Variant report

Variant	nsv1033007
Chromosome Location	chr8:87185458-87319476
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:683)
CpG islands
(count:305)
Chromatin interactive
region (count:125)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:87302190-87302818	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:87237988-87238154	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:87249730-87249762	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:87251126-87251828	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:87313199-87313488	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:87222381-87222600	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:87267265-87268652	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:87307822-87308253	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:87269106-87269601	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:87269806-87269918	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:87249992-87250780	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:87317607-87317927	HepG2	liver:	n/a	chr8:87317682-87317698
13	ATF1	chr8:87274360-87274458	K562	blood:	n/a	n/a
14	ATF3	chr8:87302234-87302791	A549	lung:	n/a	n/a
15	BHLHE40	chr8:87250154-87250425	HepG2	liver:	n/a	n/a
16	BHLHE40	chr8:87267833-87268266	HepG2	liver:	n/a	n/a
17	CBX3	chr8:87292707-87292924	K562	blood:	n/a	n/a
18	CBX3	chr8:87292590-87293043	HCT-116	colon:	n/a	n/a
19	CEBPB	chr8:87302363-87302733	A549	lung:	n/a	n/a
20	CEBPB	chr8:87302309-87302793	A549	lung:	n/a	n/a
21	CEBPB	chr8:87274635-87274945	HepG2	liver:	n/a	chr8:87274760-87274771
22	CEBPB	chr8:87259018-87259216	HepG2	liver:	n/a	chr8:87259098-87259109
23	CEBPB	chr8:87274550-87274931	MCF-7	breast:	n/a	chr8:87274760-87274771
24	CEBPB	chr8:87302198-87302848	MCF-7	breast:	n/a	n/a
25	CEBPB	chr8:87274645-87274931	Hela-S3	cervix:	n/a	chr8:87274760-87274771
26	CEBPB	chr8:87209560-87209808	HepG2	liver:	n/a	chr8:87209668-87209679
27	CEBPB	chr8:87215442-87215754	A549	lung:	n/a	n/a
28	CEBPB	chr8:87256043-87256255	K562	blood:	n/a	n/a
29	CEBPB	chr8:87196022-87196224	HepG2	liver:	n/a	chr8:87196117-87196128
30	CEBPB	chr8:87282297-87282482	K562	blood:	n/a	chr8:87282437-87282448
31	CEBPB	chr8:87224775-87224930	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:87274650-87274867	IMR90	lung:	n/a	chr8:87274760-87274771
33	CEBPB	chr8:87269121-87269709	MCF-7	breast:	n/a	chr8:87269246-87269263 chr8:87269628-87269640 chr8:87269247-87269260
34	CEBPB	chr8:87196068-87196211	K562	blood:	n/a	chr8:87196117-87196128
35	CEBPB	chr8:87302409-87302635	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:87195401-87195660	K562	blood:	n/a	n/a
37	CEBPB	chr8:87258920-87259284	HepG2	liver:	n/a	chr8:87259098-87259109
38	CEBPB	chr8:87282270-87282612	HepG2	liver:	n/a	chr8:87282437-87282448
39	CEBPB	chr8:87269317-87269533	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:87251218-87251706	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:87224730-87225127	MCF-7	breast:	n/a	n/a
42	CEBPB	chr8:87274075-87274343	A549	lung:	n/a	n/a
43	CEBPB	chr8:87317733-87317942	A549	lung:	n/a	n/a
44	CEBPB	chr8:87269244-87269623	HepG2	liver:	n/a	chr8:87269246-87269263 chr8:87269247-87269260
45	CEBPB	chr8:87301792-87302754	Hela-S3	cervix:	n/a	chr8:87301893-87301904
46	CEBPB	chr8:87302364-87302751	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:87224761-87225010	IMR90	lung:	n/a	n/a
48	CEBPB	chr8:87256017-87256246	K562	blood:	n/a	n/a
49	CEBPB	chr8:87269246-87269692	MCF-7	breast:	n/a	chr8:87269246-87269263 chr8:87269628-87269640 chr8:87269247-87269260
50	CEBPB	chr8:87302196-87302935	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:87242630-87242680	PANC-1	pancreas:	n/a
2	chr8:87243677-87243727	NH-A	brain:	n/a
3	chr8:87243983-87244033	HIPEpiC	eye:	n/a
4	chr8:87242630-87242680	AG09309	skin:	n/a
5	chr8:87226434-87226484	MCF-7	breast:	n/a
6	chr8:87242630-87242680	CMK	blood:	n/a
7	chr8:87243677-87243727	Hepatocyte	liver:	n/a
8	chr8:87243677-87243727	SK-N-SH	brain:	n/a
9	chr8:87243979-87244029	SK-N-SH	brain:	n/a
10	chr8:87243983-87244033	HRCEpiC	kidney:	n/a
11	chr8:87243677-87243727	U87	brain:	n/a
12	chr8:87242630-87242680	K562	blood:	n/a
13	chr8:87226434-87226484	ECC-1	luminal epithelium:	n/a
14	chr8:87226434-87226484	BJ	skin:	n/a
15	chr8:87243677-87243727	HepG2	liver:	n/a
16	chr8:87243677-87243727	HEK293	kidney:	embryo
17	chr8:87243677-87243727	NHDF-neo	bronchial:	n/a
18	chr8:87243677-87243727	NT2-D1	testis:	n/a
19	chr8:87242630-87242680	AG04449	skin:	fetal
20	chr8:87243983-87244033	HepG2	liver:	n/a
