Variant report

Variant	nsv611426
Chromosome Location	chr8:62036793-62179465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1129)
CpG islands
(count:733)
Chromatin interactive
region (count:42)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:62156627-62156854	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:62057926-62058090	HepG2	liver:	n/a	n/a
3	ATF1	chr8:62171026-62171196	K562	blood:	n/a	n/a
4	ATF2	chr8:62051428-62052083	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:62052340-62052731	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:62037495-62039068	GM12878	blood:	n/a	n/a
7	ATF2	chr8:62051532-62052195	GM12878	blood:	n/a	n/a
8	ATF2	chr8:62051441-62051892	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr8:62037607-62039218	GM12878	blood:	n/a	n/a
10	BACH1	chr8:62052503-62052548	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:62051701-62051898	K562	blood:	n/a	n/a
12	BACH1	chr8:62051636-62052004	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:62142024-62142192	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr8:62037354-62038189	GM12878	blood:	n/a	n/a
15	BATF	chr8:62038540-62038986	GM12878	blood:	n/a	n/a
16	BATF	chr8:62037776-62038188	GM12878	blood:	n/a	n/a
17	BATF	chr8:62115085-62115367	GM12878	blood:	n/a	n/a
18	BATF	chr8:62038583-62039039	GM12878	blood:	n/a	n/a
19	BATF	chr8:62115112-62115375	GM12878	blood:	n/a	n/a
20	BCL11A	chr8:62037818-62038064	GM12878	blood:	n/a	chr8:62038027-62038036
21	BCL11A	chr8:62079164-62079361	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr8:62038537-62039052	GM12878	blood:	n/a	chr8:62038704-62038713
23	BCL11A	chr8:62115057-62115356	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:62114990-62115367	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:62037650-62038302	GM12878	blood:	n/a	chr8:62038027-62038036
26	BCL11A	chr8:62038568-62039012	GM12878	blood:	n/a	chr8:62038704-62038713
27	BCL3	chr8:62037706-62038169	GM12878	blood:	n/a	chr8:62038027-62038036
28	BCLAF1	chr8:62038490-62039088	GM12878	blood:	n/a	chr8:62038704-62038713
29	BCLAF1	chr8:62037602-62038300	GM12878	blood:	n/a	chr8:62038027-62038036
30	BCLAF1	chr8:62051496-62052003	GM12878	blood:	n/a	chr8:62051809-62051822
31	BCLAF1	chr8:62038348-62039137	GM12878	blood:	n/a	chr8:62038704-62038713
32	BHLHE40	chr8:62172423-62172658	K562	blood:	n/a	n/a
33	BHLHE40	chr8:62051607-62052244	GM12878	blood:	n/a	chr8:62051809-62051825 chr8:62052071-62052087 chr8:62051743-62051759
34	BHLHE40	chr8:62051550-62051949	K562	blood:	n/a	chr8:62051809-62051825 chr8:62051743-62051759
35	BHLHE40	chr8:62156591-62156751	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:62037328-62039066	GM12878	blood:	n/a	n/a
37	BHLHE40	chr8:62062550-62062698	GM12878	blood:	n/a	n/a
38	BHLHE40	chr8:62059601-62059889	GM12878	blood:	n/a	n/a
39	BRCA1	chr8:62176805-62176807	GM12878	blood:	n/a	n/a
40	BRCA1	chr8:62051657-62051857	HepG2	liver:	n/a	n/a
41	BRCA1	chr8:62051636-62051920	H1-hESC	embryonic stem cell:	n/a	n/a
42	CBX3	chr8:62051393-62051997	HCT-116	colon:	n/a	n/a
43	CBX3	chr8:62114261-62114536	K562	blood:	n/a	n/a
44	CBX3	chr8:62051485-62051905	K562	blood:	n/a	n/a
45	CCNT2	chr8:62051590-62052139	K562	blood:	n/a	chr8:62052117-62052126
46	CEBPB	chr8:62145668-62145897	A549	lung:	n/a	n/a
47	CEBPB	chr8:62037626-62038387	GM12878	blood:	n/a	n/a
48	CEBPB	chr8:62174522-62174708	HepG2	liver:	n/a	chr8:62174630-62174641
49	CEBPB	chr8:62079173-62079375	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:62168419-62168738	K562	blood:	n/a	chr8:62168590-62168601

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:62052430-62052480	HRE	kidney:	n/a
2	chr8:62052430-62052480	HRE	kidney:	n/a
3	chr8:62051812-62051862	IMR90	lung:	fetal
4	chr8:62049902-62049952	HRE	kidney:	n/a
5	chr8:62052594-62052644	T-47D	breast:	n/a
6	chr8:62048493-62048543	HEK293	kidney:	embryo
7	chr8:62084457-62084507	MCF10A-Er-Src	breast:	n/a
8	chr8:62051647-62051697	T-47D	breast:	n/a
9	chr8:62052594-62052644	SK-N-SH	brain:	n/a
10	chr8:62052430-62052480	HAEpiC	amniotic membrane:	n/a
11	chr8:62051812-62051862	HRPEpiC	eye:	n/a
12	chr8:62048493-62048543	MCF-7	breast:	n/a
13	chr8:62055838-62055888	Hepatocyte	liver:	n/a
14	chr8:62084457-62084507	HCF	heart:	n/a
15	chr8:62084457-62084507	AG04449	skin:	fetal
16	chr8:62066624-62066674	AG04450	lung:	fetal
17	chr8:62052409-62052459	ProgFib	skin:	n/a
