Variant report

Variant	rs2268459
Chromosome Location	chr14:81463041-81463042
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:81453560..81454332-chr14:81462475..81463099,2	MCF-7	breast:
2	chr14:81462345..81463310-chr14:81528942..81529784,4	MCF-7	breast:
3	chr14:81462289..81463361-chr14:81629649..81631060,10	MCF-7	breast:
4	chr14:81462591..81463541-chr14:81528802..81529444,3	MCF-7	breast:
5	chr14:81462542..81463148-chr14:81629279..81630008,2	K562	blood:
6	chr14:81461329..81464418-chr14:81684245..81687408,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165417	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10145099	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1023586	0.96[ASN][1000 genomes]
rs1035144	0.87[ASN][1000 genomes]
rs11159479	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12101255	0.94[ASN][1000 genomes]
rs12101261	0.94[ASN][1000 genomes]
rs17111346	0.94[ASN][1000 genomes]
rs17111365	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs179262	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs179263	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2160215	0.96[ASN][1000 genomes]
rs2215981	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2284726	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2300516	0.98[ASN][1000 genomes]
rs2371463	0.99[ASN][1000 genomes]
rs28414437	0.86[ASN][1000 genomes]
rs3783943	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3783947	0.86[ASN][1000 genomes]
rs3783948	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3783949	0.97[ASN][1000 genomes]
rs3783950	0.97[ASN][1000 genomes]
rs4411444	0.87[ASN][1000 genomes]
rs4903961	0.96[ASN][1000 genomes]
rs56389234	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6574617	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs724170	0.99[ASN][1000 genomes]
rs8003061	0.94[ASN][1000 genomes]
rs8003515	0.98[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81455400-81463800	Weak transcription	Thymus	Thymus
2	chr14:81455800-81492200	Weak transcription	Fetal Thymus	thymus
3	chr14:81459400-81465600	Strong transcription	Dnd41	blood
4	chr14:81462600-81463200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr14:81462600-81463200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr14:81462600-81463200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr14:81462600-81463200	Flanking Active TSS	Liver	Liver
8	chr14:81462600-81463200	Enhancers	Colon Smooth Muscle	Colon
9	chr14:81462600-81463200	Active TSS	Skeletal Muscle Female	skeletal muscle
10	chr14:81462600-81463200	Enhancers	K562	blood
11	chr14:81462600-81463400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
12	chr14:81462800-81463200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr14:81462800-81463200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
14	chr14:81462800-81463200	Enhancers	Primary T cells from cord blood	blood
15	chr14:81462800-81463200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr14:81462800-81463200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:81462800-81463200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr14:81462800-81463200	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr14:81462800-81463200	Active TSS	Brain Substantia Nigra	brain
20	chr14:81462800-81463200	Enhancers	Rectal Smooth Muscle	rectum
21	chr14:81462800-81463200	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr14:81462800-81463200	Active TSS	Stomach Smooth Muscle	stomach
23	chr14:81462800-81463200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr14:81463000-81463200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:81463000-81463200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr14:81463000-81463200	Active TSS	Adipose Nuclei	Adipose
27	chr14:81463000-81463200	Flanking Active TSS	Brain Anterior Caudate	brain
28	chr14:81463000-81463200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
29	chr14:81463000-81463200	Flanking Active TSS	Psoas Muscle	Psoas
30	chr14:81463000-81463200	Bivalent/Poised TSS	Osteobl	bone
31	chr14:81463000-81467200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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