| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00123 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr1:228632930-228634320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MIXL1 | MA0662.1 | chr1:228633152-228633162 | GTTAATTAGA | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 228633200 | 228634200 | | chr1 | 228633222 | 228633907 | | chr1 | 228634060 | 228634141 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I228445 | chr1 | 228633222 | 228634355 |
|
Enhancer Sequence | TGAGGCGGGA GGATTGCTTG AGCCAGGAGT TTTGAAGCCA CAGTGAGCCT GATTAGGCGG 60
CAGAGCTAGA CCCCGTCTCA GCAAAACAAA AACAAAACAA AAACAAAAGC AAAGGTGCTT 120
CCAACAATCA GGGTGATCCT AAAATGACAG AGCAGCGTTT TGAAAATACC TCCCCGGGGC 180
TGCAATGTGA CCATTTGAGC ACTAAAAACA ACCATACAAA TGGTTAATTA GAACATGCCC 240
CATTTATAAA AGGAGGAAAG TTAACATACA CGTTTCTAAT AAGACAACAA AAGGATGGAA 300
ATAACATTGT GTTGAATTTT TGTTGATTTT GTTAAAAAGG AGCGCGTTGA CACATAGGGG 360
GATTTTGTTT CTTTAAGTTC ATGTCTGTTT ATATAAAGTT TAGGTCTGGG TGTGTGTGTG 420
TACCTGTGTA AGCAGGAAAG AGTAAACAAA ATCGAGAGCC CGGGACAAAT GCACTTAAGA 480
AGGGGCGACG GGAGGGCCAG GCTCGCCGGG CTGAGTGCTG AGGAGGGGGC GCGTCCCACC 540
CATGCAAGCC CGGAACAAAG GCGCCTGTCA CTCGTCACTC TCCACGCGGG CTGGCTCTGG 600
AAAGCCCAAA GGAAAAAACC CTCACTTTCA GGAAGAATAA GCCTCAGCCC ATGTATCTAG 660
GGAACACGTG ATGCTGCAAG AAACCAGTGA CTTAACGCGT GTAAAAGCAG GAGAGCGTCA 720
GAGGTTCTGA CCCCGGGGGA GGAGCAGACC CGCGGCAGCG TGCGGAGACT TAGCGGGCGG 780
AATCTGCCAC CAACGCAACC TGGCCCAGAG GTTTTGAACT GACCAACTGG GAGACGTCCC 840
CGAGCTTGAA TAAGGGCCTC AAAAGCTTAG CGTTTTATGC AGAGTCGCAA CCACCCAGCG 900
CTGGGAACCT GAGCCTGCAC AACCCACTAG AAAGCACCCG TGACCGTCCC CTGCGCCCGT 960
TATCCCTGCG CCCCGCACCC CTGTATCCCC GGCTTCTCTG CAGCTGTACA CCCTGCACTG 1020
CGGCGCCCCC CAGTCCCGCT GTCCGCTCCA TCGCGCAGGT CTCCAAAACG AATCCCGGCT 1080
TGGAGGGGCT CAGCGGCCCT GGGCCTGTGC GCCGTTGCGG CCGGGAGGGT CATTTTCATG 1140
CCTAAGGACC CGCCCCTTGC ACGCAACCTC GGGTAGCCAG CCGGAAACGG CGTCCCGGGC 1200
TCCAAAGGAC ATCTCTTTTT ACATTTCAGC AAAACAGCCG CACACCTTCT CCCCAGATGG 1260
CCTCTGTGCA GCCTGAAAAT GCCCGCTCCC TCCAAGTCCC TGGGCAATTG CTGGGACGCA 1320
TCTCAGAGAC TGCGCGGGGC GGAGAAGGGG TATGTGTTTG GGCCACTAAT TTGATTTTCT 1380
TGGAAACTTT 1390
|
