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

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EnhancerAtlas ID
HS049-04232 
Organism
Homo sapiens 
Tissue/cell
Fetal_spinal_cord 
Coordinate
chr19:51110620-51111960 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB1MA0018.3chr19:51111400-51111412AGTGACGTCACC+6.22
CREB1MA0018.3chr19:51111400-51111412AGTGACGTCACC-6.22
EBF1MA0154.3chr19:51111886-51111900TGTCCCTGGGGACT-6.15
RFX1MA0509.2chr19:51111546-51111562TGTCATCATGGCAACC+6.25
RFX1MA0509.2chr19:51111546-51111562TGTCATCATGGCAACC-6.25
RFX2MA0600.2chr19:51111546-51111562TGTCATCATGGCAACC-6.2
ZNF263MA0528.1chr19:51110877-51110898CGCTCCTCCCCTGCCTCCCTC-6.24
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr195111080051111288
Number: 1             
IDChromosomeStartEnd
GH19I050608chr195111134151111570
Enhancer Sequence
GGATCTTTGT CTTCGTCACC TCTCTAGTTC GCTCCCATCT GATTCACTGT CTTCTCTCTC 60
TGGTCCTGTC CCCTTTGCCT ACGAATGTAT CCTCTTTATT GCTGTTGATC CCACTGCTGC 120
ACTGTCCTCG CTGCTGCCTT CTCACAGTCC TGTCGCCGTC CCCATCCTCT TTCTCAGTCC 180
CCTGTGCCGT CGGGCGCTCC ACCTGTGACC GTGGGGTCTT TTTCTGTCCC CTCGGTGCCT 240
GTCACAACCC CTCTTGTCGC TCCTCCCCTG CCTCCCTCGC CTCAGGGCCC TTCCCCGTCT 300
CCTTCTCTTC CTGTCATCCC TGGCTCCTTC CCAGCGTCTT TTCTTCCTTC TCCGAATCGT 360
CGTCTGCTCC TCTGGGTTTG CGGCTGTTGG GGACTCTGCC CCTGGGAGAG AGAAATGCGA 420
AACGTATTTC TGGGAGCTGG AAGCTGTTTC CTCCATTTAG TCTCTGGATG TTTTCTAGGT 480
GACCACAGCC TCTTATAGGC CTGTCCTGGG GCAGAGCGGC CACCTTGAGG TCCATCAGTC 540
AGTCTGATCA TCTCTGTAGA ACCTCGAACC TCTCGCCTCG CCTCGCCTGA CGCCGTTTCC 600
TGCCCTTTAT CTCTCCCTTC AGAATTAAAA AAAAAAAAAA AAAAAAAGAC AGTCGGAAGC 660
AGCAGCGCAT GAGCCCCAAT CACCACTCTG AAACAGGTGC GCGCGGTGGC CTGCGGGCTC 720
GCGGGAGCTC ACGCGAACTC ACGCGCGAGC TCACAAGCTG CGGCGGCCGG CTAGGCGACT 780
AGTGACGTCA CCGAGGCTTG TCCCTGCCTT ATTGGCTGCC TTCGACCAGC GCGCGTTTGC 840
TGGAGTAGTC GGCCACGCCT TGCCAATCGC CAGGGGGCGC TCAGCGCTAG AGCTCCGCGA 900
CCCTGGGAGC CCTATAGAGA GACTCGTGTC ATCATGGCAA CCCTGCCCTA CCTAATTGGA 960
TACCTGCTCC AGTTGGTTGG ATCCATTACT CTGATTGGAT GCCTGGCGAG TCAAGGCTTG 1020
TATATAATTG GATGCCGGAA ATTTGGATCT TTTCTACGTT TCGCATTTCT GTCTCTTAGC 1080
CGGATTTCTT CCGCAAGCAC TGGGGATGTG GAGATTGAAA GTAACTTGAG TCTCCGTGGG 1140
GGAGTGATGG GTGTTGGGCA CGGTATGGGA ACCTGGCCCG AGTCTGCGGA CCCGATTGGC 1200
TGCTGTCTCT CAGATACAGG TCCCTTTCGT CCCGCCAAGG GGGGCCATGG AACGTAGGGC 1260
CCTCTCTGTC CCTGGGGACT GGGTGATGTC AGGGGTGATT GGCTACATCG CTCCCCAGAA 1320
GGTGAAATGG AAAAATTGAG 1340