Variant report

Variant	esv1806160
Chromosome Location	chr7:38394144-38402496
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	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
2	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
3	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
4	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
5	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
6	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
7	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
8	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
10	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
11	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
12	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
14	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a
15	CTCF	chr7:38398680-38398830	NB4	blood:	n/a	n/a
16	CTCF	chr7:38398722-38398964	Lung_OC	lung:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
17	CTCF	chr7:38398700-38398850	GM12872	blood:	n/a	n/a
18	CTCF	chr7:38398619-38399064	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
19	CTCF	chr7:38398680-38398830	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr7:38398634-38399013	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
21	CTCF	chr7:38402420-38402570	GM12864	blood:	n/a	n/a
22	CTCF	chr7:38398730-38398942	Kidney_OC	kidney:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
23	CTCF	chr7:38398660-38398810	GM12870	blood:	n/a	n/a
24	CTCF	chr7:38398644-38399160	Spleen_OC	spleen:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
25	CTCF	chr7:38393933-38394181	K562	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
26	CTCF	chr7:38394020-38394170	NHLF	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
27	CTCF	chr7:38398680-38398830	AG04449	skin:	n/a	n/a
28	CTCF	chr7:38399060-38399210	RPTEC	kidney:	n/a	n/a
29	CTCF	chr7:38399104-38399234	Gliobla	brain:	n/a	n/a
30	CTCF	chr7:38393910-38394218	MCF-7	breast:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
31	CTCF	chr7:38398660-38398810	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr7:38393848-38394271	A549	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
33	CTCF	chr7:38398680-38398830	BJ	skin:	n/a	n/a
34	CTCF	chr7:38394220-38394370	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr7:38394000-38394150	GM12874	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
36	CTCF	chr7:38393887-38394183	HepG2	liver:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
37	CTCF	chr7:38399060-38399210	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr7:38398680-38398830	HRE	kidney:	n/a	n/a
39	CTCF	chr7:38398671-38399003	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
40	CTCF	chr7:38398960-38399110	AG09319	gingival:	n/a	n/a
41	CTCF	chr7:38393855-38394198	GM13976	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
42	CTCF	chr7:38398508-38399205	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
43	CTCF	chr7:38398980-38399130	HCT-116	colon:	n/a	n/a
44	CTCF	chr7:38393980-38394178	A549	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
45	CTCF	chr7:38398693-38399003	Fibrobl	skin:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
46	CTCF	chr7:38394000-38394150	GM12875	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
47	CTCF	chr7:38398960-38399110	GM12868	blood:	n/a	n/a
48	CTCF	chr7:38398595-38399049	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
49	CTCF	chr7:38394000-38394150	GM12864	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
50	CTCF	chr7:38394000-38394150	NHDF-neo	bronchial:	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	SK-N-MC	brain:	n/a
2	chr7:38398836-38398886	MCF10A-Er-Src	breast:	n/a
3	chr7:38398839-38398889	PFSK-1	brain:	n/a
4	chr7:38398839-38398889	HRCEpiC	kidney:	n/a
5	chr7:38398836-38398886	SK-N-SH	brain:	n/a
6	chr7:38398839-38398889	HIPEpiC	eye:	n/a
7	chr7:38398839-38398889	IMR90	lung:	fetal
8	chr7:38398836-38398886	PANC-1	pancreas:	n/a
9	chr7:38398839-38398889	K562	blood:	n/a
10	chr7:38398839-38398889	RPTEC	kidney:	n/a
11	chr7:38398836-38398886	GM12878	blood:	n/a
12	chr7:38398839-38398889	SAEC	small airway:	n/a
13	chr7:38398839-38398889	HNPCEpiC	eye:	n/a
14	chr7:38398836-38398886	HCF	heart:	n/a
15	chr7:38398839-38398889	HCT-116	colon:	n/a
16	chr7:38398839-38398889	HCPEpiC	choroid plexus:	n/a
17	chr7:38398836-38398886	AG04449	skin:	fetal
18	chr7:38398839-38398889	ovcar-3	ovarian:	n/a
19	chr7:38398836-38398886	BE2_C	brain:	n/a
20	chr7:38398836-38398886	AG04450	lung:	fetal
21	chr7:38398836-38398886	T-47D	breast:	n/a
22	chr7:38398836-38398886	GM12892	blood:	n/a
23	chr7:38398839-38398889	HCF	heart:	n/a
24	chr7:38398836-38398886	HRPEpiC	eye:	n/a
25	chr7:38398839-38398889	HRPEpiC	eye:	n/a
26	chr7:38398836-38398886	SKMC	muscle:	n/a
27	chr7:38398839-38398889	LNCaP	prostate:	n/a
28	chr7:38398836-38398886	MCF-7	breast:	n/a
29	chr7:38398836-38398886	ovcar-3	ovarian:	n/a
30	chr7:38398839-38398889	SK-N-SH	brain:	n/a
31	chr7:38398839-38398889	NHDF-neo	bronchial:	n/a
32	chr7:38398839-38398889	SK-N-SH_RA	brain:	n/a
33	chr7:38398839-38398889	AG09319	gingival:	n/a
34	chr7:38398836-38398886	SK-N-SH_RA	brain:	n/a
35	chr7:38398836-38398886	GM19239	blood:	n/a
36	chr7:38398839-38398889	HCM	heart:	n/a
37	chr7:38398836-38398886	AoSMC	blood vessel:	n/a
38	chr7:38398836-38398886	H1-hESC	embryonic stem cell:	embryo
39	chr7:38398836-38398886	NHDF-neo	bronchial:	n/a
40	chr7:38398839-38398889	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:38398839-38398889	AG04449	skin:	fetal
42	chr7:38398836-38398886	RPTEC	kidney:	n/a
43	chr7:38398839-38398889	GM06990	blood:	n/a
44	chr7:38398839-38398889	MCF-7	breast:	n/a
45	chr7:38398839-38398889	NHBE	bronchial:	n/a
46	chr7:38398839-38398889	HUVEC	blood vessel:	n/a
47	chr7:38398836-38398886	K562	blood:	n/a
48	chr7:38398836-38398886	HEK293	kidney:	embryo
49	chr7:38398836-38398886	HCPEpiC	choroid plexus:	n/a
50	chr7:38398836-38398886	Hela-S3	cervix:	n/a

