Variant report

Variant	nsv435843
Chromosome Location	chr7:38386410-38397587
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	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
3	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
4	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
5	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
6	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
7	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
9	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
12	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
13	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
14	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
15	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
16	CTCF	chr7:38389540-38389690	NHEK	skin:	n/a	n/a
17	CTCF	chr7:38393916-38394198	Medullo	brain:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
18	CTCF	chr7:38389600-38389750	HCM	heart:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
19	CTCF	chr7:38389572-38389865	GM10248	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
20	CTCF	chr7:38393880-38394150	RPTEC	kidney:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
21	CTCF	chr7:38389524-38389868	GM12878	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
22	CTCF	chr7:38393919-38394193	GM12891	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
23	CTCF	chr7:38389560-38389710	AG04450	lung:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
24	CTCF	chr7:38389577-38389813	A549	lung:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
25	CTCF	chr7:38389493-38389872	K562	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
26	CTCF	chr7:38389600-38389750	HVMF	connective:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
27	CTCF	chr7:38389530-38389858	MCF-7	breast:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
28	CTCF	chr7:38389560-38389710	GM12865	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
29	CTCF	chr7:38393880-38394030	HCM	heart:	n/a	n/a
30	CTCF	chr7:38393980-38394130	K562	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
31	CTCF	chr7:38393889-38394125	ECC-1	luminal epithelium:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
32	CTCF	chr7:38394000-38394150	HVMF	connective:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
33	CTCF	chr7:38393880-38394030	GM12870	blood:	n/a	n/a
34	CTCF	chr7:38394000-38394150	AG09309	skin:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
35	CTCF	chr7:38389600-38389750	GM12867	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
36	CTCF	chr7:38394000-38394150	AG04450	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
37	CTCF	chr7:38389510-38389870	A549	lung:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
38	CTCF	chr7:38389600-38389750	NB4	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
39	CTCF	chr7:38393880-38394030	GM12872	blood:	n/a	n/a
40	CTCF	chr7:38388823-38388870	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr7:38393940-38394184	H1-hESC	embryonic stem cell:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
42	CTCF	chr7:38393901-38394188	Pancreas_OC	pancreas:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
43	CTCF	chr7:38393936-38394233	MCF-7	breast:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
44	CTCF	chr7:38393980-38394130	GM12864	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
45	CTCF	chr7:38393951-38394179	GM10266	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
46	CTCF	chr7:38393980-38394130	AoAF	blood vessel:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
47	CTCF	chr7:38394000-38394150	HUVEC	blood vessel:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
48	CTCF	chr7:38393955-38394137	ECC-1	luminal epithelium:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
49	CTCF	chr7:38393980-38394130	HL-60	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
50	CTCF	chr7:38393980-38394130	Hela-S3	cervix:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38389685-38389735	HIPEpiC	eye:	n/a
2	chr7:38389659-38389709	NHBE	bronchial:	n/a
3	chr7:38389991-38390041	H1-hESC	embryonic stem cell:	embryo
4	chr7:38389685-38389735	RPTEC	kidney:	n/a
5	chr7:38389659-38389709	Hepatocyte	liver:	n/a
6	chr7:38389685-38389735	GM06990	blood:	n/a
7	chr7:38389991-38390041	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:38389991-38390041	HEK293	kidney:	embryo
9	chr7:38389659-38389709	HNPCEpiC	eye:	n/a
10	chr7:38389685-38389735	AG09309	skin:	n/a
11	chr7:38389659-38389709	HCM	heart:	n/a
12	chr7:38389991-38390041	HCF	heart:	n/a
13	chr7:38389991-38390041	HL-60	blood:	n/a
14	chr7:38389659-38389709	HRCEpiC	kidney:	n/a
15	chr7:38389685-38389735	K562	blood:	n/a
16	chr7:38389991-38390041	HAEpiC	amniotic membrane:	n/a
17	chr7:38389685-38389735	LNCaP	prostate:	n/a
18	chr7:38389685-38389735	HUVEC	blood vessel:	n/a
19	chr7:38389659-38389709	PANC-1	pancreas:	n/a
20	chr7:38389659-38389709	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:38389991-38390041	NT2-D1	testis:	n/a
22	chr7:38389685-38389735	HepG2	liver:	n/a
23	chr7:38389685-38389735	HEEpiC	esophagus:	n/a
24	chr7:38389685-38389735	AG04449	skin:	fetal
25	chr7:38389991-38390041	NHDF-neo	bronchial:	n/a
26	chr7:38389991-38390041	K562	blood:	n/a
27	chr7:38389659-38389709	GM12878	blood:	n/a
28	chr7:38389659-38389709	Caco-2	colon:	n/a
29	chr7:38389659-38389709	CMK	blood:	n/a
30	chr7:38389659-38389709	SAEC	small airway:	n/a
31	chr7:38389685-38389735	PrEC	prostate:	n/a
32	chr7:38389991-38390041	GM19239	blood:	n/a
33	chr7:38389659-38389709	MCF10A-Er-Src	breast:	n/a
34	chr7:38389685-38389735	SK-N-SH	brain:	n/a
35	chr7:38389659-38389709	U87	brain:	n/a
36	chr7:38389659-38389709	HepG2	liver:	n/a
37	chr7:38389991-38390041	Hela-S3	cervix:	n/a
38	chr7:38389659-38389709	BJ	skin:	n/a
39	chr7:38389659-38389709	ProgFib	skin:	n/a
40	chr7:38389685-38389735	HNPCEpiC	eye:	n/a
41	chr7:38389991-38390041	GM12892	blood:	n/a
42	chr7:38389685-38389735	HCF	heart:	n/a
43	chr7:38389685-38389735	AG09319	gingival:	n/a
44	chr7:38389685-38389735	IMR90	lung:	fetal
45	chr7:38389685-38389735	GM12878	blood:	n/a
46	chr7:38389991-38390041	A549	lung:	n/a
47	chr7:38389685-38389735	MCF10A-Er-Src	breast:	n/a
48	chr7:38389659-38389709	AG04450	lung:	fetal
49	chr7:38389991-38390041	AG09319	gingival:	n/a
50	chr7:38389659-38389709	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
2	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
3	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
4	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:

