Tag | Content |
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EnhancerAtlas ID | HS054-00218 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr1:53513610-53515170 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr1:53515006-53515021 | AAGATAAAAATAGCA | + | 6.53 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 53514320 | 53514470 | chr1 | 53514656 | 53515144 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I053046 | chr1 | 53512461 | 53514419 |
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Enhancer Sequence | TAAGTATGAT GGAGCTTATA TCCTGCTAGT AGGTAGGTCT TTCAGCCCTT TCTACTCCAT 60 CTCCTGACTC AGACTCTAAA GTGCAAAGTG GTCAGACTCA CAAAACTCAG TGTTCCCCAA 120 ACAGTTGACA GACGTCTGTG GAGCAAGCTG TGTGCCACAC ACTGTCTTGT GTGCTGGAAG 180 TGCCCAGAAG AGTAAGAAAG TTCCCACGCT CAGGGCATCC ACAGATGTGT AAAAGAGTCA 240 GTGCAGCCAG AGATCCAAGG TGCCACACCT GGCTTGTGGT CAGGGGAGGA TGAAGGCAGG 300 AGCAGCCATA TCTCTCTGGG CCATCAGGGA GAGCACCACA GAGGAAGCAG CTCTTGAGCT 360 TAGTACCCAG GCGGAAAGTA GGAGTGTTCC AGGAGGAGGG AGGGGTGGCA TGAACAAAGG 420 CCTGACCTTT TACATTCCAT TTATTTGCCC ATGCTCTTCT TTTTGCCTGA CCTGTCCTTA 480 CCTGACAAAT GACTTGTCTT TCAAAATTAG CTCAGATATT ATCTCCAAGG ACCTCTTTCC 540 AAGTTGCTGG GGAGCTGTAA CCAGTCCCTC TCCTGAGCCA CGTACTGGAC TGCCAGCTTA 600 GTGCCTGTTG TGTTATGTTA GTCATAATAT GCCTCTCTCT CTTCCCTGTT AGGCTGTGAG 660 TGTCTCAAAG CATCAAAGCA CATCTTATTT GTCTTTATGT TTCCAGAATT TAGCACAGTA 720 TCTGATGTTT TTAGGTATTC TGTAAACAAC TGTTGGACTA AATTGCATTT GTCTAAAGTG 780 TGTTTATGCC TTGTATAGAT TTTCCTAGTC CCCAAATTGT CAAGGGTCCT CTTAGGCTCT 840 TCAGCTGCAG TGTTGAATGG ACTTGATATA GTGAGCTTTC TGTCAACTTG ATATATACTG 900 AGCTTTCCAT TAATAAAAAA GAAACTAAGA CGTTTCTTTC CAATGTAACT TAATTTTTTC 960 TGTTGTCTCA GTCTGGTTTG TTTTAGGTTT TATTCCTGTG GTTCTCTGGT AATTTCCAAG 1020 ATTGGATAAA ACAACTAAAT CTCACTCCCA CTTGCTTTTT TAAAATGCTT TTTCTACGTA 1080 ACCAAGCACA TTTTAGTTGA TGCCATGACA AGTGAGAAAT TTGCATCTGT GATGTTTCAG 1140 CTGAATACAC ACCATTGGCA CTGACATTTC CACTGAGCCT GCTCCAGAAA TCTGGACAGA 1200 ACAGAGGCCA CCAGTATAGG AGCTGGCTGT CATCCTCCTT CCCACCCACT GCACATGCCA 1260 TGCACAGCTT TGGCAGGCTG TTCAGACTTC ACACATCAGC TGCCTTCATT CTCTCAATTT 1320 ATCTTTGTAC TGCCCATTTT GGGGGCAAGG TGTCAGCTTA TTTTCCTTCA GCACCTGTTA 1380 ACACCCAAAG GAATTAAAGA TAAAAATAGC AGACCTTTCT ATTAATGTGC TAATGGACTT 1440 CCCTTATGCT CAGAGGATTT CCAGAGGATT TGACTGGAAA TCGTTAAATG CAGTGGAAAT 1500 TCTAATTTCA GTGTTTGGCT CCAGCAGCAA GCGTACATGA AGAACACCTA GGGGCCAGAT 1560
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