Variant report

Variant	nsv526764
Chromosome Location	chr7:102701826-102737251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1348)
CpG islands
(count:1043)
Chromatin interactive
region (count:82)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1348 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102702422-102702598	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102715075-102715689	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:102715479-102715490	K562	blood:	n/a	n/a
4	ATF2	chr7:102715018-102715634	GM12878	blood:	n/a	n/a
5	ATF3	chr7:102715170-102715696	K562	blood:	n/a	chr7:102715307-102715316
6	BACH1	chr7:102706276-102706354	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:102714777-102715487	K562	blood:	n/a	n/a
8	BACH1	chr7:102714954-102715637	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:102716301-102716459	K562	blood:	n/a	n/a
10	BCL3	chr7:102714922-102715397	A549	lung:	n/a	n/a
11	BCLAF1	chr7:102715413-102716333	GM12878	blood:	n/a	chr7:102716007-102716016 chr7:102716010-102716019 chr7:102716004-102716017 chr7:102716001-102716010 chr7:102715706-102715715 chr7:102715701-102715714
12	BHLHE40	chr7:102714705-102716143	GM12878	blood:	n/a	chr7:102715272-102715288
13	BHLHE40	chr7:102715088-102715737	HepG2	liver:	n/a	chr7:102715272-102715288
14	BHLHE40	chr7:102702515-102702570	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:102706243-102706451	K562	blood:	n/a	n/a
16	BHLHE40	chr7:102714627-102715752	K562	blood:	n/a	chr7:102715272-102715288
17	BRCA1	chr7:102715205-102715586	GM12878	blood:	n/a	n/a
18	BRCA1	chr7:102714725-102715413	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:102702403-102702680	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:102715587-102715625	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr7:102715074-102715301	HepG2	liver:	n/a	n/a
22	BRCA1	chr7:102716098-102716377	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr7:102714539-102715680	K562	blood:	n/a	n/a
24	CCNT2	chr7:102714836-102715974	K562	blood:	n/a	chr7:102715307-102715316
25	CEBPB	chr7:102723009-102723265	K562	blood:	n/a	n/a
26	CEBPB	chr7:102715102-102715566	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:102715249-102715521	K562	blood:	n/a	n/a
28	CEBPB	chr7:102714788-102715680	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:102730203-102730407	K562	blood:	n/a	chr7:102730323-102730334
30	CEBPB	chr7:102715168-102715570	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:102730200-102730410	IMR90	lung:	n/a	chr7:102730323-102730334
32	CEBPB	chr7:102717219-102717583	HepG2	liver:	n/a	chr7:102717390-102717401
33	CEBPB	chr7:102714986-102715850	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:102717346-102717520	H1-hESC	embryonic stem cell:	n/a	chr7:102717390-102717401
35	CEBPB	chr7:102723024-102723274	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:102717271-102717664	MCF-7	breast:	n/a	chr7:102717390-102717401
37	CEBPB	chr7:102730247-102730402	HepG2	liver:	n/a	chr7:102730323-102730334
38	CEBPB	chr7:102717317-102717565	A549	lung:	n/a	chr7:102717390-102717401
39	CEBPB	chr7:102715045-102715539	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:102717331-102717473	HepG2	liver:	n/a	chr7:102717390-102717401
41	CEBPB	chr7:102732719-102732818	K562	blood:	n/a	n/a
42	CEBPB	chr7:102721786-102722032	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:102715039-102715701	A549	lung:	n/a	n/a
44	CEBPB	chr7:102715268-102715408	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:102717304-102717524	K562	blood:	n/a	chr7:102717390-102717401
46	CEBPB	chr7:102715005-102715625	A549	lung:	n/a	n/a
47	CEBPB	chr7:102717239-102717672	A549	lung:	n/a	chr7:102717390-102717401
48	CEBPB	chr7:102717173-102717578	K562	blood:	n/a	chr7:102717390-102717401
49	CEBPB	chr7:102723010-102723342	MCF-7	breast:	n/a	n/a
50	CEBPB	chr7:102714951-102715703	MCF-7	breast:	n/a	n/a

(count:1043 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102715121-102715171	GM12891	blood:	n/a
2	chr7:102715617-102715667	SK-N-SH_RA	brain:	n/a
3	chr7:102716072-102716122	CMK	blood:	n/a
4	chr7:102718772-102718822	GM12891	blood:	n/a
5	chr7:102711687-102711737	NHDF-neo	bronchial:	n/a
6	chr7:102715565-102715615	NH-A	brain:	n/a
7	chr7:102715121-102715171	GM12891	blood:	n/a
8	chr7:102715617-102715667	SK-N-SH_RA	brain:	n/a
9	chr7:102716072-102716122	CMK	blood:	n/a
10	chr7:102718772-102718822	GM12891	blood:	n/a
11	chr7:102711687-102711737	NHDF-neo	bronchial:	n/a
12	chr7:102715565-102715615	NH-A	brain:	n/a
13	chr7:102718772-102718822	AG04449	skin:	fetal
14	chr7:102716072-102716122	SK-N-SH_RA	brain:	n/a
15	chr7:102715191-102715241	NB4	blood:	n/a
16	chr7:102711687-102711737	K562	blood:	n/a
17	chr7:102714871-102714921	GM06990	blood:	n/a
