| Tag | Content |
|---|
EnhancerAtlas ID | HS133-06401 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:77904660-77907280 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr11:77906077-77906092 | CAGGGGCAGAGGGCA | + | 6.1 | | REST | MA0138.2 | chr11:77905826-77905847 | GGCACTGTGCTAGGTGCTGGG | - | 6.15 | | ZNF263 | MA0528.1 | chr11:77906707-77906728 | GGGGAAGGATGGGGAGGAGGC | + | 6.26 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I078192 | chr11 | 77903073 | 77904774 | | GH11I078194 | chr11 | 77905103 | 77905358 |
|
Enhancer Sequence | AAGGACTTTG CTTCTGAAGC AACAGGAGTT GACATTTTCT GAGAACTTCC TTGTGCCCAG 60
CTCAGAGAGC CTAAGTAACC TTTATGGGAA CCAGAATGTA TCCCAGATGA GCCACATTCA 120
AAGAGTCAAA AACAACAACA ACAACAACAA AACCCAGAAT CGAACACATC ATTTCCCTCA 180
TTTCCTCATT CAGGAAGCTT CGGGTGGACC CTGAACTTTT TCTTTTCTTT TTTTGAGACA 240
GGGTCTCACT CTATCACTTA GGCTGGAGTG CAGTGGCACG ATCTTGCCTT ACTTCACCCT 300
TGACCTCCTG GGCTCGCCAC CACCCTTGGC TGGTGTTGAA CTCCTGGGCT CAAGTGATCT 360
GCCTGCCTTG GCCTCCCAAA GTGTTGGGAC TACAGGCGTG AGCCACCGCG CCCGGCCGCA 420
TCTGAGCTTG TAGCAGGTGC CCAGGTGCTT CTGAGGCATT CTGAGGCTTC TGAGCAGGCC 480
AGGATTTGGG AACCACTGAT GTCTGCCATG GTTACAACCT CTAACCAACA GTGAACTCTT 540
AAGAGGCACA CACTCTTGGC ATGAGAGATG CTAGCCACAG ACTAATAAAC CCTGGTCCTT 600
TCCTGGTGGA GCTCAGCCTG GTGAGAGAGA CAGATATTTA AACAAATGGG CCCTTTGTAT 660
CGTAACACGT GCAGCAATGG AGGTTAGGTC ACAGCTGAGA ACTAGAACAG AGCAGGGAGC 720
TCACTGGGTC TAGTACATAG TTGGGGTTCC AGAATATCTG TGATTCTGAA TAAAACTTTC 780
CAGCTTATTA TCCCAGAAAT TTAAGGCTTG TCCACACTCT AGCTCCAGTT CTCAGGCATA 840
AGAGTAGTTT TTACTGAGCC CATAAGTTTA AACACCTGTT GTCTGCTGAG TCTTATATCA 900
GGTCCTGCCT AGATTGGGCA TCGAAGCAAA GAAATGGTTC TGCGCTCCAG GAGAGGCATT 960
ACGTGTTAGA TGTTAAGAGA GCAAGCTGTG CCCATGTGAA CCTGCATGAG AGGGCTCAAA 1020
GTGGGTTGGT GTGGGACAAA GTCTTCAGGA AACAGGCCAG GTGGAGGAGA AGGGCAGAAG 1080
GAAGGCTATT ATGGCTCAGA GGAGTAAGGT AGAGATGACT CACACTGCAC CCTGCATTTG 1140
CTCATCCAGC AAATGCCTGT CTGCTGGGCA CTGTGCTAGG TGCTGGGGAT ACTGTGGTGA 1200
ACAAAACCTG AAGCTGCCCT CAAGAACCAT ATACAGCATT GGAGGGGAGG CTGACCCCAA 1260
TCAAGAAATC ATGACAAGTG CTACCAAGGA GAAGGACAAG ATGTTCTAAT TTTTAATAAG 1320
GGAGATTGAC CCAGGCAGGG AGCTCAGGTG AGGCTTCCTT GATGAAGTGA CTTTCAGCTG 1380
AGGTCTGCAG GGGGAGGGAA GAGCATACAC AAAGGCCCAG GGGCAGAGGG CACACGGTGA 1440
GCCAAGGGTG ACAGGCCGGT GTGGGCTGAG GCAGGCAGAG CCCTAGGTGT GCAGGGCTGG 1500
AGCGCGGAGA TGAGATGCTG TGCTTCGGTG GAGGGGACTG GGACCCATAC CCCACCAGCA 1560
CTAACTGATT CCAGCTGTAA TGCAAGAGGC CCCAGCGGAT TGTAGGAATT AAGGGTGGGG 1620
GATGGATTCC GGCCTGGAGG ACCAGGGCTA TTCTCACTGA GGACGGGTGC TTTAGATAGG 1680
CTTTGAAGGA AAAGACGCTT GCTTGGTTGT GTGAGAGCAT GGTGGTCGTG GGGGCCTCAG 1740
GAGATAAGGA CGTGTCAGGC AGAAGGCACA GCACACACAC GAAGTGGAGT CTAGCCAAGG 1800
GGTAGGGGAA GGAGCAGGGA GTTGAGGCAG AAAGAAAGAG TGCGAGGCAT TCTGGGACCT 1860
CTGTCGGTTC TCCCTTGGGG CCTCTTGCCC TTTCTCCACA GAGGTGTCAT TTTTTGTGTG 1920
TGCCCCATCT CATCTCCCCC ATGGAAATGA CTTGGCTGAG ACTCTGGACA GCAGCTTCTA 1980
GATCCTGCTC TTACCTGCCC TGAGAGTGGA CAGGGTCACC AGGGAGGTCT GGGGAGAGAG 2040
AAGCAAAGGG GAAGGATGGG GAGGAGGCTC ACGTAGCCTT TGTGCGATTA AAGGCGCTTA 2100
GCAACCATAG CTACAAGTCC CTGGGGTTAA TTTATTTTGA GACAGGGTCT CTTTTGCTCA 2160
GGCTGGAGTG CAGTGGGATG ATCTCCACTC GCTGCAGCCT TGAACTCCCA GGCCCAAGCG 2220
AGCCTCCCAC TTCAGCCTCC AGAGTAGCTG GCATTACAGG TGTGTGTGAC CACTCCTGGG 2280
TAATGTTTGT GTTTTTTGTA GAGACGGGCC TCGCTGTTGC TCAGGCTGGT CTTGAACTCC 2340
TGGGCTCAAG GGATCCTGCT GCCTGGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGTC 2400
ACCACGCAGG CCCCTGGCAT TTATTATGTG CCAAGTGTTG TGCTTTATTT CATCAGGATA 2460
GCTCTCAGTG AAATGACGCC CTTGCCCCAT TTCACAGATG AGAAAACTGA GGCCCAGAAA 2520
GTTTGAGTTG CTTGCCCTAA GTCTCAGCAC TCGGGGACTG CACCGGGAAC TCTTGAGCCC 2580
CGCGGTTGTC GGGCTGTGAC CTCATTCCCT GTCCTCCGCA 2620
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