Variant report

Variant	rs62018815
Chromosome Location	chr15:51058854-51058855
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELF1	chr15:51058714-51059048	HepG2	liver:	n/a	n/a
2	FOXA1	chr15:51058657-51059149	HepG2	liver:	n/a	n/a
3	RFX5	chr15:51058729-51058855	HepG2	liver:	n/a	n/a
4	FOXA2	chr15:51058715-51059006	HepG2	liver:	n/a	n/a
5	HNF4G	chr15:51058601-51059053	HepG2	liver:	n/a	chr15:51058852-51058867 chr15:51058812-51058827 chr15:51058828-51058843
6	HNF4A	chr15:51058572-51059072	HepG2	liver:	n/a	chr15:51058827-51058842 chr15:51058851-51058866
7	POLR2A	chr15:51058653-51058971	HepG2	liver:	n/a	n/a
8	EP300	chr15:51058639-51059039	HepG2	liver:	n/a	n/a
9	RXRA	chr15:51058672-51059032	HepG2	liver:	n/a	n/a
10	RAD21	chr15:51058691-51058993	HepG2	liver:	n/a	n/a
11	MYBL2	chr15:51058536-51059166	HepG2	liver:	n/a	n/a
12	HEY1	chr15:51058522-51059041	HepG2	liver:	n/a	n/a
13	ZNF263	chr15:51058710-51059010	HEK293-T-REx	kidney:	n/a	n/a
14	HNF4G	chr15:51058522-51059077	HepG2	liver:	n/a	chr15:51058852-51058867 chr15:51058812-51058827 chr15:51058828-51058843
15	SP1	chr15:51058561-51059100	HepG2	liver:	n/a	n/a
16	HNF4A	chr15:51058687-51059058	HepG2	liver:	n/a	chr15:51058827-51058842 chr15:51058851-51058866
17	JUND	chr15:51058704-51058959	HepG2	liver:	n/a	n/a
18	EP300	chr15:51058644-51059069	HepG2	liver:	n/a	n/a
19	MYBL2	chr15:51058652-51059061	HepG2	liver:	n/a	n/a
20	MXI1	chr15:51058730-51058991	HepG2	liver:	n/a	n/a
21	BHLHE40	chr15:51058775-51059006	HepG2	liver:	n/a	n/a
22	TCF12	chr15:51058677-51059043	HepG2	liver:	n/a	n/a
23	NFIC	chr15:51058711-51059007	HepG2	liver:	n/a	n/a
24	FOXA1	chr15:51058634-51059108	HepG2	liver:	n/a	n/a
25	POLR2A	chr15:51058645-51058976	HepG2	liver:	n/a	n/a
26	FOXA1	chr15:51058609-51059167	HepG2	liver:	n/a	n/a
27	TEAD4	chr15:51058622-51059099	HepG2	liver:	n/a	n/a
28	ELF1	chr15:51058688-51059007	HepG2	liver:	n/a	n/a
29	NFIC	chr15:51058664-51059081	HepG2	liver:	n/a	n/a
30	FOXA1	chr15:51058569-51059064	HepG2	liver:	n/a	n/a
31	HDAC2	chr15:51058643-51059028	HepG2	liver:	n/a	n/a
32	RCOR1	chr15:51058734-51058972	HepG2	liver:	n/a	n/a
33	YY1	chr15:51058555-51058930	HepG2	liver:	n/a	n/a
34	SMC3	chr15:51058812-51059012	HepG2	liver:	n/a	n/a
35	MAZ	chr15:51058841-51058925	HepG2	liver:	n/a	n/a
36	HNF4A	chr15:51058673-51059005	HepG2	liver:	n/a	chr15:51058827-51058842 chr15:51058851-51058866
37	REST	chr15:51058689-51059009	HepG2	liver:	n/a	n/a
38	ARID3A	chr15:51058735-51059038	HepG2	liver:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:51056442..51059084-chr15:51199726..51202707,2	MCF-7	breast:
2	chr15:51039062..51042009-chr15:51057876..51060168,3	MCF-7	breast:
3	chr15:50644661..50647207-chr15:51058214..51061180,2	MCF-7	breast:
4	chr15:51045886..51047999-chr15:51058293..51060374,2	K562	blood:
5	chr15:51056750..51061263-chr15:51087602..51092500,6	MCF-7	breast:
6	chr15:50976295..50981465-chr15:51052766..51059546,15	MCF-7	breast:
7	chr11:60926802..60929238-chr15:51056528..51059041,2	MCF-7	breast:
8	chr15:51057662..51059502-chr5:36875365..36877060,2	MCF-7	breast:
9	chr15:51054229..51056382-chr15:51058543..51060392,2	K562	blood:
10	chr15:51057335..51059727-chr6:26020365..26022635,2	MCF-7	breast:
11	chr15:51056515..51059362-chr15:51088829..51092887,6	MCF-7	breast:
12	chr15:50977319..50980700-chr15:51053372..51060901,7	MCF-7	breast:
13	chr15:51058134..51060047-chr15:51086816..51088508,2	MCF-7	breast:

