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

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EnhancerAtlas ID
HS017-21661 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr22:21102420-21104190 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFAT5MA0606.1chr22:21103261-21103271ATTTTCCATT+6.02
NFATC1MA0624.1chr22:21103261-21103271ATTTTCCATT+6.02
NFATC3MA0625.1chr22:21103261-21103271ATTTTCCATT+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 6             
ChromosomeStartEnd
chr222110381321103939
chr222110281421102884
chr222110317421103455
chr222110248221102632
chr222110310621103771
chr222110296021103031
Number: 1             
IDChromosomeStartEnd
GH22I020748chr222110283221106225
Enhancer Sequence
AACTAGCTGT GGGACTGTCA GTAAGTCAAA GCCCCTCTAT GACCAGCTAC TGCTCATTTG 60
ACTGAGGACA AGGCCAATTC CCCGAGCGGC TGTCATGCAG TCACTGCGGT GTTGCACCGT 120
CAATGGGAGA GGGCCATTTA TTCTTTCAGC ACATCCTTGC TGAGCATCTG CTGTGGTAGC 180
CACCAGGCAA ATAAGCTACA AAGCCTTGGC CTTGCGGTCA ACAGGCAGGC TGTGTGGTGT 240
GGAGCCTCGG TTCTCTACTG CAGCATACCA GCAGCCTGGT GTGGGTGAAC TGGACAGCAG 300
GAACGAAGAA CAACACCTGT GTCCACCTGG CCACCCAGTG GGAGAAGGGT GCTGGGCAAT 360
GGGATACCTG GCAGAGCCCA GGGGTGTGAG GGAGGCCTCC TGCTCTGGGG ACCACAGGGG 420
GCTCAGCCTG CAGGAGTACC AAGGACAAGG GTCTCGAGGG TGGGGGCAAG CCTGGAACAG 480
ATGCAGGCCC TGTTTACAGG CGTGAACCAA CTAATTCCCT TAAGAAGAAA TGTACAGGAG 540
TATATACATG CAGAATTGTC TCAATGGTTT TGGGGGACTC CTGGAGCTCC AGAAACCCAT 600
CCTTGGACAC TATGACGATG AAGAGTGACT AATAATCAAG TTTAAAAGGG AAGTACACTG 660
ACCAGATACC CTATTAAAAC CAGACTACTC TGGTGGGTGG AGGAGAGGGC AGATTCGGGG 720
AAGGCTGAGG CTGGGCACGG AGGGTGGGGA ATAAGCACAC TGCAGGGGAA GTGAAAGGGC 780
AGGCCTGGGG CACGCCAAGG GGACACCTGG TGGAAAAATC AAGACCGCTT CAAGCCTTTT 840
CATTTTCCAT TTCCTTCTTA GGCCAGACCT GCGTGAGAAA GTAAAAAGCT CTATCAGCTG 900
CTTTTTTTGT CCACTTAAAC TTTCTAGGCA TTAGAGGGGG CCTCCCCTCT TCAGACGACA 960
GACAGCCTTG GGACCTGAGG CCCTTTTGCT GTAAATGAAC AAAGGGAAAT AGTTTCTTGC 1020
CACTGCGTTT CCACACAGCT CTCAGGGCTC TTGGAGCTGG CTGCTCTATC CTTCCTGGAC 1080
TCCACAACCA GAAACACTTT TGAGCCTGTT TCATCTTTAA AGTGCTGCCA GGGTAAACCT 1140
CACAAGAGTT CCTCTCAGCA CACCCACTCT CTGCTAACAC AGATTCCTTC CAGAGGTATT 1200
TTTCTCATCT TTGATTCCTT TTAAGGCAAT TCTTTCCTCT CACACCCTGT GGCATTACAT 1260
GGTTTACTTC GTGGCCATCT GAGTTTCCAA ACCAGTGTTT TTGTCTGAAA GACTCCCATG 1320
CACCTACATG TGCAGCTTAT GTGGAGCTTT AATGGGACAC AAGTCCCCAA CTCTGCCTCT 1380
GCTCCACCAG CCTTGGTCAG GCCCCTGCCT TTGGGCACAG GTGCCAGCAA TGCACTTGGC 1440
ACTTAGAGAT GCTGCCATCT GGCAGCCTCC CACATCCACC ACACAAGCCC TTCCTCTCGT 1500
GAGCAGCCCC CAAGTCTTGC CACAGACCTG GCACCTCACC TGGTGTGAGC CGTCAGATGC 1560
CCTCCTTGTG CCCTGGCCAG CACTGGCCCC ACAGGCGCTC CTAACACACA GAGCAGCCTC 1620
TGAGGCATCT ATTATTCTCA GGCCCTAGAC TGATGCTTCC AGTCTCCATT CACACTAGTG 1680
CTATTTGGAT TTTGAGTTCT TCATGTCTCT GTAAAGCTTT TTTGGGAGTT TGAAGGAGCT 1740
TATGGCAATT GCCTTTTGAT GGTTTCAAGT 1770