Variant report

Variant	esv2764105
Chromosome Location	chr8:10610557-10657726
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1168)
CpG islands
(count:976)
Chromatin interactive
region (count:43)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10638845-10638952	K562	blood:	n/a	n/a
2	ARID3A	chr8:10656082-10656601	K562	blood:	n/a	n/a
3	ARID3A	chr8:10653397-10654025	K562	blood:	n/a	n/a
4	ARID3A	chr8:10631175-10631647	K562	blood:	n/a	n/a
5	ARID3A	chr8:10629194-10629470	K562	blood:	n/a	n/a
6	ARID3A	chr8:10618425-10619055	K562	blood:	n/a	n/a
7	ARID3A	chr8:10634540-10635222	K562	blood:	n/a	n/a
8	ARID3A	chr8:10657288-10657802	K562	blood:	n/a	n/a
9	ARID3A	chr8:10632964-10633416	K562	blood:	n/a	n/a
10	ARID3A	chr8:10657152-10657846	HepG2	liver:	n/a	n/a
11	ATF1	chr8:10634783-10635469	K562	blood:	n/a	n/a
12	ATF1	chr8:10657290-10657727	K562	blood:	n/a	n/a
13	ATF1	chr8:10618426-10618829	K562	blood:	n/a	n/a
14	ATF1	chr8:10629162-10629538	K562	blood:	n/a	n/a
15	ATF1	chr8:10653494-10654054	K562	blood:	n/a	n/a
16	ATF2	chr8:10641139-10641593	GM12878	blood:	n/a	n/a
17	ATF2	chr8:10646115-10646583	GM12878	blood:	n/a	n/a
18	ATF2	chr8:10641097-10641653	GM12878	blood:	n/a	n/a
19	ATF2	chr8:10646076-10646653	GM12878	blood:	n/a	n/a
20	ATF3	chr8:10657391-10657631	K562	blood:	n/a	n/a
21	ATF3	chr8:10634812-10635209	K562	blood:	n/a	n/a
22	ATF3	chr8:10657250-10657724	K562	blood:	n/a	n/a
23	BACH1	chr8:10634535-10634552	K562	blood:	n/a	n/a
24	BACH1	chr8:10618657-10618682	K562	blood:	n/a	n/a
25	BATF	chr8:10641195-10641508	GM12878	blood:	n/a	chr8:10641369-10641380
26	BATF	chr8:10646148-10646551	GM12878	blood:	n/a	chr8:10646312-10646323
27	BATF	chr8:10641154-10641577	GM12878	blood:	n/a	chr8:10641369-10641380
28	BCL11A	chr8:10641274-10641544	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:10646180-10646518	GM12878	blood:	n/a	n/a
30	BCL3	chr8:10646199-10646599	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:10629130-10629563	K562	blood:	n/a	n/a
32	BHLHE40	chr8:10633148-10633444	K562	blood:	n/a	n/a
33	BHLHE40	chr8:10648112-10648199	K562	blood:	n/a	n/a
34	BHLHE40	chr8:10646418-10646431	K562	blood:	n/a	n/a
35	BHLHE40	chr8:10618383-10618969	K562	blood:	n/a	n/a
36	BHLHE40	chr8:10657309-10657639	K562	blood:	n/a	n/a
37	BHLHE40	chr8:10653533-10653798	K562	blood:	n/a	n/a
38	BHLHE40	chr8:10634083-10635624	K562	blood:	n/a	n/a
39	BRCA1	chr8:10657228-10657844	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr8:10647677-10647797	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr8:10645582-10645644	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr8:10634548-10635220	K562	blood:	n/a	n/a
43	CBX3	chr8:10657225-10657713	K562	blood:	n/a	n/a
44	CBX3	chr8:10634712-10635188	K562	blood:	n/a	n/a
45	CBX3	chr8:10657151-10657837	HCT-116	colon:	n/a	n/a
46	CBX3	chr8:10657279-10657601	K562	blood:	n/a	n/a
47	CCNT2	chr8:10617880-10618137	K562	blood:	n/a	n/a
48	CCNT2	chr8:10618415-10618764	K562	blood:	n/a	n/a
49	CCNT2	chr8:10634549-10635416	K562	blood:	n/a	chr8:10634941-10634961
50	CCNT2	chr8:10653477-10653875	K562	blood:	n/a	chr8:10653693-10653713 chr8:10653629-10653649

