Variant report

Variant	nsv5880
Chromosome Location	chr7:102505158-102550471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:781)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102514028-102514887	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102516155-102516615	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:102509524-102509951	HepG2	liver:	n/a	n/a
4	ATF1	chr7:102533184-102533443	K562	blood:	n/a	n/a
5	ATF1	chr7:102516353-102516642	K562	blood:	n/a	n/a
6	ATF1	chr7:102531030-102531406	K562	blood:	n/a	n/a
7	ATF3	chr7:102515996-102516786	A549	lung:	n/a	n/a
8	ATF3	chr7:102516248-102516624	K562	blood:	n/a	n/a
9	ATF3	chr7:102515979-102516734	HCT-116	colon:	n/a	n/a
10	ATF3	chr7:102516058-102516843	HCT-116	colon:	n/a	n/a
11	ATF3	chr7:102516084-102516739	A549	lung:	n/a	n/a
12	BATF	chr7:102514509-102514873	GM12878	blood:	n/a	n/a
13	BATF	chr7:102514586-102514859	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:102514598-102514832	GM12878	blood:	n/a	chr7:102514741-102514750
15	BCL3	chr7:102515891-102516752	A549	lung:	n/a	chr7:102515915-102515924
16	BCL3	chr7:102515964-102516936	A549	lung:	n/a	n/a
17	BHLHE40	chr7:102516444-102516605	K562	blood:	n/a	n/a
18	BRCA1	chr7:102531852-102531897	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:102516256-102516827	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr7:102516123-102516857	HCT-116	colon:	n/a	n/a
21	CBX3	chr7:102548441-102548837	K562	blood:	n/a	n/a
22	CBX3	chr7:102514409-102515051	HCT-116	colon:	n/a	n/a
23	CBX3	chr7:102544042-102544367	K562	blood:	n/a	n/a
24	CBX3	chr7:102515992-102516945	HCT-116	colon:	n/a	n/a
25	CBX3	chr7:102516236-102516555	K562	blood:	n/a	n/a
26	CBX3	chr7:102514418-102515075	HCT-116	colon:	n/a	n/a
27	CCNT2	chr7:102533279-102533283	K562	blood:	n/a	n/a
28	CCNT2	chr7:102535855-102536087	K562	blood:	n/a	n/a
29	CEBPB	chr7:102523568-102523951	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:102516141-102516759	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:102519576-102519817	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:102515850-102516954	HCT-116	colon:	n/a	n/a
33	CEBPB	chr7:102523614-102523902	A549	lung:	n/a	n/a
34	CEBPB	chr7:102538790-102538955	K562	blood:	n/a	n/a
35	CEBPB	chr7:102534484-102534617	K562	blood:	n/a	chr7:102534514-102534527
36	CEBPB	chr7:102542534-102542881	K562	blood:	n/a	n/a
37	CEBPB	chr7:102516152-102516683	MCF-7	breast:	n/a	n/a
38	CEBPB	chr7:102533094-102533487	K562	blood:	n/a	chr7:102533281-102533292
39	CEBPB	chr7:102509560-102509706	HepG2	liver:	n/a	chr7:102509627-102509638
40	CEBPB	chr7:102516214-102516567	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:102542535-102542722	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:102525131-102525331	A549	lung:	n/a	n/a
43	CEBPB	chr7:102523488-102524042	MCF-7	breast:	n/a	n/a
44	CEBPB	chr7:102516170-102516750	A549	lung:	n/a	n/a
45	CEBPB	chr7:102525151-102525218	K562	blood:	n/a	n/a
46	CEBPB	chr7:102523485-102524118	HCT-116	colon:	n/a	n/a
47	CEBPB	chr7:102523617-102523890	K562	blood:	n/a	n/a
48	CEBPB	chr7:102512850-102513167	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:102533101-102533479	IMR90	lung:	n/a	chr7:102533281-102533292
50	CEBPB	chr7:102509541-102509825	HepG2	liver:	n/a	chr7:102509627-102509638

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102506387-102506437	HRPEpiC	eye:	n/a
2	chr7:102531568-102531618	AG04449	skin:	fetal
3	chr7:102531568-102531618	NB4	blood:	n/a
4	chr7:102506387-102506437	AG04450	lung:	fetal
5	chr7:102531568-102531618	PrEC	prostate:	n/a
6	chr7:102506387-102506437	CMK	blood:	n/a
7	chr7:102506387-102506437	HL-60	blood:	n/a
8	chr7:102531568-102531618	HCM	heart:	n/a
9	chr7:102531568-102531618	MCF10A-Er-Src	breast:	n/a
10	chr7:102506387-102506437	NHBE	bronchial:	n/a
11	chr7:102506387-102506437	HCM	heart:	n/a
12	chr7:102531568-102531618	GM19239	blood:	n/a
13	chr7:102531568-102531618	NT2-D1	testis:	n/a
