Tag | Content |
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EnhancerAtlas ID | HS180-04343 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:207885790-207886950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr1:207886264-207886275 | TAATCCAATTA | + | 6.02 | PHOX2A | MA0713.1 | chr1:207886346-207886357 | TAATCCAATTA | + | 6.02 | Phox2b | MA0681.1 | chr1:207886264-207886275 | TAATCCAATTA | + | 6.02 | Phox2b | MA0681.1 | chr1:207886346-207886357 | TAATCCAATTA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 207885856 | 207885959 | chr1 | 207886127 | 207886257 | chr1 | 207886422 | 207886537 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I207712 | chr1 | 207886141 | 207886290 |
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Enhancer Sequence | TGAGGCCTTC AGCAGGCATA GGATATAGCA AAAGAAATTC CCCCATAACT AACAAGTACT 60 CTGGAACTGT CCTTTCTACA ATGTGTCAGC CGCCTCCAGA AATCCTGCAT GGTGAGCATA 120 CCCTAAGCCA TCAGGACAAC TTTTTACCTG GGCAGGAAGT GTTCTACAGC TGTGAGCCCA 180 GCTATGACCT CAGAGGGGCT GCGTCTCTGC ACTGCATGCC CCAGGGAGAC TGGACCCCTG 240 AAGCCCCCAG ATGTACAGGT GCCTCTCTTT CCCCCTCACA TGGAAGTCTT ACTCCTGTTG 300 TTTTATTTTT TCTTCTCGTG AAATCCTGTG ATGACTTCCT GGGCCAACTC CCTCATGGCC 360 GTGTGCTGTT TCCACTTAAT CTCCAGCTTG GGGCTAAGGT ATCCTTTGTT TGTGATGAAG 420 GGTGAGTGTG ACCCAGTGTT GAGACCAAGG ACTCAGTGTG GAGAATCACT GAGTTAATCC 480 AATTAAGGAG CTGACCTAGT AGATAAGAAG TACCCAGAGA GATTAATTTA TGGAAGGGTA 540 GTTTTGAAAT AAGCGTTAAT CCAATTAAGG AGCTGACCTA GTAGATAAGA AGTACCCAGA 600 GAGATTAATT TATGGAAGGG TAGTTTTGAA ATAAGGGTAG GGACTAAGTG GCACCGCCTT 660 CAGAAAACAA TGAAAAAATG GCACATACAA CTCAATATCA GATACAAACC TAAATACAGT 720 CACTGATCTT GGGTACACAG TTGGAACTTG AAATGAATGG GTACGTATTT ATTTGGAGGC 780 AAAAGAACAT AATTTTATAA AATGTGTGCT AGAAAAAAAA GATGAATGAG ATGGAAATTG 840 TTTGCCTCAT AATAAGGCAA AGGTTGTTTT AGGAAACTTA AAACCAGTCA ATAATGGAAT 900 CTGTAATAGT GTATGAATAA CTATGTTTTA ACCCAATTAC ATATCTTCAT GTCAAGAATG 960 GCCAGTGTAA TTGTTTTGAT GCAAGATTTT TCTCAGCCAC TTTGCCAGCT GGTGACCTCT 1020 GGCCAGAAAC ATCCCTGTCC AGGCCTTGCT CTACCCAGGA TCAATGCAGG AGACACCTCA 1080 TCTACTTGGC CCACCCAGGC CGTGCCAGGC TTGTGCTCTG ATGCAGAGCC CATGGCTGCC 1140 GCGACTACAT GCTCAGCCTC 1160
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