Tag | Content |
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EnhancerAtlas ID | HS180-46932 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr8:28514730-28516140 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr8:28514913-28514934 | TCTGGCACCTTGGACAGCTCC | + | 7.58 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH08I028657 | chr8 | 28514719 | 28516422 |
| Enhancer Sequence | ATTATAGACA TGAGCCACTG TGCCCAGTCT CATTATGGAC TTTAGCAAGT ATAAGGAAGA 60 AAGTGGTTTG AATTGCTGGA TAGAGAGTTT TAAACTCAGT GGGAGGAAGA CTGGGGAGGA 120 GCTATTGGCC TTGCCAGTGC ACTGAGTAAC GCAGTCATCT CTGCATCCAC TGCCCTTTCT 180 TACTCTGGCA CCTTGGACAG CTCCACTCTG CCTGGCCCGA CTAAGTGGGC CCCACTGACC 240 TGCTGTCCAA TGACATCTTC AGCATTATGG GAACATTTTT TTTATTGTAA TATTTTAATT 300 TTGTTTAGAG CTGTAACATT CTTATGCTGT CCATCTGAGC TTCCTTTTTT ATCCTTCAAG 360 GTTTCTGGAC TACATGGTTT GGTAACAATC ATGGTTTGGT TTTTATTTTT AATGTATACA 420 TCTTTCACAT TGTACACTCT ATTTTTTTGC TTTGTAAGAG TCATCTGTGC TTATTTAAAA 480 AAAAAATTGG AAAGCACATC AAAGCATAAA GACCCGGGGG GAAAAAACCT ACCCATTATT 540 ACACAACTTG AAGCCAGTAG CATTCACATT TGGGCATATT TCTCTGTGGT ATCTTTTGGG 600 AGAGTTCCAA GCTTGGCTTG GCAGCTAGCC TTGCTTCTAT CCTGGGCTCT TTGACCTCCT 660 GGGCTTCACT CCTCCCTTAA TAGAGGTTTA CTTAATCGAC CTTCCCTTCC TCTTTCTGCC 720 TTCCCATAGA CACAATTAAA GCCAGCTGCT TGAGGATTCT GGTAACTGGT GAGGACAGCT 780 GATTCTGAGC CCGCTGGCAA GAGGGCAGGC TGAGAGGGTG GGGTTGGACT CTGGCTGATG 840 CAGGGGCACC GGGCAGGAAG CTCAGCAGCT GGGCAGGGGC CTGGACACAG GGCTGCCCGT 900 GCAGAAGCCA CGTGGTCCTG CTCTCACATT TTCCCTGCTG TTCAGAGCCA GCCAAAGCTG 960 AGGGCATATG CTTGACACCG GACGGTGGGT GGGGGGGGTC CCTCAGAAAC CAACTTCCTG 1020 CTTATTATGT CAGGCCTCAG CAGGGGATAT TTTTTCATTA TTCTCTTAAT TGTTTTGAGT 1080 AGGAACACAG TCACATGGTT CATGGAGCAG AAGTCTCCCT CCTGCTCAGC CCCATCCACC 1140 CTGTTTTCAC CCTCCCTAAT CCACTCCAGG TAATCAGCTT TTCATTTCTG TGTGTATTCA 1200 TCTAGACTTT ATTTGTGAAT ACTAAAGCAC ATAAAAATAT ATTCTATATT CTTTTTTTCC 1260 CTTCCTTGTA AACAAAAGGA AGTGTCTTAT ACACCTTTTC TGTACCTTGC TGTTCCCCCC 1320 CTGCCCCCGC ACTTATCTTG GAGACTCTAA AAATATCTGT ACCTTGAAAG TTTCCTCATG 1380 CACTCTTTTT TTGAGCTCGC TCTGTCGCCC 1410
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