Variant report

Variant	rs10038064
Chromosome Location	chr5:97972902-97972903
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:97960709..97962831-chr5:97972137..97973848,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10038307	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10039819	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10043199	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10045612	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10059259	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10065249	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10068399	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10075691	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10479181	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10479183	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10515282	0.83[ASN][1000 genomes]
rs11242242	0.94[ASN][1000 genomes]
rs11242255	0.94[ASN][1000 genomes]
rs11949924	0.83[ASN][1000 genomes]
rs11950934	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs13361670	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1421633	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1421634	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs149126	0.83[ASN][1000 genomes]
rs154197	1.00[JPT][hapmap]
rs154201	0.83[ASN][1000 genomes]
rs154203	0.83[ASN][1000 genomes]
rs154204	0.83[ASN][1000 genomes]
rs17166201	1.00[ASN][1000 genomes]
rs17661925	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2080994	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2112145	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs245444	0.83[ASN][1000 genomes]
rs27023	0.83[ASN][1000 genomes]
rs27032	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs27576	0.83[ASN][1000 genomes]
rs27577	0.83[ASN][1000 genomes]
rs36758	0.83[ASN][1000 genomes]
rs36767	0.83[ASN][1000 genomes]
rs387158	0.83[ASN][1000 genomes]
rs3907829	0.89[ASN][1000 genomes]
rs3909494	0.94[ASN][1000 genomes]
rs40175	0.85[ASN][1000 genomes]
rs4018045	0.83[ASN][1000 genomes]
rs4277375	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs457225	0.83[ASN][1000 genomes]
rs463314	0.83[ASN][1000 genomes]
rs464686	0.83[ASN][1000 genomes]
rs465312	0.83[ASN][1000 genomes]
rs467627	0.83[ASN][1000 genomes]
rs467657	0.83[ASN][1000 genomes]
rs468016	0.83[ASN][1000 genomes]
rs468238	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs59126397	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6883625	1.00[ASN][1000 genomes]
rs6895508	0.94[ASN][1000 genomes]
rs73149511	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7444475	0.89[ASN][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	nsv1016611	chr5:97873846-98035559	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv537816	chr5:97873846-98035559	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv1029509	chr5:97888644-98040172	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv882413	chr5:97918829-98022320	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1832089	chr5:97934125-97976039	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97967400-97975000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:97971600-97974000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr5:97971800-97973000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:97971800-97973000	Weak transcription	HSMMtube	muscle
5	chr5:97971800-97973200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:97971800-97973400	Weak transcription	Adipose Nuclei	Adipose
7	chr5:97971800-97973600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr5:97971800-97973600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:97971800-97974000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr5:97971800-97974000	Weak transcription	HSMM	muscle
11	chr5:97971800-97974200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:97971800-97974200	Weak transcription	NHLF	lung
13	chr5:97971800-97975000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr5:97972000-97973000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr5:97972000-97973000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:97972000-97973000	Weak transcription	NHDF-Ad	bronchial
17	chr5:97972000-97973200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr5:97972000-97973400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:97972000-97973400	Weak transcription	Osteobl	bone
20	chr5:97972000-97973600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr5:97972000-97973800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr5:97972000-97974000	Weak transcription	Small Intestine	intestine
23	chr5:97972000-97975000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:97972000-97977600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr5:97972000-97977600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr5:97972800-97974600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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