21	chr8:87243677-87243727	HEEpiC	esophagus:	n/a
22	chr8:87242630-87242680	ECC-1	luminal epithelium:	n/a
23	chr8:87243677-87243727	AoSMC	blood vessel:	n/a
24	chr8:87243983-87244033	MCF10A-Er-Src	breast:	n/a
25	chr8:87243677-87243727	BJ	skin:	n/a
26	chr8:87243979-87244029	SK-N-SH_RA	brain:	n/a
27	chr8:87226434-87226484	NHDF-neo	bronchial:	n/a
28	chr8:87242630-87242680	GM12891	blood:	n/a
29	chr8:87243677-87243727	RPTEC	kidney:	n/a
30	chr8:87243677-87243727	ovcar-3	ovarian:	n/a
31	chr8:87243979-87244029	HRPEpiC	eye:	n/a
32	chr8:87226434-87226484	HCPEpiC	choroid plexus:	n/a
33	chr8:87243677-87243727	BE2_C	brain:	n/a
34	chr8:87242630-87242680	HCPEpiC	choroid plexus:	n/a
35	chr8:87243983-87244033	T-47D	breast:	n/a
36	chr8:87242630-87242680	HMEC	breast:	n/a
37	chr8:87242630-87242680	SK-N-SH	brain:	n/a
38	chr8:87243677-87243727	Jurkat	blood:	n/a
39	chr8:87243979-87244029	Jurkat	blood:	n/a
40	chr8:87242630-87242680	HNPCEpiC	eye:	n/a
41	chr8:87243979-87244029	NH-A	brain:	n/a
42	chr8:87243979-87244029	HEEpiC	esophagus:	n/a
43	chr8:87243983-87244033	LNCaP	prostate:	n/a
44	chr8:87243677-87243727	SAEC	small airway:	n/a
45	chr8:87243983-87244033	PFSK-1	brain:	n/a
46	chr8:87242630-87242680	AG04450	lung:	fetal
47	chr8:87243979-87244029	NB4	blood:	n/a
48	chr8:87242630-87242680	HPAEpiC	pulmonary alveolar:	n/a
49	chr8:87243979-87244029	U87	brain:	n/a
50	chr8:87243979-87244029	ECC-1	luminal epithelium:	n/a

(count:125 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:87212235..87212767-chr8:87269592..87270289,2	MCF-7	breast:
2	chr8:87228877..87232522-chr8:87233381..87236697,3	MCF-7	breast:
3	chr8:87210841..87213760-chr8:87426169..87428047,2	MCF-7	breast:
4	chr8:87225336..87228071-chr8:87228709..87231733,3	MCF-7	breast:
5	chr8:87185465..87188007-chr8:87211775..87213428,2	MCF-7	breast:
6	chr8:87186174..87188770-chr8:87209763..87212500,2	MCF-7	breast:
7	chr8:87212467..87215365-chr8:87302266..87303837,2	MCF-7	breast:
8	chr8:87207485..87210641-chr8:87212300..87214518,4	MCF-7	breast:
9	chr8:87211087..87213298-chr8:87310903..87313081,2	MCF-7	breast:
10	chr8:87306259..87308296-chr8:87311144..87313010,2	MCF-7	breast:
11	chr8:87294678..87297186-chr8:87297891..87299648,2	K562	blood:
12	chr8:87234703..87239197-chr8:87353081..87358100,5	MCF-7	breast:
13	chr8:87190469..87192191-chr8:87210663..87212770,3	MCF-7	breast:
14	chr8:87302798..87305553-chr8:87314921..87316646,2	MCF-7	breast:
15	chr8:87202647..87205379-chr8:87353769..87356042,2	MCF-7	breast:
16	chr8:87198044..87200373-chr8:87209574..87213892,4	MCF-7	breast:
17	chr8:87190469..87192191-chr8:87210663..87212770,3	MCF-7	breast:
18	chr8:87189537..87192109-chr8:87199086..87201093,2	MCF-7	breast:
19	chr8:54932825..54934885-chr8:87312658..87314897,2	MCF-7	breast:
20	chr8:87306909..87311243-chr8:87354302..87356597,4	MCF-7	breast:
21	chr8:87194628..87197311-chr8:87229703..87231831,2	MCF-7	breast:
22	chr8:87187097..87192513-chr8:87353340..87357451,6	MCF-7	breast:
23	chr8:87217894..87220561-chr8:87354206..87356206,2	K562	blood:
24	chr8:87216830..87219040-chr8:87220286..87222981,2	MCF-7	breast:
25	chr8:87159966..87161535-chr8:87210569..87213255,2	MCF-7	breast:
26	chr8:87186174..87188770-chr8:87209763..87212500,2	MCF-7	breast:
27	chr8:87207725..87209616-chr8:87210524..87212253,2	MCF-7	breast:
28	chr8:87209043..87216417-chr8:87353545..87356851,10	MCF-7	breast:
29	chr8:87194678..87197306-chr8:87210652..87213144,4	MCF-7	breast:
30	chr8:87268857..87273498-chr8:87273591..87278525,6	MCF-7	breast:
31	chr8:87269276..87272026-chr8:87353907..87356009,3	MCF-7	breast:
32	chr8:87232045..87233654-chr8:87330272..87332535,2	MCF-7	breast:
33	chr8:87212192..87213055-chr8:87354638..87355564,2	MCF-7	breast:
34	chr4:2464165..2464862-chr8:87228271..87228923,2	MCF-7	breast:
35	chr8:87180089..87182207-chr8:87303826..87306523,2	MCF-7	breast:
36	chr8:87193443..87195770-chr8:87354919..87356635,3	MCF-7	breast:
37	chr8:87211087..87213298-chr8:87310903..87313081,2	MCF-7	breast:
38	chr8:87278061..87279792-chr8:87353033..87354538,2	MCF-7	breast:
39	chr8:87271961..87274632-chr8:87289481..87292404,2	MCF-7	breast:
40	chr8:87234479..87236485-chr8:87301642..87304200,2	MCF-7	breast:
41	chr8:87274382..87276397-chr8:87353174..87356496,4	MCF-7	breast:
42	chr12:132380546..132381123-chr8:87287679..87288623,2	MCF-7	breast:
43	chr8:87268554..87270621-chr8:87278313..87280560,2	MCF-7	breast:
44	chr8:87236758..87239329-chr8:87241748..87243427,2	K562	blood:
45	chr8:87272517..87276008-chr8:87285333..87287881,3	MCF-7	breast:
