EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-03879 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr1:212090270-212093080 
Target genes
Number: 9             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2808382chr1212091948hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
DUX4MA0468.1chr1:212090805-212090816TGATTGAATTA-6.14
EWSR1-FLI1MA0149.1chr1:212092241-212092259GGAAGGAAGGAAGGAAAG+10.53
EWSR1-FLI1MA0149.1chr1:212092281-212092299AGAAAGAAAGAAGGAAGG+6.56
EWSR1-FLI1MA0149.1chr1:212092233-212092251AGAAAGACGGAAGGAAGG+6.57
EWSR1-FLI1MA0149.1chr1:212092293-212092311GGAAGGAAAGAAAGAAGA+6.78
EWSR1-FLI1MA0149.1chr1:212092289-212092307AGAAGGAAGGAAAGAAAG+6.94
EWSR1-FLI1MA0149.1chr1:212092285-212092303AGAAAGAAGGAAGGAAAG+7.22
EWSR1-FLI1MA0149.1chr1:212092270-212092288GGAAGAAAGGAAGAAAGA+7.2
EWSR1-FLI1MA0149.1chr1:212092237-212092255AGACGGAAGGAAGGAAGG+7.69
EWSR1-FLI1MA0149.1chr1:212092266-212092284GGAAGGAAGAAAGGAAGA+8.26
EWSR1-FLI1MA0149.1chr1:212092245-212092263GGAAGGAAGGAAAGAAAG+8.46
EWSR1-FLI1MA0149.1chr1:212092254-212092272GAAAGAAAGGAAGGAAGG+8.57
EWSR1-FLI1MA0149.1chr1:212092258-212092276GAAAGGAAGGAAGGAAGA+8.73
EWSR1-FLI1MA0149.1chr1:212092262-212092280GGAAGGAAGGAAGAAAGG+9.25
IRF1MA0050.2chr1:212092360-212092381AGAAAGAAAAAGAAAGAAAGA-6.14
IRF1MA0050.2chr1:212092384-212092405AAAAAGAAAAAGAAAGAAAGA-6.87
IRF1MA0050.2chr1:212092422-212092443AAAAAGAAAAAGAAAGAAACA-6.8
ZNF263MA0528.1chr1:212092242-212092263GAAGGAAGGAAGGAAAGAAAG+6.03
ZNF263MA0528.1chr1:212092290-212092311GAAGGAAGGAAAGAAAGAAGA+6.53
ZNF263MA0528.1chr1:212092267-212092288GAAGGAAGAAAGGAAGAAAGA+6.56
ZNF263MA0528.1chr1:212092263-212092284GAAGGAAGGAAGAAAGGAAGA+6.63
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_27820chr1:212088149-212095215Fetal_Intestine
SE_28649chr1:212087848-212099385Fetal_Intestine_Large
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1212092520212092961
Number: 1             
IDChromosomeStartEnd
GH01I211914chr1212088252212094992
Enhancer Sequence
TAGTGATCCA CCCGCCTCGA CCTCCCAAAG CGCTGGCATT ACAGGTGTGA GCCACAACAC 60
CCAGCCTCAT TTTAAGCTTT TTCTTACGCC ACGTTGCAAC CTGAAAGGCT TTGTCCACTG 120
GACAAAGCAT CAACAGACAC TTAGAATACA GAGGGCTCTT TTTTAGCCCT TTGCAATCAC 180
ATGACGTCCA AGGGCTTGTC ACTGAACCAA TGTAACTATC TAGCACAAGA GCAGAAAGGA 240
ATCAAATCCA ACACTCTCAT TGTATAGATG AGGAAACCAA GGAACAGTGA AGTCAAGCAA 300
CTTTCCCAAG GTCATTACCA GAACAAGAAA GGAAGACACC TTCTACAAGG AAAGAGTATA 360
CAGATGGTAC ATTTTAGGAA GGGCACGGCC TGTGGAAGGT GCTAATTTCT AGATGCTACT 420
TTAGAGTATG ACTTTGATTG ATTACTTGCA AAAGTAGACC TATGCTTGTT AGTTATGCCT 480
CTTTCACCTG CTACTCCTCC ACAGTTGGTC AAGACCAAGC CCTAGTCATC CTTATTGATT 540
