Variant report

Variant	rs56881651
Chromosome Location	chr1:224835204-224835205
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:224826905..224830184-chr1:224832363..224835221,3	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10799590	0.85[EUR][1000 genomes]
rs10915684	0.86[EUR][1000 genomes]
rs10915694	0.93[EUR][1000 genomes]
rs10915696	0.81[EUR][1000 genomes]
rs12092438	0.82[EUR][1000 genomes]
rs12130499	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12132665	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs13374487	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1369846	0.87[EUR][1000 genomes]
rs1369847	0.83[EUR][1000 genomes]
rs1436169	0.83[EUR][1000 genomes]
rs1561110	0.86[EUR][1000 genomes]
rs1603917	0.85[EUR][1000 genomes]
rs1603918	0.85[EUR][1000 genomes]
rs169888	0.87[EUR][1000 genomes]
rs1965776	0.86[EUR][1000 genomes]
rs2648746	0.87[EUR][1000 genomes]
rs2936575	0.85[EUR][1000 genomes]
rs298732	0.85[EUR][1000 genomes]
rs298733	0.85[EUR][1000 genomes]
rs298734	0.85[EUR][1000 genomes]
rs298735	0.84[EUR][1000 genomes]
rs298738	0.85[EUR][1000 genomes]
rs298739	0.85[EUR][1000 genomes]
rs2993124	0.82[EUR][1000 genomes]
rs3012185	0.85[EUR][1000 genomes]
rs4147293	0.83[EUR][1000 genomes]
rs4653402	0.83[EUR][1000 genomes]
rs4653404	0.83[EUR][1000 genomes]
rs4653591	0.83[EUR][1000 genomes]
rs4653592	0.81[EUR][1000 genomes]
rs61676104	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6667034	0.85[EUR][1000 genomes]
rs6686604	0.82[EUR][1000 genomes]
rs6686633	0.82[EUR][1000 genomes]
rs67817586	0.84[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs713098	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7521396	0.86[EUR][1000 genomes]
rs7535296	0.86[EUR][1000 genomes]
rs7537973	0.85[EUR][1000 genomes]
rs7542431	0.93[EUR][1000 genomes]
rs7542995	0.94[EUR][1000 genomes]
rs7543218	0.81[EUR][1000 genomes]
rs7544312	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7545574	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014717	chr1:224551939-224885543	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv535311	chr1:224551939-224885543	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224820400-224840000	Weak transcription	Right Atrium	heart
2	chr1:224826000-224839200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:224826400-224837800	Weak transcription	NHLF	lung
4	chr1:224827000-224839800	Weak transcription	HSMM	muscle
5	chr1:224828600-224837800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:224828800-224853400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:224831600-224835600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:224832200-224839800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:224832200-224884400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:224832800-224837600	Weak transcription	Ovary	ovary
11	chr1:224832800-224838000	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr1:224832800-224869000	Weak transcription	Dnd41	blood
13	chr1:224833200-224874400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:224833400-224840600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:224833600-224837600	Weak transcription	NHDF-Ad	bronchial
16	chr1:224834600-224835600	Enhancers	Pancreas	Pancrea
17	chr1:224835000-224835400	Enhancers	Fetal Brain Male	brain
18	chr1:224835000-224835400	Enhancers	Fetal Muscle Trunk	muscle
19	chr1:224835000-224836000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:224835200-224835400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:224835200-224835600	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr1:224835200-224835600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr1:224835200-224835600	Enhancers	Brain Germinal Matrix	brain
24	chr1:224835200-224835600	Enhancers	NH-A	brain

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