Variant report

Variant	rs13278335
Chromosome Location	chr8:104384988-104384989
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EGR1	chr8:104383299-104385047	HCT-116	colon:	n/a	chr8:104383723-104383732 chr8:104383722-104383732 chr8:104383720-104383733 chr8:104383720-104383733 chr8:104383631-104383644 chr8:104384526-104384550 chr8:104383720-104383734 chr8:104383633-104383643 chr8:104383657-104383667 chr8:104383721-104383735 chr8:104383630-104383645 chr8:104383723-104383733 chr8:104383719-104383734 chr8:104383720-104383733 chr8:104383721-104383732 chr8:104383657-104383670 chr8:104383631-104383644 chr8:104383654-104383668 chr8:104383720-104383733 chr8:104383677-104383690
2	RAD21	chr8:104383970-104385893	HCT-116	colon:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
3	HDAC2	chr8:104384677-104385041	HepG2	liver:	n/a	chr8:104384891-104384900
4	MAX	chr8:104383301-104385874	HCT-116	colon:	n/a	chr8:104383634-104383644 chr8:104383467-104383476 chr8:104383465-104383473 chr8:104383661-104383670 chr8:104383466-104383477 chr8:104383465-104383478
5	GATA3	chr8:104384135-104385025	SK-N-SH	brain:	n/a	chr8:104384574-104384583
6	FOXA1	chr8:104384411-104385098	HepG2	liver:	n/a	chr8:104384916-104384928 chr8:104384888-104384900
7	SMC3	chr8:104383479-104386604	SK-N-SH	brain:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104384498-104384505 chr8:104385618-104385625
8	JUND	chr8:104384158-104385109	SK-N-SH	brain:	n/a	chr8:104384574-104384585 chr8:104384572-104384583
9	MAX	chr8:104383315-104385139	HepG2	liver:	n/a	chr8:104383634-104383644 chr8:104383467-104383476 chr8:104383465-104383473 chr8:104383661-104383670 chr8:104383466-104383477 chr8:104383465-104383478
10	GATA3	chr8:104384069-104386185	SK-N-SH	brain:	n/a	chr8:104384574-104384583
11	TEAD4	chr8:104383479-104385028	SK-N-SH	brain:	n/a	n/a
12	MAX	chr8:104383297-104385061	HCT-116	colon:	n/a	chr8:104383634-104383644 chr8:104383467-104383476 chr8:104383465-104383473 chr8:104383661-104383670 chr8:104383466-104383477 chr8:104383465-104383478
13	SIN3AK20	chr8:104384252-104385033	PFSK-1	brain:	n/a	n/a
14	E2F6	chr8:104384867-104385715	H1-hESC	embryonic stem cell:	n/a	chr8:104385185-104385202 chr8:104385091-104385100
15	POLR2A	chr8:104383590-104386072	IMR90	lung:	n/a	n/a
16	POLR2A	chr8:104384226-104385014	HUVEC	blood vessel:	n/a	n/a
17	RAD21	chr8:104384302-104386039	SK-N-SH	brain:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
18	EP300	chr8:104384263-104384999	SK-N-SH	brain:	n/a	chr8:104384891-104384901 chr8:104384575-104384584
19	POLR2A	chr8:104383527-104385057	HUVEC	blood vessel:	n/a	n/a
20	GABPA	chr8:104384321-104385131	SK-N-SH	brain:	n/a	n/a
21	JUND	chr8:104384033-104386018	SK-N-SH	brain:	n/a	chr8:104384574-104384585 chr8:104384572-104384583
22	TAF1	chr8:104383430-104385064	SK-N-SH	brain:	n/a	n/a
23	TCF12	chr8:104383394-104385161	SK-N-SH	brain:	n/a	chr8:104384891-104384900
24	NFIC	chr8:104383467-104385068	SK-N-SH	brain:	n/a	n/a
25	FOXA1	chr8:104384599-104385033	HepG2	liver:	n/a	chr8:104384916-104384928 chr8:104384888-104384900
26	PBX3	chr8:104384154-104385027	SK-N-SH	brain:	n/a	n/a
27	RAD21	chr8:104384243-104385894	IMR90	lung:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
28	TAF1	chr8:104384303-104385071	PFSK-1	brain:	n/a	n/a
29	POLR2A	chr8:104384120-104385065	PFSK-1	brain:	n/a	n/a
30	MXI1	chr8:104383388-104386158	IMR90	lung:	n/a	chr8:104383466-104383475 chr8:104383468-104383477
31	CTCF	chr8:104384980-104385130	GM12872	blood:	n/a	n/a
32	TCF12	chr8:104384123-104385043	SK-N-SH	brain:	n/a	chr8:104384891-104384900
33	RXRA	chr8:104384175-104384998	SK-N-SH	brain:	n/a	n/a
34	POLR2A	chr8:104383342-104386187	SK-N-SH	brain:	n/a	n/a
35	POLR2A	chr8:104383741-104385003	HUVEC	blood vessel:	n/a	n/a
36	JUND	chr8:104383288-104385911	SK-N-SH	brain:	n/a	chr8:104384574-104384585 chr8:104384572-104384583
37	POLR2A	chr8:104383594-104385133	HUVEC	blood vessel:	n/a	n/a
38	PBX3	chr8:104383536-104384998	SK-N-SH	brain:	n/a	chr8:104384115-104384135
39	FOXA2	chr8:104384709-104385052	HepG2	liver:	n/a	chr8:104384916-104384928 chr8:104384888-104384900
40	HEY1	chr8:104384321-104385010	HepG2	liver:	n/a	n/a
41	POLR2A	chr8:104383311-104385048	HCT-116	colon:	n/a	n/a
42	POLR2A	chr8:104383650-104386037	SK-N-SH	brain:	n/a	n/a
43	FOXA1	chr8:104384777-104385099	HepG2	liver:	n/a	chr8:104384916-104384928 chr8:104384888-104384900
44	MAX	chr8:104383326-104385031	HepG2	liver:	n/a	chr8:104383634-104383644 chr8:104383467-104383476 chr8:104383465-104383473 chr8:104383661-104383670 chr8:104383466-104383477 chr8:104383465-104383478

