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

TagContent
EnhancerAtlas ID
HS147-03518 
Organism
Homo sapiens 
Tissue/cell
NHEK 
Coordinate
chr1:167012760-167014100 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MyogMA0500.1chr1:167013258-167013269GACAGCTGCAG+6.62
Tcf12MA0521.1chr1:167013258-167013269GACAGCTGCAG+6.14
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1167013005167013714
Number: 1             
IDChromosomeStartEnd
GH01I167043chr1167012838167014050
Enhancer Sequence
TAAGGGTTCT CTCAATCTCT TTCTGGGGAA AAAAAAAAAA TCTATAAGAC AGCCCAGAAC 60
TAACATAGTT AGACCTGAGT TTGGGCTCTA TCTTTGTCAC TAACCAGCTG CATGTTCCTT 120
AACAAGTCAC TTTAATATCC CGAGCGTTGG TTTCCTCATC TGTAAACTAA GATGAATAAT 180
GCCTGGCTGA TAATGTGGCT GTGAAGATTA AAATGGGTCA TGCCTTTGAA TATGCTTTAT 240
AAAATTCAGT TCTTCTTTCA TTTCCTCAGC CGATTGCTCA TGTTCCTCTA ATACACTGTC 300
CCCACCCTGG ACAACCTCTA GCAGGTATAT GCACACCTGA AGATACTGAG ACAGGGAGAC 360
TGACTAGTTG AGATTCACTG AGGCTGATGT GTCTAGAAAG TTGCTCACTA AGTATTCCCG 420
CAGGGTGTTT GAAGCCTCTT CCTGGATGCC TGGTGAGACG AGACACTTTG AATCCACCTT 480
GCAAAGCTCC TGCTCCAAGA CAGCTGCAGC TTGTGCTCTG TAGAGCGATA TGAAATAATT 540
GCCCGTTGGC ACAATAAGCC CATCTCCTCT CCGGGCAGCA CAAAAGAAAG CTCAAAAGCA 600
TCTCCGGTTT TGATTGCCAA GTGGGGGAGG CAGTGAAAGT ACACTAAATT ATGAGTCCAG 660
GTGCCTCTCT ACAGAAATCC ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC GCAGTGGGTG 720
TTGACGTCAC CTTCGGCCAC AGGAGCTTGG AGAGGCTGGG GCCCTGACTC CCCGCGGGAT 780
CCGCTGGTAG ACCAGGGCGT GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG CTTACTCTCG 840
CCATAGACCA GACTGACAGG GGTCTGCCAA GGCTGCTGGG AATGTGGGAA GTGAACTTTA 900
GGTGGAAACA GAAAAGCTTC TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT TTTAGTTCAG 960
GAGAGAAAAA AAAAATCATA GAAGCCTGCC AAGCCAAATA AACTATGCTC AATTAAGTCT 1020
TTCAACTGTG CAATTCCTCT TGTTGATTTT ATGAGGAAAA GGGCAGAATA GAAACATGAT 1080
GGGCTTGTTT AAAATACTTC AAAAGGGAAG AACCTATATT CTCCTGCTTC CCAGACCGAC 1140
CTCTTTCGGG CTTTCCTTTC CTCCAGCCAT GCTGCAGGCC TTTCACTGTC ATCTCCTCCA 1200
TCTGTGATAA AGCTGTCCAC AGAACCCGTC CTCAGCTGCT TTCTCACCAC ACACCCTCAC 1260
TCAGGGCATG TCCTCCATGT CATGCCCCTC ATCCAGGCCT GTGACTCCCA AGGAGCTGAA 1320
TCAGCCAAAA CTCTCCCTCC 1340