Variant report

Variant	rs10498477
Chromosome Location	chr14:56180099-56180100
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	chr14:55737454..55740283-chr14:56178729..56181502,2	MCF-7	breast:
2	chr14:56178438..56180249-chr14:56182200..56183742,2	K562	blood:

Variant related genes	Relation type
ENSG00000178974	Chromatin interaction
ENSG00000258413	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10130783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10873090	0.95[ASN][1000 genomes]
rs11158049	0.95[ASN][1000 genomes]
rs11621130	0.94[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.84[MKK][hapmap];0.95[ASN][1000 genomes]
rs12431962	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12432001	0.95[ASN][1000 genomes]
rs12432019	0.95[ASN][1000 genomes]
rs12587803	0.81[ASN][1000 genomes]
rs2342585	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2342586	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2880396	0.91[ASN][1000 genomes]
rs6573055	0.91[ASN][1000 genomes]
rs7147303	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7152314	0.91[ASN][1000 genomes]
rs8015301	0.91[ASN][1000 genomes]
rs8021103	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][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	nsv832804	chr14:56083850-56277632	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv901966	chr14:56160904-56436203	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56102400-56185400	Weak transcription	Right Ventricle	heart
2	chr14:56154000-56191000	Weak transcription	Aorta	Aorta
3	chr14:56169600-56182400	Weak transcription	GM12878-XiMat	blood
4	chr14:56170000-56182400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:56170400-56182400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr14:56172200-56182200	Weak transcription	HSMM	muscle
7	chr14:56172600-56182200	Weak transcription	HSMMtube	muscle
8	chr14:56174200-56182400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr14:56174600-56182400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr14:56178000-56182400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr14:56178000-56182400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr14:56178200-56183400	Weak transcription	Left Ventricle	heart
13	chr14:56178400-56181200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:56178400-56182400	Weak transcription	NHLF	lung
15	chr14:56178600-56180600	Enhancers	Placenta	Placenta
16	chr14:56179000-56181200	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr14:56179400-56180400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr14:56179600-56180200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:56179600-56180200	Enhancers	Duodenum Mucosa	Duodenum
20	chr14:56179800-56180600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr14:56179800-56180800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr14:56179800-56181600	Weak transcription	Fetal Heart	heart
23	chr14:56179800-56188800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr14:56179800-56189000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr14:56180000-56180200	Enhancers	Primary B cells from cord blood	blood
26	chr14:56180000-56180800	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr14:56180000-56182400	Weak transcription	Adipose Nuclei	Adipose
28	chr14:56180000-56183200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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