Variant report

Variant	rs7713224
Chromosome Location	chr5:127252767-127252768
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:127251045..127254184-chr5:127417608..127420984,3	MCF-7	breast:
2	chr5:127252681..127255660-chr5:127418721..127420702,2	K562	blood:
3	chr5:127252558..127255088-chr5:127415960..127418621,2	MCF-7	breast:
4	chr5:127247758..127249668-chr5:127252486..127255400,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000064651	Chromatin interaction
ENSG00000245937	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10064259	1.00[EUR][1000 genomes]
rs10065500	1.00[EUR][1000 genomes]
rs11956483	1.00[EUR][1000 genomes]
rs2139577	1.00[EUR][1000 genomes]
rs55860273	1.00[EUR][1000 genomes]
rs57628458	1.00[EUR][1000 genomes]
rs58981401	1.00[EUR][1000 genomes]
rs60836524	1.00[EUR][1000 genomes]
rs61408727	1.00[EUR][1000 genomes]
rs6877411	1.00[EUR][1000 genomes]
rs6879972	1.00[EUR][1000 genomes]
rs6898650	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6899086	1.00[EUR][1000 genomes]
rs7710989	1.00[EUR][1000 genomes]
rs9285908	1.00[EUR][1000 genomes]
rs9327456	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033607	chr5:126385181-127304459	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1021483	chr5:126927834-127304873	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127251800-127252800	Enhancers	Stomach Mucosa	stomach
2	chr5:127252400-127252800	Enhancers	Colon Smooth Muscle	Colon
3	chr5:127252400-127253000	Enhancers	Fetal Intestine Large	intestine
4	chr5:127252400-127253000	Enhancers	Fetal Intestine Small	intestine
5	chr5:127252400-127253200	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr5:127252400-127253200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:127252400-127253200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:127252400-127253200	Flanking Active TSS	Duodenum Mucosa	Duodenum
9	chr5:127252400-127253200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr5:127252400-127253400	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr5:127252400-127253800	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr5:127252600-127252800	Enhancers	Ovary	ovary
13	chr5:127252600-127252800	Enhancers	Small Intestine	intestine
14	chr5:127252600-127253000	Enhancers	Primary T cells fromperipheralblood	blood
15	chr5:127252600-127253000	Active TSS	Primary hematopoietic stem cells	blood
16	chr5:127252600-127253000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
17	chr5:127252600-127253000	Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr5:127252600-127253000	Active TSS	Rectal Mucosa Donor 29	rectum
19	chr5:127252600-127253000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
20	chr5:127252600-127253600	Enhancers	Primary B cells from peripheral blood	blood
21	chr5:127252600-127253600	Enhancers	GM12878-XiMat	blood
22	chr5:127252600-127253600	Enhancers	Monocytes-CD14+_RO01746	blood

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