Variant report

Variant	esv1794417
Chromosome Location	chr7:102814101-102928545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:467)
CpG islands
(count:1100)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102894620-102894913	K562	blood:	n/a	n/a
2	ATF1	chr7:102894715-102894811	K562	blood:	n/a	n/a
3	ATF1	chr7:102839766-102839968	K562	blood:	n/a	n/a
4	BATF	chr7:102863528-102863901	GM12878	blood:	n/a	n/a
5	BATF	chr7:102863497-102863908	GM12878	blood:	n/a	n/a
6	BATF	chr7:102872627-102872850	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:102863536-102863866	GM12878	blood:	n/a	chr7:102863703-102863712
8	BCL3	chr7:102906588-102906815	GM12878	blood:	n/a	n/a
9	BCLAF1	chr7:102920684-102921045	GM12878	blood:	n/a	chr7:102920916-102920929
10	BHLHE40	chr7:102863630-102863788	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:102920337-102921182	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:102894632-102894890	K562	blood:	n/a	n/a
13	BRCA1	chr7:102839762-102839912	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr7:102920527-102920942	K562	blood:	n/a	n/a
15	CBX3	chr7:102904505-102904890	K562	blood:	n/a	n/a
16	CBX3	chr7:102904444-102904894	K562	blood:	n/a	n/a
17	CCNT2	chr7:102894716-102894916	K562	blood:	n/a	n/a
18	CEBPB	chr7:102913882-102914204	K562	blood:	n/a	chr7:102914022-102914033
19	CEBPB	chr7:102835869-102836152	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr7:102913801-102914217	K562	blood:	n/a	chr7:102914022-102914033
21	CEBPB	chr7:102913896-102914131	Hela-S3	cervix:	n/a	chr7:102914022-102914033
22	CEBPB	chr7:102851680-102851880	A549	lung:	n/a	n/a
23	CEBPB	chr7:102913895-102914199	HepG2	liver:	n/a	chr7:102914022-102914033
24	CEBPB	chr7:102913885-102914195	A549	lung:	n/a	chr7:102914022-102914033
25	CEBPB	chr7:102913901-102914196	H1-hESC	embryonic stem cell:	n/a	chr7:102914022-102914033
26	CEBPB	chr7:102894284-102894446	K562	blood:	n/a	n/a
27	CEBPB	chr7:102835924-102836111	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:102835797-102836162	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:102913910-102914109	K562	blood:	n/a	chr7:102914022-102914033
30	CEBPB	chr7:102913883-102914196	IMR90	lung:	n/a	chr7:102914022-102914033
31	CEBPD	chr7:102894591-102895083	K562	blood:	n/a	n/a
32	CEBPD	chr7:102894244-102894588	K562	blood:	n/a	n/a
33	CHD1	chr7:102920505-102920613	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr7:102920485-102920955	GM12878	blood:	n/a	n/a
35	CHD2	chr7:102863622-102863744	GM12878	blood:	n/a	n/a
36	CHD2	chr7:102920823-102921014	GM12878	blood:	n/a	n/a
37	CHD2	chr7:102920347-102920534	GM12878	blood:	n/a	n/a
38	CREB1	chr7:102920555-102921035	A549	lung:	n/a	n/a
39	CTCF	chr7:102923447-102923578	LNCaP	prostate:	n/a	chr7:102923504-102923520 chr7:102923503-102923521 chr7:102923505-102923526
40	CTCF	chr7:102923422-102923423	GM13977	blood:	n/a	n/a
41	CTCF	chr7:102923300-102923450	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr7:102923300-102923450	HCM	heart:	n/a	n/a
43	CTCF	chr7:102923160-102923310	HMEC	breast:	n/a	n/a
44	CTCF	chr7:102923280-102923430	BE2_C	brain:	n/a	n/a
45	CTCF	chr7:102891215-102891336	GM13976	blood:	n/a	n/a
46	CTCF	chr7:102815640-102815790	HEK293	kidney:	n/a	n/a
47	CTCF	chr7:102898085-102898154	GM20000	blood:	n/a	n/a
48	CTCF	chr7:102923152-102923184	GM20000	blood:	n/a	n/a
49	CTCF	chr7:102923455-102923539	GM20000	blood:	n/a	chr7:102923504-102923520 chr7:102923503-102923521 chr7:102923505-102923526
50	CTCF	chr7:102923260-102923410	SK-N-SH_RA	brain:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102921054-102921104	GM19239	blood:	n/a
2	chr7:102920980-102921030	RPTEC	kidney:	n/a
3	chr7:102921054-102921104	GM19239	blood:	n/a
4	chr7:102920980-102921030	RPTEC	kidney:	n/a
5	chr7:102918083-102918133	HRE	kidney:	n/a
6	chr7:102921001-102921051	AG09319	gingival:	n/a
7	chr7:102921304-102921354	HRPEpiC	eye:	n/a
8	chr7:102914896-102914946	SK-N-SH	brain:	n/a
9	chr7:102921054-102921104	SK-N-SH	brain:	n/a
10	chr7:102920962-102921012	HRE	kidney:	n/a
11	chr7:102914896-102914946	HCM	heart:	n/a
12	chr7:102920323-102920373	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:102920777-102920827	AG09309	skin:	n/a
14	chr7:102918083-102918133	K562	blood:	n/a
15	chr7:102920777-102920827	AG04450	lung:	fetal
16	chr7:102918709-102918759	HEEpiC	esophagus:	n/a
17	chr7:102918083-102918133	HL-60	blood:	n/a
18	chr7:102921054-102921104	H1-hESC	embryonic stem cell:	embryo
19	chr7:102921001-102921051	RPTEC	kidney:	n/a
20	chr7:102918709-102918759	NH-A	brain:	n/a
21	chr7:102920641-102920691	NHBE	bronchial:	n/a
22	chr7:102918083-102918133	LNCaP	prostate:	n/a
23	chr7:102921304-102921354	HNPCEpiC	eye:	n/a
24	chr7:102921643-102921693	T-47D	breast:	n/a
25	chr7:102920777-102920827	HUVEC	blood vessel:	n/a
