Variant report

Variant	rs4591731
Chromosome Location	chr5:76102513-76102514
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
2	chr5:76101619..76103504-chr5:76111998..76114759,2	K562	blood:

Variant related genes	Relation type
ENSG00000164251	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10058498	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10059976	0.87[ASN][1000 genomes]
rs12187125	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13162638	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13173178	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1529505	0.96[CEU][hapmap];1.00[CHB][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2115499	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2242995	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2243003	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2243020	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2243022	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2243026	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2243029	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2243031	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2243051	0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2243053	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2243057	0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2243059	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4380630	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs444403	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4703719	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4704365	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6453250	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6453251	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6453253	0.88[CEU][hapmap]
rs66946336	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6880329	0.96[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6887035	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6894167	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6897362	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7703930	1.00[CEU][hapmap];0.94[CHB][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7709688	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019669	chr5:75836365-76477788	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv462213	chr5:76067624-76112869	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv598682	chr5:76067624-76112869	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1015997	chr5:76079720-76129241	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1031491	chr5:76083382-76129241	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv2763908	chr5:76083394-76134777	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv598683	chr5:76086597-76129053	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv882210	chr5:76086597-76140337	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1022431	chr5:76086795-76127170	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1020397	chr5:76086795-76129241	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv598684	chr5:76086795-76130113	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1025151	chr5:76086795-76134777	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv1025061	chr5:76087544-76129241	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv1033086	chr5:76088861-76129241	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv1021460	chr5:76089512-76129241	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv1018194	chr5:76090951-76129241	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	nsv598685	chr5:76092225-76128521	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
18	nsv882211	chr5:76100536-76125577	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4591731	F2R	cis	Muscle Skeletal	GTEx
rs4591731	F2RL1	cis	multi-tissue	Pritchard
rs4591731	F2RL1	cis	Whole Blood	GTEx

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76098000-76104000	Weak transcription	Spleen	Spleen
2	chr5:76098000-76105000	Weak transcription	Right Atrium	heart
3	chr5:76099800-76102600	Enhancers	Fetal Intestine Small	intestine
4	chr5:76099800-76103400	Enhancers	Fetal Intestine Large	intestine
5	chr5:76100000-76104200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr5:76100200-76104400	Enhancers	HUVEC	blood vessel
7	chr5:76100400-76103000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:76100600-76103200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr5:76101200-76104200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr5:76101400-76102600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr5:76101400-76102600	Enhancers	K562	blood
12	chr5:76101400-76103000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:76101400-76103200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:76101400-76103800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr5:76101400-76103800	Enhancers	NHDF-Ad	bronchial
16	chr5:76101400-76104000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr5:76101400-76104200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:76101400-76104200	Enhancers	NHLF	lung
19	chr5:76101400-76104200	Enhancers	Osteobl	bone
20	chr5:76101400-76104400	Enhancers	Hela-S3	cervix
21	chr5:76101400-76104400	Enhancers	HSMMtube	muscle
22	chr5:76101400-76104600	Enhancers	HSMM	muscle
23	chr5:76101400-76105000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr5:76101400-76105400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:76101400-76107000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr5:76101400-76107400	Enhancers	NHEK	skin
27	chr5:76101600-76102600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr5:76101600-76102600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:76101600-76102600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:76101600-76102800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr5:76101600-76102800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:76101600-76104000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:76101600-76104400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:76101600-76105400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:76101600-76105400	Enhancers	HMEC	breast
36	chr5:76101600-76107000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:76101800-76102600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
38	chr5:76101800-76102600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr5:76101800-76102600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr5:76101800-76102600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr5:76101800-76102600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr5:76101800-76103000	Active TSS	A549	lung
43	chr5:76101800-76104200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:76102000-76102600	Flanking Active TSS	H9 Cell Line	embryonic stem cell
45	chr5:76102000-76103000	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr5:76102200-76102600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr5:76102200-76102600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:76102200-76102600	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr5:76102200-76102600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:76102400-76102600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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