Variant report

Variant	rs73033774
Chromosome Location	chr1:169128627-169128628
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs16861993	1.00[AMR][1000 genomes]
rs16862000	1.00[AMR][1000 genomes]
rs57461302	1.00[AMR][1000 genomes]
rs57479005	1.00[AMR][1000 genomes]
rs59561246	1.00[AMR][1000 genomes]
rs59937757	1.00[AMR][1000 genomes]
rs73035336	1.00[AMR][1000 genomes]
rs73035343	1.00[AMR][1000 genomes]
rs73035344	1.00[AMR][1000 genomes]
rs73035348	1.00[AMR][1000 genomes]
rs73035355	1.00[AMR][1000 genomes]
rs7548520	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	esv3522071	chr1:168978325-169339044	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	esv3522072	chr1:168978325-169339044	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv831858	chr1:169022383-169179068	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	esv10418	chr1:169059628-169621268	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169091800-169137600	Weak transcription	Esophagus	oesophagus
2	chr1:169096600-169137400	Weak transcription	Fetal Stomach	stomach
3	chr1:169097000-169130000	Weak transcription	Ovary	ovary
4	chr1:169100800-169141400	Weak transcription	Fetal Muscle Leg	muscle
5	chr1:169101000-169137000	Weak transcription	Primary T cells from cord blood	blood
6	chr1:169103400-169130200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:169104800-169142800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:169115800-169130400	Weak transcription	Brain Hippocampus Middle	brain
9	chr1:169116200-169130200	Weak transcription	Brain Anterior Caudate	brain
10	chr1:169116400-169139400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:169118000-169137000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:169118200-169130400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr1:169118600-169130000	Weak transcription	Liver	Liver
14	chr1:169120400-169130200	Weak transcription	A549	lung
15	chr1:169121000-169129200	Weak transcription	Lung	lung
16	chr1:169121000-169137000	Weak transcription	Psoas Muscle	Psoas
17	chr1:169121000-169140800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:169121200-169141200	Weak transcription	Left Ventricle	heart
19	chr1:169121800-169143000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr1:169122600-169130200	Weak transcription	NHEK	skin
21	chr1:169122800-169136400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr1:169124600-169130200	Weak transcription	Stomach Smooth Muscle	stomach
23	chr1:169124800-169130800	Weak transcription	Gastric	stomach
24	chr1:169124800-169138800	Weak transcription	Primary B cells from cord blood	blood
25	chr1:169125400-169130000	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:169125400-169130200	Weak transcription	Right Ventricle	heart
27	chr1:169125400-169131200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr1:169126800-169130000	Weak transcription	Fetal Heart	heart
29	chr1:169127000-169129000	Weak transcription	Stomach Mucosa	stomach
30	chr1:169127000-169130600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr1:169127200-169129200	Weak transcription	Small Intestine	intestine
32	chr1:169127200-169137200	Weak transcription	Duodenum Mucosa	Duodenum
33	chr1:169128000-169129000	Weak transcription	Fetal Intestine Small	intestine
34	chr1:169128200-169130200	Weak transcription	Fetal Intestine Large	intestine
35	chr1:169128200-169137000	Weak transcription	Aorta	Aorta

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