Variant report

Variant	nsv970916
Chromosome Location	chr7:100890266-100893923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:100893501-100893960	GM12878	blood:	n/a	n/a
2	BATF	chr7:100893617-100893947	GM12878	blood:	n/a	n/a
3	BATF	chr7:100893550-100893987	GM12878	blood:	n/a	n/a
4	CTCF	chr7:100891560-100891710	GM12864	blood:	n/a	n/a
5	CTCF	chr7:100891540-100891690	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr7:100891440-100891590	HCT-116	colon:	n/a	n/a
7	CTCF	chr7:100891460-100891610	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr7:100891594-100891647	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr7:100891460-100891610	GM12875	blood:	n/a	n/a
10	CTCF	chr7:100891500-100891650	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr7:100891520-100891670	HEK293	kidney:	n/a	n/a
12	CTCF	chr7:100891520-100891670	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr7:100891460-100891610	GM12870	blood:	n/a	n/a
14	CTCF	chr7:100891500-100891650	HepG2	liver:	n/a	n/a
15	CTCF	chr7:100891480-100891630	HAc	cerebellar:	n/a	n/a
16	CTCF	chr7:100891580-100891730	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr7:100891420-100891570	GM12872	blood:	n/a	n/a
18	CTCF	chr7:100891480-100891630	K562	blood:	n/a	n/a
19	CTCF	chr7:100891500-100891650	AG04450	lung:	n/a	n/a
20	CTCF	chr7:100891520-100891670	GM12873	blood:	n/a	n/a
21	CTCF	chr7:100891580-100891730	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr7:100891540-100891690	GM12872	blood:	n/a	n/a
23	CTCF	chr7:100891540-100891690	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:100891480-100891630	GM12878	blood:	n/a	n/a
25	CTCF	chr7:100891480-100891630	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr7:100891460-100891610	HMF	breast:	n/a	n/a
27	CTCF	chr7:100891500-100891650	GM12868	blood:	n/a	n/a
28	CTCF	chr7:100891480-100891630	A549	lung:	n/a	n/a
29	CTCF	chr7:100891520-100891670	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:100891460-100891610	GM12873	blood:	n/a	n/a
31	CTCF	chr7:100891500-100891650	HCT-116	colon:	n/a	n/a
32	EBF1	chr7:100890077-100890361	GM12878	blood:	n/a	chr7:100890237-100890248
33	EBF1	chr7:100893657-100894015	GM12878	blood:	n/a	chr7:100893853-100893862
34	EBF1	chr7:100893633-100893945	GM12878	blood:	n/a	chr7:100893853-100893862
35	EBF1	chr7:100890097-100890355	GM12878	blood:	n/a	chr7:100890237-100890248
36	EBF1	chr7:100893648-100893961	GM12878	blood:	n/a	chr7:100893853-100893862
37	FOXA2	chr7:100891437-100891738	A549	lung:	n/a	chr7:100891475-100891487
38	FOXA2	chr7:100891477-100891659	HepG2	liver:	n/a	n/a
39	IRF4	chr7:100893565-100893976	GM12878	blood:	n/a	n/a
40	MTA3	chr7:100893534-100894039	GM12878	blood:	n/a	n/a
41	NFE2	chr7:100893639-100893692	GM12878	blood:	n/a	n/a
42	NFIC	chr7:100893490-100893944	GM12878	blood:	n/a	n/a
43	PML	chr7:100893559-100894085	GM12878	blood:	n/a	n/a
44	POLR2A	chr7:100889866-100890546	GM12892	blood:	n/a	n/a
45	POLR2A	chr7:100889551-100890512	K562	blood:	n/a	n/a
46	POLR2A	chr7:100892431-100892519	HepG2	liver:	n/a	n/a
47	POLR2A	chr7:100891001-100891015	K562	blood:	n/a	n/a
48	POLR2A	chr7:100891573-100891626	HepG2	liver:	n/a	n/a
49	POLR2A	chr7:100891405-100891506	HepG2	liver:	n/a	n/a
50	POLR2A	chr7:100889978-100890373	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100890711-100890761	K562	blood:	n/a
2	chr7:100890711-100890761	HCPEpiC	choroid plexus:	n/a
3	chr7:100892699-100892749	AG10803	skin:	n/a
4	chr7:100890711-100890761	NHDF-neo	bronchial:	n/a
5	chr7:100892699-100892749	Caco-2	colon:	n/a
6	chr7:100892699-100892749	HMEC	breast:	n/a
7	chr7:100890711-100890761	HMEC	breast:	n/a
8	chr7:100892699-100892749	AG04449	skin:	fetal
9	chr7:100890711-100890761	GM12892	blood:	n/a
10	chr7:100890711-100890761	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:100892699-100892749	IMR90	lung:	fetal
12	chr7:100892699-100892749	HCPEpiC	choroid plexus:	n/a
13	chr7:100890711-100890761	HepG2	liver:	n/a
14	chr7:100892699-100892749	HRCEpiC	kidney:	n/a
15	chr7:100890711-100890761	SKMC	muscle:	n/a
16	chr7:100892699-100892749	GM06990	blood:	n/a
17	chr7:100890711-100890761	GM12891	blood:	n/a
18	chr7:100892699-100892749	HCM	heart:	n/a
19	chr7:100892699-100892749	HNPCEpiC	eye:	n/a
20	chr7:100892699-100892749	AG04450	lung:	fetal
21	chr7:100892699-100892749	A549	lung:	n/a
22	chr7:100890711-100890761	AG09319	gingival:	n/a
23	chr7:100890711-100890761	A549	lung:	n/a
24	chr7:100892699-100892749	ovcar-3	ovarian:	n/a
25	chr7:100890711-100890761	ovcar-3	ovarian:	n/a
26	chr7:100890711-100890761	AG10803	skin:	n/a
27	chr7:100890711-100890761	AG09309	skin:	n/a
28	chr7:100890711-100890761	T-47D	breast:	n/a
29	chr7:100892699-100892749	SK-N-SH_RA	brain:	n/a
30	chr7:100892699-100892749	PANC-1	pancreas:	n/a
31	chr7:100892699-100892749	ProgFib	skin:	n/a
32	chr7:100892699-100892749	NHBE	bronchial:	n/a
33	chr7:100892699-100892749	PFSK-1	brain:	n/a
34	chr7:100890711-100890761	ProgFib	skin:	n/a
35	chr7:100890711-100890761	HNPCEpiC	eye:	n/a
36	chr7:100890711-100890761	LNCaP	prostate:	n/a
37	chr7:100890711-100890761	IMR90	lung:	fetal
