Variant report

Variant	nsv519143
Chromosome Location	chr8:8296071-8328101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:417)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8314706-8315018	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8324363-8325247	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8318936-8319027	HepG2	liver:	n/a	n/a
4	ATF2	chr8:8310031-8310713	GM12878	blood:	n/a	n/a
5	ATF2	chr8:8324550-8324879	GM12878	blood:	n/a	n/a
6	ATF2	chr8:8324529-8324992	GM12878	blood:	n/a	n/a
7	ATF2	chr8:8310015-8310665	GM12878	blood:	n/a	n/a
8	BACH1	chr8:8313375-8313563	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:8310225-8310548	GM12878	blood:	n/a	n/a
10	BATF	chr8:8310182-8310550	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:8310128-8310497	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:8310249-8310487	GM12878	blood:	n/a	n/a
13	BCLAF1	chr8:8310038-8310609	GM12878	blood:	n/a	n/a
14	BCLAF1	chr8:8310124-8310538	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:8310177-8310477	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:8313428-8313566	A549	lung:	n/a	n/a
17	BHLHE40	chr8:8313440-8313517	K562	blood:	n/a	n/a
18	BHLHE40	chr8:8324440-8325002	HepG2	liver:	n/a	n/a
19	BRCA1	chr8:8313642-8313649	HepG2	liver:	n/a	n/a
20	CBX3	chr8:8298711-8299537	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:8298667-8299528	HCT-116	colon:	n/a	n/a
22	CEBPB	chr8:8313810-8313880	HepG2	liver:	n/a	chr8:8313825-8313836
23	CEBPB	chr8:8307022-8307239	MCF-7	breast:	n/a	n/a
24	CEBPB	chr8:8305274-8305363	A549	lung:	n/a	n/a
25	CEBPB	chr8:8309555-8309742	HepG2	liver:	n/a	chr8:8309599-8309610
26	CEBPB	chr8:8309467-8309731	A549	lung:	n/a	chr8:8309599-8309610
27	CEBPB	chr8:8306900-8307304	MCF-7	breast:	n/a	n/a
28	CEBPB	chr8:8313392-8313576	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:8313296-8314008	Hela-S3	cervix:	n/a	chr8:8313825-8313836
30	CEBPB	chr8:8309492-8309730	IMR90	lung:	n/a	chr8:8309599-8309610
31	CEBPB	chr8:8313772-8313879	H1-hESC	embryonic stem cell:	n/a	chr8:8313825-8313836
32	CEBPB	chr8:8313408-8313951	A549	lung:	n/a	chr8:8313825-8313836
33	CEBPB	chr8:8313314-8314082	A549	lung:	n/a	chr8:8313825-8313836
34	CEBPB	chr8:8313367-8313677	IMR90	lung:	n/a	n/a
35	CEBPB	chr8:8324596-8325001	HepG2	liver:	n/a	n/a
36	CHD2	chr8:8324676-8324913	HepG2	liver:	n/a	n/a
37	CHD2	chr8:8313285-8313945	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr8:8309880-8310497	GM12878	blood:	n/a	n/a
39	CTCF	chr8:8308183-8308224	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr8:8316400-8316550	HPF	lung:	n/a	n/a
41	CTCF	chr8:8300320-8300470	HMEC	breast:	n/a	n/a
42	CTCF	chr8:8300344-8300475	NHEK	skin:	n/a	n/a
43	CTCF	chr8:8300360-8300510	NHEK	skin:	n/a	n/a
44	CTCF	chr8:8300220-8300370	SAEC	small airway:	n/a	n/a
45	CTCF	chr8:8303180-8303330	GM12869	blood:	n/a	n/a
46	CTCF	chr8:8316620-8316770	HPF	lung:	n/a	n/a
47	CTCF	chr8:8316480-8316630	HCT-116	colon:	n/a	n/a
48	CTCF	chr8:8313500-8313650	HCPEpiC	choroid plexus:	n/a	n/a
49	CUX1	chr8:8310132-8310492	GM12878	blood:	n/a	n/a
50	CUX1	chr8:8308408-8308694	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	chr8:8318774-8318824	CMK	blood:	n/a
2	chr8:8318774-8318824	PrEC	prostate:	n/a
3	chr8:8313504-8313554	GM12892	blood:	n/a
4	chr8:8318774-8318824	K562	blood:	n/a
5	chr8:8318774-8318824	Jurkat	blood:	n/a
6	chr8:8313504-8313554	AG04450	lung:	fetal
7	chr8:8318774-8318824	HEK293	kidney:	embryo
8	chr8:8318774-8318824	RPTEC	kidney:	n/a
9	chr8:8318774-8318824	GM12878	blood:	n/a
10	chr8:8318774-8318824	HEEpiC	esophagus:	n/a
11	chr8:8313504-8313554	SK-N-MC	brain:	n/a
12	chr8:8313504-8313554	NHBE	bronchial:	n/a
13	chr8:8313504-8313554	GM12891	blood:	n/a
14	chr8:8313504-8313554	Hela-S3	cervix:	n/a
15	chr8:8313504-8313554	BE2_C	brain:	n/a
16	chr8:8313504-8313554	HMEC	breast:	n/a
17	chr8:8318774-8318824	AG09309	skin:	n/a
