Variant report

Variant	nsv1028170
Chromosome Location	chr7:100958058-101117541
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2895)
CpG islands
(count:2506)
Chromatin interactive
region (count:93)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2895 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101041212-101041406	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:100995557-100996013	K562	blood:	n/a	n/a
3	ARID3A	chr7:101034275-101034431	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:101054542-101054748	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:101029701-101030402	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:100995510-100995986	HepG2	liver:	n/a	n/a
7	ATF1	chr7:100995667-100996035	K562	blood:	n/a	n/a
8	ATF2	chr7:101045260-101045884	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:100964776-100965119	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:100965008-100965341	GM12878	blood:	n/a	n/a
11	ATF2	chr7:101034154-101034562	GM12878	blood:	n/a	n/a
12	ATF2	chr7:101045113-101045819	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:101034206-101034498	GM12878	blood:	n/a	n/a
14	ATF2	chr7:101054507-101054909	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr7:101005691-101006042	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr7:101007153-101007579	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr7:100995608-100996147	K562	blood:	n/a	n/a
18	ATF3	chr7:100964964-100965260	K562	blood:	n/a	chr7:100965121-100965130
19	ATF3	chr7:101083791-101083930	K562	blood:	n/a	n/a
20	BACH1	chr7:100964807-100965060	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:101054392-101054843	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:101080560-101080609	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:101006064-101006399	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:101006969-101007517	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr7:100978932-100978958	K562	blood:	n/a	n/a
26	BACH1	chr7:101042008-101042270	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:101045151-101045712	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:101083766-101083964	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr7:101045447-101045692	H1-hESC	embryonic stem cell:	n/a	chr7:101045565-101045572 chr7:101045573-101045582
30	BCL11A	chr7:101034127-101034558	GM12878	blood:	n/a	n/a
31	BCL3	chr7:101034235-101034520	GM12878	blood:	n/a	n/a
32	BCL3	chr7:100995424-100996093	A549	lung:	n/a	chr7:100995867-100995874
33	BCL3	chr7:101071831-101072136	GM12878	blood:	n/a	n/a
34	BCL3	chr7:101085919-101086314	GM12878	blood:	n/a	n/a
35	BCL3	chr7:101085899-101086361	GM12878	blood:	n/a	n/a
36	BCL3	chr7:101006990-101007617	A549	lung:	n/a	chr7:101007240-101007249 chr7:101007424-101007437
37	BCL3	chr7:101045065-101045790	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
38	BCL3	chr7:100995430-100996053	A549	lung:	n/a	chr7:100995867-100995874
39	BCL3	chr7:101071768-101072139	GM12878	blood:	n/a	n/a
40	BCL3	chr7:101045252-101045835	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
41	BCLAF1	chr7:100964775-100965491	GM12878	blood:	n/a	chr7:100965115-100965124
42	BHLHE40	chr7:101007335-101007606	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:101085990-101086330	K562	blood:	n/a	n/a
44	BHLHE40	chr7:101054571-101054732	K562	blood:	n/a	n/a
45	BHLHE40	chr7:100995649-100996149	K562	blood:	n/a	n/a
46	BHLHE40	chr7:100995806-100995888	HepG2	liver:	n/a	n/a
47	BHLHE40	chr7:101034158-101034493	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:100965063-100965137	GM12878	blood:	n/a	n/a
49	BHLHE40	chr7:101007069-101007443	K562	blood:	n/a	n/a
50	BHLHE40	chr7:101083725-101083894	GM12878	blood:	n/a	n/a

(count:2506 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101007442-101007492	GM19239	blood:	n/a
2	chr7:101006308-101006358	SKMC	muscle:	n/a
3	chr7:101007072-101007122	GM12892	blood:	n/a
4	chr7:100968383-100968433	GM12878	blood:	n/a
5	chr7:101079617-101079667	SK-N-MC	brain:	n/a
6	chr7:101007442-101007492	GM19239	blood:	n/a
7	chr7:101006308-101006358	SKMC	muscle:	n/a
8	chr7:101007072-101007122	GM12892	blood:	n/a
9	chr7:100968383-100968433	GM12878	blood:	n/a
10	chr7:101079617-101079667	SK-N-MC	brain:	n/a
11	chr7:101006035-101006085	HUVEC	blood vessel:	n/a
12	chr7:101006058-101006108	ECC-1	luminal epithelium:	n/a
13	chr7:100965709-100965759	Caco-2	colon:	n/a
14	chr7:100965274-100965324	GM19239	blood:	n/a
15	chr7:101049300-101049350	LNCaP	prostate:	n/a
16	chr7:101006089-101006139	PANC-1	pancreas:	n/a
17	chr7:100964669-100964719	LNCaP	prostate:	n/a
18	chr7:101054654-101054704	BJ	skin:	n/a
19	chr7:101049372-101049422	NB4	blood:	n/a
