Tag | Content |
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EnhancerAtlas ID | HS133-00432 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:16701330-16702950 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr1:16702705-16702716 | TTTGTTTACAT | - | 6.14 | Zfx | MA0146.2 | chr1:16701614-16701628 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_30493 | chr1:16701832-16702738 | Fetal_Muscle | SE_54328 | chr1:16701480-16703157 | Spleen |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016373 | chr1 | 16700142 | 16703894 |
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Enhancer Sequence | TTAATGTAGT ATCCATAGAG ATTTCTCTTC TTGAGTGTTT TTGTTTTGTT TTGTTTTTTT 60 GAGACGGAGT CTAGCTCTGT CGCCGAGGCT GGAGTGCAGT GGCGCAATCT CAGCTCGCTG 120 CAACCTCTGC CTCCCGGGTT CGAGCGATTC TCCTGCCTCA GCCTCCCAAG TAGCTGGGAT 180 TACAGGTGCT CGCCACTACA CCCAGCCAAT TTTTGTATTT TTAGTAGAGA TGGGGTTTCA 240 CTGTGTTGGC TAGGCCGGTC TCAAACTCGT GACCTCGTGA TCCGCCCGCC TCGGCCTCCC 300 AAAATGCTGG GATTACAAGC GTGAGCCACC ACGCCTGGCC TTTGAGTGTT TTTCTTAAAA 360 CCGTTTGCTC CTACCAAGCA TCCTTCTCTT TAACATCTAG CTCTGTGCAG GATATTAAGG 420 TAAAACCATG CCCCACAGAA ATTAGCAACA AACCCCAATA GTCTGTATGG AGACAGATAA 480 TTTTTTTTTC TTTTTTTTGA GAAGGAGTTT CTCTCTGTCA CCCAGGCTAG AGTGCAGTGG 540 CGCAATTTCT GCTCACTGAA CCTCTGCCTT CCGGGTTCAA GCAATTCTCA TGCCTCACCC 600 TCCCAAGTAG CTGGGACTAC AGGCTCATGT CACCATGCCC GACTCATGTT TTGTATTTTA 660 GTAGAGACGG GTTCACCATG TTGCCCAAGC TGGTCTGGAA CTCCTGAGCT CAGGCAGTCT 720 GCCCACATCG GCCTCCCAAA GTGTTAGGAT TACAGGCGTG AGCCACCGCG CCCGGTCCGA 780 GACAGAGAAT CTTGTCCTTG ACGGTGAGAC ATTTCAAAAT GCCCATCACA GTAAGCCAGC 840 CCCTCCCCCC AACAAACTCG TTCCCTTATA AAAGGAACAC AGGAAATAAC AGTCATTCCT 900 TTCTAAAAGG AATAATAAAT ATGTACAGCT AAAATTGCAT TCTTCAGGGG CCATGGCGAT 960 TAGATGAGAT TGTATAGAAG GAAAGTATGA CTTGAGTCTG GAAAGGTCAG GACTGTCACC 1020 ACTCTTCACT GACCTTGAGA ACAATTCCCA GCCCAGCCCT TCCTAGCTTA TAAAAACATT 1080 TGTGACCTTC CATATGTCAG TAGTGTTTCT GCTATCTAGT TGTTCATCTC ACTGGCGAAC 1140 AAGCGCGCAG CCTGTGGGAA GCTCCCAAGT TCCTCGGGCC CTTTTTGGAA GAGCTTCTAA 1200 GATATATGTT GTATGGCTGC CTACAGCCCA GGGGGAGTGC ATTTTTACAA TCATTAGCAG 1260 TGACCTTGTG AGGTGTAGGT GCTATTATTC CTGGTCCGGG GAGGAAATCA TGTGGTCGGT 1320 CCAGCCCTGG CTGTTAGGCC TGAGCCCACA CTCTGAGGGA CCTTTTTTGG AGCAATTTGT 1380 TTACATTTGC TTCTCACCAG ATAATTAACT AGTTAAGTGC TTTAGGATGC TTAGTTACTA 1440 GCTCCTTTGA AGCATTTCAT TTGTTTTCAC CTGGGATTGA CCTCCTGCCT CTGTAGCCTG 1500 CATGAGCTCA TAAACTGCAT CTGAGAAATT TGAACTCAGT GCTGAAGAGC CAAGCGATAA 1560 TCCTGCTCTC AGTTATAATG CTAAGAACAG TGACTACAAG TGAGATGCTG GTCGAAATCT 1620
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