| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03239 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:203494920-203496800 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr1:203495106-203495122 | CCTAAAGCAAACAAAC | + | 6.24 | | Foxd3 | MA0041.1 | chr1:203495114-203495126 | AAACAAACAAAC | - | 6.32 | | ZNF740 | MA0753.2 | chr1:203496227-203496240 | ACTCCCCCCCCAC | + | 6.25 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00433 | chr1:203492450-203498563 | Adipose_Nuclei | | SE_34957 | chr1:203495081-203496909 | HeLa | | SE_54703 | chr1:203492671-203496788 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH01I203526 | chr1 | 203495281 | 203496609 |
|
Enhancer Sequence | GGCGTGAGAT TCTAACTTCC CTCAGAAATG GGCCCACACA GGCCAGGTAC ACTGGCCCAC 60
ACTTGTAATT CCAGCACTCT GGGAGGCTGA GGTGGGAGGA TCACTTGAAC CGAGGAGGTG 120
GAGGCTGCAG TGAGCCAAGG TCATATCACT TGTACTCCAG CCTGGGCGAC AAAGTGAGAC 180
CCTGTCCCTA AAGCAAACAA ACAAACCAAA ACCTGTCAGT GACTTACTGT TTGATATCCT 240
GGTCATCATT ATGGGAAGAA ACAGAATTCT TGGTGTTCCT TACTCTAATT TATCTCTGGT 300
TTAACTTTAT GTTATGGGGA TGTGGGGGCA GTGAGGAAAG CACCAGTGTC TTTTTACGGC 360
CCAGGACATC CTAAGTACCT TACCCCAGTC CTGGCAAGCT TGCAGGACAT GCTAAAGATG 420
GGAGCCTTTA GTTGGCATCG CTTACTTGGC CTGGGATGAA GTCTTGACCT CCCATCTGGA 480
GCTAAATGTC CAAGCCAAGG GGCATCTGGG GGTGGGACTG CCCTTTGCCC AGCCACGGCC 540
TTGTGGGCTG ATGGCAGACA GTCATGTTCT TATGAGCCAC TTCCCCCAAT GGCTGACATT 600
TCATCTTTGG AGAGGAAAGC TACCAGAGTC AAAGAGGGAG GCGGGTAAGA GAGGACTAGG 660
CTATACCTTG CACGATTAGT CTTTCATAAG TAGTGTTTAA GGATCAGGAT GAAAAATTAA 720
AAAAGCAAAA AACAAAACCA GCAAGCCAAT TCCTCTCAAG AAACTTCCCT GAAAGAAAAG 780
GGAGGAAATC AATATTTAAT TCAGACTTCA TTGATTTGCA GTTTGGGTAC CACACTCAGC 840
ACTCGATTCT GTCCCGGTTT CCCAGTAAGA GATTATGGAG TCCCTGGCAA AGGATACTAA 900
AGGGCCTGAG GGAAAGGCAG CGCCAGGGAA GAGAAGCCGG GAACTTTGTC TTGAGTCAAC 960
TTTCCCCAGC TGCTCCCTGC CCCAGTGTGG GGCACCTCCC CTCCCTGAGG GCTTCGCTGA 1020
GCTGGGAGGG ATGAACCAGG CCTTCCTTGG CCCACTCCCC TGCCTCTGAG AAGAGCAGCA 1080
GCCAAACCCC CCCTCAAAGA GCTGTGTGCA CTTGACACAA ACGTGCACTC TCTCTCTCTC 1140
ACACACACAC ACACACACAC ACACTCACAC ACCACTCCTC CACTCACATA CCACACCTAC 1200
AGACACTCAC ATAAGCTCAC ACAACACACA CACTCTCACA CACACTTGCA CACCACTCCT 1260
ACACTCACAT ACCCACCTAG ACACACTCAC ATAAACTCAC ACACCAAACT CCCCCCCCAC 1320
ACACTCTCAC ACACCACTCC TACACTCACA TACCACACCT ACACACACTC ACATAAGCTC 1380
ACACACCACA CACTCACACA CTCACACACC ACTCCTACAC TCACATACCC ACCTAGACAC 1440
ACTCACATTA GCTCACACAC CACACACACT CACATTAGCT CACACACCAC ATACACTCAC 1500
ATTAGCTTAC ACAGCACACA CACTCACATA AGCTCACACA CCACACACTA CATTAGCTCA 1560
CACACCACAC ACACTCACAT TAGCTCACAC ACCACACACA CTCACATAAG CTCACACACC 1620
ACACACTACA TTAGCTCACA CACCACACAC TCACATTAGC TTATACAGCA CACGCACGGC 1680
ACACACACTC CCACACACAC ACCCTCTTAC GTACATTCAC ATACACTCCA TACCACATAC 1740
ACTACACACA CATACACCAC ACACACACAC ACACAAAATG CCCTAACTTT ACTTAACTAG 1800
CCTAAAAAAA AACCCCTAAT TTTTCAAAGA TACAAACTGA AGTATCTAGG AATGAAAAAT 1860
CATACCTGTA ACTTACTCTA 1880
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