14	chr7:102531568-102531618	BE2_C	brain:	n/a
15	chr7:102506387-102506437	NT2-D1	testis:	n/a
16	chr7:102506387-102506437	T-47D	breast:	n/a
17	chr7:102531568-102531618	Jurkat	blood:	n/a
18	chr7:102506387-102506437	LNCaP	prostate:	n/a
19	chr7:102531568-102531618	BJ	skin:	n/a
20	chr7:102531568-102531618	Hela-S3	cervix:	n/a
21	chr7:102531568-102531618	LNCaP	prostate:	n/a
22	chr7:102506387-102506437	AG04449	skin:	fetal
23	chr7:102531568-102531618	SK-N-MC	brain:	n/a
24	chr7:102506387-102506437	HMEC	breast:	n/a
25	chr7:102506387-102506437	PANC-1	pancreas:	n/a
26	chr7:102506387-102506437	MCF10A-Er-Src	breast:	n/a
27	chr7:102506387-102506437	SAEC	small airway:	n/a
28	chr7:102531568-102531618	HUVEC	blood vessel:	n/a
29	chr7:102531568-102531618	AG10803	skin:	n/a
30	chr7:102506387-102506437	BE2_C	brain:	n/a
31	chr7:102506387-102506437	AG10803	skin:	n/a
32	chr7:102531568-102531618	HAEpiC	amniotic membrane:	n/a
33	chr7:102531568-102531618	Hepatocyte	liver:	n/a
34	chr7:102506387-102506437	GM06990	blood:	n/a
35	chr7:102506387-102506437	RPTEC	kidney:	n/a
36	chr7:102531568-102531618	H1-hESC	embryonic stem cell:	embryo
37	chr7:102506387-102506437	MCF-7	breast:	n/a
38	chr7:102506387-102506437	ProgFib	skin:	n/a
39	chr7:102531568-102531618	HEK293	kidney:	embryo
40	chr7:102506387-102506437	BJ	skin:	n/a
41	chr7:102531568-102531618	RPTEC	kidney:	n/a
42	chr7:102531568-102531618	HEEpiC	esophagus:	n/a
43	chr7:102531568-102531618	T-47D	breast:	n/a
44	chr7:102531568-102531618	SKMC	muscle:	n/a
45	chr7:102506387-102506437	GM12878	blood:	n/a
46	chr7:102531568-102531618	K562	blood:	n/a
47	chr7:102531568-102531618	CMK	blood:	n/a
48	chr7:102506387-102506437	HRE	kidney:	n/a
49	chr7:102506387-102506437	SK-N-SH	brain:	n/a
50	chr7:102506387-102506437	Hepatocyte	liver:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102522158..102525265-chr7:102531503..102535074,3	K562	blood:
2	chr7:102516404..102517929-chr7:102714703..102716697,2	MCF-7	breast:
3	chr7:102489859..102491552-chr7:102503328..102506075,2	MCF-7	breast:
4	chr7:102529179..102531129-chr7:102713390..102716151,2	MCF-7	breast:
5	chr7:102497049..102499033-chr7:102503041..102505939,2	K562	blood:
6	chr7:102503409..102506375-chr7:102514987..102518844,3	K562	blood:
7	chr7:102510827..102513027-chr7:102515036..102518141,3	K562	blood:
8	chr7:102513883..102516664-chr7:102520756..102522395,2	K562	blood:
9	chr7:102501221..102503373-chr7:102515985..102518701,2	MCF-7	breast:
10	chr7:102504642..102507106-chr7:102507263..102511653,3	K562	blood:
11	chr7:102510827..102513027-chr7:102515036..102518141,3	K562	blood:
12	chr7:102537736..102539276-chr7:102622119..102624837,2	MCF-7	breast:
13	chr7:102527046..102528879-chr7:102528977..102531238,2	MCF-7	breast:
14	chr7:102517307..102518855-chr7:102521320..102524235,2	MCF-7	breast:
15	chr7:102535894..102537505-chr7:102552390..102554520,2	MCF-7	breast:
16	chr7:102501610..102503166-chr7:102508637..102510523,2	K562	blood:
17	chr7:102504642..102507106-chr7:102507263..102511653,3	K562	blood:
18	chr7:102513883..102516664-chr7:102520756..102522395,2	K562	blood:
19	chr7:102513072..102513724-chr9:129702545..129703389,2	MCF-7	breast:
20	chr7:102522158..102525265-chr7:102531503..102535074,3	K562	blood:
21	chr20:52596990..52599653-chr7:102503790..102506770,2	MCF-7	breast:
22	chr7:102517778..102519381-chr7:102714945..102717591,2	MCF-7	breast:
23	chr7:102526206..102528003-chr7:102535680..102538379,2	MCF-7	breast:
24	chr7:102526206..102528003-chr7:102535680..102538379,2	MCF-7	breast:
25	chr7:102517307..102518855-chr7:102521320..102524235,2	MCF-7	breast:
26	chr7:102527046..102528879-chr7:102528977..102531238,2	MCF-7	breast:
27	chr7:102503409..102506375-chr7:102514987..102518844,3	K562	blood:

No data

Variant related genes	Relation type
LRRC17	TF binding region
LRRC17	CpG island
ENSG00000170632	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000238324	chromatin interactions
