Tag | Content |
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EnhancerAtlas ID | HS129-00498 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:21475770-21477200 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr1:21477128-21477146 | AACTTGATTTCACTTTCC | - | 6 |
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| 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 |
GH01I021148 | chr1 | 21475116 | 21479692 |
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Enhancer Sequence | AATTCCTTCA AGGAAATTTA TCGAAATACA TCAATGAGTT AGAGTTATGA GTAAACTGTT 60 ATTCTTTTTT TTTCCCTGTA TTTTCCATAA TGATCACATA TGGCTTTTCT AGAGAAGGGG 120 GGCTTTTCTG TTTCTCAAGC AAAAAAGCCT TTTCTCTTCA TCACACTGAA AGAGAAATGA 180 ATGAAGTACT GTGTTACTGC CTATCCAGAT ATACGGTATT TTACTGGTTG CTAAGCAGCA 240 GATCCTGGTG TTTTTACATC ATGCCTATCT CTAGTCACAG GCAGAAAGGA CAGGAACTCA 300 GGCACAAACT CACCCCATCC AAATGGCAGT GTATTTCCTC TTGGGAGTGG TCCAAAGAGC 360 ACACACAGCA ACTTTAATTC TCTACTCAAA CCACTCCCCA TCTCTCACCT TAACATACCA 420 AGCAGATTTT TTATATGGAA CAGTATTCCT CACACAAGCT GCACGAAAGG GAAGACCTTT 480 TTAATCCTCT ACTATATGCC ACCCACTCCA TCTCTGAGAG ATAATTCGCA TTTAAGTATG 540 TTCACCCACC AAGCTAGAAA TCACCATCAT TCTGGACATG TATCTGTCAT CAACTGACAC 600 AGACAGGTAA GCCTTGCTGC TTTCTGAAAA TAGCCAATCC TGCTCAGTGA ATGACAGCAT 660 CAGCTAAGAT TTCTTCTACT GCAGAGAATG GGTGGGTCCC CCCACTAATG CTGTAAATTC 720 CAATACTCAG TGTCATTCCC TCCAAACAGC AGAATCTACA GTATGGAAAT TCTTCCACAA 780 GAAAAGCCCA ATTCTTGTGG CCACAACCAT TAAGAGAATC CTGAGCCAGG ACATTCTCCC 840 CAAGCTTCCC CTCCTGCTTC TTCACAGGAA CCACAGCAGC CAAGTCCTAT ACTATGCCCG 900 CCCCTGCTGC AGCAGCAGCC ATTTTTGGCT CAGCCCTGCT GCAGTCCCAG ATGAAAGCCA 960 GGACGGCAAG GACAAGATGG CAAAGGACTT TTAAAATGGA AACTCTTAAC AAAAATAACA 1020 ATGAAGCAAG CATCATAAAA AATGTTGCAA TAATATGCCA TGTCATTTAA AATAAGGCTT 1080 TAAAAAAAGA TGCCTATATT CAAGTACTTT AAACCATTTT TCATGGCGTC ATGAAAAATT 1140 TGAGGGAACC TAATTCATCA CAATGTGAGA TCAGCACTAT ACTGACACTA TGGGGAAAAC 1200 AATGCTTAAT GAGTTTAGTT TTCTACTCAA CTAACAGTTA ACAACAACTC CCTTGATTCC 1260 TGTGGAAAAT CTAAACGCAT TTCAAATTCC TCTTCACTCT CTTAAAATAA TGTAATTTAA 1320 TCTTTGCTGA ATGAAGAGCT CACAGAGAAT CAAATTTTAA CTTGATTTCA CTTTCCAAAA 1380 TAGAAGTAGC TTTACTTTGC TAATTATAAA AATAACTGGC CGGGTGCGGT 1430
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