Variant report

Variant	rs4610465
Chromosome Location	chr5:43569026-43569027
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43555077..43559335-chr5:43568297..43574840,9	MCF-7	breast:
2	chr5:43566373..43570038-chr5:43599893..43602969,4	K562	blood:
3	chr5:43555648..43560164-chr5:43568493..43574062,6	MCF-7	breast:
4	chr5:43553205..43562648-chr5:43565710..43576086,17	K562	blood:
5	chr5:43562535..43565589-chr5:43568381..43570890,3	K562	blood:
6	chr5:43565730..43567318-chr5:43568871..43570663,2	K562	blood:
7	chr5:43568689..43571180-chr5:43594322..43596361,2	MCF-7	breast:
8	chr5:43563244..43565362-chr5:43568381..43570262,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000172239	Chromatin interaction
ENSG00000112992	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10042992	1.00[ASN][1000 genomes]
rs10057103	0.85[ASN][1000 genomes]
rs10058558	0.90[ASN][1000 genomes]
rs10059912	0.90[EUR][1000 genomes]
rs10059993	0.81[EUR][1000 genomes]
rs10065689	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10065863	0.87[ASN][1000 genomes]
rs1072745	0.85[ASN][1000 genomes]
rs1072746	0.85[ASN][1000 genomes]
rs10941640	0.90[ASN][1000 genomes]
rs11949083	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11958046	0.90[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs12521249	0.91[EUR][1000 genomes]
rs12652547	0.90[ASN][1000 genomes]
rs12697457	0.90[EUR][1000 genomes]
rs13189004	0.99[ASN][1000 genomes]
rs13189484	0.87[EUR][1000 genomes]
rs13359906	0.90[EUR][1000 genomes]
rs13360902	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1366410	0.81[EUR][1000 genomes]
rs28437972	0.83[EUR][1000 genomes]
rs35881272	0.89[ASN][1000 genomes]
rs36013953	0.90[ASN][1000 genomes]
rs4072918	0.83[EUR][1000 genomes]
rs4072919	0.83[EUR][1000 genomes]
rs4073848	0.90[ASN][1000 genomes]
rs4073850	0.89[ASN][1000 genomes]
rs4073851	0.85[ASN][1000 genomes]
rs4367306	0.89[ASN][1000 genomes]
rs4386738	0.90[EUR][1000 genomes]
rs4428418	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4513704	0.89[ASN][1000 genomes]
rs4535459	0.90[EUR][1000 genomes]
rs4866752	0.88[ASN][1000 genomes]
rs4866835	0.89[EUR][1000 genomes]
rs4991951	0.84[ASN][1000 genomes]
rs55641556	0.96[ASN][1000 genomes]
rs55667604	0.90[EUR][1000 genomes]
rs55855322	0.81[EUR][1000 genomes]
rs56008952	0.89[EUR][1000 genomes]
rs56097465	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56400900	0.96[ASN][1000 genomes]
rs59224335	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60297702	0.87[EUR][1000 genomes]
rs6451718	0.89[ASN][1000 genomes]
rs6860493	0.81[EUR][1000 genomes]
rs6866325	0.85[EUR][1000 genomes]
rs6866802	0.89[EUR][1000 genomes]
rs6869933	0.89[EUR][1000 genomes]
rs6884661	0.88[EUR][1000 genomes]
rs6885679	0.80[EUR][1000 genomes]
rs6891363	0.89[EUR][1000 genomes]
rs6898866	0.92[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7701429	0.88[ASN][1000 genomes]
rs7705166	0.81[EUR][1000 genomes]
rs7706431	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7708072	0.89[ASN][1000 genomes]
rs7710125	0.89[ASN][1000 genomes]
rs7710628	0.80[EUR][1000 genomes]
rs7713479	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7715782	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7732656	0.81[EUR][1000 genomes]
rs7736615	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7737793	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9292883	0.90[ASN][1000 genomes]
rs9885189	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv881017	chr5:43444826-43731692	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	222 gene(s)	inside rSNPs	diseases
2	nsv830275	chr5:43469511-43639384	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	220 gene(s)	inside rSNPs	diseases
3	nsv881108	chr5:43527432-43800333	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
4	esv3471239	chr5:43541792-43587904	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
5	esv3471240	chr5:43541792-43587904	Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4610465	NNT	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43557800-43571400	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr5:43557800-43584600	Weak transcription	Psoas Muscle	Psoas
3	chr5:43560200-43584400	Weak transcription	K562	blood
4	chr5:43562000-43570400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr5:43564000-43574800	Weak transcription	Fetal Intestine Small	intestine
6	chr5:43564600-43571000	Weak transcription	Colon Smooth Muscle	Colon
7	chr5:43564600-43575000	Weak transcription	Fetal Stomach	stomach
8	chr5:43564600-43580200	Weak transcription	Fetal Kidney	kidney
9	chr5:43564800-43570800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr5:43564800-43571000	Weak transcription	NHDF-Ad	bronchial
11	chr5:43564800-43575400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr5:43565200-43572600	Weak transcription	Hela-S3	cervix
13	chr5:43565400-43579000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:43565400-43601800	Weak transcription	Fetal Thymus	thymus
15	chr5:43565600-43575000	Weak transcription	Fetal Muscle Leg	muscle
16	chr5:43565600-43581800	Weak transcription	Dnd41	blood
17	chr5:43566200-43590400	Weak transcription	Thymus	Thymus
18	chr5:43566400-43580200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:43566800-43586000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr5:43567000-43575000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:43567000-43575200	Weak transcription	Primary T cells from cord blood	blood
22	chr5:43567200-43575200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr5:43567200-43575200	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr5:43567200-43577000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:43567400-43602000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr5:43568000-43601800	Weak transcription	Primary B cells from peripheral blood	blood
27	chr5:43568000-43602400	Weak transcription	Pancreas	Pancrea
28	chr5:43568400-43581800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr5:43568600-43570000	Weak transcription	Left Ventricle	heart
30	chr5:43568600-43601800	Weak transcription	Fetal Brain Female	brain
31	chr5:43568800-43572400	Weak transcription	GM12878-XiMat	blood
32	chr5:43569000-43571200	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr5:43569000-43601400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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