Variant report

Variant	esv3509848
Chromosome Location	chr7:38388049-38399215
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	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
4	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
5	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
6	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
7	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
8	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
9	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
10	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
13	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
17	BHLHE40	chr7:38398804-38399002	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	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
21	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
22	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
23	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a
24	CTCF	chr7:38393910-38394218	MCF-7	breast:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
25	CTCF	chr7:38393880-38394030	GM12872	blood:	n/a	n/a
26	CTCF	chr7:38398599-38398890	H1-hESC	embryonic stem cell:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
27	CTCF	chr7:38398680-38398830	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr7:38389560-38389710	HEK293	kidney:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
29	CTCF	chr7:38389586-38389836	GM13976	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
30	CTCF	chr7:38393959-38394224	Lung_OC	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
31	CTCF	chr7:38389560-38389710	BJ	skin:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
32	CTCF	chr7:38393880-38394150	RPTEC	kidney:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
33	CTCF	chr7:38389560-38389710	AG09319	gingival:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
34	CTCF	chr7:38393931-38394196	GM13977	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
35	CTCF	chr7:38398100-38398250	GM12871	blood:	n/a	n/a
36	CTCF	chr7:38389580-38389730	GM12866	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
37	CTCF	chr7:38394000-38394150	MCF-7	breast:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
38	CTCF	chr7:38394220-38394370	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr7:38394000-38394150	GM12874	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
40	CTCF	chr7:38389520-38389523	GM12878	blood:	n/a	n/a
41	CTCF	chr7:38398680-38398830	RPTEC	kidney:	n/a	n/a
42	CTCF	chr7:38398660-38398810	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr7:38393960-38394110	GM12867	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
44	CTCF	chr7:38394040-38394190	NHDF-neo	bronchial:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
45	CTCF	chr7:38389580-38389730	GM12867	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
46	CTCF	chr7:38399080-38399230	GM12872	blood:	n/a	n/a
47	CTCF	chr7:38398680-38398830	GM12866	blood:	n/a	n/a
48	CTCF	chr7:38393960-38394110	GM12869	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
49	CTCF	chr7:38389940-38390090	GM12872	blood:	n/a	n/a
50	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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38398836-38398886	HNPCEpiC	eye:	n/a
2	chr7:38398836-38398886	HNPCEpiC	eye:	n/a
3	chr7:38389659-38389709	GM06990	blood:	n/a
4	chr7:38389659-38389709	AoSMC	blood vessel:	n/a
5	chr7:38398839-38398889	T-47D	breast:	n/a
6	chr7:38398836-38398886	PANC-1	pancreas:	n/a
7	chr7:38389991-38390041	HEEpiC	esophagus:	n/a
8	chr7:38389991-38390041	GM12892	blood:	n/a
9	chr7:38398836-38398886	NHDF-neo	bronchial:	n/a
10	chr7:38398839-38398889	HCPEpiC	choroid plexus:	n/a
11	chr7:38389685-38389735	GM12878	blood:	n/a
12	chr7:38389991-38390041	GM12878	blood:	n/a
13	chr7:38389991-38390041	NT2-D1	testis:	n/a
14	chr7:38389659-38389709	HRCEpiC	kidney:	n/a
15	chr7:38398839-38398889	HMEC	breast:	n/a
16	chr7:38389685-38389735	RPTEC	kidney:	n/a
17	chr7:38398839-38398889	HEK293	kidney:	embryo
18	chr7:38389685-38389735	ProgFib	skin:	n/a
19	chr7:38398836-38398886	NB4	blood:	n/a
20	chr7:38398836-38398886	HL-60	blood:	n/a
21	chr7:38398836-38398886	NHBE	bronchial:	n/a
22	chr7:38389991-38390041	HRPEpiC	eye:	n/a
23	chr7:38398839-38398889	AoSMC	blood vessel:	n/a
24	chr7:38389991-38390041	HL-60	blood:	n/a
25	chr7:38389659-38389709	Hela-S3	cervix:	n/a
26	chr7:38398839-38398889	NB4	blood:	n/a
27	chr7:38398839-38398889	GM12892	blood:	n/a
28	chr7:38389659-38389709	GM12878	blood:	n/a
29	chr7:38389659-38389709	BJ	skin:	n/a
30	chr7:38398839-38398889	NH-A	brain:	n/a
31	chr7:38398839-38398889	GM19239	blood:	n/a
32	chr7:38389991-38390041	NHDF-neo	bronchial:	n/a
33	chr7:38398839-38398889	Hela-S3	cervix:	n/a
34	chr7:38389685-38389735	ovcar-3	ovarian:	n/a
35	chr7:38389685-38389735	AG09309	skin:	n/a
36	chr7:38389991-38390041	HCF	heart:	n/a
37	chr7:38398836-38398886	HRPEpiC	eye:	n/a
38	chr7:38389659-38389709	HEEpiC	esophagus:	n/a
39	chr7:38389685-38389735	SAEC	small airway:	n/a
40	chr7:38389659-38389709	HUVEC	blood vessel:	n/a
41	chr7:38398836-38398886	AG09309	skin:	n/a
42	chr7:38389659-38389709	Jurkat	blood:	n/a
43	chr7:38398836-38398886	ovcar-3	ovarian:	n/a
44	chr7:38389685-38389735	GM12892	blood:	n/a
45	chr7:38398839-38398889	AG04449	skin:	fetal
46	chr7:38389685-38389735	HCF	heart:	n/a
47	chr7:38389685-38389735	BE2_C	brain:	n/a
48	chr7:38398836-38398886	Hepatocyte	liver:	n/a
49	chr7:38389659-38389709	A549	lung:	n/a
50	chr7:38389991-38390041	SK-N-SH	brain:	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	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
4	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:

