Variant report

Variant	rs2655055
Chromosome Location	chr9:98071729-98071730
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:98070196..98076913-chr9:98077454..98080836,13	K562	blood:
2	chr9:98064416..98068474-chr9:98070574..98074570,5	K562	blood:
3	chr9:98070528..98077616-chr9:98077726..98081396,9	MCF-7	breast:
4	chr9:98069917..98072451-chr9:98074616..98076565,2	MCF-7	breast:
5	chr9:98070320..98072476-chr9:98077911..98080883,2	MCF-7	breast:
6	chr9:98064416..98067357-chr9:98070574..98072936,2	K562	blood:

Variant related genes	Relation type
ENSG00000158169	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1623009	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs173339	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs242448	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2765817	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs356660	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs356661	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs356662	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs356663	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs356671	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs356685	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs356686	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3780560	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs400727	1.00[EUR][1000 genomes]
rs420089	0.80[EUR][1000 genomes]
rs4743989	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4744440	0.83[EUR][1000 genomes]
rs475413	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs607105	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs648615	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs651009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7038007	0.80[AFR][1000 genomes]
rs9299427	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831657	chr9:97959274-98204769	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98060400-98075000	Weak transcription	NHEK	skin
2	chr9:98066200-98075200	Weak transcription	Left Ventricle	heart
3	chr9:98066800-98074800	Weak transcription	Thymus	Thymus
4	chr9:98067000-98075200	Weak transcription	Lung	lung
5	chr9:98067800-98074200	Weak transcription	GM12878-XiMat	blood
6	chr9:98068400-98075200	Weak transcription	HMEC	breast
7	chr9:98068800-98075200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:98068800-98075200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr9:98068800-98075200	Weak transcription	Brain Hippocampus Middle	brain
10	chr9:98068800-98075200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr9:98068800-98075400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr9:98069000-98075000	Weak transcription	Fetal Stomach	stomach
13	chr9:98069000-98075200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:98069000-98075200	Weak transcription	Fetal Lung	lung
15	chr9:98069000-98075200	Weak transcription	HUVEC	blood vessel
16	chr9:98069000-98075200	Weak transcription	NHLF	lung
17	chr9:98069000-98077200	Weak transcription	Hela-S3	cervix
18	chr9:98069000-98077400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:98069000-98077400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr9:98069400-98075200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr9:98069400-98075200	Weak transcription	Pancreas	Pancrea
22	chr9:98069400-98075200	Weak transcription	Psoas Muscle	Psoas
23	chr9:98069800-98075000	Weak transcription	Colonic Mucosa	Colon
24	chr9:98070000-98074400	Weak transcription	Fetal Heart	heart
25	chr9:98070200-98074200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr9:98070200-98074200	Weak transcription	A549	lung
27	chr9:98070200-98075200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:98070400-98073800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:98070400-98073800	Weak transcription	Duodenum Mucosa	Duodenum
30	chr9:98070400-98074400	Weak transcription	K562	blood
31	chr9:98070400-98074800	Weak transcription	Liver	Liver
32	chr9:98070400-98075000	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr9:98070400-98075000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr9:98070400-98075000	Weak transcription	Stomach Mucosa	stomach
35	chr9:98070400-98075000	Weak transcription	HepG2	liver
36	chr9:98070400-98075200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr9:98070800-98075200	Weak transcription	Fetal Intestine Small	intestine
38	chr9:98071000-98075000	Weak transcription	Fetal Intestine Large	intestine
39	chr9:98071000-98075200	Weak transcription	Small Intestine	intestine

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