Variant report

Variant	rs74092533
Chromosome Location	chr1:76602998-76602999
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:10)

rs_ID	r²[population]
rs2631785	1.00[AMR][1000 genomes]
rs2706202	1.00[AMR][1000 genomes]
rs2783988	1.00[AMR][1000 genomes]
rs58685142	1.00[AMR][1000 genomes]
rs61685633	1.00[AMR][1000 genomes]
rs74092513	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74092517	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74092521	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74092526	1.00[AMR][1000 genomes]
rs74092528	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1488	chr1:76587622-76632635	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76557400-76605800	Weak transcription	Fetal Intestine Small	intestine
2	chr1:76575400-76606000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:76576600-76620000	Weak transcription	Primary B cells from cord blood	blood
4	chr1:76588200-76615600	Weak transcription	Left Ventricle	heart
5	chr1:76591200-76607800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:76592600-76610800	Weak transcription	Fetal Kidney	kidney
7	chr1:76592800-76605800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr1:76593000-76608200	Weak transcription	Fetal Lung	lung
9	chr1:76594200-76607400	Weak transcription	Fetal Brain Female	brain
10	chr1:76594600-76615400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:76598600-76609800	Weak transcription	Fetal Stomach	stomach
12	chr1:76599800-76620200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:76601200-76603000	Enhancers	Brain Angular Gyrus	brain
14	chr1:76601200-76603000	Enhancers	Brain Cingulate Gyrus	brain
15	chr1:76601200-76603400	Weak transcription	Psoas Muscle	Psoas
16	chr1:76601200-76604600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr1:76601400-76603800	Enhancers	Brain Anterior Caudate	brain
18	chr1:76601400-76604000	Enhancers	Brain Substantia Nigra	brain
19	chr1:76601600-76603600	Enhancers	Brain Hippocampus Middle	brain
20	chr1:76601600-76605200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:76601800-76605600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr1:76601800-76606000	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr1:76601800-76608200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:76602000-76607600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:76602400-76603200	Enhancers	Primary B cells from peripheral blood	blood
26	chr1:76602800-76603000	Enhancers	GM12878-XiMat	blood
27	chr1:76602800-76603600	Enhancers	Right Atrium	heart
28	chr1:76602800-76604600	Enhancers	Adipose Nuclei	Adipose

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