Variant report

Variant	esv1792643
Chromosome Location	chr7:87069758-87108420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:613)
CpG islands
(count:733)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:87093353-87093783	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:87105129-87105319	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:87103805-87104061	HepG2	liver:	n/a	n/a
4	ATF1	chr7:87080871-87080985	K562	blood:	n/a	n/a
5	ATF2	chr7:87103159-87104838	GM12878	blood:	n/a	chr7:87104394-87104401
6	ATF2	chr7:87075193-87075772	GM12878	blood:	n/a	n/a
7	ATF2	chr7:87075213-87075701	GM12878	blood:	n/a	n/a
8	ATF2	chr7:87103357-87104743	GM12878	blood:	n/a	chr7:87104394-87104401
9	BACH1	chr7:87104693-87104885	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:87094518-87094660	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr7:87103714-87104408	GM12878	blood:	n/a	chr7:87104368-87104377
12	BATF	chr7:87075232-87075613	GM12878	blood:	n/a	n/a
13	BATF	chr7:87103408-87104590	GM12878	blood:	n/a	chr7:87104368-87104377
14	BCL11A	chr7:87103389-87104608	GM12878	blood:	n/a	chr7:87103426-87103435
15	BCL11A	chr7:87103765-87104455	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:87075212-87075653	GM12878	blood:	n/a	chr7:87075396-87075405
17	BCL11A	chr7:87075188-87075625	GM12878	blood:	n/a	chr7:87075396-87075405
18	BCL3	chr7:87103771-87104306	GM12878	blood:	n/a	n/a
19	BCL3	chr7:87103501-87104527	GM12878	blood:	n/a	n/a
20	BCLAF1	chr7:87103241-87104577	GM12878	blood:	n/a	chr7:87103426-87103435
21	BCLAF1	chr7:87103284-87104672	GM12878	blood:	n/a	chr7:87103426-87103435
22	BHLHE40	chr7:87105560-87105599	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:87075261-87075645	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:87093399-87093797	HepG2	liver:	n/a	n/a
25	BHLHE40	chr7:87103333-87105002	GM12878	blood:	n/a	n/a
26	BRCA1	chr7:87105230-87105252	GM12878	blood:	n/a	n/a
27	BRCA1	chr7:87104037-87104253	GM12878	blood:	n/a	n/a
28	BRCA1	chr7:87093351-87093701	HepG2	liver:	n/a	n/a
29	CCNT2	chr7:87089363-87089563	K562	blood:	n/a	n/a
30	CCNT2	chr7:87105224-87105341	K562	blood:	n/a	n/a
31	CEBPB	chr7:87104253-87104485	K562	blood:	n/a	n/a
32	CEBPB	chr7:87093392-87093696	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:87104230-87104587	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:87103220-87104832	GM12878	blood:	n/a	n/a
35	CEBPB	chr7:87077625-87077807	HepG2	liver:	n/a	chr7:87077714-87077727
36	CEBPB	chr7:87104255-87104498	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr7:87104216-87104585	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:87104372-87104706	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:87104224-87104575	A549	lung:	n/a	n/a
40	CEBPB	chr7:87103821-87104498	GM12878	blood:	n/a	n/a
41	CEBPD	chr7:87104723-87105270	HepG2	liver:	n/a	n/a
42	CEBPD	chr7:87094462-87094862	HepG2	liver:	n/a	n/a
43	CHD1	chr7:87103651-87105326	GM12878	blood:	n/a	chr7:87104889-87104899
44	CHD1	chr7:87102462-87102974	GM12878	blood:	n/a	n/a
45	CHD1	chr7:87105625-87106080	GM12878	blood:	n/a	n/a
46	CHD1	chr7:87103203-87103403	GM12878	blood:	n/a	n/a
47	CHD1	chr7:87104723-87104848	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr7:87094469-87094656	HepG2	liver:	n/a	n/a
49	CHD2	chr7:87102329-87102373	GM12878	blood:	n/a	n/a
50	CHD2	chr7:87093418-87093639	HepG2	liver:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:87093634-87093684	SK-N-SH_RA	brain:	n/a
2	chr7:87093634-87093684	SK-N-SH_RA	brain:	n/a
3	chr7:87103624-87103674	HepG2	liver:	n/a
4	chr7:87104932-87104982	GM19239	blood:	n/a
5	chr7:87105293-87105343	AG09319	gingival:	n/a
6	chr7:87104724-87104774	SK-N-SH_RA	brain:	n/a
7	chr7:87105398-87105448	AoSMC	blood vessel:	n/a
8	chr7:87105416-87105466	NB4	blood:	n/a
9	chr7:87103624-87103674	PrEC	prostate:	n/a
10	chr7:87105398-87105448	IMR90	lung:	fetal
11	chr7:87104879-87104929	HRPEpiC	eye:	n/a
12	chr7:87103624-87103674	NH-A	brain:	n/a
13	chr7:87104932-87104982	NT2-D1	testis:	n/a
14	chr7:87104879-87104929	HRE	kidney:	n/a
15	chr7:87105416-87105466	GM19239	blood:	n/a
16	chr7:87105416-87105466	SKMC	muscle:	n/a
17	chr7:87104879-87104929	RPTEC	kidney:	n/a
18	chr7:87105022-87105072	A549	lung:	n/a
19	chr7:87093634-87093684	HCM	heart:	n/a
20	chr7:87093634-87093684	HEEpiC	esophagus:	n/a
21	chr7:87104724-87104774	SK-N-SH	brain:	n/a
22	chr7:87105216-87105266	AG04450	lung:	fetal
23	chr7:87102261-87102311	HIPEpiC	eye:	n/a
24	chr7:87103624-87103674	ECC-1	luminal epithelium:	n/a
25	chr7:87093634-87093684	NHDF-neo	bronchial:	n/a
26	chr7:87104879-87104929	IMR90	lung:	fetal
27	chr7:87105022-87105072	LNCaP	prostate:	n/a
28	chr7:87104879-87104929	GM06990	blood:	n/a
29	chr7:87104932-87104982	LNCaP	prostate:	n/a
30	chr7:87105398-87105448	HUVEC	blood vessel:	n/a
31	chr7:87105293-87105343	AG04450	lung:	fetal
32	chr7:87105416-87105466	NH-A	brain:	n/a
33	chr7:87104932-87104982	Hela-S3	cervix:	n/a
34	chr7:87105022-87105072	HAEpiC	amniotic membrane:	n/a
