Variant report

Variant	rs10026518
Chromosome Location	chr4:151588483-151588484
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:151586870..151590523-chr4:151590940..151593870,4	K562	blood:
2	chr4:151587714..151590523-chr4:151591747..151595848,4	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10003085	0.93[CHB][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes]
rs10004115	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10017937	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10021640	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10028040	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10034965	0.90[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10520078	0.81[JPT][hapmap]
rs1148656	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs12500679	0.82[EUR][1000 genomes]
rs12505123	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12505967	0.81[JPT][hapmap]
rs1289963	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13105060	0.93[JPT][hapmap]
rs13145482	0.80[JPT][hapmap]
rs13340305	0.97[ASN][1000 genomes]
rs17026968	0.82[EUR][1000 genomes]
rs17026978	0.82[EUR][1000 genomes]
rs17027065	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17027116	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1966844	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28379788	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28405183	0.82[EUR][1000 genomes]
rs28447376	0.82[EUR][1000 genomes]
rs28501240	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28521457	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28539520	0.90[AFR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28540258	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28544421	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28558492	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28572569	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28591543	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28627398	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28630451	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28641948	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28802622	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs294528	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3922785	0.93[CHB][hapmap];0.84[JPT][hapmap]
rs4260528	0.96[AFR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4309819	0.92[JPT][hapmap]
rs4318628	0.81[JPT][hapmap]
rs4336207	0.81[JPT][hapmap]
rs57790879	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59515357	0.82[EUR][1000 genomes]
rs61655905	0.82[EUR][1000 genomes]
rs6835367	0.93[JPT][hapmap]
rs6849364	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6858706	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72959804	0.82[EUR][1000 genomes]
rs7655913	0.96[AFR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7691319	0.82[EUR][1000 genomes]
rs7691594	0.82[EUR][1000 genomes]
rs9884181	0.81[JPT][hapmap]
rs9884732	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880256	chr4:151126725-151751369	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv817540	chr4:151228965-151858609	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv869051	chr4:151347901-151737781	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1024820	chr4:151364078-151943561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv1032070	chr4:151514664-151775259	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv880261	chr4:151521933-151588483	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv830113	chr4:151538184-151691942	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv1029861	chr4:151556384-151720601	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151487200-151655000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr4:151533400-151596200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:151571200-151601600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr4:151571200-151604600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr4:151574800-151601200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr4:151577600-151637000	Weak transcription	Primary T cells from cord blood	blood
7	chr4:151578600-151589600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:151579400-151604400	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr4:151582200-151642800	Weak transcription	Left Ventricle	heart
10	chr4:151582600-151595800	Weak transcription	Fetal Intestine Small	intestine
11	chr4:151583400-151603400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr4:151585200-151589200	Weak transcription	Ovary	ovary
13	chr4:151585200-151590200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:151586000-151589800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:151586000-151600800	Weak transcription	Primary B cells from peripheral blood	blood
16	chr4:151586400-151604800	Weak transcription	HSMM	muscle
17	chr4:151587000-151600200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:151587000-151600600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:151587000-151603400	Weak transcription	Aorta	Aorta
20	chr4:151587000-151604600	Weak transcription	Small Intestine	intestine
21	chr4:151587400-151592400	Weak transcription	Primary B cells from cord blood	blood
22	chr4:151587400-151605000	Weak transcription	GM12878-XiMat	blood

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