Tag | Content |
---|
EnhancerAtlas ID | HS048-35925 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr8:80733240-80735060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:80734413-80734431 | GGAAGGAAAGAAGGGAGG | + | 7.82 | EWSR1-FLI1 | MA0149.1 | chr8:80734409-80734427 | GGAAGGAAGGAAAGAAGG | + | 9.09 | Nr2f6(var.2) | MA0728.1 | chr8:80733957-80733972 | GAGGTCAGGAGTTCA | + | 6.22 | TCF3 | MA0522.2 | chr8:80733644-80733654 | AGCAGGTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr8:80734410-80734431 | GAAGGAAGGAAAGAAGGGAGG | + | 6.75 |
|
| 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 |
GH08I079821 | chr8 | 80733655 | 80735056 |
|
Enhancer Sequence | CGGTTCCTAC CCTCTATGTT GGCTTTCTGT ATTAAACAGT GTGTGCAGCT TCATTCCCTG 60 TGGTCTAAGG AAGGAGAGAA TGGCACGAGA AAACTGTCTC CACAGTCATG GTAACCTCTA 120 ACCTGAGCCA ATGGGTAGGA AACAGTCGCC TTTGTCAGTT GGCAAGGCAA ACCTGAGGCC 180 ATCAGGGCAT TCTGGCATAG CCACGAATAG CACACGCTCT GGAGTCAATC TGTCTGGGTT 240 GAATCCGGAC TTCTCCACTC TCTAGCTGTG TGCTCTTGGG CAAAATACTT GATCTCCCTG 300 TGAATCTGAA AAACAGTAGT AATATTTATA TACACCTCAT AAGGCTGTTG CCATGATTAA 360 CTAAGTGAAA ACACATAAAT CCATTAGAAC AGTGCCTGGA AAATAGCAGG TGTTCAATAA 420 ATGTTAGCAA TTGTTATTCT TATCTGACCT TATCTCCCAT CATAGCTCTG CACACAGCCT 480 GGAGTCCAAG CAGGGTTACT TCCCTTCTTG GCCTCTGCCA CAATTTCCCC TGCCTACTTC 540 TCCTCTCTAC CCCGACACCC ATGCTTTCAC ACATGGTGTG AGAGCCTGGA CAGCTTTACC 600 ATTTCTTTTC TTCCTAGCAA ACTTTTCTTG TATTCTTAAA GGCTCAGCTC AGGCTGGGTG 660 CAGTGGCTAA CGCCTGTAAT CCCAACACTT TAGGAAGCCG AGGTGGGTGG ATCATTTGAG 720 GTCAGGAGTT CAAGACCAGG CTGGCCAACA TGGTGAACCC TGTCTCTACC AAAAATACAA 780 AAATTAGCTG GGCGGTAGTG GCGCATGACT GTAATCCCAA TTATTCAGGA GGCTGAGGAG 840 GCAGAGGTTG GGGTGAGCCG AGATGGCACC ACTATACCCC AGTCTGGGCA ACAGAGTGAG 900 AATCTGTCTC AAAAAAAAAA AAAAAAAAAA GAGTTTAAAG GCTCAGCTCA AGCTCCCTTC 960 CTCTAGGAAA ATCTCCTTGT CCCTGACTGC CAACAGCCAG GTGTCCCTCC ACTCTGCTCT 1020 TCCAAAAGCT GTGCACAGCT CTAACCCTCG ATTGCACACT GGACTCTAAG GGCTTACTTG 1080 TGTGTTTCCT CTCACCGGAT GGGGGCTGCT ATAAGGCCAT AGGAGGGGCT CCATCAATGT 1140 TTGTTGAATG AATGGATGAA TGAGTCAGTG GAAGGAAGGA AAGAAGGGAG GGAGTGTCCC 1200 TGGAACAATC TAATTGGGAT ACTGAATTGT AATGTGTGGA GCAGGCAGTG AAGAACTCTG 1260 AGCCCAGTGA TTATTTCCTC TTCCCAAGGC TACCGCTCTC TGCTATTGGC CTAAAGACAT 1320 AAGGGCAGAC AGAGATTCAG CTAGAAACAT GGAGCAGTTA ACTTATTTAT GACTTTACAA 1380 CCCATGAGAT CTGACCACAC CAGAGGCCTG CAAGCACCCT TAAGATAGTA TCGGCAGGCC 1440 AGGCACAGTG GCTTACATCT GTAATCTCAA CACTTAGGGA GGCTGAGGCT GCAGTGAGCT 1500 ATGACTGTGC CACTACACTC CAGTCTAGGC AATAAAGTAA GACCCTGTCT CAAGAAAAAA 1560 AAAAAAAAAG ATAGCATACG TACCAAACCT CTCTTTAAGC ATGTGAATAC CTGCATTTCT 1620 CAAGAGGTAT GTTTATCCAT AGTTTTAAGA ATATCGAGTC TAGAAAGTCC ATAGCGTCCC 1680 TTGGTAGTAT TTGCTTCAGG ATACTACTCA GCAGAAATGA CCTTTCTTAA GCTGCAAATC 1740 AAGTCCATGA TTACTGTCCT CAGAATTGGT TCATTCTTTC AATCTCTGGT TCACCAAAAG 1800 CATTACATTT TGATGAACTA 1820
|