ENSG00000128606	chromatin interactions

Extended variants
information (count: 1529 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10660217	chr7:102505186-102505187	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs10659093	chr7:102505187-102505188	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs398095270	chr7:102505190-102505191	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs529713700	chr7:102505203-102505204	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375689938	chr7:102505249-102505250	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563129114	chr7:102505256-102505257	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542134322	chr7:102505329-102505330	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530861146	chr7:102505333-102505334	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552478028	chr7:102505361-102505362	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560472957	chr7:102505362-102505363	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs6942855	chr7:102505376-102505377	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs182655771	chr7:102505394-102505395	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566170390	chr7:102505440-102505441	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536343009	chr7:102505512-102505513	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs142661834	chr7:102505546-102505547	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569932948	chr7:102505556-102505557	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537372827	chr7:102505559-102505560	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs138764678	chr7:102505590-102505591	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141709409	chr7:102505614-102505615	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs75400151	chr7:102505696-102505697	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs17136137	chr7:102505713-102505714	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541352571	chr7:102505809-102505810	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376602889	chr7:102505866-102505867	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541544693	chr7:102505882-102505883	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563324676	chr7:102505903-102505904	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530545677	chr7:102505971-102505972	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79180063	chr7:102505979-102505980	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545783438	chr7:102505985-102505986	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564384043	chr7:102506012-102506013	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528349956	chr7:102506013-102506014	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201549615	chr7:102506038-102506039	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186921063	chr7:102506135-102506136	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561721815	chr7:102506138-102506139	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192284979	chr7:102506163-102506164	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375685337	chr7:102506172-102506173	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548369698	chr7:102506212-102506213	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369698282	chr7:102506227-102506228	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532644547	chr7:102506238-102506239	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148529224	chr7:102506264-102506265	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537062814	chr7:102506302-102506303	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182854814	chr7:102506353-102506354	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570811491	chr7:102506388-102506389	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76319516	chr7:102506422-102506423	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188489277	