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

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

Extended variants
information (count: 753 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:753 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552971285	chr7:38386440-38386441	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs572757404	chr7:38386441-38386442	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs146951385	chr7:38386468-38386469	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
4	rs545239987	chr7:38386490-38386491	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs58323782	chr7:38386501-38386502	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530711370	chr7:38386522-38386523	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs544450439	chr7:38386526-38386527	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs563768589	chr7:38386541-38386542	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs62445005	chr7:38386558-38386559	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs549220568	chr7:38386566-38386567	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs566019397	chr7:38386618-38386619	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs371626978	chr7:38386642-38386643	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs2736948	chr7:38386657-38386658	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs374033020	chr7:38386679-38386680	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs2735138	chr7:38386698-38386699	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs550806354	chr7:38386733-38386734	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs7787253	chr7:38386737-38386738	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs536302242	chr7:38386760-38386761	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs369081518	chr7:38386764-38386765	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs569997368	chr7:38386767-38386768	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs552794620	chr7:38386768-38386769	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs77300967	chr7:38386783-38386784	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs2736947	chr7:38386791-38386792	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs138624025	chr7:38386799-38386800	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs151210213	chr7:38386812-38386813	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs398111257	chr7:38386813-38386814	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs370631799	chr7:38386849-38386850	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs373207141	chr7:38386855-38386856	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs575659443	chr7:38386899-38386900	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs544410761	chr7:38386945-38386946	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs187447703	chr7:38386958-38386959	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs553697328	chr7:38386959-38386960	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs539046186	chr7:38386968-38386969	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs543081459	chr7:38386981-38386982	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs377384421	chr7:38386986-38386987	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs116789972	chr7:38387000-38387001	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs75757243	chr7:38387004-38387005	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
38	rs149328738	chr7:38387008-38387009	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs112800002	chr7:38387012-38387013	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs531145815	chr7:38387032-38387033	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs550869625	chr7:38387041-38387042	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs112986070	chr7:38387064-38387065	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs191486600	chr7:38387069-38387070	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs536466544	chr7:38387073-38387074	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs184801030	chr7:38387075-38387076	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs60306481	chr7:38387076-38387077	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs189998227	chr7:38387079-38387080	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs557287347	chr7:38387101-38387102	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs558626328	chr7:38387103-38387104	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs77127435	chr7:38387110-38387111	Weak transcription Enhancers Active TSS	n/a	n/a	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:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
3	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
4	chr7:38381800-38388800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
6	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:38384800-38390800	Active TSS	Thymus	Thymus
8	chr7:38385000-38388800	Weak transcription	Spleen	Spleen
9	chr7:38385600-38389000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr7:38385800-38386800	Weak transcription	Primary B cells from cord blood	blood
11	chr7:38385800-38386800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr7:38385800-38387000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:38385800-38387400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr7:38385800-38388800	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr7:38385800-38389000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr7:38385800-38389000	Weak transcription	GM12878-XiMat	blood
17	chr7:38385800-38389200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr7:38385800-38389200	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr7:38386000-38388600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr7:38386000-38388600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr7:38386000-38388800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:38386000-38389000	Weak transcription	Primary T cells from cord blood	blood
23	chr7:38386000-38389000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr7:38386000-38389000	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr7:38386000-38389200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr7:38386000-38389200	Weak transcription	K562	blood
27	chr7:38386200-38386600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr7:38386200-38386600	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr7:38386200-38388200	Enhancers	Dnd41	blood
30	chr7:38386200-38388600	Weak transcription	Fetal Thymus	thymus
31	chr7:38386400-38387400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr7:38386400-38387400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr7:38386600-38386800	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr7:38386600-38387400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr7:38386800-38387800	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr7:38386800-38388400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr7:38386800-38390600	Enhancers	Primary B cells from cord blood	blood
38	chr7:38387000-38387600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:38387400-38387800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr7:38387400-38388000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:38387400-38388200	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr7:38387400-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr7:38387600-38388000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr7:38387800-38388200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr7:38387800-38388800	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr7:38388000-38388200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:38388000-38388400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:38388200-38388600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr7:38388200-38388800	Weak transcription	Dnd41	blood
50	chr7:38388200-38389000	Weak transcription	Primary T helper cells PMA-I stimulated	--

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