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

Variant related genes	Relation type
TRGV5	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV5P	TF binding region
TRGV5	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV5P	CpG island
ENSG00000228668	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000226212	chromatin interactions
RAB5A	miRNA target sites

Extended variants
information (count: 797 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:797 , 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	rs13309318	chr7:38388066-38388067	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs11761741	chr7:38388094-38388095	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs560857399	chr7:38388109-38388110	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532739320	chr7:38388112-38388113	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs13309373	chr7:38388115-38388116	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs13309677	chr7:38388134-38388135	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs13309324	chr7:38388137-38388138	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs117896430	chr7:38388147-38388148	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs11768479	chr7:38388163-38388164	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs562565054	chr7:38388175-38388176	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs531472170	chr7:38388183-38388184	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs548272870	chr7:38388190-38388191	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs368707840	chr7:38388196-38388197	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs372315581	chr7:38388225-38388226	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs553521500	chr7:38388235-38388236	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs564841944	chr7:38388263-38388264	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs35579179	chr7:38388276-38388277	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs28634947	chr7:38388277-38388278	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs71558119	chr7:38388305-38388306	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs574961995	chr7:38388321-38388322	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs374711769	chr7:38388374-38388375	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs542431054	chr7:38388386-38388387	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs368101473	chr7:38388392-38388393	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs2534592	chr7:38388396-38388397	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs547338838	chr7:38388402-38388403	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs570756025	chr7:38388431-38388432	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs539247081	chr7:38388432-38388433	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs549606095	chr7:38388442-38388443	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs2735134	chr7:38388478-38388479	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs199627720	chr7:38388489-38388490	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs569524770	chr7:38388495-38388496	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs537905498	chr7:38388510-38388511	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs555070540	chr7:38388540-38388541	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs375380542	chr7:38388545-38388546	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs200626762	chr7:38388552-38388553	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs186317097	chr7:38388561-38388562	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs369277839	chr7:38388598-38388599	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs371389885	chr7:38388661-38388662	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs554146719	chr7:38388704-38388705	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs62445007	chr7:38388710-38388711	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376140545	chr7:38388719-38388720	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs191612253	chr7:38388735-38388736	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs182511589	chr7:38388761-38388762	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs576713149	chr7:38388763-38388764	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs13227721	chr7:38388773-38388774	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs13227725	chr7:38388777-38388778	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
47	rs564190001	chr7:38388849-38388850	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs62445008	chr7:38388851-38388852	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs546816239	chr7:38388859-38388860	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs1810378	chr7:38388889-38388890	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:341 , 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	chr7:38385800-38388800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr7:38385800-38389000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr7:38385800-38389000	Weak transcription	GM12878-XiMat	blood
13	chr7:38385800-38389200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr7:38385800-38389200	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr7:38386000-38388600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr7:38386000-38388600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr7:38386000-38388800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:38386000-38389000	Weak transcription	Primary T cells from cord blood	blood
19	chr7:38386000-38389000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr7:38386000-38389000	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr7:38386000-38389200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr7:38386000-38389200	Weak transcription	K562	blood
23	chr7:38386200-38388200	Enhancers	Dnd41	blood
24	chr7:38386200-38388600	Weak transcription	Fetal Thymus	thymus
25	chr7:38386800-38388400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr7:38386800-38390600	Enhancers	Primary B cells from cord blood	blood
27	chr7:38387400-38388200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr7:38387400-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr7:38387800-38388200	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr7:38387800-38388800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr7:38388000-38388200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr7:38388000-38388400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr7:38388200-38388600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr7:38388200-38388800	Weak transcription	Dnd41	blood
35	chr7:38388200-38389000	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr7:38388200-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:38388400-38388800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr7:38388400-38389200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:38388600-38389000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr7:38388600-38389200	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr7:38388600-38390200	Flanking Active TSS	Fetal Thymus	thymus
42	chr7:38388600-38390400	Active TSS	Primary T killer memory cells from peripheral blood	blood
43	chr7:38388600-38391000	Enhancers	Primary B cells from peripheral blood	blood
44	chr7:38388800-38389000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr7:38388800-38389200	Active TSS	Dnd41	blood
46	chr7:38388800-38389600	Enhancers	Spleen	Spleen
47	chr7:38388800-38390000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
48	chr7:38388800-38390600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
49	chr7:38388800-38390600	Active TSS	Duodenum Mucosa	Duodenum
50	chr7:38388800-38391800	Active TSS	Primary T cells fromperipheralblood	blood

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