Variant report

Variant	nsv887424
Chromosome Location	chr7:5863379-5927956
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	ARID3A	chr7:5867459-5867694	K562	blood:	n/a	n/a
2	ARID3A	chr7:5867592-5867694	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:5908686-5908892	HepG2	liver:	n/a	n/a
4	BATF	chr7:5896136-5896348	GM12878	blood:	n/a	n/a
5	BCLAF1	chr7:5896165-5896407	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:5889190-5889204	K562	blood:	n/a	n/a
7	BHLHE40	chr7:5896140-5896326	GM12878	blood:	n/a	n/a
8	BRCA1	chr7:5896176-5896337	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr7:5891846-5891857	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr7:5872758-5872976	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:5892975-5893180	HepG2	liver:	n/a	chr7:5893027-5893038
12	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
13	CEBPB	chr7:5892977-5893179	IMR90	lung:	n/a	chr7:5893027-5893038
14	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
15	CEBPB	chr7:5890492-5890732	K562	blood:	n/a	chr7:5890571-5890582
16	CEBPB	chr7:5892913-5893127	H1-hESC	embryonic stem cell:	n/a	chr7:5893027-5893038
17	CEBPB	chr7:5892955-5893172	K562	blood:	n/a	chr7:5893027-5893038
18	CEBPB	chr7:5912087-5912368	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:5890460-5890688	HepG2	liver:	n/a	chr7:5890571-5890582
20	CEBPB	chr7:5896180-5896389	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:5890535-5890604	H1-hESC	embryonic stem cell:	n/a	chr7:5890571-5890582
22	CEBPB	chr7:5891809-5891870	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:5890537-5890700	A549	lung:	n/a	chr7:5890571-5890582
24	CEBPB	chr7:5872011-5872190	K562	blood:	n/a	n/a
25	CEBPB	chr7:5890537-5890656	IMR90	lung:	n/a	chr7:5890571-5890582
26	CHD2	chr7:5894459-5894465	HepG2	liver:	n/a	n/a
27	CTCF	chr7:5880420-5880570	MCF-7	breast:	n/a	chr7:5880500-5880513 chr7:5880497-5880515
28	CTCF	chr7:5867448-5867694	MCF-7	breast:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
29	CTCF	chr7:5867417-5867737	K562	blood:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
30	CTCF	chr7:5896100-5896250	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr7:5877220-5877370	K562	blood:	n/a	n/a
32	CTCF	chr7:5896100-5896250	HFF	foreskin:	n/a	n/a
33	CTCF	chr7:5867500-5867650	GM12871	blood:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
34	CTCF	chr7:5895880-5896030	NHEK	skin:	n/a	n/a
35	CTCF	chr7:5896160-5896310	AG10803	skin:	n/a	n/a
36	CTCF	chr7:5895892-5896026	GM12892	blood:	n/a	n/a
37	CTCF	chr7:5867432-5867762	IMR90	lung:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
38	CTCF	chr7:5867453-5867697	Gliobla	brain:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
39	CTCF	chr7:5867600-5867750	RPTEC	kidney:	n/a	n/a
40	CTCF	chr7:5867100-5867250	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr7:5867560-5867710	HEEpiC	esophagus:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
42	CTCF	chr7:5867444-5867715	MCF-7	breast:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
43	CTCF	chr7:5896140-5896290	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:5867500-5867650	GM12867	blood:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
45	CTCF	chr7:5867540-5867690	GM12872	blood:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598
46	CTCF	chr7:5896093-5896386	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr7:5896076-5896406	K562	blood:	n/a	n/a
48	CTCF	chr7:5896151-5896394	ECC-1	luminal epithelium:	n/a	n/a
49	CTCF	chr7:5867420-5867570	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr7:5867520-5867670	HCM	heart:	n/a	chr7:5867583-5867599 chr7:5867582-5867600 chr7:5867584-5867597 chr7:5867577-5867598

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5865915-5865965	HNPCEpiC	eye:	n/a
2	chr7:5865915-5865965	HNPCEpiC	eye:	n/a
3	chr7:5890037-5890087	SK-N-MC	brain:	n/a
4	chr7:5919589-5919639	AoSMC	blood vessel:	n/a
5	chr7:5920535-5920585	IMR90	lung:	fetal
6	chr7:5919012-5919062	MCF10A-Er-Src	breast:	n/a
7	chr7:5886722-5886772	HepG2	liver:	n/a
8	chr7:5911900-5911950	NHBE	bronchial:	n/a
9	chr7:5887023-5887073	NT2-D1	testis:	n/a
10	chr7:5911900-5911950	SAEC	small airway:	n/a
11	chr7:5883645-5883695	PFSK-1	brain:	n/a
12	chr7:5886722-5886772	HL-60	blood:	n/a
13	chr7:5920635-5920685	Hepatocyte	liver:	n/a
14	chr7:5887023-5887073	AG04450	lung:	fetal
15	chr7:5888077-5888127	NT2-D1	testis:	n/a
16	chr7:5883645-5883695	CMK	blood:	n/a
17	chr7:5911900-5911950	SKMC	muscle:	n/a
18	chr7:5885244-5885294	AoSMC	blood vessel:	n/a
19	chr7:5863510-5863560	MCF10A-Er-Src	breast:	n/a
20	chr7:5919012-5919062	SK-N-MC	brain:	n/a
21	chr7:5920535-5920585	SK-N-SH_RA	brain:	n/a
22	chr7:5911701-5911751	NHBE	bronchial:	n/a
23	chr7:5890037-5890087	SK-N-SH	brain:	n/a
24	chr7:5863813-5863863	GM12878	blood:	n/a
25	chr7:5919583-5919633	HRE	kidney:	n/a
26	chr7:5911701-5911751	GM19239	blood:	n/a
27	chr7:5863813-5863863	HRPEpiC	eye:	n/a
28	chr7:5920635-5920685	NB4	blood:	n/a
29	chr7:5890037-5890087	ECC-1	luminal epithelium:	n/a
30	chr7:5887023-5887073	HIPEpiC	eye:	n/a
31	chr7:5911900-5911950	Jurkat	blood:	n/a
32	chr7:5911800-5911850	ProgFib	skin:	n/a
33	chr7:5919583-5919633	LNCaP	prostate:	n/a
