Variant report

Variant	rs4420183
Chromosome Location	chr10:51101356-51101357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10857543	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2015984	0.93[ASN][1000 genomes]
rs58501852	1.00[ASN][1000 genomes]
rs59632809	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6537553	0.80[ASN][1000 genomes]
rs7904589	0.81[EUR][1000 genomes]
rs7911715	0.93[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	esv2758219	chr10:50971974-51925166	Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	esv2759749	chr10:50971974-51925166	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv428232	chr10:50971974-51925166	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv895379	chr10:51022933-51187793	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv32940	chr10:51051718-51488059	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv895381	chr10:51094660-51515534	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:51051800-51102800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr10:51051800-51122000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr10:51075600-51103400	Weak transcription	Fetal Intestine Large	intestine
4	chr10:51080800-51130200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:51083200-51102800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr10:51084400-51131800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr10:51084600-51130200	Weak transcription	Fetal Lung	lung
8	chr10:51084600-51136000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr10:51084600-51136600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr10:51084600-51137800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr10:51084800-51103600	Weak transcription	Fetal Stomach	stomach
12	chr10:51085000-51103200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr10:51085000-51127200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr10:51085400-51106000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr10:51085400-51138200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr10:51085400-51138600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr10:51086200-51102800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:51087000-51103400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr10:51087000-51132000	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr10:51087200-51103200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:51087600-51122000	Weak transcription	Primary B cells from cord blood	blood
22	chr10:51087600-51122400	Weak transcription	Adipose Nuclei	Adipose
23	chr10:51089800-51120600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr10:51089800-51121800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr10:51091200-51138000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:51095000-51137200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:51097800-51103800	Weak transcription	Dnd41	blood
28	chr10:51098000-51102200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr10:51098200-51122000	Weak transcription	K562	blood
30	chr10:51100400-51104400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr10:51100600-51104400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr10:51100800-51137600	Weak transcription	Lung	lung
33	chr10:51101200-51119800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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