| Tag | Content |
|---|
EnhancerAtlas ID | HS080-01767 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr1:98981380-98982820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:98981923-98981944 | AAAAGAAAAGGGAAAGTTAAG | - | 6.22 | | TP53 | MA0106.3 | chr1:98982043-98982061 | GGCATGTCTGGACTTGCC | + | 6.23 | | TP53 | MA0106.3 | chr1:98982043-98982061 | GGCATGTCTGGACTTGCC | - | 6.31 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 98981698 | 98982246 | | chr1 | 98982290 | 98982441 |
| Enhancer Sequence | TCTAGGCTAC AAGGACTACA ATTTCTAGGC AGGTCCTACT ACTGAACTGG GCTTAGAGCC 60
AGTGGATGGG GAAAATGTGA TCTATGAGAC ACCATCTGGG GCTACCAAGG GAGTGCTTGA 120
GCTATCCCTT CCTCAATCAT AGGCTGCACA GCTCACAGCT CCAAAACAGA CCCCTTCCTT 180
CTGCTTGAGG AGAGGAGACA GAAGAGTAAA GGGGGCTTTG TCTGGAATTG TGGACACCAG 240
TTCAGCCACA GTAGGATAGG GTACCAGTCA GATTTGTGAG GTACCCATTC CAGGCCCCAG 300
CTCTCAGCTG ACATTTCTAG ACACATCAAG GCCAGAAGGG AACCTGCTAC CTTGAAGAGA 360
AGTATCCAAT CCTGGAAGGA CCCATAACAT GCTGAATAAA GAGCTCTTGG GCCCTAAATA 420
ACCAGCAGAG ATATCCCAGT ATTATGCCTT GGGCCTTGGG TGAGACTCTG AAACTTGCTG 480
GCTTCAGGTG AGACTCAGCA CTTTCCCAGC TGTGGTGACT ATAGGAAGAA ACTCCTGCTC 540
GAGAAAAGAA AAGGGAAAGT TAAGCAGATT TTGTCTTGCA CTTTAGGTAC CAGACTGTCC 600
ATAGTGGGGT AGAGCACCAA GCAGGCTCTT GGAGTCCCTG ATTCCAAACC TTGGCTCTAG 660
GATGGCATGT CTGGACTTGC CCTAGGCCAG AAGGCAGCTC ATTGCCCTGA AGGGTGAGTC 720
CTGAGCCAGG TAGCATTCAC CAAAAGTTGA CTAAAGAGAG TCCGTGGGCT TTAAAGAAAC 780
ATCAACAGTT GCCTGGAAAG ACTCCTCATG GGTGTGTGGT GGTACCCACA GAGTGAGGCT 840
CCTTTGCATA TGAAAAGGGA GGGAAGAGTG GGAAGGACTG CATCTCATGG TTTGAGTGCC 900
AGCTCAGCCA CACTACAACA GAATACCAAG GAGACTTCTA AGGTTTTTTA CTGTAATCTC 960
TGCCTCCCAG GTGACACTTC TGGGTACAGC TGGGGCCTGG GGGGAACTTG CTGCACTGAA 1020
AGGAAGGATA CAAGCCTGGC TGGCTTCATT ACCTGCTGAT TGTAGAGCCC CAGGGCCTTG 1080
AGCGAATACA GGCAGTAGTC AGGTAATGGT TACTATTGGC CTTGGATGAA CCTCAGTGCT 1140
ATGCTTGCTT CAGGTCTGAC CCAGCACAGT CCTCCCTGTG GTGGTAGCCA CAGGGGTGCT 1200
TGTGTCACAC CACCCCCAGT TCTAGGCAGC TCAGAACCAA GACACTCCAT TTATTTGTGA 1260
GAAAGTAAGG GAAGAGAACA AAAGTCTCAG CCTGGTAATA CAGAGAATTC TTCCACATCT 1320
TATGCAACAC CATCTAGGAG GTACCTCCAT GAGTCTGCAA GAATCACAGC ATTATTAGGT 1380
TTGGGGTGCC CAGTAATGCA GATATGGTTT ATATCACAAC ACCCAAGTCC TTTCAAATAC 1440
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