35	chr7:87105398-87105448	HCT-116	colon:	n/a
36	chr7:87105022-87105072	AG09309	skin:	n/a
37	chr7:87103624-87103674	PANC-1	pancreas:	n/a
38	chr7:87102261-87102311	HEEpiC	esophagus:	n/a
39	chr7:87105216-87105266	SK-N-MC	brain:	n/a
40	chr7:87105216-87105266	MCF10A-Er-Src	breast:	n/a
41	chr7:87105416-87105466	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:87105398-87105448	HepG2	liver:	n/a
43	chr7:87102261-87102311	SK-N-MC	brain:	n/a
44	chr7:87104724-87104774	NH-A	brain:	n/a
45	chr7:87104879-87104929	HCT-116	colon:	n/a
46	chr7:87105398-87105448	MCF10A-Er-Src	breast:	n/a
47	chr7:87105022-87105072	GM12878	blood:	n/a
48	chr7:87103624-87103674	GM12892	blood:	n/a
49	chr7:87105416-87105466	RPTEC	kidney:	n/a
50	chr7:87102261-87102311	HRCEpiC	kidney:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:86848248..86850327-chr7:87074296..87076315,2	MCF-7	breast:
2	chr7:87051942..87054838-chr7:87071863..87073802,2	K562	blood:
3	chr7:87075903..87078103-chr7:87080060..87082449,2	K562	blood:
4	chr7:87073633..87076529-chr7:87078114..87081650,4	K562	blood:
5	chr7:87075903..87078103-chr7:87080060..87082449,2	K562	blood:
6	chr7:87105847..87108201-chr7:87108317..87110707,2	K562	blood:
7	chr7:86972942..86975537-chr7:87069538..87072015,2	MCF-7	breast:
8	chr7:87043780..87045715-chr7:87084104..87086345,2	MCF-7	breast:
9	chr7:87064330..87066764-chr7:87067722..87070554,3	K562	blood:
10	chr7:87073633..87076529-chr7:87078114..87081650,4	K562	blood:
11	chr7:86568193..86568776-chr7:87081301..87082150,2	MCF-7	breast:
12	chr7:87060366..87063144-chr7:87081442..87083012,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CROT-1	chr7:87105081-87107196	NONHSAT121834

No data

Variant related genes	Relation type
ABCB4	TF binding region
ABCB4	CpG island
ENSG00000005471	chromatin interactions
ENSG00000182165	chromatin interactions
ENSG00000005469	chromatin interactions
ENSG00000135185	chromatin interactions

Extended variants
information (count: 1397 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs31675	chr7:87069758-87069759	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557588658	chr7:87069766-87069767	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs575897289	chr7:87069783-87069784	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs536232867	chr7:87069799-87069800	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs554637288	chr7:87069827-87069828	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs31676	chr7:87069880-87069881	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs571415336	chr7:87069911-87069912	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372998981	chr7:87069923-87069924	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs374958970	chr7:87069939-87069940	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs111569203	chr7:87069967-87069968	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs369105736	chr7:87070041-87070042	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11768036	chr7:87070089-87070090	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs11767995	chr7:87070096-87070097	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs144857113	chr7:87070102-87070103	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373379133	chr7:87070125-87070126	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs542590454	chr7:87070141-87070142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs45487294	chr7:87070147-87070148	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs45447995	chr7:87070217-87070218	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs45560434	chr7:87070220-87070221	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs546651835	chr7:87070247-87070248	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs377439413	chr7:87070266-87070267	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs45533331	chr7:87070298-87070299	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs184036543	chr7:87070299-87070300	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs45541342	chr7:87070301-87070302	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569516957	chr7:87070320-87070321	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188592077	chr7:87070355-87070356	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs555320667	chr7:87070383-87070384	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs564878697	chr7:87070433-87070434	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533780102	chr7:87070487-87070488	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs193166661	chr7:87070494-87070495	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11971900	chr7:87070557-87070558	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs544380594	chr7:87070649-87070650	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370186709	chr7:87070723-87070724	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs372408612	chr7:87070724-87070725	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs367689432	