Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:70505048..70507568-chr14:70516082..70518702,2	MCF-7	breast:
2	chr14:70248801..70250348-chr14:70516038..70518090,2	K562	blood:

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

rs_ID	r²[population]
rs11623433	0.87[EUR][1000 genomes]
rs11625977	0.87[EUR][1000 genomes]
rs11627233	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11627445	0.88[EUR][1000 genomes]
rs11629254	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17107778	0.87[EUR][1000 genomes]
rs17175297	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17175346	0.88[EUR][1000 genomes]
rs17175444	0.88[EUR][1000 genomes]
rs17765078	0.87[EUR][1000 genomes]
rs2125745	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41285486	0.87[EUR][1000 genomes]
rs61977411	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61977413	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61977415	0.87[EUR][1000 genomes]
rs61977417	0.88[EUR][1000 genomes]
rs61977419	0.83[EUR][1000 genomes]
rs61977420	0.87[EUR][1000 genomes]
rs61977422	0.87[EUR][1000 genomes]
rs61977423	0.88[EUR][1000 genomes]
rs61977424	0.88[EUR][1000 genomes]
rs61977425	0.88[EUR][1000 genomes]
rs61977426	0.88[EUR][1000 genomes]
rs7150941	0.87[EUR][1000 genomes]
rs7161025	0.87[EUR][1000 genomes]
rs8013407	0.88[EUR][1000 genomes]
rs8013867	0.88[EUR][1000 genomes]
rs8020358	0.87[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	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70511200-70518200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:70511600-70519000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:70512800-70535600	Weak transcription	Psoas Muscle	Psoas
4	chr14:70513200-70519200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr14:70513200-70520000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:70514200-70518000	Strong transcription	Skeletal Muscle Female	skeletal muscle
7	chr14:70514600-70531200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr14:70515800-70520000	Weak transcription	Fetal Brain Female	brain
9	chr14:70516000-70518800	Weak transcription	Gastric	stomach
10	chr14:70516600-70518000	Strong transcription	HSMMtube	muscle
11	chr14:70517000-70525200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr14:70517200-70519400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr14:70517800-70518800	Weak transcription	HepG2	liver
14	chr14:70517800-70519200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:70517800-70526200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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