Tag | Content |
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EnhancerAtlas ID | HS007-12221 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr4:4462440-4463810 |
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) |
FOS | MA0476.1 | chr4:4462724-4462735 | AATGAGTCAGA | - | 6.32 | LMX1B | MA0703.2 | chr4:4463088-4463099 | TTAATTAAAAT | - | 6.62 | RARA | MA0729.1 | chr4:4462867-4462885 | AAGGTCTAAAGGTTAATT | + | 6.55 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I004460 | chr4 | 4462338 | 4465366 |
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Enhancer Sequence | TCCTTATTCC AATGCTCCTT AGGATCTTGT TCTATTAGTT ACTTAGGCTT GGGATGGCAA 60 CCATGAGAGA ATGGACTCTG TCCGAGGGAA GACCCAACAG TGAGACAAAG GCGCTAAGCC 120 AGCAAGCTCG ATCCCCTCTC CCCAACCCCA GCCCACCTCC AACACCAGAT GAATGGCTCC 180 CCTCTGGGGA GGAGCCAGAG TGGCAAGCAG AGGGGCCAAA GCCTTAGGTT CATCCCTACT 240 AGGAACCTTC TCATCGGAAA TAGAGGCTAA CGGGGTCAGG GACAAATGAG TCAGAAAGGT 300 ACCAACTCAG TGAATATGTA CCCTGCAGAC AGAACAGACC TAGAAATGAC TAGTTCCAAG 360 AACATTCGAT TAACATCCTC CTACTCTATA TTTTGATTTA ATGGAAACTC AGCTCAGTGA 420 AATTGAAAAG GTCTAAAGGT TAATTTGATA AAACTGATTA TTTAATTAAA AGGTAATGTT 480 CCTTTAGGAA ACATTATATA TATACATTAA CCTTCTAAAT TGAAAATTGA CAGTATGGTT 540 ATTCTATTAG TAAGAACAAC AGAAACCAAG GAAGTTTTTT CTCCCAGATT GTTTTGTTGC 600 CAGGATATTG TGGAAAAAGT CCATCTACCA GAAGTGGAGA CATTATTTTT AATTAAAATC 660 ATTCAGAGAT CTAGCCACAG GCTATCTAGG TTACATGCTG TTCTGCTCTA GTAAAATGTC 720 ATTATTAAAA AAAAATTAAA TGGGTCAATA AAGTCTGAGC TCTACATTCT GGAAAAAATT 780 ACAGCTTCCT AATTATGTCA AACTAACAAA GCCTCATAGG TCTGAAGGCA GTATTTCTAC 840 ACATATTCTT TCAATTCCAT GATCATACTC CACATAAAAT GTTCCTAGGA GCAGGCCAAG 900 GCTAGCACAT TGCACTGGGA GGGCAGAAGA GTAAAAAAGA AAGGCTTTAA GCAGTCTACC 960 ACCTTTGGGA GGGAGAACTT GATGAGAGAC AATAAGGGTG GTCTTTCTCC ACCTGGACAG 1020 AACCTGGGCT ACCGGGGGGA ATGCTTATTC CCTAATCCTC ATGTTTCTGT GGGAACCAAC 1080 TTCCCCAAAT GACACCTTGC CTCCTCCCAG AGCCTCCTCC CTCTGGCCCC CTCGCAGAAA 1140 GCATGGGGTG TGCATATAGT CACCACACCT TTCTCTCCTC TCTTTTACCT ACTTAGAGAC 1200 AGCAGAGGTT CCGCTCTGTT CCTCTCTCTC CTATGTTGCA AAGGGGCCTG TCCCTGCTGT 1260 CTGTGCTCCA GGGGCTGCGG CTGCGCAGTG GCACTAATGC CTGAGTGTGT CTAATTCAAG 1320 AGCAGAGTAT CAACAAGGCC ACCCGCCTGC AAACCAAAGC TTTGTTTGCT 1370
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