| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04586 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr13:49305130-49306800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr13:49306296-49306315 | CAGCGCCCTCTGTTGGCCC | - | 6.47 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 49305362 | 49305702 | | chr13 | 49306000 | 49306182 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH13I048729 | chr13 | 49303985 | 49306580 |
| Enhancer Sequence | GTATAGGAAG AGGAGGAAGA AGAATCTAGC AACTGACATA ATGCAGACCC TTAACAGAGA 60
TGCAGGGCTA CAACCCATCT TGTGCTGCTG CTGAGGCCCA GGGAGGAGCC ACCTGGGTGC 120
CCAGAGCTGT GCTGGGCAGA CACAGGGCAA TTCAGCCCTG TGGGAGACAC ACAGGTCTCC 180
ACAGGAGGCA GCAGTTTTTT AGCACGGGAA TTCATCAGGC TTGGGCACCT GCTGGGGAGG 240
AGATGGAAAC ACAGTCAATA CATCTCATCA TCAAAAACAG GAAGGAAACG AAACATTTTG 300
GAAGTCATTG AAAGGCAGGT TTTATGTTAA TTTGAAATAA AATGTTTGCT TAACCGACTG 360
CTCTCTGAAG ACTTCTTGAT TTGGTATTTG GAGACAGACA TCACCCTGAC GTACATTAGG 420
AGGCCTGTGA TCTTAGGCTT GTTCCAGCTG TGATTCACTT CACGTCTGAT TCACTTCATC 480
ATTTATGCAA TTTGTCATCA GGTTATCTGA AAGCTGAGTA AAACCTCTCA TATCCTCATG 540
AGTTCCTCTC ATATCCTTAT GAGTTCTATC TATTGTTAGA TAGAACTACA TGAACAGAAG 600
CTCTTTGAGT CCTCAATCAT TTTTAAGAGT GCAAAGAGGT CTTAAGACCA AAATGATCGC 660
AATCTGCTTT GAGTCCTCAA TCATTTTTAA GAGTGCAAAG AGGTCTTAAG ACCAAAATGA 720
TCGCAATCTG CTGACCTACT TTGGGCAAGA TGACATACTC TCACCTTTTC TGTTCATTCT 780
CTTTAGCCTT CAGAGCAGAC CTGTAAGAGC CTAGATTTCC AGCGTATGGA AAGCAAAAAG 840
GAGGCTCAGA GTAAAGCCGC ACCTCTAATA AGGGATAAAG CTGGGATTGG ACATCACTTT 900
CTCTGCTCTA CCCATTTTGC TGCACTGTCT CTTAGCATCC ATTGTGGCAA AAAGAAGTTT 960
TATGGAAGAG AAAGCAAGCC GCAAACATTA GAGATTTTGC AAGAGGCAAG CTTCACTCTC 1020
CAATACTTGC TGAAAAATAT TCTCTGTGCT CCTCGGTCTC CAAAGAAGGA GACTAATTTA 1080
GTTCAAAAAG AGAGATCTCT GTCCGCGGCT CAGCCCTGGG TGTCGGGGTT CCAGGCGTCG 1140
CTGGGTCTGG GCGCGCCACG TCTGCACAGC GCCCTCTGTT GGCCCCTCTC TGCTCCAGCC 1200
GGCACTTGGT CTAGCCTGGC CACCTTAGAT GCTCCCTTTA GATGCTTTCT GGTGAGCGTC 1260
TCTAGGGACC ACAGCATCTT ACTAGGGCTT GGGCATTCCT CTGGGGGCAA CTGGGCTTTT 1320
ATACAAATAT ACAAGGTTGC CCTCAACAGC TAACCCTCCC TGCGGGCCAC TCCTAGTTTG 1380
CAGCTCCATC TTTTCTGCGT TATTTTTCAC ATCCAGAACT CAGAACACAC ACAGAGAACC 1440
GCCCTCTCCA CTCTTGTCAT TGAGAAGGAA GCCTGGTGTG AACTTCAGAC TTACACAAAC 1500
CTAGATTTGA ATCCAGGCCC TCTGCCCTGC AAATGACTTA ACCTTTCTGA GCCCCACTCT 1560
TCTCAGTTTT AGAATGGAAA TGCTAGTATT TACCTTGTAG GGTTATTGGG CGCCTAAAGC 1620
ACTTGGCACA GGAATGAACG GTGTTGGTTT CCAGTTTCCC ATGTCTGCTG 1670
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