Variant report

Variant	esv3478171
Chromosome Location	chr7:38385100-38398748
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	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
2	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
3	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
4	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
5	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
6	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
7	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
8	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
9	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
10	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
11	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
13	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
15	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
16	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
19	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
21	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
22	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
23	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
24	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
25	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
26	CHD2	chr7:38385235-38385424	GM12878	blood:	n/a	n/a
27	CTCF	chr7:38393886-38394185	H1-hESC	embryonic stem cell:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
28	CTCF	chr7:38385260-38385410	GM06990	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
29	CTCF	chr7:38394000-38394150	AG09319	gingival:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
30	CTCF	chr7:38385238-38385525	LNCaP	prostate:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
31	CTCF	chr7:38385400-38385550	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr7:38385360-38385510	GM12870	blood:	n/a	n/a
33	CTCF	chr7:38385220-38385533	GM12891	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
34	CTCF	chr7:38398700-38398850	HCM	heart:	n/a	n/a
35	CTCF	chr7:38385231-38385503	NHEK	skin:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
36	CTCF	chr7:38393960-38394110	HEK293	kidney:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
37	CTCF	chr7:38389560-38389710	AG09309	skin:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
38	CTCF	chr7:38385680-38385830	AG10803	skin:	n/a	n/a
39	CTCF	chr7:38398680-38398830	NHEK	skin:	n/a	n/a
40	CTCF	chr7:38385400-38385550	HFF	foreskin:	n/a	n/a
41	CTCF	chr7:38389637-38389839	IMR90	lung:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
42	CTCF	chr7:38394000-38394150	SAEC	small airway:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
43	CTCF	chr7:38393960-38394110	GM12872	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
44	CTCF	chr7:38389600-38389750	NB4	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
45	CTCF	chr7:38389521-38389898	Gliobla	brain:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
46	CTCF	chr7:38389570-38389844	ProgFib	skin:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
47	CTCF	chr7:38398660-38398810	GM12870	blood:	n/a	n/a
48	CTCF	chr7:38394000-38394150	HBMEC	blood vessel:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
49	CTCF	chr7:38393880-38394030	HCM	heart:	n/a	n/a
50	CTCF	chr7:38389560-38389710	WERI-Rb-1	eye:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38389991-38390041	MCF10A-Er-Src	breast:	n/a
2	chr7:38389991-38390041	MCF10A-Er-Src	breast:	n/a
3	chr7:38389685-38389735	GM19239	blood:	n/a
4	chr7:38389991-38390041	HRPEpiC	eye:	n/a
5	chr7:38389685-38389735	HEEpiC	esophagus:	n/a
6	chr7:38389685-38389735	GM12878	blood:	n/a
7	chr7:38389659-38389709	Hela-S3	cervix:	n/a
8	chr7:38389659-38389709	ovcar-3	ovarian:	n/a
9	chr7:38389685-38389735	ProgFib	skin:	n/a
10	chr7:38389659-38389709	AG09309	skin:	n/a
11	chr7:38389991-38390041	NHBE	bronchial:	n/a
12	chr7:38389991-38390041	NHDF-neo	bronchial:	n/a
13	chr7:38389991-38390041	HUVEC	blood vessel:	n/a
14	chr7:38389991-38390041	Hela-S3	cervix:	n/a
15	chr7:38389685-38389735	HL-60	blood:	n/a
16	chr7:38389685-38389735	Hepatocyte	liver:	n/a
17	chr7:38389685-38389735	HNPCEpiC	eye:	n/a
18	chr7:38389685-38389735	NHDF-neo	bronchial:	n/a
19	chr7:38389685-38389735	NH-A	brain:	n/a
20	chr7:38389685-38389735	MCF10A-Er-Src	breast:	n/a
21	chr7:38389659-38389709	AG04449	skin:	fetal
22	chr7:38389991-38390041	SK-N-SH	brain:	n/a
23	chr7:38389659-38389709	HCM	heart:	n/a
24	chr7:38389685-38389735	HIPEpiC	eye:	n/a
25	chr7:38389659-38389709	HRE	kidney:	n/a
26	chr7:38389991-38390041	K562	blood:	n/a
27	chr7:38389685-38389735	HMEC	breast:	n/a
28	chr7:38389991-38390041	HRCEpiC	kidney:	n/a
29	chr7:38389991-38390041	HEK293	kidney:	embryo
30	chr7:38389991-38390041	A549	lung:	n/a
31	chr7:38389685-38389735	K562	blood:	n/a
32	chr7:38389659-38389709	HNPCEpiC	eye:	n/a
33	chr7:38389991-38390041	NT2-D1	testis:	n/a
34	chr7:38389659-38389709	Jurkat	blood:	n/a
35	chr7:38389685-38389735	AoSMC	blood vessel:	n/a
36	chr7:38389685-38389735	IMR90	lung:	fetal
37	chr7:38389659-38389709	GM19239	blood:	n/a
38	chr7:38389685-38389735	ovcar-3	ovarian:	n/a
39	chr7:38389659-38389709	AoSMC	blood vessel:	n/a
40	chr7:38389685-38389735	HCF	heart:	n/a
41	chr7:38389991-38390041	GM12892	blood:	n/a
42	chr7:38389685-38389735	HCPEpiC	choroid plexus:	n/a
43	chr7:38389991-38390041	HRE	kidney:	n/a
44	chr7:38389991-38390041	CMK	blood:	n/a
45	chr7:38389991-38390041	HCM	heart:	n/a
46	chr7:38389659-38389709	Hepatocyte	liver:	n/a
47	chr7:38389685-38389735	BJ	skin:	n/a
48	chr7:38389659-38389709	HCT-116	colon:	n/a
49	chr7:38389659-38389709	HMEC	breast:	n/a
50	chr7:38389659-38389709	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
2	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
3	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
4	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
5	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
6	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
7	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
2	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
3	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
4	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
5	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
6	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
7	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181

