Variant report

Variant	esv2753233
Chromosome Location	chr7:25655060-25771160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:598)
CpG islands
(count:488)
Chromatin interactive
region (count:34)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:25659901-25660223	K562	blood:	n/a	n/a
2	ATF1	chr7:25756095-25756295	K562	blood:	n/a	n/a
3	ATF1	chr7:25683567-25683652	K562	blood:	n/a	n/a
4	ATF1	chr7:25766630-25766860	K562	blood:	n/a	n/a
5	BACH1	chr7:25756216-25756397	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr7:25704214-25704582	GM12878	blood:	n/a	n/a
7	BATF	chr7:25704238-25704562	GM12878	blood:	n/a	n/a
8	BCL3	chr7:25682953-25683301	GM12878	blood:	n/a	n/a
9	BCL3	chr7:25682517-25682771	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:25695097-25695298	K562	blood:	n/a	n/a
11	BHLHE40	chr7:25683491-25683740	K562	blood:	n/a	n/a
12	BHLHE40	chr7:25659845-25660257	K562	blood:	n/a	n/a
13	BHLHE40	chr7:25760146-25760272	K562	blood:	n/a	n/a
14	CCNT2	chr7:25687546-25687747	K562	blood:	n/a	n/a
15	CEBPB	chr7:25730959-25731096	HepG2	liver:	n/a	chr7:25731013-25731024 chr7:25731013-25731026 chr7:25731013-25731026
16	CEBPB	chr7:25762767-25763389	K562	blood:	n/a	chr7:25762870-25762883 chr7:25762870-25762881
17	CEBPB	chr7:25763133-25763236	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:25683034-25683304	HepG2	liver:	n/a	chr7:25683091-25683103
19	CEBPB	chr7:25703628-25703731	K562	blood:	n/a	n/a
20	CEBPB	chr7:25734476-25734772	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:25730949-25731176	A549	lung:	n/a	chr7:25731013-25731024 chr7:25731013-25731026 chr7:25731013-25731026
22	CTCF	chr7:25764333-25764378	K562	blood:	n/a	n/a
23	CTCF	chr7:25714560-25714710	HMF	breast:	n/a	n/a
24	CTCF	chr7:25725740-25725890	GM12871	blood:	n/a	n/a
25	CTCF	chr7:25760040-25760190	A549	lung:	n/a	chr7:25760132-25760141
26	CTCF	chr7:25760080-25760230	GM12868	blood:	n/a	chr7:25760132-25760141
27	CTCF	chr7:25760000-25760150	GM12866	blood:	n/a	chr7:25760132-25760141
28	CTCF	chr7:25760020-25760170	AG04450	lung:	n/a	chr7:25760132-25760141
29	CTCF	chr7:25760040-25760190	HFF	foreskin:	n/a	chr7:25760132-25760141
30	CTCF	chr7:25760060-25760210	GM12864	blood:	n/a	chr7:25760132-25760141
31	CTCF	chr7:25760100-25760250	GM12870	blood:	n/a	chr7:25760132-25760141
32	CTCF	chr7:25760040-25760190	SAEC	small airway:	n/a	chr7:25760132-25760141
33	CTCF	chr7:25760040-25760190	HA-sp	spinal cord:	n/a	chr7:25760132-25760141
34	CTCF	chr7:25712220-25712370	BJ	skin:	n/a	chr7:25712323-25712341 chr7:25712324-25712340 chr7:25712325-25712338 chr7:25712318-25712339
35	CTCF	chr7:25759960-25760306	GM12878	blood:	n/a	chr7:25760132-25760141
36	CTCF	chr7:25712100-25712250	HCM	heart:	n/a	n/a
37	CTCF	chr7:25748800-25748950	AG09319	gingival:	n/a	n/a
38	CTCF	chr7:25760043-25760237	Fibrobl	skin:	n/a	chr7:25760132-25760141
39	CTCF	chr7:25712292-25712403	Hela-S3	cervix:	n/a	chr7:25712323-25712341 chr7:25712324-25712340 chr7:25712325-25712338 chr7:25712318-25712339
40	CTCF	chr7:25760060-25760210	GM12869	blood:	n/a	chr7:25760132-25760141
41	CTCF	chr7:25714580-25714730	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr7:25714620-25714770	RPTEC	kidney:	n/a	n/a
43	CTCF	chr7:25764400-25764550	GM12869	blood:	n/a	n/a
44	CTCF	chr7:25748780-25748930	AG04450	lung:	n/a	n/a
45	CTCF	chr7:25714480-25714630	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr7:25760060-25760210	GM12872	blood:	n/a	chr7:25760132-25760141
47	CTCF	chr7:25760060-25760210	HPAF	blood vessel:	n/a	chr7:25760132-25760141
48	CTCF	chr7:25759998-25760258	MCF-7	breast:	n/a	chr7:25760132-25760141
49	CTCF	chr7:25760061-25760215	GM10266	blood:	n/a	chr7:25760132-25760141
50	CTCF	chr7:25760069-25760242	Medullo	brain:	n/a	chr7:25760132-25760141

