Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:130243320..130247146-chr4:130247624..130250769,3	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10518546	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11943511	1.00[EUR][1000 genomes]
rs13102645	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13109938	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13128188	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13130195	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13149187	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17014599	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17014611	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17014614	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17014727	0.86[EUR][1000 genomes]
rs17367613	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34010234	0.86[EUR][1000 genomes]
rs34466472	1.00[EUR][1000 genomes]
rs34864289	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34955650	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34974459	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35004602	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35255990	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35524133	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35918555	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71613929	0.86[EUR][1000 genomes]
rs71613931	0.86[EUR][1000 genomes]
rs71613934	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534538	chr4:129799138-130431688	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv830058	chr4:130136025-130315471	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv879932	chr4:130167642-130264517	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr4:130246000-130251000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:130247400-130248800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr4:130247800-130248800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:130247800-130248800	Enhancers	Fetal Muscle Leg	muscle
5	chr4:130248000-130248600	Enhancers	Fetal Kidney	kidney
6	chr4:130248000-130248800	Enhancers	Adipose Nuclei	Adipose
7	chr4:130248000-130249000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr4:130248000-130249000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr4:130248200-130248600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:130248200-130248600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:130248200-130248800	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr4:130248400-130248600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:130248400-130248600	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr4:130248400-130248600	Enhancers	Stomach Smooth Muscle	stomach
15	chr4:130248400-130249600	Enhancers	Primary hematopoietic stem cells	blood

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