GAATTAGGAG CAAAATCTAG GTTCTAGTCC TCCTAATTCT ACTACTTACA AGTTGCCTCA 600
CCTTAGGAAC GCCATTTAAC TGCTGTCTCC TTATTTTCCC AGTCTGGCCT TGTCCTCACC 660
GTTGTGGGGT ATCAGGCAAG ATAAAGCACA CAAAGTCTCT CTGCATGCCG GAGAGCATTT 720
TGCAGCATGA GGAGATGTTT TCTGCCCCAC CTATGTACTA GAATCCTCCA AGGAGCCCGT 780
AATGTGAGTG TAGGGGTCAG GGGCAGGCTG GTGACTGGAT GCTTTTGTTT AAGTTCCACC 840
AGTGATTTTG ATGCACATCC AAATGTGGAA ACCACTGACA AAGTACAAAA GACAAACAGG 900
AGAAGAGAAA TAAATTGTGA GCTAAAGATG CAGGCATGTT TTAAGCTCTC TTTAGAGTGG 960
ATAACTAAGG GCCAACTTAG AGAACAATTA AATTGCCCAT CTTTTTCAAG GTACCTGAAA 1020
CCCTAATCTC AAGTCCCTTT TTTCTTCCTG GAAAAGATGT ATATGACTTC AATTACATTA 1080
CTTTTCTTAC CTAGCAATCT AAACACACAC TGAAGATTTC ACACGCACAC ACACACACAC 1140
ACACACACAC ACACACACAC ACTTCGTGAA TCATCTCTGC CTGGTTGCAT GCTGAAGTCA 1200
GATTCCGAGT AATGTCTGTT ATTCTTTAAC CTCTGAGTAA TCACTCTGGC CCTGGTCTGC 1260
TCTTTATCGT CCAGGAAAAC AATCTGATCA AGCCTTGGAT GATGGATTCA TAGTTGCTCA 1320
AGTCTCCAGA GTGCTGTATA AACCAGACTA TTAATTTATT CCATGGGGAT ATTCTGTGAA 1380
AGTCCTACTT CTCCTTTTTA ATAATTGAGT GGCCTCGAGC AAGTCACTCA ATCTCTCTAG 1440
GTCTCTAAGA TGATTATGAT CACTAAGCAT CACTCTTTAC AAAGTATTTC CTTCTTTGTG 1500
ACATCTCTCT TTAAAATGTC AGTTGAATGT TCTCAGAAAC TTGTTGCAGT GGGCATAACA 1560
TTAAAGAAAA TGGGTAAGAA TGAGAACAAT GAATTTAAGG AACATTTCAT TCAGTCCATG 1620
GGACACCAGA GTGGACAGCT GTGACTTGTG TCTGCTCAGC ACTTCTTCTG CTCTTCAGGG 1680
GACAGAACTT CCTTCCATGG GGGAACTGCT CCTTTCTTCT TCCACCTGGT TGTGAGGAGG 1740
CTGCTGATCA AAGGACCCTG GCCTCCTCTT CTTCGGCCAC AGGGGTGGGC ATGTGACCCT 1800
GATTCAACCG TAATAACAAC CTACTCACCT AGCCACAGTG ATTGATCTGG GAATTCATCC 1860
AAGGATCAAT CTGAAAAGAG AGAGAGAGAG AGAAAAGAAG AAAGAAAGAA AGAAAGAAAG 1920
AAAGACAGAA AGAAAGAAAG AAAGAAAGAA AAGAAAGAAA GAAAGAAAGA CGGAAGGAAG 1980
GAAGGAAAGA AAGGAAGGAA GGAAGAAAGG AAGAAAGAAA GAAGGAAGGA AAGAAAGAAG 2040
AACAAGAAAG AAAGGAAGAA GGAAAGAAAG AAGAAAAGAA AGAAAGAGAG AGAAAGAAAA 2100
AGAAAGAAAG AAAGAAAAAG AAAAAGAAAG AAAGAAAGAC AAAGAAAGAA AGAAAAAGAA 2160
AAAGAAAGAA ACAAAGGGAA AGAAAGAAAA AGCAAGCCAG GGATTTTTCT AAATTAAGCT 2220
TGTAGGGAAA AGTATCTTCC CTTTCTGGTC AAGGCGCTTT ATCAATATGA CCCCATGTGC 2280
CACATGAGAA GGCTGGGAGG ACAAGGCCAC CAGCCAGAAG GAAGAAGAAA TGAGGCAGTG 2340
AGAGACAGAG ATGGAAACAA GGAAAGGGTC TGTGGTGTCG AGTTCCCAGG TCTGACTCTT 2400
CCTGGCGTCA TCTGGCAATT GTTCTTTTGA TTCCTCGAGC TACCCCAGAG CTTTCCCCAA 2460
AAGTCACTCT CTCTTTTTTT CTCACTTAGG TCAGTTTGTT TTAGAATTTC TACCACTTGC 2520
AACTTAGTCT TGATGAACAG AAACTCTCCG ACAGTTTTCC TCTCAACTAT ACCTTAAAAG 2580
AAACGTGGTC CCAAATTTGA GGCTCTATGT CCTCTTGTCA CCTGGCCCTT GACGGCAGCC 2640
AGTCTTGCCT TGCTTTCTGC AAGCTGCACC TTGTTCACCC ACGCCAGGCC AAGCAGTGAC 2700
TCTCGTGATT CTTCACCTCC CCTTTTCAGA TCTTTACTTC CCCACTTTCC CCACTGCATT 2760
GTGTAAGATC TCATTCTTAT AATAAATACC TTAGTCCATA ATAATCAGTG 2810