34	chr7:5885244-5885294	AG04450	lung:	fetal
35	chr7:5919589-5919639	PrEC	prostate:	n/a
36	chr7:5863813-5863863	AG10803	skin:	n/a
37	chr7:5887023-5887073	Hepatocyte	liver:	n/a
38	chr7:5890037-5890087	PFSK-1	brain:	n/a
39	chr7:5865915-5865965	SKMC	muscle:	n/a
40	chr7:5919583-5919633	MCF-7	breast:	n/a
41	chr7:5911900-5911950	K562	blood:	n/a
42	chr7:5863510-5863560	SAEC	small airway:	n/a
43	chr7:5911701-5911751	Caco-2	colon:	n/a
44	chr7:5911701-5911751	HMEC	breast:	n/a
45	chr7:5885244-5885294	T-47D	breast:	n/a
46	chr7:5865915-5865965	H1-hESC	embryonic stem cell:	embryo
47	chr7:5911900-5911950	NT2-D1	testis:	n/a
48	chr7:5911701-5911751	GM12878	blood:	n/a
49	chr7:5887023-5887073	K562	blood:	n/a
50	chr7:5911800-5911850	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:5895754..5896691-chr7:6036473..6037181,2	MCF-7	breast:
2	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
3	chr7:5877192..5879014-chr7:6172405..6175361,2	K562	blood:
4	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
5	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
6	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
7	chr7:5921888..5923776-chr7:6615172..6617060,2	K562	blood:
8	chr7:5896217..5898583-chr7:97641356..97642858,2	MCF-7	breast:
9	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
10	chr7:5464152..5466960-chr7:5862123..5864390,2	MCF-7	breast:
11	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
12	chr3:107149613..107150322-chr7:5862636..5863385,2	NB4	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118944
2	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118948
3	lnc-OCM-3	chr7:5879580-5879706	NONHSAT118944
4	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118942
5	lnc-OCM-3	chr7:5878701-5878783	NONHSAT118942
6	lnc-OCM-3	chr7:5878820-5878850	NONHSAT118948
7	lnc-RSPH10B-1	chr7:5911384-5911681	NONHSAT118956
8	lnc-OCM-3	chr7:5893738-5893857	NONHSAT118944
9	lnc-OCM-3	chr7:5870812-5870914	NONHSAT118942
10	lnc-OCM-3	chr7:5880321-5880487	NONHSAT118944

Variant related genes	Relation type
OCM	TF binding region
ZNF815P	TF binding region
RN7SL556P	TF binding region
OCM	CpG island
ZNF815P	CpG island
RN7SL556P	CpG island
ENSG00000272953	chromatin interactions
ENSG00000182095	chromatin interactions
ENSG00000273125	chromatin interactions

Extended variants
information (count: 4135 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4135 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2287588	chr7:5863379-5863380	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186370581	chr7:5863380-5863381	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs115989272	chr7:5863384-5863385	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs567740838	chr7:5863404-5863405	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs377545544	chr7:5863413-5863414	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs575264948	chr7:5863416-5863417	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs536290806	chr7:5863422-5863423	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs62455923	chr7:5863423-5863424	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs189316348	chr7:5863441-5863442	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540525656	chr7:5863443-5863444	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs373018939	chr7:5863456-5863457	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs565138074	chr7:5863468-5863469	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576983930	chr7:5863476-5863477	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs73345307	chr7:5863526-5863527	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs562873479	chr7:5863540-5863541	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs571646887	chr7:5863559-5863560	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555893291	chr7:5863565-5863566	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs530112757	chr7:5863593-5863594	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538603516	chr7:5863606-5863607	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs115432150	chr7:5863608-5863609	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560104854	chr7:5863619-5863620	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs527638910	chr7:5863673-5863674	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs552456339	chr7:5863681-5863682	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571098227	chr7:5863686-5863687	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs531828156	chr7:5863722-5863723	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs550333288	chr7:5863725-5863726	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs368518705	chr7:5863733-5863734	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568890202	chr7:5863740-5863741	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536352232	chr7:5863758-5863759	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs556960347	chr7:5863763-5863764	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs34605620	chr7:5863770-5863771	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs554647612	chr7:5863771-5863772	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs77075633	