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

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EnhancerAtlas ID
HS180-01833 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:57772840-57774220 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr1:57773221-57773232CCACACCCTCT+6.02
Klf12MA0742.1chr1:57773219-57773234GGCCACACCCTCTTT+6.05
Klf1MA0493.1chr1:57773219-57773230GGCCACACCCT+6.32
PHOX2AMA0713.1chr1:57773024-57773035TAATTAGATTA-6.32
PROP1MA0715.1chr1:57773024-57773035TAATTAGATTA-6.14
Phox2bMA0681.1chr1:57773024-57773035TAATTAGATTA-6.32
SP4MA0685.1chr1:57773443-57773460TAGGCCACACCCCCTTT+6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr15777307757773509
Number: 1             
IDChromosomeStartEnd
GH01I057306chr15777250057778001
Enhancer Sequence
AATACCTTCT CTTTTGTGCT TTCATTTCAT CTTCATGGTG CTGTCCTCAT TTTACCATGG 60
TTGGAGATGA TATAAGCCAC AGATTTTCCA GCTAAATAGG ACTGGACTCC ATGCCTTTTG 120
AGTCCAAGAT CTCTTCTGTA CCTTGTAAAT ACCACCTGAC TTCTGGCTCT ATATTATGCT 180
ACCTTAATTA GATTATCAGC CCTAGTACAG GTACTGCCAC CCTGAATGAT AGTGAAAGAG 240
CAGGACCTCT TGCTAGTAGG TGAGTTGCCC ACAATCTTCC CCACTCCTCC CCAGCTGGTG 300
AGACCACACC TCCTTCACCA TCTGTTGAAT CTAGACCGCA CCTCCCAGAC CACACCTCCT 360
TCTCCATCCG CTGAGTCTAG GCCACACCCT CTTTCCCTTT CTGTTGAATC TAGGCCACAC 420
TCCCTTTCCT GTCTGTTGAA TCTGGACCAC ACCCCGTTTC CTGTCTGCTG AACCTAGGCC 480
ACACCTTCTT TGCCTGTCTG TTGAATCCAG ACCACATCCC CTTCCCTGTC TGTTGAATCT 540
AGACTACACC CCCTTTCGTA TCTGTTGAAT CTAGGCCACA CCTCCTTTCC TGTTTGTTGA 600
ATTTAGGCCA CACCCCCTTT CCTGTATGTT GAATATAGAC CATACTCTCT TCCCTGTCAA 660
TTCAATCTAG ACCACACCTC CTAGACCACC TTCTTTCCCT AGCTATGGAA TCTAGATCAC 720
ACCTCCCAGA CCAGGTCTCC TTCTCCATCT GCTGAATCTA GACTACACCT CCTGTCCAAT 780
CTGTTGAATC TCTGCACCTT TGCCCAGCCA CCTGATGAGA GCTGTGGGGT CACTAACCTG 840
AATAATAGTG CTTTTTCCCT CTCTGGAGGG AACTTTAACC TTAGCTCATT AAAATTTACA 900
GTCTAAATTA AAAGTATTCT TTAGAGATAA AAAGACCAAA ATAAAGATAA CAGAATACTA 960
AATGGCTTCC AAGAGCCAAA CTAGTAGGTC AGTTCATCCA GATTTGTAAT TGAGTTATCC 1020
CTAAAAAATG AGCCAGCCTT GATTAGGTGC CCATTAGCTT TCAGCTTCCA GAGAGCAGCA 1080
AGCTAGTCCT GCAAACAGTC ATTCTCTTGA CATCTGTGAT TCTCTAGATA TTACCAGTTA 1140
ACGTCCATGC AAGGAGGAAT GGATATATGA TCAGAAGAAG CATGAAAAGA TCTCCTCCTC 1200
TCAGGAATTC CAGGGGGAAA CACCCACAGA AAATCACAAG GCTGAAAAAA ACTGGTATAT 1260
CAAATACTCC TTTGAAAAAT TTTATGAAAG CTGTGAACAC TTTCCCAAAG CTCAAGTCAA 1320
GAACTTAACA TGTAAAGTGG GGATTTAAAA AAAAATTCAA AAAGGAAACA AAAACCCAAT 1380