Variant report

Variant	esv1811068
Chromosome Location	chr7:38390909-38400548
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	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
2	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
3	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
4	BATF	chr7:38397936-38398227	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	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
10	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
11	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
12	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
13	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
14	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
16	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a
17	CTCF	chr7:38394220-38394370	GM12868	blood:	n/a	n/a
18	CTCF	chr7:38398733-38398965	HepG2	liver:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
19	CTCF	chr7:38398720-38398870	GM12869	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
20	CTCF	chr7:38398720-38398870	HAc	cerebellar:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
21	CTCF	chr7:38398680-38398830	GM12874	blood:	n/a	n/a
22	CTCF	chr7:38393980-38394130	HRE	kidney:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
23	CTCF	chr7:38398624-38399024	A549	lung:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
24	CTCF	chr7:38399104-38399234	Gliobla	brain:	n/a	n/a
25	CTCF	chr7:38398619-38399064	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
26	CTCF	chr7:38393660-38393810	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr7:38398700-38398850	HMEC	breast:	n/a	n/a
28	CTCF	chr7:38399060-38399210	RPTEC	kidney:	n/a	n/a
29	CTCF	chr7:38393855-38394198	GM13976	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
30	CTCF	chr7:38393939-38394212	LNCaP	prostate:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
31	CTCF	chr7:38393920-38394070	GM12873	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
32	CTCF	chr7:38398680-38398830	GM12864	blood:	n/a	n/a
33	CTCF	chr7:38393959-38394224	Lung_OC	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
34	CTCF	chr7:38398680-38398830	BE2_C	brain:	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	chr7:38398677-38398888	H1-hESC	embryonic stem cell:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
37	CTCF	chr7:38399060-38399210	GM12865	blood:	n/a	n/a
38	CTCF	chr7:38393920-38394070	HFF	foreskin:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
39	CTCF	chr7:38399060-38399210	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr7:38394000-38394150	NHDF-neo	bronchial:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
41	CTCF	chr7:38398716-38399000	MCF-7	breast:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
42	CTCF	chr7:38398681-38399005	MCF-7	breast:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
43	CTCF	chr7:38393980-38394130	BJ	skin:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
44	CTCF	chr7:38398684-38399019	GM12878	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
45	CTCF	chr7:38393880-38394030	HCM	heart:	n/a	n/a
46	CTCF	chr7:38394040-38394190	NHDF-neo	bronchial:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
47	CTCF	chr7:38398680-38398830	HVMF	connective:	n/a	n/a
48	CTCF	chr7:38398680-38398830	HMF	breast:	n/a	n/a
49	CTCF	chr7:38398682-38399055	Gliobla	brain:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
50	CTCF	chr7:38393919-38394198	Fibrobl	skin:	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	HCPEpiC	choroid plexus:	n/a
2	chr7:38398836-38398886	HEEpiC	esophagus:	n/a
3	chr7:38398839-38398889	HCF	heart:	n/a
4	chr7:38398839-38398889	NHBE	bronchial:	n/a
5	chr7:38398836-38398886	A549	lung:	n/a
6	chr7:38398836-38398886	HL-60	blood:	n/a
7	chr7:38398836-38398886	BJ	skin:	n/a
8	chr7:38398836-38398886	PrEC	prostate:	n/a
9	chr7:38398839-38398889	HAEpiC	amniotic membrane:	n/a
10	chr7:38398836-38398886	GM12878	blood:	n/a
11	chr7:38398839-38398889	T-47D	breast:	n/a
12	chr7:38398836-38398886	BE2_C	brain:	n/a
13	chr7:38398836-38398886	ovcar-3	ovarian:	n/a
14	chr7:38398836-38398886	Caco-2	colon:	n/a
15	chr7:38398839-38398889	HRCEpiC	kidney:	n/a
16	chr7:38398839-38398889	GM12892	blood:	n/a
17	chr7:38398839-38398889	BE2_C	brain:	n/a
18	chr7:38398836-38398886	RPTEC	kidney:	n/a
19	chr7:38398836-38398886	HCT-116	colon:	n/a
20	chr7:38398836-38398886	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:38398839-38398889	SK-N-SH	brain:	n/a
22	chr7:38398839-38398889	HRPEpiC	eye:	n/a
23	chr7:38398836-38398886	Hela-S3	cervix:	n/a
24	chr7:38398836-38398886	U87	brain:	n/a
25	chr7:38398839-38398889	ECC-1	luminal epithelium:	n/a
26	chr7:38398836-38398886	ProgFib	skin:	n/a
27	chr7:38398836-38398886	SK-N-SH_RA	brain:	n/a
28	chr7:38398839-38398889	SAEC	small airway:	n/a
29	chr7:38398836-38398886	HNPCEpiC	eye:	n/a
30	chr7:38398836-38398886	MCF-7	breast:	n/a
31	chr7:38398839-38398889	A549	lung:	n/a
32	chr7:38398839-38398889	SK-N-SH_RA	brain:	n/a
33	chr7:38398839-38398889	H1-hESC	embryonic stem cell:	embryo
34	chr7:38398836-38398886	SAEC	small airway:	n/a
35	chr7:38398839-38398889	ovcar-3	ovarian:	n/a
36	chr7:38398836-38398886	NB4	blood:	n/a
37	chr7:38398836-38398886	T-47D	breast:	n/a
38	chr7:38398836-38398886	GM12891	blood:	n/a
39	chr7:38398836-38398886	NH-A	brain:	n/a
40	chr7:38398836-38398886	HMEC	breast:	n/a
41	chr7:38398839-38398889	NHDF-neo	bronchial:	n/a
42	chr7:38398839-38398889	HCT-116	colon:	n/a
43	chr7:38398836-38398886	HIPEpiC	eye:	n/a
44	chr7:38398839-38398889	LNCaP	prostate:	n/a
45	chr7:38398839-38398889	NH-A	brain:	n/a
46	chr7:38398836-38398886	SKMC	muscle:	n/a
47	chr7:38398839-38398889	Hela-S3	cervix:	n/a
48	chr7:38398836-38398886	HCM	heart:	n/a
49	chr7:38398836-38398886	AG09309	skin:	n/a
50	chr7:38398836-38398886	AG09319	gingival:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
2	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
3	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
4	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180

