Variant report

Variant	nsv611675
Chromosome Location	chr8:87187050-87302328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:538)
CpG islands
(count:305)
Chromatin interactive
region (count:109)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr8:87269106-87269601	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:87237988-87238154	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:87251126-87251828	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:87222381-87222600	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:87249730-87249762	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:87267265-87268652	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:87249992-87250780	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:87269806-87269918	HepG2	liver:	n/a	n/a
10	ATF1	chr8:87274360-87274458	K562	blood:	n/a	n/a
11	ATF3	chr8:87302234-87302791	A549	lung:	n/a	n/a
12	BHLHE40	chr8:87267833-87268266	HepG2	liver:	n/a	n/a
13	BHLHE40	chr8:87250154-87250425	HepG2	liver:	n/a	n/a
14	CBX3	chr8:87292590-87293043	HCT-116	colon:	n/a	n/a
15	CBX3	chr8:87292707-87292924	K562	blood:	n/a	n/a
16	CEBPB	chr8:87209560-87209808	HepG2	liver:	n/a	chr8:87209668-87209679
17	CEBPB	chr8:87216681-87216880	HepG2	liver:	n/a	chr8:87216817-87216828
18	CEBPB	chr8:87258920-87259284	HepG2	liver:	n/a	chr8:87259098-87259109
19	CEBPB	chr8:87196068-87196211	K562	blood:	n/a	chr8:87196117-87196128
20	CEBPB	chr8:87256043-87256255	K562	blood:	n/a	n/a
21	CEBPB	chr8:87224706-87225063	A549	lung:	n/a	n/a
22	CEBPB	chr8:87224760-87224960	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:87274730-87274836	HepG2	liver:	n/a	chr8:87274760-87274771
24	CEBPB	chr8:87195401-87195660	K562	blood:	n/a	n/a
25	CEBPB	chr8:87224730-87225127	MCF-7	breast:	n/a	n/a
26	CEBPB	chr8:87269308-87269515	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:87224791-87225031	K562	blood:	n/a	n/a
28	CEBPB	chr8:87251218-87251706	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:87274645-87274931	Hela-S3	cervix:	n/a	chr8:87274760-87274771
30	CEBPB	chr8:87269246-87269692	MCF-7	breast:	n/a	chr8:87269246-87269263 chr8:87269628-87269640 chr8:87269247-87269260
31	CEBPB	chr8:87224658-87225114	MCF-7	breast:	n/a	n/a
32	CEBPB	chr8:87274075-87274343	A549	lung:	n/a	n/a
33	CEBPB	chr8:87209639-87209709	IMR90	lung:	n/a	chr8:87209668-87209679
34	CEBPB	chr8:87301802-87301962	HepG2	liver:	n/a	chr8:87301893-87301904
35	CEBPB	chr8:87274550-87274931	MCF-7	breast:	n/a	chr8:87274760-87274771
36	CEBPB	chr8:87269121-87269709	MCF-7	breast:	n/a	chr8:87269246-87269263 chr8:87269628-87269640 chr8:87269247-87269260
37	CEBPB	chr8:87256017-87256246	K562	blood:	n/a	n/a
38	CEBPB	chr8:87269244-87269623	HepG2	liver:	n/a	chr8:87269246-87269263 chr8:87269247-87269260
39	CEBPB	chr8:87269304-87269571	K562	blood:	n/a	n/a
40	CEBPB	chr8:87269317-87269533	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:87302309-87302793	A549	lung:	n/a	n/a
42	CEBPB	chr8:87282294-87282594	IMR90	lung:	n/a	chr8:87282437-87282448
43	CEBPB	chr8:87224726-87225047	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:87224775-87224930	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:87302196-87302935	A549	lung:	n/a	n/a
46	CEBPB	chr8:87269300-87269537	A549	lung:	n/a	n/a
47	CEBPB	chr8:87211798-87212460	MCF-7	breast:	n/a	n/a
48	CEBPB	chr8:87215458-87215759	HepG2	liver:	n/a	n/a
49	CEBPB	chr8:87301764-87302059	A549	lung:	n/a	chr8:87301893-87301904
50	CEBPB	chr8:87282299-87282618	A549	lung:	n/a	chr8:87282437-87282448

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:87243983-87244033	HAEpiC	amniotic membrane:	n/a
2	chr8:87243677-87243727	LNCaP	prostate:	n/a
3	chr8:87243983-87244033	SK-N-SH	brain:	n/a
4	chr8:87243677-87243727	HUVEC	blood vessel:	n/a
5	chr8:87243983-87244033	MCF-7	breast:	n/a
6	chr8:87243677-87243727	RPTEC	kidney:	n/a
7	chr8:87243979-87244029	SAEC	small airway:	n/a
8	chr8:87243983-87244033	AoSMC	blood vessel:	n/a
9	chr8:87242630-87242680	LNCaP	prostate:	n/a
10	chr8:87243983-87244033	NHDF-neo	bronchial:	n/a
11	chr8:87243983-87244033	NHBE	bronchial:	n/a
12	chr8:87242630-87242680	AG09309	skin:	n/a
13	chr8:87243979-87244029	HCPEpiC	choroid plexus:	n/a
14	chr8:87243677-87243727	HEEpiC	esophagus:	n/a
15	chr8:87243979-87244029	H1-hESC	embryonic stem cell:	embryo
16	chr8:87243983-87244033	Jurkat	blood:	n/a
