Variant report

Variant	nsv888679
Chromosome Location	chr7:87057699-87101407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:389)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

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	ATF1	chr7:87080871-87080985	K562	blood:	n/a	n/a
3	ATF1	chr7:87068362-87068484	K562	blood:	n/a	n/a
4	ATF2	chr7:87075213-87075701	GM12878	blood:	n/a	n/a
5	ATF2	chr7:87075193-87075772	GM12878	blood:	n/a	n/a
6	BACH1	chr7:87094518-87094660	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr7:87075232-87075613	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:87075212-87075653	GM12878	blood:	n/a	chr7:87075396-87075405
9	BCL11A	chr7:87075188-87075625	GM12878	blood:	n/a	chr7:87075396-87075405
10	BHLHE40	chr7:87093399-87093797	HepG2	liver:	n/a	n/a
11	BHLHE40	chr7:87075261-87075645	GM12878	blood:	n/a	n/a
12	BRCA1	chr7:87093351-87093701	HepG2	liver:	n/a	n/a
13	BRCA1	chr7:87065015-87065221	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr7:87089363-87089563	K562	blood:	n/a	n/a
15	CEBPB	chr7:87077625-87077807	HepG2	liver:	n/a	chr7:87077714-87077727
16	CEBPB	chr7:87093392-87093696	HepG2	liver:	n/a	n/a
17	CEBPD	chr7:87094462-87094862	HepG2	liver:	n/a	n/a
18	CHD2	chr7:87093418-87093639	HepG2	liver:	n/a	n/a
19	CHD2	chr7:87094469-87094656	HepG2	liver:	n/a	n/a
20	CHD2	chr7:87088175-87088219	K562	blood:	n/a	n/a
21	CHD2	chr7:87094526-87094716	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr7:87075152-87075611	GM12878	blood:	n/a	n/a
23	CREB1	chr7:87075045-87075699	GM12878	blood:	n/a	n/a
24	CTCF	chr7:87081693-87081853	HepG2	liver:	n/a	n/a
25	CTCF	chr7:87081780-87081930	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr7:87081449-87082122	A549	lung:	n/a	n/a
27	CTCF	chr7:87081700-87081850	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr7:87081657-87081912	IMR90	lung:	n/a	n/a
29	CTCF	chr7:87094640-87094790	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:87081700-87081850	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr7:87077700-87077850	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr7:87081680-87081830	SAEC	small airway:	n/a	n/a
33	CTCF	chr7:87081511-87082024	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:87094710-87094790	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:87069044-87069073	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:87081640-87081790	HEK293	kidney:	n/a	n/a
37	CTCF	chr7:87081580-87081850	RPTEC	kidney:	n/a	n/a
38	CTCF	chr7:87081760-87081910	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr7:87081728-87081848	Gliobla	brain:	n/a	n/a
40	CTCF	chr7:87094720-87094870	HEK293	kidney:	n/a	n/a
41	CTCF	chr7:87081740-87081890	NHLF	lung:	n/a	n/a
42	CTCF	chr7:87081721-87081874	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr7:87081700-87081850	AG04449	skin:	n/a	n/a
44	CTCF	chr7:87081712-87081869	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:87081724-87081860	HepG2	liver:	n/a	n/a
46	CTCF	chr7:87081486-87082027	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:87094620-87094770	HepG2	liver:	n/a	n/a
48	CTCF	chr7:87094660-87094810	A549	lung:	n/a	n/a
49	CTCF	chr7:87094773-87094787	HepG2	liver:	n/a	n/a
50	CTCF	chr7:87081720-87081870	AG10803	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:87093634-87093684	HepG2	liver:	n/a
2	chr7:87093634-87093684	MCF-7	breast:	n/a
3	chr7:87093634-87093684	HRCEpiC	kidney:	n/a
4	chr7:87093634-87093684	SK-N-SH_RA	brain:	n/a
5	chr7:87093634-87093684	HCT-116	colon:	n/a
