Tag | Content |
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EnhancerAtlas ID | HS180-14172 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr14:20895270-20896490 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr14:20896137-20896147 | ACCACTTGAG | + | 6.02 | SPIC | MA0687.1 | chr14:20895990-20896004 | AGAAAGAGGAAGCA | + | 6.04 | ZNF263 | MA0528.1 | chr14:20895933-20895954 | GGAGAAAGAAGAGAAAGAAAA | + | 6.03 | ZNF263 | MA0528.1 | chr14:20895930-20895951 | GAGGGAGAAAGAAGAGAAAGA | + | 6.42 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28028 | chr14:20895260-20896705 | Fetal_Intestine | SE_29051 | chr14:20895241-20896718 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 20895383 | 20896384 | chr14 | 20895931 | 20896136 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I020426 | chr14 | 20894921 | 20897612 |
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Enhancer Sequence | AGCATGGCAC ATGTATACAT ATGTAACTAA CCTGCACATT GGGCACATGT ACCCTAAAAC 60 TTAAAGTATA ATAATAATAA AATAAAATAA ATTAAAAAAA AAAAAAGAAA AAGAAAATTG 120 ACCTAAACAC ACACAAAAAA ACTGACCCTT TTTTGCTCTC AGCTGTCCAG TAGGCAGAAA 180 TGGAAAGAGC AGACAGGAAG GATAGAGGTG AGTCATAGAG GGCGGGAATA CACAATCATT 240 AAGTGAAAGC CATTATCCTC AGGAAGGCTC CAGAGAAGAG AGTAGGTGGC AAGAGCAGCA 300 GAATTATCTG AAAAGCCTCT GGAATACCCA CTTCCTCTTT GCTATGGAGA AACAGGGCAT 360 GGCATGCCCC ACTTCTTTCT GTTTCAAATG CATTCCCCCT TCTCTAATGG GTGAGACTCT 420 AGGCAGCCTT TAAGATCCAG TTCAAAATAC ACCCATCGGA TGACACCTTT CCTAACAGAA 480 GCCTTCCTGA GCAGAGTTCA CTGCTCTATC CTCTGGGCTC TCGCAAGACT CGTCCATACA 540 TGTAAGTCCA CTCAAAATTT GTATTTGTTT ATGTCTATCT GCTGGTCAGG AGCTCTCTGA 600 CCTCTGTATC TTGGTGCCTC CTACAGTGCC TGCCACACAG TAGGTAATTA ATAACTGTGT 660 GAGGGAGAAA GAAGAGAAAG AAAAAAGAGA GGCAGTGGGG AGAGCAGGAT GGGGGAAGAG 720 AGAAAGAGGA AGCACCTGAC TACCTTCCCT GGCCAAGATA AAGGGAAATG GATTTAAAAA 780 TAACTCTGGG GGAAAGGAAC TGAAAGGGGG AAATGACTTT TCTGAGTCTT GTCTGCTTCT 840 CACTCTTCTC TCCCCCCACA TCCTCTCACC ACTTGAGACC TCAGGCAACA ACGGTCTCAT 900 TTTCACTCCT GATTCCTCAG TTTGCCCAAA AGAAAGAAGG CACACAGGCT TCTGACTTCT 960 TCCACCCCAT CTCCTTAAAC CTCAGATCAT CTGTTTTTCC ACTGTGGGCC TCTCCCTCCT 1020 TGGCCTCTGC CCCCATCATC TTTCCCACAC AACACTCCTG CCACATGGCC CTGGGGGGCC 1080 CGTCAGGCCT CTCAGGCCCC TGTGCCGTGC ATGTCCATGT GGGAGCTTCT GCCTCAGAAG 1140 GAAACCAAGA GGTTCTCAGG GGCAGCCTGT GGTGTCTCGC TGGGAAACGC TAGACCAGGC 1200 CTACAAAGTT ACCCGGGAGA 1220
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