20	chr7:101006308-101006358	MCF10A-Er-Src	breast:	n/a
21	chr7:101006019-101006069	GM19239	blood:	n/a
22	chr7:100965200-100965250	SKMC	muscle:	n/a
23	chr7:100964669-100964719	HAEpiC	amniotic membrane:	n/a
24	chr7:100964799-100964849	HCM	heart:	n/a
25	chr7:101006052-101006102	HMEC	breast:	n/a
26	chr7:101049300-101049350	AG04449	skin:	fetal
27	chr7:101006573-101006623	SK-N-MC	brain:	n/a
28	chr7:100965680-100965730	Jurkat	blood:	n/a
29	chr7:100964799-100964849	HEEpiC	esophagus:	n/a
30	chr7:101006035-101006085	PANC-1	pancreas:	n/a
31	chr7:100964734-100964784	PrEC	prostate:	n/a
32	chr7:101006063-101006113	AoSMC	blood vessel:	n/a
33	chr7:101006963-101007013	ProgFib	skin:	n/a
34	chr7:101005910-101005960	GM19239	blood:	n/a
35	chr7:100965198-100965248	SK-N-SH	brain:	n/a
36	chr7:101079617-101079667	GM19239	blood:	n/a
37	chr7:100966076-100966126	GM12891	blood:	n/a
38	chr7:101017354-101017404	PrEC	prostate:	n/a
39	chr7:100958103-100958153	HNPCEpiC	eye:	n/a
40	chr7:101005846-101005896	HEK293	kidney:	embryo
41	chr7:100965200-100965250	K562	blood:	n/a
42	chr7:100964966-100965016	HRPEpiC	eye:	n/a
43	chr7:101007442-101007492	AG04449	skin:	fetal
44	chr7:100964669-100964719	BE2_C	brain:	n/a
45	chr7:101007072-101007122	ECC-1	luminal epithelium:	n/a
46	chr7:101049300-101049350	CMK	blood:	n/a
47	chr7:101007603-101007653	GM12891	blood:	n/a
48	chr7:101006089-101006139	GM12892	blood:	n/a
49	chr7:100964669-100964719	MCF10A-Er-Src	breast:	n/a
50	chr7:101006308-101006358	SAEC	small airway:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:101043147..101045492-chr7:101051053..101052921,2	K562	blood:
2	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
3	chr7:100948583..100953192-chr7:100953249..100959954,9	MCF-7	breast:
4	chr7:100965612..100969667-chr7:101005034..101007660,3	MCF-7	breast:
5	chr15:65596698..65597638-chr7:100964826..100965617,2	HCT-116	colon:
6	chr7:101067571..101069515-chr7:101079650..101082212,2	MCF-7	breast:
7	chr7:100958176..100959175-chr7:101150758..101151564,2	MCF-7	breast:
8	chr7:101083863..101087245-chr7:101089520..101092470,3	K562	blood:
9	chr7:100957376..100960174-chr7:100960338..100962294,2	K562	blood:
10	chr7:100953764..100956279-chr7:100958212..100960386,3	K562	blood:
11	chr7:100964942..100967208-chr7:101081876..101083958,2	MCF-7	breast:
12	chr7:101031371..101033701-chr7:101034998..101036873,2	K562	blood:
13	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
14	chr7:101084569..101086934-chr7:101141583..101143364,2	MCF-7	breast:
15	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
16	chr7:100943319..100945510-chr7:100956650..100958675,2	K562	blood:
17	chr7:100989055..100991707-chr7:100994198..100995736,2	MCF-7	breast:
18	chr7:100950840..100954191-chr7:100963498..100966604,5	MCF-7	breast:
19	chr7:100967257..100969650-chr7:100972376..100975221,2	K562	blood:
20	chr7:101037193..101039012-chr7:101045881..101047459,2	MCF-7	breast:
21	chr7:101083724..101084446-chr7:101150709..101151315,2	MCF-7	breast:
22	chr7:101012360..101015108-chr7:101017249..101019175,2	K562	blood:
23	chr7:101015968..101018340-chr7:101024306..101026455,2	MCF-7	breast:
24	chr7:101054544..101055233-chr7:101150595..101151343,2	K562	blood:
25	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
26	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
27	chr7:101015968..101018340-chr7:101024306..101026455,2	MCF-7	breast:
28	chr7:101006939..101007476-chr7:101083770..101084337,2	K562	blood:
29	chr7:100950629..100953061-chr7:100957040..100959763,3	K562	blood:
30	chr7:100957376..100960174-chr7:100960338..100962294,2	K562	blood:
31	chr7:101016391..101018815-chr7:101033017..101035506,2	K562	blood:
32	chr7:101100607..101102049-chr7:101150824..101151606,9	MCF-7	breast:
33	chr7:100954257..100956157-chr7:100957247..100959809,2	MCF-7	breast:
34	chr7:101006908..101008057-chr7:101150804..101151679,7	MCF-7	breast:
35	chr7:101007762..101011060-chr7:101013667..101017793,3	K562	blood:
36	chr7:101007762..101011060-chr7:101013667..101017793,3	K562	blood:
37	chr7:100941519..100944089-chr7:100963395..100965508,2	K562	blood:
38	chr12:132413848..132415692-chr7:101084473..101086964,2	MCF-7	breast:
39	chr7:100964128..100967078-chr7:100972257..100974815,3	MCF-7	breast:
40	chr7:101006530..101007875-chr7:101054200..101055148,9	MCF-7	breast:
41	chr7:101006441..101008974-chr7:101023704..101025266,2	MCF-7	breast:
42	chr7:101006932..101008338-chr7:101181516..101182765,6	K562	blood:
43	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
44	chr7:100964710..100967141-chr7:101003077..101007417,4	MCF-7	breast:
45	chr7:101006939..101007476-chr7:101083770..101084337,2	K562	blood:
46	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
