Variant report

Variant	esv3509850
Chromosome Location	chr7:38386827-38398625
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	chr7:38393104-38393312	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	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
6	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
7	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
8	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
9	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
10	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
12	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
16	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
17	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
18	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
19	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
20	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
21	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
22	CTCF	chr7:38394020-38394170	BE2_C	brain:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
23	CTCF	chr7:38393939-38394212	LNCaP	prostate:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
24	CTCF	chr7:38394000-38394150	GM12874	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
25	CTCF	chr7:38389586-38389815	NHEK	skin:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
26	CTCF	chr7:38394000-38394150	HPAF	blood vessel:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
27	CTCF	chr7:38394000-38394150	GM12873	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
28	CTCF	chr7:38393948-38394212	LNCaP	prostate:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
29	CTCF	chr7:38393940-38394090	WERI-Rb-1	eye:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
30	CTCF	chr7:38393980-38394130	HUVEC	blood vessel:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
31	CTCF	chr7:38393736-38393795	GM13977	blood:	n/a	n/a
32	CTCF	chr7:38389560-38389710	BJ	skin:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
33	CTCF	chr7:38393980-38394130	HRPEpiC	eye:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
34	CTCF	chr7:38394000-38394150	BE2_C	brain:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
35	CTCF	chr7:38393788-38394244	K562	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
36	CTCF	chr7:38393980-38394130	GM12867	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
37	CTCF	chr7:38393855-38394198	GM13976	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
38	CTCF	chr7:38393980-38394130	AG04449	skin:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
39	CTCF	chr7:38398508-38399205	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
40	CTCF	chr7:38389515-38389845	Spleen_OC	spleen:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
41	CTCF	chr7:38389300-38389450	HMF	breast:	n/a	n/a
42	CTCF	chr7:38389600-38389750	GM12870	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
43	CTCF	chr7:38389568-38389830	H1-hESC	embryonic stem cell:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
44	CTCF	chr7:38393889-38394208	GM19238	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
45	CTCF	chr7:38389614-38389793	LNCaP	prostate:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
46	CTCF	chr7:38389594-38389779	MCF-7	breast:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
47	CTCF	chr7:38389556-38389825	GM10266	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
48	CTCF	chr7:38393880-38394030	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr7:38389940-38390090	GM12872	blood:	n/a	n/a
50	CTCF	chr7:38389600-38389750	GM12872	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38389685-38389735	HepG2	liver:	n/a
2	chr7:38389659-38389709	AG10803	skin:	n/a
3	chr7:38389991-38390041	RPTEC	kidney:	n/a
4	chr7:38389685-38389735	Hela-S3	cervix:	n/a
5	chr7:38389659-38389709	AG04450	lung:	fetal
6	chr7:38389991-38390041	SAEC	small airway:	n/a
7	chr7:38389685-38389735	K562	blood:	n/a
8	chr7:38389685-38389735	H1-hESC	embryonic stem cell:	embryo
9	chr7:38389659-38389709	HMEC	breast:	n/a
10	chr7:38389685-38389735	RPTEC	kidney:	n/a
11	chr7:38389659-38389709	K562	blood:	n/a
12	chr7:38389685-38389735	SK-N-SH_RA	brain:	n/a
13	chr7:38389991-38390041	SK-N-SH	brain:	n/a
14	chr7:38389991-38390041	NT2-D1	testis:	n/a
15	chr7:38389991-38390041	PANC-1	pancreas:	n/a
16	chr7:38389659-38389709	GM12891	blood:	n/a
17	chr7:38389659-38389709	PANC-1	pancreas:	n/a
18	chr7:38389991-38390041	HNPCEpiC	eye:	n/a
19	chr7:38389685-38389735	AG10803	skin:	n/a
20	chr7:38389991-38390041	NHDF-neo	bronchial:	n/a
21	chr7:38389659-38389709	IMR90	lung:	fetal
22	chr7:38389685-38389735	HIPEpiC	eye:	n/a
23	chr7:38389659-38389709	HRE	kidney:	n/a
24	chr7:38389991-38390041	NHBE	bronchial:	n/a
25	chr7:38389685-38389735	GM19239	blood:	n/a
26	chr7:38389685-38389735	SK-N-SH	brain:	n/a
27	chr7:38389991-38390041	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:38389991-38390041	LNCaP	prostate:	n/a
29	chr7:38389659-38389709	SAEC	small airway:	n/a
30	chr7:38389685-38389735	T-47D	breast:	n/a
31	chr7:38389659-38389709	HCM	heart:	n/a
32	chr7:38389685-38389735	GM12878	blood:	n/a
33	chr7:38389659-38389709	AG09309	skin:	n/a
34	chr7:38389685-38389735	HEEpiC	esophagus:	n/a
35	chr7:38389991-38390041	ProgFib	skin:	n/a
36	chr7:38389659-38389709	Hepatocyte	liver:	n/a
37	chr7:38389659-38389709	MCF10A-Er-Src	breast:	n/a
38	chr7:38389685-38389735	MCF10A-Er-Src	breast:	n/a
39	chr7:38389659-38389709	GM12892	blood:	n/a
40	chr7:38389659-38389709	HEK293	kidney:	embryo
41	chr7:38389685-38389735	HNPCEpiC	eye:	n/a
42	chr7:38389685-38389735	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:38389991-38390041	Caco-2	colon:	n/a
44	chr7:38389991-38390041	HRCEpiC	kidney:	n/a
45	chr7:38389659-38389709	NH-A	brain:	n/a
46	chr7:38389659-38389709	NHDF-neo	bronchial:	n/a
47	chr7:38389991-38390041	U87	brain:	n/a
48	chr7:38389991-38390041	HEEpiC	esophagus:	n/a
49	chr7:38389685-38389735	SK-N-MC	brain:	n/a
50	chr7:38389991-38390041	HAEpiC	amniotic membrane:	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	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
4	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:

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

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
ENSG00000228668	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000226212	chromatin interactions
RAB5A	miRNA target sites

Extended variants
information (count: 837 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:837 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370631799	chr7:38386849-38386850	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs373207141	chr7:38386855-38386856	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs575659443	chr7:38386899-38386900	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs544410761	chr7:38386945-38386946	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs187447703	chr7:38386958-38386959	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs553697328	chr7:38386959-38386960	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs539046186	chr7:38386968-38386969	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs543081459	chr7:38386981-38386982	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs377384421	chr7:38386986-38386987	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116789972	chr7:38387000-38387001	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs75757243	chr7:38387004-38387005	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs149328738	chr7:38387008-38387009	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs112800002	chr7:38387012-38387013	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs531145815	chr7:38387032-38387033	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs550869625	chr7:38387041-38387042	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs112986070	chr7:38387064-38387065	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs191486600	chr7:38387069-38387070	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs536466544	chr7:38387073-38387074	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs184801030	chr7:38387075-38387076	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs60306481	chr7:38387076-38387077	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs189998227	chr7:38387079-38387080	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs557287347	chr7:38387101-38387102	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs558626328	chr7:38387103-38387104	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs77127435	chr7:38387110-38387111	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs75304934	chr7:38387154-38387155	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs116085085	chr7:38387176-38387177	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs574538832	chr7:38387238-38387239	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs540087591	chr7:38387263-38387264	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs559775478	chr7:38387264-38387265	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372001312	chr7:38387290-38387291	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573302792	chr7:38387299-38387300	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs2735137	chr7:38387330-38387331	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564892660	chr7:38387360-38387361	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs13310780	chr7:38387377-38387378	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2534589	chr7:38387391-38387392	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs575074188	chr7:38387404-38387405	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs192294285	chr7:38387456-38387457	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184580507	chr7:38387482-38387483	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546927002	chr7:38387483-38387484	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553835643	chr7:38387504-38387505	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148545430	chr7:38387509-38387510	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141814580	chr7:38387511-38387512	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189417133	chr7:38387520-38387521	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs56242205	chr7:38387548-38387549	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
45	rs375438635	chr7:38387565-38387566	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181976615	chr7:38387571-38387572	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537857646	chr7:38387574-38387575	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554886830	chr7:38387583-38387584	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs386712325	chr7:38387610-38387611	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189089003	chr7:38387611-38387612	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 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:336 , 50 per page) page: 1 2 3 4 5 6 7

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	chr7:38385800-38387000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr7:38385800-38387400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr7:38385800-38388800	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr7:38385800-38389000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr7:38385800-38389000	Weak transcription	GM12878-XiMat	blood
15	chr7:38385800-38389200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr7:38385800-38389200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr7:38386000-38388600	Weak transcription	Primary B cells from peripheral blood	blood
18	chr7:38386000-38388600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr7:38386000-38388800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:38386000-38389000	Weak transcription	Primary T cells from cord blood	blood
21	chr7:38386000-38389000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr7:38386000-38389000	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr7:38386000-38389200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr7:38386000-38389200	Weak transcription	K562	blood
25	chr7:38386200-38388200	Enhancers	Dnd41	blood
26	chr7:38386200-38388600	Weak transcription	Fetal Thymus	thymus
27	chr7:38386400-38387400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr7:38386400-38387400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:38386600-38387400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr7:38386800-38387800	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr7:38386800-38388400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr7:38386800-38390600	Enhancers	Primary B cells from cord blood	blood
33	chr7:38387000-38387600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr7:38387400-38387800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr7:38387400-38388000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr7:38387400-38388200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr7:38387400-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:38387600-38388000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:38387800-38388200	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr7:38387800-38388800	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr7:38388000-38388200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr7:38388000-38388400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr7:38388200-38388600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr7:38388200-38388800	Weak transcription	Dnd41	blood
45	chr7:38388200-38389000	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr7:38388200-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:38388400-38388800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr7:38388400-38389200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr7:38388600-38389000	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr7:38388600-38389200	Weak transcription	H9 Cell Line	embryonic stem cell

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