38	chr7:100890711-100890761	ECC-1	luminal epithelium:	n/a
39	chr7:100892699-100892749	BJ	skin:	n/a
40	chr7:100890711-100890761	Caco-2	colon:	n/a
41	chr7:100892699-100892749	HL-60	blood:	n/a
42	chr7:100892699-100892749	HEK293	kidney:	embryo
43	chr7:100892699-100892749	SK-N-MC	brain:	n/a
44	chr7:100892699-100892749	MCF-7	breast:	n/a
45	chr7:100890711-100890761	H1-hESC	embryonic stem cell:	embryo
46	chr7:100890711-100890761	NH-A	brain:	n/a
47	chr7:100892699-100892749	HepG2	liver:	n/a
48	chr7:100892699-100892749	CMK	blood:	n/a
49	chr7:100890711-100890761	HEEpiC	esophagus:	n/a
50	chr7:100890711-100890761	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:100858946..100862708-chr7:100892771..100897292,5	MCF-7	breast:
2	chr7:100804987..100809107-chr7:100886873..100890454,4	MCF-7	breast:
3	chr7:100859409..100862433-chr7:100893851..100895703,4	K562	blood:
4	chr7:100860572..100862632-chr7:100892717..100896862,3	K562	blood:
5	chr7:100888737..100891690-chr7:100902094..100903966,2	MCF-7	breast:
6	chr7:100878550..100881686-chr7:100893113..100895457,3	MCF-7	breast:
7	chr7:100888574..100891028-chr7:100920575..100922314,2	MCF-7	breast:
8	chr7:100883935..100885996-chr7:100893008..100895659,3	K562	blood:
9	chr7:100858478..100862757-chr7:100884994..100890276,15	MCF-7	breast:
10	chr7:100859374..100863045-chr7:100885733..100890781,8	K562	blood:
11	chr7:100892265..100894287-chr7:100903598..100905585,2	K562	blood:
12	chr7:100859400..100864017-chr7:100886115..100890578,15	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLDN15-1	chr7:100893301-100895582	NONHSAT122458

No data

Variant related genes	Relation type
FIS1	TF binding region
FIS1	CpG island
ENSG00000106400	chromatin interactions
ENSG00000128564	chromatin interactions
ENSG00000214253	chromatin interactions
ENSG00000106404	chromatin interactions
ENSG00000106397	chromatin interactions

Extended variants
information (count: 138 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:138 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547471902	chr7:100890272-100890273	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs565877106	chr7:100890322-100890323	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs191915536	chr7:100890372-100890373	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs146619070	chr7:100890378-100890379	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs148840045	chr7:100890489-100890490	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs559958005	chr7:100890521-100890522	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs527568404	chr7:100890575-100890576	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs199769501	chr7:100890578-100890579	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs6953615	chr7:100890579-100890580	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs201782281	chr7:100890580-100890581	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs67265371	chr7:100890581-100890582	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs61527805	chr7:100890582-100890583	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs35434716	chr7:100890583-100890584	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529295708	chr7:100890616-100890617	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs372230907	chr7:100890619-100890620	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs2410799	chr7:100890620-100890621	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs145188251	chr7:100890631-100890632	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs146372776	chr7:100890635-100890636	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs569885303	chr7:100890654-100890655	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs35689623	chr7:100890709-100890710	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs539979036	chr7:100890712-100890713	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs537357894	chr7:100890750-100890751	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs551986854	chr7:100890820-100890821	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs567099147	chr7:100890850-100890851	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs201112811	chr7:100890913-100890914	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs556041806	chr7:100891010-100891011	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs573517568	chr7:100891064-100891065	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs556056893	chr7:100891112-100891113	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs555935256	chr7:100891127-100891128	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181807507	chr7:100891147-100891148	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538854004	chr7:100891162-100891163	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150924386	chr7:100891174-100891175	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11765891	chr7:100891263-100891264	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12333731	chr7:100891272-100891273	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs368541409	chr7:100891285-100891286	