Variant report

Variant	esv3420137
Chromosome Location	chr7:6522252-6524800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:619)
CpG islands
(count:732)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6522729-6523152	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:6523743-6524104	HepG2	liver:	n/a	n/a
3	ATF1	chr7:6522614-6523091	K562	blood:	n/a	chr7:6522795-6522809
4	BACH1	chr7:6522707-6524156	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr7:6523560-6524076	GM12878	blood:	n/a	chr7:6523584-6523593 chr7:6523577-6523586
6	BHLHE40	chr7:6523023-6523223	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:6523724-6524027	K562	blood:	n/a	n/a
8	BHLHE40	chr7:6523737-6524032	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:6522661-6523249	K562	blood:	n/a	n/a
10	BRCA1	chr7:6523097-6523257	HepG2	liver:	n/a	n/a
11	BRCA1	chr7:6523740-6524015	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr7:6523641-6524002	K562	blood:	n/a	n/a
13	CBX3	chr7:6522425-6523098	K562	blood:	n/a	n/a
14	CCNT2	chr7:6522695-6524016	K562	blood:	n/a	chr7:6523867-6523876
15	CEBPB	chr7:6522695-6523055	K562	blood:	n/a	n/a
16	CEBPB	chr7:6522679-6523144	Hela-S3	cervix:	n/a	n/a
17	CEBPD	chr7:6523570-6524010	HepG2	liver:	n/a	n/a
18	CHD1	chr7:6522457-6524240	IMR90	lung:	n/a	chr7:6523177-6523187
19	CHD1	chr7:6522373-6524009	GM12878	blood:	n/a	chr7:6523177-6523187
20	CHD2	chr7:6522778-6524038	GM12878	blood:	n/a	chr7:6523177-6523187
21	CHD2	chr7:6523052-6523261	HepG2	liver:	n/a	chr7:6523177-6523187
22	CHD2	chr7:6522741-6524064	Hela-S3	cervix:	n/a	chr7:6523177-6523187
23	CHD2	chr7:6523642-6524163	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr7:6522853-6523897	K562	blood:	n/a	chr7:6523177-6523187
25	CHD2	chr7:6523487-6523922	HepG2	liver:	n/a	n/a
26	CREB1	chr7:6523494-6524081	GM12878	blood:	n/a	n/a
27	CREB1	chr7:6522677-6523409	GM12878	blood:	n/a	chr7:6523138-6523151 chr7:6522796-6522809
28	CREB1	chr7:6523520-6524045	K562	blood:	n/a	n/a
29	CREB1	chr7:6522542-6523409	HepG2	liver:	n/a	chr7:6523138-6523151 chr7:6522796-6522809
30	CREB1	chr7:6522541-6523412	HepG2	liver:	n/a	chr7:6523138-6523151 chr7:6522796-6522809
31	CREB1	chr7:6523417-6524012	A549	lung:	n/a	n/a
32	CREB1	chr7:6521848-6522407	HepG2	liver:	n/a	n/a
33	CREB1	chr7:6523725-6523897	A549	lung:	n/a	n/a
34	CREB1	chr7:6522673-6523342	K562	blood:	n/a	chr7:6523138-6523151 chr7:6522796-6522809
35	CREB1	chr7:6522686-6523405	A549	lung:	n/a	chr7:6523138-6523151 chr7:6522796-6522809
36	CREB1	chr7:6523425-6524131	HepG2	liver:	n/a	n/a
37	CTBP2	chr7:6523706-6524272	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr7:6522659-6522908	K562	blood:	n/a	n/a
39	CTCF	chr7:6522720-6522870	HMF	breast:	n/a	n/a
40	CTCF	chr7:6522740-6522890	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr7:6523739-6523945	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr7:6523782-6523874	GM12878	blood:	n/a	n/a
43	CTCF	chr7:6522580-6522730	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr7:6522660-6522810	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr7:6522757-6522767	GM12878	blood:	n/a	n/a
46	CTCF	chr7:6522740-6522890	NHEK	skin:	n/a	n/a
47	CTCF	chr7:6523604-6523679	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr7:6522520-6522670	HepG2	liver:	n/a	n/a
49	CTCF	chr7:6522680-6522830	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr7:6523760-6523910	SK-N-SH_RA	brain:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6523611-6523661	HCF	heart:	n/a
2	chr7:6523282-6523332	A549	lung:	n/a
3	chr7:6523611-6523661	HRE	kidney:	n/a
4	chr7:6523810-6523860	HIPEpiC	eye:	n/a
5	chr7:6523917-6523967	RPTEC	kidney:	n/a
6	chr7:6523886-6523936	AG09319	gingival:	n/a
7	chr7:6522842-6522892	HUVEC	blood vessel:	n/a
8	chr7:6522802-6522852	SAEC	small airway:	n/a
9	chr7:6522842-6522892	HCPEpiC	choroid plexus:	n/a
10	chr7:6523968-6524018	K562	blood:	n/a
11	chr7:6523810-6523860	HRCEpiC	kidney:	n/a
12	chr7:6522802-6522852	NT2-D1	testis:	n/a
13	chr7:6523611-6523661	SKMC	muscle:	n/a
14	chr7:6523611-6523661	Hepatocyte	liver:	n/a
15	chr7:6523253-6523303	HCM	heart:	n/a
16	chr7:6523691-6523741	ECC-1	luminal epithelium:	n/a
17	chr7:6523691-6523741	HCT-116	colon:	n/a
18	chr7:6523896-6523946	ECC-1	luminal epithelium:	n/a
19	chr7:6523810-6523860	IMR90	lung:	fetal
20	chr7:6523896-6523946	HRPEpiC	eye:	n/a
21	chr7:6522842-6522892	ECC-1	luminal epithelium:	n/a
22	chr7:6523888-6523938	Jurkat	blood:	n/a
23	chr7:6523810-6523860	AG09309	skin:	n/a
24	chr7:6523917-6523967	NH-A	brain:	n/a
25	chr7:6523810-6523860	AG10803	skin:	n/a
26	chr7:6523917-6523967	HRPEpiC	eye:	n/a
27	chr7:6523810-6523860	ProgFib	skin:	n/a
28	chr7:6523282-6523332	HRE	kidney:	n/a
29	chr7:6523917-6523967	LNCaP	prostate:	n/a
30	chr7:6523282-6523332	GM06990	blood:	n/a
31	chr7:6523691-6523741	BE2_C	brain:	n/a
32	chr7:6523691-6523741	BJ	skin:	n/a