18	chr8:8318774-8318824	AG04450	lung:	fetal
19	chr8:8313504-8313554	NT2-D1	testis:	n/a
20	chr8:8313504-8313554	A549	lung:	n/a
21	chr8:8318774-8318824	SK-N-SH	brain:	n/a
22	chr8:8313504-8313554	Hepatocyte	liver:	n/a
23	chr8:8313504-8313554	PFSK-1	brain:	n/a
24	chr8:8318774-8318824	SK-N-SH_RA	brain:	n/a
25	chr8:8313504-8313554	SKMC	muscle:	n/a
26	chr8:8318774-8318824	AoSMC	blood vessel:	n/a
27	chr8:8313504-8313554	MCF-7	breast:	n/a
28	chr8:8313504-8313554	ECC-1	luminal epithelium:	n/a
29	chr8:8313504-8313554	RPTEC	kidney:	n/a
30	chr8:8318774-8318824	HCM	heart:	n/a
31	chr8:8313504-8313554	H1-hESC	embryonic stem cell:	embryo
32	chr8:8318774-8318824	BJ	skin:	n/a
33	chr8:8313504-8313554	SK-N-SH	brain:	n/a
34	chr8:8313504-8313554	BJ	skin:	n/a
35	chr8:8318774-8318824	NT2-D1	testis:	n/a
36	chr8:8313504-8313554	SAEC	small airway:	n/a
37	chr8:8318774-8318824	PANC-1	pancreas:	n/a
38	chr8:8318774-8318824	SKMC	muscle:	n/a
39	chr8:8313504-8313554	IMR90	lung:	fetal
40	chr8:8318774-8318824	HMEC	breast:	n/a
41	chr8:8318774-8318824	NHBE	bronchial:	n/a
42	chr8:8313504-8313554	HCM	heart:	n/a
43	chr8:8318774-8318824	GM12892	blood:	n/a
44	chr8:8318774-8318824	GM12891	blood:	n/a
45	chr8:8313504-8313554	SK-N-SH_RA	brain:	n/a
46	chr8:8313504-8313554	ovcar-3	ovarian:	n/a
47	chr8:8318774-8318824	BE2_C	brain:	n/a
48	chr8:8313504-8313554	GM12878	blood:	n/a
49	chr8:8318774-8318824	Caco-2	colon:	n/a
50	chr8:8313504-8313554	HNPCEpiC	eye:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8299017..8300539-chr8:8317523..8321166,3	MCF-7	breast:
2	chr8:8145200..8147453-chr8:8312155..8314860,2	MCF-7	breast:
3	chr8:8308652..8310168-chr8:8314593..8316228,2	MCF-7	breast:
4	chr8:8317671..8320936-chr8:8323021..8325939,5	MCF-7	breast:
5	chr8:8310535..8312786-chr8:8315430..8317371,2	MCF-7	breast:
6	chr8:8298645..8300548-chr8:8312022..8313794,2	MCF-7	breast:
7	chr8:8298645..8300548-chr8:8312022..8313794,2	MCF-7	breast:
8	chr8:8241273..8244866-chr8:8311320..8315481,8	MCF-7	breast:
9	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
10	chr8:8242477..8244553-chr8:8320092..8324260,3	MCF-7	breast:
11	chr8:8242907..8245706-chr8:8295976..8300172,6	MCF-7	breast:
12	chr8:8301355..8304096-chr8:8318371..8320187,2	MCF-7	breast:
13	chr8:8242445..8245313-chr8:8297878..8301672,4	MCF-7	breast:
14	chr8:8306469..8311532-chr8:8316315..8320180,6	MCF-7	breast:
15	chr8:8312145..8315725-chr8:8317532..8320911,6	MCF-7	breast:
16	chr8:8317141..8321564-chr8:8323708..8327409,4	MCF-7	breast:
17	chr8:8151768..8153956-chr8:8305542..8308270,3	MCF-7	breast:
18	chr8:8307359..8308990-chr8:8310543..8313387,3	MCF-7	breast:
19	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
20	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
21	chr8:8237866..8240823-chr8:8310722..8313327,2	MCF-7	breast:
22	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
23	chr8:8241927..8245169-chr8:8316549..8319625,5	MCF-7	breast:
24	chr8:8242160..8245521-chr8:8318713..8321604,3	MCF-7	breast:
25	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
26	chr8:8308652..8310168-chr8:8314593..8316228,2	MCF-7	breast:
27	chr8:8307359..8308990-chr8:8310543..8313387,3	MCF-7	breast:
28	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
29	chr8:8311665..8315626-chr8:8317447..8320934,9	MCF-7	breast:
30	chr8:8307087..8309406-chr8:8317216..8320167,2	MCF-7	breast:
31	chr8:8243810..8245986-chr8:8307375..8310131,2	MCF-7	breast:
32	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
33	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
34	chr8:8241777..8245267-chr8:8311182..8314962,7	MCF-7	breast:
35	chr8:8310535..8312786-chr8:8315430..8317371,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-2	chr8:8314419-8314592	ENSG00000254153
2	lnc-PRAGMIN.1-2	chr8:8318630-8318847	ENSG00000254153
3	lnc-PRAGMIN.1-2	chr8:8315919-8316036	ENSG00000254153
4	lnc-PRAGMIN.1-8	chr8:8327533-8327591	NONHSAT124876