18	chr8:62052043-62052093	IMR90	lung:	fetal
19	chr8:62051647-62051697	SAEC	small airway:	n/a
20	chr8:62052409-62052459	MCF-7	breast:	n/a
21	chr8:62048493-62048543	BE2_C	brain:	n/a
22	chr8:62051812-62051862	AG09319	gingival:	n/a
23	chr8:62049902-62049952	HNPCEpiC	eye:	n/a
24	chr8:62052430-62052480	HEEpiC	esophagus:	n/a
25	chr8:62052207-62052257	HNPCEpiC	eye:	n/a
26	chr8:62051812-62051862	HIPEpiC	eye:	n/a
27	chr8:62066624-62066674	U87	brain:	n/a
28	chr8:62049902-62049952	SKMC	muscle:	n/a
29	chr8:62052207-62052257	HMEC	breast:	n/a
30	chr8:62084457-62084507	MCF-7	breast:	n/a
31	chr8:62049902-62049952	AoSMC	blood vessel:	n/a
32	chr8:62084457-62084507	HNPCEpiC	eye:	n/a
33	chr8:62052043-62052093	NHDF-neo	bronchial:	n/a
34	chr8:62049902-62049952	GM19239	blood:	n/a
35	chr8:62051647-62051697	Caco-2	colon:	n/a
36	chr8:62052430-62052480	SK-N-SH	brain:	n/a
37	chr8:62055838-62055888	AG04450	lung:	fetal
38	chr8:62084457-62084507	AG04450	lung:	fetal
39	chr8:62051647-62051697	BJ	skin:	n/a
40	chr8:62055838-62055888	PFSK-1	brain:	n/a
41	chr8:62052207-62052257	Jurkat	blood:	n/a
42	chr8:62084457-62084507	PANC-1	pancreas:	n/a
43	chr8:62055838-62055888	NHDF-neo	bronchial:	n/a
44	chr8:62051647-62051697	NHDF-neo	bronchial:	n/a
45	chr8:62051812-62051862	SK-N-SH_RA	brain:	n/a
46	chr8:62052207-62052257	PrEC	prostate:	n/a
47	chr8:62051647-62051697	HRE	kidney:	n/a
48	chr8:62084457-62084507	HRCEpiC	kidney:	n/a
49	chr8:62052430-62052480	SKMC	muscle:	n/a
50	chr8:62051812-62051862	LNCaP	prostate:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:62156582..62157132-chr8:62381389..62382258,2	MCF-7	breast:
2	chr8:62044721..62047676-chr8:62048656..62051008,2	MCF-7	breast:
3	chr8:62051294..62051870-chr8:62381197..62381952,2	MCF-7	breast:
4	chr8:61589463..61592430-chr8:62051338..62054107,2	K562	blood:
5	chr8:61786507..61789220-chr8:62034568..62037339,2	K562	blood:
6	chr8:62034256..62037126-chr8:62040343..62042185,2	K562	blood:
7	chr8:61567081..61569634-chr8:62050277..62052303,2	K562	blood:
8	chr8:62051677..62052206-chr8:62381213..62382143,4	K562	blood:
9	chr8:62077514..62080405-chr8:62083367..62084892,2	K562	blood:
10	chr8:62129510..62131097-chr8:62132892..62135202,2	K562	blood:
11	chr8:62077514..62079078-chr8:62082702..62084867,2	K562	blood:
12	chr8:62156501..62157309-chr8:62475663..62476458,3	K562	blood:
13	chr8:62036289..62038012-chr8:62049623..62051509,2	MCF-7	breast:
14	chr8:62155417..62156246-chr8:62381440..62381973,2	MCF-7	breast:
15	chr8:62156250..62157004-chr8:62428078..62428760,2	MCF-7	breast:
16	chr7:95064221..95064952-chr8:62154095..62154615,2	Hela-S3	cervix:
17	chr8:62039342..62040905-chr8:62046486..62048457,2	MCF-7	breast:
18	chr8:62119495..62121970-chr8:62122752..62125031,2	K562	blood:
19	chr8:62034871..62036799-chr8:62043503..62045064,2	K562	blood:
20	chr8:62171421..62173455-chr8:62175789..62177372,2	K562	blood:
21	chr8:62156269..62156884-chr8:62475900..62476409,2	MCF-7	breast:
22	chr8:62077514..62079078-chr8:62082702..62084867,2	K562	blood:
23	chr8:62119495..62121970-chr8:62122752..62125031,2	K562	blood:
24	chr8:62034256..62037126-chr8:62040343..62042185,2	K562	blood:
25	chr22:39566536..39567354-chr8:62099186..62100100,2	MCF-7	breast:
26	chr8:62039342..62040905-chr8:62046486..62048457,2	MCF-7	breast:
27	chr8:62042411..62044649-chr8:62046602..62048940,2	K562	blood:
28	chr8:62050920..62052213-chr8:62152653..62153352,3	MCF-7	breast:
29	chr8:62156345..62157248-chr8:62475582..62476441,2	MCF-7	breast:
30	chr8:62156342..62157143-chr8:62381140..62382022,5	K562	blood:
31	chr8:62036289..62038012-chr8:62049623..62051509,2	MCF-7	breast:
32	chr8:62044721..62047676-chr8:62048656..62051008,2	MCF-7	breast:
33	chr8:62156342..62157195-chr8:62380225..62380826,2	MCF-7	breast:
34	chr8:61564289..61566085-chr8:62064724..62067710,2	K562	blood:
35	chr8:62042411..62044649-chr8:62046602..62048940,2	K562	blood:
36	chr8:62034871..62036799-chr8:62043503..62045064,2	K562	blood:
37	chr8:62050920..62052213-chr8:62152653..62153352,3	MCF-7	breast:
38	chr8:62129510..62131097-chr8:62132892..62135202,2	K562	blood:
39	chr8:62156322..62157217-chr8:62381101..62382114,8	MCF-7	breast:
40	chr8:62077514..62080405-chr8:62083367..62084892,2	K562	blood:
41	chr8:62112094..62114817-chr8:62114903..62119963,4	K562	blood:
42	chr8:62171421..62173455-chr8:62175789..62177372,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPH-8	chr8:62042686-62042861	l_3611_chr8:62041271-62042861_whiteBloodCell
