| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01353 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:54583330-54585320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:54584972-54584993 | ATCTGCTTTCTCTTTTAAATT | + | 6.13 | | MEF2A | MA0052.3 | chr1:54584997-54585009 | TTTATTTTTAGA | - | 6.07 | | RARA | MA0729.1 | chr1:54585070-54585088 | CCTTGAACTCTTGGCCTC | - | 6.36 | | RREB1 | MA0073.1 | chr1:54583384-54583404 | AGGGTTGGGTAGGTTTGGGG | - | 6.19 | | RREB1 | MA0073.1 | chr1:54583412-54583432 | GGGGGTGGGGTGGGCGGTGG | - | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I054117 | chr1 | 54583670 | 54585410 |
|
Enhancer Sequence | CAAACAAAGC TCTTTCTTCT GCAGAGAGCC TTGGTCACAG CATCAAGTAA GGGCAGGGTT 60
GGGTAGGTTT GGGGTGAGGT CTGGGGGTGG GGTGGGCGGT GGAGGGGTGG AATGCAGCTA 120
GTGAAGAATG CAGTAGAGTC CCTACAGATC CTCCAACAGT GGCAGTTGAA ATGCCTGAGA 180
GGGGAGAGGA CTTAGCCAAG GTCACTCAGC CAGATCTGGG CCTCCTGACC ACCGCCCAGC 240
TGCCCAGAGG AGGCCTTTTG GCTCACTCTC TCCTCTCCAA GCTCTCCTGC AAGGGCTCTT 300
GGGATTACCA TGTCTTTGCA CCATTCTGCA AATCTGACTC CATGCTCACT GGGCATCATG 360
CTTCCTGGTC TGTGCTAGGT CTAGGCTGGG CACTGGGGAT GCAGAAGTGT GAGTCAGCCA 420
CGGTGACTCA AGGAATCACC GAGACACCTG CAGAAATATT CCTTGGGCAG CGGGTTGGTA 480
CCATCACACA CTCCTAGCCT CCAACCGCAC TTACTTCTTC CACTGACTCT GGTTGGCTCA 540
CCCATTCCTG GGCCTCTCAG GAGCAGTTAA GGGGCTCTTC CCTTGCCTAA GCCCTCCAAC 600
TGCACCCTCA CCTCCTATAC TCACAGATGG CCTTGCCGCC CATGCCACAA ACAATATAAG 660
CATCTCATAG CAGCTCCCTC CCCCTCCCCC TGCAGGAACA CGAGCTGCAC TGTCGTGTTC 720
TCAGAGGCTG TGCTGTCCTG TCACTGCCCG CCCCTCCCCT TGTGCTCCAG CCCCTGCCTC 780
CCACTCTGTA ACAGGCCTTG CTCTACTTCA ATGTCCACCT CTCGCCCCCT TCCTTAGCTT 840
TTCCCGTCAG TATTTAAATG CACTTAAAGC CTTTCCATCC TCAACAAACA AAACCAAACA 900
GACAGAAACC AGGGTCACCA TCCACTAAAT CAGCCCCCTC CACCCTCACC GGTGCTCCAG 960
CTCCTCCTCG CCTCTCTCCT GCTTGAGAAA GGCCACACTT CTCCAGGGAG CCACGACTCT 1020
CACTCTCTTA GCTCCTCTCC TCAACTCCTC CTCGGCCCTA TCTTCACTTG CCCGGGTCAC 1080
AGTGCTGTCC TCATTCCTAA TTATGAATCA AGGCTGTGGG TCCCTTCCCA GACTGGCGGC 1140
TGCCACATCA CCACTACCCT CCTAGATCTC AGGCTGTTGT GGGCTCCTCT CCATTCATCC 1200
AGCTATTATT TAAGTAGCTA TTTTTCTGTG TCGGTCACTG GGCTTGAGTC TAGTGACTCA 1260
GTGATGAGCA AGAGGATCAG GATCTGCCTT CCAGAGTGCA AGGACAAGGG GATCCTCGGA 1320
GGTCCTGCTC TAATGCCCCT CCTCTCCCCG CAACACACAC CCTCTCCTGA TCATCTCAGC 1380
TACACGCTGA TGACTGTCAG AGCCTAGCTT CTGCCCCGAC TTTCCCCCAA GCTCCACATC 1440
CACACCTCTA ACTACTTGGG GGACAATTCC ACCTGCATGG TCCACAGGCA ACTCAGACTT 1500
GCAAGGTCCA AACCAAACGA GTTCTGCTCC TTAAATTTCC CCCCTTCCCC TATACCAAGG 1560
GCGGAGCCAC CATTCACACA ACTCACAAGC CATAAACTTG GGAGACATTT TTCACTCCTC 1620
CCTCCAGCCC CACATTCCAA CCATCTGCTT TCTCTTTTAA ATTTCATTTT ATTTTTAGAG 1680
ACACTGTCTT GCTCTGTCAC CCAGGCTGGT GTGCAGTGGC ATGATCATGG CTCATTGCAG 1740
CCTTGAACTC TTGGCCTCAA GCTATCCTCC TGCCTCAGCC TCCTGAGTTG CTAAGAATAC 1800
AGGCTCAAGA TATTGCACCC AGCCCACCTT CCTTCTAAAT CAGTGGCATT GTCCTTGCCA 1860
CGGCCACTGA CCTAGGCTCA CGTCACTGAG ACACTCTCCA GCCCATCTTC CACATCCAGT 1920
CTTGTGCCCT CCAAGCCATT GTATGGACAT AGCTAGAGAG GTCAAAAGTA AGCCCGAACA 1980
GCCCAAATGT 1990
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