| Tag | Content |
|---|
EnhancerAtlas ID | HS007-07656 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr18:33614830-33616250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr18:33615270-33615282 | GAACAAACAATC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr18 | 33615027 | 33615304 | | chr18 | 33615993 | 33616094 |
| Enhancer Sequence | CATTCTCGAG GAGCAACCAG AAGCCCAACC TTCTCATATA CTAAGTCACA ACTGATCAAA 60
CTTTACAAAC CTGTGCCATG CCACTGTATA ACCTGGTTTG TCTGTTTAAA TTGCTGTCTA 120
CCACTTTTCA TGATTTTGCA AGTTGCTGGC ATGGAATAAA AATAAGAAGA GATGGCTATA 180
ACAGAGACCA GCTTCTGGTT TTCAGGCTCC TTGTCTGGTT AGATAAACCA CAGTGTACAA 240
CTGGTTAAGA TATCGGGACC CTATCCTAAC ATTCAGTCCT GTCTCTTTTG TACCCATCCT 300
TGCCCTCTCA ATCCCACCCA CAAAATAGAT TGGTATTGTT CAATCCAGAT TTTTGCCTTC 360
CCAGTGTCAA ATGAGTTTAG AAACTCAAAT TTGTATTATC TAATTGGGAG ATTGCCTGCA 420
TCACTTTTGA ATGGGTACCT GAACAAACAA TCCTTTCACT GCACTTTTAC TATGTGCTAC 480
ACACTATTCC AAGCACTTTA CATACATTAT CTCAATCCTA ACAATATGTC TCTATTTGGC 540
AGCTGAACAA ACAAAGCCAA AAACATTATT TGCCCTCAGG GAAATAATGA GGAAGAGATA 600
AGCCAGGATT GGAATCCAAA AAGTCCAACA GCCAAGCAAA TCCCTCTTAA CAACTAGACC 660
ATGCTTCCTG TCATAATTAA AAGGGCATGT TAATCTTTGA GACTCAAAAG TAGCAACTGA 720
AAAGAAGAAA AAGATAAAAC AATGCAAAAC AAAAAGTAGC AACTGAAATA AAAATATTTT 780
ACAATGTTAG CAGCATTATT CACAATAGCC AAGAGTTAAG AGCAACCTAA CCCACTGATC 840
AATGAATAAA CAAAATGTGA ATTATATATT CAATAAAGTA TTATTCAGCC TTATAGAAGA 900
AGGAAATGTT GACGCATGTT ACAACATGGA TGAATCTCCA GGACATCATG CCAGGTGAAA 960
TAATCGAGTC ATGAAAAAAG ACAAACCACT GTATGATTCT ACTTATTGGA GGTACTCAAA 1020
TTCATAGAAA AAAAGAGTAG AAGGATAGTT GCCAAAGGCT GTGGGAATGG GAGGAGAATA 1080
GGAAATTATT CATGGGTACA GAGTCTCAGT TTTGCAAAAT GAACAGTTCT GGAAACTGGC 1140
TACACAACAA TGTACTTAAC ACTACTGGAC TGTACACGGA AAAAATGAAG ATGGTAAATA 1200
ATATTTATTA CCACAAAAAC AAAAAAAATG TTTTTGTTTT TTTTGTTTGA GACAAGTTCT 1260
GTCTCCCAGA CTAAAGGCTC ACTGCAGCCT CGACCTCCTG GGCTCTAGCA ATCCTCCTGC 1320
CTCAGCTTCC AAGTAGCTGG AACCACAGGC ACACGCCACC ATGCCTGGCT AATTTTTTAA 1380
ATTTTTTGTA GAGATAAGGT CTTACTTTGT TGCCCAGGCT 1420
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