| Tag | Content |
|---|
EnhancerAtlas ID | HS007-14148 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr5:179715680-179717150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr5:179715992-179716005 | GAATTAATTATTC | + | 6.46 |
| | | 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 |
| GH05I180289 | chr5 | 179716621 | 179716750 |
| Enhancer Sequence | CCTACCACAT TTATTCTCCC ATTTAGCTTT GTCTTTACCA AACATTTACT GGGCACCCAC 60
TGTGTAATTA GTATCCCAAA AAATAATGAA TGAAATGACA TGATATTTAG GATTTGCTTG 120
AAAATAATTA TGGGTGGTAA GGGTGCAAGT GGATACCATT AGAGATGAAA CAAGATTGGT 180
CAGGAGTTAA TAACTGTTAA AGCAGGACAC TATTCTGTTT ATTTTGTATA TGTTTGAAAG 240
TTCCCATAAT AAAAGTTAAA ATAAAAAGAA TGATGTTGAA ACTGGTTCAT ACAATCAAGT 300
ACAAAGTATC AGGAATTAAT TATTCTGAAG GAAAATTATG TAAAAATGGC ACCTTCCTAA 360
CCAAGTGTGA GGTGTAACTA CTGTATGTAT GTAGACCAAA AATAGTTGCC CTATTGGCAA 420
ATCAATAGTC TCAAGAAGAA AAAAAATCTG GTCTCTGTTT TATCTTATGC CTCATGAAAA 480
CAACTGGTTT ACTCGCTATT AACTGGTTTG TCTGGTCCTT TTCTTTATCC AGAAAATTAA 540
GAATATTTTA TCTTAGACAC ATTCAAGTAT CCCCTCTGTT GTTTATTTAC GGGACCAAAT 600
AAACAGATTT TAATCTGTGA ACAAATTAAA GTCCTGGCAC CCTGAAAATT AAATTGCCAG 660
GAAAATCAAA GCTGTCAAAA GAGAAGTCTA TGCAAAAATA GTATTGTTTT TAACTCTGCA 720
GGATCCTTTT GAAGAAAAAA AAAAGTTAAA TGGAGGAAAA CATTAAATAG ATTGGTGGTC 780
ATTCTTCCAG AACAAGTTAA AAGCCAAAAG AGAATACTCA GAGCTGAGGG ACCCAGGAAA 840
GAATCCTTAT CTGGGAAGTG ATCTGGGTTC GAACTCCACT CACCAGCTGC TTGCTAAGAA 900
ACAGACTACT TAGACTCCTG AGCTTCCGTT TCCACAGGGC TCCAGTTACA ATCAAATGAG 960
TATCTGGGCT GGCACCTGGG CAAACAGGGC CTGGCTCCCC TGGCCTTAGG CTACCTTTCC 1020
TGCTCTCCTC ACAGCTCCTC CCTCCCACAC AGCCAGTCCT GGAGGATGAC GATCCTGCAA 1080
CCAAGCTGAA TGAATCTGTA TTTGGCTTGG CTCACAGCAT TAAAAAAAAA TTTAATTAGC 1140
TATTGCCAAC ATTTAAAAAT CAGAACAAAT GTGGAGTGCT GCCTTCCTTT TTAGAGACAG 1200
GGTCTTGCTC TGTCACCCAG GCTGGAGCAC AGTGGTGTGA TCATAGCTCA CTGCAGGCTC 1260
CAAATCCTGG GCTCATGGGA TCCTTCCACC TCAGCCTCCC AAGCAGCTAG GACTACAGGT 1320
GGATGCCACC ACACCTAGCT AATTTCTTAA AATTTTTTGT AGAGACAGAT CTCGCTACGT 1380
TGCCCAGGCT GGTCTTGAAC TCCTGGCCTG AAGTGATCCT CCCACATCAG CCTCCCAAAG 1440
TGTCTTGAAA TTACTGGCGT GAGCCATGGC 1470
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