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

TagContent
EnhancerAtlas ID
HS180-25651 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr2:30733760-30734940 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CrxMA0467.1chr2:30734734-30734745CTAATCCTCTT-6.62
FOSL1MA0477.1chr2:30734159-30734170CATGAGTCACC-6.62
HNF4GMA0484.1chr2:30734025-30734040TGAACTTTGGGCTTT-6.09
JUNDMA0491.1chr2:30734159-30734170CATGAGTCACC-6.02
TCF7L2MA0523.1chr2:30733846-30733860TTTCTTTGAAGTTT-6.2
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr23073437630734545
chr23073473330734838
Number: 1             
IDChromosomeStartEnd
GH02I030511chr23073396530734547
Enhancer Sequence
CTTTCTTCAT TTTATTTTCC CACAAGAACA TGTTATTGTT TCCTGATTGC AGTATTTATT 60
GTCTTTTTGA AAATGTTAAA GATAGTTTTC TTTGAAGTTT TCTTTTCCCC TGAATAGTTT 120
ATTTCCTTCA AGTATACTTT TTTTTCTGTT TAATTTAGTC TCTAATGTCA TGTTAGAGTG 180
TTTGCTCAGA AGTCTCATTA TCTGTTCCTA ATAAAAAATG GGTGATTTAG AAAGCCAGTA 240
GAGGCTTGCA CGTAGGTGAG GCTTGTGAAC TTTGGGCTTT ACTGAGGGGT GATTTATGTG 300
GGCTGTTTAT TAGGGAATCC CTCAATGTTT CTGTATTTTC GAACTCCTGA CCTCAAGTGA 360
TCTGACCGCC TCGGCCTCCC AAAGTGCTAG GATTACAGGC ATGAGTCACC GCGCCTGGCC 420
TGTTTCTGTA TTTTTGTCTT TCCTCATAGC CTGGTCAGAC ATCCCAGAGA GTACACTCCT 480
GTCTTCTGCC TAGGACTGTG CTGTTCAATA CTGTGGCCAC TACCCACATG TAGCTATTTA 540
AATTGAAATA TAATTAAGTT AAAAATTCAT TTCTTCAATG GCACTAGCCA CATTTCAGAT 600
GCTCAATAGC TACATGTAGC TAATGGCTGC AGTTTTGGAC AGCATAACTA GGGAACATTT 660
CCATCATTGC AGAATATTCT ATAGGACAAC TGGCATAGGA CCAAAGATCT TGTTGCCAGC 720
CATCTGAGAG CTCATCCAGG GAAGATGGTC TGAGGTTTTA GCATTCAGGA TTCAGCATGT 780
ATATGGTCAC TTAATCCCAC TGTTCTTAGA GTGGTGACCA TGCCCTAAAC TGTGCATTTC 840
CTAATTGGGA AACTCTGTTT TACCTTCTCT AGAGAATAGA CATGCAAGTT TATGCTGCGG 900
TAGGAGAGGG ACAGTTACCC AGAGGTGCAG AGAGAGAAGG GAATCTAGGA ATCCACCTGC 960
CCCTCACTCA TTACCTAATC CTCTTTATTT TGGCAAACTG CCATTCATCT CCATTTGCAT 1020
CCAGCAGTAC CTGATGCTTC CGCCTCCTAG GCCTTAGGAG GATTCTGTGG GTTTGTTTTC 1080
AACTTTTTCC TCTGCTGGCT TACACTTTGT CTTTGCAGGT CAGCCAGGAT AGTCAACATT 1140
TGGCTTTCTG CTTTCCAGCT TTTAAAATGT TGTTCTTTTT 1180