Tag | Content |
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EnhancerAtlas ID | HS048-01968 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:108224730-108226100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MNX1 | MA0707.1 | chr1:108225489-108225499 | GGTAATTAAA | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_35587 | chr1:108222451-108229404 | HepG2 | SE_64423 | chr1:108224463-108233000 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 108225113 | 108225462 | chr1 | 108225751 | 108226089 | chr1 | 108225057 | 108225600 |
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Enhancer Sequence | CTGTTTTATT GTTGTTCTAC TTTGCCATAT TTCTAATCTG GGAATTTACT AATCTAAATA 60 ATGTAAGGGA TTCTAGAAAA TTTTGGCTAT AAATGGTTGA GTCAAATATG TTCCTATTGA 120 CATACTACAA ATACAAAAAT GCATTTCCCT GAGGGGAGAA GAAAGAAAAA ATACATTAAA 180 AAAATAACAC TTATAAAGGT TAAGTAATTT TTCTGAAACA GCAATACTAT AACTCACACA 240 AAATAAGACA AAAATATTAT GTTCACAGTC ATATACCCCT ACTGAAAATA ATAGAGAAAG 300 TCACTTCTAA ATATTATTGC AGGGAGTCCT CTGCAAAGGA TATTGTCTTG GGAAAGTCAG 360 AACTATTAAA AAGTAAACCA GAACCCCTGT TTTTTTAATG GCTTCAAATT TGTTCTGTAG 420 TTAAAAGATT TAAACTAGTC TCAGGACACA AGTGAGGCAA TTTCTAGCCA GAGGCAACAA 480 AGCTCCTATA AATCTTAAAC AGCTCATAAA CTGGCAATGC TACCATGGGT GTGGTTTCAG 540 TTATAAACTA TAATGCTTTG AAAACTAAAC TTTACAACTA GGTGAATACC ACTTATGATA 600 GGAAAACAAA ATGAAACACA TAGTCCAGAT TATTTTCCAG CAAAGCTACT CTATTTCTCA 660 TGTTCCCCTT GGTTTATCAT CAAGTTCGTG TATTTGGAAT CCTTTAACTG TGAATACCTT 720 TTACTCACAA CAAAAGGATC ACATACATAA AAAATCTTTG GTAATTAAAC TGTGGAAAGA 780 AGGCATTGCA TAATGGATGA AAAATAATTA TACTAACATA ATGACAGGGC AAATCTCACA 840 ATGCTAAATA GAAAACAACT GAACGTTTTC TGCAGACAAA TAATTGGTCT CCGGAGAGGA 900 AACTTGTCAC AAAGTCCCCA AAAAACATGC TGCTATTATA AAATAGCATG GATATAGAAT 960 TAAGAAATTT TCTCTGATGG AGGGTGGGTA CCAGTTGTCT GGTTTATGCT CTCCCCTACT 1020 TACTTAGAAA ACAGTGATTT TTAAGTGGCA GCTAGCTGGC TGGTTTTCTT ACTAGATTTA 1080 CAAAGGAACA CAGGGAGGGT GCTGGATATG TGAGCATTAA CCAGGCACCC TGAGGCTGTT 1140 CAGTAAGCAA ATAACCAGCT CAACTGCTGA CTGTGGAAAG AGTGCAATGC TGGTAGTTGC 1200 TGGTAGTTAC TCATGTGAAT GATTTACACG TTAGACCATG ACCTCCTGGT CACACATTAT 1260 ACACCAAATT ATGAGGAACA AAGGCCAACA ATATGCCTCA CTTTCCACAG CAATTCCCAT 1320 ATCCTTTCAT AAGCACTTAG CTGAAGCCAT AATTATGGAA GGTTTAATCA 1370
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