Variant report

Variant	esv3509849
Chromosome Location	chr7:38387277-38398525
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	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
3	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
4	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
5	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
6	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
7	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
8	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
9	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
10	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:38398493-38398682	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	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
17	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
18	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
19	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
20	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
21	CTCF	chr7:38393920-38394191	MCF-7	breast:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
22	CTCF	chr7:38389580-38389730	GM12864	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
23	CTCF	chr7:38389570-38389815	GM20000	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
24	CTCF	chr7:38389515-38389845	Spleen_OC	spleen:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
25	CTCF	chr7:38389510-38389870	A549	lung:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
26	CTCF	chr7:38394000-38394150	MCF-7	breast:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
27	CTCF	chr7:38394200-38394350	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr7:38389560-38389710	HCFaa	heart:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
29	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
30	CTCF	chr7:38389600-38389750	GM12866	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
31	CTCF	chr7:38389600-38389750	HCM	heart:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
32	CTCF	chr7:38389600-38389750	AG04450	lung:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
33	CTCF	chr7:38393911-38394223	GM12878	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
34	CTCF	chr7:38394220-38394370	HVMF	connective:	n/a	n/a
35	CTCF	chr7:38394000-38394150	GM12866	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
36	CTCF	chr7:38389600-38389750	NHDF-neo	bronchial:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
37	CTCF	chr7:38394000-38394150	NB4	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
38	CTCF	chr7:38394000-38394150	WI-38	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
39	CTCF	chr7:38389560-38389710	HepG2	liver:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
40	CTCF	chr7:38393880-38394030	HCT-116	colon:	n/a	n/a
41	CTCF	chr7:38393980-38394130	Hela-S3	cervix:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
42	CTCF	chr7:38393940-38394090	GM12871	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
43	CTCF	chr7:38393980-38394130	SAEC	small airway:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
44	CTCF	chr7:38393960-38394110	HEK293	kidney:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
45	CTCF	chr7:38389600-38389750	GM12870	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
46	CTCF	chr7:38389569-38389862	GM13977	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
47	CTCF	chr7:38393880-38394030	GM06990	blood:	n/a	n/a
48	CTCF	chr7:38389431-38390041	K562	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
49	CTCF	chr7:38393980-38394130	HEK293	kidney:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
50	CTCF	chr7:38389600-38389750	MCF-7	breast:	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	IMR90	lung:	fetal
2	chr7:38389685-38389735	HCPEpiC	choroid plexus:	n/a
3	chr7:38389659-38389709	PFSK-1	brain:	n/a
4	chr7:38389991-38390041	HL-60	blood:	n/a
5	chr7:38389685-38389735	BJ	skin:	n/a
6	chr7:38389991-38390041	GM12892	blood:	n/a
7	chr7:38389991-38390041	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:38389991-38390041	NHBE	bronchial:	n/a
9	chr7:38389991-38390041	SK-N-SH	brain:	n/a
10	chr7:38389685-38389735	A549	lung:	n/a
11	chr7:38389659-38389709	HAEpiC	amniotic membrane:	n/a
12	chr7:38389991-38390041	NT2-D1	testis:	n/a
13	chr7:38389685-38389735	ovcar-3	ovarian:	n/a
14	chr7:38389659-38389709	H1-hESC	embryonic stem cell:	embryo
15	chr7:38389685-38389735	RPTEC	kidney:	n/a
16	chr7:38389659-38389709	GM12891	blood:	n/a
17	chr7:38389991-38390041	GM12891	blood:	n/a
18	chr7:38389685-38389735	AG09319	gingival:	n/a
19	chr7:38389991-38390041	AG10803	skin:	n/a
20	chr7:38389685-38389735	HCM	heart:	n/a
21	chr7:38389991-38390041	RPTEC	kidney:	n/a
22	chr7:38389685-38389735	U87	brain:	n/a
23	chr7:38389659-38389709	Jurkat	blood:	n/a
24	chr7:38389659-38389709	HCF	heart:	n/a
25	chr7:38389659-38389709	NHBE	bronchial:	n/a
26	chr7:38389991-38390041	AG09319	gingival:	n/a
27	chr7:38389991-38390041	K562	blood:	n/a
28	chr7:38389659-38389709	HNPCEpiC	eye:	n/a
29	chr7:38389659-38389709	AG10803	skin:	n/a
30	chr7:38389685-38389735	HEEpiC	esophagus:	n/a
31	chr7:38389659-38389709	AG09319	gingival:	n/a
32	chr7:38389991-38390041	BE2_C	brain:	n/a
33	chr7:38389991-38390041	Hela-S3	cervix:	n/a
34	chr7:38389659-38389709	Hepatocyte	liver:	n/a
35	chr7:38389659-38389709	K562	blood:	n/a
36	chr7:38389991-38390041	SK-N-SH_RA	brain:	n/a
37	chr7:38389685-38389735	MCF10A-Er-Src	breast:	n/a
38	chr7:38389991-38390041	NB4	blood:	n/a
39	chr7:38389991-38390041	PFSK-1	brain:	n/a
40	chr7:38389685-38389735	BE2_C	brain:	n/a
41	chr7:38389659-38389709	PrEC	prostate:	n/a
42	chr7:38389685-38389735	SK-N-MC	brain:	n/a
43	chr7:38389659-38389709	U87	brain:	n/a
44	chr7:38389685-38389735	SAEC	small airway:	n/a
45	chr7:38389991-38390041	LNCaP	prostate:	n/a
46	chr7:38389659-38389709	HRE	kidney:	n/a
47	chr7:38389685-38389735	AG10803	skin:	n/a
48	chr7:38389685-38389735	NH-A	brain:	n/a
49	chr7:38389659-38389709	IMR90	lung:	fetal
50	chr7:38389659-38389709	SKMC	muscle:	n/a