5	lnc-AC068020.1-4	chr8:8322957-8323060	NONHSAT124875

No data

Variant related genes	Relation type
ENSG00000254153	TF binding region
ENSG00000254153	CpG island
ENSG00000254153	chromatin interactions
ENSG00000182319	chromatin interactions

Extended variants
information (count: 2005 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:2005 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2976846	chr8:8296071-8296072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569509757	chr8:8296076-8296077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541247098	chr8:8296113-8296114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557879507	chr8:8296117-8296118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs73664613	chr8:8296118-8296119	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs543548178	chr8:8296161-8296162	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs75764856	chr8:8296162-8296163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs74689412	chr8:8296208-8296209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542924643	chr8:8296223-8296224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs41393948	chr8:8296230-8296231	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528661512	chr8:8296252-8296253	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs551598871	chr8:8296254-8296255	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112229488	chr8:8296280-8296281	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182668381	chr8:8296308-8296309	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530865786	chr8:8296370-8296371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550667283	chr8:8296371-8296372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115302686	chr8:8296400-8296401	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs575666815	chr8:8296414-8296415	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs75420961	chr8:8296431-8296432	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150413230	chr8:8296511-8296512	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2921084	chr8:8296531-8296532	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs187647568	chr8:8296543-8296544	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557940842	chr8:8296601-8296602	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577924993	chr8:8296605-8296606	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537109777	chr8:8296609-8296610	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs578209240	chr8:8296658-8296659	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540521736	chr8:8296677-8296678	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557041299	chr8:8296690-8296691	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77567375	chr8:8296692-8296693	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112737793	chr8:8296712-8296713	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559785462	chr8:8296722-8296723	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111665891	chr8:8296727-8296728	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs573526496	chr8:8296729-8296730	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545298010	chr8:8296748-8296749	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs77090853	chr8:8296771-8296772	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs531025025	chr8:8296774-8296775	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs117286626	chr8:8296779-8296780	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79986505	chr8:8296784-8296785	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138119540	chr8:8296789-8296790	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547019930	chr8:8296793-8296794	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566755389	chr8:8296794-8296795	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534875406	