EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-41719 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr20:32297280-32298360 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs13042148chr2032298286hg19
TF binding sites/motifs
Number: 28             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF13MA0657.1chr20:32298316-32298334GAACCACGCCCCCTTCAC+6.08
KLF13MA0657.1chr20:32298208-32298226GAACCACGCCCCCTTCCG+6.42
KLF13MA0657.1chr20:32298279-32298297GAACCACGCCCCCTTCTG+7.4
KLF14MA0740.1chr20:32298209-32298223AACCACGCCCCCTT+6.91
KLF14MA0740.1chr20:32298243-32298257AACCACGCCCCCTT+6.91
KLF14MA0740.1chr20:32298280-32298294AACCACGCCCCCTT+6.91
KLF14MA0740.1chr20:32298317-32298331AACCACGCCCCCTT+6.91
KLF16MA0741.1chr20:32298210-32298221ACCACGCCCCC+6.14
KLF16MA0741.1chr20:32298244-32298255ACCACGCCCCC+6.14
KLF16MA0741.1chr20:32298281-32298292ACCACGCCCCC+6.14
KLF16MA0741.1chr20:32298318-32298329ACCACGCCCCC+6.14
SP1MA0079.4chr20:32297563-32297578TAAACCACGCCCCTC+6.54
SP3MA0746.2chr20:32298209-32298222AACCACGCCCCCT+6.09
SP3MA0746.2chr20:32298243-32298256AACCACGCCCCCT+6.09
SP3MA0746.2chr20:32298280-32298293AACCACGCCCCCT+6.09
SP3MA0746.2chr20:32298317-32298330AACCACGCCCCCT+6.09
SP4MA0685.1chr20:32298207-32298224TGAACCACGCCCCCTTC+6.22
SP4MA0685.1chr20:32298241-32298258TGAACCACGCCCCCTTC+6.22
SP4MA0685.1chr20:32298278-32298295TGAACCACGCCCCCTTC+6.22
SP4MA0685.1chr20:32298315-32298332TGAACCACGCCCCCTTC+6.22
SP4MA0685.1chr20:32297563-32297580TAAACCACGCCCCTCCC+6.27
SP8MA0747.1chr20:32298210-32298222ACCACGCCCCCT+6.52
SP8MA0747.1chr20:32298244-32298256ACCACGCCCCCT+6.52
SP8MA0747.1chr20:32298281-32298293ACCACGCCCCCT+6.52
SP8MA0747.1chr20:32298318-32298330ACCACGCCCCCT+6.52
ZNF263MA0528.1chr20:32297645-32297666CCTTCCCCCACCCCCACCTCT-6.14
ZNF263MA0528.1chr20:32297681-32297702CCTTCCCCCACTCCCACCTCC-6.75
ZNF263MA0528.1chr20:32298182-32298203TCTTCCCCAACCCCCTCCTCT-6.83
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr203229735332297590
chr203229767432297991
Number: 1             
IDChromosomeStartEnd
GH20I033708chr203229674832298991
Enhancer Sequence
CATTTCACTA CAGAGTGATT TTTAAAAACA ATCTTTGCCC CAGAGAGCAG CACATGCATT 60
GATTTTTGGG AACCATGAAA TTACAGATGG AAAAACTGAG AGGAAAGTGA CCTTCCCAAG 120
GTCACAGAGG GACTGGTGAG TCACAGAACT CAGACATGCA AAAGAGCCAA GAGCTTATCA 180
TCTTAATCAC CTCCACCCCA ACCTCTATAC AGAACCAGGG CCCCCTCCTC TAGCCCCACC 240
TCTATACAGA AACACGCCCC TCCACCCACC CCTACCTCTA GAATAAACCA CGCCCCTCCC 300
CACCCCCACC TCTACACTGA ACCACGCCCC TTCACCCACC CATACTTCTA CACTGAACCA 360
CGTCCCCTTC CCCCACCCCC ACCTCTACAC GGAACCAGGC CCCTTCCCCC ACTCCCACCT 420
CCACACTGAA CCACGCTCTT TCCCCACTCC TAACTCTACA CTGAACCACG CCCTTTCTCC 480
CACTCCTACC TCTATACAGA ACCACGCCCT TCTGCCACTC AAAACTCTAC ACTGACCCAC 540
ACCCCTTCCC CCACTCCTAC CTCTACACTG AGCCACGCCC TTGTCCCCAC TCATAACTCT 600
ACACTGAACC ACACCCCTTC CCCGACTCCC ACCTCTATCC AGAACCACGC CCTTCCCCCA 660
CTCCCACCTC TATCCAGAAC CACGCCCTTT CCCCACTCCT ACCTCTATAC AGAACCACAC 720
CCCTTCCCCC ACTCCCACCT CTACAATGAA CCACGCCCTT TCCCCCACTC CCACCTCTAT 780
CCAGAACCAC GCCCTTTCCC CCACTCCTAC CTCCATACAG AACCACACCT CTTCTCCTAC 840
TCCTACCTCT ACACTGAATC ACGCCCCTTC CCCCACTCCT ACCTCTATAC TGAAACAAGC 900
CCTCTTCCCC AACCCCCTCC TCTACACTGA ACCACGCCCC CTTCCGTCAC CACCTCTGTA 960
CTGAACCACG CCCCCTTCCA TCACCCCCAC CTCTGTACTG AACCACGCCC CCTTCTGTCA 1020
CCCCCACCTC TGTGCTGAAC CACGCCCCCT TCACTACCCC CATCTCGGGA GGATCTTTAC 1080