Variant report

Variant	rs4737254
Chromosome Location	chr8:69128538-69128539
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:69126795..69128703-chr8:69131275..69133013,2	K562	blood:

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs7014680	0.91[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs73265339	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73265346	0.96[AMR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3331644	chr8:68806705-69189171	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1028889	chr8:69026806-69308725	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv890976	chr8:69100070-69155563	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69075000-69130800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr8:69086000-69141600	Weak transcription	Fetal Muscle Leg	muscle
3	chr8:69103200-69141400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr8:69103200-69141800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr8:69104800-69132800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:69105400-69141400	Weak transcription	Brain Hippocampus Middle	brain
7	chr8:69106400-69129800	Weak transcription	Adipose Nuclei	Adipose
8	chr8:69109600-69129800	Weak transcription	Left Ventricle	heart
9	chr8:69115400-69129600	Weak transcription	Fetal Stomach	stomach
10	chr8:69116800-69135000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:69120600-69140000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:69122200-69138400	Weak transcription	Fetal Lung	lung
13	chr8:69123000-69130000	Weak transcription	HUVEC	blood vessel
14	chr8:69123600-69128800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:69124000-69132800	Weak transcription	Pancreas	Pancrea
16	chr8:69125800-69141200	Weak transcription	Brain Substantia Nigra	brain
17	chr8:69126200-69129800	Weak transcription	Lung	lung
18	chr8:69127000-69129800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:69127200-69128800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr8:69127200-69132800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:69127400-69129800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:69127400-69135000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr8:69127400-69136400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:69127600-69129800	Weak transcription	Fetal Brain Male	brain
25	chr8:69127600-69130000	Weak transcription	Fetal Brain Female	brain
26	chr8:69127600-69131800	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr8:69127600-69135400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr8:69127800-69131800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr8:69128400-69141400	Weak transcription	Brain Anterior Caudate	brain

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