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

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EnhancerAtlas ID
HS180-27012 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr2:106886000-106887150 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs66569888chr2106886967hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr2:106886660-106886674AACCACGCCCACCT+6.28
KLF5MA0599.1chr2:106886646-106886656GCCCCGCCCC+6.02
RREB1MA0073.1chr2:106886674-106886694ACCGAACCCACCCCCCACCG+6.48
SP1MA0079.4chr2:106886658-106886673CAAACCACGCCCACC+7.02
SP3MA0746.2chr2:106886660-106886673AACCACGCCCACC+6.28
SP4MA0685.1chr2:106886658-106886675CAAACCACGCCCACCTA+6.77
SP8MA0747.1chr2:106886661-106886673ACCACGCCCACC+6.32
Number: 1             
IDChromosomeStartEnd
GH02I106269chr2106885857106887256
Enhancer Sequence
GCGTTATTAA ACTTTAAACC ACATGAAAGA AGAATATGAA ATAGTCTCCG CTCAGAGTGA 60
AAATGATGAG TAACTGTTGG TAGACAATAC CAGTAAAGAC ACAGTGAATT GGCAAAAACG 120
GACCCCTAAG CGACGGTGCC CTGAGGAGTC ACGGAAGTTC GGGTGAAGAG TGCGGGGCCT 180
GGGCAGGAAG TTCCTGGGAG TGGTTTGAAC AAACGGTCCT GCAAGGTCAG CCAGACGGGG 240
AGCGTGCTTC AGGGAGACAG CGAGTTCAGC GCTCGGTGGA GCAGCACCGT CGGCCAGGTG 300
CATGGTCACT GAACAGAGGA GCCCAGGCCC ACAGCCAACA GGAACACGGG AAGTGACTGG 360
CCCATGTACT AGAAGTCGTA TTTACTCTGT GTCCGTCAAC CCGCGCCAGC TGTCAGCTCA 420
CGGCTCTCGG CCGCCTTTGG GTGGAGGGAG GGCGTTGCCA GAGCAGCATC ATAAAGTACA 480
TAGGTCTGCC CACGTCGGGA CGCGTGGGTC CGCGTCTGCA GGTTCCTATC GCTCCCCGTT 540
TTCTGAATAT TGGGAGATAT TCCACACCCT GGTCACACTC CCTAACCCAG CTCGCTCCAG 600
GCGTCCCACG CTCAGCGTTC AGGGTCACCT CCCTGCACCC TGGCCGGCCC CGCCCCACCA 660
AACCACGCCC ACCTACCGAA CCCACCCCCC ACCGAACCAA GCCTGGCGGA TCCTGCTTCA 720
TCAAACCACG TCCACTCGGT GGCTCCTAAC TGGGCCAAAG CCCGCTGCCC CTCCGCACCA 780
GCTGGGGTCC TACTTCTCCA TCAGGCTCAT TACGCACTTC AGTTTTCTTT CCCTAACATG 840
TTATAAGCAC TTTAAGGGCG GAGCCAGTGC CTGTGGGATA CTTTCAATAT CCCTTGAAGA 900
AATGAATGAC ATAATTGCCC CTTCCCAATC CTGATCACCC CAAAGATGGG GCCAGCTGTC 960
CTCACTGAGG CCAGGAGACT CTCAGGAATG TGAGTCCTGC TAACCCTTAA AGGGACACTT 1020
ACAGAGCAAG AGTAGCAACA GTGAGAAGAG GGTGGGGTGT CCCGTCACAG CCCTTAGCAC 1080
ATGTCCGCAG AGCAAAGCTA GGTGGCTCCC AGCCCTCGGG GCAGCAACAC AGGCCCGCAC 1140
CTCCACTGCC 1150