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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS105-34101
Organism
Homo sapiens
Tissue/cell
IMR90
Coordinate
chr17:40314340-40315060
Target genes
Number: 27
Name
Ensembl ID
EIF1
ENSG00000173812
HAP1
ENSG00000173805
JUP
ENSG00000173801
LEPREL4
ENSG00000141696
FKBP10
ENSG00000141756
NT5C3L
ENSG00000141698
RP11
ENSG00000259623
KLHL11
ENSG00000178502
ACLY
ENSG00000131473
CNP
ENSG00000173786
KAT2A
ENSG00000108773
RAB5C
ENSG00000108774
STAT5B
ENSG00000173757
STAT5A
ENSG00000126561
STAT3
ENSG00000168610
PTRF
ENSG00000177469
ATP6V0A1
ENSG00000033627
AC067852.1
ENSG00000256929
NAGLU
ENSG00000108784
HSD17B1
ENSG00000108786
COASY
ENSG00000068120
MLX
ENSG00000108788
PSMC3IP
ENSG00000131470
TUBG1
ENSG00000131462
CNTNAP1
ENSG00000108797
VPS25
ENSG00000131475
CCDC56
ENSG00000183978
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr17
40314461
40314541
Enhancer Sequence
TGCAGGGTGA AGGGATGCAG GTGAGTTCAT GGAGCATTAA TACCTGAGCC TATAACTTGG 60
GCTGGAATCC TCCTGTCATT GGGCAGGCGG AGAGCAGGGG GAGACAAAGC TCTAGGGTCT 120
GTAAGATGGG AAACCTAAAC TCCTTAGCCT GGTTCTGAGG CCCCTGTGTA ACTCTCCAGC 180
CTCATCCTGC CCCTTGCCCC ATCTTGGTAC GGAGCTTCTC TTTGGTGTCT GAACACAGCA 240
TCCCTCTGGT TTTCATGCCT TTCAACAATT GTTTTTGTTT TTTTTTTTGA GATGGGGTCT 300
CACTCTGTTG CCCAGGGTGG AGTGCAGTGG TGTGCTCTCA GCTCACTGCA ACCTCTGTCT 360
CCGAGGTTCA AGCAATTCTC CTGTCTCAGC CTTCCGAGTA ACTGGGATTA CAGGTGTGCA 420
CCACCACGCC TGGCTAATTT TTGTATTTTT AGTAGAGATG GGGTTTTGCC ATATTGGCCA 480
GGCTGGTCTC GAACTCCTGA CCTCAGGTGA TCCACCCTCA TCAGCCTCCC AAAGTACTGG 540
GATTACAGGC ATGAACCACC ATGCCCAGCT CAATAACTGT TTTGCTCCAC TCTTCAAGAT 600
CCCACCCACC CTTTAAGAAG CAACCCAAGC ATCCCCTCCT CTGCAAGGAA GTCGAGTGAG 660
CACCTTCCTC TTCTACCACA GAGTCCTGTT CTTGTCTGTC ATGGTATTTA GCATCTGGAA 720