18	chr7:102715131-102715181	SK-N-MC	brain:	n/a
19	chr7:102716072-102716122	HRE	kidney:	n/a
20	chr7:102716002-102716052	NHDF-neo	bronchial:	n/a
21	chr7:102715145-102715195	AG04449	skin:	fetal
22	chr7:102715131-102715181	ProgFib	skin:	n/a
23	chr7:102714871-102714921	NHDF-neo	bronchial:	n/a
24	chr7:102716072-102716122	PrEC	prostate:	n/a
25	chr7:102715565-102715615	HCM	heart:	n/a
26	chr7:102715559-102715609	SK-N-SH	brain:	n/a
27	chr7:102714871-102714921	K562	blood:	n/a
28	chr7:102715129-102715179	GM12878	blood:	n/a
29	chr7:102715145-102715195	HCF	heart:	n/a
30	chr7:102715232-102715282	HCF	heart:	n/a
31	chr7:102715129-102715179	NHDF-neo	bronchial:	n/a
32	chr7:102715204-102715254	H1-hESC	embryonic stem cell:	embryo
33	chr7:102718772-102718822	SK-N-MC	brain:	n/a
34	chr7:102715617-102715667	HRPEpiC	eye:	n/a
35	chr7:102716072-102716122	HCPEpiC	choroid plexus:	n/a
36	chr7:102715204-102715254	RPTEC	kidney:	n/a
37	chr7:102715121-102715171	LNCaP	prostate:	n/a
38	chr7:102718772-102718822	BE2_C	brain:	n/a
39	chr7:102715565-102715615	CMK	blood:	n/a
40	chr7:102715131-102715181	U87	brain:	n/a
41	chr7:102715204-102715254	NH-A	brain:	n/a
42	chr7:102715131-102715181	Caco-2	colon:	n/a
43	chr7:102715121-102715171	HCF	heart:	n/a
44	chr7:102715565-102715615	SK-N-SH_RA	brain:	n/a
45	chr7:102715559-102715609	NH-A	brain:	n/a
46	chr7:102715232-102715282	U87	brain:	n/a
47	chr7:102714871-102714921	IMR90	lung:	fetal
48	chr7:102716072-102716122	NHBE	bronchial:	n/a
49	chr7:102715204-102715254	SK-N-SH_RA	brain:	n/a
50	chr7:102715204-102715254	MCF-7	breast:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:102714451..102716302-chr7:102729810..102731727,2	MCF-7	breast:
2	chr7:102734288..102735154-chr7:102937317..102937869,2	K562	blood:
3	chr7:102706745..102709062-chr7:102713643..102715718,3	MCF-7	breast:
4	chr15:59225405..59226269-chr7:102715959..102716628,2	Hela-S3	cervix:
5	chr7:102608423..102610942-chr7:102700411..102702582,3	K562	blood:
6	chr7:102712172..102716042-chr7:102726342..102729326,4	K562	blood:
7	chr7:102613006..102614516-chr7:102715583..102717366,2	K562	blood:
8	chr7:102715242..102717974-chr7:105515259..105517980,2	MCF-7	breast:
9	chr7:102611593..102615684-chr7:102700169..102704441,4	K562	blood:
10	chr7:102673845..102676724-chr7:102700499..102703034,2	K562	blood:
11	chr7:102714071..102718258-chr7:102757961..102760938,3	K562	blood:
12	chr7:102714786..102716772-chr7:102789401..102791256,2	MCF-7	breast:
13	chr7:102705659..102708585-chr7:102755906..102758111,2	K562	blood:
14	chr7:102711380..102713849-chr7:102713852..102716556,3	MCF-7	breast:
15	chr7:102715561..102717346-chr7:102754713..102757374,2	MCF-7	breast:
16	chr7:102733228..102736205-chr7:102789279..102791780,2	MCF-7	breast:
17	chr7:102620399..102622083-chr7:102705547..102707771,2	K562	blood:
18	chr7:102715186..102716937-chr7:102734053..102736983,2	K562	blood:
19	chr7:102715317..102716101-chrX:11775950..11776939,2	Hela-S3	cervix:
20	chr7:102724225..102725917-chr7:102730430..102732210,2	MCF-7	breast:
21	chr7:102696664..102700307-chr7:102700461..102702793,3	K562	blood:
22	chr7:102718865..102720397-chr7:102721163..102723713,2	K562	blood:
23	chr7:102733221..102734992-chr7:102757778..102759973,2	MCF-7	breast:
24	chr7:102700472..102704073-chr7:102705229..102707917,4	K562	blood:
25	chr7:102676967..102679361-chr7:102702578..102705004,2	K562	blood:
26	chr20:53057077..53059223-chr7:102716078..102718486,2	MCF-7	breast:
27	chr7:102704633..102706824-chr7:102709048..102710835,2	MCF-7	breast:
28	chr22:20193823..20194749-chr7:102715063..102715854,2	HCT-116	colon:
29	chr7:102713351..102719247-chr7:102725221..102729310,7	MCF-7	breast:
30	chr7:102714716..102718005-chr7:102734624..102737524,3	MCF-7	breast:
31	chr7:102430529..102431497-chr7:102702527..102703245,2	K562	blood:
32	chr7:102720886..102723558-chr7:102788067..102789895,2	K562	blood:
33	chr7:102724225..102725917-chr7:102730430..102732210,2	MCF-7	breast:
34	chr7:102722298..102724318-chr7:102734038..102736793,2	K562	blood:
35	chr7:102714473..102716689-chr7:102731603..102733946,2	MCF-7	breast:
36	chr7:102714451..102716302-chr7:102729810..102731727,2	MCF-7	breast:
37	chr7:102713351..102719247-chr7:102725221..102729310,7	MCF-7	breast:
38	chr7:102714725..102717201-chr7:102788241..102791780,5	K562	blood:
39	chr7:102710661..102713218-chr7:102714768..102717114,2	K562	blood:
40	chr7:102732929..102734759-chr7:102789421..102792163,3	K562	blood:
41	chr7:102714408..102716045-chr7:102987929..102989478,2	MCF-7	breast:
42	chr7:102708220..102712161-chr7:102714525..102717019,5	K562	blood:
43	chr7:102702765..102704335-chr7:102714764..102716771,2	MCF-7	breast:
44	chr7:102714022..102717631-chr7:102788669..102792237,6	MCF-7	breast:
45	chr7:102389656..102391894-chr7:102702213..102705034,2	MCF-7	breast:
46	chr7:102389494..102391981-chr7:102714130..102716680,2	MCF-7	breast:
47	chr7:102704923..102706991-chr7:102714522..102716456,2	MCF-7	breast:
48	chr1:247495212..247495870-chr7:102715654..102716186,2	Hela-S3	cervix:
49	chr7:102691392..102694110-chr7:102703544..102706469,2	K562	blood:
50	chr7:102668956..102671176-chr7:102710132..102712664,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAPEPLD-3	chr7:102729111-102730057	NONHSAT122533

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ARMC10	hsa-miR-1	chr7:102727113-102727134

Variant related genes	Relation type
CRYZP1	TF binding region
ARMC10	TF binding region
FBXL13	TF binding region
CRYZP1	CpG island
ARMC10	CpG island
FBXL13	CpG island
ENSG00000222011	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000005302	chromatin interactions
ENSG00000235354	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000236226	chromatin interactions
ENSG00000161048	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000230257	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000233025	chromatin interactions
ENSG00000105819	chromatin interactions
ENSG00000161057	chromatin interactions
ENSG00000236499	chromatin interactions
ENSG00000255198	chromatin interactions

Extended variants
information (count: 1273 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1273 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7809075	chr7:102701826-102701827	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576272502	chr7:102701840-102701841	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs182042824	chr7:102701885-102701886	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs186465660	chr7:102701896-102701897	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs80025428	chr7:102701937-102701938	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs571496622	chr7:102701985-102701986	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs200293769	chr7:102702039-102702040	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs538490632	chr7:102702071-102702072	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs146474414	chr7:102702087-102702088	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs573304751	chr7:102702100-102702101	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs140837500	chr7:102702124-102702125	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs370840667	chr7:102702129-102702130	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs147423949	chr7:102702144-102702145	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs555401358	chr7:102702162-102702163	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs573712608	chr7:102702202-102702203	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs10236966	chr7:102702307-102702308	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs563070601	chr7:102702339-102702340	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs533663800	chr7:102702400-102702401	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs376576904	chr7:102702430-102702431	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs369635063	chr7:102702436-102702437	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs373552279	chr7:102702441-102702442	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs376437982	chr7:102702443-102702444	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs369709619	chr7:102702456-102702457	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs372649141	chr7:102702472-102702473	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs375908944	chr7:102702473-102702474	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs555229016	chr7:102702484-102702485	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs555070558	chr7:102702485-102702486	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs545319695	chr7:102702488-102702489	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs560739066	chr7:102702491-102702492	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs371911493	chr7:102702492-102702493	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs11977138	chr7:102702514-102702515	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs60322290	chr7:102702522-102702523	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs142959690	chr7:102702547-102702548	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs200634872	chr7:102702549-102702550	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs560934359	chr7:102702570-102702571	Weak transcription Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs533491741	chr7:102702604-102702605	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs531363072	chr7:102702621-102702622	