Variant report

Variant	esv1811927
Chromosome Location	chr7:99904607-99922335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:176)
CpG islands
(count:366)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:176 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:99922294-99922458	GM12878	blood:	n/a	n/a
2	BATF	chr7:99921263-99921667	GM12878	blood:	n/a	n/a
3	BATF	chr7:99915667-99915855	GM12878	blood:	n/a	n/a
4	BATF	chr7:99921172-99921850	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:99922169-99922589	GM12878	blood:	n/a	chr7:99922216-99922225
6	BCL11A	chr7:99921092-99921910	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:99915597-99915943	GM12878	blood:	n/a	chr7:99915669-99915678
8	BCL11A	chr7:99921061-99921746	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:99915598-99915786	GM12878	blood:	n/a	chr7:99915669-99915678
10	BHLHE40	chr7:99918692-99918940	HepG2	liver:	n/a	n/a
11	EBF1	chr7:99922050-99922565	GM12878	blood:	n/a	chr7:99922279-99922288 chr7:99922279-99922288 chr7:99922278-99922289 chr7:99922279-99922289
12	EBF1	chr7:99922267-99922272	GM12878	blood:	n/a	n/a
13	EBF1	chr7:99919792-99920123	GM12878	blood:	n/a	n/a
14	EBF1	chr7:99921178-99921996	GM12878	blood:	n/a	n/a
15	EBF1	chr7:99904888-99905056	GM12878	blood:	n/a	n/a
16	EBF1	chr7:99921189-99921874	GM12878	blood:	n/a	n/a
17	EBF1	chr7:99922035-99922479	GM12878	blood:	n/a	chr7:99922279-99922288 chr7:99922279-99922288 chr7:99922278-99922289 chr7:99922279-99922289
18	EBF1	chr7:99918743-99919003	GM12878	blood:	n/a	n/a
19	EBF1	chr7:99915877-99916141	GM12878	blood:	n/a	n/a
20	EP300	chr7:99919834-99920074	GM12878	blood:	n/a	n/a
21	EP300	chr7:99921053-99921627	GM12878	blood:	n/a	n/a
22	EP300	chr7:99921232-99921538	GM12878	blood:	n/a	n/a
23	EP300	chr7:99918766-99918994	GM12878	blood:	n/a	n/a
24	EP300	chr7:99905052-99905213	GM12878	blood:	n/a	n/a
25	EP300	chr7:99921742-99921902	GM12878	blood:	n/a	n/a
26	EP300	chr7:99915777-99916098	GM12878	blood:	n/a	n/a
27	EP300	chr7:99921673-99922007	GM12878	blood:	n/a	n/a
28	EP300	chr7:99904894-99905235	GM12878	blood:	n/a	n/a
29	EP300	chr7:99918587-99919063	GM12878	blood:	n/a	n/a
30	FOSL2	chr7:99915631-99916059	HepG2	liver:	n/a	n/a
31	FOSL2	chr7:99921215-99921536	HepG2	liver:	n/a	n/a
32	FOSL2	chr7:99904948-99905235	HepG2	liver:	n/a	n/a
33	FOXM1	chr7:99921964-99922500	GM12878	blood:	n/a	n/a
34	GABPA	chr7:99905001-99905230	Hela-S3	cervix:	n/a	n/a
35	GATA2	chr7:99921148-99921402	K562	blood:	n/a	n/a
36	HEY1	chr7:99913433-99913669	K562	blood:	n/a	n/a
37	HEY1	chr7:99915599-99915795	K562	blood:	n/a	n/a
38	IRF4	chr7:99922256-99922572	GM12878	blood:	n/a	n/a
39	IRF4	chr7:99919841-99920180	GM12878	blood:	n/a	n/a
40	IRF4	chr7:99921088-99922075	GM12878	blood:	n/a	n/a
41	IRF4	chr7:99921036-99922083	GM12878	blood:	n/a	n/a
42	IRF4	chr7:99904902-99905329	GM12878	blood:	n/a	n/a
