Variant report

Variant	rs1870109
Chromosome Location	chr8:110407381-110407382
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:110397376..110399556-chr8:110407254..110410081,2	K562	blood:
2	chr8:110399789..110401392-chr8:110406709..110408339,2	K562	blood:
3	chr8:110399789..110401948-chr8:110406839..110408656,2	K562	blood:
4	chr8:110403524..110405569-chr8:110405749..110408596,2	K562	blood:

Extended variants
information (count: 125 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10088918	0.98[ASN][1000 genomes]
rs10097258	0.98[ASN][1000 genomes]
rs10098672	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10099126	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10101522	0.98[ASN][1000 genomes]
rs1037695	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10458302	0.95[ASN][1000 genomes]
rs10955518	0.98[ASN][1000 genomes]
rs12334438	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12550601	0.98[ASN][1000 genomes]
rs12680439	0.96[ASN][1000 genomes]
rs13252234	0.98[ASN][1000 genomes]
rs13254245	0.98[ASN][1000 genomes]
rs13254461	0.98[ASN][1000 genomes]
rs13258279	0.95[ASN][1000 genomes]
rs13262995	0.95[ASN][1000 genomes]
rs13264576	0.95[ASN][1000 genomes]
rs13264587	0.95[ASN][1000 genomes]
rs13266285	0.97[ASN][1000 genomes]
rs13266293	0.95[ASN][1000 genomes]
rs13266374	0.96[ASN][1000 genomes]
rs13266838	0.96[ASN][1000 genomes]
rs13267428	0.97[ASN][1000 genomes]
rs13268429	0.97[ASN][1000 genomes]
rs13278812	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1379363	0.98[ASN][1000 genomes]
rs1379364	0.98[ASN][1000 genomes]
rs1379365	0.98[ASN][1000 genomes]
rs1379369	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1379370	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1457284	0.84[EUR][1000 genomes]
rs1457287	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1457289	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1457290	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1457291	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1457292	0.98[ASN][1000 genomes]
rs1457293	0.98[ASN][1000 genomes]
rs1458920	0.96[ASN][1000 genomes]
rs1471124	0.81[EUR][1000 genomes]
rs1471125	0.81[EUR][1000 genomes]
rs1585294	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1624114	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1673390	0.83[EUR][1000 genomes]
rs1673393	0.83[EUR][1000 genomes]
rs1673397	0.81[EUR][1000 genomes]
rs1673398	0.81[EUR][1000 genomes]
rs1673400	0.81[EUR][1000 genomes]
rs1673401	0.81[EUR][1000 genomes]
rs1673403	0.81[EUR][1000 genomes]
rs1673404	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1673405	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1673407	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1673408	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16879470	0.96[ASN][1000 genomes]
rs1783142	0.81[EUR][1000 genomes]
rs1783143	0.81[EUR][1000 genomes]
rs1783144	0.84[EUR][1000 genomes]
rs1783145	0.81[EUR][1000 genomes]
rs1783149	0.81[EUR][1000 genomes]
rs1783152	0.81[EUR][1000 genomes]
rs1783163	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1783164	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1783165	0.80[ASN][1000 genomes]
rs1824193	0.98[ASN][1000 genomes]
rs1870107	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1870108	0.98[ASN][1000 genomes]
rs2061294	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2061295	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2124982	0.98[ASN][1000 genomes]
rs2199120	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2349436	0.98[ASN][1000 genomes]
rs2349759	0.92[ASN][1000 genomes]
rs2349761	0.99[ASN][1000 genomes]
rs2607638	0.81[EUR][1000 genomes]
rs2607639	0.80[EUR][1000 genomes]
rs2844251	0.82[EUR][1000 genomes]
rs2844252	0.81[EUR][1000 genomes]
rs2844253	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2926224	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2926228	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2926238	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2980569	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2980582	0.84[EUR][1000 genomes]
rs2980583	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4348463	0.98[ASN][1000 genomes]
rs4604408	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4734212	0.98[ASN][1000 genomes]
rs4735130	0.85[ASN][1000 genomes]
rs4735133	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4735134	0.95[ASN][1000 genomes]
rs6469256	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6469257	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6469260	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6469261	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6469262	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6651203	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6982748	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6987198	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6993467	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6993552	0.98[ASN][1000 genomes]
rs6999505	0.96[ASN][1000 genomes]
rs7002606	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7002926	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7014589	0.95[ASN][1000 genomes]
rs7015262	0.95[ASN][1000 genomes]
rs7016609	0.96[ASN][1000 genomes]
rs714995	0.81[EUR][1000 genomes]
rs7818553	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7819141	0.98[ASN][1000 genomes]
rs7819151	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs897838	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs897839	0.98[ASN][1000 genomes]
rs921959	0.98[ASN][1000 genomes]
rs9297425	0.98[ASN][1000 genomes]
rs9642806	0.97[ASN][1000 genomes]
rs964307	0.98[ASN][1000 genomes]
rs9656793	0.98[ASN][1000 genomes]
rs9656882	0.98[ASN][1000 genomes]
rs965930	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891273	chr8:110219735-110475874	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv891279	chr8:110268104-110450092	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv891280	chr8:110346363-110465481	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	esv1845153	chr8:110397738-110421793	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1832336	chr8:110397738-110437384	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1018510	chr8:110403496-110504029	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs1870109	RP11-419L20.2	cis	Thyroid	GTEx
rs1870109	PKHD1L1	cis	Thyroid	GTEx
rs1870109	PKHD1L1	Cis_1M	lymphoblastoid	RTeQTL
rs1870109	PKHD1L1	cis	multi-tissue	Pritchard
rs1870109	PKHD1L1	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110406000-110408600	Weak transcription	K562	blood
2	chr8:110407000-110407400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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