Variant report

Variant	rs1127615
Chromosome Location	chr5:179660774-179660775
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:179660175..179662984-chr5:180235591..180238303,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000131446	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11743530	0.94[ASN][1000 genomes]
rs11743623	0.94[ASN][1000 genomes]
rs11955394	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11956696	0.89[ASN][1000 genomes]
rs13164011	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13190345	0.94[ASN][1000 genomes]
rs17080153	0.88[ASN][1000 genomes]
rs33979712	0.89[ASN][1000 genomes]
rs33998980	1.00[ASN][1000 genomes]
rs6869542	0.88[ASN][1000 genomes]
rs6872534	0.88[ASN][1000 genomes]
rs6885325	0.88[ASN][1000 genomes]
rs6898670	0.89[ASN][1000 genomes]
rs6898872	0.89[ASN][1000 genomes]
rs7702792	0.88[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	nsv948909	chr5:179249099-179772640	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	nsv1033706	chr5:179402769-179806356	Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	esv2758032	chr5:179534477-179729944	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	esv2759398	chr5:179534477-179729944	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv1023914	chr5:179649883-180040672	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv537983	chr5:179649883-180040672	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179650200-179669000	Weak transcription	Fetal Brain Male	brain
2	chr5:179651600-179678000	Weak transcription	Fetal Heart	heart
3	chr5:179653000-179662800	Weak transcription	Brain Hippocampus Middle	brain
4	chr5:179653600-179662400	Weak transcription	Brain Substantia Nigra	brain
5	chr5:179653600-179714600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:179653800-179662000	Weak transcription	Fetal Thymus	thymus
7	chr5:179654000-179661800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:179654400-179660800	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:179654800-179660800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr5:179655000-179679600	Weak transcription	Stomach Mucosa	stomach
11	chr5:179655200-179663200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr5:179655400-179712600	ZNF genes & repeats	Liver	Liver
13	chr5:179655800-179661600	ZNF genes & repeats	Lung	lung
14	chr5:179655800-179666400	ZNF genes & repeats	Aorta	Aorta
15	chr5:179655800-179675400	Strong transcription	Primary B cells from cord blood	blood
16	chr5:179656200-179675000	Strong transcription	Skeletal Muscle Female	skeletal muscle
17	chr5:179656600-179703000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
18	chr5:179656800-179660800	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr5:179656800-179666000	Weak transcription	NH-A	brain
20	chr5:179657200-179660800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr5:179657200-179668000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:179657400-179660800	Weak transcription	Right Ventricle	heart
23	chr5:179657400-179661200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr5:179657400-179661200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr5:179657400-179662000	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr5:179657400-179663000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr5:179657400-179669200	Strong transcription	Fetal Stomach	stomach
28	chr5:179657400-179669200	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr5:179657400-179673600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:179657400-179674400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:179657600-179667800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr5:179657800-179660800	Weak transcription	Osteobl	bone
33	chr5:179657800-179661400	Strong transcription	Brain Germinal Matrix	brain
34	chr5:179657800-179662000	Weak transcription	Small Intestine	intestine
35	chr5:179657800-179674400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:179657800-179697000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr5:179658000-179660800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:179658000-179662000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr5:179658000-179663200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr5:179658000-179667600	Weak transcription	NHLF	lung
41	chr5:179658200-179662400	Weak transcription	Psoas Muscle	Psoas
42	chr5:179658200-179663200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
43	chr5:179658400-179662000	Strong transcription	Stomach Smooth Muscle	stomach
44	chr5:179658400-179665800	Strong transcription	Adipose Nuclei	Adipose
45	chr5:179658400-179668200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:179658400-179669600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr5:179658400-179670600	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr5:179658400-179670800	Strong transcription	Fetal Muscle Leg	muscle
49	chr5:179658400-179672600	Strong transcription	Thymus	Thymus
50	chr5:179658400-179679200	Strong transcription	Primary T cells from cord blood	blood

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