| Tag | Content |
|---|
EnhancerAtlas ID | HS094-00451 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:24620510-24621980 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:24621502-24621520 | GCAAGGCAGGAAGGAAAC | + | 6.2 | | ZNF263 | MA0528.1 | chr1:24621321-24621342 | GGGGGAGGGAAAGGGAGGGAT | + | 6.04 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26668 | chr1:24619434-24622898 | Esophagus | | SE_35109 | chr1:24619287-24622930 | HeLa | | SE_36021 | chr1:24619590-24622512 | HMEC | | SE_64493 | chr1:24619475-24622503 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I024293 | chr1 | 24619544 | 24622505 |
|
Enhancer Sequence | CGGTATTATT TCCCCCATCT TACAGGTGAG ACTCAGGAAG GCAAAGTGAC TCACCCTAAA 60
GTATGCGGCC AAGACAGTCT CCAAGGACTT TCTGGCTCTT TGGCCCGTGA TCTTAACCTC 120
TACCTGAGTT TGTATCAAAT ATGGCACCAA AATGTGGTTG TAGTCCTACA GTTAGGGAAC 180
TGGGCCCCGA GTTTGGCCAT GGCTCTCACC CTGTGCGATC TGGGCAGTCA CGTCACCTCT 240
CTGAGCCTAG GTTTCCTCTT GAGTTTAGCA TGAGGGCCGG AGGAGGAAAC GTGTGTGTCT 300
ATTAATGCCT GGGATGGATA AGGCTCCATA AGGGTCAGCT ACCATATTCT TTTGCTGTTG 360
TTGGTACTGT TAGGCTTTAT TGGTGGAGTG ATGAAATCAC CGTCTACACA GACACAAACA 420
TCAGGGCATT GGGAAACCTC TTCGTACTGG ATGTGCCACA GGCGAGATTT GATCATACAT 480
TCTCCAATTT CTTCCAGATC CTGAGTCATG AAAAGGTGGG CTGAGTCATG CCTGGGGCTT 540
CCATTTTGCT TATACTGAGC CATTACGTTG TGAAATCTTT AGTAAGTAGC AGGAGCTTTA 600
ATGGAAAGCA AATTAAACTC ATCCCCCAGT TTGCTGGGGG TGTGGAAGCC CGTCCGGGAA 660
GCTCATAGTG ATCATAGCAT GGAGCCTGGA GCTCTTGGAA GGAAAGGGGT TTGAGAAGTC 720
CTAGGTCTTC CTCCCCGCCT TTCCTTTTTC TTTTTAATAA TGTGTTTTCT TCAGCCTGTG 780
ATAAATGACT GGGAGTGGAA GATGCCCAGT AGGGGGAGGG AAAGGGAGGG ATGTTGTTTA 840
CTTATCTGGG AGCACATCGC CAAGACAAAG CTTGGAGTTC TAATACTCTC CAGTGCGTGA 900
CCCACTTCCC TCTGTGGCCC AGAGCAAGTA TCGCCCTGAT TTGCTGGTGA CTCTGCAATA 960
ATCACCTCCC TCAAACTTCC ACACCTCTCC CAGCAAGGCA GGAAGGAAAC ACCACGCCTG 1020
GCCTTGGGCA ATCCCAGGGA CCAGCCAGGA TTCCATTAAC CCCAGAAGTG AACCCTGGAT 1080
TCCATTGGTC AGGCCCCACC CCCCAACTTC GTTGGGCTTC CTTGGGTAAT TTATGAGCTT 1140
CTCCACTTTG GCTGTTATTA TTCGCCTCTT GTTAATGAGC AGGCTTAGGG CATTCAGGAT 1200
TTCCTTAGTC AGTGATTCCT CCTTCTGGAG TAGTCTGTCT TTGGACTTTT ATAGGTCGTT 1260
AACAGCCTTG CAAAGTCTGA CACTGTACCA GGCAACTGGG TTTCTTTACT GGAAAGGAAA 1320
AGGGGGAGGC TGAGGGACGG ATGGAAGCTA CTTCAGGTCA AGGGGGGCTC TTGCTCACCA 1380
CAGGACATAA GCTCACCATT TTCTGTCCCA AGGGGACAAA CACGACACAC GCGGCTACAG 1440
GGGACTGAGG AGATTTTGTA TCTGCATTCA 1470
|
