-10282867
36	CTCF	chr8:10282820-10282970	HEK293	kidney:	n/a	chr8:10282850-10282866 chr8:10282932-10282940 chr8:10282844-10282865 chr8:10282932-10282945 chr8:10282929-10282947 chr8:10282849-10282867
37	CTCF	chr8:10282528-10282594	Gliobla	brain:	n/a	n/a
38	CTCF	chr8:10274580-10274730	SAEC	small airway:	n/a	n/a
39	CTCF	chr8:10282820-10282970	GM12865	blood:	n/a	chr8:10282850-10282866 chr8:10282932-10282940 chr8:10282844-10282865 chr8:10282932-10282945 chr8:10282929-10282947 chr8:10282849-10282867
40	CTCF	chr8:10274900-10275050	GM12870	blood:	n/a	n/a
41	CTCF	chr8:10275360-10275510	K562	blood:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
42	CTCF	chr8:10275360-10275510	GM12870	blood:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
43	CTCF	chr8:10282673-10283039	NHEK	skin:	n/a	chr8:10282850-10282866 chr8:10282932-10282940 chr8:10282844-10282865 chr8:10282932-10282945 chr8:10282929-10282947 chr8:10282849-10282867
44	CTCF	chr8:10275250-10275590	GM12892	blood:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
45	CTCF	chr8:10275660-10275810	HCPEpiC	choroid plexus:	n/a	chr8:10275779-10275787
46	CTCF	chr8:10282800-10282950	HA-sp	spinal cord:	n/a	chr8:10282850-10282866 chr8:10282932-10282940 chr8:10282844-10282865 chr8:10282932-10282945 chr8:10282929-10282947 chr8:10282849-10282867
47	CTCF	chr8:10275380-10275530	BE2_C	brain:	n/a	chr8:10275429-10275445 chr8:10275430-10275451 chr8:10275428-10275446
48	CTCF	chr8:10252120-10252270	BE2_C	brain:	n/a	n/a
49	CTCF	chr8:10282440-10282590	HCM	heart:	n/a	n/a
50	CTCF	chr8:10282800-10282950	AG09319	gingival:	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	NH-A	brain:	n/a
2	chr8:10261798-10261848	NH-A	brain:	n/a
3	chr8:10262628-10262678	GM19239	blood:	n/a
4	chr8:10283795-10283845	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:10286243-10286293	HPAEpiC	pulmonary alveolar:	n/a
6	chr8:10283858-10283908	NH-A	brain:	n/a
7	chr8:10273890-10273940	NH-A	brain:	n/a
8	chr8:10283221-10283271	H1-hESC	embryonic stem cell:	embryo
9	chr8:10268916-10268966	AG04449	skin:	fetal
10	chr8:10262020-10262070	Hela-S3	cervix:	n/a
11	chr8:10282549-10282599	NB4	blood:	n/a
12	chr8:10262159-10262209	IMR90	lung:	fetal
13	chr8:10259065-10259115	AG09319	gingival:	n/a
14	chr8:10282809-10282859	GM12892	blood:	n/a
15	chr8:10282607-10282657	MCF-7	breast:	n/a
16	chr8:10253076-10253126	AG04449	skin:	fetal
17	chr8:10282809-10282859	HRPEpiC	eye:	n/a
18	chr8:10261972-10262022	GM12892	blood:	n/a
19	chr8:10261641-10261691	AG04449	skin:	fetal
20	chr8:10262221-10262271	AG09319	gingival:	n/a
21	chr8:10268916-10268966	HMEC	breast:	n/a
22	chr8:10283152-10283202	BE2_C	brain:	n/a
23	chr8:10273890-10273940	PFSK-1	brain:	n/a
24	chr8:10259065-10259115	SK-N-SH	brain:	n/a
25	chr8:10261798-10261848	CMK	blood:	n/a
26	chr8:10273726-10273776	GM12878	blood:	n/a
27	chr8:10273691-10273741	HCPEpiC	choroid plexus:	n/a
28	chr8:10262221-10262271	HNPCEpiC	eye:	n/a
29	chr8:10282549-10282599	PrEC	prostate:	n/a
30	chr8:10283858-10283908	U87	brain:	n/a
31	chr8:10283221-10283271	HL-60	blood:	n/a
32	chr8:10283152-10283202	HRCEpiC	kidney:	n/a
33	chr8:10273691-10273741	ProgFib	skin:	n/a
34	chr8:10283275-10283325	SK-N-SH_RA	brain:	n/a
35	chr8:10282607-10282657	AG04450	lung:	fetal
36	chr8:10262221-10262271	IMR90	lung:	fetal
37	chr8:10283858-10283908	AoSMC	blood vessel:	n/a
38	chr8:10282549-10282599	SK-N-MC	brain:	n/a
39	chr8:10282549-10282599	AG04450	lung:	fetal
40	chr8:10282809-10282859	AoSMC	blood vessel:	n/a
41	chr8:10283275-10283325	CMK	blood:	n/a
42	chr8:10283152-10283202	U87	brain:	n/a
43	chr8:10262221-10262271	AG04449	skin:	fetal
44	chr8:10273726-10273776	AG10803	skin:	n/a
45	chr8:10273691-10273741	HCF	heart:	n/a
46	chr8:10275927-10275977	HNPCEpiC	eye:	n/a
47	chr8:10282607-10282657	NHDF-neo	bronchial:	n/a
48	chr8:10261641-10261691	HUVEC	blood vessel:	n/a
49	chr8:10273691-10273741	A549	lung:	n/a
50	chr8:10283858-10283908	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:10277398..10280414-chr8:10281254..10284079,3	K562	blood:
2	chr8:10293147..10295471-chr8:10296811..10299239,2	K562	blood:
3	chr8:10271744..10274704-chr8:10275996..10278041,2	MCF-7	breast:
4	chr8:9898874..9899812-chr8:10282419..10282930,2	K562	blood:
