| Tag | Content |
|---|
EnhancerAtlas ID | HS133-17288 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr2:95998640-96000800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RELA | MA0107.1 | chr2:95999761-95999771 | GGAAATTCCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 95999089 | 95999238 | | chr2 | 95999501 | 96000056 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I095333 | chr2 | 95998773 | 96002010 |
| Enhancer Sequence | TAAATGGGAA TCACAATTAC ATCCTTGGGG GTCTTCCAGA CTTAGGGACA AAGGGACAAG 60
ACAAATGTGA AGATGCTTAA TAAAATGTAA AGTTATGTGA ATGTGAAATG CCCTGTCTCG 120
CGTGAGTTCT GTGACAGCCT CTGCTGGGCC TCACTTGTCT CACCTGTGAA ATGGGAGTTG 180
GGGTAAAATC ACTGTAGCTC CCCTACTCTG CATGCAGTCA CGCTGCAGCT AGAGTGGTTG 240
TTATAGAGAA AACAAAAACC AAACGAATGC TCCCTTGCTC TGAGGATAAA TCCCCGGCCA 300
CAGACTTGGC CATGCCCTTA TAACTGTTTG ACTATCTGCC TGCACCTCTA GAGTGTAAGC 360
TCCTTGAGGC CAGGGCCGCA GCTGCAGCAT GTAGTGCCAC ATCTGGCAGG CACAGAGTCG 420
ACTTGGGAAG TATTTGTCAA ATGAGTAAAT GCATGAACCT AGGCCTCTTC TAACTCTGAA 480
ATCTTACATC CCTCCGGATT GAGAAAAGAA TCAAAAGCCA TTCTACCACT ACTGCTGCGG 540
GAAACAGACT GCCCTGGACC CTGACTCCTC TCCTGTGGTG GCCTCACCAG GGCCCGCCCT 600
CGGTCAACCT AGCCTCGAAG AAGGGAATGC TTGGGTGTTT CCAGAGACTC CTCAGAGCAC 660
GTGCTCAGGA TAGAGTCCTG ATGCTTCTAG AGACCGTATG GGCAAGTCCT GTAGCCTCTG 720
TTGGTTGCAA TTGTGACAGC TCGTAGGAGC ATGGTGAGGA TTCAATGATA CTATGTCAGT 780
GAGTGCCTAG GACAGTGCCT GGCACATGGT AAGCAGCAAT GAATGACACT GCTGCTATCC 840
ATTATTATTA CCCAATTCCC TCACTGAACG CAGAGGGCAT GATGGGTGGC TGAGTCCTCC 900
CAGCTTCCTT GAGGCAAAGG TGGGACTTGG ATAGGGGGCG TCTCACTCCT GCCCAGCACC 960
CTGGCTGCTC CCCTGCTGCT TTCTGACTCA GACCCCAAGG TTGTGATTCC CAAGTCATTC 1020
GTCTGCATTC AGCTGACACA GGCCATCTGC AAGACACACA CCTCTCTGAG CTGTCAGAAG 1080
ACACTGCAGA AGCTGAGATC CTGGCATCAA GCGTCCCAGA TGGAAATTCC CCAAGACACC 1140
CTTGGGCCCT CGGCTCAAGT TCAAACAAAG AAATGCTTAT GTTCAGAGAT CTTCACAGAT 1200
CACCAGCGAG GATGTGACTT GAGAACACTT TGCGTCAGCA TCATAAAACA TGAGGATTGA 1260
TGACCCGTGT GAGTGGGGCG AGTGCCAGGG GAACACAGGC TCTGAGTTGG CCGGCCGTGC 1320
TTCCTGCATA CACTCTGTGC AGAGGGTGCC AGCCTAGACT GGCGGGGGGG TTAGAATAGC 1380
ACCGCACTAG TTAGCATGTC CCATAGGACC CTGTTTACAG CACACTTGCA TGGGCATGTG 1440
TGCACCTGGT TCTCATGACA ATATGCAGGG TGGGCAGGGG TTAAGGAATG CTTCCCCACT 1500
TTGGGGATGA AGGAAACTGA GGCTCAAGGA GGTGCGAAGC CAGGCAGCTG AGGTCACACA 1560
GCCTTGGATC TCCCTACCGT CACTATCCTC CCCTCTTGCC AGCAGAGAGA GGTGGGAAAG 1620
CCACGTTCAG CCAAAACCCA GAAATTTACC CAGAGAAACT CACAAACCAA CATGGTGGGC 1680
CTTGTACAAA CTCTAAGAGT ATGAAGAGAA GAGCTACAGC TGGCCTTACC CAGTCCTGCC 1740
ATGCTGGGAC TGGTCAGCTC CCCTGCACTG AATCTGGGTA GGGGCATGAA AAGACACAAG 1800
ATGGGATGAG AAATCCTCCA CATGGGAGAG GAAATGGGAA CCTTTCATCA CTGGGGACCA 1860
GGAAGCAGGG TGAGGGGCTC ACAGGACAAG CTGGCCTCAA ACGTTCCCCT TCCATTGCCT 1920
GTTCAATGTT ACTAGATACT TGCAGACCTC TGGCAGAACA GATGGGGACT TGGATATACC 1980
TTGTAAGGGG ATGGGGGCAT GAAGACAGAT TCGTTCCCCT GACCAAGGGG GAATCAAACA 2040
GGTCACTGAG CGCTCAAAGG AGAATATTCC CAGAGCTATG CAGTGAGGGG CCTGCTACCA 2100
CAGTAACACT TGGGCATGTG TCAAGTCCCC ACTTGGCCAA GTAGCTTGGT CTTCTCCTAC 2160
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