No data

Variant related genes	Relation type
SPPL2A	TF binding region
ENSG00000138600	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000092439	Chromatin interaction
ENSG00000081014	Chromatin interaction
ENSG00000167987	Chromatin interaction
ENSG00000241130	Chromatin interaction
ENSG00000164190	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000243027	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10467	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10519285	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1052457	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11630124	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11633905	0.89[EUR][1000 genomes]
rs11635800	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11637164	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11637308	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12324521	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17702595	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28472713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61751063	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62017255	1.00[EUR][1000 genomes]
rs62017256	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62017257	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62017259	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018760	0.85[EUR][1000 genomes]
rs62018762	1.00[EUR][1000 genomes]
rs62018763	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018764	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018765	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018798	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62018799	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018800	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018801	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018802	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018803	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018809	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018810	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018812	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62018813	1.00[EUR][1000 genomes]
rs62018814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7167416	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72740496	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72742304	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72742306	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72742311	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8037489	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8040136	1.00[EUR][1000 genomes]
rs8042462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053966	chr15:50715572-51133186	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
2	nsv542383	chr15:50715572-51133186	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
5	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
6	nsv1051990	chr15:50745814-51133186	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv457134	chr15:50770868-51184583	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
8	nsv471242	chr15:50770868-51184583	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
9	nsv569396	chr15:50770868-51184583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
10	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
12	nsv1048621	chr15:50775451-51115535	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv1047039	chr15:50782070-51187804	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
14	nsv542385	chr15:50782070-51187804	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
16	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
17	nsv1036081	chr15:50818569-51097229	Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
18	nsv1055112	chr15:50822035-51133186	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
19	nsv1042372	chr15:50846461-51208891	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
20	nsv542386	chr15:50846461-51208891	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
21	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
22	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
23	nsv904212	chr15:50979738-51132170	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
24	nsv904213	chr15:51011402-51119731	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
25	nsv1044320	chr15:51016364-51074061	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
26	nsv457137	chr15:51019117-51117524	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
27	nsv569402	chr15:51019117-51117524	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
28	nsv529339	chr15:51048579-51270372	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51058000-51059000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
2	chr15:51058000-51059000	Flanking Active TSS	Stomach Smooth Muscle	stomach
3	chr15:51058200-51059000	Enhancers	Lung	lung
4	chr15:51058200-51059000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr15:51058400-51059000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr15:51058400-51059000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr15:51058400-51059000	Enhancers	Colonic Mucosa	Colon
8	chr15:51058400-51059000	Enhancers	Fetal Intestine Small	intestine
9	chr15:51058400-51059000	Enhancers	Left Ventricle	heart
10	chr15:51058400-51059000	Enhancers	Pancreas	Pancrea
11	chr15:51058400-51059000	Enhancers	Right Ventricle	heart
12	chr15:51058400-51059200	Active TSS	HepG2	liver
13	chr15:51058400-51059400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr15:51058400-51059400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr15:51058400-51059400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr15:51058400-51059400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr15:51058400-51059400	Enhancers	Fetal Heart	heart
18	chr15:51058400-51059400	Weak transcription	Osteobl	bone
19	chr15:51058400-51059600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr15:51058400-51059600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:51058400-51059600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:51058400-51059600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr15:51058400-51059800	Weak transcription	Aorta	Aorta
24	chr15:51058400-51059800	Weak transcription	Esophagus	oesophagus
25	chr15:51058400-51059800	Enhancers	Stomach Mucosa	stomach
26	chr15:51058400-51059800	Weak transcription	NHEK	skin
27	chr15:51058400-51059800	Weak transcription	NHLF	lung
28	chr15:51058400-51060000	Weak transcription	Right Atrium	heart
29	chr15:51058400-51060400	Enhancers	GM12878-XiMat	blood
30	chr15:51058400-51061000	Weak transcription	NHDF-Ad	bronchial
31	chr15:51058400-51066800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr15:51058600-51059000	Enhancers	Fetal Muscle Trunk	muscle
33	chr15:51058600-51059000	Enhancers	Psoas Muscle	Psoas
34	chr15:51058600-51059400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr15:51058600-51059400	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr15:51058600-51059600	Weak transcription	Adipose Nuclei	Adipose
37	chr15:51058600-51059600	Weak transcription	Small Intestine	intestine
38	chr15:51058600-51059600	Weak transcription	Hela-S3	cervix
39	chr15:51058600-51059600	Weak transcription	HMEC	breast
40	chr15:51058600-51059600	Weak transcription	K562	blood
41	chr15:51058600-51060000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr15:51058600-51060000	Enhancers	Liver	Liver
43	chr15:51058600-51070200	Weak transcription	Fetal Intestine Large	intestine
44	chr15:51058800-51059000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr15:51058800-51059000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr15:51058800-51059200	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr15:51058800-51059200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr15:51058800-51059200	Weak transcription	A549	lung
49	chr15:51058800-51059600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr15:51058800-51060000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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