Variant report

Variant	rs2207527
Chromosome Location	chr1:184442196-184442197
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:184434578..184437265-chr1:184439841..184442761,2	MCF-7	breast:
2	chr1:184427992..184429921-chr1:184441519..184443422,2	MCF-7	breast:
3	chr1:184440449..184442376-chr1:184450326..184452605,2	MCF-7	breast:
4	chr1:184355623..184357608-chr1:184441118..184443754,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000271387	Chromatin interaction
ENSG00000116667	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10399817	0.95[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs10911610	0.84[CHB][hapmap]
rs11810399	0.80[CEU][hapmap]
rs12117823	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.96[TSI][hapmap];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12120604	0.95[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];0.88[ASN][1000 genomes]
rs12121612	0.95[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs12127697	0.87[CEU][hapmap];0.89[CHB][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12129904	1.00[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12138103	1.00[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12141469	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12143271	0.87[EUR][1000 genomes]
rs1535132	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16823195	0.95[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];0.91[ASN][1000 genomes]
rs16823197	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16823238	0.95[CHB][hapmap];0.96[CHD][hapmap];0.88[GIH][hapmap];0.86[JPT][hapmap];0.96[ASN][1000 genomes]
rs2180072	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2207526	0.95[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs58231072	0.91[ASN][1000 genomes]
rs61825202	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61825204	0.86[EUR][1000 genomes]
rs61825205	0.87[EUR][1000 genomes]
rs6659261	0.95[CHB][hapmap];0.85[CHD][hapmap];0.87[GIH][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs6683932	0.95[CHB][hapmap];0.85[CHD][hapmap];0.88[GIH][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs6693408	0.87[CEU][hapmap];0.89[CHB][hapmap];1.00[GIH][hapmap];0.90[TSI][hapmap];0.87[EUR][1000 genomes]
rs7513091	0.87[CEU][hapmap];0.89[CHB][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7525267	0.96[ASN][1000 genomes]
rs7548188	0.95[ASN][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	nsv530079	chr1:183797938-184639971	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	esv2756618	chr1:184393343-184674343	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2207527	TDRD5	cis	parietal	SCAN

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184425400-184442200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:184427400-184443800	Weak transcription	Esophagus	oesophagus
3	chr1:184427400-184444000	Weak transcription	Lung	lung
4	chr1:184427400-184448400	Weak transcription	Fetal Muscle Leg	muscle
5	chr1:184429000-184454800	Weak transcription	Aorta	Aorta
6	chr1:184429400-184449600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:184429600-184442200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr1:184430600-184444000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:184430600-184449800	Weak transcription	Right Ventricle	heart
10	chr1:184430600-184450000	Weak transcription	Fetal Stomach	stomach
11	chr1:184431400-184446400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr1:184431800-184447600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr1:184432000-184443400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr1:184433200-184442200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:184433600-184449600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr1:184433800-184443600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:184436800-184442400	Weak transcription	Left Ventricle	heart
18	chr1:184436800-184442400	Weak transcription	Ovary	ovary
19	chr1:184436800-184444000	Weak transcription	Pancreas	Pancrea
20	chr1:184438000-184450600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr1:184439200-184453600	Weak transcription	Fetal Brain Female	brain
22	chr1:184440600-184445800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:184440800-184442600	Enhancers	Fetal Heart	heart
24	chr1:184440800-184446200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr1:184441000-184442200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:184441000-184442200	Weak transcription	Psoas Muscle	Psoas
27	chr1:184441000-184443000	Enhancers	Fetal Brain Male	brain
28	chr1:184441000-184443800	Weak transcription	Right Atrium	heart
29	chr1:184441000-184445000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr1:184441000-184452000	Weak transcription	Colonic Mucosa	Colon
31	chr1:184441600-184443800	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr1:184441600-184443800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:184441800-184442800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr1:184441800-184442800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:184441800-184447400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:184442000-184442600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr1:184442000-184442600	Enhancers	Placenta Amnion	Placenta Amnion
38	chr1:184442000-184442800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:184442000-184448400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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