Variant report

Variant	rs59442924
Chromosome Location	chr12:29434334-29434335
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERGIC2-2	chr12:29433351-29434475	ENSG00000245593
2	lnc-ERGIC2-2	chr12:29433351-29434475	ENSG00000257176.1
3	lnc-ERGIC2-2	chr12:29433349-29434475	NONHSAT027487

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs56224606	0.87[AFR][1000 genomes]
rs57967706	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58244411	0.87[AFR][1000 genomes]
rs58552561	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59173481	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59368526	0.95[AFR][1000 genomes]
rs60044892	0.95[AFR][1000 genomes]
rs60675725	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60697326	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61447708	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7342354	0.92[AFR][1000 genomes]
rs74076684	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74076962	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74077152	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078140	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078141	0.90[AFR][1000 genomes]
rs74078380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078381	1.00[AFR][1000 genomes];1.00[AMR][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	nsv532233	chr12:29009388-29496179	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv995123	chr12:29095272-29571558	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1053641	chr12:29268813-29854413	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29417200-29465400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr12:29420400-29435000	Weak transcription	HUVEC	blood vessel
3	chr12:29422000-29455600	Weak transcription	Left Ventricle	heart
4	chr12:29422000-29465000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr12:29422200-29434800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr12:29422400-29434400	Weak transcription	Fetal Kidney	kidney
7	chr12:29424600-29435200	Weak transcription	Colon Smooth Muscle	Colon
8	chr12:29424800-29434800	Weak transcription	Dnd41	blood
9	chr12:29425000-29434400	Weak transcription	Fetal Stomach	stomach
10	chr12:29425200-29435600	Weak transcription	Brain Hippocampus Middle	brain
11	chr12:29426600-29434400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr12:29426600-29440600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:29426800-29436200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr12:29426800-29440600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:29426800-29472800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr12:29427000-29435200	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr12:29427000-29452200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:29427200-29527400	Weak transcription	Small Intestine	intestine
19	chr12:29427800-29438400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr12:29429000-29460200	Weak transcription	Primary T cells from cord blood	blood
21	chr12:29429200-29463600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr12:29429400-29460400	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr12:29431800-29434800	Weak transcription	HSMMtube	muscle
24	chr12:29432200-29442800	Weak transcription	Psoas Muscle	Psoas
25	chr12:29432400-29434400	Weak transcription	Adipose Nuclei	Adipose
26	chr12:29432400-29438400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr12:29432600-29434400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:29432600-29434800	Weak transcription	HSMM	muscle
29	chr12:29432600-29435000	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr12:29432600-29436600	Weak transcription	NH-A	brain
31	chr12:29432800-29434400	Weak transcription	Osteobl	bone
32	chr12:29432800-29434600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr12:29432800-29434600	Weak transcription	NHDF-Ad	bronchial
34	chr12:29432800-29445800	Weak transcription	Primary B cells from cord blood	blood
35	chr12:29433400-29434800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr12:29433400-29435400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:29433400-29436000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:29433400-29436400	Enhancers	Primary hematopoietic stem cells	blood
39	chr12:29433600-29435400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr12:29434200-29449600	Weak transcription	Primary neutrophils fromperipheralblood	blood

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