Variant report

Variant	rs17159467
Chromosome Location	chr5:100125658-100125659
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10515265	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10515266	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10515267	1.00[ASN][1000 genomes]
rs1423381	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17159344	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159370	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159464	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159534	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17159602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159616	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159626	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17160705	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17160732	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs17160771	1.00[JPT][hapmap]
rs17160844	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2544911	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2544912	1.00[CEU][hapmap]
rs2544914	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2544915	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2544917	1.00[EUR][1000 genomes]
rs2544919	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2548272	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2548277	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2561524	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2561525	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2561526	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2725118	1.00[EUR][1000 genomes]
rs2725123	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs3776165	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs3776166	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs3776173	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3857364	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6595534	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6878151	1.00[ASN][1000 genomes]
rs6897681	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73775624	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs768777	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7725476	1.00[ASN][1000 genomes]
rs980901	1.00[EUR][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	nsv948969	chr5:99534096-100133827	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv1021183	chr5:99625857-100221426	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1017420	chr5:99745775-100133140	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv537825	chr5:99745775-100133140	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv1023765	chr5:99915011-100733755	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
6	esv2762532	chr5:100041758-100136552	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:100114000-100136400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:100118200-100126000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr5:100118600-100126000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:100124600-100126200	Weak transcription	Fetal Lung	lung
5	chr5:100125200-100126000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:100125200-100126200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr5:100125200-100126400	Enhancers	Placenta Amnion	Placenta Amnion
8	chr5:100125400-100125800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr5:100125400-100125800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr5:100125400-100125800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr5:100125400-100126000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:100125400-100126200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:100125400-100126200	Enhancers	Spleen	Spleen
14	chr5:100125400-100126400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:100125400-100126400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr5:100125400-100126400	Enhancers	Brain Cingulate Gyrus	brain
17	chr5:100125400-100126400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr5:100125400-100126400	Enhancers	Pancreas	Pancrea
19	chr5:100125400-100126800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr5:100125400-100127400	Enhancers	Dnd41	blood
21	chr5:100125600-100125800	Enhancers	Adipose Nuclei	Adipose
22	chr5:100125600-100126000	Enhancers	Brain Substantia Nigra	brain
23	chr5:100125600-100126200	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr5:100125600-100126200	Flanking Active TSS	GM12878-XiMat	blood
25	chr5:100125600-100126400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:100125600-100126400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:100125600-100126400	Enhancers	Fetal Intestine Large	intestine
28	chr5:100125600-100126400	Enhancers	Placenta	Placenta
29	chr5:100125600-100126400	Enhancers	Fetal Thymus	thymus
30	chr5:100125600-100126400	Enhancers	HUVEC	blood vessel
31	chr5:100125600-100126400	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr5:100125600-100126800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr5:100125600-100127200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr5:100125600-100127200	Enhancers	A549	lung
35	chr5:100125600-100127400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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