EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS002-02622 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr12:98863790-98865210 
Target genes
Number: 2             
NameEnsembl ID
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr12:98864930-98864947AGGAACAACGTGTTCCT+6.93
ArMA0007.3chr12:98864930-98864947AGGAACAACGTGTTCCT-7.05
ESRRBMA0141.3chr12:98864073-98864084AATGACCTTGA-6.32
EsrrgMA0643.1chr12:98864074-98864084ATGACCTTGA-6.02
NR3C1MA0113.3chr12:98864930-98864947AGGAACAACGTGTTCCT+6.23
NR3C1MA0113.3chr12:98864930-98864947AGGAACAACGTGTTCCT-6.35
NR3C2MA0727.1chr12:98864930-98864947AGGAACAACGTGTTCCT+6.11
NR3C2MA0727.1chr12:98864930-98864947AGGAACAACGTGTTCCT-6.19
RORAMA0071.1chr12:98864075-98864085TGACCTTGAT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr129886406098864142
Number: 1             
IDChromosomeStartEnd
GH12I098470chr129886407798865403
Enhancer Sequence
GGGATTACAG GCATGAGCCA CCGCGCCCGG CTGGATGGAC TCCTATCTAA AGCCAATCAA 60
TCTTTGTCAT TCCCTAGGAT TTTTGTAACT GAAGCTGAAC AAAGATTTAT TTATTCTCTG 120
TTGGTGAGGC CAGGAGATGG TGAGACTCAG GAACTGCTAG TGGCCACATT TCTTGCTATG 180
TAAAGAAAGC TTTTCTAAGA GAAAGAAGTT AACAACACAG AGAGAGAAAC AGAATTGAGA 240
GACTGAGAAA AGAAGACCTA GCAGCACTCA AATCACCTGT TCCAATGACC TTGATACCAC 300
CTGCCACTCA TCCTTCTCAG TGTGAGCCTT CCAGTAAGTC CCCTTCTTTT TGCCTAAGTT 360
GGTTTAAGTT GGGGTTCTAG AGGGTGGGGG TGGGAGGAGG GAGAGCATCA GGAAGAATAG 420
CTAATGGATG CTGGGGCTTA ATACCTAGGT GATGTGCTGA TCTGTGCAGC AAACTACCGT 480
GGCAGACATT TACCTATGTA ACAAGCGTGC ACATCCTGCA CATGTACCCC TGAACTTAAA 540
AGTTGGAAGA AAAACAAAAC TTGCAACAAC CCCTAAAAAA TAATAAGCTG GGTTTCTAAA 600
CCTTTCCTCC AAATGGGTCT TGACTGATGT ATTCTCACAC AACTCTATGC TTCCCCTAGC 660
ACAGCACTGA TGACTGAGCT GTAATTGCTG GGTGCTTGTC TACCTGTCTA CCTCTCTGTC 720
CAGAAGACAG TGGCTTTCAG GTTCATGCAT TCTGCCCATC GCTGGGGCAC TCAACTGAGA 780
GGGAAGGAAG TGGGGATGCA CTCAATACAC ACAGGTAGGA TTGCGACAAC CATGTGTGTA 840
CTTCATAACC CTGAGCCCTG AACCACAGAT GATTTACTCG AGCTGGGCCA CAGTCTCCCT 900
GTAGCAATTT GGGACTGAGT CATACAAAGA TTGGACACTG AAACTCCTTC ACACAAATAA 960
TAGCACTCTT CAGAGGATGT TATTAGCCTC TGGCTAGTAA GGGGCCCCAA GCTGTCTTCT 1020
GCGAATTCTC TAAGAACCTC TAATATTCCT CCAACAAGCT TGCAAGGTCA TTTCTGCTTC 1080
CTAAAGCCAA AAGAAACTGA ACTAATACAC ACCCCAAAAT ATTGTAGTTT CTGTGTGAGC 1140
AGGAACAACG TGTTCCTCAT TATAGCTCCA AGGCCAGCAC GGTCCCTAAT CAGAACTCAC 1200
TGAACACCTG ATGAATGCCT GCAGCTCACT GCACTGAGTG GGAGATGCTC CTCCCACTTA 1260
GATAGGGATT TTTTTTTTTT TTAACTCTCT TGCCTTCAAG GTCCTGCGCA CATCTGCCCT 1320
GGCCTTGGTC TCCCTGTGTT GTCAGCTACA GTGGCCAGTG TGTCCTCTGT AGGGTACATC 1380
ACATCCCTGC TCAAGAATGC ATGTTAGAGA CTAGAAGTAC 1420