47	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
48	chr7:100964752..100967137-chr7:100978107..100980737,2	MCF-7	breast:
49	chr7:100887243..100887763-chr7:100958276..100958965,2	MCF-7	breast:
50	chr7:101037193..101039012-chr7:101045881..101047459,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABL5-1	chr7:100998850-100999006	ucscGeneNc_uc003uyp_2
2	lnc-RABL5-1	chr7:100995310-100996633	ucscGeneNc_uc003uyp_2
3	lnc-ZNHIT1-1	chr7:100964396-100964425	NR_110115
4	lnc-RABL5-2	chr7:101032149-101032361	NONHSAT122467

No data

Variant related genes	Relation type
RABL5	TF binding region
ENSG00000233683	TF binding region
COL26A1	TF binding region
RABL5	CpG island
ENSG00000233683	CpG island
COL26A1	CpG island
ENSG00000160963	chromatin interactions
ENSG00000180447	chromatin interactions
ENSG00000233683	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000232301	chromatin interactions
ENSG00000128581	chromatin interactions
ENSG00000177192	chromatin interactions
ENSG00000255992	chromatin interactions
ENSG00000232445	chromatin interactions

Extended variants
information (count: 7012 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:7012 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200501903	chr7:100958059-100958060	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs550602095	chr7:100958097-100958098	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540842299	chr7:100958107-100958108	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184390500	chr7:100958263-100958264	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11544858	chr7:100958270-100958271	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs189271108	chr7:100958295-100958296	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs143488810	chr7:100958300-100958301	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs62483513	chr7:100958324-100958325	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550271124	chr7:100958348-100958349	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368093551	chr7:100958363-100958364	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373822049	chr7:100958389-100958390	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376870854	chr7:100958401-100958402	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571787938	chr7:100958403-100958404	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201765206	chr7:100958410-100958411	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547989963	chr7:100958426-100958427	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs376378313	chr7:100958437-100958438	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs148720859	chr7:100958526-100958527	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs369051540	chr7:100958563-100958564	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs373806259	chr7:100958571-100958572	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377036032	chr7:100958595-100958596	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184027289	chr7:100958610-100958611	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147162873	chr7:100958715-100958716	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs548608002	chr7:100958717-100958718	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374004645	chr7:100958728-100958729	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569584612	chr7:100958752-100958753	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138544006	chr7:100958797-100958798	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs188615117	chr7:100958832-100958833	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs181684223	chr7:100958854-100958855	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs202033034	chr7:100958885-100958886	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs534438892	chr7:100958925-100958926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs149244924	chr7:100958936-100958937	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs542007717	chr7:100958947-100958948	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs574557449	chr7:100958953-100958954	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73180986	chr7:100958965-100958966	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs563457947	chr7:100958986-100958987	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs576473957	chr7:100959120-100959121	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs144464195	chr7:100959172-100959173	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs527890557	chr7:100959222-100959223	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs532650989	chr7:100959232-100959233	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148471256	