Tag | Content |
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EnhancerAtlas ID | HS098-54651 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:37901120-37902430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr8:37901856-37901873 | GGGAACATCCTGTTCTG | + | 6.07 | NR3C1 | MA0113.3 | chr8:37901856-37901873 | GGGAACATCCTGTTCTG | - | 6.07 | NR3C2 | MA0727.1 | chr8:37901856-37901873 | GGGAACATCCTGTTCTG | - | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_28068 | chr8:37900877-37901802 | Fetal_Intestine | SE_29061 | chr8:37900885-37902282 | Fetal_Intestine_Large | SE_47750 | chr8:37901046-37901806 | Pancreas | SE_47750 | chr8:37902100-37902552 | Pancreas |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I038042 | chr8 | 37900502 | 37902690 |
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Enhancer Sequence | CCCAAAGTGC TGGGATAACA GGTGTGAGCT ATCACACCTG GCCTGAAGCC AATTTTCAAA 60 GAAACTGACC TATTCCCTCC CATGCCAGGG CCTCAGAGGG AGAGGCTGCC GATCGTCCCC 120 ATCTGGTATC CAGCAGCTTC ATAAGACCCC TGGCCCCTGA GAAATGTTGG GATCTTGGTT 180 CTCTTTGTGG AGGTCAGCGG TTGCGGGGCA GAGGTAAAGA AAAGTCTTGG ACTGAGTGTG 240 CTCTGCATCT CTCACCAGGA TTTCCACCCC GGCAGTTCTG TCCTGCTTGT TAAATAGACC 300 ATCCAGCCAG AAAAGCCACC CAGACACATG TGATTCCTCC CTGGACTGTG TGGCGAGGAG 360 GGAGGGAAGA CCGAGATTCT GGCATGTCGG CGTATTTACC TCCAGGTTAA CAGGGAGCTG 420 CCTCAGAGCT GGAGTTCAGA TTGTCCAGGG TGTTTTGCTC ACTGGCTGTT GGCTTGGATC 480 TGAGCAGAAG CATTTGGACC TCCCCCACCC CGGCCCTGTT GTGAAATGCT CTCCCTCTCC 540 CTGGAATGGG AACAGCAGTT CTAGGAATTC CATCCTCGTA CTCTCACTAA GCCTCACGTC 600 CCCACATCCA ATGGAAGAAT GCTTCTGCCA AAGGAACCCC AGGGGAAAGT GAGGGCCATG 660 CGCGGCTCAG TTTACAGAAG TCCTATCCAG CCGCAGAGTA TGGGCACTGG AGGGCTATGG 720 GGAAGCGCTC AAGGCAGGGA ACATCCTGTT CTGACAAGCA CCCAGAAGTC TAAGACCTCC 780 TAATTTTTCC AGCTGAGAGT GTTAGCTAAG GGGTGGTAGC CTGGTCTGCC TTACTAATTT 840 TATTTTATTT TGTAGAGACA GGGTCTCACT CTATCACCCA GGCTAGAGTA CAGTAGCATG 900 ATCCCAGCTC ACTGCAGCCT CAAACTCCTG GGCTAAAGCG ATCCTCCTGC CTCAGCCTCT 960 GGAGTAGCTG GGATCATAGG CGCACGCCAT CATGCCAGGC TACTTTTTAA ATTTTTTGTA 1020 GAGATGGGGG TCTCACTGTG TTGCCCAGGC TGGTCTCAAA CTCCTGGCCT CAAGCAATTC 1080 TCATGCCTTG GCCTCCCAAA GCATTGTGAT TGCAGGCATG ATCCAGCCTT GCTAATTTTA 1140 AACAGTAGGA GGCATTTAGG ATTGGAGTCG AGGTGGGTTA GGTTGGCCTC TGGACGGCTG 1200 TGAGGGGACA GCCTTTCTGG GCCTCAGTTT CCTCTTCTGC AAGGTGAAGC TCCTGCGTGG 1260 GGAGTTGTAA GGGGGAATAA GACCTAGCAC GTCAGGCTGT GAGCACAGAC 1310
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