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:25734378-25734428	SK-N-MC	brain:	n/a
2	chr7:25765894-25765944	Hela-S3	cervix:	n/a
3	chr7:25703841-25703891	CMK	blood:	n/a
4	chr7:25702848-25702898	SKMC	muscle:	n/a
5	chr7:25766144-25766194	HEEpiC	esophagus:	n/a
6	chr7:25703841-25703891	HEK293	kidney:	embryo
7	chr7:25765894-25765944	MCF10A-Er-Src	breast:	n/a
8	chr7:25734378-25734428	Jurkat	blood:	n/a
9	chr7:25702709-25702759	BE2_C	brain:	n/a
10	chr7:25703644-25703694	AoSMC	blood vessel:	n/a
11	chr7:25766144-25766194	AoSMC	blood vessel:	n/a
12	chr7:25702709-25702759	HRCEpiC	kidney:	n/a
13	chr7:25765894-25765944	AoSMC	blood vessel:	n/a
14	chr7:25765894-25765944	SK-N-SH_RA	brain:	n/a
15	chr7:25702709-25702759	GM19239	blood:	n/a
16	chr7:25765894-25765944	HNPCEpiC	eye:	n/a
17	chr7:25765894-25765944	HepG2	liver:	n/a
18	chr7:25734378-25734428	HMEC	breast:	n/a
19	chr7:25734378-25734428	GM12891	blood:	n/a
20	chr7:25667952-25668002	NHBE	bronchial:	n/a
21	chr7:25734378-25734428	HCF	heart:	n/a
22	chr7:25702848-25702898	AG09319	gingival:	n/a
23	chr7:25766144-25766194	GM12878	blood:	n/a
24	chr7:25703644-25703694	BE2_C	brain:	n/a
25	chr7:25765894-25765944	PFSK-1	brain:	n/a
26	chr7:25703644-25703694	SK-N-MC	brain:	n/a
27	chr7:25765894-25765944	U87	brain:	n/a
28	chr7:25667952-25668002	HRCEpiC	kidney:	n/a
29	chr7:25766144-25766194	HL-60	blood:	n/a
30	chr7:25667952-25668002	CMK	blood:	n/a
31	chr7:25667952-25668002	NH-A	brain:	n/a
32	chr7:25766144-25766194	ECC-1	luminal epithelium:	n/a
33	chr7:25703841-25703891	AG10803	skin:	n/a
34	chr7:25765894-25765944	AG10803	skin:	n/a
35	chr7:25766144-25766194	NHBE	bronchial:	n/a
36	chr7:25703841-25703891	SK-N-SH_RA	brain:	n/a
37	chr7:25703841-25703891	IMR90	lung:	fetal
38	chr7:25703644-25703694	GM19239	blood:	n/a
39	chr7:25702709-25702759	AG10803	skin:	n/a
40	chr7:25734378-25734428	Caco-2	colon:	n/a
41	chr7:25703644-25703694	HL-60	blood:	n/a
42	chr7:25667952-25668002	BE2_C	brain:	n/a
43	chr7:25702709-25702759	GM12892	blood:	n/a
44	chr7:25703841-25703891	HEEpiC	esophagus:	n/a
45	chr7:25667952-25668002	Hepatocyte	liver:	n/a
46	chr7:25702709-25702759	PrEC	prostate:	n/a
47	chr7:25703841-25703891	HCT-116	colon:	n/a
48	chr7:25702848-25702898	HUVEC	blood vessel:	n/a
49	chr7:25667952-25668002	ovcar-3	ovarian:	n/a
50	chr7:25703841-25703891	NT2-D1	testis:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:25743441..25745908-chr7:25764496..25766130,2	K562	blood:
2	chr7:25660475..25663311-chr7:25663363..25666015,2	K562	blood:
3	chr7:25688424..25690991-chr7:25691761..25694010,2	K562	blood:
4	chr7:25743441..25745908-chr7:25764496..25766130,2	K562	blood:
5	chr7:25708676..25711169-chr7:25713723..25715607,2	K562	blood:
6	chr7:25727130..25728806-chr7:25729659..25731798,2	K562	blood:
7	chr7:25751339..25752861-chr7:25879316..25882224,2	MCF-7	breast:
8	chr7:25692948..25694538-chr7:25698709..25701163,2	K562	blood:
9	chr7:25649000..25651876-chr7:25686289..25688697,2	MCF-7	breast:
10	chr7:25746547..25750029-chr7:25750386..25754973,4	K562	blood:
11	chr7:25767131..25769460-chr7:25770576..25772527,2	K562	blood:
12	chr7:25767131..25769460-chr7:25770576..25772527,2	K562	blood:
13	chr7:25660475..25663311-chr7:25663363..25666015,2	K562	blood:
14	chr7:25708676..25711169-chr7:25713723..25715607,2	K562	blood:
15	chr7:25661025..25663705-chr7:25665924..25668424,2	K562	blood:
16	chr7:25716769..25719426-chr7:25720470..25723064,3	K562	blood:
17	chr7:25727130..25728806-chr7:25729659..25731798,2	K562	blood:
18	chr7:25746547..25750051-chr7:25750386..25754973,6	K562	blood:
19	chr7:25769376..25771048-chr7:25790503..25792672,2	K562	blood:
20	chr7:25687389..25689932-chr7:25703208..25705047,2	K562	blood:
21	chr7:25760089..25760596-chr7:25891195..25891843,2	K562	blood:
22	chr7:25688424..25690991-chr7:25691761..25694010,2	K562	blood:
23	chr7:25759879..25760410-chr7:25891017..25891630,2	MCF-7	breast:
24	chr7:25687389..25689932-chr7:25703208..25705047,2	K562	blood:
25	chr7:25661025..25663705-chr7:25665924..25668424,2	K562	blood:
26	chr7:25692948..25694538-chr7:25698709..25701163,2	K562	blood:
27	chr7:25300000..25302398-chr7:25671728..25673940,2	K562	blood:
28	chr7:25767407..25769460-chr7:25770576..25772766,2	K562	blood:
29	chr7:25767407..25769460-chr7:25770576..25772766,2	K562	blood:
30	chr7:25715255..25718154-chr7:25720732..25722618,2	MCF-7	breast:
31	chr7:25715255..25718154-chr7:25720732..25722618,2	MCF-7	breast:
32	chr7:25746547..25750051-chr7:25750386..25754973,6	K562	blood:
33	chr7:25746547..25750029-chr7:25750386..25754973,4	K562	blood:
34	chr7:25716769..25719426-chr7:25720470..25723064,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPVF-10	chr7:25668891-25669198	ucscGeneNc_uc003sxp_1
2	lnc-NPVF-5	chr7:25697580-25697713	ENSG00000223561.2
3	lnc-NPVF-5	chr7:25701290-25701351	ENSG00000223561.2
4	lnc-NPVF-11	chr7:25729200-25729579	NONHSAT119599
5	lnc-NPVF-10	chr7:25664105-25664238	ucscGeneNc_uc003sxp_1
6	lnc-NPVF-5	chr7:25701290-25701351	ENSG00000223561.2
7	lnc-NPVF-5	chr7:25696691-25697713	ENSG00000223561.2
8	lnc-NPVF-10	chr7:25667815-25667876	ucscGeneNc_uc003sxp_1
9	lnc-NPVF-5	chr7:25702366-25702561	ENSG00000223561.2
10	lnc-NPVF-5	chr7:25702366-25702673	ENSG00000223561.2
11	lnc-NPVF-5	chr7:25701290-25701351	ENSG00000223561.2
12	lnc-NPVF-5	chr7:25697580-25697713	ENSG00000223561.2

