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

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EnhancerAtlas ID
HS182-09870 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr17:72673680-72675010 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:72674244-72674262TCTTGCTTCCTTCCTCCT-6.04
EWSR1-FLI1MA0149.1chr17:72674240-72674258CCCTTCTTGCTTCCTTCC-7.02
RORAMA0071.1chr17:72674569-72674579TGACCTTGAT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177267409172674939
chr177267374472674303
Number: 1             
IDChromosomeStartEnd
GH17I074677chr177267372572674539
Enhancer Sequence
CTATTGTCAG CTCAGGAACA AACAAGAAAG CCAAGAAAAG CTAGCTGCTC CCTGTATAAT 60
ATTTCCACTG GCTTGTTTTC CTCTCTTGCT TGCTCTGAAG GCTTACAGAT AAACAAATGA 120
AGTGTATATT ACATCACTGG CAATCTGGTG CCGTCTGGGA CTCCTTTGGC TGATAGGTCG 180
GTCCTGCCCA GATCCCAGAG CAGGCAGCTG GTGTGGGGAG TGGTGGTGCC TGCTAGTTCT 240
CTTAGGATAA CCTCAGCAGG AAATGATGGT GACTCAGTCC AGCGCCTCAA AGTCGTTTTC 300
CAAACTCTCC AGGCTTTCCT CTCCTAAGCA TCCTTTCCTT TAATTTGTGG TCCCTGGGGC 360
CTTTTGTGAG AAAATGTCTG AGACTCACTT GTGTTGCTGC CCTAATGTTT CCTCTTATAA 420
GCTGTTCTAG GGAGGGACGT CCTTCAGTTT CAGGGCAGGA AACTCCGCCT TACTGGGTGG 480
AAGTAAACAG CCAGAGGTGA GCACCAGGCT GGAGAATTGT TGAAGTGGGC ATTTGAAGTG 540
GCTCTAAATT TATCCCAATA CCCTTCTTGC TTCCTTCCTC CTCTTCTCAG GCAAGAGAAA 600
CAGTCTGTAG AGACTGCGAG TGCGAATGGA GATCACAGCT CCTTGTTAAC TCACTCAGGC 660
AATGTAGTTC CCAGCTGGGA GTGGCCCTGG ACATCCTCCT ATCTCTTAAC CAGAGGAGGT 720
TTTCTGGGGC CAAGAGAGAC AGCTCCAAGC AAACAGATCT GGAAAATATT AACCCCTAAC 780
TGATGACACC AGGCCTCACC CTGCTCCTAA AGGGAGCAAG GCCTTGAGTG GTGCAGTGAA 840
AATAACTTGA GACGTGCAGG GCTCAAGAAT TCTCCCAGCA CATGGTTCCT GACCTTGATT 900
TCTAAGTCAG CTCCCTCCCT TCTCATTTGC TTATCAGCGC CTTTTCATTT GCTTATTAGC 960
ACCTTCTCAT TTGCTTATTA GCAGACAGTT TCTACCCATC AACATGAGGA TGCTATTTAA 1020
TCATTTGTGC TTTTGCAAAT GCACATGCTT TTAGGTATCT GAAACCAAGC TGTGCTTAAG 1080
TTCAAATTTT CTCTTACTTG CTAGCCTTCT GCCCCTGGCC ACCACACACA CAGACACACA 1140
GACACACACA CACACACACA CACACATGCC TGCACATGCA CACATACGCA CCCTTCCTCT 1200
CATGAGCTGT GGGCAGGGCC AGTGATCATC CGTTTTTGTT CTCTGTCTCC CCTTAGCTTT 1260
TGTTATGAGC CTTTTAAAAG CAAAGCAGGC TGGGTGCAGT GGCTTAGTCC TGTAATCCCA 1320
GCACTTTGGG 1330