Variant report

Variant	rs61979448
Chromosome Location	chr14:81269223-81269224
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1016507	0.86[AFR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11623023	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12431821	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12432357	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12434564	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12880014	0.86[AMR][1000 genomes]
rs12880075	0.80[ASN][1000 genomes]
rs12886388	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12888082	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12891585	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12896065	0.86[AMR][1000 genomes]
rs1458993	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs172920	0.88[EUR][1000 genomes]
rs17542615	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17613911	0.83[AMR][1000 genomes]
rs17614081	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1797670	0.80[AFR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1992973	0.84[AMR][1000 genomes]
rs2044737	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs2044738	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2217174	0.83[EUR][1000 genomes]
rs2217176	0.82[EUR][1000 genomes]
rs228110	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs228111	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs228118	0.88[EUR][1000 genomes]
rs228120	0.88[EUR][1000 genomes]
rs228121	0.88[EUR][1000 genomes]
rs228125	0.88[EUR][1000 genomes]
rs2371416	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2556601	0.87[EUR][1000 genomes]
rs2556605	0.84[EUR][1000 genomes]
rs2596118	0.84[AMR][1000 genomes]
rs35540104	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4523859	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61979449	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61979451	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61979452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs66492142	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7141130	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs71416852	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7143407	0.86[AFR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7148368	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7148618	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7150858	0.87[ASN][1000 genomes]
rs7153979	0.82[EUR][1000 genomes]
rs7154132	0.82[EUR][1000 genomes]
rs7154373	0.82[EUR][1000 genomes]
rs728444	0.82[EUR][1000 genomes]
rs759916	0.84[EUR][1000 genomes]
rs759917	0.83[EUR][1000 genomes]
rs8003784	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8006507	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8006864	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8021137	0.84[EUR][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:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81192800-81305400	Weak transcription	Primary B cells from cord blood	blood
2	chr14:81246800-81271600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr14:81251800-81282600	Weak transcription	A549	lung
4	chr14:81256400-81271000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr14:81259400-81274000	Weak transcription	Aorta	Aorta
6	chr14:81259400-81274000	Weak transcription	Pancreas	Pancrea
7	chr14:81259400-81274200	Weak transcription	Thymus	Thymus
8	chr14:81259400-81278400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:81264800-81269400	Weak transcription	Fetal Lung	lung
10	chr14:81265600-81277200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr14:81265600-81284400	Weak transcription	Fetal Thymus	thymus
12	chr14:81265800-81274600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:81267400-81273800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:81267400-81284200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:81267400-81284800	Weak transcription	HSMM	muscle
16	chr14:81269000-81269800	Strong transcription	Dnd41	blood

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