Tag | Content |
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EnhancerAtlas ID | HS182-12583 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr2:97621380-97623610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr2:97622164-97622175 | GACAGCTGCTG | + | 6.14 | Nr5a2 | MA0505.1 | chr2:97622997-97623012 | TCTGGCCTTGAAGTC | - | 6.08 | TFAP4 | MA0691.1 | chr2:97621989-97621999 | ATCAGCTGTT | - | 6.02 | Tcf12 | MA0521.1 | chr2:97622164-97622175 | GACAGCTGCTG | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 97621567 | 97621661 | chr2 | 97622818 | 97623438 | chr2 | 97623107 | 97623405 |
| Enhancer Sequence | CACTGCAGCC TGGGCAACAA GAGCGAAACT TCGTTCCAAA AATAAATAAA TAAATAAGCG 60 AGTGTTACCA CAGGCAGAAA CTCAGGGATC CCATAATGGC CCTGCTTGCT ACCTCCGCTT 120 GCTCTTTATT TTGGGGGGCA GATGCAGCCA GCTGGAAGGC TCAGCCCTCT CCATACTTCA 180 GAACTGCTGG GTTTATTGCA CCTGGGCTTC AACCCTGGCC TGTTCCTCCA GGAAGAGAAG 240 CTAGTGGCAA AACAAGAGGC GGGGCTGCCG GGCCTCCGGG AGAAGCTGAG CCTCATCCAC 300 CTCCTTCTTC CCCTGCCTGC TGGATATTCA TGGAGGAACG GCCTGGCCCA TGCATCGGGC 360 TTGTGGAAAG CACGCTGGTC CTCGCACCAA CAGTGGCAGA TGCACCCAGA GGACAAACGC 420 ACACCCCAAT GTCCTTGCAA ATACTGTGAG GGGCCTATGA CTAACTGAGC AGGGCAGACA 480 AACTCCACCC TTCCAACTTC CGCCCCCGAG TGGGATGTGG GCTTTGGTCC TGACACTTTT 540 CCATGCAGGA GCATTGGATT TCCTTTTGAA TTACTGTCAA GGGTGGAGGA AAAAAGTTCA 600 GCTCCTGCAA TCAGCTGTTA TCAGCTTCCG TCATAATGAC ATGTGACTGT GGTGGCAGGG 660 GACTGACCCT GGGATGCACA GCTAGCTTGG TGATGGATGA GCAGGTCATC TGGACCACAT 720 GCACTCCCAA GGCAGGCTCC CCGGGAAGAG GGTTCTTGCA CATAAACCTG GATAGGTCCA 780 ACAGGACAGC TGCTGGGACG CAGACGCCAA GCCCACCCAA GCTCGCTCTG CAGTCTGAAA 840 CAAACTGCTT AATTTGTGCT ATTGCCTACT TTGTTCAGAG GGAAGAAAGA TATTTTCCCC 900 CTTTCACAGA AAGGTAAGGA GAAGTGAATC TATTTCAAGA GTTGATTTTT TAAAAAATGG 960 CATTTACTTT CCTCTCTTCT AATGATAAAA ATGATATACG TTCACTGTAG AAAGTTAGGA 1020 ATATAAAGGT GGTATAACGA GGAAAATGAA AACCTAGCTG TCAGCTCCCA CAGCATGAAC 1080 TTTCTCCCAC CCAAGTACTA ACCAGGCCGG GCCCTGCTCA GCCTCTGAGA TGAGAGAACA 1140 TCCAGCATGT TCAGGGTGGC ATGGCCACAG ACCACAGCAG CAACTTTGTG TATGGAATTG 1200 GACTGACAGC TTTTTATTTA TTATTATTTT TTGAGACAGG GTCTCACTCT GTTGCCCAGG 1260 CTGGAGTGCA CTGGCATGAT CACGGCTCAC TGCAGCCTCA ACCTCCCTAG GCTCAAGCAA 1320 TTGTCCCTTC TCAGCCTGCT GAGTAGCTGG GACCACAGGT GTGCTATCAC CCATGGCTCA 1380 TTTTTTTTTT GCATTTTTTT GGGTTGAGAC GGGGTTTCTC CATGTTGGCC AGGCTGCTCT 1440 AGAACTCCTG AGCTCAAGCG ATCCTCCCAA AGTGCTGGGA TTATAGGCAT GAGCCACCAT 1500 GCCCCGGCTG ACTGCTTCTT AAGAGATCCC CTTGTCACCC GCCTCCATGG CCATGTTTCT 1560 GGCTGAATAT GGTAAGGTTA TTATTGAATG ACTGACTAGT GTTTTCCCAC TCTTATGTCT 1620 GGCCTTGAAG TCCTTGGCAC AAGGAGGAAA TGAAAGATGA CCCAGGGCTA AATGGTGACC 1680 TCCAGGAAGT GGGCCTCGCC ACTGCCCGGC AGAGGTCCCA GGACTGAGAC CGAGTCACAC 1740 AGCGGGCATT CCCTCCAGAA AGCCCAAAGC CGATTCCCAA GACTGCAGAT CTGAGGCACT 1800 GGCAACACCC TCTCTACTGA GCCTCATTAG CATATCTGAG GGAGGAGGGT CTGAAACCCT 1860 CACTCCAGGG AAGCTGGGCA GCCACCTGGC CCCATTTGGC AGGCCTGCTC TGATCCCAGG 1920 TCACCGCTCC ATGGGCCATC TCATCTGTCA AACACTTCCT GCACGCCATC CACTCTAGGA 1980 CAGAAAACCT GCTGTCGGCA CAAACTCCAA GGCTGAAGCA GCCCAGGAAG ACGCCTTCCT 2040 TTCTCCGCTG TTCACCTCAG TTCCTGCCCA GACATTCTTT GGCTCTCTCC TTTCTCCAGC 2100 TCTTTCTTCT TTTCACCATC TATCTATTTA TTAAATACCT TTCCAACATG GTGATGTGAA 2160 CCCTTACTAA TGTTCTTACA CTCAGACCCA ATAACCTCAC ACTGCAGCTA TGAACACATT 2220 TTAGACCTCC 2230
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