26	chr7:102914896-102914946	Caco-2	colon:	n/a
27	chr7:102920777-102920827	HIPEpiC	eye:	n/a
28	chr7:102920323-102920373	AoSMC	blood vessel:	n/a
29	chr7:102921001-102921051	A549	lung:	n/a
30	chr7:102920641-102920691	ProgFib	skin:	n/a
31	chr7:102920962-102921012	GM06990	blood:	n/a
32	chr7:102918709-102918759	Hela-S3	cervix:	n/a
33	chr7:102920323-102920373	HRPEpiC	eye:	n/a
34	chr7:102920980-102921030	SK-N-MC	brain:	n/a
35	chr7:102921052-102921102	HRPEpiC	eye:	n/a
36	chr7:102921001-102921051	HepG2	liver:	n/a
37	chr7:102921001-102921051	NB4	blood:	n/a
38	chr7:102920641-102920691	Jurkat	blood:	n/a
39	chr7:102921001-102921051	NHDF-neo	bronchial:	n/a
40	chr7:102921054-102921104	IMR90	lung:	fetal
41	chr7:102920771-102920821	SK-N-MC	brain:	n/a
42	chr7:102914896-102914946	AG09309	skin:	n/a
43	chr7:102920641-102920691	A549	lung:	n/a
44	chr7:102920323-102920373	Hepatocyte	liver:	n/a
45	chr7:102921513-102921563	AG09319	gingival:	n/a
46	chr7:102918083-102918133	BE2_C	brain:	n/a
47	chr7:102924808-102924858	PrEC	prostate:	n/a
48	chr7:102920962-102921012	Hela-S3	cervix:	n/a
49	chr7:102920777-102920827	H1-hESC	embryonic stem cell:	embryo
50	chr7:102921442-102921492	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:102789896..102791786-chr7:102883525..102886485,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAPEPLD-5	chr7:102920280-102920411	NONHSAT122547
2	lnc-NAPEPLD-5	chr7:102918669-102918793	NONHSAT122547

No data

Variant related genes	Relation type
S100A11P1	TF binding region
DPY19L2P2	TF binding region
S100A11P1	CpG island
DPY19L2P2	CpG island
ENSG00000161048	chromatin interactions

Extended variants
information (count: 1489 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs397842194	chr7:102814114-102814115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs3987912	chr7:102814123-102814124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139457034	chr7:102814139-102814140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs3987913	chr7:102814153-102814154	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs541531948	chr7:102814166-102814167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs397842195	chr7:102814168-102814169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140134054	chr7:102827211-102827212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62480132	chr7:102827257-102827258	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs569178021	chr7:102827288-102827289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539746646	chr7:102827326-102827327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551320125	chr7:102827351-102827352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs62480133	chr7:102827359-102827360	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs192497203	chr7:102827382-102827383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116117934	chr7:102827407-102827408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77619467	chr7:102827419-102827420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62480134	chr7:102827431-102827432	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs539736777	chr7:102827441-102827442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556416265	chr7:102827493-102827494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577966352	chr7:102827509-102827510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4265122	chr7:102827544-102827545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184676203	chr7:102827655-102827656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs3987898	chr7:102827715-102827716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571319973	chr7:102827717-102827718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189196618	chr7:102827751-102827752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538738000	chr7:102827789-102827790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571982658	chr7:102827796-102827797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375751956	chr7:102827815-102827816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs3987899	chr7:102827832-102827833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs3987900	chr7:102827851-102827852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542290363	chr7:102827861-102827862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556971600	chr7:102827867-102827868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377042518	chr7:102827868-102827869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561002245	chr7:102827934-102827935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531325737	chr7:102828029-102828030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375903526	chr7:102828115-102828116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4336542	