Tag | Content |
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EnhancerAtlas ID | HS105-49749 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr20:32652640-32654100 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr20:32653667-32653679 | ACTATAAATAGC | + | 6.11 | MEF2B | MA0660.1 | chr20:32653667-32653679 | ACTATAAATAGC | + | 6.74 | MITF | MA0620.2 | chr20:32653170-32653188 | GCAGGTCACATGACTAAG | + | 6.16 | MITF | MA0620.2 | chr20:32653170-32653188 | GCAGGTCACATGACTAAG | - | 6.16 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_10041 | chr20:32648369-32652819 | CD14 | SE_18636 | chr20:32648578-32655130 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I034064 | chr20 | 32652661 | 32654294 |
|
Enhancer Sequence | TTATCCTAAT TCTGGGAGGT TGGTATAATT TCCGTTTTGC AGTTGAGGAC TCTGAGGCCC 60 AGCAAGTGAA AGGATATGGC CACAGTTACA GTTTCAAGTG ATAGGTCTCG GATTGGAACT 120 CAGTCCTGTC GGACTCTAGG GCCTGAGCTA TTTTTGCTAT TTCATGTGCA TTTGTCCTTT 180 GTTACTAAGA AATCGTTTTT AAAAAACAGG TTCCCAGAGA GGGGGCTTCT TGAAAAGCAA 240 GTAGAGCAGA AGACTGGTGA GCACGGTGTT TCCCAGCATC TCCACAGTGC CAGCACAGAG 300 GAGGACACTC AAGAAATGTT TGTTAAGTGA GTGAAGGAGA TAGGAAGTGG GTAATAATAG 360 AAATTGGCAT AATCCATATT CTTTGATAGT ACATTACAGA TGCAACAGAG CGCTTTCACA 420 TCAATTAGCC TATTTGATTC TTGTATCAGA CCTGAAAGGT AATCAGGGAA GAGATTATTT 480 CTGTTTTCGG ATTAAAGACA AGAAGGCCTA GGGAAGTTAA ATGACTTGTT GCAGGTCACA 540 TGACTAAGAA CAGCAGAGCC AAGGCCAAGC CTTCTGGACC TGTAGCCTGC ACTGCTTACA 600 CTTCACCCAT CCAGGAGCTT TTGCTGTTTG ACATGCAGGG AGCTGACTCA TGAGAGTGGG 660 AATGGTCAGG AACTAAAGAG CATTCCTTGG GAAATTAGTC CTGTCTGGCC AGTAACAATC 720 ATTTGGGCAC TGCTAATGAA CCAGGGCTTG GCCAGTTTAA TGAGATTAAT AGATGTTCTG 780 TCATCCCTGG CCGCCTGGTA AAAGCAGGAG CCTCTGGACC AAGGAGGCCC TGGACACTGA 840 TGAGTCTAAT TGCTTGACTT TCTCCAGAAA TAGTCTTCCC ATCACTAGTA GCTGTTTTCC 900 TTCTGAACCA CCCGGATGTC CCCAGGGTTA TCTAAGGGCA GAGAGCTGGC CACAGGCTGC 960 TGTGACCCTC ATCCCCATGC AGGAGAATAA GGCCAGAGGG GTCCAGCAGG ACTGAACCAA 1020 GACAGAGACT ATAAATAGCA TTGGGGGCAT CAAGACCTAA AGCAGCAGCT CCTCCCTTGA 1080 AATGAGTATT TCAGGAGGAA GAGATTTAGT GCTGGGGAGG ATTTACAGAG TTCTCTGAGT 1140 GCCTGAGACT AGACTTGATC TGATAGGATT TGGAGCACAT GAGGGGTGAC ATGGCAGAGT 1200 TTTAGAGTGT TAAGACAGCC ATTGAGACAG TGGAATGGAG AGTGTCGAGT AAGAAGCCTT 1260 GATTCAGGAC CCCTAGCTAC ACTCCCCTCA CCAGCTGGTT GACCTTAAGT AAGTCACTTA 1320 TCTTTGCTGA TCCTCTTTTT TTTTTTTTTT TTTTCATTTA TAAAATGGGG CGGGATGGGT 1380 GCAGTGGCTT ATGCCTGTAA TCCCAGCAGT TTGGGAAGCA AAGGAGGGTG GATCAGGAGT 1440 TCGAGACCAG CCTGACTAGC 1460
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