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10643634-10643684	Jurkat	blood:	n/a
2	chr8:10657514-10657564	SKMC	muscle:	n/a
3	chr8:10635419-10635469	GM06990	blood:	n/a
4	chr8:10646690-10646740	HCPEpiC	choroid plexus:	n/a
5	chr8:10621935-10621985	Hepatocyte	liver:	n/a
6	chr8:10622887-10622937	GM19239	blood:	n/a
7	chr8:10623344-10623394	HEK293	kidney:	embryo
8	chr8:10635419-10635469	NB4	blood:	n/a
9	chr8:10650046-10650096	HCT-116	colon:	n/a
10	chr8:10617394-10617444	HRPEpiC	eye:	n/a
11	chr8:10635419-10635469	Caco-2	colon:	n/a
12	chr8:10621935-10621985	NHDF-neo	bronchial:	n/a
13	chr8:10621935-10621985	HRPEpiC	eye:	n/a
14	chr8:10657514-10657564	HUVEC	blood vessel:	n/a
15	chr8:10622887-10622937	GM12878	blood:	n/a
16	chr8:10646690-10646740	SK-N-SH_RA	brain:	n/a
17	chr8:10621935-10621985	HCF	heart:	n/a
18	chr8:10617394-10617444	SKMC	muscle:	n/a
19	chr8:10646690-10646740	BJ	skin:	n/a
20	chr8:10621874-10621924	AG09319	gingival:	n/a
21	chr8:10621935-10621985	LNCaP	prostate:	n/a
22	chr8:10649960-10650010	BJ	skin:	n/a
23	chr8:10646690-10646740	HEK293	kidney:	embryo
24	chr8:10621935-10621985	AG04450	lung:	fetal
25	chr8:10649960-10650010	LNCaP	prostate:	n/a
26	chr8:10623344-10623394	HRCEpiC	kidney:	n/a
27	chr8:10649960-10650010	AG09309	skin:	n/a
28	chr8:10621935-10621985	IMR90	lung:	fetal
29	chr8:10623344-10623394	SAEC	small airway:	n/a
30	chr8:10622887-10622937	ProgFib	skin:	n/a
31	chr8:10621935-10621985	GM12878	blood:	n/a
32	chr8:10623344-10623394	Hepatocyte	liver:	n/a
33	chr8:10646690-10646740	T-47D	breast:	n/a
34	chr8:10646690-10646740	HMEC	breast:	n/a
35	chr8:10657514-10657564	NB4	blood:	n/a
36	chr8:10646690-10646740	PrEC	prostate:	n/a
37	chr8:10650046-10650096	PANC-1	pancreas:	n/a
38	chr8:10623344-10623394	U87	brain:	n/a
39	chr8:10617063-10617113	U87	brain:	n/a
40	chr8:10622805-10622855	PrEC	prostate:	n/a
41	chr8:10649960-10650010	Caco-2	colon:	n/a
42	chr8:10621801-10621851	RPTEC	kidney:	n/a
43	chr8:10621801-10621851	Hela-S3	cervix:	n/a
44	chr8:10635419-10635469	GM19239	blood:	n/a
45	chr8:10622805-10622855	IMR90	lung:	fetal
46	chr8:10623344-10623394	GM19239	blood:	n/a
47	chr8:10643634-10643684	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:10635419-10635469	H1-hESC	embryonic stem cell:	embryo
49	chr8:10617063-10617113	HCT-116	colon:	n/a
50	chr8:10643634-10643684	MCF-7	breast:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:10621941..10624619-chr8:10627842..10631333,3	K562	blood:
2	chr8:10647998..10650941-chr8:10651803..10654879,3	K562	blood:
3	chr8:10635373..10637028-chr8:10639267..10640869,2	MCF-7	breast:
4	chr8:10611693..10613429-chr8:10616715..10619425,2	K562	blood:
5	chr8:10447404..10448576-chr8:10655982..10656998,11	MCF-7	breast:
6	chr8:10635373..10637028-chr8:10639267..10640869,2	MCF-7	breast:
7	chr8:10644063..10645864-chr8:10646300..10647918,2	K562	blood:
