Variant report

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10465835	0.83[AMR][1000 genomes]
rs10465836	0.82[CEU][hapmap];0.90[EUR][1000 genomes]
rs11206981	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11206989	0.85[CHB][hapmap];0.83[AMR][1000 genomes]
rs11206992	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs12563280	0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12565136	0.85[CHB][hapmap]
rs12566131	0.86[CHB][hapmap]
rs12568992	1.00[JPT][hapmap]
rs155291	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs155293	0.85[CHB][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17115222	1.00[JPT][hapmap]
rs17115233	0.83[CEU][hapmap];0.90[EUR][1000 genomes]
rs17115240	0.81[EUR][1000 genomes]
rs1857739	0.83[AMR][1000 genomes]
rs1857741	0.83[AMR][1000 genomes]
rs1857742	0.83[AMR][1000 genomes]
rs4124453	0.83[CEU][hapmap];0.90[EUR][1000 genomes]
rs61767495	0.97[ASN][1000 genomes]
rs61767496	1.00[ASN][1000 genomes]
rs61767497	0.89[ASN][1000 genomes]
rs61767499	0.86[ASN][1000 genomes]
rs61767500	0.86[ASN][1000 genomes]
rs61767501	0.86[ASN][1000 genomes]
rs61767502	0.86[ASN][1000 genomes]
rs66474646	0.90[EUR][1000 genomes]
rs66665045	0.81[EUR][1000 genomes]
rs72672662	0.81[EUR][1000 genomes]
rs72672669	0.81[EUR][1000 genomes]
rs72672676	0.90[EUR][1000 genomes]
rs72672678	0.81[EUR][1000 genomes]
rs7530049	0.85[CHB][hapmap];0.83[AMR][1000 genomes]
rs7530255	0.83[AMR][1000 genomes]
rs7533282	0.81[CEU][hapmap];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57623200-57635400	Weak transcription	Fetal Intestine Small	intestine
2	chr1:57624000-57644800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:57631800-57636400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:57631800-57636800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr1:57632000-57636400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr1:57632000-57636600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr1:57632000-57636600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr1:57632000-57637000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:57632000-57637400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:57632000-57637800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:57632200-57636000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:57632200-57636200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:57632200-57636400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr1:57633400-57639800	Weak transcription	Fetal Intestine Large	intestine
15	chr1:57634200-57636800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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