| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00669 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:24132770-24134620 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:24133163-24133175 | GTATGTTTGTTT | + | 6.37 |
|
| | 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 |
| GH01I023807 | chr1 | 24134101 | 24134250 |
|
Enhancer Sequence | ATCATCTCCC TCCCCGCCCC TGCTCAAGAC TCTCTGTTAG CTTCCCAGCT CAGTCTGAAA 60
GAGTCAAAGT CCTACAAGGC CCCCGATCTG GCCTTCCTCT AACCCTGACA TCTCTGCCCC 120
CCTCTCCTCA GTCACACTGC TCCCGCCACA TGCCTCCTCC TGATCCCTGA ACACAGCAAG 180
CACACTCCTC CCTCAGGGCT CTGCGCCTGC TTTCCTGGGT GGGGCTCCCT TCCCTCCCCC 240
TCCCTGCTAG GGATCCGCAG GGCTCACTCC CTCGCTTCCC TCAGGTCTCT CTCAAATGCT 300
ACCTTCTGAG TGAGGCCACT CTACAGAAAG GCCTGGCACT GCCTTAACCT GCTTCATTTT 360
TTCTCCACAG TGTTTATGAA CACCTGGCCT GCTGTATGTT TGTTTATTTA TTATCTGTCT 420
CATAGTACTA GAGTGTCAGC CTCATGAGGG CAGAGACTCT GTTTTGGTCA CAGCTGAATC 480
CTTAATGCTG AGAACAGTGC CTAGCACACT AGGCACCGTT AGGTTAGGTT TTAATAGGTG 540
AATAAATGGT CTTACAATGT GCTATTTACA CGCCTGTAAT CTTCCATCTG TCTTCCCCAC 600
CCACCATAAC ATGAGCTCCC AGAGGGCAGG GATTGGGTCT TGTTACCATT GTCTAAGTCA 660
GCACTTAACC TGGCACATCG ATCCATATTT CCGAAGTAAC TGATGGAAGA GGGAGGTCAG 720
AGGAAGCTAC TGCCAGACGT CACACAGCTC AACCTGTTCC CTGATAAATT TTCAAAAAGG 780
GGATTCTGAG ATATCACTGC CATGAAACAG AGAAGCACAG AGGAGCAGGA GTGTCCTGAG 840
CGTGATCAGG ATGAAGTTTT GCCTCAGACT CACCTCAGCT GTGCAGAATT CCCCTTTACC 900
TGCCTGGCAA GGCATAGGAG AGGAAGTCAC TCTTCCTGTC TGCCTGGCTG GGAAACGCAT 960
GAGCTGAAGG AAAGCCCAGG AACCAGGGCA GGGTATCACA GTAAGCTGAA AAATGAGGAG 1020
ACCACAGAAC TACGAACCTT AACCTTGACA GCCACAACTC TGAGGAAACC GACCCAGAAC 1080
ATAACAGACT CACCTGGCTT AGACACGAAC CTCTAGGGGA TAATTGAGAG GAAAAAAAAA 1140
GTGGCTGGAA CTGCCATCAC TATCCTAGAG ATGGAAGGTT AGGCCAATGC TACAGCAAGG 1200
TAGCTGTGGT CAGACACTAA GAATGCTCCT TCTATCTGGC TGCCAGCCAA TGGATCTCCA 1260
TTCTGGACCA GCCCACGAGA AGCAAACCTC AAAGGAAACT AATCTGAGGT CTTAGCTCAA 1320
TCTGTGGGGA ACGGCATTAA AGCCTCTCCC TCTGAGTGAC CTCTGCTAGC TTCTCTACCT 1380
CCTGCTTCCT CATCTGCTTC TGCTACACAC CCGCACACTG AAAACCCTGT ATATTGTATG 1440
AGTCCTCCCT GAACCCCACA TCAGTCCTGA GGTGCAATTC TGCCTAGTCA TCTTTCCTCT 1500
TCCCTCAACA GCAGCTTACT TTATGTTCTT CAAGCTTCAC TGAGGCCTCT TTTGCAAATC 1560
CTCCCAGATC TCCTCAGCTG GGATGGGGCC CCTCTAGGCT TCCTGAGCCC CATGCTTCCT 1620
CCCTTCATGG CATCTGTCAT AATGCAGTGG GATTGCCATG TAACTCCCTT GACTGTCTCC 1680
CCAACACAGA GCTGTACACT TCACATCTGG GCAGGGTCAC CATGACTGTG TCCACCATTG 1740
CCAGCTTGGA ACCTGGCATA CTGGCATCAG TAAATGTTTG CTGAAAGAAT AAATGATAAC 1800
AAGCTGTCCT GCCCACCGTG ACCTTTGGGA GAATGGGCAT ATGCTTTTGA 1850
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