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

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EnhancerAtlas ID
HS062-10959 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr22:50936260-50937490 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr22:50936797-50936816CAGTGCCCCCTTCTGGAAA-6.79
EWSR1-FLI1MA0149.1chr22:50936898-50936916CCTGCCTTCATCCCTTCC-7.36
HLFMA0043.2chr22:50937369-50937381TGTTATGTAATG-6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr225093662550937431
chr225093694550937290
Number: 2             
IDChromosomeStartEnd
GH22I050497chr225093622250936310
GH22I050498chr225093657850937500
Enhancer Sequence
TTCCTGCTCG GCGAGCCACA CAGCTAGAAT CATCTCACCA GCCAGGGCCT CTGCCCGTGG 60
TTCTTGTGCA GCTCTGGAGA GCTGCTCTTC CCATCCAAAG GTCTTCGATC CCCTACAGTC 120
CACAGTTCCC AGTTCTCCCC TCCACGTGCA TGGAAGCAGG ACACCCCAAT CTCATCTCTT 180
TTTTTGTTTC TTTTAAGAAA CCAGGTCTTG CTCTGTTGCC ATGCTGGGAG TGCAGGGGTG 240
CAATTAGAGC TCACTGCAGC CTCGAACTCC TGGCTCAAGT GATCCTCCTG CCTCAGCCTC 300
CTGAGTAGCT GGGACTACAC GTTCAGGCCA CCACATCTGG CTACATTTTA AATTTTTTTT 360
TTTGTAGAGA GAAGCTCTTG CTATGTTGCC CAGGTGGTCT TGAACCCCTG GCCTCAAGTG 420
ATCCTTTTGT GGCTTCCCAA AGTGCTAGGA TTACAGGAGT GACCGCTGTG CCTGGTCGTC 480
TCACCTTCTT TTGACATGGA GCCCCAGCCT TGGGAGGCAG ATGCTGAACC GTGTCCACAG 540
TGCCCCCTTC TGGAAATTCT CCACAAGCCA AGGTTTTGGA CAGCTCCAAT GTCTGGGGCT 600
ATGGCATTTC AGGCGGGAAG TCTCTGCAGA GAGCAGTACC TGCCTTCATC CCTTCCTAGA 660
TATTAATTCA CTTTCAGACA CATACTGAGC AGCTAGTGTG AGCTGTTACG GTGCTGGCTC 720
TGCAGACAGA GCTGCAGCGA AGACAGACGC CAACCCCACC CTCACACAGC CAATCCTGTG 780
CTAGTTTTTT CTGTAGAACC ACCACTGGGT TTCCAGTTGG TCTGGGTTAT CTGGTGAACT 840
CAGAGACTTT CGCTGTCTTC TGGACACTCC ACAACAGTCC AATCACCTGC GGGGACCCTG 900
ACCTCTGCAA ACCTCCGGGG GGTGGTTCCT TGGTTGGCCG CCCTCCTCTG ACGGCTCCGC 960
CTCCCTGCCG AGCCCTGGGA TCGTCCTCCC TGGCTCCTGC CTTCTCTCTC ATAGGATCTC 1020
ATTTGTTCTG ACACACTTAT TCTCAAGCCC AGTAGTTACT CTTGAATATT GCTTATAGAG 1080
GTGTGTTTCC TTGAATATTC AAGCATATGT GTTATGTAAT GGGTAATAAT AAAGTAGGAA 1140
TGTGCATATA TGAATCAGCA CAAAATAACT AAAAAAAATC CCATCTCCAA AGTCACTGAC 1200
TATTGACAAA TTCTGGACCT ACTTCTCCGT 1230