8	chr8:10628530..10631997-chr8:10633640..10636320,4	K562	blood:
9	chr8:10515210..10517092-chr8:10648053..10650432,2	K562	blood:
10	chr8:10648353..10650941-chr8:10651549..10653303,2	K562	blood:
11	chr8:10447773..10448295-chr8:10656037..10656649,2	MCF-7	breast:
12	chr8:10444773..10445405-chr8:10656129..10656744,2	MCF-7	breast:
13	chr8:10637227..10639658-chr8:10641198..10643629,3	K562	blood:
14	chr8:10517902..10518777-chr8:10655034..10655826,2	K562	blood:
15	chr8:10634439..10636776-chr8:10637920..10639941,2	K562	blood:
16	chr8:10654838..10657527-chr8:10667570..10669417,2	K562	blood:
17	chr8:10655273..10657441-chr8:10673003..10675779,2	MCF-7	breast:
18	chr8:10634439..10636776-chr8:10637920..10639941,2	K562	blood:
19	chr8:10615706..10617702-chr8:10620374..10622044,2	K562	blood:
20	chr8:10633410..10636281-chr8:10695946..10698229,2	K562	blood:
21	chr8:10616130..10621063-chr8:10631004..10634975,5	K562	blood:
22	chr8:10631743..10634256-chr8:10658449..10660185,2	K562	blood:
23	chr8:10648269..10650512-chr8:10653379..10655643,2	K562	blood:
24	chr8:10628530..10631997-chr8:10633640..10636320,4	K562	blood:
25	chr8:10621941..10624619-chr8:10627842..10631333,3	K562	blood:
26	chr8:10622933..10625831-chr8:10627358..10629898,3	K562	blood:
27	chr8:10615706..10617702-chr8:10620374..10622044,2	K562	blood:
28	chr8:10616130..10621063-chr8:10631004..10634975,5	K562	blood:
29	chr8:10611693..10613429-chr8:10616715..10619425,2	K562	blood:
30	chr8:10647998..10650941-chr8:10651803..10654879,3	K562	blood:
31	chr8:10622933..10625831-chr8:10627358..10629898,3	K562	blood:
32	chr8:10648269..10650512-chr8:10653379..10655643,2	K562	blood:
33	chr8:10613644..10615982-chr8:10616006..10618005,2	MCF-7	breast:
34	chr8:10613644..10615982-chr8:10616006..10618005,2	MCF-7	breast:
35	chr8:10615290..10617626-chr8:10678525..10680394,2	K562	blood:
36	chr8:10592393..10594061-chr8:10610774..10613759,2	K562	blood:
37	chr8:10640744..10643813-chr8:10646247..10648006,3	K562	blood:
38	chr8:10651485..10654382-chr8:10658663..10661335,2	K562	blood:
39	chr8:10591978..10593893-chr8:10610774..10613689,2	K562	blood:
40	chr8:10648353..10650941-chr8:10651549..10653303,2	K562	blood:
41	chr8:10620237..10621942-chr8:10624836..10626716,2	K562	blood:
42	chr8:10644063..10645864-chr8:10646300..10647918,2	K562	blood:
43	chr8:10620237..10621942-chr8:10624836..10626716,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf74-1	chr8:10611712-10611828	ENSG00000248896
2	lnc-C8orf74-4	chr8:10649122-10649238	ucscGeneNc_uc003wtg_1
3	lnc-C8orf74-1	chr8:10628705-10628902	ENSG00000248896
4	lnc-C8orf74-1	chr8:10621847-10622233	ENSG00000248896
5	lnc-C8orf74-1	chr8:10622680-10622686	NONHSAT125014
6	lnc-C8orf74-4	chr8:10624234-10624550	ucscGeneNc_uc003wtg_1
7	lnc-C8orf74-1	chr8:10621847-10622667	NONHSAT125014
8	lnc-PINX1-1	chr8:10615296-10618693	NONHSAT125016
9	lnc-C8orf74-1	chr8:10611712-10611828	NONHSAT125014

