Variant report

Variant	rs73337306
Chromosome Location	chr5:127433880-127433881
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:127425561..127430012-chr5:127430548..127434724,5	K562	blood:
2	chr5:127432707..127435327-chr5:127438169..127440618,3	K562	blood:
3	chr5:127432801..127435148-chr5:127441508..127443788,3	K562	blood:
4	chr5:127429085..127432949-chr5:127432984..127436984,4	MCF-7	breast:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10519973	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10519974	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1368270	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17697126	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17697290	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17764718	0.97[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3805604	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4835938	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4835939	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4835942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4836362	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4836365	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55763377	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58395264	0.98[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58597384	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62373688	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62373689	0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62373694	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6867078	0.98[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7379655	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9800302	0.98[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][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	esv1813981	chr5:127327649-127437401	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv4993	chr5:127405214-127445622	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	esv1825644	chr5:127427533-127450581	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127421400-127436400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:127421400-127450200	Weak transcription	Fetal Thymus	thymus
3	chr5:127421600-127466800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:127422000-127434200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr5:127423000-127436600	Weak transcription	HSMMtube	muscle
6	chr5:127423600-127436400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr5:127423600-127444800	Weak transcription	Fetal Stomach	stomach
8	chr5:127423600-127494000	Weak transcription	K562	blood
9	chr5:127425800-127445000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr5:127429200-127436000	Weak transcription	Left Ventricle	heart
11	chr5:127429600-127436000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:127429800-127436000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr5:127430000-127441000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr5:127430800-127436000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:127431200-127434800	ZNF genes & repeats	A549	lung
16	chr5:127431400-127435600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:127431600-127435000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr5:127432200-127435200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:127432400-127454600	Weak transcription	Fetal Kidney	kidney
20	chr5:127432600-127437200	Weak transcription	NHDF-Ad	bronchial
21	chr5:127433600-127434000	ZNF genes & repeats	Psoas Muscle	Psoas
22	chr5:127433600-127434400	ZNF genes & repeats	Dnd41	blood
23	chr5:127433600-127435000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
24	chr5:127433600-127435400	Weak transcription	Fetal Heart	heart
25	chr5:127433800-127435000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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