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

TagContent
EnhancerAtlas ID
HS129-19668 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr2:61686660-61688080 
Target genes
Number: 11             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs778138chr261687214hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxq1MA0040.1chr2:61687370-61687381AATAAACAATT-6.02
HSF1MA0486.2chr2:61687358-61687371GAAAATTCCAGAA-6.17
IRF2MA0051.1chr2:61687300-61687318TCTTTGGTTTTGCTTTCC-6
NFAT5MA0606.1chr2:61687354-61687364AATGGAAAAT-6.02
NFATC1MA0624.1chr2:61687354-61687364AATGGAAAAT-6.02
NFATC3MA0625.1chr2:61687354-61687364AATGGAAAAT-6.02
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_60516chr2:61645792-61699770DHL6
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr26168683561687959
Number: 1             
IDChromosomeStartEnd
GH02I061459chr26168673661688385
Enhancer Sequence
GCAGTTTGGG AGGCCAAGAC GGGCGGATCA CTTCAGGTCA AGAGTTCGAA ACCAGCCTGG 60
CCAACACGGT GAAACCCCGT CTCTACTAAA AATACAAAAG AATTAGCCGA GCGTGGTGGC 120
AGGCACCTGT AATCCCAGCT ACTCAGGAGG CTGAGGCAGG AGAATCGCTT GAACCCGGGA 180
GGCGAAGGCT GCAGTGAGCT GATATTAAGC CACTGCACTC CAGCCTGGGC TACAGAGCCA 240
AAAAAAAAAA AAGGCCAGGC ACAGTGACTC ACACCTGTAA TCGTAGCACT TTGGGAGGCC 300
AAGGTGGGCA GATCACCTGA GGTCAGGAGA TCAAGACCAT CCTGATTAAC ACGGTAAAAC 360
CCCATCTCTA CTAAAAATAC AAAAAAATTA GCTGGACATG GTGGCGGACG CCTGTAGTCC 420
CAGCCACTCG GGTGGCTGAG GGAGGAGAAT GGCGTCAACC CAGGAAGCAG AACTTGCAGT 480
GAGCCGAGAT CGCACCACTG CACTCCAGCC TGAGCGACAG AGCAAGACTC CATCTCAGAA 540
AAAAGATACT TGAAAACAGT TTTATGTTGG CTTTTTTTGA GCACCCACAT ATTACTTAGT 600
TTCCAAGCTT ATTAAGAAAT TACAATAGTC TCCCTTATTA TCTTTGGTTT TGCTTTCCAT 660
AGTTAACCAC AGTCACTATG GTCCAAAAAT ATTAAATGGA AAATTCCAGA AATAAACAAT 720
TCATAAGTTT TAAATTGCCA TTCCGAGTGG CATGATGAAA TCTTGTGCCG TCCCGTCTAG 780
GATGTGAATC ATCCTTTTGT CCAGCATATC CAGGCTGCAC ATGCAACCTA CCCATTAAGT 840
CACTAAGTAG CTGTCCTGGT TATCAGATCC ACTGTGGCAC TACACAATGC TTGTATTCAA 900
GTAACCCTTA CTTTACCCAA TAATGGCCCC AAAGTGCAAG AGCAGCGATA CTAGTAATTC 960
AGATATGCCA AAGAAAAGCT TATTTGAAGT GAAAAGGTGA AAGTTCTTAA AATAATGAGA 1020
AAAAAAACAG TATATAGGGT ACAGCACTAT CTGTGGTTTG AGGTATCCAC TGGAAGTCTC 1080
AGAACACATT CCACTTGGAT AAGGGGGGAA TACTGTATAC CCTTTTTCTC CTCAAAAGAA 1140
ATCTTACATA GAATTTCGAT TCATAAAACA GGTAGAAGGC CGGGTGTGGC AGCTCATGCC 1200
TGTAATCCCA GTACTTTGGG AGGCCGAGGC AAGTGGATCA CGAGTTCAGG AGATCGAGAC 1260
CATCCTGGCC AACATGGAGA AACTCTGTCT CTACTAAAAA CATAAAAATT AGCTGGGCAT 1320
AGTGACGCAC GCCTGTAGTC CCAGGTACTC GAGAGGCTGA GGCAGGACAA TCACTTGAAC 1380
CTGGGAGGTG GAGGTCCAGG AAGCCAAGAT CGCGCCACTG 1420