Tag | Content |
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EnhancerAtlas ID | HS076-01226 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:25944830-25946430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr1:25946025-25946036 | TTCTTATCTTT | + | 6.62 | HNF4G | MA0484.1 | chr1:25944957-25944972 | TGCACTTTGCACCTT | - | 6.05 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 25945335 | 25945579 | chr1 | 25945896 | 25946000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I025619 | chr1 | 25946165 | 25947830 |
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Enhancer Sequence | ATGGACTCAG CCCCCAAACT CCTCCCACCA ACTGCCCCCT CTAAGGAGAG AAGACCCTCT 60 GGCGCTCCCA CCCCTTTCCC TTGCCTCAGT CACTCCTGGT CCCAGGTCTA CTTCTGGCCC 120 TGCAGACTGC ACTTTGCACC TTCCCCTTTC CTCCCAAATG TCCCACCTTC TTTCCTCCCT 180 ACACAGTTTC CCACCACTCG GGTCAGTTAA TCGTCCCCAC CGTGACAGAT GGCAGCTGAA 240 CCCCTAGACC AACTGCCCCC TCACTCCCAG ACTCTGGTAT GTCGTATCCA ACCCCCAGGC 300 CCAGTGAGCT CCACTCCTTC CCTTTGTGGA GTTGCTAATG AGAGTGGAGT TCAGGTTCCT 360 TAGTGCACCC TCTTTTTGCA TTTGTGGACA CAGAGCCACT GGTCCCATTC TTTTTCACTG 420 TGTGACCTTA AGTCCAAAAC CCCTATAGGA CCTGCTTACC TAAAAACCCA GGATTTAAGG 480 GGGTATTTGG TGTCCTGCAA ATATTTTGTA ATCTAGTAAG CAACCTACAA ACCAGAGGAT 540 GTTGTGCATT CTGTTTCTAT TGAGCTTATT GAGCTTCAGA ACAATTGTAC ACAATTGTAC 600 ATAATTGCAT ATGATGCAGG AAGAGATGAT AAAGCAGTGG TCATATTACA GAAGCTCCGA 660 GGTTATTGGC ATAATGAAGC AGATCTTGAG CTGGTTCCCT GTAGGGATTG TACCAGGAGG 720 GATTTAGAAG GATCACTTTA AGTCTGAGTC TTAGTTTAAG AAATCAAAAG CAAACACAGC 780 CTCACAAGGC TTGAAGACAG TTGCCAGCTT GCCACTGCCA CTAAATATTC TGCTGGACCA 840 CTGTTAGAAC TGCCTGCGTG CGGATGGTGC CCAGCAATGC AGAGGGGGCT GCAGTGACAC 900 CCCCAGGCCA CGAGGGGGCC GTGGGCAAGC TGTGGGCCAG GGTCTCCTCC CTAGAAACGA 960 GAGGATGCTC TCCCCTCCCC ATGGACTCAA AGGAAAGAAA GGGCTGCTTC TGCCTGGACT 1020 TCTTGATTTG CTGCGAAGAA GTCAGCAGTT CGACCCTGAT TTCCAGGAAG AGCAGGCAGC 1080 AAGGATCAGG ACCTGCCCTG TCAAGACCTG CTCAGAGCCG ATGGAGGGCT TAGCCAGATT 1140 ATCCCCTTCT CCTTGTCTGA ACCATCCTCC CTTCCAGCGC CCACCTCTCT TCCACTTCTT 1200 ATCTTTTCTG TTACTCTGTT TGGAGACTTA ACTAGCAATC ACAGGACATT TTGTGAAGTT 1260 ACAGTAGGAA GCCACAGGGA AACTGAGTGC TTGGTGTGTA TGTGTGTGTG CATGTTTGTG 1320 TGCTCTCAGT TTCCAGATTC CTGTTGAAAT CTCAGGTTGA GTGACAGCTG GAACTTGCAG 1380 TAGCTAAGTA AGGGGCATTC ATTTCTCCCT TTCTTGTTAA GGAACTACGC TGTTGAATAC 1440 TCACTTGGAC CACCCATAGC TCTTTCTCAA AGCTGCTTCT GAGCACAGTG GCTCTTTTTG 1500 CCCCTCTCGA CCTCCCAGTA GGGCAGTGAC CCCCAGTGAA ATTACATATA AATTGCATGC 1560 ATGCAGTTTT TCATGGGGCA TCCAGAGGTG CCATCAGATT 1600
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