5	chr8:10274936..10276062-chr8:10331610..10332507,4	MCF-7	breast:
6	chr8:10281970..10284229-chr8:10318464..10320467,2	K562	blood:
7	chr8:10275131..10275838-chr8:10399365..10400272,2	MCF-7	breast:
8	chr8:10290739..10292284-chr8:10294138..10295858,2	K562	blood:
9	chr8:10277398..10280414-chr8:10281254..10284079,3	K562	blood:
10	chr8:10271744..10274704-chr8:10275996..10278041,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS55-4	chr8:10268611-10269075	NONHSAT124981
2	lnc-MSRA-1	chr8:10291182-10295822	ENSG00000261451.1
3	lnc-RP1L1-8	chr8:10281418-10284043	NONHSAT124985
4	lnc-MSRA-1	chr8:10293466-10295495	NONHSAT124987

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

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

Extended variants
information (count: 2652 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:2652 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17151892	chr8:10250758-10250759	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150246339	chr8:10250767-10250768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568179256	chr8:10250768-10250769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533959154	chr8:10250802-10250803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553675863	chr8:10250804-10250805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367543620	chr8:10250816-10250817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539084456	chr8:10250830-10250831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs28507213	chr8:10250849-10250850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs192742838	chr8:10250862-10250863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541572833	chr8:10250895-10250896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555407997	chr8:10250926-10250927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573788588	chr8:10250938-10250939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115834510	chr8:10250972-10250973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540800508	chr8:10250999-10251000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138922535	chr8:10251012-10251013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532845740	chr8:10251042-10251043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546472594	chr8:10251074-10251075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562880033	chr8:10251075-10251076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184133487	chr8:10251079-10251080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570236779	chr8:10251080-10251081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548414657	chr8:10251095-10251096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149434790	chr8:10251139-10251140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs28712068	chr8:10251145-10251146	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs2001337	chr8:10251154-10251155	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs113462278	chr8:10251155-10251156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539354347	chr8:10251156-10251157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11782297	chr8:10251190-10251191	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs2001338	chr8:10251217-10251218	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs535403715	chr8:10251235-10251236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11249999	chr8:10251265-10251266	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572091744	chr8:10251266-10251267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540869627	chr8:10251286-10251287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115581853	chr8:10251307-10251308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577472880	chr8:10251309-10251310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114746057	chr8:10251345-10251346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563167488	chr8:10251356-10251357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143857716	chr8:10251371-10251372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544474945	chr8:10251395-10251396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542188998	chr8:10251433-10251434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562079480	