17	chr8:87243983-87244033	HEK293	kidney:	embryo
18	chr8:87243677-87243727	HRE	kidney:	n/a
19	chr8:87243983-87244033	GM12891	blood:	n/a
20	chr8:87243983-87244033	SK-N-SH_RA	brain:	n/a
21	chr8:87243983-87244033	PANC-1	pancreas:	n/a
22	chr8:87243677-87243727	SK-N-MC	brain:	n/a
23	chr8:87243983-87244033	HEEpiC	esophagus:	n/a
24	chr8:87243677-87243727	HPAEpiC	pulmonary alveolar:	n/a
25	chr8:87226434-87226484	PANC-1	pancreas:	n/a
26	chr8:87226434-87226484	ProgFib	skin:	n/a
27	chr8:87242630-87242680	Caco-2	colon:	n/a
28	chr8:87226434-87226484	A549	lung:	n/a
29	chr8:87226434-87226484	AoSMC	blood vessel:	n/a
30	chr8:87243979-87244029	ProgFib	skin:	n/a
31	chr8:87226434-87226484	SK-N-MC	brain:	n/a
32	chr8:87243983-87244033	AG04449	skin:	fetal
33	chr8:87226434-87226484	HRE	kidney:	n/a
34	chr8:87243979-87244029	HMEC	breast:	n/a
35	chr8:87243983-87244033	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:87242630-87242680	NT2-D1	testis:	n/a
37	chr8:87243983-87244033	HRE	kidney:	n/a
38	chr8:87243677-87243727	AG09319	gingival:	n/a
39	chr8:87226434-87226484	SK-N-SH_RA	brain:	n/a
40	chr8:87243983-87244033	AG09309	skin:	n/a
41	chr8:87226434-87226484	HepG2	liver:	n/a
42	chr8:87242630-87242680	RPTEC	kidney:	n/a
43	chr8:87243979-87244029	GM19239	blood:	n/a
44	chr8:87242630-87242680	Jurkat	blood:	n/a
45	chr8:87243979-87244029	HPAEpiC	pulmonary alveolar:	n/a
46	chr8:87243677-87243727	NH-A	brain:	n/a
47	chr8:87226434-87226484	SAEC	small airway:	n/a
48	chr8:87243979-87244029	GM12892	blood:	n/a
49	chr8:87226434-87226484	K562	blood:	n/a
50	chr8:87243677-87243727	AG09309	skin:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:87212467..87215365-chr8:87302266..87303837,2	MCF-7	breast:
2	chr8:87159966..87161535-chr8:87210569..87213255,2	MCF-7	breast:
3	chr8:87268857..87273498-chr8:87273591..87278525,6	MCF-7	breast:
4	chr8:87227505..87230392-chr8:87231801..87233486,2	MCF-7	breast:
5	chr8:87240918..87243039-chr8:87246023..87247777,2	MCF-7	breast:
6	chr8:87212248..87212786-chr8:87354095..87354895,2	MCF-7	breast:
7	chr8:87207725..87209616-chr8:87210524..87212253,2	MCF-7	breast:
8	chr8:87234479..87236485-chr8:87301642..87304200,2	MCF-7	breast:
9	chr8:87212248..87212786-chr8:87354095..87354953,3	MCF-7	breast:
10	chr8:87211913..87212449-chr8:87355263..87355967,3	MCF-7	breast:
11	chr8:87272517..87276008-chr8:87285333..87287881,3	MCF-7	breast:
12	chr8:87187644..87190858-chr8:87193352..87196070,3	MCF-7	breast:
13	chr8:87207485..87210641-chr8:87212300..87214518,4	MCF-7	breast:
14	chr8:87274382..87276397-chr8:87353174..87356496,4	MCF-7	breast:
15	chr12:132380546..132381123-chr8:87287679..87288623,2	MCF-7	breast:
16	chr8:87265391..87268035-chr8:87353561..87357477,4	MCF-7	breast:
17	chr8:87177733..87179455-chr8:87185682..87188485,3	MCF-7	breast:
18	chr8:87210841..87213760-chr8:87426169..87428047,2	MCF-7	breast:
19	chr8:87228877..87232522-chr8:87233381..87236697,3	MCF-7	breast:
20	chr8:87190469..87192191-chr8:87210663..87212770,3	MCF-7	breast:
21	chr8:87272517..87276008-chr8:87285333..87287881,3	MCF-7	breast:
22	chr4:2464165..2464862-chr8:87228271..87228923,2	MCF-7	breast:
23	chr8:87284882..87289524-chr8:87353482..87357704,5	MCF-7	breast:
24	chr8:87213959..87216666-chr8:87241758..87244737,2	MCF-7	breast:
25	chr8:87211087..87213298-chr8:87310903..87313081,2	MCF-7	breast:
26	chr8:87278061..87279792-chr8:87353033..87354538,2	MCF-7	breast:
27	chr8:87186174..87188770-chr8:87209763..87212500,2	MCF-7	breast:
28	chr8:87187218..87190589-chr8:87353304..87356196,4	MCF-7	breast:
29	chr8:87274626..87278061-chr8:87304076..87307581,3	MCF-7	breast:
30	chr8:87185465..87188007-chr8:87211775..87213428,2	MCF-7	breast:
31	chr8:87232831..87235143-chr8:87256917..87258574,2	MCF-7	breast:
32	chr8:87217991..87221144-chr8:87354089..87356606,3	MCF-7	breast:
33	chr8:87187097..87192513-chr8:87353340..87357451,6	MCF-7	breast:
34	chr8:87232831..87235143-chr8:87256917..87258574,2	MCF-7	breast:
35	chr8:87268857..87273498-chr8:87273591..87278525,6	MCF-7	breast:
36	chr8:87227505..87230392-chr8:87231801..87233486,2	MCF-7	breast:
37	chr8:87216830..87219040-chr8:87220286..87222981,2	MCF-7	breast:
38	chr8:87271961..87274632-chr8:87289481..87292404,2	MCF-7	breast:
39	chr8:87265105..87267783-chr8:87353436..87357347,3	MCF-7	breast:
40	chr8:87186174..87188770-chr8:87209763..87212500,2	MCF-7	breast:
41	chr8:87267716..87270046-chr8:87281008..87283289,2	MCF-7	breast:
42	chr8:87225336..87228071-chr8:87228709..87231733,3	MCF-7	breast:
43	chr8:87196093..87197608-chr8:87352930..87355663,2	MCF-7	breast:
44	chr8:87291428..87296035-chr8:87300622..87304072,4	MCF-7	breast:
45	chr8:87236758..87239329-chr8:87241748..87243427,2	K562	blood:
46	chr8:87214685..87217092-chr8:87228293..87229889,2	MCF-7	breast:
47	chr8:87228971..87230907-chr8:87353906..87356164,2	MCF-7	breast:
48	chr8:87212235..87212767-chr8:87269592..87270289,2	MCF-7	breast:
49	chr8:87234703..87239197-chr8:87353081..87358100,5	MCF-7	breast:
50	chr8:87198044..87200373-chr8:87209574..87213892,4	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 3772 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:3772 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6470428	chr8:87187050-87187051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs13272356	chr8:87187077-87187078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs554489515	chr8:87187086-87187087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143784598	chr8:87187095-87187096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs13272593	chr8:87187113-87187114	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs371453945	chr8:87187151-87187152	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs540930879	chr8:87187155-87187156	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs187370694	chr8:87187161-87187162	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs532679344	chr8:87187191-87187192	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs4076881	chr8:87187195-87187196	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs56199972	chr8:87187274-87187275	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531850041	chr8:87187277-87187278	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs5892978	chr8:87187289-87187290	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs201398533	chr8:87187302-87187303	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs576063405	chr8:87187315-87187316	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs4076880	chr8:87187342-87187343	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs112195608	chr8:87187432-87187433	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs527730362	chr8:87187448-87187449	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs547380954	chr8:87187471-87187472	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs576410506	chr8:87187474-87187475	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs74376050	chr8:87187481-87187482	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs75992684	chr8:87187482-87187483	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs540963202	chr8:87187503-87187504	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs570445489	chr8:87187510-87187511	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs67157692	chr8:87187522-87187523	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556343482	chr8:87187567-87187568	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs569715587	chr8:87187575-87187576	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs371796600	chr8:87187590-87187591	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs189995193	chr8:87187611-87187612	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs67613864	chr8:87187645-87187646	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs398047340	chr8:87187647-87187648	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs142846149	chr8:87187697-87187698	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs114782580	chr8:87187708-87187709	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs541061804	chr8:87187719-87187720	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs113162925	chr8:87187727-87187728	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577488906	chr8:87187767-87187768	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs111911780	chr8:87187776-87187777	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs140931328	chr8:87187832-87187833	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs541663393	chr8:87187839-87187840	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs62512385	