6	chr7:87093634-87093684	NH-A	brain:	n/a
7	chr7:87093634-87093684	A549	lung:	n/a
8	chr7:87093634-87093684	BJ	skin:	n/a
9	chr7:87093634-87093684	HNPCEpiC	eye:	n/a
10	chr7:87093634-87093684	HUVEC	blood vessel:	n/a
11	chr7:87093634-87093684	SK-N-MC	brain:	n/a
12	chr7:87093634-87093684	Caco-2	colon:	n/a
13	chr7:87093634-87093684	H1-hESC	embryonic stem cell:	embryo
14	chr7:87093634-87093684	NHBE	bronchial:	n/a
15	chr7:87093634-87093684	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:87093634-87093684	Hepatocyte	liver:	n/a
17	chr7:87093634-87093684	Hela-S3	cervix:	n/a
18	chr7:87093634-87093684	GM19239	blood:	n/a
19	chr7:87093634-87093684	GM12878	blood:	n/a
20	chr7:87093634-87093684	CMK	blood:	n/a
21	chr7:87093634-87093684	HCM	heart:	n/a
22	chr7:87093634-87093684	SKMC	muscle:	n/a
23	chr7:87093634-87093684	LNCaP	prostate:	n/a
24	chr7:87093634-87093684	AG10803	skin:	n/a
25	chr7:87093634-87093684	NT2-D1	testis:	n/a
26	chr7:87093634-87093684	GM06990	blood:	n/a
27	chr7:87093634-87093684	ProgFib	skin:	n/a
28	chr7:87093634-87093684	HIPEpiC	eye:	n/a
29	chr7:87093634-87093684	NB4	blood:	n/a
30	chr7:87093634-87093684	Jurkat	blood:	n/a
31	chr7:87093634-87093684	SAEC	small airway:	n/a
32	chr7:87093634-87093684	GM12892	blood:	n/a
33	chr7:87093634-87093684	NHDF-neo	bronchial:	n/a
34	chr7:87093634-87093684	AoSMC	blood vessel:	n/a
35	chr7:87093634-87093684	HEK293	kidney:	embryo
36	chr7:87093634-87093684	U87	brain:	n/a
37	chr7:87093634-87093684	ovcar-3	ovarian:	n/a
38	chr7:87093634-87093684	BE2_C	brain:	n/a
39	chr7:87093634-87093684	T-47D	breast:	n/a
40	chr7:87093634-87093684	PFSK-1	brain:	n/a
41	chr7:87093634-87093684	GM12891	blood:	n/a
42	chr7:87093634-87093684	SK-N-SH	brain:	n/a
43	chr7:87093634-87093684	HMEC	breast:	n/a
44	chr7:87093634-87093684	PANC-1	pancreas:	n/a
45	chr7:87093634-87093684	MCF10A-Er-Src	breast:	n/a
46	chr7:87093634-87093684	HEEpiC	esophagus:	n/a
47	chr7:87093634-87093684	HRE	kidney:	n/a
48	chr7:87093634-87093684	HCPEpiC	choroid plexus:	n/a
49	chr7:87093634-87093684	AG09309	skin:	n/a
50	chr7:87093634-87093684	HL-60	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:87075903..87078103-chr7:87080060..87082449,2	K562	blood:
2	chr7:87058152..87059942-chr7:87060909..87063593,2	MCF-7	breast:
3	chr7:87073633..87076529-chr7:87078114..87081650,4	K562	blood:
4	chr7:87064944..87067466-chr7:87067483..87069471,2	MCF-7	breast:
5	chr7:86568193..86568776-chr7:87081301..87082150,2	MCF-7	breast:
6	chr7:87064330..87066764-chr7:87067722..87070554,3	K562	blood:
7	chr7:86848274..86850901-chr7:87061443..87064403,3	MCF-7	breast:
8	chr7:87064944..87067466-chr7:87067483..87069471,2	MCF-7	breast:
9	chr7:86972942..86975537-chr7:87069538..87072015,2	MCF-7	breast:
10	chr7:86973632..86975242-chr7:87056633..87058680,2	MCF-7	breast:
11	chr7:87064330..87066764-chr7:87067722..87070554,3	K562	blood:
12	chr7:86848248..86850327-chr7:87074296..87076315,2	MCF-7	breast:
13	chr7:87056485..87058052-chr7:87059900..87061514,2	K562	blood:
14	chr7:87051942..87054838-chr7:87071863..87073802,2	K562	blood:
15	chr7:87059548..87061142-chr7:87062685..87064346,3	K562	blood:
16	chr7:87060366..87063144-chr7:87081442..87083012,2	MCF-7	breast:
17	chr7:87048856..87050665-chr7:87056840..87059034,2	MCF-7	breast:
18	chr7:87043780..87045715-chr7:87084104..87086345,2	MCF-7	breast:
19	chr7:87075903..87078103-chr7:87080060..87082449,2	K562	blood:
20	chr7:87058152..87059942-chr7:87060909..87063593,2	MCF-7	breast:
21	chr7:87073633..87076529-chr7:87078114..87081650,4	K562	blood:

No data

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

Extended variants
information (count: 1593 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6956661	chr7:87057699-87057700	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553788726	chr7:87057743-87057744	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs142336600	chr7:87057771-87057772	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs77202119	chr7:87057780-87057781	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs545973503	chr7:87057814-87057815	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs150774798	chr7:87057838-87057839	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs575913001	chr7:87057894-87057895	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs537792944	chr7:87057901-87057902	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs138082355	chr7:87057910-87057911	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs180949315	chr7:87057918-87057919	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs45451204	chr7:87057938-87057939	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs45506995	chr7:87058048-87058049	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs369398287	chr7:87058054-87058055	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530066983	chr7:87058070-87058071	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs17149586	chr7:87058110-87058111	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs528178549	chr7:87058152-87058153	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs45482600	chr7:87058158-87058159	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186001731	chr7:87058194-87058195	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs527824682	chr7:87058232-87058233	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs191028247	chr7:87058233-87058234	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143755218	chr7:87058393-87058394	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs45462893	chr7:87058418-87058419	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs550462474	chr7:87058439-87058440	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs568670290	chr7:87058474-87058475	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs553923830	chr7:87058524-87058525	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535382634	chr7:87058546-87058547	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs45466200	chr7:87058570-87058571	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs183207326	chr7:87058689-87058690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539191556	chr7:87058716-87058717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115356434	chr7:87058726-87058727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187530482	chr7:87058879-87058880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76495580	chr7:87058904-87058905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555200210	chr7:87058974-87058975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573901907	chr7:87059013-87059014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574979344	chr7:87059059-87059060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560321612	chr7:87059060-87059061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527765184	chr7:87059067-87059068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546292708	chr7:87059077-87059078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140591958	chr7:87059137-87059138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs31670	chr7:87059164-87059165	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs550399666	chr7:87059182-87059183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542389355	chr7:87059215-87059216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373766488	chr7:87059220-87059221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369943105	chr7:87059229-87059230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201172032	chr7:87059230-87059231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs57819699	chr7:87059231-87059232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73705206	chr7:87059232-87059233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550243869	chr7:87059242-87059243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58654815	chr7:87059243-87059244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565565182	chr7:87059268-87059269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

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	chr7:87037400-87064800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:87040800-87072400	Weak transcription	Aorta	Aorta
6	chr7:87040800-87085600	Weak transcription	Psoas Muscle	Psoas
7	chr7:87044600-87064600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:87047000-87078000	Strong transcription	Primary B cells from cord blood	blood
9	chr7:87050800-87059800	Weak transcription	Left Ventricle	heart
10	chr7:87051200-87085600	Weak transcription	Fetal Heart	heart
11	chr7:87052200-87072000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr7:87054600-87059600	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr7:87055800-87060200	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr7:87055800-87075000	Weak transcription	GM12878-XiMat	blood
15	chr7:87056200-87075200	Strong transcription	Primary B cells from peripheral blood	blood
16	chr7:87057600-87061200	Strong transcription	HepG2	liver
17	chr7:87059600-87061200	Strong transcription	Skeletal Muscle Female	skeletal muscle
18	chr7:87059800-87061000	Strong transcription	Left Ventricle	heart
19	chr7:87060200-87062200	Strong transcription	Skeletal Muscle Male	skeletal muscle
20	chr7:87060800-87061000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:87061000-87066200	Weak transcription	Left Ventricle	heart
22	chr7:87061200-87064000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr7:87061200-87064800	Weak transcription	HepG2	liver
24	chr7:87062200-87070400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr7:87064000-87069200	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr7:87064600-87065000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:87064600-87065000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:87064600-87065600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:87064600-87077800	Weak transcription	Spleen	Spleen
30	chr7:87064800-87065200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr7:87064800-87065200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:87064800-87065400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:87064800-87065400	Enhancers	NH-A	brain
34	chr7:87064800-87065400	Enhancers	NHDF-Ad	bronchial
35	chr7:87064800-87066800	Strong transcription	HepG2	liver
36	chr7:87065000-87077800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:87065200-87067600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr7:87065200-87068000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:87066200-87066800	Strong transcription	Left Ventricle	heart
40	chr7:87066800-87072000	Weak transcription	HepG2	liver
41	chr7:87066800-87085600	Weak transcription	Left Ventricle	heart
42	chr7:87068000-87069400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:87068800-87069200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:87068800-87069200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:87069000-87069600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:87069200-87071800	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr7:87069400-87071800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:87070400-87072800	Strong transcription	Skeletal Muscle Male	skeletal muscle
49	chr7:87071800-87072800	Strong transcription	Skeletal Muscle Female	skeletal muscle
50	chr7:87071800-87073200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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