EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-14000 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr22:43075800-43077520 
Target genes
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr22:43077422-43077440CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr22:43077062-43077080CATTTCTTCCTTTCCTCC-6.08
EWSR1-FLI1MA0149.1chr22:43077434-43077452CCTTCCTCCCTCCCTCCC-7.28
EWSR1-FLI1MA0149.1chr22:43077430-43077448CCTTCCTTCCTCCCTCCC-8.32
EWSR1-FLI1MA0149.1chr22:43077418-43077436TTTTCCTTCCTTCCTTCC-9.07
EWSR1-FLI1MA0149.1chr22:43077426-43077444CCTTCCTTCCTTCCTCCC-9.47
IRF1MA0050.2chr22:43077390-43077411TCTTTCTTTCTCTTTCTTTCT+6.76
IRF1MA0050.2chr22:43077374-43077395TCTTTCTTTCTTTTTCTCTTT+6.96
NR2C2MA0504.1chr22:43076473-43076488TGGGGTCAAAGGTGA+6.3
Nr2f6MA0677.1chr22:43076474-43076488GGGGTCAAAGGTGA+6.4
RxraMA0512.2chr22:43076474-43076488GGGGTCAAAGGTGA+6.77
TEAD1MA0090.2chr22:43076765-43076775CACATTCCAT+6.02
ZNF263MA0528.1chr22:43077077-43077098TCCTCCTCACTCTTCTCCCCT-6.12
ZNF263MA0528.1chr22:43077121-43077142CTCCTCTCTTCCTCCTTCCCC-6.33
ZNF263MA0528.1chr22:43077418-43077439TTTTCCTTCCTTCCTTCCTTC-6.56
ZNF263MA0528.1chr22:43077062-43077083CATTTCTTCCTTTCCTCCTCC-6.57
ZNF263MA0528.1chr22:43077074-43077095TCCTCCTCCTCACTCTTCTCC-6.79
ZNF263MA0528.1chr22:43077429-43077450TCCTTCCTTCCTCCCTCCCTC-6.86
ZNF263MA0528.1chr22:43077065-43077086TTCTTCCTTTCCTCCTCCTCA-6.88
ZNF263MA0528.1chr22:43077425-43077446TCCTTCCTTCCTTCCTCCCTC-7.08
ZNF263MA0528.1chr22:43077118-43077139CTTCTCCTCTCTTCCTCCTTC-7.18
ZNF263MA0528.1chr22:43077433-43077454TCCTTCCTCCCTCCCTCCCTC-7.29
ZNF263MA0528.1chr22:43077422-43077443CCTTCCTTCCTTCCTTCCTCC-7.42
ZNF263MA0528.1chr22:43077437-43077458TCCTCCCTCCCTCCCTCCTTT-7.97
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_27285chr22:43076358-43077107Esophagus
SE_42360chr22:43076132-43077172Lung
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr224307667743076928
chr224307665243077001
chr224307707243077204
Number: 1             
IDChromosomeStartEnd
GH22I042679chr224307592043077428
Enhancer Sequence
CGTGGATGGC TGTACCACCC TGAATACGCA CAATCTCATC TGATAAATTA CCCAGTCTAG 60
GGTATTTCTT CATAGCAGTG TGAAAATGGA GTAATACACT GACCTTACCT CACACTTCCC 120
ATCTCATTAT TATTATTTTA ATTTAGTCAT GGTAAAACAA GCCTGGTGCA GTGGTTCGCT 180
TCTGTAATTT CTACACTTTG AGAGGCTGAT GCCAGAGGAT TGGTTGAGGC CAGGAGTTAG 240
AGACCAGCCT CAGCAACATA GCAAGACCCT CTCTCTATTA AAAAATAATA AGACCGGGTG 300
CAGCGGCTCA TGCCTGAATT TCAGCACTCT GGGAGGCATT TTGAGCCACT GCACTCCAGC 360
CTGGGTAACA GAGCGAGACC CTGGCTCAAA ACACAAAAAA ATTGTGGTAA AATATACACA 420
AGATAAAAAT CGATCCTTCT GGCCATGTGT AAGTGTACAG TTCAGGAGTG TTCAGTGCAT 480
TCACATTGTT GTGGGGAGTC ATGCTCTTTA TTTTGAATAT TACCCTGCAG GGTTGTGGAG 540
GTGTGCATTT CTTGTTTCTC ACTGAGCCTT CACTGTGATC AATCCCTGTT GTTTCCTCCC 600
AGACTCAAAT AGAATGAACG CCCCCTGATA TTTTAGCCTG GAGGGGATCA CATTTGGGGA 660
CTTTAGACCA AGCTGGGGTC AAAGGTGATG TTCCACCACC CTTTGCCTTC AGCCCCCAGC 720
CTGGCTCAGC AGCACAGGAG AGGACTGCTG GGTGGGCTTC CTCCATGACC TAGTGGAGGA 780
TCTTCCAGGG CAGAGTAGGC CCTTATTGTC TCTGAGATAC CCCTCCACCC AGAAACAGCT 840
GGTCCAGCAG CATGGTGGTG GCATGACCTC CTGAAGGCTC AGGTACAACC CCAGTTGGGA 900
GGAAACACGC TGAAAAGATG AGGCTCTGTC TTGTAGGATA CAGTGTGTGG TGACTCAGAG 960
ACCCGCACAT TCCATGACAG AACACACAGC CAGGAATCAT GACTGCACTG AGTCATCACC 1020
CACAGAATTG TCATTTCCGG TTCCTGAAAC TTGGAGCTCT GCTGGGGTAA AGGTCTTGGT 1080
CCCCAAGAGA GGAGTGTTTC TACCAGCAGA CAACAATGGT TCCACTTAGT CAGAAGCTGA 1140
GATTGCCACC TGGCCATGTT AGGCTCCTTA TCCACTGAAC CAAAAACGCA TGCACACACA 1200
CGCAAAAGAA AATAATGCAC GCACACTCAC AAACGTATAC GTATTTTACT CATACATACA 1260
TACATTTCTT CCTTTCCTCC TCCTCACTCT TCTCCCCTCC TGTCTAACTT CCTATTGTCT 1320
TCTCCTCTCT TCCTCCTTCC CCGGATTTAT TTCAGCATTG ATGTTGGTGA TTAAGTTTAA 1380
AATGTATTAT ATAAATATTT TATATATATT TAACTACTTA ATTTTTTTTT TGAGACATGG 1440
TTTTGCCATG TTGCCCGGGC TGGTCTCGAA CTCCTGAGCT CAAGGGATCC GCCTGCCTTG 1500
GCCTCCCAAA GTGCTAGGAT TATAGGCATG AGCCACCATG CCTGGCCTAT ACATCTATAC 1560
ATTTTCTTTG CTTTTCTTTC TTTCTTTTTC TCTTTCTTTC TCTTTCTTTC TTTCTTTCTT 1620
TTCCTTCCTT CCTTCCTTCC TCCCTCCCTC CCTCCTTTTT TTTTTTTTTT TTTTCTGGAG 1680
TCTCGCTCTG TCACCCAGGC TGGAGTGCAA TGACGTGATC 1720