Variant report

Variant	esv2761351
Chromosome Location	chr7:100967098-101135398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2235)
CpG islands
(count:1711)
Chromatin interactive
region (count:81)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2235 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101054542-101054748	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:101041212-101041406	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101034275-101034431	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:100995557-100996013	K562	blood:	n/a	n/a
5	ARID3A	chr7:100995510-100995986	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:101029701-101030402	HepG2	liver:	n/a	n/a
7	ATF1	chr7:100995667-100996035	K562	blood:	n/a	n/a
8	ATF2	chr7:101034154-101034562	GM12878	blood:	n/a	n/a
9	ATF2	chr7:101054507-101054909	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:101007153-101007579	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:101034206-101034498	GM12878	blood:	n/a	n/a
12	ATF2	chr7:101005691-101006042	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:101045113-101045819	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:101045260-101045884	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:101083791-101083930	K562	blood:	n/a	n/a
16	ATF3	chr7:100995608-100996147	K562	blood:	n/a	n/a
17	BACH1	chr7:101042008-101042270	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:101080560-101080609	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:101045151-101045712	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:101006969-101007517	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:101006064-101006399	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:100978932-100978958	K562	blood:	n/a	n/a
23	BACH1	chr7:101083766-101083964	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:101054392-101054843	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr7:101034127-101034558	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:101045447-101045692	H1-hESC	embryonic stem cell:	n/a	chr7:101045565-101045572 chr7:101045573-101045582
27	BCL3	chr7:101034235-101034520	GM12878	blood:	n/a	n/a
28	BCL3	chr7:101085899-101086361	GM12878	blood:	n/a	n/a
29	BCL3	chr7:100995430-100996053	A549	lung:	n/a	chr7:100995867-100995874
30	BCL3	chr7:101085919-101086314	GM12878	blood:	n/a	n/a
31	BCL3	chr7:101045065-101045790	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
32	BCL3	chr7:101045252-101045835	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
33	BCL3	chr7:101006990-101007617	A549	lung:	n/a	chr7:101007240-101007249 chr7:101007424-101007437
34	BCL3	chr7:101071768-101072139	GM12878	blood:	n/a	n/a
35	BCL3	chr7:100995424-100996093	A549	lung:	n/a	chr7:100995867-100995874
36	BCL3	chr7:101071831-101072136	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:101007069-101007443	K562	blood:	n/a	n/a
38	BHLHE40	chr7:100995806-100995888	HepG2	liver:	n/a	n/a
39	BHLHE40	chr7:101034158-101034493	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:101007335-101007606	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:101085990-101086330	K562	blood:	n/a	n/a
42	BHLHE40	chr7:101006937-101007505	HepG2	liver:	n/a	n/a
43	BHLHE40	chr7:101054571-101054732	K562	blood:	n/a	n/a
44	BHLHE40	chr7:101083725-101083894	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:100995649-100996149	K562	blood:	n/a	n/a
46	BRCA1	chr7:101030201-101030430	HepG2	liver:	n/a	n/a
47	BRCA1	chr7:101034222-101034342	GM12878	blood:	n/a	n/a
48	BRCA1	chr7:100996299-100996395	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr7:101034269-101034281	HepG2	liver:	n/a	n/a
50	CBX3	chr7:101052757-101053143	K562	blood:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101005910-101005960	NT2-D1	testis:	n/a
2	chr7:101005846-101005896	BE2_C	brain:	n/a
3	chr7:101006052-101006102	GM19239	blood:	n/a
4	chr7:101005910-101005960	NT2-D1	testis:	n/a
5	chr7:101005846-101005896	BE2_C	brain:	n/a
6	chr7:101006052-101006102	GM19239	blood:	n/a
7	chr7:101005910-101005960	HepG2	liver:	n/a
8	chr7:101006363-101006413	ProgFib	skin:	n/a
9	chr7:101006058-101006108	HUVEC	blood vessel:	n/a
10	chr7:101005832-101005882	HCPEpiC	choroid plexus:	n/a
11	chr7:101005832-101005882	ovcar-3	ovarian:	n/a
12	chr7:101017354-101017404	T-47D	breast:	n/a
13	chr7:101006019-101006069	SK-N-SH_RA	brain:	n/a
14	chr7:101006573-101006623	HCPEpiC	choroid plexus:	n/a
15	chr7:101007442-101007492	SKMC	muscle:	n/a
16	chr7:101129980-101130030	AoSMC	blood vessel:	n/a
17	chr7:101055912-101055962	Caco-2	colon:	n/a
18	chr7:101007190-101007240	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:100993034-100993084	SK-N-SH_RA	brain:	n/a
20	chr7:101132009-101132059	Hela-S3	cervix:	n/a
21	chr7:101005832-101005882	HAEpiC	amniotic membrane:	n/a
22	chr7:101006058-101006108	GM12878	blood:	n/a