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs11505859	chr7:102702634-102702635	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs189280548	chr7:102702644-102702645	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs180944906	chr7:102702667-102702668	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs549734278	chr7:102702710-102702711	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs529956386	chr7:102702781-102702782	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs201508113	chr7:102702782-102702783	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs369248586	chr7:102702860-102702861	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs138834782	chr7:102702894-102702895	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs538919928	chr7:102702900-102702901	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs185952499	chr7:102703007-102703008	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs75554890	chr7:102703059-102703060	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs75993700	chr7:102703061-102703062	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs75836657	chr7:102703062-102703063	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1211 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102679200-102713800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:102684200-102708000	Weak transcription	Pancreas	Pancrea
3	chr7:102692800-102712800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr7:102694800-102702000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr7:102700400-102702400	Weak transcription	Liver	Liver
6	chr7:102701200-102702200	Enhancers	Aorta	Aorta
7	chr7:102701600-102702800	Enhancers	HUVEC	blood vessel
8	chr7:102701800-102702000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr7:102701800-102702000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:102701800-102702000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:102701800-102702200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:102701800-102702200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:102701800-102702200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:102701800-102702200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:102701800-102702200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:102701800-102702200	Enhancers	Ovary	ovary
17	chr7:102701800-102702800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr7:102701800-102702800	Enhancers	K562	blood
19	chr7:102702000-102702800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr7:102702000-102702800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr7:102702000-102702800	Enhancers	NH-A	brain
22	chr7:102702200-102702600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:102702200-102713800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr7:102702200-102714600	Weak transcription	Ovary	ovary
25	chr7:102702600-102702800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:102702600-102702800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:102702600-102702800	Enhancers	Liver	Liver
28	chr7:102706000-102706200	Weak transcription	K562	blood
29	chr7:102706200-102706800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:102706400-102706600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:102706400-102706800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr7:102706800-102714000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr7:102708000-102708200	ZNF genes & repeats	Pancreas	Pancrea
34	chr7:102708200-102709200	Weak transcription	Pancreas	Pancrea
35	chr7:102708400-102709400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:102708600-102709000	Enhancers	Fetal Lung	lung
37	chr7:102709000-102714200	Weak transcription	Fetal Lung	lung
38	chr7:102709200-102710200	Enhancers	Pancreas	Pancrea
39	chr7:102709400-102710000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:102710200-102711400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:102710200-102713800	Weak transcription	Pancreas	Pancrea
42	chr7:102710200-102714400	Weak transcription	Brain Angular Gyrus	brain
43	chr7:102711200-102711400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:102711200-102711400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:102711400-102714000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:102711400-102714400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:102712800-102713000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:102712800-102713000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:102712800-102713000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr7:102712800-102713000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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