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

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EnhancerAtlas ID
HS180-42238 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr6:52976660-52978190 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RESTMA0138.2chr6:52977628-52977649ACCATGACCCAGGACAGCGCC+6.33
ZNF263MA0528.1chr6:52977315-52977336CCTTCCCCACCCTCCAGCTCC-6.07
ZNF263MA0528.1chr6:52977318-52977339TCCCCACCCTCCAGCTCCTCC-6.41
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr65297709952978012
chr65297701752978121
Number: 1             
IDChromosomeStartEnd
GH06I053111chr65297667552978470
Enhancer Sequence
TTTCCTATCA GATATTCTTC CTGTACTCTC GCCCCTTCCC AATCAAAACG CTGGCATCAG 60
GTTAGTCTGA GGCACAACCT TCCTCTGTTA TCCACAAGTT GTGACCTTCT AAACTTTCTA 120
CAGCCTGCTG TCTCTGGCAA GGGTGATGAA CTCAAACACC TGTGAAGGTC CAGAGGACAC 180
CACAAGTGAG TGAGGTGGAC CAGGTGTGCA GGCAGTGGCA AGCCAGACCC TGTGTCTCTT 240
GCCTGAAAGG GAAGCGGCTA CTCAGCTTCC GTTCGAAGAT TCTCTATAAG GCCTGACCTT 300
CCTATTTTTA AAGAGAAGCT GGAAATCCAT GTTGTTTGTG AAATGTTGTA TGCTTAACCA 360
AACTCAAGTT TAAAAGGAAA AAAATAAAAA CACGATACAG GTCAAACAAA AGCCATCTGC 420
AGGATGAGTG GAATCGGCCA ATTTTTGACC CTTGGTATGC AGGTTAAAGC CCAAATAATA 480
AACTTTGCAT TCTAGGTCTG TACAGGTTTG ACACTAACCT ACCTTTCCAG CTCGCCTCCT 540
GCTCCTCCTC CAGGTCTGCT CCTAGCCAAG AATAGTTCTG GTTCCCAGGA CACCCAAAGC 600
CCCTCCCTAC CCCTGCCCCT TTGCTCTGCT GGCATCTGGA ATGCTCTTTC TCTCACCTTC 660
CCCACCCTCC AGCTCCTCCT GGAAGTTCTA CTATTCCTCC TGGAGGCTTT CCACAGTTTA 720
ACTCCAGCCA ATGAATGATT AAATAATTAC ACACAATCTA CTCCCCCTGG GCCTCCAGGG 780
CACTCTCAAA GAGCTCTGTT TCACCTGTGT TTACTTTCTA CCACATCCTG GCCAGTGCCA 840
CACCTCAGAA GGCTTCAGAG AAAAATTGTG ACTAACTGAC TTGTGTCACT TCTCTCCTAC 900
TAAATCATAA GCAAGTTGTC TGCAGAGCCC CCCACTGCCA GCTCCTTGCC CCAGCTCCTC 960
CCACCACCAC CATGACCCAG GACAGCGCCT TATAGGTCCC AGATGACTGT CAAGGCTTCT 1020
TGAAAGCTTT GGCTCTAAGG GATTAAACTG GAAGACTGCA GCTGATTAAC TCACTAGGTT 1080
TAAATTAAGT TCTTGGGCTT GCTGCAAGCA GAGCAAAACT CTCCCGTCTC TCTGCAGCCC 1140
CTTCTCAGGC CTCTGCTCTC TTTGTGGGCA TGGCCAGTGT CTCTTAGCTG CATCCTGGGT 1200
CACTCAAGGT CTCAGGGTAG GAGAGCTGGA TGTACAAATC ACACCCTCAT CCTCCTGGGG 1260
GAGTGGATCC AGGTGCTGGT GGAGGGATGC CAGCATCACC TGGAAGCAGA AAGTTATGCC 1320
CTGAGGGAGC TGTCCCTTGT TTGACTAATC CAAATTAATA CCACTATTAT TGTCTTACAG 1380
TGTTAGGGCC ATGAGAGGCC ATATAGCCAT TTAGACTGAA GGAGGAAACC GAGACCCAGA 1440
GAAGCATGAT TTGCCCAAAG ACAGGGTAAG GGTGAACTCT AGATAGGATC CAGGACATCT 1500
AACTCCAACT CTGGAGACTT TTTTCCACTA 1530