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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS105-14748
Organism
Homo sapiens
Tissue/cell
IMR90
Coordinate
chr11:67263070-67263640
Target genes
Number: 28
Name
Ensembl ID
KDM2A
ENSG00000173120
ADRBK1
ENSG00000173020
ANKRD13D
ENSG00000172932
SSH3
ENSG00000172830
POLD4
ENSG00000175482
7SK
ENSG00000201684
AP003419.11
ENSG00000256514
CLCF1
ENSG00000175505
RAD9A
ENSG00000172613
TBC1D10C
ENSG00000175463
CARNS1
ENSG00000172508
PPP1CA
ENSG00000172531
RPS6KB2
ENSG00000175634
AP003419.16
ENSG00000255949
PTPRCAP
ENSG00000213402
CORO1B
ENSG00000172725
TMEM134
ENSG00000172663
AIP
ENSG00000110711
PITPNM1
ENSG00000110697
CDK2AP2
ENSG00000167797
GSTP1
ENSG00000084207
NDUFV1
ENSG00000167792
NUDT8
ENSG00000167799
RPL37P2
ENSG00000239559
RP11
ENSG00000227620
FAM86C2P
ENSG00000160172
NDUFS8
ENSG00000110717
TCIRG1
ENSG00000110719
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
INSM1
MA0155.1
chr11:67263415-67263427
TGCCAGGGGGCA
+
6.62
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr11
67263327
67263393
Enhancer Sequence
CGGCTGGGGG AAGGAGGGCA AGGTCAGCAG GGGCCGGCCA GGTGGCTCTC CTGTCTTCTC 60
ACCCAGGGCT CCCCGCACCT CTGCCATCTT CCTGTGGCCC CTCTGGTCAG GTCCTGGCTG 120
AGGCTGCACT GTGGCATTCT CTCCTCTCAG CCCAGTGGCC AGCTGCACTC CTGCCAGAAT 180
GCCTGTTGCC ACCGCCCCAA ACGCTGCACA CCTGTGCCCA ACACAGGCCC GCTTGGCCCA 240
TACATACCTG GGCATGCCCC GCAATAAATG TCTGCAGCAC ACCCCACACA GATGCAGCAG 300
CGCACACATG CTGGCTGCTT GTATGGCAGC ACACCAGCAT CATGCTGCCA GGGGGCACCC 360
TCTCTAGCTT GGCTAACCAC CCCCACCCAA CTTCTAGGCC CAGGAGGTCA GAGGGTCCTG 420
GGGATCCAGA CCCCCCCAGG GGGAAGGAGC GCCTGGTCCT GGGAGTGGTG GCCTGAGAGG 480
TTTTCCATCG TCTGGGAGCC TCCTCATGTC TTCTGCTACC TCCTCCCTTC CTGTGTGTGC 540
CCTCCTCCTT CTCCCCTTTA TCTTGTTTGG 570