Tag | Content |
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EnhancerAtlas ID | HS104-48879 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr5:139708520-139709990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr5:139708604-139708625 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_32120 | chr5:139709160-139709715 | Gastric | SE_38075 | chr5:139708725-139710047 | HUVEC | SE_49431 | chr5:139709246-139709696 | Right_Atrium |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I140329 | chr5 | 139709385 | 139709786 |
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Enhancer Sequence | TGCTGGGATT ACAGACATGA CCCACTGTTC TGGCCCCAGA AACCCTTGAG CTCTAAGGAG 60 TTGCTCTCTA AGATCTTTTT TCTTTTTTTC TTTCTTTTTT TTTTTTAAGA GATAGGGTCT 120 TGCTCTGTTG CCTAGGCTGG AGTGCAGCAG TGTGATTATA GCTCACTGCA ACCTCAAACT 180 CCTGGGCTCA AAGGATCCTC CCACCTCAGC CTCCCAAGTA GCTAGAACTG CAGGTACATG 240 CCACCACATC AGGCTAATGT TTACATTTTT TTTTTTCTGG TAGAGATGAG GGTCTCACTA 300 TGTTGCCCAG GCTGGCCTCG AACTCCTGGC CTCAAGTGAT TATTCTGCCT CAGCCTCCCA 360 AAGTGCTAGG AATCCAGGTG TGAGCGACTG TGTCCAGCCA TTAAGTTCCT GTTAGTATTA 420 TTTCTCCATC ATATTATTTC TGGATATGGG AAAAGAGAAA ACAACTGTGG GACAGAGAGC 480 TCATTTAGGA ATGTAGCTTA GTGTTTACAG TGAAGGTTTG AAAATTAGGC TCCTTGAGTT 540 TACATTCTGC CTTTACCACT TTCCTTAGGC ATACATTTAA CATCTCTCAA TTGCTTCTCA 600 ATTTTCCTCA TCTATAACAC GGATACAGTA AGTTGTGTTG AGATGTAAAT GAGATAGTGC 660 CTGTAAAGTG TGCAGCCCAG TGTGCGATAC ATACTGAGCA TTCCATGAAA TGTTAAATGT 720 TTATTAAGCG AATAATGATT ATTATGAACA CTATAAAAGA AAGTTTCTCA AAGGAGGCTG 780 AAAGGGGAGC CCAGAGAGAA GAGGTAGATG CTTTTTAGTG CTCAGGGAGG GCCAGATTTC 840 TTCTGACAGC CCGTCTTGAG AAATGGCTGC AGGTTCAGAG GCTCCTAGGG CCACTGTATA 900 AACCAAGAAG ATGCCCAGAG GAGCTCCAGA GGACCTCTGC TGAAGGGAAT TCCCATGAGA 960 AACAGGGGTA GAGGAGCGAG CAGTTGAAAG GCAGGAAGCC CTGAGCCTGC AGGAAACATT 1020 AGCTGGAGAA ACAAAGTGTG CTTGGAAAAG CCCAGCTCAG GACAAGAGCT TGAGACTGAA 1080 AGCTTGGAAG CAGGAAAGGG AGCCCCAGGA GAGTTCAAAG TAACTCACTA CTCCAGTTAT 1140 TTCTGATGTC TTTATTATTC TCTCTGATTA CCACAGATAA TACATTGGTA CTTCATAGAA 1200 CTTTATGCAA TGCAAATAGC AAAGGAGTTC CCTATTCAAG TTTTTAAATT TTTTTTTTTT 1260 TTTTTTTTTT AGACAGGGCC TCACTCTGTC ACCCAGGCTG GAGTGCAGTG GTACAACACA 1320 GCTCACTGCA GCCTCAACGT CCTAGGCTGA AGTGATCCTC CTGCCTCAGC CTCCCAAGTA 1380 GCTGGGATTA CAAGCACACA CCATCATGCC TGGCTAATTT TTTTTTTTTT TTTTTTTTTT 1440 TTTTGAGATG GAATCTTACT CTGTTGCCCA 1470
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