46	chr8:87301270..87304931-chr8:87353185..87356602,8	MCF-7	breast:
47	chr8:87211913..87212449-chr8:87355263..87355967,3	MCF-7	breast:
48	chr8:87227505..87230392-chr8:87231801..87233486,2	MCF-7	breast:
49	chr8:87267716..87270046-chr8:87281008..87283289,2	MCF-7	breast:
50	chr8:87227505..87230392-chr8:87231801..87233486,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0D2-1	chr8:87212370-87212451	ENSG00000253699.1
2	lnc-ATP6V0D2-1	chr8:87192647-87192848	ENSG00000253699.1
3	lnc-ATP6V0D2-1	chr8:87198876-87198935	ENSG00000253699.1
4	lnc-ATP6V0D2-1	chr8:87208116-87208230	ENSG00000253699.1
5	lnc-ATP6V0D2-1	chr8:87224424-87224465	ENSG00000253699.1

No data

Variant related genes	Relation type
ENSG00000253699	TF binding region
SLC7A13	TF binding region
ENSG00000253699	CpG island
SLC7A13	CpG island
ENSG00000139725	chromatin interactions
ENSG00000253699	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000187735	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000254231	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000123124	chromatin interactions
ENSG00000164893	chromatin interactions

Extended variants
information (count: 4558 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:4558 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566134918	chr8:87185512-87185513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs193153429	chr8:87185515-87185516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551745815	chr8:87185518-87185519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571881222	chr8:87185541-87185542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545615518	chr8:87185567-87185568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs58965951	chr8:87185578-87185579	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557296592	chr8:87185581-87185582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572181996	chr8:87185582-87185583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10088392	chr8:87185606-87185607	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs536754981	chr8:87185646-87185647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs59777373	chr8:87185655-87185656	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs573369982	chr8:87185671-87185672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531192401	chr8:87185702-87185703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10107622	chr8:87185716-87185717	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs575476885	chr8:87185739-87185740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544466544	chr8:87185752-87185753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4596629	chr8:87185763-87185764	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs111592105	chr8:87185785-87185786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540036812	chr8:87185829-87185830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550433360	chr8:87185837-87185838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532224846	chr8:87185839-87185840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547196263	chr8:87185863-87185864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs71525038	chr8:87185871-87185872	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs4596630	chr8:87185901-87185902	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs367797275	chr8:87185903-87185904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377195472	chr8:87185909-87185910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568809901	chr8:87185913-87185914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531129594	chr8:87185919-87185920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551217196	chr8:87185942-87185943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549190080	chr8:87185959-87185960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569781714	chr8:87185970-87185971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112573241	chr8:87185971-87185972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7825380	chr8:87185977-87185978	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7846210	chr8:87185987-87185988	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs537842705	chr8:87186006-87186007	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556944816	chr8:87186009-87186010	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs184791552	chr8:87186025-87186026	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs142802921	chr8:87186029-87186030	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs552872682	chr8:87186061-87186062	