Variant report

Variant	rs41258005
Chromosome Location	chr1:213037685-213037686
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PBX3	chr1:213037676-213037802	GM12878	blood:	n/a	n/a
2	WRNIP1	chr1:213037506-213037784	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:213031674..213033675-chr1:213035938..213038632,2	MCF-7	breast:
2	chr1:213032255..213037228-chr1:213037322..213040248,4	K562	blood:

Variant related genes	Relation type
FLVCR1	TF binding region
ENSG00000162769	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs2047288	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2047291	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2088256	1.00[AFR][1000 genomes]
rs3738799	1.00[AMR][1000 genomes]
rs3738801	1.00[AMR][1000 genomes]
rs3768549	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41275386	1.00[AMR][1000 genomes]
rs41296666	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296668	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296674	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296676	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296678	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296680	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41297452	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300027	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300033	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300035	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300043	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300979	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41301029	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs41307644	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs41307646	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs41314540	1.00[AMR][1000 genomes]
rs41314542	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56300028	0.85[AMR][1000 genomes]
rs58746017	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73079880	0.85[AMR][1000 genomes]
rs73079886	0.85[AMR][1000 genomes]
rs73079887	0.85[AMR][1000 genomes]
rs7521050	1.00[AMR][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	nsv1011186	chr1:213005165-213069563	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1013705	chr1:213005344-213064209	Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv1008383	chr1:213025546-213114894	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv998261	chr1:213029814-213064209	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv998979	chr1:213029814-213073013	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1007129	chr1:213037244-213083261	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213032600-213046400	Weak transcription	Ovary	ovary
2	chr1:213032600-213049200	Weak transcription	Right Atrium	heart
3	chr1:213032600-213073000	Weak transcription	Colonic Mucosa	Colon
4	chr1:213032600-213073000	Weak transcription	Esophagus	oesophagus
5	chr1:213032800-213046400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr1:213032800-213048000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr1:213032800-213056800	Weak transcription	Fetal Thymus	thymus
8	chr1:213032800-213057800	Weak transcription	Placenta	Placenta
9	chr1:213032800-213061800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:213032800-213062000	Weak transcription	Psoas Muscle	Psoas
11	chr1:213033400-213038200	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
12	chr1:213033400-213046800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:213033400-213046800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr1:213033600-213046800	Weak transcription	Liver	Liver
15	chr1:213033600-213048600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr1:213033600-213062000	Weak transcription	Thymus	Thymus
17	chr1:213034400-213041200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:213034400-213044800	Weak transcription	HSMMtube	muscle
19	chr1:213034400-213046200	Weak transcription	Fetal Lung	lung
20	chr1:213034400-213046600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr1:213034400-213046600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr1:213034400-213048200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr1:213034400-213048400	Weak transcription	Brain Hippocampus Middle	brain
24	chr1:213034400-213058000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr1:213034400-213068000	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:213034600-213039000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:213034600-213039600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:213034600-213041400	Weak transcription	Fetal Stomach	stomach
29	chr1:213034600-213044200	Weak transcription	Aorta	Aorta
30	chr1:213034600-213044800	Weak transcription	Left Ventricle	heart
31	chr1:213034600-213044800	Weak transcription	Pancreas	Pancrea
32	chr1:213034600-213046000	Weak transcription	HMEC	breast
33	chr1:213034600-213046400	Weak transcription	Brain Anterior Caudate	brain
34	chr1:213034600-213046400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr1:213034600-213046600	Weak transcription	Primary B cells from peripheral blood	blood
36	chr1:213034600-213046800	Weak transcription	Primary B cells from cord blood	blood
37	chr1:213034600-213046800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr1:213034600-213046800	Weak transcription	NHDF-Ad	bronchial
39	chr1:213034600-213047400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:213034600-213048000	Weak transcription	Spleen	Spleen
41	chr1:213034600-213048600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr1:213034600-213048600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr1:213034600-213049200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr1:213034600-213049200	Weak transcription	Lung	lung
45	chr1:213034600-213049400	Weak transcription	Gastric	stomach
46	chr1:213034600-213056200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr1:213034600-213057000	Weak transcription	Brain Substantia Nigra	brain
48	chr1:213034600-213057000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr1:213034600-213057200	Weak transcription	Right Ventricle	heart
50	chr1:213034600-213061800	Weak transcription	Fetal Heart	heart

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