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

TagContent
EnhancerAtlas ID
HS102-02467 
Organism
Homo sapiens 
Tissue/cell
HuCCT1 
Coordinate
chr1:221996460-222001000 
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:221999882-221999900GAAAGAAAGAAAGGAAGA+6.22
EWSR1-FLI1MA0149.1chr1:221999886-221999904GAAAGAAAGGAAGAAAGA+6.22
EWSR1-FLI1MA0149.1chr1:221999901-221999919AGAAAGAAAGAAGGAAGG+6.56
EWSR1-FLI1MA0149.1chr1:222000059-222000077GGGAGGGAGGGAGGAAGG+7.28
EWSR1-FLI1MA0149.1chr1:222000063-222000081GGGAGGGAGGAAGGAAGA+7.39
EWSR1-FLI1MA0149.1chr1:221999905-221999923AGAAAGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr1:222000067-222000085GGGAGGAAGGAAGAAAGA+7
EWSR1-FLI1MA0149.1chr1:221999913-221999931GGAAGGAAGGAAGGAAAA+9.07
EWSR1-FLI1MA0149.1chr1:221999909-221999927AGAAGGAAGGAAGGAAGG+9.09
FOSL2MA0478.1chr1:222000249-222000260GGGTGACTCAG+6.02
IRF1MA0050.2chr1:221999850-221999871AGAAAGAAAGAGAAAGAAAGA-6.76
IRF1MA0050.2chr1:221999955-221999976AGAAAGAAAGAGAAAGAAAGA-6.76
JUNBMA0490.1chr1:222000249-222000260GGGTGACTCAG+6.02
Nr2f6(var.2)MA0728.1chr1:221999616-221999631GAGGTCAAGAGTTCG+6.24
ZNF263MA0528.1chr1:222000065-222000086GAGGGAGGAAGGAAGAAAGAG+6.07
ZNF263MA0528.1chr1:221999914-221999935GAAGGAAGGAAGGAAAAAGGA+6.17
ZNF263MA0528.1chr1:222000068-222000089GGAGGAAGGAAGAAAGAGAGA+6.24
ZNF263MA0528.1chr1:222000061-222000082GAGGGAGGGAGGAAGGAAGAA+6.41
ZNF263MA0528.1chr1:221999910-221999931GAAGGAAGGAAGGAAGGAAAA+6.56
ZNF263MA0528.1chr1:222000072-222000093GAAGGAAGAAAGAGAGAAAGA+6.58
ZNF263MA0528.1chr1:222000057-222000078GAGGGAGGGAGGGAGGAAGGA+7.29
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_35982chr1:221999806-222001200HMEC
SE_52249chr1:222000163-222000869Skeletal_Muscle_Myoblast
SE_55946chr1:221996685-221998843u87
SE_55946chr1:221999901-222005096u87
SE_64045chr1:221999986-222000869HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1221997414221997699
chr1222000173222000483
Number: 2             
IDChromosomeStartEnd
GH01I221824chr1221997414221997750
GH01I221826chr1221999933222001478
Enhancer Sequence
TTGTTTATTG ATTAAATATT TAACAGAATT GGATCATCAT TTGGTCTCTG GCCCAGCATA 60
TCAGTGGTAG GAGTTAATCA AAAGGATCAT TTGCCCCAGA AGAGTGGCTT TCAAATTTAG 120
CATGCATTGG AATCCCCCTG GAGGGCTTGT TAACACAGAT TATTGAACTC TACCCCGAGA 180
GTTTCTGATT CAGTAGGTCT TGGGTTGGCT TGAGAATTTG CATTTCTAGC AAACTTTCAG 240
GTGATGCTGA TGCTGCTGGT CCAGGGACCA CGCTTTGAGT GAGAACCACG GGACGAGAGA 300
AACCACTGAA GAGCAGAGAT TCATTTTGAA GACTACACCA TAGGAAGGAG GCAGAAAGTA 360
