Tag | Content |
---|
EnhancerAtlas ID | HS048-01090 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:41509700-41511140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:41510119-41510137 | GGAAGGCAGGCAGGCAAG | + | 6.45 | EWSR1-FLI1 | MA0149.1 | chr1:41510115-41510133 | GGCAGGAAGGCAGGCAGG | + | 7.44 |
|
| 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 |
GH01I041044 | chr1 | 41509803 | 41512830 |
|
Enhancer Sequence | GGTTTGAAAT TTTTAAAATA AAACATTGGA GAAAAAAGTA GTAGTCTCAA CTTAGGTAGG 60 AAAGCTTAAT GGGATATGAA ATCTCCCTGA GCTTTGGGTG ACTACCTGCT ATATCGGAAG 120 TGCATGGTCA GTTGGGCCAG GACTCTAAGT GGTAGGGTAG TGTGGAGACA AGGATATAGG 180 AAAGGGGGAG GGCCAGTAAG CACCCAGATA ACAGAGGTGG TACCTATGTA TGTCTAGCAG 240 AAGCGTGTAG CCAGGCAGAA GGGCAGGAGT CATAAATACC AGATCCAAAG GGCAAAGCAA 300 AAGACAGCTC TTGTACAGAT CGAGCTCTTT GGCAGAGGTT TAGGTAAGTA ATCAGAAAAA 360 CACAGGAAAT GATAATATCA GAGGTGGGGC AAAGGGTCAG TAAGGCAGGC AAGCAGGCAG 420 GAAGGCAGGC AGGCAAGCAG GCAGAAAGGA TACACTAAGA AGCACAGAGG AATTAGAAGT 480 TTAGGCAAGG CTCTGGCTTG TCTGGGCATA GTTAAAGGCT AATTTCAGGG AAGCAAATAG 540 AAACTAGAGT GAGAGCAGAC AAGTTGCTGA GCACCCACGA TGAGAAACAG CTTAAGAGCA 600 GAGGAGGACA CAAAAAGTGG GCTCAATCTG TCTGAAAATG GGGAAGGGAG AGGTAGCAGC 660 TAATGGCAGA ATGTGATACC TTGGTCTTTG TTTCTCTTAG TTGGTGAGGC AAGAAGAGTC 720 TGGCTAAAGT TTGCTTCCTC TTATCTAGTG GCTGAATCAG AGAGATGTAA ATTGGGGCAG 780 AATTCCCAGG AAAGGTCATG CCCCGGTCCC AAACCACTTT TGGGACTGCA GGCCCATGAG 840 GTACATCCTT ACCAGTCTCT GAATGCTGCT ACCAGTATGT TTCTCTCACT TCTTAATGAT 900 GGCATTCCAT TTAAGAATTC GGAGTTCCTA TTTCTTTGAG AAATCTCTTT TTAAACTAGC 960 AGCTACATTC ATGGATGTGC TAACCCCCAT TCATGCATCC ATTCTTTCAG AATCCCAGGT 1020 AGGCCTAACT TTCACGTCTG AAATGTAGAT CAGAGTTCCT GAATGCCTAA CTGGAGGTAT 1080 TTAAAACTTG CCTTTGTCTG GACCAGCTCT ACCATGCCCA GTCCAGACTC CCAGTGCAAC 1140 ATTCTAACTG CAAGTCAGAA TGCCTTTTTC TTTTCTCAGA GACTCTGGTA CTGAAAGAAA 1200 GCAATCTAGC ATGGGTTAGG TGAGGAGAAG TTCCCTCCAT AGAAAAGGAT CAGCCAGGGG 1260 ATCATAGAAA TGGCTGCAGG GATCAGATGG TCTGGCCCCC ACAGAGTATT TAAAATTCAG 1320 GTATCTTTTT GACCTGCTTG CAAGTCACAT AAGCAATACG GATTTGGGTA CAGAAGTATC 1380 TATGAGGGAA AGGGGGAAGG AGAATGGGGG AACAGTCACT TCCCTGGGCA CATTCTCTAG 1440
|