| Tag | Content |
|---|
EnhancerAtlas ID | HS051-21908 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr5:73686700-73688130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr5:73686855-73686866 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr5:73686855-73686866 | TTTCTGGGAAA | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29084 | chr5:73687896-73693335 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I074390 | chr5 | 73686821 | 73693607 |
|
Enhancer Sequence | TCTAATCATT TACTGGAAAT TCCTGGGTAA TGTGCAGGAA AACCAACCTT GACAGAAAGA 60
TGATTGGTAC TGGACAGCTC CTGAAAAATA CAGTGAGGCT GGGGAGAAGG GCAGTGCCCC 120
AACAGCGCTA TTCCTGGAAG CCCAAGAAAT CACAATTTCT GGGAAAAAAA AAAAAAAAAA 180
GTATGCAGAG CAAAGCAAAC ACATGGGTTG CTGTATTTTG TGGTTGCCTC TTTTTCGCCT 240
TGGCTCATTT TTTCTATTGG TTATTTTTTT CTAACTGATT AGTAAAAGCT CAAAGCTTAA 300
CAACACCTGG CATTTACATC ACATTTTTTC CCTCTATTTG TTTGCCTTTC AAGATTTTTG 360
TGAAATTTTA TGACACATAG AAGTTCTCAT TGTTTGTGTG ATAAAGTATA ACAGTCATCT 420
TTTTTTTTTA ATGATTCTTG GCTTTGGTAT CTTGCTTGGA AACGCTTTTT CTACCCCCCA 480
AAACACCAAA ATTATTCACT CATATTTTAT TTAACCTATA CATTTTTATC TTTTATAATT 540
GTTAAAAGGA AAATTACAGA TAAATTAAAT TTAACAGAGT TTAACTGAGC AAAGAACGGT 600
TTGCAAATAG GCACCTCCCC CACCACCAGA ATAGACTCAG AGACACTCCA GCGCTGCATG 660
TGATCAAAGA GAATTTACAG ACAGAAAAAA AAAGTGATGC TAGAAACAGC CTGATTGGTT 720
ACAGCTCTGT GTTTGCCTTA TTTGAACCTG GTTTGAACTA TCAGCTGCCT TTGGTTGGCT 780
AAAGCTTGGC GATTTGTATG AGTAGGTTGC AGTCTGTTTA CACATCCAGC TGGGTTTCAG 840
TTCACTATAT ATGGAGGAAA CTTTAGACCA AAAGTCTCAT ATGTAAGGAG ACAGCTTTGG 900
GCTAAACTTA ATTTAACATA ATTATTAAAT TGATCGAATT TGTGTGTGTG TGTGTCATGT 960
ATGAGGTAGT GATATAAATG GTTTGTACCA ATTGGTTGAT CATTCTTCCC AACACCATTT 1020
ATAGATTTAT CCAGTCTTTT TTTTACTGAT TAGAAATAAT ATTTTTTTTT TTTTTTTTTT 1080
TTGAGACGGA GTCTCGCTCT TTCAACCCAG GCGGGGCTGC AGCGGCGCTA TCACTGCTCA 1140
CTGCAAGCTC CGCCTCCCGG GTTCACGCCA TTCTCCTGCC TCAGGCTCCT GAGTAGCTGG 1200
GATTACAGGC GCCCGCCACC GCGCCCAGCT AGTTTTTTGT ATTTTTAGTA GAGACGGGGT 1260
TTCACCGTGT TAGCCAAGAT GGTCTCGATC TCCTGACCTC GTGATCCACC CGCCTCGGCC 1320
TTCCAAAGTG CTGGGATTAC AGGCGTAAGC CACCGCGCCC GGCCTTATTG TATACCAAAA 1380
CAACACAAAT ACACAAGGGT ACATACATAC ATAGCCTTGG GTATGTTCTG 1430
|
