Variant report

Variant	rs72756744
Chromosome Location	chr1:239701208-239701209
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11806179	1.00[AFR][1000 genomes]
rs72754685	1.00[AFR][1000 genomes]
rs72756710	1.00[AFR][1000 genomes]
rs72758703	1.00[AFR][1000 genomes]
rs72758706	1.00[AFR][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	nsv1002301	chr1:239182255-239774393	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv549435	chr1:239375010-239974006	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv3377526	chr1:239623743-240111639	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv873351	chr1:239636613-240324200	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:239699200-239702400	Enhancers	Stomach Smooth Muscle	stomach
2	chr1:239699200-239702600	Enhancers	Rectal Smooth Muscle	rectum
3	chr1:239699400-239702600	Weak transcription	Pancreas	Pancrea
4	chr1:239699400-239703200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:239699600-239703600	Enhancers	Colon Smooth Muscle	Colon
6	chr1:239700000-239702200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr1:239700000-239703000	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr1:239700200-239702600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:239700400-239701800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr1:239700400-239701800	Enhancers	Fetal Lung	lung
11	chr1:239700400-239702800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:239700400-239704000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:239700600-239702000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:239700600-239702600	Enhancers	Fetal Stomach	stomach
15	chr1:239700600-239702800	Enhancers	Ovary	ovary
16	chr1:239700600-239703400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:239700800-239701400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:239700800-239701600	Weak transcription	Right Atrium	heart
19	chr1:239700800-239703800	Enhancers	Primary hematopoietic stem cells	blood
20	chr1:239701000-239702600	Weak transcription	Fetal Muscle Trunk	muscle
21	chr1:239701200-239701400	Enhancers	Fetal Intestine Small	intestine
22	chr1:239701200-239701600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:239701200-239702000	Enhancers	Adipose Nuclei	Adipose
24	chr1:239701200-239702200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:239701200-239702600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:239701200-239702600	Enhancers	Fetal Brain Male	brain
27	chr1:239701200-239703000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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