chr7:87070725-87070726	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs139243442	chr7:87070748-87070749	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs556115015	chr7:87070763-87070764	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550973559	chr7:87070795-87070796	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs562984312	chr7:87070814-87070815	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs184228171	chr7:87070908-87070909	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs188637876	chr7:87070909-87070910	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs45484095	chr7:87070944-87070945	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs191600418	chr7:87070981-87070982	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540278428	chr7:87071051-87071052	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs35183818	chr7:87071058-87071059	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547913880	chr7:87071103-87071104	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs45624341	chr7:87071112-87071113	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs45545433	chr7:87071121-87071122	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs569322355	chr7:87071243-87071244	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530332021	chr7:87071302-87071303	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:602 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86980000-87085600	Weak transcription	Right Ventricle	heart
2	chr7:87019800-87079400	Strong transcription	Liver	Liver
3	chr7:87024800-87093200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:87040800-87072400	Weak transcription	Aorta	Aorta
5	chr7:87040800-87085600	Weak transcription	Psoas Muscle	Psoas
6	chr7:87047000-87078000	Strong transcription	Primary B cells from cord blood	blood
7	chr7:87051200-87085600	Weak transcription	Fetal Heart	heart
8	chr7:87052200-87072000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:87055800-87075000	Weak transcription	GM12878-XiMat	blood
10	chr7:87056200-87075200	Strong transcription	Primary B cells from peripheral blood	blood
11	chr7:87062200-87070400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr7:87064600-87077800	Weak transcription	Spleen	Spleen
13	chr7:87065000-87077800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:87066800-87072000	Weak transcription	HepG2	liver
15	chr7:87066800-87085600	Weak transcription	Left Ventricle	heart
16	chr7:87069200-87071800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr7:87069400-87071800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:87070400-87072800	Strong transcription	Skeletal Muscle Male	skeletal muscle
19	chr7:87071800-87072800	Strong transcription	Skeletal Muscle Female	skeletal muscle
20	chr7:87071800-87073200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:87072000-87073800	Strong transcription	HepG2	liver
22	chr7:87072400-87072800	Genic enhancers	Aorta	Aorta
23	chr7:87072600-87073600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:87072800-87077800	Weak transcription	Aorta	Aorta
25	chr7:87072800-87079000	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr7:87072800-87079200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr7:87073200-87087000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:87073800-87076400	Weak transcription	HepG2	liver
29	chr7:87074200-87074600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:87074600-87079000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:87075000-87075600	Enhancers	GM12878-XiMat	blood
32	chr7:87075200-87075600	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr7:87075200-87075600	Genic enhancers	Primary B cells from peripheral blood	blood
34	chr7:87075600-87081800	Weak transcription	GM12878-XiMat	blood
35	chr7:87075600-87094800	Strong transcription	Primary B cells from peripheral blood	blood
36	chr7:87076400-87081600	Strong transcription	HepG2	liver
37	chr7:87076600-87077000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr7:87076800-87077200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:87077000-87078400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr7:87077600-87078000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:87077600-87078000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:87077600-87078000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr7:87077800-87078000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:87077800-87078000	ZNF genes & repeats	Aorta	Aorta
45	chr7:87077800-87078000	Enhancers	Spleen	Spleen
46	chr7:87077800-87078200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:87077800-87078200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:87078000-87079000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:87078000-87079000	Weak transcription	Primary B cells from cord blood	blood
50	chr7:87078000-87087400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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