| Tag | Content |
|---|
EnhancerAtlas ID | HS092-37685 | Organism | Homo sapiens | Tissue/cell | HFF | Coordinate | chr8:146073650-146075180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr8:146074039-146074054 | ACTGCTGAGTCAGAG | - | 6.05 |
| | | 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 |
| GH08I144848 | chr8 | 146073461 | 146075179 |
| Enhancer Sequence | ATTGCATTCC AGACTGGATG ATGGGGAGAC CTTGTCTCAA AAAAAAAGGA AAATTTCAAT 60
ATCCATTAAA AAAATATCAT TGGAGGCCAG GCTCGGTGGC TCATGCCTGT AATCCCAGCT 120
GCCTGGGAGG CTGAGACATG AGAATTGCTT GAACCTGGGA GGCAGAGGTT GCAATGAGTC 180
GAGATCGTGC CACTGCACAC CAGCCTGGGC AACAGGAGTG AAACTCCCGT CTCAAAAAAA 240
AAAAAAGATG GTATTGGAAC ACAGCCATAT ACATTTGTTT ACGTATTGTG TGACTGCTTT 300
CAAGCCACCA TGGCAGGGTG GACAGAAACT TCATGGCCCA CAAAATCTAA AATGTTTACT 360
CTCTGGCCCT TTGTGGGAAG AGTTTGCTCA CTGCTGAGTC AGAGGAAGTG GCCTCTAAGT 420
CTGCTCCACG CTGTAGGGAT CTCAAGTCCA ACTGGATCAT GTCTGCCCTG ATTAAAACCC 480
CACTGCTCCC CCTTGCCCCA GTGGAATGAC CAAAATCCTG TGTGTGGCCT TGAGGCCAGC 540
CGCTGTCCCT GCACTTGATC CCCCATCCCT CAATCCCCTA TACTCGGGCA GTGCCAGCCC 600
CAGTCCCAGG AATGGCCCAC TCCCCTGCCT GTGTCTCATA AGCTGTCTTT TCATGGCTGT 660
GTCTTGATTT GCCTGGGTCC CCGCTTGAGA CAAGCCCAAG GGTTCACAGA TGAATTGAGG 720
CAAACACAGA TTCCCAATGA GAGACGGCGA GAGGTCAGCC TGAGGACCGA GGGCAGGTCC 780
ATGCTCTGGG CTCCACACAG GCTTTGCTAA GCAGCTGGGA GAAGCAGAAG GATGGGGCTG 840
TCCCTAAAGC TGCTGTTCCT GCAGGGCCAG GGCCAGTGAG TGAGAAAGGC AACATGGTCC 900
CAGCTGCCCC AGCCCCATCC ACATCTGGGG ACAGAGAATG CAGGAAGTGG CTGGTCATAT 960
TCCTGATCCG ATGACAGTGG GGGGACAGTG CCTTCGGGGA GAGAGAAGGG CTTTACCTGG 1020
AACTCAGTGA GGGTGGGACA AAGCTGAGTG ATCGACCAGA TGGCAGGACC CACAAGCATG 1080
CACCTTAGAG GGCACCTGGG CTCCTCCCAG AGTCTACTGA CCCCACCCCC AGGTACTCCT 1140
CTGTACCCTG ACATGTCAGA ACTGCCCATG GAGGGATGAG GAAGAAATCC AGGCTAGTGG 1200
AGGAGACAAC CCAAAAACTG CAGACAAGAC AAACAGCCAA GCAACCCCAG GCACTCAAAG 1260
ACAAGGGGAG GTTTCTCAGC AGAGAACAGA CTAGACATGG TCCAGAAGTG CTCCACGGAG 1320
GCAGGAACAG TCAGCTGGAA GCCAGCTGAC CGAAAATGGC TCTGCAGAGA CCGAGCACCA 1380
AGGCCCCTCC TGGAACACAG TTATGCTGGA AGCTGCAAAG CTGGCTACAA CCCCTGCACA 1440
CACCTGCCCT AGAGGCACCC GGGAGAGGTC CCTGCCACCA ACTCCACCCT GGTGACAGCC 1500
TCTCTGCTGG GCTCTAGCCT CCTCCCTTGC 1530
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