Variant report

Variant	nsv1026480
Chromosome Location	chr7:26090236-26128758
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:26124122-26124308	K562	blood:	n/a	n/a
2	BACH1	chr7:26124155-26124371	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:26118646-26118885	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr7:26101253-26101643	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:26118652-26118870	K562	blood:	n/a	n/a
6	BHLHE40	chr7:26101304-26101622	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:26114648-26114915	HepG2	liver:	n/a	chr7:26114765-26114778 chr7:26114767-26114776 chr7:26114761-26114782 chr7:26114766-26114775 chr7:26114767-26114776 chr7:26114768-26114777
8	BHLHE40	chr7:26101343-26101531	K562	blood:	n/a	n/a
9	BHLHE40	chr7:26114567-26114951	K562	blood:	n/a	chr7:26114765-26114778 chr7:26114767-26114776 chr7:26114761-26114782 chr7:26114766-26114775 chr7:26114767-26114776 chr7:26114768-26114777
10	BHLHE40	chr7:26114691-26114850	GM12878	blood:	n/a	chr7:26114765-26114778 chr7:26114767-26114776 chr7:26114761-26114782 chr7:26114766-26114775 chr7:26114767-26114776 chr7:26114768-26114777
11	CBX3	chr7:26092227-26093181	HCT-116	colon:	n/a	n/a
12	CCNT2	chr7:26114596-26114921	K562	blood:	n/a	n/a
13	CCNT2	chr7:26118676-26118851	K562	blood:	n/a	n/a
14	CEBPB	chr7:26121149-26121727	MCF-7	breast:	n/a	n/a
15	CEBPB	chr7:26118459-26118991	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:26118723-26118989	K562	blood:	n/a	n/a
17	CEBPB	chr7:26113403-26113603	HepG2	liver:	n/a	chr7:26113507-26113518
18	CEBPB	chr7:26113425-26113625	H1-hESC	embryonic stem cell:	n/a	chr7:26113507-26113518
19	CEBPB	chr7:26122768-26123153	MCF-7	breast:	n/a	n/a
20	CHD1	chr7:26101346-26101348	GM12878	blood:	n/a	n/a
21	CREB1	chr7:26118585-26118928	A549	lung:	n/a	n/a
22	CTCF	chr7:26101440-26101590	HAc	cerebellar:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
23	CTCF	chr7:26101400-26101550	GM12873	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
24	CTCF	chr7:26118552-26118904	A549	lung:	n/a	n/a
25	CTCF	chr7:26118640-26118790	GM12873	blood:	n/a	n/a
26	CTCF	chr7:26118620-26118770	AG09319	gingival:	n/a	n/a
27	CTCF	chr7:26118540-26118690	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr7:26101400-26101550	GM12871	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
29	CTCF	chr7:26122860-26123010	NHEK	skin:	n/a	n/a
30	CTCF	chr7:26101460-26101610	GM12867	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
31	CTCF	chr7:26118640-26118790	AG09309	skin:	n/a	n/a
32	CTCF	chr7:26101400-26101550	NHLF	lung:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
33	CTCF	chr7:26101400-26101550	HEK293	kidney:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
34	CTCF	chr7:26101420-26101570	AG04450	lung:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
35	CTCF	chr7:26101420-26101570	SK-N-SH_RA	brain:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
36	CTCF	chr7:26118575-26118790	LNCaP	prostate:	n/a	n/a
37	CTCF	chr7:26101368-26101632	Fibrobl	skin:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
38	CTCF	chr7:26118541-26118894	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:26101400-26101550	AoAF	blood vessel:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
40	CTCF	chr7:26118513-26118856	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:26118620-26118770	AG04450	lung:	n/a	n/a
42	CTCF	chr7:26101440-26101590	MCF-7	breast:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
43	CTCF	chr7:26101372-26101629	HUVEC	blood vessel:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
44	CTCF	chr7:26118600-26118750	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr7:26101400-26101550	HA-sp	spinal cord:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
46	CTCF	chr7:26118600-26118750	HCT-116	colon:	n/a	n/a
47	CTCF	chr7:26118600-26118750	HL-60	blood:	n/a	n/a
48	CTCF	chr7:26101340-26101636	GM19240	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
49	CTCF	chr7:26101400-26101550	GM12868	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
50	CTCF	chr7:26101396-26101593	H1-hESC	embryonic stem cell:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:26112215-26112265	H1-hESC	embryonic stem cell:	embryo
2	chr7:26112215-26112265	Caco-2	colon:	n/a
3	chr7:26112215-26112265	HNPCEpiC	eye:	n/a
4	chr7:26112215-26112265	Hela-S3	cervix:	n/a
5	chr7:26112215-26112265	HCT-116	colon:	n/a
6	chr7:26119300-26119350	Hepatocyte	liver:	n/a
7	chr7:26112215-26112265	Hepatocyte	liver:	n/a
8	chr7:26119300-26119350	NT2-D1	testis:	n/a
9	chr7:26119300-26119350	HRCEpiC	kidney:	n/a
10	chr7:26112215-26112265	NT2-D1	testis:	n/a
11	chr7:26112215-26112265	GM12891	blood:	n/a