33	chr7:6523253-6523303	AG04450	lung:	fetal
34	chr7:6522802-6522852	AG10803	skin:	n/a
35	chr7:6523896-6523946	PrEC	prostate:	n/a
36	chr7:6523253-6523303	AG09309	skin:	n/a
37	chr7:6523691-6523741	AG09309	skin:	n/a
38	chr7:6523968-6524018	GM06990	blood:	n/a
39	chr7:6523282-6523332	NH-A	brain:	n/a
40	chr7:6522842-6522892	AG09319	gingival:	n/a
41	chr7:6523917-6523967	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:6523253-6523303	IMR90	lung:	fetal
43	chr7:6523691-6523741	HL-60	blood:	n/a
44	chr7:6523691-6523741	IMR90	lung:	fetal
45	chr7:6523888-6523938	GM12891	blood:	n/a
46	chr7:6523886-6523936	SAEC	small airway:	n/a
47	chr7:6522842-6522892	GM12891	blood:	n/a
48	chr7:6523888-6523938	MCF10A-Er-Src	breast:	n/a
49	chr7:6523611-6523661	HL-60	blood:	n/a
50	chr7:6523888-6523938	PrEC	prostate:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6522590..6525464-chr7:6629667..6631342,2	K562	blood:
2	chr7:6521681..6526038-chr7:6526623..6531331,7	K562	blood:
3	chr7:6523333..6525416-chr7:6628158..6630053,2	K562	blood:
4	chr7:6509730..6517655-chr7:6520090..6524473,18	K562	blood:
5	chr7:6485398..6489202-chr7:6520855..6525273,5	MCF-7	breast:
6	chr7:6142905..6144683-chr7:6522279..6524664,2	MCF-7	breast:
7	chr7:6523102..6525727-chr7:6628447..6631086,2	MCF-7	breast:
8	chr6:27857335..27860257-chr7:6521676..6523586,2	MCF-7	breast:
9	chr7:6521171..6524635-chr7:6615181..6617344,3	K562	blood:
10	chr7:6486201..6489628-chr7:6522463..6525039,4	MCF-7	breast:
11	chr1:107863835..107864489-chr7:6521954..6522744,2	MCF-7	breast:
12	chr7:6522385..6525546-chr7:6675389..6679461,5	MCF-7	breast:
13	chr1:153507926..153508844-chr7:6523134..6524128,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000269781	TF binding region
DAGLB	TF binding region
KDELR2	TF binding region
ENSG00000269781	CpG island
DAGLB	CpG island
KDELR2	CpG island
ENSG00000146576	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000231359	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000205903	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73674121	chr7:6522323-6522324	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556627008	chr7:6522329-6522330	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs200817664	chr7:6522345-6522346	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs202109275	chr7:6522350-6522351	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs574952425	chr7:6522370-6522371	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs145751266	chr7:6522411-6522412	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs368349971	chr7:6522463-6522464	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs201968306	chr7:6522464-6522465	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs201936540	chr7:6522472-6522473	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs567971611	chr7:6522474-6522475	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs201381963	chr7:6522475-6522476	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs10525658	chr7:6522485-6522486	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs182775513	chr7:6522499-6522500	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs77456823	chr7:6522532-6522533	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs540904922	chr7:6522580-6522581	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs565180449	chr7:6522606-6522607	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs371708138	chr7:6522628-6522629	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs113336623	chr7:6522636-6522637	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs55669539	chr7:6522637-6522638	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs34123172	chr7:6522643-6522644	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs397817878	chr7:6522649-6522650	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs532529752	chr7:6522677-6522678	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs544240029	chr7:6522700-6522701	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs562975568	chr7:6522713-6522714	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs530191521	chr7:6522715-6522716	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs549217456	chr7:6522729-6522730	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs79216842	chr7:6522754-6522755	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs528406645	chr7:6522756-6522757	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs546867093	chr7:6522791-6522792	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs190693582	chr7:6522829-6522830	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs538635482	chr7:6522903-6522904	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs115435732	chr7:6522965-6522966	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs142660495	chr7:6522994-6522995	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs3833678	