GAAAGAAGCA CTCCACTGCA TAAAGCTGAA ACTGGCATCC AGGAATGAGA GATACCAGGC 420
AAGCTTTGGA TGATTACAGG AAATAACTTC TCAAAGGTAA AAAATGAAGT CAGATCTCCT 480
TACACCTATA GTAGCTTTTT TAAAGTTCCC ATTTCATCAA GAATCAAGAC AAGGATCATA 540
AAGGAAATTG TCTTTGAGGC TGCATGCCCT ACCTGATTGC TCTTGAACTG GAACTCAGCC 600
AGCCTAGTTG CTTATTTCCA AGGTTAGCCA TAAACTGTGC AGATGTGTGA GAAATTGCCC 660
ACTACTGAAG ATGACTCTTG TGAATAGTCT CTGGTGTGTG GCTGCAAGGG AAGGGTTTTC 720
TTTTCCCAAG ATGTTTGTCT TTTCCCAAGT TCTCCACCAC TTATCCACAG ATGCTACTTG 780
TGACACATAC AGTTAGCCTC TGAACTGAGA TACAGAGCAT CGATGTCACC TTCTCCTCAA 840
AAACTTTGGC ACATCTTAGT TATCTCTGTG GTCTCAGGAT GGAGCATTAG GTGCCACCTG 900
AATGCTGGAG AAAGCTTCCT CACTGAAAAG GATTTGAGAG CAGAGAAAAG CGCTCATTTG 960
TCAGGCTTCT GTGGAACTTG ATTTTCTGTG CCTGATTGTC ACTACGTCAC TCTGCTCTGA 1020
GTCAGTCATC AGGAGTCCCC TGACTGCCCA GTGCCCAGTG ATGGGCAGCT TTGACTTGCA 1080
CTGAGTAGAG GATGGAAGGG AGGTGACCCA CAGAGGTTGA CTGTTTACCC AGTCTCCATC 1140
ATGGGGATTT TCTTGGCCAC ACTCTGCTAA AACTGACTCA TGAAGAAGAC AGCAAGCCAA 1200
CAGTTCATGG GAGGTAGAAC TGTTTCTATT GTTCACATGT CATTTGGCTC AGCTGAATCA 1260
TCTCCTCCAC AACTCAGAAA GGAAGGTGCT TCCATCAACA CCTTCTTCAT TTGGGGGAAG 1320
GGATGGAGTG GGAATTTTCA GGACCTACCT CATTCCTATA CCTTTCCCAC TCCAAAGAGA 1380
GAAGAATGAC TTTGGTTATC AGACACACTG GCTATTCCTC TACTGGGCAG GGTAAAAACT 1440
CAAGGTCACT CACTTCTCCT ACATGCTCCC CCATTTCCTG ATTCTTCTTG AACTAGCCTT 1500
TATTTCAGAG CAATGGGTCA GTCTCTGTGG GTCAACCCCT TGGTGGGACC ACCTCAGAGC 1560
AGGGAGGACT GATCTCCAGC TTCTCAGCCT GGGACTGGGT GGATAAGTCC ACCTTGTAGG 1620
GAAGACTTGG CTCTCTATAA TTCTGAGTGG GAGGTCAGAA ACCCAGCTAT ATTCTCTAGT 1680
CTTCTAATTG TTACAGAAAG TCAAACAGAA CTAATGTTGC AATCCTCATT TAACAATATG 1740
TGTATCTTTT ATCAACCAGA ATCCTCAAGG AGAAGCAAGG TGGGCATTAG GATCTGGGAC 1800
CAGCCCTCCT CCCCAGCAAC TCCCTCACTC TCAATTCCCA AGAAGTTCTG AGGCTGACAC 1860
TTTCCCATAC ATTCTTCTCT TGTGCCAGGA TTTATCAGGA GGTGTGGAGG TTTGTTGGGA 1920
GCAGGACAGT GTAGGCAGGA AAGGGACTGA GACTTGGCAC TAGACATGCC CTTCAGAGTG 1980
GGACAGGCCA AGCTAACAGG AGAGGTTGGA GAAGGCACAG GTGCAAGGAG TTCAGCCTTC 2040
CACATAGCGA TTCAGCTAAG TAGCTGGCAC CAGGTGCTCC AAGTGGAATT GCAAATTATG 2100
CCAAAACATG AGCAGGGCCC ACTGAAAATT GGGGGCAGGT AATTTTTGGA ATTCAGGGCA 2160
GGGTGCCAGC CTCTGGCAGA TTTGTTCCCC AGAAATCCAG ACCCCAACAC TAAACTAAGA 2220
TACAGAGCTA AAGACTCCCC TGATCTTAAC CTCAGATAAG GAGAGAGGTA CTGATATGGA 2280
CAAGAGACAG GGAAATACTG GGTAGAAGAA GGCAGTTCCC TGGCAAAGGC CCCACCCTCA 2340
AGCCTGGAAA CCCATGGCCC TAAATAGAAA CAGGCATTTC TCTTTTTGCA CCCAAATGTT 2400
GCCTTCTGGC CCACCATGCC CCACTATCTC ATACCCATAT AAACCCCAAA TCCCATGCTC 2460
