| Tag | Content |
|---|
EnhancerAtlas ID | HS129-03709 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:228197880-228199320 |
Target genes | | Number: 26 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:228198190-228198201 | CCACACCCTCC | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGAGACCATG GCTCCATCTG AGAACAATCC CCAGGCACAC CCGCACTCCA GGGCACTCTG 60
AGCACCTCTC CCTTCTTCCC ATGTCTGGGT TAACGGAATC TTGTCATCTC CCCAGGGACC 120
CCACCAGGAC CCTAGAGGTG GGCCTGTGCC TCCCGCCACC GCCTCCCCAG GGTCCAAGCC 180
CACTTCAGGG CTTGCAACTG GATTTTGTTC ATCTTTCAAG TCCCTCTGCT GCCTTTACCA 240
GACTGGGCTG TGGCACTCCC GCCACGGCCA CCTCCTGCTT CCGTTCTCAG TCCTGGCCCT 300
CCCCTGGGAC CCACACCCTC CCAGCCACCT GGAGTTGCTG CCAGGCCTGG CCATAGCCAC 360
CGTCGCTGCC TAGTGGAGCA CAGCAAGCTC CACCCCTTAC CCAGCCCTGC TCTCCCTCTC 420
AGGCCGTTCC TTCTGCCCGG CCGTCACCAG CTCCTGCTGG ACTATGGGAT CCCAAGCACA 480
GAGGCCTGGC TGCTTGCAGA TGGCCACCCC AGTTGTCCCA GCGAAGTGCA GTGTGGGCTG 540
TGTCCAGCCT TTTGCCTGCC CCTGGCCTGC TCCACAGCCT CGCTCATGCT CCCTCCAGGG 600
TCTCCCTCAC ATCCCTCTGG GCCTCGAGCT TGTCACTATG ACAGAAACAC ATCATGACCT 660
CCATTTTTAT AGGGCACCTC ACACAGCCCT CAACAGAAGA TGTAGGCCCT TTCAGGCCCC 720
CACTCTCCTA CACACTCATG GGTGCAAACA ACCTCCTGGG CACAAGAGCT CAGCCCCTCC 780
TCCTAGCCCT TCATGGGCTG GAGGGCCAGC ACACTTGGAG GCCCTGCTCA GCCAGTGTCT 840
GCACTGCACC ACCGCCAGGC ACTTCGCCCC TGTGTCCTCA GTCCTGGTGG GCCTCATTGT 900
GGTGGGGAGA CAGCCTGACT GGAAGAGGGG TCGGGTGAAG AGGCAGCTTA GAGAGGCAGG 960
AGCCAGGAAA GGGTGCAGGA GAGAAGGAGC TCGGCTGGAA TGATGGGTCA GGCATACGTG 1020
TGTGGTGTGT GGGCAGGTGG CTGCAGCATG GGTGTTTCGG GGACTGAGAG GGGCCAGTCG 1080
AGCAGGGCAG GGACATGGCC CAGGGTACCC AGAAGCTCAG ATGGGAAGGG CCTTGTGATA 1140
GGAGGGATGG TTGCCACTCC CAGAGTCACC CTGCCTCCAC ATTAGCCTGC CACTGGCCCA 1200
CTCCCTCTGC AGGCCTGGCC TCACCCTAGC CCCTTCTTCC TTCTCCCTTC GCCCGCATCT 1260
GTCTGTGTCT CTCTGTCTCT GTTTCTCTCT TCCCTGCCTC TGTCCCTCCA TATCTCCATA 1320
CCTTTGTCTC TCAGTTTCTC CCTGTCTGTC TCTCTCTCTT CCCTGTATCT GTCTCTGCCC 1380
GTCTCTGTCT CTATCTCTCT GTGTCTGTCT CTCTCTTTCA GTCTTTGTCC TGTCTCTCTC 1440
|
