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

TagContent
EnhancerAtlas ID
HS196-05889 
Organism
Homo sapiens 
Tissue/cell
ZR75-1 
Coordinate
chr10:79604230-79606070 
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr10:79605368-79605386GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr10:79605356-79605374GGAGGGAAGAAGGGAAGG+6.56
EWSR1-FLI1MA0149.1chr10:79605348-79605366GGAGGGAAGGAGGGAAGA+6.96
EWSR1-FLI1MA0149.1chr10:79605352-79605370GGAAGGAGGGAAGAAGGG+7.14
EWSR1-FLI1MA0149.1chr10:79605372-79605390GGAAGGAAGGAAGGGGAG+7.43
EWSR1-FLI1MA0149.1chr10:79605364-79605382GAAGGGAAGGAAGGAAGG+8.32
EWSR1-FLI1MA0149.1chr10:79605360-79605378GGAAGAAGGGAAGGAAGG+8.7
IRF1MA0050.2chr10:79605387-79605408GAGGAGAAAGAGAAAGAGAGA-6.24
KLF4MA0039.3chr10:79604411-79604422GGAGGGTGTGG-6.32
ZNF263MA0528.1chr10:79605374-79605395AAGGAAGGAAGGGGAGGAGAA+6.26
ZNF263MA0528.1chr10:79605333-79605354GGAAGAGGGAGAAATGGAGGG+6.27
ZNF263MA0528.1chr10:79605349-79605370GAGGGAAGGAGGGAAGAAGGG+6.42
ZNF263MA0528.1chr10:79605373-79605394GAAGGAAGGAAGGGGAGGAGA+6.51
ZNF263MA0528.1chr10:79605369-79605390GAAGGAAGGAAGGAAGGGGAG+6.58
ZNF263MA0528.1chr10:79605361-79605382GAAGAAGGGAAGGAAGGAAGG+6.66
ZNF263MA0528.1chr10:79605383-79605404AGGGGAGGAGAAAGAGAAAGA+6.68
ZNF263MA0528.1chr10:79605427-79605448GAGGGAGAGAGGGAGGGAGGA+6.89
ZNF263MA0528.1chr10:79605357-79605378GAGGGAAGAAGGGAAGGAAGG+7.01
ZNF263MA0528.1chr10:79605353-79605374GAAGGAGGGAAGAAGGGAAGG+7.34
ZNF263MA0528.1chr10:79605419-79605440AAAGGAGGGAGGGAGAGAGGG+7.3
ZNF263MA0528.1chr10:79605386-79605407GGAGGAGAAAGAGAAAGAGAG+7.53
ZNF263MA0528.1chr10:79605377-79605398GAAGGAAGGGGAGGAGAAAGA+7.57
ZNF263MA0528.1chr10:79605423-79605444GAGGGAGGGAGAGAGGGAGGG+7.96
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_00876chr10:79603894-79605214Adrenal_Gland
SE_26983chr10:79604146-79605411Esophagus
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr107960452579604686
chr107960470779605273
Number: 1             
IDChromosomeStartEnd
GH10I077842chr107960238579610136
Enhancer Sequence
CCAGAATCAG GTTATGTAAA TCGGACCTAA AGACTCTCAA AAGCCCTAGG GTGACCCTCC 60
ATGGTGTAGG GTCCCCCCGC ATCCCATGCA AGTACCTAAT ATGTCTAGCA CTGGTCTAGG 120
GGCTGGTGAT GCCAGACAGG ACAGAAAGAC GCTGTGCCCT GTGGGCCTTT TATCCTAATT 180
TGGAGGGTGT GGACACACAG ATAGGCCAAA TAAAGTAACT TCAGAGCAAG GTAAGAACTA 240
TCAAGAAAAT AAAAAATAAA ACAGAATAAT GGGCTGGAGA GAGCCATCTG AGCAGCAGAG 300
TGGAGGTCTG TGAGGGAGGC TAAGGCTGAA GAGGCTTCTT GAAGAAGGCG ACTTCAGAGG 360
CAAATGAAGA AGAGCAGCGA GAGCACACTG GGCAGAGAGG GGGGCAGGGT CAAAGGCCCA 420
GAGGCAGGGC CTGCAGGCGT GTTCTAGAGA CAGAGAGGGG CAAGGCGGAG TAGCAAGAGC 480
CCAATGCACA GGGGGAGGTG GGTTCAAAGG GGACCTGGAG AAGTGGGTGT GGGCATGGGG 540
GTGGCCATGG CCGCAGGCCT CACAGTGAAG ACTGTCTCCT GAGTGAGACA GGAAGCTGTG 600
GAGGGTTTTA AGCTAGACAG CATTCTACTC TAAATGACAG GCACTAAAGT TCATTTGGGG 660
TGCTGTTATA GAGAAAAAAA CAAACCAAGA AGATGAGTTA AGAGGTTGCC AGGGGGGCTG 720
CTGGCTTTGG CTAAGCACCT CATGGGATCT GAGCCCTGGG GTGAGTCACT CCACCTCTCT 780
GGGTTTCAGC TTCCGGATTC CTCAAATGCC CAGGCTAGAC CAGGAAAGCT TGTCTGGCCC 840
TTCCAGCTCC AACAGCCGAG GAATCACCTG GCTCATTCAG TGGCAGCCTG GTTTATCAAG 900
CGTTTGCAGC CTAGAGAACC AGAAGCTGGG ACGATGGAAC ACTCCCTTTG GAATTAGGGT 960
CAGCTCTCAA TAAACACGAA AAACACAAAA AGCAAAAGAG GGCTTAATTT AAAAGTCAGA 1020
ATCATAGCAA CAAGAAAGTA AGGTCTTCCT CTAAGACCTA AGCATTAGAT TCTAGGACTG 1080
TAGACTCTTA AAGAGGAAGT CAAGGAAGAG GGAGAAATGG AGGGAAGGAG GGAAGAAGGG 1140
AAGGAAGGAA GGAAGGGGAG GAGAAAGAGA AAGAGAGAGA AAGAAAGGGA AAGGAGGGAG 1200
GGAGAGAGGG AGGGAGGATT GGTTCATTTC AGGCTCATTC TTTTTCCTTT ATTTATTTTT 1260
AAAGCAGAAC ATTTTCTTTC AAGGGAAATC TTACTAGTAC ACCAAAAATA CAGAACTTAT 1320
TTTAAAAAGC AGTACACAGG TATCTCAGGC AGTCAAAATC TTCACTGTTT TGTAAAATGG 1380
CATCACTGTT GCAAAACAGG AATGCACACT GAGAAACAGA ACCTCACTGA CAGTGCCCAC 1440
TCTACATCTA AAATCTTTCT TTAAAAAAAA AAAAAAAAAA AAAAAGCCCT GGCCAGGCAC 1500
AGTGGCACAT GCCTGTAATC CCAGCACTTT GGGAAGCCGA GGTAGGCGGA TCACCTGAGG 1560
TCAGGAGTTT GAGACCAGCC TGACCAACAT GGTGAAACCT TGTCTCTACT AAACATACAA 1620
AAATTAGCTG GGCGTGGTGG CGGGCACCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAG 1680
GAGAATTGCT TGAACCCAGG ATGCGGAGGT GGCAGTGAGC CGAGATCACG CCATGGCACT 1740
CCAGCCTGGG TGACAAGCGC GAGACTTCGT CTCAAAAAAA AGACGAAGAA TGGGCTCACC 1800
ATGACTATAC TGGGTCAGTG AAGGACAGTC CTGACATCTG 1840