2	lnc-ASPH-4	chr8:62177183-62177418	ENSG00000254222.1
3	lnc-ASPH-8	chr8:62041272-62041385	l_3611_chr8:62041271-62042861_whiteBloodCell
4	lnc-ASPH-8	chr8:62041386-62041570	l_3611_chr8:62041271-62042861_whiteBloodCell
5	lnc-CHD7-5	chr8:62041283-62041594	l_3610_chr8:62040284-62041594_adrenal
6	lnc-CHD7-5	chr8:62040285-62040474	l_3610_chr8:62040284-62041594_adrenal

No data

Variant related genes	Relation type
NPM1P6	TF binding region
NPM1P6	CpG island
ENSG00000105854	chromatin interactions
ENSG00000213881	chromatin interactions
ENSG00000171316	chromatin interactions

Extended variants
information (count: 3381 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3381 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3864667	chr8:62036793-62036794	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371566764	chr8:62036794-62036795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114432711	chr8:62036799-62036800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9643525	chr8:62036855-62036856	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552167341	chr8:62036860-62036861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112503277	chr8:62037010-62037011	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs560813360	chr8:62037017-62037018	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs574299614	chr8:62037018-62037019	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs528066995	chr8:62037020-62037021	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs578096307	chr8:62037086-62037087	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs543661482	chr8:62037125-62037126	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs557919305	chr8:62037134-62037135	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs568113160	chr8:62037169-62037170	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs563958813	chr8:62037177-62037178	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs535564048	chr8:62037178-62037179	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs73257915	chr8:62037196-62037197	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs569455961	chr8:62037219-62037220	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs139783122	chr8:62037221-62037222	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs75540104	chr8:62037259-62037260	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs539990614	chr8:62037378-62037379	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs533900501	chr8:62037403-62037404	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs555364279	chr8:62037408-62037409	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs573763645	chr8:62037462-62037463	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs544285060	chr8:62037468-62037469	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs562672283	chr8:62037478-62037479	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs575344922	chr8:62037479-62037480	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs115518906	chr8:62037506-62037507	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs144480728	chr8:62037589-62037590	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs113570547	chr8:62037627-62037628	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs528386424	chr8:62037643-62037644	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs372623289	chr8:62037687-62037688	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs146143637	chr8:62037707-62037708	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs573199242	chr8:62037728-62037729	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs528928984	chr8:62037734-62037735	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs560035102	chr8:62037816-62037817	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs569018571	chr8:62037847-62037848	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs532225177	chr8:62037865-62037866	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs577610078	chr8:62037883-62037884	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs375875893	chr8:62037891-62037892	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs574297847	chr8:62037933-62037934	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs184086058	chr8:62037944-62037945	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs567025090	