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs548612169	chr8:87186062-87186063	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs558701005	chr8:87186065-87186066	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs575560584	chr8:87186087-87186088	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs35715881	chr8:87186107-87186108	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs78878376	chr8:87186137-87186138	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs574382188	chr8:87186168-87186169	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs375295060	chr8:87186186-87186187	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs35332272	chr8:87186215-87186216	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559894558	chr8:87186255-87186256	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs576553319	chr8:87186268-87186269	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs545460629	chr8:87186315-87186316	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	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
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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21990379	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	19805367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87180000-87187400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:87185400-87186000	Enhancers	HepG2	liver
3	chr8:87185800-87186200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr8:87186000-87186200	Flanking Active TSS	HepG2	liver
5	chr8:87186000-87186400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:87186000-87186400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr8:87186000-87186400	Enhancers	Gastric	stomach
8	chr8:87186000-87186600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:87186000-87186800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr8:87186200-87186400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr8:87186200-87188400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr8:87186200-87189200	Enhancers	HepG2	liver
13	chr8:87186400-87186600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:87186400-87187400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:87186600-87186800	Enhancers	A549	lung
16	chr8:87186600-87187200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:87186600-87188400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr8:87186800-87187800	Weak transcription	A549	lung
19	chr8:87186800-87188400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr8:87187000-87189800	Enhancers	Hela-S3	cervix
21	chr8:87187200-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:87187400-87187600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:87187400-87188000	Enhancers	HUVEC	blood vessel
24	chr8:87187400-87188200	Enhancers	HMEC	breast
25	chr8:87187400-87188400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:87187600-87188200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr8:87187600-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:87187600-87188200	Enhancers	NHEK	skin
29	chr8:87187600-87189000	Enhancers	Fetal Lung	lung
30	chr8:87187600-87189800	Enhancers	Placenta Amnion	Placenta Amnion
31	chr8:87187800-87188000	Enhancers	A549	lung
32	chr8:87187800-87188000	Enhancers	HSMMtube	muscle
33	chr8:87187800-87188000	Enhancers	NH-A	brain
34	chr8:87187800-87188200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr8:87187800-87188400	Enhancers	HSMM	muscle
36	chr8:87187800-87189400	Enhancers	Osteobl	bone
37	chr8:87187800-87190000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr8:87188000-87188200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:87188000-87188400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:87188000-87188400	Flanking Active TSS	HSMMtube	muscle
41	chr8:87188000-87188600	Enhancers	Fetal Brain Female	brain
42	chr8:87188000-87189000	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr8:87188000-87189200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:87188000-87189200	Flanking Active TSS	A549	lung
45	chr8:87188000-87189200	Flanking Active TSS	NH-A	brain
46	chr8:87188000-87189400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr8:87188000-87189400	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr8:87188000-87189400	Flanking Active TSS	HUVEC	blood vessel
49	chr8:87188200-87188400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr8:87188200-87188600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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