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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS139-09700
Organism
Homo sapiens
Tissue/cell
Myotube
Coordinate
chr11:64693410-64694050
Target genes
Number: 30
Name
Ensembl ID
BAD
ENSG00000002330
ESRRA
ENSG00000173153
TRMT112
ENSG00000173113
PRDX5
ENSG00000126432
AP001092.4
ENSG00000237410
NRXN2
ENSG00000110076
RASGRP2
ENSG00000068831
PYGM
ENSG00000068976
SF1
ENSG00000168066
MAP4K2
ENSG00000168067
MEN1
ENSG00000133895
CDC42BPG
ENSG00000171219
EHD1
ENSG00000110047
ATG2A
ENSG00000110046
PPP2R5B
ENSG00000068971
GPHA2
ENSG00000149735
ARL2
ENSG00000213465
SNX15
ENSG00000110025
SAC3D1
ENSG00000168061
NAALADL1
ENSG00000168060
CDCA5
ENSG00000146670
ZFPL1
ENSG00000162300
C11orf2
ENSG00000149823
AP003068.6
ENSG00000187066
AP003068.9
ENSG00000254501
TM7SF2
ENSG00000149809
ZNHIT2
ENSG00000174276
MRPL49
ENSG00000149792
FAU
ENSG00000149806
SYVN1
ENSG00000162298
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
Tcf12
MA0521.1
chr11:64693882-64693893
CAGCAGCTGTT
-
6.32
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr11
64693997
64694047
Enhancer Sequence
CTGGCTGCTG GCCACTGGGG GAACCGAACC CCCGAGGGGA CCAGCAGGGC CATGGGGAGG 60
GGTGGGAGGC AGCGGGCAGC TGCCAAGAGA GAGAGTTTGG ATACCCCTCC AGGCTAGGTT 120
CTCCGCCATC AGAACTGACC CCAGCCCTCC AGCCCTCTCT GCTGACACAT GGCCTGACTG 180
GCCTGTCATC CTTAGAGGTG GGACATCCGA AGGTGGTGCC ACCCTAGGGG CAGACCAAGG 240
CCAAGGGTGG GGCCCATAGC CTGGGTTCCA GGGGGCCACT ATCAGCCCAG CCAGCTGCCA 300
GATCCCTGGA GCAGGCGCTT GGCAGGGTTC CCTGGGATCA CCACATAGGT CCCTTCCCCA 360
GCCTTGGGCC ATAGGGCCAG ACTGGCCAAG CCTGAGGACA CCGTAGAGAT CCTTGGCCCT 420
GAACCCCTCC CCATTTCTGG CCCTTAGAAC AGGGTGCCAC CTGAGAGGGA GGCAGCAGCT 480
GTTTGGGGCA CCTGTGGAAA GCTGCTGCAT CCAGGATTTG TGATCTTGCT TTAAAACTCA 540
GGCCATCATA CTCTCTGAGC CTGGATTAGG AGGAAGAAAA GCAACCCTCA ACCCCCAGGA 600
ATGGAGGAAG GGACAGTAGT TGTTTGCTGT CTGCAAGGAG 640