Variant related genes	Relation type
TRGV5	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV5	CpG island
TRGV4	CpG island
TRGV3	CpG island
ENSG00000249978	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000226212	chromatin interactions

Extended variants
information (count: 674 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4078668	chr7:38390909-38390910	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191396337	chr7:38390912-38390913	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs183963381	chr7:38390917-38390918	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187811908	chr7:38390939-38390940	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558869630	chr7:38390942-38390943	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369743893	chr7:38390972-38390973	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539724465	chr7:38390981-38390982	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs58730250	chr7:38390982-38390983	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs1808312	chr7:38390989-38390990	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs554428889	chr7:38391006-38391007	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574575747	chr7:38391013-38391014	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs59611922	chr7:38391017-38391018	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs372816352	chr7:38391049-38391050	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs193268436	chr7:38391050-38391051	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs57448903	chr7:38391080-38391081	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs386712327	chr7:38391085-38391086	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs112260069	chr7:38391088-38391089	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs531148996	chr7:38391147-38391148	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs544897248	chr7:38391167-38391168	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs561297980	chr7:38391172-38391173	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs185059299	chr7:38391173-38391174	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs59852119	chr7:38391190-38391191	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs73694034	chr7:38391192-38391193	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs200337170	chr7:38391199-38391200	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs566601154	chr7:38391206-38391207	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545035497	chr7:38391226-38391227	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72496141	chr7:38391255-38391256	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs568880595	chr7:38391259-38391260	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143959604	chr7:38391269-38391270	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548485134	chr7:38391270-38391271	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146427526	chr7:38391311-38391312	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372961297	chr7:38391313-38391314	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553025213	chr7:38391316-38391317	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2540198	chr7:38391317-38391318	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs373356485	chr7:38391369-38391370	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58353432	chr7:38391439-38391440	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs575597383	chr7:38391468-38391469	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544545557	chr7:38391474-38391475	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561661606	chr7:38391487-38391488	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574914572	chr7:38391516-38391517	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374153854	chr7:38391543-38391544	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201897035	chr7:38391544-38391545	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs3999879	chr7:38391547-38391548	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs564185776	chr7:38391557-38391558	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567160886	chr7:38391575-38391576	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529808258	chr7:38391578-38391579	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188724516	chr7:38391590-38391591	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531350952	chr7:38391627-38391628	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs548168768	chr7:38391636-38391637	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs2735131	chr7:38391669-38391670	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
2	chr7:38388600-38391000	Enhancers	Primary B cells from peripheral blood	blood
3	chr7:38388800-38391800	Active TSS	Primary T cells fromperipheralblood	blood
4	chr7:38388800-38394200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:38389200-38392800	Active TSS	GM12878-XiMat	blood
6	chr7:38389600-38391200	Active TSS	Dnd41	blood
7	chr7:38389600-38391400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
8	chr7:38389600-38391600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr7:38389600-38392800	Weak transcription	Spleen	Spleen
10	chr7:38389600-38413800	Weak transcription	K562	blood
11	chr7:38390400-38391200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr7:38390600-38391000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr7:38390600-38391200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr7:38390600-38391200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:38390600-38391200	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr7:38390600-38391200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:38390600-38391400	Weak transcription	Primary T cells from cord blood	blood
18	chr7:38390600-38391400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:38390600-38391400	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr7:38390600-38392600	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr7:38390600-38392800	Weak transcription	Primary B cells from cord blood	blood
22	chr7:38390600-38392800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr7:38390600-38392800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr7:38390600-38393400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr7:38390600-38393600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr7:38390600-38394600	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr7:38390800-38391200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr7:38390800-38391800	Weak transcription	Fetal Thymus	thymus
29	chr7:38390800-38392800	Weak transcription	Thymus	Thymus
30	chr7:38391000-38391200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr7:38391000-38392800	Weak transcription	Primary B cells from peripheral blood	blood
32	chr7:38391200-38391400	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr7:38391200-38391400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
34	chr7:38391200-38391400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr7:38391200-38391400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:38391200-38391600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr7:38391200-38391600	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr7:38391200-38391600	Flanking Active TSS	Dnd41	blood
39	chr7:38391200-38394200	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr7:38391400-38391600	Enhancers	Primary T cells from cord blood	blood
41	chr7:38391400-38391600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr7:38391400-38391600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr7:38391400-38391600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:38391400-38392600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr7:38391400-38393400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr7:38391400-38396600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr7:38391600-38391800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr7:38391600-38391800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr7:38391600-38391800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:38391600-38392200	Weak transcription	Primary T cells from cord blood	blood

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