Variant report

Variant	rs456938
Chromosome Location	chr5:70933791-70933792
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:70929199..70932384-chr5:70932859..70936890,5	MCF-7	breast:
2	chr5:70930390..70934601-chr5:70935196..70939070,4	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs157049	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs277936	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs277938	0.84[ASN][1000 genomes]
rs277976	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs277978	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs277979	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs277980	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs277981	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs277996	0.81[EUR][1000 genomes]
rs277999	0.81[EUR][1000 genomes]
rs278000	0.81[EUR][1000 genomes]
rs278001	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs544779	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034703	chr5:70391173-70995695	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv830340	chr5:70797113-70967110	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv532805	chr5:70916228-71020967	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv328811	chr5:70928971-70936086	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs456938	BDP1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70884800-70934800	Weak transcription	Fetal Brain Male	brain
2	chr5:70895800-70937800	Weak transcription	Colonic Mucosa	Colon
3	chr5:70897400-70933800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:70897800-70944800	Weak transcription	Small Intestine	intestine
5	chr5:70898200-70944200	Weak transcription	Osteobl	bone
6	chr5:70898400-70935400	Weak transcription	NHDF-Ad	bronchial
7	chr5:70898400-70955000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:70898600-70948400	Weak transcription	Brain Germinal Matrix	brain
9	chr5:70900000-70944800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr5:70900200-70945200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr5:70906600-70952400	Weak transcription	Stomach Mucosa	stomach
12	chr5:70909000-70938200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr5:70912400-70936600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr5:70912600-70941800	Weak transcription	Colon Smooth Muscle	Colon
15	chr5:70912600-70943800	Weak transcription	A549	lung
16	chr5:70913000-70934200	Weak transcription	Fetal Brain Female	brain
17	chr5:70914200-70938000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr5:70914200-70948800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:70915400-70950800	Weak transcription	NHLF	lung
20	chr5:70917000-70936400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr5:70917000-70945000	Weak transcription	Hela-S3	cervix
22	chr5:70917200-70937800	Weak transcription	Aorta	Aorta
23	chr5:70917200-70942000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:70917400-70942600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr5:70918000-70942400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:70919400-70934800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr5:70919800-70955000	Weak transcription	HUVEC	blood vessel
28	chr5:70923200-70936400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr5:70923200-70937600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr5:70925400-70950600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr5:70926600-70954000	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr5:70927000-70939600	Strong transcription	Fetal Intestine Large	intestine
33	chr5:70927000-70939800	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr5:70927000-70954000	Strong transcription	Dnd41	blood
35	chr5:70927000-70954200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr5:70927200-70934800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:70927200-70937800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr5:70927200-70940200	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr5:70927400-70938200	Weak transcription	Spleen	Spleen
40	chr5:70927600-70940000	Strong transcription	Liver	Liver
41	chr5:70927600-70940200	Strong transcription	Duodenum Mucosa	Duodenum
42	chr5:70927800-70935800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:70928000-70940200	Strong transcription	Primary B cells from peripheral blood	blood
44	chr5:70928000-70940200	Strong transcription	Adipose Nuclei	Adipose
45	chr5:70928000-70940200	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr5:70928200-70934000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:70928200-70935600	Strong transcription	Ovary	ovary
48	chr5:70928600-70934000	Weak transcription	Fetal Heart	heart
49	chr5:70928600-70935000	Weak transcription	Brain Angular Gyrus	brain
50	chr5:70928600-70943800	Weak transcription	Thymus	Thymus

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