23	chr7:101017354-101017404	Hepatocyte	liver:	n/a
24	chr7:101005910-101005960	GM12891	blood:	n/a
25	chr7:101006063-101006113	GM12891	blood:	n/a
26	chr7:101006573-101006623	HepG2	liver:	n/a
27	chr7:101006063-101006113	HEEpiC	esophagus:	n/a
28	chr7:101005910-101005960	NHDF-neo	bronchial:	n/a
29	chr7:100968383-100968433	BJ	skin:	n/a
30	chr7:101006363-101006413	GM12892	blood:	n/a
31	chr7:101006052-101006102	HEEpiC	esophagus:	n/a
32	chr7:101005832-101005882	CMK	blood:	n/a
33	chr7:101017354-101017404	PrEC	prostate:	n/a
34	chr7:101007603-101007653	PANC-1	pancreas:	n/a
35	chr7:101006089-101006139	GM12891	blood:	n/a
36	chr7:101006052-101006102	HMEC	breast:	n/a
37	chr7:101079617-101079667	ProgFib	skin:	n/a
38	chr7:100993034-100993084	HL-60	blood:	n/a
39	chr7:101049300-101049350	Hepatocyte	liver:	n/a
40	chr7:101007072-101007122	PANC-1	pancreas:	n/a
41	chr7:101005846-101005896	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:101007442-101007492	GM06990	blood:	n/a
43	chr7:101007442-101007492	BE2_C	brain:	n/a
44	chr7:101006089-101006139	RPTEC	kidney:	n/a
45	chr7:101006363-101006413	HMEC	breast:	n/a
46	chr7:101005846-101005896	HCT-116	colon:	n/a
47	chr7:101006308-101006358	HMEC	breast:	n/a
48	chr7:101007072-101007122	NHDF-neo	bronchial:	n/a
49	chr7:101007603-101007653	SK-N-SH_RA	brain:	n/a
50	chr7:101054654-101054704	HCF	heart:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:101007762..101011060-chr7:101013667..101017793,3	K562	blood:
2	chr7:100964710..100967141-chr7:101003077..101007417,4	MCF-7	breast:
3	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
4	chr7:101068095..101068916-chr7:101150848..101151469,2	MCF-7	breast:
5	chr7:101039985..101042024-chr7:101043789..101046579,2	MCF-7	breast:
6	chr7:101006811..101007905-chr7:101150693..101151800,11	K562	blood:
7	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
8	chr7:101084569..101086934-chr7:101141583..101143364,2	MCF-7	breast:
9	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
10	chr7:101083863..101087245-chr7:101089520..101092470,3	K562	blood:
11	chr7:101083863..101087245-chr7:101089520..101092470,3	K562	blood:
12	chr7:101006530..101007875-chr7:101054200..101055148,9	MCF-7	breast:
13	chr7:101006862..101007822-chr7:101083395..101084349,8	MCF-7	breast:
14	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
15	chr7:101054216..101055052-chr7:101150685..101151359,3	MCF-7	breast:
16	chr7:101023195..101025977-chr7:101028738..101030293,2	K562	blood:
17	chr7:100949900..100952097-chr7:100994165..100995851,2	MCF-7	breast:
18	chr7:101012360..101015108-chr7:101017249..101019175,2	K562	blood:
19	chr7:101006939..101007476-chr7:101083770..101084337,2	K562	blood:
20	chr7:101037193..101039012-chr7:101045881..101047459,2	MCF-7	breast:
21	chr7:101067571..101069515-chr7:101079650..101082212,2	MCF-7	breast:
22	chr7:101006862..101007822-chr7:101083395..101084349,8	MCF-7	breast:
23	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
24	chr7:101006939..101007476-chr7:101083770..101084337,2	K562	blood:
25	chr7:100967257..100969650-chr7:100972376..100975221,2	K562	blood:
26	chr7:101054544..101055233-chr7:101150595..101151343,2	K562	blood:
27	chr7:101006530..101007875-chr7:101054200..101055148,9	MCF-7	breast:
28	chr7:101112161..101112969-chr7:101150803..101151689,2	MCF-7	breast:
29	chr7:101006746..101007872-chr7:101054217..101055171,4	K562	blood:
30	chr7:101006441..101008974-chr7:101023704..101025266,2	MCF-7	breast:
31	chr7:100964752..100967137-chr7:100978107..100980737,2	MCF-7	breast:
32	chr7:101015968..101018340-chr7:101024306..101026455,2	MCF-7	breast:
33	chr7:101012360..101015108-chr7:101017249..101019175,2	K562	blood:
34	chr7:100989055..100991707-chr7:100994198..100995736,2	MCF-7	breast:
35	chr7:100812436..100814522-chr7:100976453..100978919,2	MCF-7	breast:
36	chr7:101022613..101024114-chr7:101025793..101027679,2	MCF-7	breast:
37	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
38	chr7:101067571..101069515-chr7:101079650..101082212,2	MCF-7	breast:
39	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
40	chr7:101016391..101018815-chr7:101033017..101035506,2	K562	blood:
41	chr7:100964942..100967208-chr7:101081876..101083958,2	MCF-7	breast:
42	chr7:100965612..100969667-chr7:101005034..101007660,3	MCF-7	breast:
43	chr7:101039985..101042024-chr7:101043789..101046579,2	MCF-7	breast:
44	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
45	chr7:101005587..101007184-chr7:101013675..101015580,2	MCF-7	breast:
46	chr7:101031371..101033701-chr7:101034998..101036873,2	K562	blood:
47	chr7:101131107..101133497-chr7:101133742..101135419,2	K562	blood:
48	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
49	chr7:100967257..100969650-chr7:100972376..100975221,2	K562	blood:
50	chr7:101032377..101034733-chr7:101037402..101040388,2	MCF-7	breast:

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

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

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
ENSG00000233683	chromatin interactions
ENSG00000255992	chromatin interactions
ENSG00000160963	chromatin interactions
ENSG00000128581	chromatin interactions
ENSG00000232445	chromatin interactions
ENSG00000177192	chromatin interactions

Extended variants
information (count: 7376 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:7376 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573495572	chr7:100967111-100967112	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs540206436	chr7:100967177-100967178	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs113786612	chr7:100967198-100967199	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532305484	chr7:100967222-100967223	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs561716985	chr7:100967267-100967268	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs189163643	chr7:100967288-100967289	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550701811	chr7:100967299-100967300	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs192508995	chr7:100967316-100967317	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs550437765	chr7:100967354-100967355	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs72292126	chr7:100967382-100967383	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs545565902	chr7:100967384-100967385	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541505352	chr7:100967385-100967386	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs61529309	chr7:100967401-100967402	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs61350123	chr7:100967403-100967404	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550277592	chr7:100967404-100967405	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200138500	chr7:100967405-100967406	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570076628	chr7:100967459-100967460	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34522084	chr7:100967512-100967513	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs555841840	chr7:100967522-100967523	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566742112	chr7:100967545-100967546	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs527618071	chr7:100967556-100967557	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs77096771	chr7:100967574-100967575	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369921842	chr7:100967592-100967593	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546969328	chr7:100967651-100967652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs568124517	chr7:100967663-100967664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375585771	chr7:100967693-100967694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs567608727	chr7:100967701-100967702	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145353664	chr7:100967721-100967722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557056296	chr7:100967779-100967780	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182450626	chr7:100967780-100967781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374501432	chr7:100967868-100967869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186627203	chr7:100967916-100967917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191782077	chr7:100967979-100967980	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573480940	chr7:100968012-100968013	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370370989	chr7:100968043-100968044	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74989639	chr7:100968058-100968059	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573680556	chr7:100968089-100968090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548612807	chr7:100968098-100968099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs545744375	chr7:100968168-100968169	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs62483514	chr7:100968171-100968172	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs73180998	chr7:100968238-100968239	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs184046792	chr7:100968272-100968273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542211039	chr7:100968304-100968305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7799285	chr7:100968363-100968364	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs560135184	chr7:100968384-100968385	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs148843392	chr7:100968424-100968425	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs569452549	chr7:100968449-100968450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs115101288	chr7:100968501-100968502	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566803688	chr7:100968508-100968509	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs568087609	chr7:100968513-100968514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1967 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100965800-100967200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:100965800-100967400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:100965800-100973200	Weak transcription	Right Atrium	heart
4	chr7:100966200-100969800	Weak transcription	Fetal Muscle Leg	muscle
5	chr7:100966600-100967400	Flanking Active TSS	HepG2	liver
6	chr7:100967000-100967400	Enhancers	Fetal Intestine Large	intestine
7	chr7:100967200-100967400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:100967400-100967600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:100967400-100967600	Enhancers	HepG2	liver
10	chr7:100967600-100969000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:100969000-100969200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:100969200-100969400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:100970000-100970200	Enhancers	Fetal Muscle Leg	muscle
14	chr7:100973200-100973600	Enhancers	Right Atrium	heart
15	chr7:100973400-100973600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:100973400-100973600	Bivalent Enhancer	Adipose Nuclei	Adipose
17	chr7:100973400-100973600	Flanking Active TSS	Lung	lung
18	chr7:100973400-100973800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:100973400-100973800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr7:100973400-100973800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr7:100973400-100973800	Enhancers	Fetal Muscle Trunk	muscle
22	chr7:100973400-100973800	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr7:100973400-100974000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:100973600-100973800	Enhancers	NHEK	skin
25	chr7:100973600-100980600	Weak transcription	Right Atrium	heart
26	chr7:100973800-100975400	Weak transcription	Lung	lung
27	chr7:100973800-100976200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:100973800-100976200	Weak transcription	NHEK	skin
29	chr7:100973800-100977400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr7:100974000-100976000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:100975600-100976400	Enhancers	HepG2	liver
32	chr7:100976000-100976400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:100976000-100976600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr7:100976000-100976800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr7:100976200-100976600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:100976200-100976600	Enhancers	Fetal Kidney	kidney
37	chr7:100976200-100976800	Enhancers	NHEK	skin
38	chr7:100976400-100977400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:100977400-100977600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:100977400-100978200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr7:100982400-100983800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:100983800-100984000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:100984000-100990800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:100990800-100991200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:100990800-100991400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:100991000-101006000	Weak transcription	Right Atrium	heart
47	chr7:100991200-100991400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:100991400-100992800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:100991400-100993000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:100992800-100993000	Enhancers	Stomach Mucosa	stomach

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