Tag | Content |
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EnhancerAtlas ID | HS040-02417 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:153487480-153489270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr1:153489251-153489262 | TGCCTGAGGCT | - | 6.32 | ZEB1 | MA0103.3 | chr1:153487619-153487630 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr1:153488263-153488284 | GGAGGAGGACTGGAAAGGGGT | + | 6.3 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_02992 | chr1:153487818-153488496 | Bladder | SE_23261 | chr1:153487446-153489480 | Colon_Crypt_1 | SE_23926 | chr1:153487531-153487754 | Colon_Crypt_2 | SE_23926 | chr1:153487791-153489348 | Colon_Crypt_2 | SE_25303 | chr1:153487485-153489518 | Colon_Crypt_3 | SE_28418 | chr1:153487633-153489575 | Fetal_Intestine | SE_36529 | chr1:153487745-153488859 | HMEC | SE_52579 | chr1:153487618-153489518 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 153488459 | 153488748 | chr1 | 153488088 | 153488813 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I153514 | chr1 | 153487077 | 153489449 |
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Enhancer Sequence | TCGCTTGAAC CCGGGAGGCG GAAGTTGCAG GGAGGCGGAA GTTGCAGTGA GCCGAGATTG 60 CACCACTGCA CCCCAGCCTG GTGACAAAGC GAGACTCCAT CTAAAAAAAA AGAACCACCT 120 CCACCTCCTT CCCTCTGCAC CCACCTGCCC TGTGAGGTGT GCCGGCCTCC AGGCAGGGTG 180 GGCACCCATT GGGCACTGGA GGCGTAGCCC TGAGGGCCCA ACAAAATGAT TAATTTTTGT 240 TTCTTTTACA AGCAGAGAAA TTTGAACATA ATCATAATGA ATCTATCATA GTGAATTCAT 300 CTTGGCTTGT ATTTGTCTTT ATACCAATGC AGTCATGAAA TGTTATTTTT AATATTTTTC 360 TATGAAGGAA AGCGCCCACA GAGCCAAAAG TGCTGGGGCC TGTGGAAGTC ATAAGGCCCT 420 AGGTAACCCA TGAGGAACTC AGTCTCAGGC TTTGCATGCT GCAGAGAATG ATCAGAATTG 480 GAGGGCCCAT CCCTCCCTTC TCCTGGGTGT AGGACTGCAC CGCCACCTGA AGCCTTCAGA 540 GCCACGCAGC CTGGCTCAGG AAAGCTGCAT CTGCACTCTT CAGTGCCAGG GAACTAAAGG 600 CTGGGGCTTC CTATGCGAGG TGCAGAGCTC CCAGAGGAGC AGGCACACAG ACCATGACAG 660 GAGGCGGGGT AAGAGGCATT CATTGAAAGG TGCATCTGTG TAGGATTCTT CCTAGCTGAA 720 AACCCTAAAC TGAGCCTGGA GGCAGGAGAG GGGCTTTCTG ATGCTGTGGC TCTTCCTTCC 780 TGTGGAGGAG GACTGGAAAG GGGTCCCTTG GGGCCCTCCC CAGCCTCCCT CATTCTTCTG 840 GACAGAGGGC TGGGCTGCTG TCCCCTGGAC TTGGGGAGGA CACAGGCAGG GAAGCTGGGT 900 GCTCAGAGGA CAGAGAAAGG ATCTCCTTGG ACAGCCCACT GAGCAATGGC AAGTGGCTCG 960 CCAGGTTTCT CCTTCTCTGC TCCCTGCTCT CTTGTCACAC CCTTCCTGGT ATGAAGCAAG 1020 ACAAGCTCCG GTAGTGAGCC CCTCCCTGAC TCCCTCGCCC TAGGCACTGC CTATAATGGG 1080 GTGGGGCAAA ACAGCTCCCT TCTCCCAGCT TCCTCTTCAG GCTCCACTGG GTCTGTCCCT 1140 GCTCACCACC TGGACTAGGT CCCTAGGTGT CAGGACAGCT GGAGCTGTCT CCAGGTGTGT 1200 CATCATCACT GGCATCCTGG CCACCCAGGA GCCATACCTA GGTATCCTAG ACCCCCTCTC 1260 TAGGCTCCAT CCTACCTCCT CCCACCCTGT TACCCTATAG CCAACAAACC CTGCATGTTC 1320 ATCCTTGGGC ACACGTCTGC CCTCTTCCTG CTACCCTACT CCACCCCAGG TCACATCCTC 1380 ATTCTCTCAC CGACCCAGGG CACCAGCCTC CTGGCGGGGG GCTCTGCCTC CACTCCAGGA 1440 CCCCTTCTCC AGGCTCCAGG TCTCCTTGAA GTCCAGGTTT TCATCACATC ACCATTCTGT 1500 TCAACCTTCA CCTACTTCAC GGCTTAGAGA TGAGGCTTTC AAACATCTGT TTATTCCTAG 1560 AACCTTTCTT TAAAATAAAA CCTTATGAGG AAGCCTGATA TATGAAAAAT ACAGGGCTCT 1620 GGCTGAAATG GGGTAAGGGA CCAGGAGTCT CACCCACGTG AGCCACTACC CCCTCAAGAG 1680 GAAGCCCTTA AGTTGCCTCT GAAGATCCAC TAGAGCTCTT GAAGTTCCTA TTAGTATCCT 1740 ATTATTAGTG GGGACAAAAC TAAAGTGATA GTGCCTGAGG CTGTTAGGGA 1790
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