| Tag | Content |
|---|
EnhancerAtlas ID | HS145-06335 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr12:125092700-125094110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr12:125093263-125093274 | ATGACCTTGAC | - | 6.32 | | Esrrg | MA0643.1 | chr12:125093263-125093273 | ATGACCTTGA | - | 6.02 | | TCF7L2 | MA0523.1 | chr12:125093799-125093813 | GGACTTCAAAGGAA | + | 6.11 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09620 | chr12:125092318-125094236 | CD14 | | SE_23633 | chr12:125087499-125095065 | Colon_Crypt_1 | | SE_49901 | chr12:125091618-125098478 | RPMI-8402 | | SE_57235 | chr12:125091592-125093704 | VACO_400 | | SE_57235 | chr12:125093812-125097482 | VACO_400 | | SE_57418 | chr12:125091747-125093761 | VACO_503 | | SE_57418 | chr12:125093883-125095052 | VACO_503 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I124607 | chr12 | 125091939 | 125094677 |
|
Enhancer Sequence | ATAAAAAGAT TGTGAAGACC GAACAGTCAC CCCATACTCC ACGCCCAGTT TACCCTACTG 60
TTAGCATCTG ACATTAGTAT GATACATTGT TTAGAATTTT GTGGGGGAGG AGACAGTGTC 120
TTGCTCTGTT ACCCAAGCTG GAGTGCAGTG GTGCAAACAT GGCTCACTGC AGCCTCAACC 180
TCCCAGGCTC AAGCAACACT CCTGCTTCAG CCTCCCAAAT AACTGGGACT GCATGTGCAC 240
GCCACCATGC CTCGCTAATT CTTTTTGTTG TTGTTAGAGA TAGGGTTTCG TTCTGTTGCC 300
TAAAATGGTC TGGAACTCCT GGGCTCAAGG GATCCTCCAG CCTCGCCCTC CCAAAGTGCT 360
GGTATTACAG GCGTGAGTCA CTGCCCCGGC CCATTTTTCA CAATTAAGGA ACCAGTGTGG 420
ATACATTAGT ATCAACTGAC ATCTGCCTGT TTCAATCTCA CTTCTTCCCC AGGGCCCCAG 480
GTGGCATCTG TCTTTGGCCT TCTCGAGGCT CCTCCGAGCC TCTGGGCTGG ATAGTTTCTC 540
AGACTCACCT TGGTTTTGAT TTGATGACCT TGACAGTTTC GAGGCAGGTG ACCTTGACAG 600
TTTCGAGGCT TGCTGGTCAC GGAGCTGCAG GATGCGCCTG CATTGGGATT GGTCTGATGT 660
TTTTCTCATG ATGAGACTGG GGTGACGGTT TGAGAGAATT TTTCAAGCCA AGTGGGTGCA 720
GGAGACCCAT GAAGGCCCCT CCCGCTGATC TTTTGAGGAA TATGTATTTC TATCTGTGCA 780
TTTCTGCTTG TGTGTTCCTA AGCTACTCCC TGGAAGGACA CACAGACACT GGGAACTGAA 840
GATGCTTCTG GGGCGGGCAC GCGGGCCCCT GAAGACAAAG TCGGAGAGAT GCATGCTTTG 900
CAATGTGTGC CCCGTTGGTA CCGATTGAAA AAGTTATTTA ACTACACGTA TACGAGACTG 960
AACTGTGTGT GTACATTTTA AAATAAAACA AAACGTGCTT CCTGTTCTGC GGCCTCTGCC 1020
CCTCCCCTCG GCAGCCCTGA GGCTTGGCCA GGGTCCAGGA GGAAGGCGCG GGGAACAGGT 1080
TGGCCCAGTC AGCTGGCTGG GACTTCAAAG GAAAGCGCCG CTGGGGCCCA CCTGGGGCGC 1140
AGCGGAGCAC CTCCCACAGA GGGAAGGAAA TGCCAGCCCT GGGGCGACCT CAGAACATCT 1200
GCAGGGACAA GGGTGTGTCA GGCCACCTGG GCAAGCGCTT TACCTCTCTG TGCCTCGGTT 1260
TGCTCATCTG GGAATTGGGG ATGTTGAGAG CACCTGAGTC CCAGCACTGC TGTGAGGGTG 1320
AACGTGATCC TGAACGCCAA GGGCTTGGCT AGGCTTTTCA CGCGTGCTCT TCACACCGAG 1380
AATACAATCA AGCCCCACAC CCACCCCCAG 1410
|
