Variant report

Variant	rs73607736
Chromosome Location	chr8:19730281-19730282
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs60165673	1.00[AMR][1000 genomes]
rs73597632	1.00[AMR][1000 genomes]
rs73597633	1.00[AMR][1000 genomes]
rs73601525	0.83[AMR][1000 genomes]
rs73601530	0.83[AMR][1000 genomes]
rs73601536	0.83[AMR][1000 genomes]
rs7832264	0.83[AMR][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	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv610759	chr8:19561997-20068842	Enhancers Strong transcription Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv890631	chr8:19712564-19756813	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv498082	chr8:19722435-19873112	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19718600-19732200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:19725200-19731200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:19726400-19732400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:19728000-19732800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:19728200-19731200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:19728200-19731800	Enhancers	H9 Cell Line	embryonic stem cell
7	chr8:19728200-19733400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:19728200-19734000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr8:19728400-19733600	Enhancers	Duodenum Mucosa	Duodenum
10	chr8:19728600-19733600	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr8:19728800-19730400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:19728800-19731200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:19728800-19733200	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr8:19728800-19733200	Weak transcription	Adipose Nuclei	Adipose
15	chr8:19729000-19733600	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr8:19729200-19731600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:19729400-19731600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr8:19729600-19730600	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr8:19729600-19730800	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr8:19730000-19730600	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr8:19730000-19732600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr8:19730200-19731200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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