Variant report

Variant	rs2622269
Chromosome Location	chr9:116398827-116398828
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:116398646..116400904-chr9:116412622..116414433,2	MCF-7	breast:
2	chr9:116392305..116395161-chr9:116397306..116400059,2	MCF-7	breast:
3	chr9:116382976..116384778-chr9:116398456..116400066,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000227482	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1411672	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1679671	0.90[EUR][1000 genomes]
rs2039224	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2622265	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2622268	0.84[AMR][1000 genomes]
rs2812397	0.81[AMR][1000 genomes]
rs4582632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs589248	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs590963	0.84[AMR][1000 genomes]
rs591354	0.84[AMR][1000 genomes]
rs6478026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs659498	1.00[AMR][1000 genomes];0.97[EUR][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	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription 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 miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv893748	chr9:116308709-116421786	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
4	nsv893749	chr9:116378759-116439749	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	esv2560176	chr9:116397318-116399163	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	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	chr9:116385800-116402600	Weak transcription	Stomach Mucosa	stomach
2	chr9:116389800-116402800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:116392600-116399000	Enhancers	Fetal Muscle Leg	muscle
4	chr9:116393400-116399400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:116393600-116399000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr9:116394600-116399000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr9:116396000-116399200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:116396200-116399000	Enhancers	Adipose Nuclei	Adipose
9	chr9:116396200-116399000	Enhancers	HSMM	muscle
10	chr9:116396200-116399400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:116396200-116399400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:116397000-116399600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr9:116397200-116400400	Weak transcription	Rectal Smooth Muscle	rectum
14	chr9:116397200-116401200	Weak transcription	Spleen	Spleen
15	chr9:116397600-116403000	Weak transcription	Fetal Heart	heart
16	chr9:116397800-116400800	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:116398000-116399000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:116398000-116399000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:116398200-116399000	Flanking Active TSS	HepG2	liver
20	chr9:116398400-116399000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr9:116398400-116399000	Enhancers	NHLF	lung
22	chr9:116398600-116399000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
23	chr9:116398800-116399000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:116398800-116399000	Enhancers	Osteobl	bone
25	chr9:116398800-116401200	Weak transcription	Fetal Stomach	stomach
26	chr9:116398800-116410200	Weak transcription	Right Atrium	heart

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