Variant related genes	Relation type
TRGV5	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV5P	TF binding region
TRGV5	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV5P	CpG island
ENSG00000249978	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000226212	chromatin interactions
RAB5A	miRNA target sites
SERTAD3	miRNA target sites

Extended variants
information (count: 965 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556877591	chr7:38385102-38385103	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs13307706	chr7:38385109-38385110	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs13307707	chr7:38385112-38385113	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs13307440	chr7:38385130-38385131	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs576834448	chr7:38385134-38385135	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs13307331	chr7:38385143-38385144	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs190822284	chr7:38385145-38385146	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs13307714	chr7:38385149-38385150	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs540743904	chr7:38385150-38385151	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs111885782	chr7:38385158-38385159	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs13307372	chr7:38385162-38385163	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs13307717	chr7:38385173-38385174	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs532775824	chr7:38385175-38385176	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs549393569	chr7:38385198-38385199	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs200779905	chr7:38385227-38385228	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs529191665	chr7:38385245-38385246	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs548874130	chr7:38385247-38385248	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs62445003	chr7:38385255-38385256	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs62445004	chr7:38385260-38385261	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
20	rs139625300	chr7:38385266-38385267	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs375994707	chr7:38385307-38385308	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs386712321	chr7:38385336-38385337	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs368435694	chr7:38385337-38385338	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs111530608	chr7:38385364-38385365	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs148285231	chr7:38385384-38385385	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs577467672	chr7:38385401-38385402	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs371743546	chr7:38385415-38385416	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs556640306	chr7:38385418-38385419	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs111644200	chr7:38385420-38385421	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs559878706	chr7:38385423-38385424	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs142475202	chr7:38385429-38385430	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs368709830	chr7:38385434-38385435	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs76792064	chr7:38385442-38385443	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs117765166	chr7:38385445-38385446	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs541648061	chr7:38385449-38385450	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs564005302	chr7:38385451-38385452	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs117916024	chr7:38385452-38385453	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs377028456	chr7:38385455-38385456	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs562904826	chr7:38385463-38385464	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs386712323	chr7:38385470-38385471	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs74633917	chr7:38385472-38385473	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs73694031	chr7:38385475-38385476	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs78943824	chr7:38385483-38385484	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs142065651	chr7:38385493-38385494	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs386712324	chr7:38385505-38385506	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs375723414	chr7:38385516-38385517	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs111848856	chr7:38385534-38385535	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs369716119	chr7:38385542-38385543	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs548141122	chr7:38385546-38385547	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs146341763	chr7:38385553-38385554	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	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
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:38381400-38385400	Weak transcription	Adipose Nuclei	Adipose
3	chr7:38381400-38385600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
5	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
6	chr7:38381800-38388800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr7:38382000-38385200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr7:38382000-38385600	Weak transcription	Pancreas	Pancrea
9	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
10	chr7:38382600-38385200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr7:38383600-38385200	Enhancers	Dnd41	blood
12	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:38383800-38386000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:38383800-38386200	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr7:38384000-38385200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:38384000-38386000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:38384200-38385600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
18	chr7:38384200-38385600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr7:38384200-38385800	Enhancers	Primary B cells from cord blood	blood
20	chr7:38384200-38385800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:38384200-38385800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr7:38384200-38385800	Enhancers	GM12878-XiMat	blood
23	chr7:38384200-38386000	Enhancers	Primary B cells from peripheral blood	blood
24	chr7:38384200-38386000	Enhancers	Primary hematopoietic stem cells	blood
25	chr7:38384200-38386000	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr7:38384400-38385200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr7:38384400-38385400	Enhancers	K562	blood
28	chr7:38384600-38385800	Flanking Active TSS	Fetal Thymus	thymus
29	chr7:38384800-38385400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr7:38384800-38385800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:38384800-38385800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr7:38384800-38386200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:38384800-38386400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr7:38384800-38390800	Active TSS	Thymus	Thymus
35	chr7:38385000-38385200	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr7:38385000-38385400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr7:38385000-38385400	Enhancers	Fetal Muscle Leg	muscle
38	chr7:38385000-38385800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:38385000-38388800	Weak transcription	Spleen	Spleen
40	chr7:38385200-38385600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr7:38385200-38385600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr7:38385200-38385800	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr7:38385200-38386000	Enhancers	Primary T cells from cord blood	blood
44	chr7:38385200-38386200	Flanking Active TSS	Dnd41	blood
45	chr7:38385400-38385800	Enhancers	Adipose Nuclei	Adipose
46	chr7:38385400-38386000	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr7:38385400-38386000	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr7:38385400-38386000	Enhancers	Brain Cingulate Gyrus	brain
49	chr7:38385400-38386000	Genic enhancers	K562	blood
50	chr7:38385600-38385800	Enhancers	Primary T cells fromperipheralblood	blood

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