Variant report

Variant	rs2697923
Chromosome Location	chr11:47363215-47363216
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:47352349..47353915-chr11:47361681..47363878,2	MCF-7	breast:
2	chr11:47362701..47365249-chr11:47372942..47374468,2	K562	blood:
3	chr11:47359409..47362242-chr11:47362245..47364967,2	MCF-7	breast:
4	chr11:47362842..47365902-chr11:47366345..47370723,5	K562	blood:
5	chr11:47362758..47365324-chr11:47366232..47368748,4	MCF-7	breast:
6	chr11:47357637..47360736-chr11:47361620..47364167,4	K562	blood:
7	chr11:47289590..47291966-chr11:47362403..47364981,2	K562	blood:
8	chr11:47204720..47207139-chr11:47362825..47364900,2	K562	blood:
9	chr11:47288601..47291966-chr11:47362403..47364981,3	K562	blood:
10	chr11:47358496..47361439-chr11:47361620..47365193,4	K562	blood:
11	chr11:47362680..47364496-chr11:47377424..47380369,2	K562	blood:
12	chr11:47362842..47364563-chr11:47366345..47368440,2	K562	blood:
13	chr11:47355176..47357449-chr11:47361021..47363432,2	K562	blood:
14	chr11:47354148..47357317-chr11:47361021..47366088,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000025434	Chromatin interaction
ENSG00000165912	Chromatin interaction
ENSG00000110514	Chromatin interaction
ENSG00000134571	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10838696	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11039130	0.82[CHB][hapmap]
rs11039138	0.80[CEU][hapmap];1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs11039139	1.00[ASN][1000 genomes]
rs11039149	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11039159	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11039162	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11039165	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11039182	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11039183	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11606683	0.84[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11988	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2167080	1.00[ASN][1000 genomes]
rs2278890	0.81[CEU][hapmap]
rs2596407	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2856653	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3824869	0.84[CEU][hapmap]
rs7116451	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs749067	0.84[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7944419	0.83[ASN][1000 genomes]
rs7944584	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897323	chr11:47182926-47460306	Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv917316	chr11:47232210-47448882	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
3	esv3330173	chr11:47289256-47450681	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
4	esv3416377	chr11:47289276-47450651	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
5	nsv832141	chr11:47333180-47520993	Flanking Active TSS Genic enhancers Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	nsv554209	chr11:47353498-47364127	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	9 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	chr11:47343200-47370600	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr11:47351400-47375600	Weak transcription	Primary B cells from cord blood	blood
3	chr11:47352400-47364000	Weak transcription	Lung	lung
4	chr11:47352600-47366000	Weak transcription	Brain Germinal Matrix	brain
5	chr11:47353600-47375400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr11:47354000-47369800	Weak transcription	Right Atrium	heart
7	chr11:47354800-47372800	Weak transcription	Gastric	stomach
8	chr11:47356800-47367200	Strong transcription	Right Ventricle	heart
9	chr11:47358400-47363600	Enhancers	Placenta	Placenta
10	chr11:47358400-47364000	Genic enhancers	Fetal Heart	heart
11	chr11:47359800-47363600	Strong transcription	Left Ventricle	heart
12	chr11:47361000-47364000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr11:47361200-47364200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:47361400-47363600	Weak transcription	Spleen	Spleen
15	chr11:47361400-47364000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr11:47361800-47363600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:47362400-47364600	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr11:47362800-47363400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:47362800-47363600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:47362800-47363800	Weak transcription	Fetal Intestine Small	intestine
21	chr11:47363000-47366600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr11:47363200-47363400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:47363200-47363400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:47363200-47363400	Enhancers	Hela-S3	cervix

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