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

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EnhancerAtlas ID
HS073-09664 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr22:21102460-21104190 
Target genes
Number: 3             
NameEnsembl ID
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
GACCAGCTAC TGCTCATTTG ACTGAGGACA AGGCCAATTC CCCGAGCGGC TGTCATGCAG 60
TCACTGCGGT GTTGCACCGT CAATGGGAGA GGGCCATTTA TTCTTTCAGC ACATCCTTGC 120
TGAGCATCTG CTGTGGTAGC CACCAGGCAA ATAAGCTACA AAGCCTTGGC CTTGCGGTCA 180
ACAGGCAGGC TGTGTGGTGT GGAGCCTCGG TTCTCTACTG CAGCATACCA GCAGCCTGGT 240
GTGGGTGAAC TGGACAGCAG GAACGAAGAA CAACACCTGT GTCCACCTGG CCACCCAGTG 300
GGAGAAGGGT GCTGGGCAAT GGGATACCTG GCAGAGCCCA GGGGTGTGAG GGAGGCCTCC 360
TGCTCTGGGG ACCACAGGGG GCTCAGCCTG CAGGAGTACC AAGGACAAGG GTCTCGAGGG 420
TGGGGGCAAG CCTGGAACAG ATGCAGGCCC TGTTTACAGG CGTGAACCAA CTAATTCCCT 480
TAAGAAGAAA TGTACAGGAG TATATACATG CAGAATTGTC TCAATGGTTT TGGGGGACTC 540
CTGGAGCTCC AGAAACCCAT CCTTGGACAC TATGACGATG AAGAGTGACT AATAATCAAG 600
TTTAAAAGGG AAGTACACTG ACCAGATACC CTATTAAAAC CAGACTACTC TGGTGGGTGG 660
AGGAGAGGGC AGATTCGGGG AAGGCTGAGG CTGGGCACGG AGGGTGGGGA ATAAGCACAC 720
TGCAGGGGAA GTGAAAGGGC AGGCCTGGGG CACGCCAAGG GGACACCTGG TGGAAAAATC 780
AAGACCGCTT CAAGCCTTTT CATTTTCCAT TTCCTTCTTA GGCCAGACCT GCGTGAGAAA 840
GTAAAAAGCT CTATCAGCTG CTTTTTTTGT CCACTTAAAC TTTCTAGGCA TTAGAGGGGG 900
CCTCCCCTCT TCAGACGACA GACAGCCTTG GGACCTGAGG CCCTTTTGCT GTAAATGAAC 960
AAAGGGAAAT AGTTTCTTGC CACTGCGTTT CCACACAGCT CTCAGGGCTC TTGGAGCTGG 1020
CTGCTCTATC CTTCCTGGAC TCCACAACCA GAAACACTTT TGAGCCTGTT TCATCTTTAA 1080
AGTGCTGCCA GGGTAAACCT CACAAGAGTT CCTCTCAGCA CACCCACTCT CTGCTAACAC 1140
AGATTCCTTC CAGAGGTATT TTTCTCATCT TTGATTCCTT TTAAGGCAAT TCTTTCCTCT 1200
CACACCCTGT GGCATTACAT GGTTTACTTC GTGGCCATCT GAGTTTCCAA ACCAGTGTTT 1260
TTGTCTGAAA GACTCCCATG CACCTACATG TGCAGCTTAT GTGGAGCTTT AATGGGACAC 1320
AAGTCCCCAA CTCTGCCTCT GCTCCACCAG CCTTGGTCAG GCCCCTGCCT TTGGGCACAG 1380
GTGCCAGCAA TGCACTTGGC ACTTAGAGAT GCTGCCATCT GGCAGCCTCC CACATCCACC 1440
ACACAAGCCC TTCCTCTCGT GAGCAGCCCC CAAGTCTTGC CACAGACCTG GCACCTCACC 1500
TGGTGTGAGC CGTCAGATGC CCTCCTTGTG CCCTGGCCAG CACTGGCCCC ACAGGCGCTC 1560
CTAACACACA GAGCAGCCTC TGAGGCATCT ATTATTCTCA GGCCCTAGAC TGATGCTTCC 1620
AGTCTCCATT CACACTAGTG CTATTTGGAT TTTGAGTTCT TCATGTCTCT GTAAAGCTTT 1680
TTTGGGAGTT TGAAGGAGCT TATGGCAATT GCCTTTTGAT GGTTTCAAGT 1730