Tag | Content |
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EnhancerAtlas ID | HS148-00043 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:7550900-7552430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr1:7551354-7551370 | GCTTGTTTACTTAAGG | - | 7.43 | FOXP2 | MA0593.1 | chr1:7551887-7551898 | TTTGTTTACTT | - | 6.62 | HSF1 | MA0486.2 | chr1:7551519-7551532 | TTCCGGAATGTTC | + | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I007490 | chr1 | 7550829 | 7552540 |
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Enhancer Sequence | TCTCTCAGGC AGGATGCTCT TTCCTGGGAA GACTTTGGGC CTCCAGGCTG AGGACATAAC 60 CCCAAAGCAG TTTAGGACTT CTGGCTTCGG TAGCAAAGAT ATTTCCTTCT GTGCTTGTCT 120 CTTCCCCACT CCAGCTCCGA TCCATTGACT CAGCTTTTGT TCTGTGAATG TCATTTTCTT 180 TGAATTTGTG TGAGTTTTGT TGTTTGCAAA TAACCTAATG AAACTCCTTC TGTTCCCTTC 240 CAAAACAAAA AGGAGGCTCT AGCATGGTCT ACCTCCACAT CTGAACTCCT CCAAGCTTTT 300 CTGATGGTGT TTGGGCTGTA CAGCACCCTG AGAGACCACC CCCGGCCTCC ATGTACCCCC 360 TGCCATCACC TGAGCCGCAC TCACCAAGGC AGAGCCGGGA GGACTCCACC CACCCTCTTT 420 CCTGTTCATA AGGTTTCTCA AGGAGCCTCT TGATGCTTGT TTACTTAAGG ACGGGCACGG 480 GTGAACTCTC ACCCCCACCT GGTGATTTCA CAAACACAAA CCATAGAGGG GAAGGCTATT 540 TCTCTCACTT TCTGGAAAAG GCCAAAACTA ACCCTGAATC CCCCCGCCCA TGTTTAGAGT 600 AGACACAGAG GGAAGATGGT TCCGGAATGT TCTGCGTGTA CTGCCGATTG TCCAATTGCT 660 TAAAACAGGG CTTGGCGTGC ATTGTTTTGG TCATTAGTTA ACCAATCTGG GCGGGGAAAA 720 AGGCAGAGCG TTAAATAATT ACAAGCACTT CGGTGATTTT TTTTTCTACT GACTAAGGTT 780 AAAATGAATA GTGTTGATCC GTTGCCCAGG CAGCAGGCTT GTTAAAGGAA ATGGTATTTA 840 AAATGATTTT TGAGCCAAAG CAATTTGGCT GCTTCAAGGC ATCCTTTATC TTTTGCTTTC 900 AAGAGGATAA TAATGTTTAA AAACGAAGTC ACTCATACCA TTTCCTGTCG CGAAGCCAGC 960 TCAGTGATGG GCAGAGCTTC CTCTGGGTTT GTTTACTTGC TCCATGATGG AAAATGCAAA 1020 CTTAATGGGC TCCCTTCTGC CGAGGCTTTG GTGTTCCGAC GAAACAAAGA CCCATGCTGC 1080 TGCCGAATCT GTGTCCACAG CTCTGGCCAG CTCACCCTGG AAGTCTTGAT TGCCACATTG 1140 TGGATGTCAG AATGTCACCT GCTTGGTTAG AGCTTCTAAA CAGGAGGCTC AAGGCCACTC 1200 CCTGGCTCTA GGGTGGAGTC GAGGAAACCT GTCTAGGATG GGACACGCTC CCACTAGGCT 1260 CAGGGTGCCC TCCCGTCCAA GAGCATGATG GTCACCCCAG CTGGGAAGTT GCTAAGCAAG 1320 TCCTCCTTGG TAGAGCGTCT TTCCCATCAT CCTCTGCGAG GAAGGCCAGG GCGATACACT 1380 CAGCTTATAG AGTGAAGTCG GCAGAAAGCA CAACTTCTCA GTGAAGAGGA TAAAAGGAAG 1440 GCACTACGGG GGCCCAGGAC CTGCTCTGCC CTGCTTAGGG CTGGGCAGGG CTTACGGGCG 1500 TGACATGCAT AGAGGCTCAG AAGAGCTGGC 1530
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