Variant report

Variant	esv1797814
Chromosome Location	chr7:38389957-38404408
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	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
2	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
3	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
4	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
5	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
6	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
7	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
8	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
10	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
11	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
14	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
16	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
17	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
18	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
19	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
20	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
21	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
23	CHD1	chr7:38402581-38402583	GM12878	blood:	n/a	n/a
24	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a
25	CHD2	chr7:38403060-38403224	GM12878	blood:	n/a	n/a
26	CTCF	chr7:38393980-38394130	HCPEpiC	choroid plexus:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
27	CTCF	chr7:38403120-38403270	GM12870	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
28	CTCF	chr7:38393922-38394186	GM19239	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
29	CTCF	chr7:38398680-38398830	BJ	skin:	n/a	n/a
30	CTCF	chr7:38394000-38394150	NHDF-neo	bronchial:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
31	CTCF	chr7:38398320-38398470	GM12872	blood:	n/a	n/a
32	CTCF	chr7:38393980-38394130	HUVEC	blood vessel:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
33	CTCF	chr7:38403160-38403310	BE2_C	brain:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
34	CTCF	chr7:38393904-38394212	K562	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
35	CTCF	chr7:38394000-38394150	GM12864	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
36	CTCF	chr7:38398980-38399130	HCT-116	colon:	n/a	n/a
37	CTCF	chr7:38393880-38394030	HA-sp	spinal cord:	n/a	n/a
38	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
39	CTCF	chr7:38389484-38390023	GM19240	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
40	CTCF	chr7:38389466-38390000	GM19238	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
41	CTCF	chr7:38398703-38399023	GM19239	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
42	CTCF	chr7:38393880-38394030	HCT-116	colon:	n/a	n/a
43	CTCF	chr7:38403060-38403284	T-47D	breast:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
44	CTCF	chr7:38398644-38399160	Spleen_OC	spleen:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
45	CTCF	chr7:38399060-38399210	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr7:38398619-38399064	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
47	CTCF	chr7:38398680-38398830	SAEC	small airway:	n/a	n/a
48	CTCF	chr7:38394220-38394370	GM12868	blood:	n/a	n/a
49	CTCF	chr7:38403091-38403327	LNCaP	prostate:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
50	CTCF	chr7:38394000-38394150	HUVEC	blood vessel:	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	MCF-7	breast:	n/a
2	chr7:38398839-38398889	A549	lung:	n/a
3	chr7:38398839-38398889	SKMC	muscle:	n/a
4	chr7:38398839-38398889	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:38398836-38398886	T-47D	breast:	n/a
6	chr7:38398839-38398889	T-47D	breast:	n/a
7	chr7:38398836-38398886	PFSK-1	brain:	n/a
8	chr7:38398836-38398886	HCF	heart:	n/a
9	chr7:38403507-38403557	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:38389991-38390041	SK-N-SH	brain:	n/a
11	chr7:38398836-38398886	NHBE	bronchial:	n/a
12	chr7:38398836-38398886	AG09319	gingival:	n/a
13	chr7:38398839-38398889	K562	blood:	n/a
14	chr7:38398839-38398889	ProgFib	skin:	n/a
15	chr7:38403507-38403557	GM12891	blood:	n/a
16	chr7:38398836-38398886	PANC-1	pancreas:	n/a
17	chr7:38389991-38390041	ovcar-3	ovarian:	n/a
18	chr7:38403507-38403557	SK-N-MC	brain:	n/a
19	chr7:38389991-38390041	HCT-116	colon:	n/a
20	chr7:38403507-38403557	SK-N-SH_RA	brain:	n/a
21	chr7:38398836-38398886	AG04450	lung:	fetal
22	chr7:38403507-38403557	PANC-1	pancreas:	n/a
23	chr7:38389991-38390041	ECC-1	luminal epithelium:	n/a
24	chr7:38403507-38403557	H1-hESC	embryonic stem cell:	embryo
25	chr7:38398839-38398889	SAEC	small airway:	n/a
26	chr7:38398836-38398886	Caco-2	colon:	n/a
27	chr7:38398836-38398886	HEK293	kidney:	embryo
28	chr7:38398836-38398886	HAEpiC	amniotic membrane:	n/a
29	chr7:38389991-38390041	LNCaP	prostate:	n/a
30	chr7:38389991-38390041	NB4	blood:	n/a
31	chr7:38389991-38390041	PFSK-1	brain:	n/a
32	chr7:38398839-38398889	BE2_C	brain:	n/a
33	chr7:38403507-38403557	Caco-2	colon:	n/a
34	chr7:38398836-38398886	SK-N-SH	brain:	n/a
35	chr7:38398839-38398889	Caco-2	colon:	n/a
36	chr7:38403507-38403557	GM19239	blood:	n/a
37	chr7:38403507-38403557	RPTEC	kidney:	n/a
38	chr7:38398839-38398889	GM19239	blood:	n/a
39	chr7:38389991-38390041	GM12878	blood:	n/a
40	chr7:38398836-38398886	HL-60	blood:	n/a
41	chr7:38398836-38398886	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:38403507-38403557	HRE	kidney:	n/a
43	chr7:38398839-38398889	HCT-116	colon:	n/a
44	chr7:38389991-38390041	AG04450	lung:	fetal
45	chr7:38398839-38398889	NHBE	bronchial:	n/a
46	chr7:38398839-38398889	HRPEpiC	eye:	n/a
47	chr7:38389991-38390041	HRPEpiC	eye:	n/a
48	chr7:38403507-38403557	HRCEpiC	kidney:	n/a
49	chr7:38389991-38390041	HNPCEpiC	eye:	n/a
50	chr7:38398836-38398886	AG04449	skin:	fetal

