EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS055-04881 
Organism
Homo sapiens 
Tissue/cell
FT33 
Coordinate
chr20:288910-291980 
Target genes
Number: 9             
NameEnsembl ID
TF binding sites/motifs
Number: 20             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr20:290776-290794CCTTCTCCCCTTCCTTCC-6.65
EWSR1-FLI1MA0149.1chr20:290788-290806CCTTCCTTCCCTCCCTCT-6.94
EWSR1-FLI1MA0149.1chr20:290780-290798CTCCCCTTCCTTCCTTCC-7.43
EWSR1-FLI1MA0149.1chr20:290784-290802CCTTCCTTCCTTCCCTCC-9.47
KLF16MA0741.1chr20:291228-291239GCCCCGCCCCC+6.02
KLF5MA0599.1chr20:291228-291238GCCCCGCCCC+6.02
RFX1MA0509.2chr20:291135-291151CGTTGCCATAGAAACC+6.63
RFX1MA0509.2chr20:291135-291151CGTTGCCATAGAAACC-6.66
RFX2MA0600.2chr20:291135-291151CGTTGCCATAGAAACC+7.13
RFX2MA0600.2chr20:291135-291151CGTTGCCATAGAAACC-7.14
RFX5MA0510.2chr20:291135-291151CGTTGCCATAGAAACC-7.08
RFX5MA0510.2chr20:291135-291151CGTTGCCATAGAAACC+7.21
SP1MA0079.4chr20:291225-291240GAGGCCCCGCCCCCC+6.52
SP3MA0746.2chr20:291227-291240GGCCCCGCCCCCC+6.11
SP4MA0685.1chr20:291225-291242GAGGCCCCGCCCCCCAG+6.04
ZNF263MA0528.1chr20:290776-290797CCTTCTCCCCTTCCTTCCTTC-6.6
ZNF263MA0528.1chr20:290766-290787CCCTCCCTCCCCTTCTCCCCT-6.81
ZNF263MA0528.1chr20:290784-290805CCTTCCTTCCTTCCCTCCCTC-7.27
ZNF263MA0528.1chr20:290772-290793CTCCCCTTCTCCCCTTCCTTC-7.35
ZNF263MA0528.1chr20:290793-290814CTTCCCTCCCTCTCTTCCTCC-7.59
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_04571chr20:289111-292182Brain_Anterior_Caudate
SE_05672chr20:288550-292373Brain_Cingulate_Gyrus
SE_06604chr20:288859-292008Brain_Hippocampus_Middle
SE_07456chr20:288751-292193Brain_Hippocampus_Middle_150
SE_08506chr20:288447-292351Brain_Inferior_Temporal_Lobe
SE_29860chr20:289076-292911Fetal_Muscle
SE_54219chr20:289529-291501Spleen
SE_64903chr20:288518-291179NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr20290672290826
Number: 1             
IDChromosomeStartEnd
GH20I000307chr20288611292808
Enhancer Sequence
CCTAACATCC TGTATCAGAC CCTCTTACAC CGTCCGTTAC CTCCCTGGCC TCTCCTTCAG 60
CAGTTACTCG GGTGCAATGA TATACTTATT TGTGCCATGG TTTGATTGAT ATCTGCCTCT 120
GCCTCTCCAC TTTGAGCTCC CTGAGGGCAG GAACCAGTCT CTTTTGGCTC ACGGTTATAG 180
CTTGAGCAAT TAGCACTATG CCTGGCACAG AGTAAAGCCT AATAAATATT TATTGCATGC 240
ATGATCTAGA ATCACTTGGC TGAGGTTACA GATTAAGACA CGTGTCTACT TGTCCTTCTT 300
TAATATACTT AACATACCTT AGCACTCTGT CATTGACACA TACTGAACAA GGGCTTATTC 360
ATTCATCTTT TAAAAGCTAA CTCACTCTTT TAGTTTTCCC ACCTTTGATA AGGGAGGATA 420
GGACCTGGGA GGTCAGGCCC TCGGTTTACT AGCTCATCCT CCTCTATTTC TCTGAGAGCA 480
TAAAATCACT GGAAGTCAGC CAGCATGCCC CATGGCACTG TGAGGCACAG GGGAGAAGCA 540
CCAGGCTCCT GGATTCTGAA TGCGTGGCTT TGAAGCCTGG CAAGAGTGGC CCCTTCCCTG 600
AGTCCCCCAC CACCCCTCCC CTTGGGGCGA GGATTCTGCA GGCATGAGAA GTGCCCACCC 660
AGAGTCTGTG CCTATGCCTT CTAGAACACG CTCTGATACC CGATAATTCC CTTCCAAAAT 720
