Variant report

Variant	rs1951705
Chromosome Location	chr4:74570643-74570644
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:74558633..74562298-chr4:74570528..74572669,3	MCF-7	breast:
2	chr4:74548585..74551184-chr4:74569612..74572509,2	MCF-7	breast:
3	chr4:74570144..74571742-chr4:74963833..74965447,2	K562	blood:
4	chr4:74563931..74567096-chr4:74570167..74572895,3	K562	blood:
5	chr4:74568145..74570838-chr4:74686420..74688170,2	K562	blood:
6	chr4:74569886..74571730-chr4:74572414..74575134,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000081041	Chromatin interaction

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10025373	0.98[ASN][1000 genomes]
rs10029200	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10938089	0.98[ASN][1000 genomes]
rs10938091	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11722921	0.98[ASN][1000 genomes]
rs11938646	0.98[ASN][1000 genomes]
rs1247605	0.96[ASN][1000 genomes]
rs1247607	0.96[ASN][1000 genomes]
rs1247608	0.96[ASN][1000 genomes]
rs1247611	0.96[ASN][1000 genomes]
rs1247620	0.96[ASN][1000 genomes]
rs1247633	0.98[ASN][1000 genomes]
rs1247634	0.96[ASN][1000 genomes]
rs1247635	0.98[ASN][1000 genomes]
rs1247639	0.96[ASN][1000 genomes]
rs1247687	0.96[ASN][1000 genomes]
rs1247689	0.98[ASN][1000 genomes]
rs12508451	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1261935	0.98[ASN][1000 genomes]
rs12642878	0.90[ASN][1000 genomes]
rs12643076	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs12643148	0.96[ASN][1000 genomes]
rs12646031	0.98[ASN][1000 genomes]
rs12649614	0.90[ASN][1000 genomes]
rs1269764	0.96[ASN][1000 genomes]
rs1269766	0.96[ASN][1000 genomes]
rs1358594	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1406498	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1528910	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1528912	0.98[ASN][1000 genomes]
rs1528913	0.98[ASN][1000 genomes]
rs1729722	0.98[ASN][1000 genomes]
rs1745246	0.98[ASN][1000 genomes]
rs1951702	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.98[ASN][1000 genomes]
rs1951703	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1951704	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.98[ASN][1000 genomes]
rs2091587	0.95[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2141467	0.96[ASN][1000 genomes]
rs2141468	0.98[ASN][1000 genomes]
rs2178291	0.96[ASN][1000 genomes]
rs2367273	0.98[ASN][1000 genomes]
rs2886918	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs3796679	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs4127802	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.98[ASN][1000 genomes]
rs4259030	0.97[ASN][1000 genomes]
rs4568212	0.98[ASN][1000 genomes]
rs4637366	0.92[ASN][1000 genomes]
rs4694633	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56785010	0.98[ASN][1000 genomes]
rs61101665	0.96[ASN][1000 genomes]
rs6446950	0.90[ASN][1000 genomes]
rs6446951	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[JPT][hapmap];0.98[ASN][1000 genomes]
rs6446953	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs6446954	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs6818711	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs6836038	1.00[CEU][hapmap];0.98[ASN][1000 genomes]
rs6857472	0.98[ASN][1000 genomes]
rs720702	0.92[ASN][1000 genomes]
rs72865497	0.96[ASN][1000 genomes]
rs72865502	0.96[ASN][1000 genomes]
rs7655660	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs7656501	0.82[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs7656608	0.98[ASN][1000 genomes]
rs7657356	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs7657358	0.96[ASN][1000 genomes]
rs7660448	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7660923	0.90[ASN][1000 genomes]
rs7665606	0.90[ASN][1000 genomes]
rs7678280	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs7678307	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs7681924	0.90[ASN][1000 genomes]
rs7681932	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7682745	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7683759	0.90[ASN][1000 genomes]
rs7689702	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs942051	0.96[ASN][1000 genomes]
rs9991585	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.95[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	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1008104	chr4:74468434-74621952	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1012198	chr4:74487793-74621952	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv537139	chr4:74487793-74621952	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv1005231	chr4:74555497-74680079	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74566800-74571400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:74566800-74574600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:74566800-74575400	Enhancers	HMEC	breast
4	chr4:74567200-74570800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:74567400-74572000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr4:74567400-74572200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr4:74567800-74574000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr4:74568000-74570800	Enhancers	Osteobl	bone
9	chr4:74568000-74573800	Enhancers	NHEK	skin
10	chr4:74568000-74574400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr4:74568200-74574800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:74568200-74574800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:74568400-74570800	Enhancers	NHDF-Ad	bronchial
14	chr4:74568400-74572200	Enhancers	HSMM	muscle
15	chr4:74568400-74574600	Enhancers	NHLF	lung
16	chr4:74568600-74572000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:74568800-74572000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:74569200-74571000	Enhancers	Psoas Muscle	Psoas
19	chr4:74569200-74571400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr4:74569200-74572200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:74569200-74576400	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr4:74569400-74570800	Weak transcription	Right Atrium	heart
23	chr4:74569600-74572200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:74569600-74572400	Enhancers	HSMMtube	muscle
25	chr4:74569800-74571000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:74569800-74571000	Enhancers	Adipose Nuclei	Adipose
27	chr4:74569800-74571000	Flanking Active TSS	A549	lung
28	chr4:74569800-74571200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr4:74569800-74571400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr4:74569800-74576200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:74570000-74570800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:74570000-74570800	Enhancers	Liver	Liver
33	chr4:74570000-74571000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr4:74570000-74571000	Enhancers	Placenta Amnion	Placenta Amnion
35	chr4:74570000-74571000	Enhancers	Stomach Mucosa	stomach
36	chr4:74570000-74571200	Enhancers	Primary hematopoietic stem cells	blood
37	chr4:74570000-74571400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:74570000-74571400	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr4:74570000-74571600	Enhancers	Small Intestine	intestine
40	chr4:74570000-74571800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:74570000-74571800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:74570000-74572200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr4:74570000-74575200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:74570200-74570800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
45	chr4:74570200-74570800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr4:74570200-74570800	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr4:74570200-74571000	Enhancers	Placenta	Placenta
48	chr4:74570200-74571000	Enhancers	Ovary	ovary
49	chr4:74570200-74571000	Enhancers	Spleen	Spleen
50	chr4:74570200-74571400	Enhancers	H1 Cell Line	embryonic stem cell

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