chr7:102828151-102828152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs562751942	chr7:102828176-102828177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2909165	chr7:102828264-102828265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533388137	chr7:102828276-102828277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537597380	chr7:102828281-102828282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367635067	chr7:102828299-102828300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551655494	chr7:102828327-102828328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373704535	chr7:102828328-102828329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4266582	chr7:102828337-102828338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs117020235	chr7:102828393-102828394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143151927	chr7:102828401-102828402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369864588	chr7:102828402-102828403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79984934	chr7:102828404-102828405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567637200	chr7:102828451-102828452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192569552	chr7:102828464-102828465	Weak transcription	n/a	n/a	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
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21510904	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102813800-102814200	Enhancers	K562	blood
2	chr7:102827200-102827800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr7:102827400-102827800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:102827800-102828800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr7:102828800-102830400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr7:102829000-102830200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:102835400-102836200	Enhancers	Liver	Liver
8	chr7:102835400-102836600	Enhancers	Hela-S3	cervix
9	chr7:102835800-102836200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:102839600-102840400	Enhancers	K562	blood
11	chr7:102850600-102850800	Weak transcription	Fetal Lung	lung
12	chr7:102850800-102851000	Enhancers	Fetal Lung	lung
13	chr7:102851000-102851400	Flanking Active TSS	Fetal Lung	lung
14	chr7:102851200-102851800	Enhancers	K562	blood
15	chr7:102863800-102864000	Enhancers	GM12878-XiMat	blood
16	chr7:102864000-102866400	Weak transcription	GM12878-XiMat	blood
17	chr7:102865800-102867200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:102866400-102867000	Enhancers	GM12878-XiMat	blood
19	chr7:102867200-102871800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:102871800-102872200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:102875600-102876600	Enhancers	Liver	Liver
22	chr7:102876600-102881000	Weak transcription	Liver	Liver
23	chr7:102881000-102881800	Enhancers	Liver	Liver
24	chr7:102881200-102881600	Enhancers	A549	lung
25	chr7:102881600-102884600	Weak transcription	A549	lung
26	chr7:102884200-102886400	Weak transcription	Right Atrium	heart
27	chr7:102884600-102885000	Active TSS	A549	lung
28	chr7:102894200-102894400	Enhancers	K562	blood
29	chr7:102894400-102894800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:102894400-102895000	Flanking Active TSS	K562	blood
31	chr7:102894600-102894800	Enhancers	Fetal Heart	heart
32	chr7:102895000-102895400	Enhancers	K562	blood
33	chr7:102906200-102907000	Enhancers	K562	blood
34	chr7:102906600-102907600	Enhancers	Fetal Heart	heart
35	chr7:102907400-102919400	Weak transcription	Fetal Brain Male	brain
36	chr7:102907800-102908600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:102907800-102919600	Weak transcription	Fetal Thymus	thymus
38	chr7:102907800-102920000	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr7:102908000-102914200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr7:102908000-102915800	Weak transcription	Dnd41	blood
41	chr7:102908600-102911600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr7:102909200-102909400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr7:102909400-102920200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:102910600-102919600	Weak transcription	Fetal Stomach	stomach
45	chr7:102912800-102915000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:102912800-102918800	Weak transcription	Fetal Brain Female	brain
47	chr7:102913000-102919600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:102913000-102920000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr7:102913200-102914800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:102914200-102915200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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