Variant report

Variant	rs7664299
Chromosome Location	chr4:166153649-166153650
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10015885	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10024370	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16999615	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17842697	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2048604	0.89[EUR][1000 genomes]
rs28575657	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3817246	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3901797	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3932270	0.82[EUR][1000 genomes]
rs4690809	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4691180	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6830714	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7685245	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7692029	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7699872	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[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	nsv1022210	chr4:165792630-166251612	Genic enhancers Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv537337	chr4:165792630-166251612	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv1021905	chr4:165852926-166212878	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv533191	chr4:165879671-166171638	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv881168	chr4:165975122-166196438	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv980271	chr4:166140782-166154486	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166129600-166154400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:166129600-166196800	Weak transcription	Pancreas	Pancrea
3	chr4:166130400-166176800	Weak transcription	Fetal Intestine Small	intestine
4	chr4:166130600-166200800	Weak transcription	Lung	lung
5	chr4:166131600-166162800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:166131600-166165800	Weak transcription	Gastric	stomach
7	chr4:166131600-166196800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr4:166132000-166156400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr4:166132200-166193800	Weak transcription	Fetal Brain Female	brain
10	chr4:166135800-166159000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr4:166136000-166176800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:166137600-166162800	Weak transcription	NH-A	brain
13	chr4:166137800-166194200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:166138000-166157200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:166138000-166161600	Weak transcription	HSMMtube	muscle
16	chr4:166138200-166168800	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr4:166138400-166185600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:166142800-166165800	Weak transcription	Esophagus	oesophagus
19	chr4:166142800-166176800	Weak transcription	Duodenum Mucosa	Duodenum
20	chr4:166143600-166156600	Weak transcription	Fetal Muscle Leg	muscle
21	chr4:166143800-166159400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:166144000-166153800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:166144000-166156600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:166144000-166159400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr4:166144000-166161200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr4:166144000-166162400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:166144000-166163200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr4:166144000-166165000	Weak transcription	Primary B cells from cord blood	blood
29	chr4:166144000-166165400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:166144000-166176000	Weak transcription	Brain Hippocampus Middle	brain
31	chr4:166144200-166155800	Weak transcription	HepG2	liver
32	chr4:166144200-166160200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:166144200-166168800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr4:166144200-166168800	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr4:166144200-166168800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr4:166144600-166153800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:166144600-166159200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr4:166144600-166159200	Weak transcription	Brain Anterior Caudate	brain
39	chr4:166144600-166159200	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr4:166144600-166159800	Weak transcription	Adipose Nuclei	Adipose
41	chr4:166144600-166218800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:166144800-166159200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr4:166144800-166159400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:166144800-166159400	Weak transcription	Liver	Liver
45	chr4:166144800-166176200	Weak transcription	Primary hematopoietic stem cells	blood
46	chr4:166145800-166153800	Weak transcription	HMEC	breast
47	chr4:166146400-166160600	Weak transcription	Rectal Smooth Muscle	rectum
48	chr4:166147000-166159200	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr4:166147000-166165400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:166147000-166176400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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