| Tag | Content |
|---|
EnhancerAtlas ID | HS133-04904 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:104614880-104616750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr10:104615508-104615520 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr10:104615512-104615524 | GTTTGTTTGTTT | + | 6.32 | | NFE2L1 | MA0089.2 | chr10:104616707-104616722 | ACTGCTGTGTCATCC | - | 6.21 | | Nfe2l2 | MA0150.2 | chr10:104616709-104616724 | TGCTGTGTCATCCTA | - | 6.17 | | Nr2f6(var.2) | MA0728.1 | chr10:104615133-104615148 | CGAACTCTTGACCTC | - | 6.24 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I102855 | chr10 | 104615042 | 104616510 |
|
Enhancer Sequence | GTCTTTAGAA TGACTAATTG AAGGAAGTAC TTTTCCTTTT TTTTTTTTTT TTTTGAGACG 60
GAGTCTAGCT CTGTCGCCAG GCTGGAGTGT AGTGGTGTGA TCTTGGCTCA CTGCAACTTC 120
CGCCTCCTGG GTTCAAGTGA TTCTCCCGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGC 180
ACGCACCACC ACACCTGGCT ATTTTTGTAT TCTTAGTAGA GATGAGGTTT CACCATGTTG 240
GCCAGGCTGG TCTCGAACTC TTGACCTCAT GATCTGCCTG CATCAGCCTT CCAAAGTGCT 300
GGGATTACAG GCGTGAGCCA CCGCTCCTGG CAGCATTGCT TCTTGAGCAG TCTCCACATA 360
GCTATTTTGT TTGATTAGCT GAGAATTTCA TGTGTAAAAA ACTCATTCCA CAGTATTCAT 420
TTAACAAATA CTTATTGGGT GTCTGCTATG TGCCAGGAAC TGCTCTAGGT ACACGGAATA 480
AACAAAACTA AATCCCTCTA CTTGGGAAGT TTACATTTTA GTGAAGAGAC AGACGATAAA 540
CAAGTGAAAC AGAAAAAAAT CAGGTGGTGG TAAATCCTGT GAAGCAAAAT TAATCTGGGA 600
ATAGAGAGTG ATGAAAGGGT TAATCTTTGT TTGTTTGTTT GTTTTGAGAC AGAGGAGGAG 660
TCCCACTAGC TCTGTCACCC AGGCTAAAGT GCAGTGGCCC GATCTCGGGC TCACTGCAAC 720
CTCTGCCTCC TGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTATA 780
GGCGCCTGCC ACCACACCCA GCTAATTTTT GTGTTTTTAG TAGAGATGGG GTTTCACCAT 840
GTTGGCCAGG CTGGTCTCAA ACTCCTGACC TCAAGTGATC CTTCCCGCTT TGGCCCCCTA 900
AAGTGCTGGG ATTACAGGCA TGAGCCACCA CACCCGGTCG AAAGGGTTAA TCTTAAACAG 960
ATGATCAGGG AAGGGGTCTC TGGGGAGAGA GCCTGTGAGG AGAAACACAC TGACATTTGC 1020
CCACAGCATA ATGAGTGGTT ATGACTCATA GGCTTGTCTC TTGCATGCCT GCGCTTCTCC 1080
TCCTCCATTT GAGTTGTGTG CTTAGTGAGG GTCCATTGTG TTTTTTTCTA AACATCATGT 1140
GTCTGTGGGC TGGGCGCAGT GGCTCATGCC TGTAATCCTA ACACTTTGGG AGGCCGAGGC 1200
AGGATTGCTT AAGCCCAGGG GTTCGAGACC AGCCTGGGCC ACATAGTGAT ATCTTGTCTC 1260
TGTAAAAAAA GGAAAAAAAA AAAGAATGAA AACAATTTTT TAAATGTGTG TATGGCACTT 1320
ATGCTTACAG TTGCAACTAC GTAATTTAAT GAAATAATAC GAAAAATGAA ATATGAGTAC 1380
CAAAAAAGAG GGTTGCTATT GCTATGAAAA CTAAGTTGAA AATCAGAAAC ACTTGTTGAA 1440
GATGAGTAGC TAAGACAAAT TGTTATTGAG TTAATTATGA ACAAGTTAAT GGTAAAAGCC 1500
TAGGAGAAAA ATTTATAGAA ATCTAAAAAG ATTCTGTAGT GAAGATTGTT TTACAGGTGT 1560
ATTCAAGATG TTCTTCCATT TTAAAGAAAG CAAAACTAGA AATCTCAGAT GGTATGTTAT 1620
GTGTCTGGTC TGTTTATGTA GGAAAGTGAT GCAGAATGCC AATGAATATA TCAAGGAAAA 1680
GCCTTGGCTT TACATTACAA CAGCCCCTGC CTTCAAGGCA ACCACAACTC CCATTGAGTC 1740
TGTTTTCTAA ATGTCTCACA AATCCTTTGT TTCTTTTTTT CTTGGCTACT TCTGTGTTTC 1800
AGGCCATCCT CATTCCTTGC TTAGAGTACT GCTGTGTCAT CCTAACCAAT CTCTCTGCCT 1860
CATTCCCCAC 1870
|