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

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

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
ENSG00000226212	chromatin interactions
ENSG00000249978	chromatin interactions
RAB5A	miRNA target sites

Extended variants
information (count: 794 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:794 , 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	rs372001312	chr7:38387290-38387291	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs573302792	chr7:38387299-38387300	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	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
4	rs564892660	chr7:38387360-38387361	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs13310780	chr7:38387377-38387378	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs2534589	chr7:38387391-38387392	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs575074188	chr7:38387404-38387405	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs192294285	chr7:38387456-38387457	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184580507	chr7:38387482-38387483	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546927002	chr7:38387483-38387484	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553835643	chr7:38387504-38387505	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148545430	chr7:38387509-38387510	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141814580	chr7:38387511-38387512	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189417133	chr7:38387520-38387521	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs56242205	chr7:38387548-38387549	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
16	rs375438635	chr7:38387565-38387566	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181976615	chr7:38387571-38387572	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537857646	chr7:38387574-38387575	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554886830	chr7:38387583-38387584	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs386712325	chr7:38387610-38387611	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189089003	chr7:38387611-38387612	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542104428	chr7:38387621-38387622	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs555789039	chr7:38387629-38387630	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372567652	chr7:38387631-38387632	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553724286	chr7:38387638-38387639	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576975000	chr7:38387643-38387644	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545050937	chr7:38387644-38387645	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558646926	chr7:38387653-38387654	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530786655	chr7:38387692-38387693	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575613403	chr7:38387695-38387696	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374685362	chr7:38387701-38387702	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544229267	chr7:38387713-38387714	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2534590	chr7:38387731-38387732	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs530370720	chr7:38387739-38387740	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373442378	chr7:38387754-38387755	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181121352	chr7:38387762-38387763	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2736946	chr7:38387763-38387764	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs144946632	chr7:38387769-38387770	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369928078	chr7:38387775-38387776	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552268852	chr7:38387787-38387788	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569006112	chr7:38387803-38387804	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531310546	chr7:38387823-38387824	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs57798381	chr7:38387824-38387825	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568335047	chr7:38387858-38387859	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs140067125	chr7:38387859-38387860	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554035372	chr7:38387908-38387909	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs377732398	chr7:38387911-38387912	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539263279	chr7:38387912-38387913	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558606353	chr7:38387934-38387935	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs77084610	chr7:38387941-38387942	Weak transcription Enhancers 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:322 , 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	chr7:38385800-38387400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr7:38385800-38388800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr7:38385800-38389000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr7:38385800-38389000	Weak transcription	GM12878-XiMat	blood
14	chr7:38385800-38389200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr7:38385800-38389200	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr7:38386000-38388600	Weak transcription	Primary B cells from peripheral blood	blood
17	chr7:38386000-38388600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr7:38386000-38388800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr7:38386000-38389000	Weak transcription	Primary T cells from cord blood	blood
20	chr7:38386000-38389000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr7:38386000-38389000	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr7:38386000-38389200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr7:38386000-38389200	Weak transcription	K562	blood
24	chr7:38386200-38388200	Enhancers	Dnd41	blood
25	chr7:38386200-38388600	Weak transcription	Fetal Thymus	thymus
26	chr7:38386400-38387400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr7:38386400-38387400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr7:38386600-38387400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr7:38386800-38387800	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr7:38386800-38388400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr7:38386800-38390600	Enhancers	Primary B cells from cord blood	blood
32	chr7:38387000-38387600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:38387400-38387800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr7:38387400-38388000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr7:38387400-38388200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr7:38387400-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr7:38387600-38388000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr7:38387800-38388200	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr7:38387800-38388800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr7:38388000-38388200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr7:38388000-38388400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr7:38388200-38388600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr7:38388200-38388800	Weak transcription	Dnd41	blood
44	chr7:38388200-38389000	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr7:38388200-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr7:38388400-38388800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr7:38388400-38389200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:38388600-38389000	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr7:38388600-38389200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr7:38388600-38390200	Flanking Active TSS	Fetal Thymus	thymus

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