Variant report

Variant	rs2570370
Chromosome Location	chr1:226607385-226607386
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:226599163..226601499-chr1:226605058..226607870,2	MCF-7	breast:
2	chr1:226607208..226608718-chr1:226613102..226615218,2	K562	blood:
3	chr1:226595173..226597286-chr1:226606354..226609716,3	MCF-7	breast:
4	chr1:226607208..226609606-chr1:226610785..226615218,4	K562	blood:

Variant related genes	Relation type
ENSG00000143799	Chromatin interaction
ENSG00000270287	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1104893	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1341333	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1341335	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1341336	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1397550	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1417765	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1805414	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1828445	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1828446	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1858548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1858549	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1858550	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1865220	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1865221	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1865222	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2027439	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2048424	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2048426	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2136875	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2249844	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2570368	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2570369	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2666427	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2666428	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2695235	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2695236	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2695237	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2695238	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2695239	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2695240	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793376	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2793377	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2793378	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2793380	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2793382	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2793654	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2793655	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2793657	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3219090	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3219112	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3219119	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3754376	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs907186	0.83[ASN][1000 genomes]
rs9426568	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][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	nsv832770	chr1:226465130-226655512	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv832781	chr1:226570901-226750697	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226596200-226622600	Weak transcription	Right Atrium	heart
2	chr1:226602800-226616200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:226606000-226616200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr1:226606200-226612000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr1:226606200-226616000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:226606400-226607600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:226606600-226608600	Enhancers	Brain Cingulate Gyrus	brain
8	chr1:226606800-226607400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:226607000-226607400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:226607000-226607400	Active TSS	Brain Angular Gyrus	brain
11	chr1:226607000-226607400	Active TSS	Brain Anterior Caudate	brain
12	chr1:226607000-226607400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
13	chr1:226607000-226607400	Active TSS	Brain Substantia Nigra	brain
14	chr1:226607000-226607400	Enhancers	Fetal Brain Male	brain
15	chr1:226607000-226607400	Bivalent Enhancer	HMEC	breast
16	chr1:226607000-226607400	Flanking Active TSS	HSMMtube	muscle
17	chr1:226607000-226607600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:226607000-226607600	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr1:226607000-226607600	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr1:226607000-226607600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:226607000-226607600	Flanking Active TSS	Brain Hippocampus Middle	brain
22	chr1:226607000-226608200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:226607200-226607400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr1:226607200-226607400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr1:226607200-226607400	Flanking Active TSS	HSMM	muscle
26	chr1:226607200-226607400	Flanking Bivalent TSS/Enh	Osteobl	bone
27	chr1:226607200-226607600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr1:226607200-226608600	Enhancers	Sigmoid Colon	Sigmoid Colon

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