chr7:5863789-5863790	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533740243	chr7:5863800-5863801	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs558589601	chr7:5863806-5863807	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577049199	chr7:5863817-5863818	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112164499	chr7:5863827-5863828	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556320879	chr7:5863861-5863862	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs542742704	chr7:5863862-5863863	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148823901	chr7:5863903-5863904	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560168335	chr7:5863939-5863940	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs180763841	chr7:5863947-5863948	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs116308948	chr7:5863972-5863973	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs564661562	chr7:5863975-5863976	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs532013644	chr7:5863992-5863993	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs113839044	chr7:5864001-5864002	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs186446344	chr7:5864002-5864003	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs565138657	chr7:5864029-5864030	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs74923259	chr7:5864030-5864031	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs571884627	chr7:5864040-5864041	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	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
Urothelial carcinoma	21177765	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
Schizophrenia	21346763	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5862000-5864000	Flanking Active TSS	Dnd41	blood
2	chr7:5862200-5863400	Active TSS	iPS-18 Cell Line	embryonic stem cell
3	chr7:5862200-5863400	Active TSS	Primary T cells from cord blood	blood
4	chr7:5862200-5863400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:5862200-5863400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr7:5862200-5863400	Active TSS	Fetal Brain Female	brain
7	chr7:5862200-5863400	Active TSS	Fetal Kidney	kidney
8	chr7:5862200-5863400	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr7:5862200-5863600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:5862200-5863600	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr7:5862200-5863600	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr7:5862200-5863600	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr7:5862200-5863600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:5862200-5863600	Active TSS	Colon Smooth Muscle	Colon
15	chr7:5862200-5863800	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr7:5862200-5863800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:5862200-5863800	Flanking Active TSS	Adipose Nuclei	Adipose
18	chr7:5862200-5863800	Active TSS	Rectal Smooth Muscle	rectum
19	chr7:5862200-5864200	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr7:5862200-5864200	Active TSS	Brain Angular Gyrus	brain
21	chr7:5862200-5864400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
22	chr7:5862400-5863400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr7:5862400-5863400	Active TSS	H9 Cell Line	embryonic stem cell
24	chr7:5862400-5863400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:5862400-5863400	Active TSS	Fetal Intestine Large	intestine
26	chr7:5862400-5863600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:5862400-5863600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr7:5862400-5863800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:5862400-5863800	Active TSS	A549	lung
30	chr7:5862600-5863400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:5862600-5863400	Active TSS	Muscle Satellite Cultured Cells	--
32	chr7:5862600-5863400	Active TSS	Gastric	stomach
33	chr7:5862600-5863400	Active TSS	HUVEC	blood vessel
34	chr7:5862600-5863600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
35	chr7:5862600-5863600	Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr7:5862600-5863600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:5862600-5863600	Active TSS	Stomach Mucosa	stomach
38	chr7:5862600-5863600	Active TSS	K562	blood
39	chr7:5862600-5864200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:5862800-5863400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:5862800-5863400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
42	chr7:5862800-5863400	Flanking Active TSS	Esophagus	oesophagus
43	chr7:5862800-5863400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
44	chr7:5862800-5863400	Flanking Active TSS	Placenta	Placenta
45	chr7:5862800-5863400	Flanking Active TSS	Right Ventricle	heart
46	chr7:5862800-5863400	Bivalent/Poised TSS	HepG2	liver
47	chr7:5862800-5863400	Flanking Active TSS	HMEC	breast
48	chr7:5862800-5863600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
49	chr7:5862800-5863600	Flanking Active TSS	Colonic Mucosa	Colon
50	chr7:5863000-5863400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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