43	IRF4	chr7:99915527-99915967	GM12878	blood:	n/a	n/a
44	IRF4	chr7:99915577-99916202	GM12878	blood:	n/a	n/a
45	JUND	chr7:99918718-99918846	HepG2	liver:	n/a	n/a
46	NFIC	chr7:99921977-99922473	GM12878	blood:	n/a	n/a
47	NFIC	chr7:99921983-99922389	GM12878	blood:	n/a	n/a
48	NFIC	chr7:99915486-99915969	GM12878	blood:	n/a	n/a
49	NR2F2	chr7:99915613-99915872	K562	blood:	n/a	n/a
50	PAX5	chr7:99920984-99922569	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99912131-99912181	Hela-S3	cervix:	n/a
2	chr7:99905331-99905381	HAEpiC	amniotic membrane:	n/a
3	chr7:99904850-99904900	MCF10A-Er-Src	breast:	n/a
4	chr7:99905334-99905384	HRPEpiC	eye:	n/a
5	chr7:99905331-99905381	K562	blood:	n/a
6	chr7:99904875-99904925	HMEC	breast:	n/a
7	chr7:99904875-99904925	GM19239	blood:	n/a
8	chr7:99912131-99912181	GM12891	blood:	n/a
9	chr7:99918120-99918170	LNCaP	prostate:	n/a
10	chr7:99904850-99904900	GM12892	blood:	n/a
11	chr7:99904875-99904925	GM12892	blood:	n/a
12	chr7:99918120-99918170	HMEC	breast:	n/a
13	chr7:99912131-99912181	SK-N-MC	brain:	n/a
14	chr7:99912131-99912181	U87	brain:	n/a
15	chr7:99904850-99904900	HCM	heart:	n/a
16	chr7:99918120-99918170	NB4	blood:	n/a
17	chr7:99904850-99904900	SK-N-SH_RA	brain:	n/a
18	chr7:99918120-99918170	BJ	skin:	n/a
19	chr7:99904875-99904925	Caco-2	colon:	n/a
20	chr7:99904850-99904900	NT2-D1	testis:	n/a
21	chr7:99904850-99904900	NB4	blood:	n/a
22	chr7:99918120-99918170	A549	lung:	n/a
23	chr7:99904875-99904925	NHDF-neo	bronchial:	n/a
24	chr7:99918120-99918170	HL-60	blood:	n/a
25	chr7:99912131-99912181	NB4	blood:	n/a
26	chr7:99905334-99905384	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:99904875-99904925	LNCaP	prostate:	n/a
28	chr7:99904875-99904925	HRCEpiC	kidney:	n/a
29	chr7:99918120-99918170	MCF10A-Er-Src	breast:	n/a
30	chr7:99905334-99905384	CMK	blood:	n/a
31	chr7:99918120-99918170	GM12878	blood:	n/a
32	chr7:99912131-99912181	AoSMC	blood vessel:	n/a
33	chr7:99905334-99905384	MCF10A-Er-Src	breast:	n/a
34	chr7:99918120-99918170	RPTEC	kidney:	n/a
35	chr7:99905331-99905381	NH-A	brain:	n/a
36	chr7:99905331-99905381	NB4	blood:	n/a
37	chr7:99905334-99905384	U87	brain:	n/a
38	chr7:99905334-99905384	ovcar-3	ovarian:	n/a
39	chr7:99905331-99905381	H1-hESC	embryonic stem cell:	embryo
40	chr7:99918120-99918170	BE2_C	brain:	n/a
41	chr7:99905331-99905381	HEEpiC	esophagus:	n/a
42	chr7:99904850-99904900	AG04449	skin:	fetal
43	chr7:99912131-99912181	HIPEpiC	eye:	n/a
44	chr7:99918120-99918170	SK-N-SH	brain:	n/a
45	chr7:99905334-99905384	Jurkat	blood:	n/a
46	chr7:99904875-99904925	HCM	heart:	n/a
47	chr7:99905334-99905384	RPTEC	kidney:	n/a
48	chr7:99905334-99905384	K562	blood:	n/a
49	chr7:99905331-99905381	AG09309	skin:	n/a
50	chr7:99904875-99904925	CMK	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GATS-2	chr7:99913916-99914300	expReg_chr7_6439_-
2	lnc-GATS-1	chr7:99907941-99908299	expReg_chr7_6426_-