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

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

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
ENSG00000226212	chromatin interactions

Extended variants
information (count: 584 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2192680	chr7:38394144-38394145	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571817813	chr7:38394158-38394159	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs530475093	chr7:38394182-38394183	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs577245912	chr7:38394213-38394214	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs374177035	chr7:38394214-38394215	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs550670616	chr7:38394302-38394303	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs181242556	chr7:38394311-38394312	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs574437452	chr7:38394332-38394333	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs142991046	chr7:38394339-38394340	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs145966554	chr7:38394363-38394364	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs139541280	chr7:38394379-38394380	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs538945319	chr7:38394399-38394400	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs149232631	chr7:38394401-38394402	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs144450347	chr7:38394427-38394428	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs183533144	chr7:38394434-38394435	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs148474647	chr7:38394472-38394473	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs573679522	chr7:38394497-38394498	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs369105337	chr7:38394564-38394565	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371784033	chr7:38394565-38394566	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs189480992	chr7:38394569-38394570	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs78434912	chr7:38394588-38394589	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
22	rs559606761	chr7:38394597-38394598	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369354685	chr7:38394623-38394624	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs573158071	chr7:38394625-38394626	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs181954263	chr7:38394652-38394653	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187361544	chr7:38394657-38394658	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532506176	chr7:38394671-38394672	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550387831	chr7:38394679-38394680	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs561065844	chr7:38394724-38394725	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113553920	chr7:38394745-38394746	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
31	rs192126115	chr7:38394762-38394763	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140499395	chr7:38394769-38394770	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs73357300	chr7:38394802-38394803	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs552462811	chr7:38394806-38394807	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs56085620	chr7:38394831-38394832	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs386712331	chr7:38394838-38394839	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs112465930	chr7:38394848-38394849	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs370220286	chr7:38394865-38394866	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs149150067	chr7:38394889-38394890	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs111441633	chr7:38394890-38394891	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs573840531	chr7:38394892-38394893	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs144463982	chr7:38394900-38394901	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs113905990	chr7:38394907-38394908	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs112066355	chr7:38394909-38394910	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs552900332	chr7:38394971-38394972	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs36069651	chr7:38394981-38394982	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs572922224	chr7:38394990-38394991	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs181531120	chr7:38394996-38394997	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs565604540	chr7:38395037-38395038	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554105048	chr7:38395058-38395059	Weak transcription Enhancers Strong transcription	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:256 , 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	chr7:38388800-38394200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:38389600-38413800	Weak transcription	K562	blood
4	chr7:38390600-38394600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr7:38391200-38394200	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr7:38391400-38396600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr7:38392000-38394200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:38392000-38394600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr7:38392400-38398200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:38392800-38394200	Enhancers	Primary B cells from peripheral blood	blood
11	chr7:38392800-38394400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr7:38392800-38394400	Flanking Active TSS	Dnd41	blood
13	chr7:38393200-38394400	Enhancers	GM12878-XiMat	blood
14	chr7:38393200-38394600	Enhancers	Fetal Thymus	thymus
15	chr7:38393600-38394400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr7:38393600-38395400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr7:38393600-38395400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr7:38393600-38395800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:38393800-38394200	Weak transcription	Spleen	Spleen
20	chr7:38393800-38394400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
21	chr7:38393800-38396000	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr7:38393800-38396200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:38393800-38398000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr7:38394000-38394400	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr7:38394000-38395600	Enhancers	Primary T cells fromperipheralblood	blood
26	chr7:38394000-38396400	Weak transcription	Primary T cells from cord blood	blood
27	chr7:38394000-38397000	Weak transcription	Primary B cells from cord blood	blood
28	chr7:38394000-38397400	Weak transcription	Thymus	Thymus
29	chr7:38394200-38394400	Enhancers	Spleen	Spleen
30	chr7:38394200-38395000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:38394200-38395200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:38394200-38396200	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr7:38394200-38397600	Weak transcription	Primary B cells from peripheral blood	blood
34	chr7:38394400-38395600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr7:38394400-38396200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr7:38394400-38396600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr7:38394400-38397000	Enhancers	Dnd41	blood
38	chr7:38394400-38397800	Weak transcription	GM12878-XiMat	blood
39	chr7:38394400-38398200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr7:38394400-38402200	Weak transcription	Spleen	Spleen
41	chr7:38394600-38395000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr7:38394600-38395000	Weak transcription	Fetal Thymus	thymus
43	chr7:38394600-38397600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr7:38395000-38395600	Enhancers	Fetal Thymus	thymus
45	chr7:38395000-38398200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr7:38395000-38400000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:38395200-38398200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:38395400-38396200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr7:38395400-38396400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr7:38395600-38396400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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