| Tag | Content |
|---|
EnhancerAtlas ID | HS133-29551 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:117511220-117513380 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr7:117511802-117511818 | GATTAAGTAAACAAAT | + | 7.48 | | FOXP2 | MA0593.1 | chr7:117511806-117511817 | AAGTAAACAAA | + | 6.62 | | ZNF263 | MA0528.1 | chr7:117512183-117512204 | CCTCCTCCCCGTTTCTCCTTC | - | 6.09 | | ZNF263 | MA0528.1 | chr7:117511932-117511953 | CTTTCTTTTTCCTCGTCCTTC | - | 6.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_61408 | chr7:117506521-117516081 | HBL1 |
|
Enhancer Sequence | CAAAATGCAT AAAACGCCTC TGATTTTTAA GGAGCAATTG TGATGACACA TATCACTCCT 60
CTACACTAGC TTTCCTTTCA CTTAAAAATC AGTCTATAGG TCAAGCGGCT GATATGAGAG 120
AACCATGCCT TATTAAGTCA AAACTATTTG GAGAACTAAA ATAAAAGGCC CAATTTACTA 180
CAAAAGCCAT CATCAAAATT TTACTAAAAA TTCAGAAATT ATTACTGGTT TTTAAACTAC 240
TAGATGAAGA ATCCTTATTG CATCTCGCAA CCCTAAAGGA TTCTATGGAA ATAGCAAAGA 300
AGGTTCACTT TCGCAGATTT TCCATGGCTC TGCCCATTAA CAAGGGTGAA ATTATCAAAT 360
CCCCAACTAT CAGCAGTGAA AATCAGACTT GAACATTTTA AACAGAAGAG AGGGAACACT 420
GACCTTGTTA ACACAGAAAT CTGCCTGGCG TCCTGGGTTT TGTTTACGAT CTAACCAAAC 480
AAAACTATAT ATCAGCTCTA CAGACCATCA GTCAGATGTT TGTGTTTGGG TTAATTGTCA 540
GGTGATTAAA ATATTGAGGG TAACAGAAAC CCATTCTGAG TGGATTAAGT AAACAAATTC 600
AACCTTTCTG GGGAACAAGA AACACACCAC ACACACACAC ACACACACAC ACCCTCTTTC 660
TTTTTCGTCC TTCCCCTTCA CACACACACA CACACACACA CACACACACC CTCTTTCTTT 720
TTCCTCGTCC TTCCCCTTCC CACCTTTTGG GGATGAAGGC ACCAAATCAT TTCCACTTGC 780
CAGAGAGCCT TGTCTCAATA GCTAGTTTCC TTACTGTGCC CCACAGAGGG GAGCTGATTC 840
ACATAAGTGG GCAGGTTTCG TTTGAAATCT TAAAGTTCTC ATTTTCTATG CAAAGAATGG 900
AAACTCAATT TTCCCAAAAG TTCAAATCAA AACTTGCCAG TTTTACAAGT GGAAATTAGC 960
AGTCCTCCTC CCCGTTTCTC CTTCCATTGC CAGGCTCAGC TCCTCTCACC CCAAGTACCT 1020
TCCTCCACAT CTCTCCTCTC CCTCTCCAGA AAGCCCTACC TCCAGAGGGT GGGAGGAAGT 1080
TAAAGCGGCC CCCGCTGTTT ACGCCCGGCC CTGCCCTCTC CTGCACTGAT TCTGCTCAGG 1140
TCTTGATAGG AAGAGGGGGG CGTCCACGCC CCGCTCGCTC CATCCCACCC CATCCTTCGG 1200
CGGGAGCAGC CAGATCTGGC CAAGAGTGGG AGGCGCTCCC AGATCTGCCT TTCTCTGCAG 1260
CTCCTTGCAG CTCCTGCGAA GCTGCTTCCC AAACACCGAG AACCTTTTCC ACCCAGGAAA 1320
TGTGGGTCCA GCCCTTCCCC AAAGTAGAGG CTGGAAACCA CCAGCGAGTC TCTACACCGG 1380
AATATTAAGG GGGTGAAAGT AAGGACCAGT CAAGAATGGT AGCGCATTCG GCCTCTAGAC 1440
TCCAGAGAAG GAGAACAATG TCTTGAAACC AGGTGCAGAA CCTCCACCTC TCCTGAGCAT 1500
CGTCTCGGGA AGAACCAATC CATCCACCCC ACCCCAATCA CTACCACCAA GTAATGGGGC 1560
AGCAGGCTGC TAGGACCTAA AGCGCTGGCC TCAGCGGCAG CAGCGCCCAC ATCTGGACAC 1620
GGCCCTCTCC CAGTGGGCCT CCCGAAGGCA CAGGACCAGA TGCACACAAT GGGCATCCCC 1680
ACACCTGCTG GGCGATGGCC CACCTCCCCC AAGCTGCTCT CCCGGGTCCG CTGAGCGGTA 1740
CCAGGCACCC CCGAGACACG CGCTGGCAAC CACGCGCGCA GCGAGAGGTG AACAATGGGG 1800
GGTCAAATTC GCCAGGAAAC ACGTCCCAGC CTTCTCCCCC GGCCAGAAGC GACCGCAGCG 1860
GAGGGAGTGG GCATAGGGGT CGCACTGGAC GCAGACAGGG AGCTGGGAGA ACCGGGCGAC 1920
CCGGGGCCGC TTCCCGTGGG GCGCGGAAGG GACAGGAGGG ATCCCCAGCC AGGGTGGCCG 1980
CTCCGCTCCC CCCCGCGGCC TCCGCCGTGT GGGCATCCCG AGGAAGGGGG GCCCCGATGA 2040
AGGGGCACCG GAGAGTCCCG GGCTTACGGA ACGCCCCGGG GGTGCGAAGT CGGGTCCGGC 2100
TGGGACCCCG GCGCCGCCCC CGGCCCGCGT CTACACTAGC CCCGCGCCCG CCCCGGGAAC 2160
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