No data

Variant related genes	Relation type
SPDYE3	TF binding region
SPDYE3	CpG island

Extended variants
information (count: 499 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367782549	chr7:99904696-99904697	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs577809009	chr7:99904709-99904710	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs3991499	chr7:99904724-99904725	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs9784931	chr7:99904759-99904760	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs372284946	chr7:99904768-99904769	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs2405477	chr7:99904827-99904828	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs10262442	chr7:99904832-99904833	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs2405476	chr7:99904834-99904835	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554781976	chr7:99904840-99904841	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs183879448	chr7:99904859-99904860	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs572010769	chr7:99904873-99904874	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs2405473	chr7:99904885-99904886	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs188599114	chr7:99904909-99904910	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs560565985	chr7:99904949-99904950	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs191899061	chr7:99904967-99904968	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs3991498	chr7:99904969-99904970	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs184509800	chr7:99904992-99904993	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532071442	chr7:99905033-99905034	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs547974402	chr7:99905052-99905053	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs540105733	chr7:99905078-99905079	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs566116845	chr7:99905123-99905124	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536964656	chr7:99905142-99905143	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548884944	chr7:99905224-99905225	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs570093854	chr7:99905230-99905231	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs151094890	chr7:99905243-99905244	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558825627	chr7:99905288-99905289	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs577276513	chr7:99905303-99905304	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs139853451	chr7:99905321-99905322	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs111312383	chr7:99905325-99905326	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
30	rs571873525	chr7:99905349-99905350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542544978	chr7:99905379-99905380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554419053	chr7:99905400-99905401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143930404	chr7:99905453-99905454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543394302	chr7:99905456-99905457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146873825	chr7:99905458-99905459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs28680963	chr7:99905475-99905476	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs540737751	chr7:99905478-99905479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560026144	chr7:99905479-99905480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530296597	chr7:99905491-99905492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548946020	chr7:99905513-99905514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570356065	chr7:99905519-99905520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563626806	chr7:99905530-99905531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531190963	chr7:99905583-99905584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552543470	chr7:99905585-99905586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570727318	chr7:99905601-99905602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28401739	chr7:99905684-99905685	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs190175040	chr7:99905694-99905695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565564199	chr7:99905699-99905700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140844048	chr7:99905705-99905706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554482394	chr7:99905711-99905712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
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
Acute lymphoblastic leukemia	21339820	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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99870200-99916800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:99870200-99932800	Weak transcription	Ovary	ovary
3	chr7:99870400-99917000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:99870400-99917000	Weak transcription	Fetal Muscle Leg	muscle
5	chr7:99870400-99917600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:99870400-99923400	Weak transcription	Fetal Intestine Large	intestine
7	chr7:99870400-99932600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:99870600-99916800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:99870600-99923400	Weak transcription	Spleen	Spleen
10	chr7:99870600-99926200	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr7:99870600-99932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr7:99871000-99917000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr7:99871000-99923000	Weak transcription	Brain Germinal Matrix	brain
14	chr7:99874400-99932800	Weak transcription	Brain Angular Gyrus	brain
15	chr7:99880400-99917800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr7:99884400-99916000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:99887400-99932800	Weak transcription	Brain Anterior Caudate	brain
18	chr7:99889400-99915000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:99890200-99914200	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr7:99890400-99917000	Weak transcription	Fetal Brain Female	brain
21	chr7:99893600-99914200	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr7:99893600-99917000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr7:99893600-99917800	Weak transcription	Lung	lung
24	chr7:99893600-99918000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:99896400-99917000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:99896600-99924600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr7:99896600-99931800	Weak transcription	K562	blood
28	chr7:99897600-99933200	Weak transcription	Pancreas	Pancrea
29	chr7:99898000-99932800	Weak transcription	Brain Substantia Nigra	brain
30	chr7:99901200-99923400	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr7:99902000-99916800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:99902400-99914800	Weak transcription	Primary B cells from peripheral blood	blood
33	chr7:99902400-99914800	Weak transcription	Fetal Thymus	thymus
34	chr7:99902400-99915000	Weak transcription	Thymus	Thymus
35	chr7:99902800-99932800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr7:99903000-99916800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:99903200-99916800	Weak transcription	Fetal Intestine Small	intestine
38	chr7:99903400-99914800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:99903800-99918000	Weak transcription	Adipose Nuclei	Adipose
40	chr7:99904600-99905000	Strong transcription	Dnd41	blood
41	chr7:99904600-99905400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr7:99904600-99905800	Strong transcription	Fetal Muscle Trunk	muscle
43	chr7:99904600-99905800	Strong transcription	Fetal Stomach	stomach
44	chr7:99905000-99917000	Weak transcription	Dnd41	blood
45	chr7:99905200-99909400	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr7:99905400-99914200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr7:99905600-99917000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:99905800-99916600	Weak transcription	Fetal Stomach	stomach
49	chr7:99905800-99918000	Weak transcription	Fetal Muscle Trunk	muscle
50	chr7:99909200-99910000	Enhancers	Primary neutrophils fromperipheralblood	blood

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