chr8:10251440-10251441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527779652	chr8:10251483-10251484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140274677	chr8:10251507-10251508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116493000	chr8:10251537-10251538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532929679	chr8:10251546-10251547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549687822	chr8:10251576-10251577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112243879	chr8:10251578-10251579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535139684	chr8:10251592-10251593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190638765	chr8:10251600-10251601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565684292	chr8:10251607-10251608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77200739	chr8:10251648-10251649	Weak transcription Enhancers	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:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr8:10233800-10252400	Weak transcription	Fetal Brain Male	brain
4	chr8:10235200-10252400	Weak transcription	Brain Hippocampus Middle	brain
5	chr8:10235400-10256800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:10236200-10252600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr8:10236200-10255800	Weak transcription	Pancreas	Pancrea
8	chr8:10236200-10255800	Weak transcription	Right Ventricle	heart
9	chr8:10240400-10256000	Weak transcription	Adipose Nuclei	Adipose
10	chr8:10240400-10256800	Weak transcription	Left Ventricle	heart
11	chr8:10242000-10255800	Weak transcription	Brain Germinal Matrix	brain
12	chr8:10244800-10251200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:10245000-10253400	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr8:10247800-10251000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr8:10248000-10253200	Weak transcription	Spleen	Spleen
16	chr8:10248200-10252400	Weak transcription	HepG2	liver
17	chr8:10248200-10253200	Weak transcription	Liver	Liver
18	chr8:10248400-10255000	Weak transcription	Fetal Brain Female	brain
19	chr8:10249000-10251200	Weak transcription	Primary T cells from cord blood	blood
20	chr8:10249000-10258200	Enhancers	Fetal Muscle Leg	muscle
21	chr8:10249000-10275200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr8:10249800-10251200	Enhancers	Fetal Muscle Trunk	muscle
23	chr8:10250000-10251800	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr8:10250000-10252600	Weak transcription	NHDF-Ad	bronchial
25	chr8:10250000-10255400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr8:10250200-10252400	Weak transcription	HSMMtube	muscle
27	chr8:10250200-10252600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:10250200-10252600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr8:10250200-10252600	Weak transcription	HSMM	muscle
30	chr8:10250200-10252800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr8:10250400-10252400	Weak transcription	NHLF	lung
32	chr8:10251000-10253600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr8:10251200-10251400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:10251200-10252000	Weak transcription	Fetal Muscle Trunk	muscle
35	chr8:10251200-10255200	Enhancers	Primary T cells from cord blood	blood
36	chr8:10251400-10251600	Enhancers	Brain Anterior Caudate	brain
37	chr8:10251400-10251600	Enhancers	Right Atrium	heart
38	chr8:10251600-10252400	Weak transcription	Right Atrium	heart
39	chr8:10251600-10253200	Weak transcription	Brain Anterior Caudate	brain
40	chr8:10252000-10252400	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr8:10252000-10258200	Enhancers	Fetal Muscle Trunk	muscle
42	chr8:10252200-10253400	Enhancers	Brain Cingulate Gyrus	brain
43	chr8:10252200-10254000	Enhancers	Brain Angular Gyrus	brain
44	chr8:10252400-10252600	Enhancers	Fetal Thymus	thymus
45	chr8:10252400-10253600	Enhancers	Brain Hippocampus Middle	brain
46	chr8:10252400-10253600	Enhancers	Right Atrium	heart
47	chr8:10252400-10253600	Enhancers	NHLF	lung
48	chr8:10252400-10253800	Enhancers	Fetal Brain Male	brain
49	chr8:10252400-10253800	Enhancers	HSMMtube	muscle
50	chr8:10252400-10257200	Enhancers	HepG2	liver

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