GTCACTAAGT TAATTCACAG GGCTCTTTGT GGGCCTCATC CCTGGCTTCA TCTCACCTGA 780
GGGCAAACTA TACTGCCTGA TGCACATCTT ATAGACCTGA GCCTTGGGCC TCAAGATAGC 840
TGTTTGCAGG TGACAGCTAG GTGTTGACCC ATGCATGCTA GCTCCATCAC TGATGGGATG 900
AGAGGTAGCT GGATAAGGGA TGGATACAGG TTCCAGGGGA CAGGTCTCCT TGGGCCTACA 960
CATTCTGGCA CATAACTCCA AGGGTCTTAG AATTCTAATT TGAACATGGC CTTCCAGGTT 1020
GTTAGAGGAT ATATCCATCA AGGAAGAAAA CAGAACATAT TTCATTTAAC ACTTGCTGGA 1080
CTGTTGTATA ATTTCTAACT ATAGAGACAT ATGGTATATG GGCCTCCAAC TCTACTCTTG 1140
TTCTGAGCCC CACAAATGCC CATTTGGTTC TGTCATTTCT TTGCATAGAC AAGCTACATA 1200
ACCTCTCTGA ACTTCAGTTT CCTGAGCAGG AAAATGGGTC TATGGTAATA ACTACATTAT 1260
CAGGGCTGGT GAGAAAATGA AATAAAATAA TCCATGTCAA GGGCTTGAGA AGAATGCCCT 1320
CTGGCTGTCG TCTCCTATGA CTTCCTGTAT GATCTCCAAA CTGCTCTCTT TGCAGGGTTT 1380
CAACACGGCT GCTCCCTCCT GCCTCCTTAC CCACAGCCAA TAACCTCCCC ATTCTCTCCA 1440
CCTAGTCAAA TCCCACCGTC TTCAATTGTG ATAATAGCTG GTTGATTGCA CGTTTACTAC 1500
GTTTCAGGCA TTGTATTAAG AACTTTCCAT GCATTAACTC AGTTCTGACA CCAACTCGAT 1560
GAAGCAGGCA CTGTTTATTA TTCCCCAAAC ACAAAGACAC AGGGATCTGG AGACTGGAAG 1620
CACTGGCGGC TGCAAGTGGC AGGGCTGGCG GGGTGTGAAG CCGGAGAGGA GTCTTTCTGC 1680
AGTCAGGCCT CCCAAATCCC GGGATGGAAT CAAGGAGCCT TTGGCTGTCC CACCCCTCCT 1740
CCTCCAAGCC CCCAAATCCA AGTCTGTTAT ATCCCGTCAG CTCTGCGGGC CTGCCTGTGA 1800
CTTTCAGCCC AAGGGGGCGG GCACTTCGTG TCACGCCACG TTGTCCACAT CATCGACCCT 1860
CCCTCCCCTT CTCCCCTTCC TTCCTTCCCT CCCTCTCTTC CTCCCATTGA GTGCCAGTTC 1920
TGTGCCAAGC TTTGCTGTTC AAAATGTTAC GAGTGGAGAA GTCAGGGAAG GATGGAATTA 1980
TAGGTGTTTC TTCTTCATAC CTTTCTGTTT GGCTGATTTT TTTTCAAATG AGCACGCAGG 2040
CCCGGTTCCT CAAACCCACT TCCAATGTGG CATTGCTGGG TTGGTTTGGT CCAAGGAAAG 2100
CCCTGTCTCC TTAACTCCCA GCCCCCACGC CTCCTCCGCC GGCCCCCAAA TCCAGGCCGC 2160
CCTGCCCCCT CCGGAAAGGG GAGTTGGGGG CGAGCGCCGA AATCTGAGTG GCTCTTTCAA 2220
GCCTCCGTTG CCATAGAAAC CGGCCGCACA GGCCGATGCT GTCCATTACA CCATCCTCTA 2280
GCCTCGCAGC CAATGGACTC CGAGCTCCAT CGCCAGAGGC CCCGCCCCCC AGCTCTGGGG 2340
AGTCCACCAA TCAGCAGGTC CCGTGACTTA GAGCCCTGCC CTCGGCCCAG GGACACCACC 2400
AATGCGCTTC GACCCTGCCC TCCTTCTCTT CGGTGTAACA AGAAGACTCG ATATTTTTTT 2460
TTTTTTTTTT AGGAATTCTC CAGATCAGAA GGAATTGGCA GTAAGGCCTC TGTCAGCTGC 2520
ACCCTGAATA ATCTTTGGCT GCTATTTTAT TTAAGGAGAG CAAAACTGTT TCAATTACGC 2580
AACAATATAT ACCATTCTCT ACTAAAACAA TTTTAGGAAA TGAAAATGTA GGCAATGGGA 2640
TGATATAGTC TGCTCTATAT GAATGTCTTT CATTATAGGT ATTTTAATTT AACTTAAAAT 2700
GATCAAGGAA CTAGTCATCT TTCCTTTGTA TTTCAAATGC ATACAAAATT AAAGATACCG 2760
AGTTTTTTGA TGCAGAGTTC ATGAGACATT GACTTAATTA GTTGGTAGGC AACTTTTACT 2820
GAACCATCTA ATTCCTGGTT CAGAACATTA CAACTGGAGG ATAAATGAAT ATTTCTCTTA 2880
ATCCATGGAA GAAATTCTGT TTTTGAGGCG GGCTGCGTAA ATGGCTCTGA CACTCTGGAG 2940
TCTAAATAAA CCAAATGTGT TTTTAAAACC CGTTTGCCAT TACAAAAAAA AAACTTCAAT 3000
TTTTTAGAAC ACTTTTAGAT TTACAGAAAA ATTGTGAATA TAAAGTTCCC GTCTACCCCA 3060
GCCACCCACC 3070