chr7:100959269-100959270	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577219577	chr7:100959274-100959275	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs571311020	chr7:100959279-100959280	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs559855126	chr7:100959291-100959292	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs59453200	chr7:100959297-100959298	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs58660040	chr7:100959365-100959366	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs548832388	chr7:100959424-100959425	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs186078136	chr7:100959443-100959444	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537382743	chr7:100959469-100959470	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs570832019	chr7:100959483-100959484	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551733244	chr7:100959502-100959503	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:2471 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100951800-100964000	Weak transcription	Fetal Heart	heart
2	chr7:100952200-100964000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr7:100952400-100959200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr7:100952400-100964000	Weak transcription	Liver	Liver
5	chr7:100952400-100964000	Weak transcription	Right Ventricle	heart
6	chr7:100952400-100964200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr7:100952400-100964200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr7:100952400-100964400	Weak transcription	Psoas Muscle	Psoas
9	chr7:100952400-100964400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr7:100952400-100964400	Weak transcription	NHLF	lung
11	chr7:100952600-100958200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr7:100952600-100958200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr7:100952600-100964000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:100952600-100964000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr7:100952600-100964000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:100952600-100964000	Weak transcription	Colonic Mucosa	Colon
17	chr7:100952600-100964000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:100952600-100964000	Weak transcription	Esophagus	oesophagus
19	chr7:100952600-100964000	Weak transcription	HUVEC	blood vessel
20	chr7:100952600-100964400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:100952600-100964400	Weak transcription	Gastric	stomach
22	chr7:100953200-100958200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:100953200-100962400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr7:100953200-100964200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr7:100953400-100958200	Strong transcription	H1 Cell Line	embryonic stem cell
26	chr7:100953800-100960200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr7:100953800-100964000	Weak transcription	Colon Smooth Muscle	Colon
28	chr7:100953800-100964200	Weak transcription	Left Ventricle	heart
29	chr7:100954200-100959400	Weak transcription	Adipose Nuclei	Adipose
30	chr7:100954200-100964000	Weak transcription	HepG2	liver
31	chr7:100954600-100964400	Weak transcription	NHEK	skin
32	chr7:100954800-100958200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:100954800-100960200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:100955000-100959400	Weak transcription	Brain Anterior Caudate	brain
35	chr7:100955000-100964000	Weak transcription	HMEC	breast
36	chr7:100955000-100964400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:100955000-100964400	Weak transcription	K562	blood
38	chr7:100955200-100958200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:100955200-100958400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr7:100955200-100958400	Weak transcription	Fetal Muscle Leg	muscle
41	chr7:100955200-100958600	Weak transcription	Primary B cells from peripheral blood	blood
42	chr7:100955200-100959400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr7:100955200-100962600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:100955200-100964200	Weak transcription	Primary B cells from cord blood	blood
45	chr7:100955200-100964200	Weak transcription	Primary T cells from cord blood	blood
46	chr7:100955400-100964000	Weak transcription	Brain Angular Gyrus	brain
47	chr7:100955400-100964000	Weak transcription	Stomach Mucosa	stomach
48	chr7:100955400-100964000	Weak transcription	Hela-S3	cervix
49	chr7:100955600-100959400	Weak transcription	Brain Substantia Nigra	brain
50	chr7:100955600-100960800	Weak transcription	Placenta Amnion	Placenta Amnion

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