No data

Variant related genes	Relation type
ENSG00000252565	TF binding region
ENSG00000252565	CpG island
ENSG00000252565	chromatin interactions
ENSG00000253695	chromatin interactions
ENSG00000258724	chromatin interactions
ENSG00000254093	chromatin interactions
HSPA1B	miRNA target sites

Extended variants
information (count: 2640 )
Associated
traits (count: 149 )

Variant overlapped rSNPs/rCNVs (count:2640 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565161413	chr8:10610557-10610558	Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs577049001	chr8:10610566-10610567	Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs192586069	chr8:10610569-10610570	Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs560843411	chr8:10610570-10610571	Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs529850851	chr8:10610574-10610575	Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs559631755	chr8:10610612-10610613	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs146691745	chr8:10610634-10610635	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs566586302	chr8:10610666-10610667	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs558482023	chr8:10610681-10610682	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs185641623	chr8:10610707-10610708	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs552235519	chr8:10610731-10610732	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs568802181	chr8:10610732-10610733	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs537837276	chr8:10610739-10610740	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs77332704	chr8:10610754-10610755	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs12335139	chr8:10610781-10610782	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs536851914	chr8:10610809-10610810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572678602	chr8:10610810-10610811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114593114	chr8:10610821-10610822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190435570	chr8:10610828-10610829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558997151	chr8:10610838-10610839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566537369	chr8:10610861-10610862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140306831	chr8:10610910-10610911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544162284	chr8:10610921-10610922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192916672	chr8:10610927-10610928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529911654	chr8:10610942-10610943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554252152	chr8:10610946-10610947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540501783	chr8:10610951-10610952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150976436	chr8:10611009-10611010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574018975	chr8:10611029-10611030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543083471	chr8:10611067-10611068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35414136	chr8:10611073-10611074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552034327	chr8:10611078-10611079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549790691	chr8:10611104-10611105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140838179	chr8:10611105-10611106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533657202	chr8:10611106-10611107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184469315	chr8:10611108-10611109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150156433	chr8:10611114-10611115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555081678	chr8:10611155-10611156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115260735	chr8:10611177-10611178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536973128	chr8:10611215-10611216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553613028	chr8:10611290-10611291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76061241	chr8:10611297-10611298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367554748	chr8:10611335-10611336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539218665	chr8:10611353-10611354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371388464	chr8:10611355-10611356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574686956	chr8:10611368-10611369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575301340	chr8:10611380-10611381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79412488	chr8:10611381-10611382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376018069	chr8:10611384-10611385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532509822	chr8:10611387-10611388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:149)

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
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Osteosarcoma	21215367	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD

Chromatin state (count:1290 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10609600-10614000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:10609600-10616200	Weak transcription	Primary T cells from cord blood	blood
3	chr8:10610000-10621400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:10610200-10610800	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
5	chr8:10610400-10610600	Bivalent Enhancer	Esophagus	oesophagus
6	chr8:10610400-10610600	ZNF genes & repeats	HepG2	liver
7	chr8:10610400-10614200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:10610600-10620400	Weak transcription	HepG2	liver
9	chr8:10610800-10622200	Weak transcription	Primary B cells from cord blood	blood
10	chr8:10610800-10662000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr8:10611200-10624400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:10612600-10612800	Weak transcription	Pancreas	Pancrea
13	chr8:10612600-10617600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr8:10612600-10621600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:10612800-10621600	Weak transcription	Spleen	Spleen
16	chr8:10613200-10613400	ZNF genes & repeats	Aorta	Aorta
17	chr8:10613200-10622600	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr8:10613400-10621600	Weak transcription	Aorta	Aorta
19	chr8:10613600-10614800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:10613600-10614800	Enhancers	HMEC	breast
21	chr8:10613600-10618400	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr8:10613600-10618800	Weak transcription	Fetal Muscle Leg	muscle
23	chr8:10613800-10617800	Weak transcription	Ovary	ovary
24	chr8:10614000-10614800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:10614000-10614800	Enhancers	Esophagus	oesophagus
26	chr8:10614000-10614800	Enhancers	Placenta	Placenta
27	chr8:10614200-10614400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:10614200-10614800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:10614200-10614800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:10614200-10614800	Enhancers	Hela-S3	cervix
31	chr8:10614200-10614800	Enhancers	NHEK	skin
32	chr8:10614200-10616600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr8:10614200-10621400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr8:10614400-10614800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:10614400-10634200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:10614600-10616600	Weak transcription	K562	blood
37	chr8:10614800-10616000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:10614800-10616800	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr8:10614800-10617200	Weak transcription	Esophagus	oesophagus
40	chr8:10614800-10617400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:10614800-10617600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:10614800-10617600	Weak transcription	HMEC	breast
43	chr8:10614800-10617600	Weak transcription	NHEK	skin
44	chr8:10614800-10617800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr8:10614800-10618400	Weak transcription	Placenta	Placenta
46	chr8:10614800-10618600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:10614800-10621400	Weak transcription	Left Ventricle	heart
48	chr8:10614800-10621400	Weak transcription	Lung	lung
49	chr8:10614800-10621800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr8:10614800-10622000	Weak transcription	Hela-S3	cervix

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