Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:51271422..51272928-chr13:51274925..51277429,2	K562	blood:

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs2245243	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2246135	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2794462	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2794463	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2812231	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2812232	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3116599	1.00[ASW][hapmap]
rs3121212	1.00[ASW][hapmap]

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	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
2	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753864	chr13:51136699-51375199	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1037350	chr13:51272518-51447354	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51268400-51277200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr13:51269400-51296800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr13:51270600-51276200	Enhancers	Fetal Heart	heart
4	chr13:51271800-51281800	Weak transcription	Lung	lung
5	chr13:51272800-51275800	Weak transcription	Right Ventricle	heart
6	chr13:51272800-51277200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr13:51272800-51281800	Weak transcription	Brain Hippocampus Middle	brain
8	chr13:51272800-51285600	Weak transcription	Fetal Stomach	stomach
9	chr13:51274200-51276000	Enhancers	Fetal Thymus	thymus
10	chr13:51274200-51276200	Enhancers	Dnd41	blood
11	chr13:51274800-51275800	Weak transcription	Fetal Intestine Small	intestine
12	chr13:51274800-51276600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr13:51274800-51277800	Weak transcription	Thymus	Thymus
14	chr13:51275000-51275800	Weak transcription	Fetal Lung	lung
15	chr13:51275000-51276200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr13:51275000-51278200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr13:51275600-51275800	Enhancers	Right Atrium	heart
18	chr13:51275600-51275800	Enhancers	Stomach Mucosa	stomach
19	chr13:51275600-51276200	Enhancers	Fetal Muscle Leg	muscle
20	chr13:51275600-51276200	Enhancers	Left Ventricle	heart
21	chr13:51275600-51276600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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