No data

Variant related genes	Relation type
ENSG00000239622	TF binding region
ENSG00000223561	TF binding region
ENSG00000239622	CpG island
ENSG00000223561	CpG island
ENSG00000223561	chromatin interactions

Extended variants
information (count: 4209 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4209 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73691311	chr7:25655065-25655066	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577385095	chr7:25655070-25655071	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs79403492	chr7:25655081-25655082	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs146188743	chr7:25655085-25655086	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs17152030	chr7:25655093-25655094	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs188865231	chr7:25655152-25655153	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs561759506	chr7:25655183-25655184	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs567872539	chr7:25655201-25655202	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs575288943	chr7:25655218-25655219	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs368508302	chr7:25655278-25655279	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs181994867	chr7:25655326-25655327	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs139056758	chr7:25655331-25655332	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs546503607	chr7:25655356-25655357	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs527400922	chr7:25655369-25655370	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs12700650	chr7:25655407-25655408	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs546763779	chr7:25655428-25655429	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144046989	chr7:25655487-25655488	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568872247	chr7:25655532-25655533	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187058715	chr7:25655547-25655548	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28723687	chr7:25655560-25655561	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs571283706	chr7:25655572-25655573	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540021446	chr7:25655592-25655593	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553332155	chr7:25655610-25655611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191120246	chr7:25655648-25655649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542718919	chr7:25655686-25655687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76897625	chr7:25655713-25655714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145968976	chr7:25655736-25655737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182365217	chr7:25655738-25655739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558208641	chr7:25655761-25655762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs578069733	chr7:25655763-25655764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115797603	chr7:25655770-25655771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560098379	chr7:25655849-25655850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529154724	chr7:25655850-25655851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186596237	chr7:25655851-25655852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140150818	chr7:25655852-25655853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552592597	chr7:25655895-25655896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531312679	chr7:25655924-25655925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551137016	chr7:25655951-25655952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571310808	chr7:25655952-25655953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527406338	chr7:25655955-25655956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191348095	chr7:25655961-25655962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566975789	chr7:25655968-25655969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371206211	chr7:25655989-25655990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535717148	chr7:25656020-25656021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73085994	chr7:25656115-25656116	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs569236344	chr7:25656124-25656125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537834712	chr7:25656143-25656144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182593380	chr7:25656144-25656145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372316561	chr7:25656153-25656154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557903344	chr7:25656165-25656166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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

Chromatin state (count:1206 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25653000-25655800	Enhancers	Fetal Thymus	thymus
2	chr7:25653000-25657200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr7:25653200-25657600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:25653200-25657600	Enhancers	Primary T cells from cord blood	blood
5	chr7:25653400-25656200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:25653400-25659600	Enhancers	Primary B cells from peripheral blood	blood
7	chr7:25653600-25655400	Enhancers	Right Ventricle	heart
8	chr7:25653600-25655600	Enhancers	Right Atrium	heart
9	chr7:25653600-25655800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:25653600-25655800	Enhancers	Left Ventricle	heart
11	chr7:25653600-25655800	Enhancers	Spleen	Spleen
12	chr7:25653600-25657400	Enhancers	Primary hematopoietic stem cells	blood
13	chr7:25653600-25657600	Enhancers	Adipose Nuclei	Adipose
14	chr7:25653800-25655200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr7:25653800-25656200	Enhancers	Fetal Heart	heart
16	chr7:25654000-25655400	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr7:25654000-25655800	Enhancers	Brain Hippocampus Middle	brain
18	chr7:25654000-25656000	Enhancers	Fetal Muscle Leg	muscle
19	chr7:25654200-25655200	Enhancers	Fetal Kidney	kidney
20	chr7:25654200-25655400	Enhancers	Fetal Lung	lung
21	chr7:25654200-25655600	Enhancers	Ovary	ovary
22	chr7:25654200-25655800	Enhancers	Brain Anterior Caudate	brain
23	chr7:25654400-25655200	Enhancers	Placenta	Placenta
24	chr7:25654400-25655200	Enhancers	Fetal Stomach	stomach
25	chr7:25654400-25656400	Enhancers	Primary B cells from cord blood	blood
26	chr7:25654400-25657200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr7:25654600-25655200	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr7:25654600-25655400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr7:25654600-25655600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:25654600-25655600	Enhancers	Aorta	Aorta
31	chr7:25654600-25656000	Enhancers	Thymus	Thymus
32	chr7:25654800-25655200	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr7:25654800-25655600	Enhancers	Primary T cells fromperipheralblood	blood
34	chr7:25654800-25655600	Enhancers	Fetal Muscle Trunk	muscle
35	chr7:25654800-25656600	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr7:25655000-25655200	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr7:25655000-25655200	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr7:25655000-25655400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:25655000-25655600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:25655000-25655600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr7:25655000-25655600	Enhancers	Lung	lung
42	chr7:25655000-25655800	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr7:25655200-25655600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
44	chr7:25655200-25656400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr7:25655200-25656600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr7:25655200-25656800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr7:25655200-25657200	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr7:25655200-25657400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr7:25655200-25659600	Weak transcription	Fetal Stomach	stomach
50	chr7:25655200-25660000	Weak transcription	Placenta	Placenta

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