No.	Distal block	Cell Line	Cell type
1	chr8:104384537..104387363-chr8:104425771..104427328,2	MCF-7	breast:
2	chr8:104309661..104313454-chr8:104382208..104385836,8	MCF-7	breast:
3	chr8:104383486..104387596-chr8:104393672..104397600,4	K562	blood:
4	chr8:104384521..104386453-chr8:104425627..104427344,2	K562	blood:
5	chr8:104309966..104312210-chr8:104383451..104386900,3	MCF-7	breast:
6	chr8:104382282..104385358-chr8:104387344..104390689,3	K562	blood:
7	chr8:104382634..104385222-chr8:104394415..104397249,2	K562	blood:
8	chr8:104382707..104385620-chr8:104427062..104430016,2	MCF-7	breast:
9	chr8:104085750..104086680-chr8:104384771..104385796,4	K562	blood:
10	chr8:104382288..104384118-chr8:104384150..104386828,2	MCF-7	breast:
11	chr8:104383757..104385653-chr8:104425622..104427492,3	K562	blood:
12	chr8:104384840..104386401-chr8:104401334..104403233,2	K562	blood:
13	chr8:104384672..104387548-chr8:104409163..104411650,2	K562	blood:
14	chr8:104384922..104387635-chr8:104403443..104406734,3	MCF-7	breast:

Variant related genes	Relation type
CTHRC1	TF binding region
ENSG00000266289	Chromatin interaction
ENSG00000164933	Chromatin interaction
ENSG00000247081	Chromatin interaction
ENSG00000164930	Chromatin interaction
ENSG00000164932	Chromatin interaction
ENSG00000164934	Chromatin interaction
ENSG00000207399	Chromatin interaction