chr8:8296814-8296815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149537310	chr8:8296816-8296817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537273127	chr8:8296817-8296818	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558347530	chr8:8296837-8296838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556767554	chr8:8296839-8296840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs373759084	chr8:8296889-8296890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532427065	chr8:8296894-8296895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573719168	chr8:8296919-8296920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535866107	chr8:8296924-8296925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8294000-8298600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:8295800-8297400	Enhancers	Primary B cells from peripheral blood	blood
3	chr8:8295800-8297600	Enhancers	Primary B cells from cord blood	blood
4	chr8:8296000-8296800	Enhancers	Stomach Mucosa	stomach
5	chr8:8296000-8296800	Enhancers	GM12878-XiMat	blood
6	chr8:8296000-8297000	Enhancers	Fetal Intestine Small	intestine
7	chr8:8296200-8296400	Enhancers	Fetal Lung	lung
8	chr8:8296200-8296800	Enhancers	Fetal Intestine Large	intestine
9	chr8:8296200-8303000	Enhancers	Placenta Amnion	Placenta Amnion
10	chr8:8296400-8296600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:8296400-8296600	Enhancers	Duodenum Mucosa	Duodenum
12	chr8:8296400-8296800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:8296400-8296800	Enhancers	Esophagus	oesophagus
14	chr8:8296400-8300000	Weak transcription	Fetal Lung	lung
15	chr8:8296600-8296800	Enhancers	Gastric	stomach
16	chr8:8296600-8297800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr8:8296600-8298200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:8296800-8298200	Weak transcription	Stomach Mucosa	stomach
19	chr8:8296800-8298600	Weak transcription	Esophagus	oesophagus
20	chr8:8296800-8298800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:8296800-8298800	Weak transcription	Gastric	stomach
22	chr8:8296800-8300400	Weak transcription	Fetal Intestine Large	intestine
23	chr8:8297000-8297400	Weak transcription	Fetal Intestine Small	intestine
24	chr8:8297400-8299600	Enhancers	Fetal Intestine Small	intestine
25	chr8:8297800-8300600	Enhancers	Duodenum Mucosa	Duodenum
26	chr8:8298200-8298800	Enhancers	Stomach Mucosa	stomach
27	chr8:8298200-8298800	Enhancers	NHEK	skin
28	chr8:8298200-8300800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:8298200-8302400	Enhancers	Placenta	Placenta
30	chr8:8298600-8300600	Enhancers	HMEC	breast
31	chr8:8298600-8300800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:8298600-8300800	Enhancers	Esophagus	oesophagus
33	chr8:8298600-8301000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:8298800-8299000	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr8:8298800-8299000	Flanking Active TSS	Stomach Mucosa	stomach
36	chr8:8298800-8299200	Enhancers	Lung	lung
37	chr8:8298800-8299200	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr8:8298800-8299400	Enhancers	Fetal Thymus	thymus
39	chr8:8298800-8299400	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr8:8298800-8299600	Enhancers	HSMMtube	muscle
41	chr8:8298800-8299800	Flanking Active TSS	NHEK	skin
42	chr8:8298800-8300600	Enhancers	Gastric	stomach
43	chr8:8298800-8300600	Enhancers	Pancreas	Pancrea
44	chr8:8298800-8300800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:8298800-8302200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:8299000-8299200	Enhancers	Stomach Mucosa	stomach
47	chr8:8299200-8299600	Flanking Active TSS	Stomach Mucosa	stomach
48	chr8:8299400-8299800	Enhancers	Lung	lung
49	chr8:8299400-8300000	Enhancers	Fetal Kidney	kidney
50	chr8:8299400-8301800	Weak transcription	Fetal Thymus	thymus

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