12	chr7:26112215-26112265	GM12878	blood:	n/a
13	chr7:26119300-26119350	NHBE	bronchial:	n/a
14	chr7:26112215-26112265	NH-A	brain:	n/a
15	chr7:26112215-26112265	SK-N-SH	brain:	n/a
16	chr7:26119300-26119350	HEK293	kidney:	embryo
17	chr7:26119300-26119350	Jurkat	blood:	n/a
18	chr7:26119300-26119350	H1-hESC	embryonic stem cell:	embryo
19	chr7:26119300-26119350	Hela-S3	cervix:	n/a
20	chr7:26119300-26119350	A549	lung:	n/a
21	chr7:26112215-26112265	NHBE	bronchial:	n/a
22	chr7:26112215-26112265	HCPEpiC	choroid plexus:	n/a
23	chr7:26119300-26119350	PFSK-1	brain:	n/a
24	chr7:26119300-26119350	MCF-7	breast:	n/a
25	chr7:26112215-26112265	ProgFib	skin:	n/a
26	chr7:26112215-26112265	AG09309	skin:	n/a
27	chr7:26112215-26112265	GM12892	blood:	n/a
28	chr7:26112215-26112265	ECC-1	luminal epithelium:	n/a
29	chr7:26119300-26119350	HUVEC	blood vessel:	n/a
30	chr7:26119300-26119350	PANC-1	pancreas:	n/a
31	chr7:26112215-26112265	HMEC	breast:	n/a
32	chr7:26119300-26119350	MCF10A-Er-Src	breast:	n/a
33	chr7:26119300-26119350	K562	blood:	n/a
34	chr7:26119300-26119350	T-47D	breast:	n/a
35	chr7:26119300-26119350	ProgFib	skin:	n/a
36	chr7:26119300-26119350	ovcar-3	ovarian:	n/a
37	chr7:26112215-26112265	AG04449	skin:	fetal
38	chr7:26112215-26112265	SK-N-MC	brain:	n/a
39	chr7:26112215-26112265	SAEC	small airway:	n/a
40	chr7:26112215-26112265	HEEpiC	esophagus:	n/a
41	chr7:26112215-26112265	GM06990	blood:	n/a
42	chr7:26112215-26112265	CMK	blood:	n/a
43	chr7:26119300-26119350	HepG2	liver:	n/a
44	chr7:26119300-26119350	IMR90	lung:	fetal
45	chr7:26112215-26112265	BE2_C	brain:	n/a
46	chr7:26119300-26119350	HCT-116	colon:	n/a
47	chr7:26112215-26112265	NB4	blood:	n/a
48	chr7:26112215-26112265	PANC-1	pancreas:	n/a
49	chr7:26119300-26119350	GM12892	blood:	n/a
50	chr7:26112215-26112265	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:26111175..26113730-chr7:26115998..26118801,2	MCF-7	breast:
2	chr7:26100956..26102621-chr7:26104473..26107390,2	K562	blood:
3	chr7:26112064..26114800-chr7:26118641..26120981,2	K562	blood:
4	chr7:25989381..25991698-chr7:26116313..26118529,2	K562	blood:
5	chr7:26122863..26125751-chr7:26125996..26128926,3	K562	blood:
6	chr7:26127526..26133053-chr7:26238305..26241600,7	MCF-7	breast:
7	chr7:26122904..26124526-chr7:26129160..26131846,3	MCF-7	breast:
8	chr7:26035423..26036364-chr7:26100860..26101483,2	MCF-7	breast:
9	chr7:26121372..26122991-chr7:26241151..26242996,2	MCF-7	breast:
10	chr7:26122079..26124239-chr7:26127253..26128768,2	MCF-7	breast:
11	chr7:26110644..26115952-chr7:26225900..26230055,7	K562	blood:
12	chr7:26127005..26130353-chr7:26231092..26235350,4	MCF-7	breast:
13	chr7:26118254..26119023-chr7:26227436..26228387,2	MCF-7	breast:
14	chr7:26108059..26110541-chr7:26114751..26116494,2	K562	blood:
15	chr7:26125058..26127925-chr7:26238815..26242707,3	MCF-7	breast:
16	chr7:26102797..26105180-chr7:26108229..26111038,2	K562	blood:
17	chr7:25990246..25992488-chr7:26100564..26102799,3	MCF-7	breast:
18	chr7:26124079..26126684-chr7:26237086..26240273,4	MCF-7	breast:
19	chr7:26093464..26095409-chr7:26225078..26227432,2	K562	blood:
20	chr7:25989811..25992726-chr7:26096097..26097704,2	MCF-7	breast:
21	chr7:26114537..26124611-chr7:26235125..26244089,23	MCF-7	breast:
22	chr7:26120022..26122895-chr7:26235605..26238728,3	MCF-7	breast:
23	chr7:26119926..26122266-chr7:26227984..26229588,2	MCF-7	breast:
24	chr7:25990207..25991830-chr7:26094178..26097069,2	MCF-7	breast:
25	chr7:26112064..26114800-chr7:26118641..26120981,2	K562	blood:
26	chr7:26120079..26121816-chr7:26128176..26130468,2	K562	blood:
27	chr7:26127176..26132084-chr7:26132908..26137367,5	K562	blood:
28	chr7:26116496..26120025-chr7:26124167..26127570,3	MCF-7	breast:
29	chr7:26108042..26110669-chr7:26111318..26113129,2	K562	blood:
30	chr7:26123870..26125696-chr7:26226783..26229178,2	MCF-7	breast:
31	chr7:26122995..26125751-chr7:26126126..26128926,3	K562	blood:
32	chr7:26111175..26113730-chr7:26115998..26118801,2	MCF-7	breast:
33	chr7:25935063..25935626-chr7:26100854..26101524,2	K562	blood:
34	chr7:25934813..25935616-chr7:26101041..26101955,3	MCF-7	breast:
35	chr7:26035382..26036550-chr7:26101032..26101905,6	MCF-7	breast:
36	chr7:26120211..26123074-chr7:26126513..26128042,2	MCF-7	breast:
37	chr7:26117592..26119094-chr7:26231606..26233177,2	MCF-7	breast:
38	chr7:26120079..26121816-chr7:26128176..26130468,2	K562	blood:
39	chr7:26111985..26114950-chr7:26225900..26229450,4	K562	blood:
40	chr7:26117230..26119075-chr7:26243956..26245762,2	K562	blood:
41	chr7:26118648..26123140-chr7:26237417..26242169,5	K562	blood:
42	chr7:26117300..26119853-chr7:26222397..26224212,2	MCF-7	breast:
43	chr6:8102268..8102945-chr7:26101163..26101679,2	HCT-116	colon:
44	chr7:26125161..26128089-chr7:26129488..26132458,4	MCF-7	breast:
45	chr7:26100956..26102621-chr7:26104473..26107390,2	K562	blood:
46	chr7:26127085..26136794-chr7:26224123..26230309,16	K562	blood:
47	chr7:26122995..26125751-chr7:26126126..26128926,3	K562	blood:
48	chr7:26126882..26129598-chr7:26130419..26133130,2	K562	blood:
49	chr7:26126753..26129598-chr7:26130419..26132828,3	K562	blood:
50	chr7:26117990..26136794-chr7:26219781..26234338,53	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPA2B1-2	chr7:26112307-26112316	XLOC_006385
2	lnc-HNRNPA2B1-2	chr7:26109126-26109421	XLOC_006385
3	lnc-HNRNPA2B1-3	chr7:26097439-26098434	XLOC_006384
4	lnc-HNRNPA2B1-2	chr7:26109126-26109421	XLOC_006385
5	lnc-HNRNPA2B1-3	chr7:26101163-26101262	XLOC_006384
6	lnc-HNRNPA2B1-3	chr7:26097832-26098434	NONHSAT119611

Variant related genes	Relation type
ENSG00000266430	TF binding region
ENSG00000266430	CpG island
ENSG00000122566	chromatin interactions
ENSG00000050344	chromatin interactions
ENSG00000124802	chromatin interactions
ENSG00000265818	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000199085	chromatin interactions
ZNF700	miRNA target sites
ZEB1	miRNA target sites
EP300	miRNA target sites
LRRFIP1	miRNA target sites

Extended variants
information (count: 1170 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1170 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185596880	chr7:26090239-26090240	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs187774196	chr7:26090250-26090251	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs544135650	chr7:26090257-26090258	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs191245391	chr7:26090261-26090262	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs77747400	chr7:26090284-26090285	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs566965440	chr7:26090298-26090299	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs571724825	chr7:26090314-26090315	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs184024739	chr7:26090316-26090317	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs577615005	chr7:26090323-26090324	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs539838347	chr7:26090362-26090363	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs532161898	chr7:26090379-26090380	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs534558195	chr7:26090423-26090424	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs552424277	chr7:26090458-26090459	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs528951415	chr7:26090463-26090464	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs542466824	chr7:26090481-26090482	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs569139605	chr7:26090494-26090495	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs188365226	chr7:26090507-26090508	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs112677570	chr7:26090516-26090517	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs111310762	chr7:26090530-26090531	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs533401849	chr7:26090558-26090559	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs546636468	chr7:26090580-26090581	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs566958832	chr7:26090603-26090604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149275916	chr7:26090623-26090624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34665047	chr7:26090685-26090686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548780898	chr7:26090690-26090691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568741186	chr7:26090706-26090707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537648195	chr7:26090716-26090717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116413615	chr7:26090724-26090725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76033670	chr7:26090727-26090728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533787969	chr7:26090759-26090760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554948875	chr7:26090818-26090819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553463685	chr7:26090852-26090853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181614434	chr7:26090884-26090885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542775951	chr7:26090885-26090886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111318988	chr7:26090892-26090893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6944128	chr7:26090924-26090925	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs544467860	chr7:26090927-26090928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116274480	