Tag | Content |
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EnhancerAtlas ID | HS180-00009 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:959850-960780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:960688-960706 | CCTCCCTTCCTCCCTGCC | - | 6.68 | KLF14 | MA0740.1 | chr1:959982-959996 | GGCCACGCCCCTCA | + | 6.17 | SP3 | MA0746.2 | chr1:959982-959995 | GGCCACGCCCCTC | + | 6.18 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_24817 | chr1:960122-960782 | Colon_Crypt_3 | SE_57930 | chr1:959358-960218 | VACO_9m | SE_57930 | chr1:960298-960726 | VACO_9m | SE_69072 | chr1:955444-963640 | H9 |
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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 |
GH01I001023 | chr1 | 958815 | 961479 |
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Enhancer Sequence | CTCCCAGGGC ACAGGATGGC GTCTGGGCAG CCCCTAGTCT TCAGAAGCTA CCCCTGAGAC 60 CACAGGGTCC CACCTTGTAT GGGAACCCCA TCCTGGAGAC AAAGGCCCCT CCGAGCTCCC 120 CAGGTCGGGG AGGGCCACGC CCCTCACCAC CCCTGCCCGG ACACCGCCTG AGGTGCACCT 180 GCTGCTGGGC CACACCTGGA CTCAGCTCTA CTGAGGACTT CCTTTCCTCA GTTTCTCACC 240 TGGCCCTGCC AGATCTTCCT GGCCCTGCCC AGCCAAGGCC CCTCCCCCAG TCAACAACCC 300 TCAGAAAGGC TCCTCCCCCC TTCTCTGCCT AGGGAGCCAC ATTCCTGGCA TAACTAAGAC 360 AGGTATGTGT CCCTCCCTCT GCGCCACCTT TGGGCGGGGG AGGCCCGCTG CTCCCTCCGG 420 AAGGAGACCC CCGCCCCTGC TTTGTCAGGG AAGTGGCCTG GCCTCCGCAG TGCCAGCTGC 480 CCAGGGCTGG CGGCTGAGCG GGCGACTCCT CCGGCCCTCG CCACCCTGTC CTGTCTGGGC 540 ACTGCCCATG CCCTCCCAGC CCACCTCACA AAGGCTGGTC CTAGAGCCTC CCTGAAGCCC 600 CCAGGAGGGA CTCCTGGCTG AGGGCCGGCC AGGCCGCCCG GGGCCCATCC CTCCCTGCTA 660 GGAGCCAGGA GCAGAGAAAG GGAGTGTTGT CTGCCCCTGC CGGGGCCTGG CACAGGGACA 720 GGGCAGGGGG CCAGGGTCAG AGTGAGTCTG GCGCCTTCCC AGCCCGGCCC TGCCCAGCTC 780 TGAAGCCCGG GGTCCCGGCG GCCTAGTCCC GGGCCCGCCT GTATTCCGGC GTGTGCACCC 840 TCCCTTCCTC CCTGCCTGGC CAGCTGCCTA GGCCTCAGGA CGGCAGTCCT AGGGGAAGCC 900 CAGAGTCCCA CGGCACCGGG GACAGCATCG 930
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