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

TagContent
EnhancerAtlas ID
HS111-01905 
Organism
Homo sapiens 
Tissue/cell
KB 
Coordinate
chr16:31415010-31416330 
Target genes
TF binding sites/motifs
Number: 32             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr16:31416104-31416122CCTTCCCTCCCTCCCTTC-6.02
EWSR1-FLI1MA0149.1chr16:31416128-31416146CCCTCCCTCCCTCTTTCC-6.03
EWSR1-FLI1MA0149.1chr16:31416186-31416204CTTCCCTCCCTTCCCTCC-6.27
EWSR1-FLI1MA0149.1chr16:31416100-31416118CTTCCCTTCCCTCCCTCC-6.33
EWSR1-FLI1MA0149.1chr16:31416157-31416175CTTCCCTTCCTCTCTTCC-6.35
EWSR1-FLI1MA0149.1chr16:31416105-31416123CTTCCCTCCCTCCCTTCC-6.36
EWSR1-FLI1MA0149.1chr16:31416169-31416187TCTTCCTCCCTTTCTCCC-6.36
EWSR1-FLI1MA0149.1chr16:31416173-31416191CCTCCCTTTCTCCCTTCC-6.69
EWSR1-FLI1MA0149.1chr16:31416117-31416135CCTTCCTTTCTCCCTCCC-6.85
EWSR1-FLI1MA0149.1chr16:31416148-31416166CCTTCCTTTCTTCCCTTC-6.85
EWSR1-FLI1MA0149.1chr16:31416113-31416131CCTCCCTTCCTTTCTCCC-6.89
EWSR1-FLI1MA0149.1chr16:31416161-31416179CCTTCCTCTCTTCCTCCC-6.89
EWSR1-FLI1MA0149.1chr16:31416177-31416195CCTTTCTCCCTTCCCTCC-6.89
EWSR1-FLI1MA0149.1chr16:31416109-31416127CCTCCCTCCCTTCCTTTC-7.08
EWSR1-FLI1MA0149.1chr16:31416136-31416154CCCTCTTTCCCTCCTTCC-7.12
EWSR1-FLI1MA0149.1chr16:31416140-31416158CTTTCCCTCCTTCCTTTC-7.36
EWSR1-FLI1MA0149.1chr16:31416144-31416162CCCTCCTTCCTTTCTTCC-8.61
ZNF263MA0528.1chr16:31416105-31416126CTTCCCTCCCTCCCTTCCTTT-6.11
ZNF263MA0528.1chr16:31416181-31416202TCTCCCTTCCCTCCCTTCCCT-6.1
ZNF263MA0528.1chr16:31416177-31416198CCTTTCTCCCTTCCCTCCCTT-6.21
ZNF263MA0528.1chr16:31416109-31416130CCTCCCTCCCTTCCTTTCTCC-6.32
ZNF263MA0528.1chr16:31416100-31416121CTTCCCTTCCCTCCCTCCCTT-6.39
ZNF263MA0528.1chr16:31416124-31416145TTCTCCCTCCCTCCCTCTTTC-6.43
ZNF263MA0528.1chr16:31416136-31416157CCCTCTTTCCCTCCTTCCTTT-6.51
ZNF263MA0528.1chr16:31416160-31416181CCCTTCCTCTCTTCCTCCCTT-6.56
ZNF263MA0528.1chr16:31416112-31416133CCCTCCCTTCCTTTCTCCCTC-6.61
ZNF263MA0528.1chr16:31416116-31416137CCCTTCCTTTCTCCCTCCCTC-6.76
ZNF263MA0528.1chr16:31416120-31416141TCCTTTCTCCCTCCCTCCCTC-6.77
ZNF263MA0528.1chr16:31416182-31416203CTCCCTTCCCTCCCTTCCCTC-6
ZNF263MA0528.1chr16:31416186-31416207CTTCCCTCCCTTCCCTCCCTC-7.03
ZNF263MA0528.1chr16:31416157-31416178CTTCCCTTCCTCTCTTCCTCC-7.13
ZNF263MA0528.1chr16:31416132-31416153CCCTCCCTCTTTCCCTCCTTC-8.13
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr163141504931416145
Number: 1             
IDChromosomeStartEnd
GH16I031404chr163141546731416630
Enhancer Sequence
ACTTCCTAAC CCTGGGTCAG CACAGCTCTT CTCAGAGGCT GAGGGAGGCT CCAGGGAAAG 60
GGGCTACCAA GGGGCATGTC GGGGCTGCAG GGAGAACCTC CCCCCGGGGT GCTCCTGGTT 120
GCCTCGCTGC CAGTCTCCCT GATATAGGAC TAGGCTCCTC TGCAGCTATG CCTCCCCTTT 180
GCCTGGTTCT GCAGAGCCTG GACCCCAGGA CCCCTCCCCA CCCCACAGCA GCCAGAGGCC 240
CGGGCTTTGG CTCAGACACA TCAGGCTCCC ATCCTGGCTC CCCGTGAGCT ACTCTGGGTG 300
TAACCCTGGG GTGATGGGCT CTAAGTCTCA GTAACTCTCA GATGAAGATA AGCTCACAGC 360
TTAGGATTGA GATCATGTGT GTGGGGTGCT CAGCCCGGGG CACGTAGGAG GTGTCGGATA 420
AATGCCTGAG GTTTTATCAG AGAATGGAGT AGTCAGGGAC TCAGGAATTG TCACCCAAGG 480
TCGTCCTGGT GCCTTTCTCC CCACTCACCT CCTCTCCCGC ATCCCTCACC CCTGCGCACC 540
CCCTGTGCTA CCCAGGCACT CACCGTGGGC CTGCCCCGTG CACATGCAGT CTATTCCTAA 600
AACGATGTAG GAGGTGGGAC CCCCGAGAAA GGCATGTGGT TCTTGTAGGA AGGAGCTGGG 660
CTGACGGTCG GGGATCCTTG GCTTCCTGCA CACACCCCTG GGAGCAGCCC TGGGGTGGTG 720
CTAGAATTTG GCTTAAACAA GAGATGCTCC CACCAAACGC ACCCTCTTTA CTTCTGGGAG 780
GCTCTTCTGC CTTGAACGGT GGCCCCTTGT GACTCAGCAA CCCAGAGGAA GGCCTCCGTC 840
TGTCCTGTAA GTTTAAAGTC ACACGGGAGT GTCCCATTCT GGAGTCTCCA CCTCACCCCT 900
CAAAGTTCTT CCAGTGGTGG GGCCTGGGGA AAAAAATGAA TGAGGCAGGG GTGACCGAGT 960
GGTTCTCACC AACTCCAGTC CTGCTCTCAT GCCCAGACTG CAGGAAATTT CCCAGCAGCC 1020
TTTGCTCCCC AGAGCCAAGC CCATCTCAGG GCTGGACTCA GCCAAGGATT GGACCTCCCT 1080
GCTGCCGGTC CTTCCCTTCC CTCCCTCCCT TCCTTTCTCC CTCCCTCCCT CTTTCCCTCC 1140
TTCCTTTCTT CCCTTCCTCT CTTCCTCCCT TTCTCCCTTC CCTCCCTTCC CTCCCTCACT 1200
TCATTTCTTC TCTCACTCTG TTTTGTATTT TAGACAGAGT CTTGCTCTGT TGCTCAGGCT 1260
GGAGTGCAAT GGCACAATCT TGGCTTACTG CCACCTCCAT CTTCTGGGTT CCTGGATTCT 1320