Variant report

Variant	rs4737935
Chromosome Location	chr8:69916491-69916492
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	GATA3	chr8:69916410-69917042	SK-N-SH	brain:	n/a	n/a
2	GATA3	chr8:69916429-69917011	SK-N-SH	brain:	n/a	n/a
3	PBX3	chr8:69916465-69916930	SK-N-SH	brain:	n/a	n/a

Variant related genes	Relation type
ENSG00000253658	TF binding region

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10093389	1.00[JPT][hapmap]
rs10504435	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11985132	1.00[CEU][hapmap]
rs12545358	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12545420	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12549168	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.85[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12550286	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12550397	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12675555	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12675576	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16935176	1.00[CEU][hapmap]
rs16935336	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16935360	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16935363	1.00[JPT][hapmap]
rs1974974	1.00[JPT][hapmap]
rs4737936	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55729603	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6990230	0.86[ASN][1000 genomes]
rs6999385	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6999406	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73683795	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73683796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73683801	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7819411	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7819425	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7825661	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7827405	1.00[CEU][hapmap]

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	nsv1031633	chr8:69766575-70322790	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv33049	chr8:69836813-69943360	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69879600-69917200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:69906400-69928400	Weak transcription	HSMM	muscle
3	chr8:69908600-69920400	Weak transcription	Osteobl	bone
4	chr8:69914000-69917800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:69914200-69919200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:69915800-69916600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr8:69916200-69917800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:69916200-69918000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:69916200-69918200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:69916200-69918200	Enhancers	Fetal Brain Male	brain
11	chr8:69916200-69919200	Enhancers	Brain Germinal Matrix	brain
12	chr8:69916400-69917600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:69916400-69918200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr8:69916400-69918200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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