| Tag | Content |
|---|
EnhancerAtlas ID | HS043-15238 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr15:80126240-80127420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr15:80126317-80126331 | AAGACAAGATAATT | + | 6.61 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 80126748 | 80127217 | | chr15 | 80127254 | 80127387 |
| Enhancer Sequence | AGTTTGCTGC TACTAGCCTA ACAATCCTCT CAGGAATGAT GGAGAATACA CCTCGGAATT 60
GTCTGCCAAA GGGTTGGAAG ACAAGATAAT TTATCCACTG GCTTCTAATC CACACTGGCC 120
AAGCATTCAT TACCCCTTGA GGTGTTAACT ACAACACACT TCCAGGTTTG TACATGCACC 180
AGAATGACTG AGAAGGTCCT TGCAAGGGTC TCACTCAGAT GTGACATTCC AGGGCTGAAA 240
ATCATGCAGG TGAGGAGAAC TGCTGTCTGG CTTCACCTGT ATGCAGCCAG TCTGCTGTAC 300
CCAATGGCTG GAGGGAAAAA AGTGGTCTGA AAGGATGTAG GTACAGGACA AGGGGTGTCC 360
AACATGCACA TCCACGCAGG ATTTACCAAC AGAGAGCCAG AATGGCTCTT TAGTCGCCGC 420
CACCATCCTT CTCCAGGTTG TATTAGAAAA AAAGAGATTA AGCAGACTCT TTGAAGAAAG 480
AGGACTTATA AGTGTAAGGG TGCTGTGACA TTTTCCTTCC CCTCCCCACG ATTCCCTGCC 540
ATCACTCCAA GCCAAGTAAA GGCTGCTTCA GAGTATGGAA GTGTTTGCCA AAAGAGGAAT 600
CTACCTCCTG GCAGAATCAG ACACCCTGGT GCTACTGTTA GCTCTGGGAG GAGAGGAACA 660
GCAGTTCCTG GGAGAATGTG ACACGTGACT TCCAGCACTT GGGGAAGTAG CAGAACTCTG 720
ACAGTTGTGG ACTGTCTGGA GCAGCCCTCA AGAGTAGCAT GGGAGCAGGT GACACTTCCA 780
GTCTGGCGTG CAGCCAATTA CCTATTTAGT CGAGTAGTCA CCTCAAGTGG AACTATTAAT 840
AGACTCAAGT CATCCTGAAA GGACTTGGTC AAGAAGGCTG CCACTGGGCT AGGGAACTTC 900
AGGAGTGTGC TTCTGCAGGG CAGGATCTGA GCGGAGACTG TCAGAAGTAA GCTAGAGAAT 960
GGTACAATAC ACACAGTGCC AGCAGAGGTT CTCCATAAAA ACCACAAAGG AAATCTAAGA 1020
AAATCCACTG GGCATTTGAC ACACAGAAGG CACTGATGGC CAGGTTATAC TAGCACTGAT 1080
TCGAGGTGGC TTTGCCTTTC TCCTTGACTG TCAGAACCTT CAAAGCCATT AGACAGGTTG 1140
TGGAGCAAGG AAAATGAAAT TCTACACCAA GACTACGTCT 1180
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