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
2	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
3	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
4	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
5	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
6	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
7	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924

Variant related genes	Relation type
TRGV2	TF binding region
TRGV5	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV5P	TF binding region
TRGV2	CpG island
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: 997 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:997 , 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	rs566275692	chr7:38389987-38389988	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs141122766	chr7:38389989-38389990	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs551601176	chr7:38389991-38389992	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs189430581	chr7:38389992-38389993	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs533758664	chr7:38389998-38389999	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs536700056	chr7:38390008-38390009	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs115674221	chr7:38390010-38390011	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs370367398	chr7:38390023-38390024	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs2534594	chr7:38390036-38390037	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs181477327	chr7:38390038-38390039	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs535902176	chr7:38390047-38390048	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs553210541	chr7:38390057-38390058	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs376633394	chr7:38390059-38390060	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs573220268	chr7:38390060-38390061	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs376182276	chr7:38390082-38390083	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs2735132	chr7:38390083-38390084	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs185760602	chr7:38390095-38390096	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs199904798	chr7:38390103-38390104	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs189746318	chr7:38390190-38390191	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182323979	chr7:38390194-38390195	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543901341	chr7:38390225-38390226	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs7798750	chr7:38390248-38390249	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7798751	chr7:38390253-38390254	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373951475	chr7:38390258-38390259	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs143112617	chr7:38390269-38390270	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs7779898	chr7:38390270-38390271	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs571476019	chr7:38390301-38390302	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537261110	chr7:38390330-38390331	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550633866	chr7:38390350-38390351	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs35804924	chr7:38390360-38390361	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78075983	chr7:38390364-38390365	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552533062	chr7:38390370-38390371	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs112917202	chr7:38390371-38390372	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200880453	chr7:38390430-38390431	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538207206	chr7:38390437-38390438	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536240643	chr7:38390454-38390455	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs552733402	chr7:38390472-38390473	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs188731769	chr7:38390485-38390486	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374630157	chr7:38390533-38390534	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558908057	chr7:38390542-38390543	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs575496171	chr7:38390584-38390585	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12533305	chr7:38390596-38390597	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs371817531	chr7:38390605-38390606	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs60704973	chr7:38390653-38390654	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554099501	chr7:38390658-38390659	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs191079290	chr7:38390661-38390662	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs386712326	chr7:38390671-38390672	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs3999877	chr7:38390673-38390674	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs183291833	chr7:38390685-38390686	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs12533331	chr7:38390693-38390694	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 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:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
2	chr7:38384800-38390800	Active TSS	Thymus	Thymus
3	chr7:38386800-38390600	Enhancers	Primary B cells from cord blood	blood
4	chr7:38388600-38390200	Flanking Active TSS	Fetal Thymus	thymus
5	chr7:38388600-38390400	Active TSS	Primary T killer memory cells from peripheral blood	blood
6	chr7:38388600-38391000	Enhancers	Primary B cells from peripheral blood	blood
7	chr7:38388800-38390000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:38388800-38390600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
9	chr7:38388800-38390600	Active TSS	Duodenum Mucosa	Duodenum
10	chr7:38388800-38391800	Active TSS	Primary T cells fromperipheralblood	blood
11	chr7:38388800-38394200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:38389000-38390000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:38389000-38390200	Active TSS	Primary T helper naive cells from peripheral blood	blood
14	chr7:38389000-38390400	Active TSS	Primary T helper cells PMA-I stimulated	--
15	chr7:38389000-38390400	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr7:38389000-38390600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:38389200-38390400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
18	chr7:38389200-38390600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:38389200-38392800	Active TSS	GM12878-XiMat	blood
20	chr7:38389400-38390400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr7:38389400-38390400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:38389600-38390200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr7:38389600-38390400	Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr7:38389600-38390600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
25	chr7:38389600-38391200	Active TSS	Dnd41	blood
26	chr7:38389600-38391400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr7:38389600-38391600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr7:38389600-38392800	Weak transcription	Spleen	Spleen
29	chr7:38389600-38413800	Weak transcription	K562	blood
30	chr7:38389800-38390000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
31	chr7:38389800-38390400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
32	chr7:38389800-38390600	Active TSS	Primary T cells from cord blood	blood
33	chr7:38390000-38390200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr7:38390000-38390600	Active TSS	Primary T helper cells fromperipheralblood	blood
35	chr7:38390200-38390400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:38390200-38390400	Active TSS	Fetal Thymus	thymus
37	chr7:38390200-38390600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr7:38390200-38390600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
39	chr7:38390400-38390600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr7:38390400-38390600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr7:38390400-38390600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr7:38390400-38390600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr7:38390400-38390600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:38390400-38390600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
45	chr7:38390400-38390600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
46	chr7:38390400-38390600	Flanking Active TSS	Fetal Thymus	thymus
47	chr7:38390400-38390600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
48	chr7:38390400-38391200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr7:38390600-38390800	Active TSS	Primary hematopoietic stem cells short term culture	blood
50	chr7:38390600-38390800	Active TSS	Fetal Thymus	thymus

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