Extended variants
information (count: 80 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10089343	0.83[ASN][1000 genomes]
rs10090069	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10093100	0.81[AMR][1000 genomes]
rs10093198	0.81[AMR][1000 genomes]
rs10094939	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10096207	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10097121	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10100283	0.81[AMR][1000 genomes]
rs10101517	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10102413	0.83[ASN][1000 genomes]
rs10105195	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10105450	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10106795	0.83[ASN][1000 genomes]
rs10108112	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10109642	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10112317	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10112450	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10112941	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10112952	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10113160	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10113367	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1061196	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11779349	0.83[ASN][1000 genomes]
rs11785583	0.83[ASN][1000 genomes]
rs11985002	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12707777	0.83[ASN][1000 genomes]
rs13255562	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13257958	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13258345	0.83[ASN][1000 genomes]
rs13263611	0.83[ASN][1000 genomes]
rs13266347	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13266642	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13273192	0.83[ASN][1000 genomes]
rs13282967	0.83[ASN][1000 genomes]
rs17205821	0.83[ASN][1000 genomes]
rs17228538	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17802416	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17802518	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17804088	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17804149	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28437723	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28811720	1.00[ASN][1000 genomes]
rs28862349	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2948449	0.83[ASN][1000 genomes]
rs3104026	0.83[ASN][1000 genomes]
rs34208282	0.83[ASN][1000 genomes]
rs35225263	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35392014	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57237927	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6468866	0.83[ASN][1000 genomes]
rs6985718	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6989714	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6990501	0.83[ASN][1000 genomes]
rs71520811	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72675443	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72675444	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72675445	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7464317	0.83[ASN][1000 genomes]
rs7818129	0.81[AMR][1000 genomes]
rs7820626	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7839421	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7845210	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs827528	0.83[ASN][1000 genomes]
rs827537	0.83[ASN][1000 genomes]
rs827538	0.83[ASN][1000 genomes]
rs827546	0.83[ASN][1000 genomes]
rs951826	0.83[ASN][1000 genomes]
rs973242	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1016395	chr8:104327541-104473005	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1023048	chr8:104355188-104872701	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv539705	chr8:104355188-104872701	ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv1021345	chr8:104361854-104879684	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv1032085	chr8:104362187-104878345	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv1033477	chr8:104369940-104439632	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	nsv539706	chr8:104369940-104439632	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv1034183	chr8:104369940-104814008	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	nsv539707	chr8:104369940-104814008	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13278335	FZD6	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104383400-104385000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr8:104383400-104385000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr8:104383400-104385000	Active TSS	Fetal Kidney	kidney
4	chr8:104383400-104385000	Active TSS	Placenta Amnion	Placenta Amnion
5	chr8:104383400-104385400	Active TSS	Aorta	Aorta
6	chr8:104383400-104386400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:104383400-104386600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:104383600-104385200	Active TSS	NH-A	brain
9	chr8:104383800-104385000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:104383800-104385000	Bivalent/Poised TSS	Psoas Muscle	Psoas
11	chr8:104383800-104385200	Bivalent Enhancer	Stomach Mucosa	stomach
12	chr8:104383800-104385400	Flanking Active TSS	HepG2	liver
13	chr8:104384000-104385000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
14	chr8:104384000-104385600	Flanking Active TSS	NHDF-Ad	bronchial
15	chr8:104384000-104386000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
16	chr8:104384000-104386000	Flanking Active TSS	Osteobl	bone
17	chr8:104384200-104385000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
18	chr8:104384200-104385200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr8:104384200-104385400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:104384200-104385400	Enhancers	A549	lung
21	chr8:104384200-104385800	Enhancers	Brain Cingulate Gyrus	brain
22	chr8:104384200-104386400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:104384200-104394800	Weak transcription	GM12878-XiMat	blood
24	chr8:104384200-104399800	Weak transcription	Primary T cells from cord blood	blood
25	chr8:104384400-104385000	Enhancers	Fetal Thymus	thymus
26	chr8:104384400-104385200	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr8:104384400-104385200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:104384400-104385400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr8:104384400-104385400	Weak transcription	Liver	Liver
30	chr8:104384400-104385600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
31	chr8:104384400-104385600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr8:104384400-104385600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:104384400-104385600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:104384400-104385600	Enhancers	Brain Substantia Nigra	brain
35	chr8:104384400-104385600	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr8:104384400-104388000	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr8:104384400-104388000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:104384400-104412200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr8:104384600-104385000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr8:104384600-104385000	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr8:104384600-104385200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:104384600-104385400	Weak transcription	K562	blood
43	chr8:104384600-104385600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
44	chr8:104384600-104385600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:104384600-104385600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr8:104384600-104385600	Enhancers	Brain Anterior Caudate	brain
47	chr8:104384600-104385600	Enhancers	Brain Hippocampus Middle	brain
48	chr8:104384600-104385600	Enhancers	Fetal Stomach	stomach
49	chr8:104384600-104385600	Flanking Active TSS	HSMM	muscle
50	chr8:104384600-104386000	Flanking Active TSS	HUVEC	blood vessel

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