Variant report

Variant	rs10505010
Chromosome Location	chr8:102543765-102543766
allele	C/T
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	RUNX3	chr8:102543726-102543978	GM12878	blood:	n/a	n/a
2	BATF	chr8:102543688-102543904	GM12878	blood:	n/a	chr8:102543823-102543834

Variant related genes	Relation type
ENSG00000253991	TF binding region

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10955256	0.82[AMR][1000 genomes]
rs11776316	0.81[CEU][hapmap];0.83[CHB][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11783704	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13255911	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13263539	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17397776	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs17397811	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17476242	0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1880634	0.82[AMR][1000 genomes]
rs1880635	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2127034	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2127035	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34216075	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6984360	0.84[CEU][hapmap];0.83[CHB][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs922466	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024652	chr8:101802121-102587124	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	186 gene(s)	inside rSNPs	diseases
2	nsv539699	chr8:101802121-102587124	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription 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	186 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102527000-102551200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:102527000-102551400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:102527200-102555400	Weak transcription	Fetal Intestine Small	intestine
4	chr8:102527200-102556800	Weak transcription	Fetal Intestine Large	intestine
5	chr8:102528400-102550600	Weak transcription	Esophagus	oesophagus
6	chr8:102533800-102550200	Weak transcription	HMEC	breast
7	chr8:102533800-102551400	Weak transcription	Pancreas	Pancrea
8	chr8:102536000-102550200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:102536800-102550200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr8:102538200-102550400	Weak transcription	Placenta	Placenta
11	chr8:102539200-102550200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:102539800-102550200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:102541400-102544200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr8:102541600-102544600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:102541600-102545400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr8:102542200-102544400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr8:102542200-102545200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr8:102542400-102550200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:102542600-102545400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:102542600-102545400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr8:102542600-102549800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:102542600-102550200	Weak transcription	NHEK	skin
23	chr8:102542600-102550400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr8:102542800-102544200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:102543200-102544000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr8:102543200-102544600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr8:102543400-102543800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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