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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS139-39492
Organism
Homo sapiens
Tissue/cell
Myotube
Coordinate
chr3:183757160-183758310
Target genes
Number: 22
Name
Ensembl ID
KLHL24
ENSG00000114796
YEATS2
ENSG00000163872
MAP6D1
ENSG00000180834
RP11
ENSG00000234371
PARL
ENSG00000175193
ABCC5
ENSG00000114770
EEF1A1P8
ENSG00000223529
HTR3E
ENSG00000238020
DVL3
ENSG00000161202
AP2M1
ENSG00000161203
ABCF3
ENSG00000161204
VWA5B2
ENSG00000145198
ALG3
ENSG00000214160
ECE2
ENSG00000145194
CAMK2N2
ENSG00000163888
PSMD2
ENSG00000175166
EIF4G1
ENSG00000114867
FAM131A
ENSG00000175182
CLCN2
ENSG00000114859
POLR2H
ENSG00000163882
THPO
ENSG00000090534
CHRD
ENSG00000090539
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr3
183757279
183757523
Enhancer Sequence
GTGTGTTTTT TTAAGTCTAT CAGACAACAT GTGAAATGTA GGGGAAGAGA AAGAAGGGGC 60
CAAAATCTAT TAGAAGGAAT TATAGAAAAA CAGAGATTAA CTTCCTAAAT CCAGCTACTC 120
TGGACTTAAG CTTCAGAAAT TAATGTGCCA AAACTAGGCC TCTCCTGCTT AAAGAGCGCA 180
GCCTTTTGTT ACACCCTGAC GTATGACTCA TTCATCATTA AGTACTTAGA GTGTTAACAT 240
AATCCTGCAT TACCGTTAAA GTATCTGTGT TGCAATTTGA GTTGATGTAC CCTTAATCAT 300
GCTAAGAAAA GAACATAAGG CCAAGGGAAG CACATTTGAA AATGACATCT ACTTTACTTG 360
AGAGGAACAC AAATGCCCCC GTATGAACTG GAAAGTGCCT TTTCCTAACA CTTGTCTTAT 420
TATTTCGAAG GTCTTTGCCT AGGGAGCACT AGCTGCCTTG CACAAGTTGA GGCTCTACTG 480
TGCCCTTGGA CATGAGAGCT AAGGCATTTG TTGGTTCAGA AAGCACCTAT TTGAGGGCAA 540
CTTAACTACA CTCAAACATC ATATTTTCTT TTTCGCAACG ATTTATTTCC ATTTCTTTCA 600
TTTATTCTAC TACTTTCTAT CTGTAGCTCA TATTTCCCAA ATCATGACCA TCTAGGAGTA 660
AAAATAGACT CACAAAATGG TTCACTAAAT AATATTTCTC TGGCTTCTCC TCTCCACTGC 720
TCTTTCCCAA ACTCCTTCGG CTCCCTCTGG TCACTGTAGA TGCCCAAAGG GTGGCAAGGT 780
TGCTAATGTC CACTAGAGGT AGTGCTAGTG CCTGCCAAAG GTTCTACCCC ACATTAGCTG 840
CAAGAGTATC TGCTCTCTCA GAGCCATAGC CATGGTCGGG ACTGGATCCT GGAGCTACAG 900
AGGCTCCCAG CTGGATGCTG CAACCCCAGG ACCAGCTGTC ACTCGCTTTT TTCTTTCAGT 960
TCCACTGGGA CTCCAGAGGG GCCCATGGGC ATCTGGGGTG TTAAATCAGA AATACCCTGC 1020
AATACTCTGA ATCCCTCCTG TCACTCAGGC CCATGGTCTT CAAACCAAAT TGTGTCCCTT 1080
CATTCTCTTT TTAGGATGCA TTTTGTTTTT GTTTTTGTTT TTCCAAGAAG ATCTTTTGCT 1140
CCTCAGTTTC 1150