chr8:87187847-87187848	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs531729988	chr8:87187851-87187852	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs181626233	chr8:87187949-87187950	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs113891481	chr8:87187968-87187969	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs561889480	chr8:87187969-87187970	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs186398239	chr8:87187988-87187989	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs190120475	chr8:87187994-87187995	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs76405657	chr8:87188009-87188010	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs13259716	chr8:87188084-87188085	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs533271215	chr8:87188178-87188179	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs13267261	chr8:87188180-87188181	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	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:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87180000-87187400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:87186200-87188400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr8:87186200-87189200	Enhancers	HepG2	liver
4	chr8:87186400-87187400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:87186600-87187200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:87186600-87188400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr8:87186800-87187800	Weak transcription	A549	lung
8	chr8:87186800-87188400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr8:87187000-87189800	Enhancers	Hela-S3	cervix
10	chr8:87187200-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:87187400-87187600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:87187400-87188000	Enhancers	HUVEC	blood vessel
13	chr8:87187400-87188200	Enhancers	HMEC	breast
14	chr8:87187400-87188400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:87187600-87188200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr8:87187600-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:87187600-87188200	Enhancers	NHEK	skin
18	chr8:87187600-87189000	Enhancers	Fetal Lung	lung
19	chr8:87187600-87189800	Enhancers	Placenta Amnion	Placenta Amnion
20	chr8:87187800-87188000	Enhancers	A549	lung
21	chr8:87187800-87188000	Enhancers	HSMMtube	muscle
22	chr8:87187800-87188000	Enhancers	NH-A	brain
23	chr8:87187800-87188200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:87187800-87188400	Enhancers	HSMM	muscle
25	chr8:87187800-87189400	Enhancers	Osteobl	bone
26	chr8:87187800-87190000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr8:87188000-87188200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:87188000-87188400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr8:87188000-87188400	Flanking Active TSS	HSMMtube	muscle
30	chr8:87188000-87188600	Enhancers	Fetal Brain Female	brain
31	chr8:87188000-87189000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr8:87188000-87189200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:87188000-87189200	Flanking Active TSS	A549	lung
34	chr8:87188000-87189200	Flanking Active TSS	NH-A	brain
35	chr8:87188000-87189400	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:87188000-87189400	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr8:87188000-87189400	Flanking Active TSS	HUVEC	blood vessel
38	chr8:87188200-87188400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:87188200-87188600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr8:87188200-87188600	Enhancers	Adipose Nuclei	Adipose
41	chr8:87188200-87188800	Enhancers	Colon Smooth Muscle	Colon
42	chr8:87188200-87189000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr8:87188200-87189000	Enhancers	Fetal Heart	heart
44	chr8:87188200-87189200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr8:87188200-87189200	Flanking Active TSS	NHEK	skin
46	chr8:87188200-87189400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr8:87188200-87189400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr8:87188200-87189400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr8:87188200-87189400	Enhancers	Brain Cingulate Gyrus	brain
50	chr8:87188200-87189400	Flanking Active TSS	HMEC	breast

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