chr7:102506423-102506424	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193097201	chr7:102506427-102506428	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550661964	chr7:102506462-102506463	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6968559	chr7:102506464-102506465	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs141910675	chr7:102506486-102506487	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185567189	chr7:102506532-102506533	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556798352	chr7:102506541-102506542	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102470000-102516400	Weak transcription	Pancreas	Pancrea
2	chr7:102500600-102513800	Weak transcription	Aorta	Aorta
3	chr7:102500600-102514200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr7:102500600-102518400	Weak transcription	Left Ventricle	heart
5	chr7:102501000-102505800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:102501000-102511200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:102501000-102512200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr7:102501200-102506800	Weak transcription	Fetal Kidney	kidney
9	chr7:102501200-102515800	Weak transcription	Gastric	stomach
10	chr7:102501200-102530800	Weak transcription	Ovary	ovary
11	chr7:102502000-102508800	Weak transcription	HepG2	liver
12	chr7:102502400-102507400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr7:102502600-102516200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr7:102503000-102506000	Enhancers	A549	lung
15	chr7:102503600-102506400	Weak transcription	Fetal Lung	lung
16	chr7:102503600-102506400	Weak transcription	Fetal Stomach	stomach
17	chr7:102503800-102513800	Weak transcription	Brain Substantia Nigra	brain
18	chr7:102504400-102512400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr7:102504600-102505600	Enhancers	HUVEC	blood vessel
20	chr7:102504600-102507200	Strong transcription	K562	blood
21	chr7:102504600-102513000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr7:102504800-102506000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr7:102504800-102516200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr7:102505200-102505600	Enhancers	Stomach Mucosa	stomach
25	chr7:102505600-102511000	Weak transcription	HUVEC	blood vessel
26	chr7:102506000-102507000	Weak transcription	A549	lung
27	chr7:102506000-102507000	Weak transcription	HSMM	muscle
28	chr7:102506000-102507400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:102506400-102507000	Enhancers	Fetal Stomach	stomach
30	chr7:102506400-102508000	Enhancers	Fetal Lung	lung
31	chr7:102506600-102506800	Weak transcription	Fetal Muscle Leg	muscle
32	chr7:102506800-102507400	Enhancers	Fetal Kidney	kidney
33	chr7:102506800-102507600	Enhancers	Fetal Muscle Leg	muscle
34	chr7:102507000-102507400	Enhancers	A549	lung
35	chr7:102507000-102507600	Weak transcription	Fetal Stomach	stomach
36	chr7:102507000-102507600	Enhancers	HSMM	muscle
37	chr7:102507200-102508000	Genic enhancers	K562	blood
38	chr7:102507400-102507600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr7:102507400-102512400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:102507400-102512400	Weak transcription	A549	lung
41	chr7:102507400-102519400	Weak transcription	Fetal Kidney	kidney
42	chr7:102507600-102508000	Enhancers	Fetal Stomach	stomach
43	chr7:102507600-102509200	Weak transcription	Fetal Muscle Leg	muscle
44	chr7:102507600-102512200	Weak transcription	HSMM	muscle
45	chr7:102508000-102508600	Weak transcription	K562	blood
46	chr7:102508000-102522200	Weak transcription	Fetal Stomach	stomach
47	chr7:102508000-102529200	Weak transcription	Fetal Lung	lung
48	chr7:102508600-102514800	Strong transcription	K562	blood
49	chr7:102508800-102510600	Enhancers	HepG2	liver
50	chr7:102510600-102512400	Weak transcription	HepG2	liver

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