| Tag | Content |
|---|
EnhancerAtlas ID | HS043-04090 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr1:227107330-227108800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr1:227108639-227108650 | AAGTAAACAAA | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 227108144 | 227108613 | | chr1 | 227108126 | 227108648 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I226918 | chr1 | 227106400 | 227109773 |
| Enhancer Sequence | CTAATGGGAC CGGATGGCTC AAGAGCTTTT GAGAACACTG GTGTCCAATA TTTCATTTGA 60
AGTTGTTGAG TAGATCTCCT CCACTCCCCT GAGGGGTTGG TGCCAGGCTG GACAGGGACA 120
GCACACAGAT GGTGAGACAG CCCACAAGCT GAATTCTCCA CTTGCAGAGG CTGAGAACCA 180
GCGATGACTG TAAATGTGAG TCTCTGCCCG CCTTCTGCCC TGGCCTCCCT CCTGAGAACT 240
GGCCAGACTT TTGAGGAGGA ATTTAGACTT CCAAAGGGTG GAGAATAGAA GTTTCATCCA 300
GTCTTATCTA GGGAAGCTCC CGCTGACATC CAAATTACAT AATAAACACG GCCAGTAAAA 360
TACTACTGCT ACTACTATCA TAAAATAAAA TAAGGAATTA AGTAGATAGG TCAGGAATTT 420
GGCCCCTTAA AACACTGAGG CCAGAGAGAT TACACAGTGT GCCTCAGGGA TGTTTTGCTC 480
TGTTCTCAGG TTATCTGGCT CCTATTCCTT GTGTCCTCAG TCCTTGCCTG GGAAGAGAGT 540
GCAGTGAGCA GGGTAGCTCC TCACCCCCTC TCCTCAGGTA CCAGGTGCTC CTGGGCCCTC 600
AAGGGCTCAG CTCTTCCCTC CGCAGCTCCT GCAGGGGCTG TTGGGTTTAT CAGAGACTGG 660
TTCTGTCAAA GAGCTGAGCT CAGGGGAACA TTTTGGGGGA GTGAGGTTCC TACCACCTTG 720
GAGATAGCTT TTTCCAAACA AGGGGAAGCA TTTGAGAAAT ATGTTCATTA GTAAGTTCGT 780
CAGTGGTCAT AAAGATATTT TGTCTGATGG CAGAAGGCCT GAATCTTTGT TCCCATAAAA 840
GACTTACTCC TCTAACCAGA AGAATAAACG AAAGGTGGTG AGACACTGGG GACATCTGGG 900
CAGCCATGGA GAAAGAGTTT GTGGATCTGA CCCACTGTTC TCCTCTTGTC CAGATAAGGA 960
CGTGTGTTTG TGTGTTGACT GGTGAGGACA GGAGGAGGTT TCCTGAGTGC AGAGTGCCAA 1020
AGCACAAAGC CTGAGATAAA AAGGCATAAA TAGACCTAGA GCCTGACCCA GAGCCAGGCC 1080
CAGTGTCCTT GGGCTGGTAG GACTTGCAGG CCAGGTCCCA GATGGGGAGG GGGTACTGGG 1140
GCTGAGCAGC TGCTATGGAA ATTTCCATGG GCTGTACACC AGCTCTTGGT AAGCTCTTGC 1200
ACTCAGCATG GCATGGGGAG GACATGGGTT ATGAAAGAGG CACAAGACTT AGTCCAAGCT 1260
TATAAGGAGC TAGGCCTCTA GAGAAAAAAC TCAGGCTTGC CAAAGCAGCA AGTAAACAAA 1320
CAGGTTGGAA AATTTTGAAA CAAAGTTGTA AATAAGGTCA AGGCATGGAA CCAGTCAAGA 1380
AAAGTCAATA TCGTATTCCA GTTATTAGAA CCTCATTTCA CCTTCTAAGG ACAATGTTGA 1440
AAATACAAAC TTCACATTAA GATAAAAATG 1470
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