chr7:6522996-6522997	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs541592394	chr7:6523037-6523038	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs568632547	chr7:6523056-6523057	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs147782569	chr7:6523060-6523061	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs554776749	chr7:6523076-6523077	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs372778935	chr7:6523115-6523116	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs375995662	chr7:6523185-6523186	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs573364702	chr7:6523202-6523203	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs540610549	chr7:6523232-6523233	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs563269738	chr7:6523240-6523241	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs577418710	chr7:6523247-6523248	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs544640678	chr7:6523282-6523283	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs61732206	chr7:6523283-6523284	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs12113832	chr7:6523298-6523299	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs542323830	chr7:6523312-6523313	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs560968720	chr7:6523339-6523340	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs376176215	chr7:6523348-6523349	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6503600-6522800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:6507600-6522400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:6507800-6522600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:6510200-6522400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:6510200-6522600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:6513200-6522400	Weak transcription	Aorta	Aorta
7	chr7:6513200-6522400	Weak transcription	Lung	lung
8	chr7:6514000-6522400	Weak transcription	Thymus	Thymus
9	chr7:6517000-6522600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:6518800-6522400	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr7:6518800-6522400	Enhancers	Left Ventricle	heart
12	chr7:6519400-6522400	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:6519400-6522400	Enhancers	Stomach Mucosa	stomach
14	chr7:6519400-6522600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr7:6519800-6522400	Transcr. at gene 5' and 3'	NH-A	brain
16	chr7:6520400-6522400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:6520400-6522400	Weak transcription	Psoas Muscle	Psoas
18	chr7:6520400-6522600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:6520800-6524600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr7:6521000-6522400	Weak transcription	Fetal Brain Female	brain
21	chr7:6521200-6522400	Weak transcription	Esophagus	oesophagus
22	chr7:6521200-6522600	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr7:6521200-6522800	Flanking Active TSS	Liver	Liver
24	chr7:6521400-6522400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:6521400-6522400	Enhancers	Primary T cells fromperipheralblood	blood
26	chr7:6521400-6522400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr7:6521400-6522400	Weak transcription	Gastric	stomach
28	chr7:6521400-6522600	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr7:6521400-6522800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr7:6521400-6524000	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr7:6521400-6524200	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr7:6521400-6524200	Active TSS	Pancreas	Pancrea
33	chr7:6521600-6522400	Enhancers	Fetal Brain Male	brain
34	chr7:6521600-6522400	Active TSS	HepG2	liver
35	chr7:6521600-6524600	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr7:6521800-6522400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr7:6521800-6522400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:6521800-6522400	Enhancers	Brain Substantia Nigra	brain
39	chr7:6521800-6522600	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:6521800-6522600	Enhancers	Brain Cingulate Gyrus	brain
41	chr7:6521800-6522600	Flanking Active TSS	Duodenum Mucosa	Duodenum
42	chr7:6521800-6524400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr7:6522000-6522400	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
44	chr7:6522000-6522400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr7:6522000-6522400	Enhancers	Brain Angular Gyrus	brain
46	chr7:6522000-6522400	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr7:6522000-6522400	Flanking Active TSS	Fetal Intestine Small	intestine
48	chr7:6522000-6522400	Flanking Active TSS	Fetal Kidney	kidney
49	chr7:6522000-6522400	Transcr. at gene 5' and 3'	Placenta	Placenta
50	chr7:6522000-6522400	Enhancers	Rectal Smooth Muscle	rectum

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