chr7:26090928-26090929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78965500	chr7:26090932-26090933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546993295	chr7:26090939-26090940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560080823	chr7:26090975-26090976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79787274	chr7:26091002-26091003	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs576172750	chr7:26091028-26091029	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs576890346	chr7:26091034-26091035	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs144482165	chr7:26091081-26091082	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs569002476	chr7:26091106-26091107	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs558709322	chr7:26091107-26091108	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs538054957	chr7:26091181-26091182	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs551243201	chr7:26091189-26091190	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs571541752	chr7:26091221-26091222	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Breast cancer	18852474	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26090000-26090600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
2	chr7:26090200-26091800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr7:26090600-26091000	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr7:26091000-26091200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr7:26091200-26091600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
6	chr7:26091600-26099800	Weak transcription	Gastric	stomach
7	chr7:26091800-26092200	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr7:26092200-26092800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr7:26092200-26093400	Enhancers	HMEC	breast
10	chr7:26092400-26093400	Enhancers	NHEK	skin
11	chr7:26092400-26093800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:26092600-26093200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:26092800-26093800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr7:26093800-26098000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:26094200-26095200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:26095000-26095200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
17	chr7:26095000-26095400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
18	chr7:26096400-26096600	ZNF genes & repeats	Aorta	Aorta
19	chr7:26096400-26097000	Enhancers	Pancreas	Pancrea
20	chr7:26096600-26096800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr7:26096800-26097000	Enhancers	Lung	lung
22	chr7:26096800-26097800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr7:26097000-26100200	Weak transcription	Pancreas	Pancrea
24	chr7:26097800-26098200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr7:26097800-26098200	Enhancers	Spleen	Spleen
26	chr7:26098000-26098200	Bivalent Enhancer	Left Ventricle	heart
27	chr7:26098000-26098200	Bivalent Enhancer	K562	blood
28	chr7:26098000-26098800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:26098200-26098600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr7:26098200-26101200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr7:26098600-26100200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr7:26098800-26100000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:26100000-26101000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr7:26100000-26101800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:26100200-26100600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:26100200-26100600	Enhancers	Pancreas	Pancrea
37	chr7:26100200-26100600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr7:26100200-26100800	Enhancers	Fetal Muscle Leg	muscle
39	chr7:26100200-26101000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr7:26100200-26101000	Enhancers	Dnd41	blood
41	chr7:26100200-26101400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:26100200-26101400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:26100200-26101400	Enhancers	Colon Smooth Muscle	Colon
44	chr7:26100200-26101400	Enhancers	Fetal Stomach	stomach
45	chr7:26100200-26101800	Enhancers	Brain Germinal Matrix	brain
46	chr7:26100400-26100800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr7:26100400-26101000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:26100400-26101400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr7:26100400-26101400	Enhancers	Primary hematopoietic stem cells	blood
50	chr7:26100400-26101400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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