| Tag | Content |
|---|
EnhancerAtlas ID | HS133-06493 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:100509510-100511090 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:100510271-100510289 | TCTTGCCTCCTTCCTCCC | - | 6.04 | | EWSR1-FLI1 | MA0149.1 | chr11:100510267-100510285 | CCTGTCTTGCCTCCTTCC | - | 6.29 | | FOXP2 | MA0593.1 | chr11:100509951-100509962 | TTTGTTTACTT | - | 6.62 | | Stat4 | MA0518.1 | chr11:100509989-100510003 | TTTCCAGGAAGTAG | + | 6.23 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I100638 | chr11 | 100509223 | 100510814 |
|
Enhancer Sequence | GCAGTAATTG TGCAAGAACA CTCTAAACCA CATTTGAGAA ATGCAAAGTG CAGTGTAGGG 60
CACGATGTCA CTAACCTTCA GCATAACCTT AACCTCATGG AGTCCCCATA CACAGGGTTG 120
TTCTCCCCAT CTTAGATGTG CTACTAGCTA AAAGTCATCC AACCTGGTCA TGGCCTAACA 180
TCTTCTGGAA CTGGGGATTA CAAAGAATCT AAAATTCCAT TCTCTCTATT GTTAACATAA 240
CCCTTGAGTC CAGATTACCT CTCTCTTCAG GGAAATAAAT TCATAGGAGT TGCAGGACAA 300
GGAACAGATC ACAAACACAT TTCTATTTTA TTCCTGTCTC ATGGAAAAAG AGCAAGCTAG 360
AAATGTAAAC GTCAGTGAAA CATTCCTCGG ACCTTAGATG AGAGGTGTTA CATAAACACG 420
TTTTCAGCTG AGCCTGAAAA ATTTGTTTAC TTACAAACTT TCTATACAAC CCTGACGGCT 480
TTCCAGGAAG TAGCCTCTCT CTTCATTAGA AAATTCTTCA CAGGACTTGC TTCAGAGCCT 540
GCCCGCTCTT GTTTTTCAGT TCTCTTGACA TGTGACCCAT TCTTTGAGAA GCTTGTTTGT 600
TTATGCTGCA GTGCATCATC CATTTTCCCA CTGCCAAGGC GGCTCTGCTC TCATGTGAAT 660
CAGAGATCGC TGGACTGCTC TGACCTAGAG GTCCGCACAC GGCCCCCTCC CCAGCTTCTC 720
CTAACTGCAG CATTTGCTCT TCTGTTTTCT TTGACTTCCT GTCTTGCCTC CTTCCTCCCC 780
TGTACTCTTT CTTTAGTCCC AAACCTCCCT ACTGTTTGTC TCTCTGCTTG ATTCACCTTT 840
ATTTTTTATT GTATATATTT AAGGTATACA ACATGATTTT TCTATATACG TAGTGAAATT 900
GTTACTACAG TGAAGCAAAT TTATATGACC ATCATCTCGC ATAGTTACTC TTTTTGTGAG 960
TGTGGAAAGA GCACCCAAAA TCTACTACTC TCTTAGAAGG TTTCCAGTGT ACAATATAAT 1020
GTTATAATTA TCGTTGTCAT GTTGTACACT AAATCTCTAA TTTTAATTAT GCTATCAAGA 1080
GATTACCTCT CTTCTCACCT GTCAAAATGA GTGGAAATTA AGTCCCCCTA GTCTCTCCCA 1140
TTCTTCTCTA ATCTCCCCAG CTGGCCCCAG CCTCGCAAAC TAAAAGAAAA AACAATTTCA 1200
TCAAGCTCCT CTGGGGCGAA ACAATGAATA AGATATTGTT CAGCTTTACA TCTCAGAAAC 1260
CCTTCCCCCA GTGATTTGCA AGCAGTAACT TATGTTTAAT TAGCTCTTGG ATTGAATTTG 1320
GAGTCATTGG TTTGGCCAGA TAATGAAGTT CCCAATTAAT GTCACAATAT AGATTATAAT 1380
CTGATCCTTA TGGTTGGGCT CTTTCCTCAG TTATAACCAA TATTTTTATG TGATGAACCA 1440
TTTTCTGGGC TCCACTACTA AAAATAAACT TTTATACACT AAGAGATGAA AGAATCTAAA 1500
GTTTGTTTAG GGAACCGAAG TCTCCCAGTA GTTGGATGCT CACAGTTCCC TTGAAATTAA 1560
ACGATATCAA ATTACCATAT 1580
|
