| Tag | Content |
|---|
EnhancerAtlas ID | HS129-05375 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr10:101519470-101521250 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr10:101519713-101519729 | CACTGAGTAAACATTC | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34343 | chr10:101517664-101522120 | HCT-116 |
|
Enhancer Sequence | ACATGAGACT TGGTGGGGGC CAAACAAACC GTATCCAAAG CATAGTATTC TGCCCCTGAC 60
CCCCCAATCC CATGTCCTTC TCACATTACA AAATATAATC TTCCCATCCC CAAAGTCTTA 120
ACTTGTTCTA GCATCAATTC AAAAGTCCAA AGCCTCATCT GAGACTCAAG GTAAGTTCCT 180
TACAGCTGTG AGCCTATGAA ATGAAACATA TTATTTGCTT CCAAGATACA GTGGTGGTAC 240
AGGCACTGAG TAAACATTCC TGTTCCAAAA AGGAGAAATC AAAGAAAGGG GGCAATAGGC 300
CCCGTGCAAA TCTGAACCCC AGCAGGACAG ACATTAAACC TTAAAGCTCT AAAATCTACT 360
TTAACTTCAC ATCCTACAAC CTGAACACAC TGGTGTAAGG AGTGGGCTCC AAAGCCTTAT 420
GCAGTTCTGT CCCCGCAGCT TTTCTGGGCA TGGCTCAAGT GAGCTGCTCT CATGGGTTAG 480
AGTTGAATGC CTGTGACTTT TCCAGGCTGA GGGTGCGTGC TGTTGATGGT TCTACCATCC 540
AAGGTCTGGA GGGCAGTGGC CATGTTCCCA CAACTCCATT AGGAAGTTCC CCAGTGGGGA 600
CTCTGCAGGG GTTCCAACCC CACATTTCTG CTTTGCATTG CCTTAGTAGA GTCTCTGTGG 660
GGACTGCCCC TGTGGCAGGC TTTTACCTGG GCACTCAGGC TTTCTAATAC TCCTCTGAAA 720
TCTAAGTGGA AGCTGGCAAG CCATGACTTG CATTCTGTGT GCCTGCAGAC TTAACACGGA 780
AGTTACCAAG GCTTATAGCC TACATCCTCC AGAGAGGCTG GAGCCAGAAG AGCTGGGATG 840
CAGGGAGCAG CATCCTGAGG CAGGAGCCAC ACAGCAGCAG CACCTGGGAT TGTCCCTCAA 900
ACTATTCCAT CCTCCTAGGC CTCTAGGCCT TTGATAAGAG GGGTAGCCTT GAAGATTTCT 960
GAAATGGCTT CATAGCCTTT TTCTCATTGT TCTGACACCT GGCTCCCTTT TATCATTGCT 1020
AATCTCTCTA GCAAGTGATT GGACTCGGCT AATCCAATAT TCTTGGATTC CTCTCCTGAA 1080
AATGCCCTTT CCTTCTCTAC CACACGGCCA GGCTTCAAAT TCGCTAAATT TTTATTCTCT 1140
GCTTTTAAGT TCTGACTTTA GGTCATTCCT TTGTTCACAT ATTTGATTGT AGGTTGTTAG 1200
AAGCAGCCAC ACTTTGTTTT TTTTGGAGAC AGGGTCTTGC TCTGTCACCC AGGCTGGAGC 1260
AGTGGCAGGA TTATGACTCA CTGCAGCCTT GATCTCCTGG GATGAAATGA TCCTCCCACC 1320
TCAGCCTCCC AGTAGCTGGA ACTACAGGCA CATACCACCA CACCCAGCTA ATTAAAGAAA 1380
AAAAAATGTA AAGTTGGAGG ACTCACTGTG TTGCCTAGGC TGGTCTCAAA CTCCTGGGCT 1440
CAAATGATCC TCCTGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACCATG 1500
CCTGGCCTCA CCACTTATTG AACGCTTTGC TGCTTAGAAA GGCGTGGCCT TTACTGTCTG 1560
TATTTCTGTC AGCACTTTGG CCACAACCGC TCACACAGTC TAATAAATCC CAAACTTTCC 1620
CTTATCTTCC TGTTTTCTTC TGAGCCTTCT AAACTCTTCC AACTTTTGCC CATTACCCAG 1680
TTCCAAAGCC ACTTCCACAT TTTCAAGTAT CTTTATAGCA ACCACCCTCT CCTTGGTACC 1740
AGTTGTCTTC CTTAGTTCAT TTGTGTTGCT ATAAATGCCT 1780
|