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372916605	chr7:100891287-100891288	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542513396	chr7:100891299-100891300	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369084040	chr7:100891301-100891302	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10953330	chr7:100891308-100891309	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186226079	chr7:100891313-100891314	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562904031	chr7:100891356-100891357	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189042314	chr7:100891368-100891369	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113858398	chr7:100891396-100891397	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
44	rs534811906	chr7:100891439-100891440	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs376280284	chr7:100891448-100891449	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs567038088	chr7:100891515-100891516	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs575544842	chr7:100891547-100891548	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs534413665	chr7:100891569-100891570	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs10249192	chr7:100891571-100891572	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs567948303	chr7:100891578-100891579	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19214233	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100888600-100893800	Weak transcription	Gastric	stomach
2	chr7:100888800-100890800	Weak transcription	Primary T cells from cord blood	blood
3	chr7:100888800-100892200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:100888800-100893600	Weak transcription	HUVEC	blood vessel
5	chr7:100888800-100894600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:100888800-100894600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:100888800-100894600	Weak transcription	Aorta	Aorta
8	chr7:100888800-100894600	Weak transcription	Esophagus	oesophagus
9	chr7:100888800-100894600	Weak transcription	Fetal Kidney	kidney
10	chr7:100889000-100890400	Enhancers	Fetal Brain Female	brain
11	chr7:100889000-100890400	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr7:100889000-100890800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr7:100889000-100892000	Weak transcription	Primary B cells from cord blood	blood
14	chr7:100889000-100892600	Weak transcription	Lung	lung
15	chr7:100889000-100893600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr7:100889000-100893800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr7:100889000-100893800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr7:100889000-100893800	Weak transcription	Colonic Mucosa	Colon
19	chr7:100889000-100893800	Weak transcription	Right Atrium	heart
20	chr7:100889000-100894200	Weak transcription	Osteobl	bone
21	chr7:100889000-100894400	Weak transcription	HSMM	muscle
22	chr7:100889000-100894600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr7:100889000-100894600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr7:100889000-100894600	Weak transcription	HSMMtube	muscle
25	chr7:100889000-100894600	Weak transcription	NH-A	brain
26	chr7:100889200-100890400	Genic enhancers	Brain Substantia Nigra	brain
27	chr7:100889200-100890800	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr7:100889200-100890800	Weak transcription	Fetal Muscle Trunk	muscle
29	chr7:100889200-100890800	Weak transcription	Fetal Muscle Leg	muscle
30	chr7:100889200-100890800	Weak transcription	Left Ventricle	heart
31	chr7:100889200-100890800	Weak transcription	Rectal Smooth Muscle	rectum
32	chr7:100889200-100891800	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr7:100889200-100891800	Strong transcription	GM12878-XiMat	blood
34	chr7:100889200-100892400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr7:100889200-100892800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:100889200-100893600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr7:100889200-100893600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:100889200-100893600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr7:100889200-100893600	Weak transcription	Brain Hippocampus Middle	brain
40	chr7:100889200-100893600	Strong transcription	Fetal Stomach	stomach
41	chr7:100889200-100893600	Weak transcription	NHDF-Ad	bronchial
42	chr7:100889200-100893800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr7:100889200-100893800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr7:100889200-100893800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr7:100889200-100893800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr7:100889200-100893800	Weak transcription	Fetal Heart	heart
47	chr7:100889200-100893800	Weak transcription	Ovary	ovary
48	chr7:100889200-100893800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr7:100889200-100893800	Weak transcription	NHLF	lung
50	chr7:100889200-100894400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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