chr8:62037971-62037972	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs201416197	chr8:62038009-62038010	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs200712934	chr8:62038014-62038015	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs201853150	chr8:62038017-62038018	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs377075377	chr8:62038136-62038137	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs542598603	chr8:62038158-62038159	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs551919782	chr8:62038177-62038178	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs112488646	chr8:62038249-62038250	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555675961	chr8:62038281-62038282	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:599 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62034000-62037000	Enhancers	GM12878-XiMat	blood
2	chr8:62034400-62051400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:62036200-62036800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:62036200-62037400	Enhancers	HMEC	breast
5	chr8:62036200-62037800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr8:62036400-62038000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:62036800-62037400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:62037000-62039600	Flanking Active TSS	GM12878-XiMat	blood
9	chr8:62037200-62037800	Enhancers	Primary B cells from cord blood	blood
10	chr8:62037200-62038000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr8:62037200-62039200	Enhancers	Primary B cells from peripheral blood	blood
12	chr8:62037400-62037600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:62037400-62038200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
14	chr8:62037400-62038200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr8:62037600-62038200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr8:62037800-62038000	Bivalent Enhancer	Primary T cells from cord blood	blood
17	chr8:62037800-62038200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:62037800-62038400	Flanking Active TSS	Primary B cells from cord blood	blood
19	chr8:62038000-62039800	Enhancers	Primary T cells from cord blood	blood
20	chr8:62038400-62039000	Enhancers	Primary B cells from cord blood	blood
21	chr8:62038400-62039000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
22	chr8:62038600-62039000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr8:62038600-62039000	Enhancers	Pancreas	Pancrea
24	chr8:62038800-62039000	Enhancers	Fetal Thymus	thymus
25	chr8:62039000-62044000	Weak transcription	Primary B cells from cord blood	blood
26	chr8:62039000-62051400	Weak transcription	Pancreas	Pancrea
27	chr8:62039200-62043800	Weak transcription	Primary B cells from peripheral blood	blood
28	chr8:62039600-62041400	Enhancers	GM12878-XiMat	blood
29	chr8:62041400-62043600	Weak transcription	GM12878-XiMat	blood
30	chr8:62043600-62044400	Enhancers	GM12878-XiMat	blood
31	chr8:62043800-62045000	Enhancers	Primary B cells from peripheral blood	blood
32	chr8:62044000-62045000	Enhancers	Primary B cells from cord blood	blood
33	chr8:62044400-62044600	Genic enhancers	GM12878-XiMat	blood
34	chr8:62044400-62044800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr8:62044400-62044800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr8:62044400-62044800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:62044600-62045000	Enhancers	GM12878-XiMat	blood
38	chr8:62045000-62045200	Weak transcription	GM12878-XiMat	blood
39	chr8:62045200-62045600	Strong transcription	GM12878-XiMat	blood
40	chr8:62045600-62051400	Weak transcription	GM12878-XiMat	blood
41	chr8:62050600-62051400	Enhancers	Fetal Intestine Large	intestine
42	chr8:62050800-62051400	Enhancers	K562	blood
43	chr8:62051000-62051400	Enhancers	Fetal Brain Male	brain
44	chr8:62051000-62052600	Enhancers	Fetal Heart	heart
45	chr8:62051200-62051400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
46	chr8:62051200-62051400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr8:62051200-62051400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:62051200-62051400	Enhancers	Primary hematopoietic stem cells	blood
49	chr8:62051200-62051400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr8:62051200-62051400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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