| Tag | Content |
|---|
EnhancerAtlas ID | HS129-00894 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:38582760-38584230 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr1:38583486-38583504 | GGCGTGCCTGAGCATGTC | + | 6.36 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I038117 | chr1 | 38583122 | 38583462 |
|
Enhancer Sequence | ACTTACCTAC CTGAAAGATA TGGAATTTGG AGCAGGAACC TGGGTTCCAG TCCTGTCTGC 60
TCCCTTGATT AAGTTACTTA TCCTTCCTTG GCTCAGCTTC CTAGTATAAA GCAGGGAAAA 120
TAAAACCTAT GTCTTTGGGT TATTGTAAAG ATTAGGCAAG GGAAACTTAG GCAAAATCTC 180
TTTGTCATCT GAGAGGGGAT GTCCATTTAA TTGGCATGTC AGTAGGGCAG GCATATTGTC 240
CATTTCACAG GTGAGGAGCT TGAGGCCTGG AGAGGGTGGA TGACCTGAAG AAGAAGCTGG 300
CAGCATCACC AGGCAGGGCT GCATGGCAAC TGGGGCTGCT TCTCTCTCTG CCACTACAGG 360
ATCCTGGCTC CCTCACACCA CCCCCATGCT GATGCCCCAC ACGGGCTGCA ACAAGCCCTG 420
CTGGCCTGGC TCCATTTCTG GGTGTGAAAT TTGGCTGAGT CGGCACCTGG TAGAATGGAG 480
CAATTGCTAT CCTGGAGCCT GGGGCCTGGG ACAGGGCCAA TGCGCAGACC AAGGGTTGAT 540
GGGCGGATCT GACCAAGGGT TGGTGGGTGG GCCTGGCGGG CTTGGCCAGG GAACTCGCCA 600
AAGCTGGGCA GCTGGCAGGA GTGGGGCAGG AGAGGGCCTG GCTTGAGGAC AGCCACTCAG 660
GGAAGCTGAG ACCCAGGGCC TAAGCTCAAA ACAGAGCCCA GCAGCATGAG TGTCTGCCTG 720
GTTGCTGGCG TGCCTGAGCA TGTCGGCCGG TGTCTCCGAG CTTGTCTTTG TGTGTGTGCA 780
CGTGTCTAAG GGTATGCTGG GTGCGTGTGT TCTTATAAAT GAGTGTGCAT GTCTATCAGT 840
GCAAGAGCTG GTGCACCCAT GTAGTTGTGC ACATCTGTGT ACCAAGGTGT GTCTGTGTCA 900
GTGTGAGCCT ACACATCTGT GTATAAGCAA ACTTCTTGCA TGCATACATC TGTCAGTATC 960
CGTGTGTGTC TGTGCATTTC TGCCTGTATC TGCAAATGTC TGCTTGTGCA CTGTCCATGC 1020
AGGTAGGTCC ACACTGGTGT GTGTCTGATG ACCTCTGTCA GTATCTGCGG ACATGAGTCT 1080
GTGCTTTCTG TTAGCATCTG TGCAAGTGTC ATCTACGTCT ATGAGCATGT TTGTTCTTTC 1140
CAGTGCCTCT ATGTGTCTTG TACCTGTATG TAAATCTGTC CATGCCTGTC GTGAGTGTCT 1200
CTGCAGCTGT GCCTGTATGT TGGTGTATTT TGCAGTGTGT ACATCTAGTG AGGGTATTGG 1260
TATTCACTTC AGGATGCAGG CATGGCTGTC TCAGGGTGAG CAGGATGGAA TCTTCCCTGT 1320
GTCTGCAGTG GCTCCCGGTC ATCACTTCCA TCTTTGCGCT GTGGCTGAGG CCTCCTGGAC 1380
TCTCATGTTC CTTTCCTCTG CTTGAAGGGA AGCTTTGCTC AAGGTTTCCC AGGGTGCTGC 1440
CTCTGACAGG ACCAGGCCCT GGTGTCCCTG 1470
|