CACAAGTAGA TGAGCAGAGG CAGAAAAGTG GGCCTGGCAG AGAAGGAGAG AAAAGAAGGA 2520
ATATCTGAAC ATCAAGAGGA GTTCATCTGG GGATGGTTGG AGAGGAGACT GGCTGCAGGA 2580
CAGCCAAACT CCAGGTGAAG ATCATTCTTC CTACTTCATC CCCTCTTCAG CTCCCCATCC 2640
CTCCAGCTGA GAGCCATCTC CATCTGACAA CAAAGTCCCC TGCATTTGCC AACCTTCAAT 2700
TCGTCCATGT GACCTAATTC GTCCTGGATA CTGAACAAGG ACTCAGGTAC CAAGAGGGCA 2760
CTGAGCTGGT TAACACTTAA GCCATCTGCA GACAGCAGAG CTAAAAGAGC ACTGTAACAC 2820
ACCCACCTGG GCTTTGGGAG TTGCAGGCAC CCACCCCTAG ATGCTACCAT GGAGCCTGAG 2880
CCCAAAAGTG CTTGTCCTGG CTCTTGCACC TGCCCGTCTG CATGCTCCCA CTCCTATAAG 2940
GGAGGTAAGG CAGCTGAACA GACAAGCCAC ACCCCTGTTG CATGTTCTGT GAGGGGGGTC 3000
AGGGAACTCT CCCATTTCAG GAAAATCAAG AGCAAGACAA GATGGTTGAA CCAAGGATGA 3060
GATGAGAACC AAGGTCGAAA AGTGCAACTC ATGGCTGGGC GCGGTGGCTC ATGCCTGTAA 3120
TCCCAGCACT TTGGGAGGCC GAGGTGGGTG GATCACGAGG TCAAGAGTTC GAGACCAGAC 3180
TGACCAACAT GGTGAAACCC TGTCTCTACT AAAAATACAA AAATTAGCTG AGCATGGTGG 3240
TGCACGTCTG TAATCCCAGC TACTCAGGAG GCTGAGGCAG GAGAATCGCT TCAACCTGGG 3300
AGGCAGAGGT TGCAGTGAGC CGAGATGGCG CCATTGCACT CAAGCCTGGG TGACAGAGTG 3360
AAACTCCATT TTGAAGGAAA GAAAGAAAGA AGAAAGAAAG AGAAAGAAAG AAAAGAAAGA 3420
AAGAAAGAAA GAAAGGAAGA AAGAAAGAAA GAAGGAAGGA AGGAAGGAAA AAGGAAAAGA 3480
AAGAAAGAGA GAGAGAGAAA GAAAGAGAAA GAAAGAAAGA AGGAAAGAAA GAAAGAAAGA 3540
AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAAGAGAG 3600
GGAGGGAGGG AGGAAGGAAG AAAGAGAGAA AGAAAGAAGG AAAAGTGCAA CACTCTTCAG 3660
TGTTTCCCAG GAAGAAGTTT GGGTATAGGA GTTTTGTAAT TACAGTGGGA ATGTTATTCG 3720
ACTAGAGAGT TGCAACCCAG GGGTGGGGGC GGAAGCCCAC TGAGGACCCC TAGGCCAAAT 3780
CAAGAGTGAG GGTGACTCAG GTGACACACA GGGAGCCCAG TGGTCAGCTG GTTCAACCTA 3840
ATCTGGAGAA TGACTCAACA CCAGGATGCC ACTGCTGTTG GGGGAGGAGG AGGAAGTGCT 3900
AAACCCGCTT CAATATTTCC TGTCTTAAGC CCACATTGTT CTGGGGATTG AGATCTGAAG 3960
TTGAGGGGTT GGGGGTCAGT GAATCTGGCT ATAGACATTG TAGATCTGCA GATGGAGGGC 4020
ATGAAACAGG CTGAAACTGC TGCAATATGT ACTCACCCTG AGGGCCTGAG GACCTAGATG 4080
ATCATCTTAA TTTAGATTGC TCCTTGGCCC ACACAGACAT GATAGTGCCT GCAGACAGTG 4140
GCTCTGGCAC TGGCACCCAT GGTAGCAGTT GGCCTCATTG TGATGGGAAA GCCTCCAGCT 4200
CCCTCCAAGA TGCAGTTAGG GTTTCTGGTC TCATTCTTGG AAGAGTTTTG TTGGATGAAT 4260
TAAACTGGAA TCATCTTCCT TTCCCAGGAA ACTGTTGTCT CTTTTGTCTG CTCTGCCTCT 4320
GGGTGAAATC TGTAGTCCTT ACTTGCTGCT ATTTTCTACC ATCCTAATAA TAGCTCATTG 4380
TTAGGCAGAC ATGACGCAAA TACATTTCTC ACTATCTTGG GAGATTTGGG GGGGGGGTCT 4440
TACCTTCTTA TTTAAGTTCT TTGTTTAATT ATTTAATTCT TTTCTTTTCT TTTTTTTTTT 4500
TTTTTAGTTT GTTCTCTTTG TTTGCCCTTA GTTGGTAAAG 4540