Variant report

Variant	rs2331403
Chromosome Location	chr14:68316915-68316916
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:68314860..68317034-chr14:68333283..68336153,3	MCF-7	breast:
2	chr14:68315642..68318719-chr14:68330973..68334711,3	MCF-7	breast:
3	chr14:68315532..68317270-chr14:68325905..68327762,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000182185	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10130919	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10133239	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10135927	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10137614	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10137930	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10141638	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10146380	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10150007	0.85[EUR][1000 genomes]
rs10483805	0.90[ASN][1000 genomes]
rs10873208	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11158697	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11620947	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11622521	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11622535	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11623756	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11626590	0.83[EUR][1000 genomes]
rs11626769	0.85[EUR][1000 genomes]
rs11626778	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11627100	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11627417	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11627565	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11844492	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11847628	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17783094	0.83[EUR][1000 genomes]
rs17783124	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17783160	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs181572	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs181575	0.93[ASN][1000 genomes]
rs1956345	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1956346	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1956347	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1956348	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2235962	0.90[ASN][1000 genomes]
rs2235963	0.90[ASN][1000 genomes]
rs2235965	0.90[ASN][1000 genomes]
rs2295108	0.90[ASN][1000 genomes]
rs28373844	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28604984	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28623567	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35272075	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4284565	0.82[EUR][1000 genomes]
rs4402486	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4569184	0.90[ASN][1000 genomes]
rs55999745	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7149482	0.83[EUR][1000 genomes]
rs7154635	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7159109	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7160196	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs72723196	0.83[EUR][1000 genomes]
rs72725103	0.86[EUR][1000 genomes]
rs72725114	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8003431	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8004611	0.80[EUR][1000 genomes]
rs8006089	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8010086	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8011690	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8012974	0.85[EUR][1000 genomes]
rs8017013	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8018709	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs932555	0.83[AMR][1000 genomes];0.91[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	nsv1042536	chr14:68136913-68343198	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv542122	chr14:68136913-68343198	Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1054697	chr14:68202004-68345982	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 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	chr14:68287600-68317800	Weak transcription	Spleen	Spleen
2	chr14:68287800-68318200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr14:68294600-68318200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr14:68300600-68336200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr14:68303200-68318200	Weak transcription	Ovary	ovary
6	chr14:68303200-68331800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr14:68311400-68325800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr14:68313200-68318000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr14:68313200-68324400	Weak transcription	Gastric	stomach
10	chr14:68313200-68326400	Weak transcription	Pancreas	Pancrea
11	chr14:68313200-68333400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr14:68313200-68333800	Weak transcription	Primary T cells from cord blood	blood
13	chr14:68313400-68322200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr14:68313800-68320600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr14:68313800-68324600	Weak transcription	Esophagus	oesophagus
16	chr14:68314000-68331400	Weak transcription	Dnd41	blood
17	chr14:68315200-68317800	Weak transcription	Thymus	Thymus
18	chr14:68315800-68318800	Weak transcription	Primary B cells from cord blood	blood
19	chr14:68316400-68318000	Weak transcription	Fetal Stomach	stomach
20	chr14:68316600-68319000	Enhancers	Placenta	Placenta
21	chr14:68316600-68321600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr14:68316800-68317200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:68316800-68319800	Enhancers	Primary hematopoietic stem cells	blood
24	chr14:68316800-68321400	Enhancers	Primary hematopoietic stem cells short term culture	blood

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