Tag | Content |
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EnhancerAtlas ID | HS167-02743 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr2:43122220-43123750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr2:43122240-43122252 | TTTATTTTTAGA | - | 6.07 | TCF7L2 | MA0523.1 | chr2:43123101-43123115 | AGAGATCAAAGCCA | + | 6.08 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 43122430 | 43122548 | chr2 | 43122695 | 43122773 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I042896 | chr2 | 43123581 | 43124846 |
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Enhancer Sequence | CTATTTTTAT TATTTATTTA TTTATTTTTA GAGATGGGGT CTCATTATGT TGCCTAGGCT 60 GGTCTAAAAC TCCTGGGCTC AAGTGATTCT TGCATCTCAG CTTCCCAAAG TGCTAGGATT 120 ACAGGTGTTG AGCCCACACG CCTAGCCACA TGGCTATTTA GTGAGTGGCA GAGGATGGTG 180 TATGAATTCA GCTCTTCCTA TGCTAAGTCT ACAGGATGTG TCCCCTCCCA CACTGCCCCT 240 GGCCCTTCTG ACTCAGGGAC ACCAGTGTGG TTTATGCTCA TCTGTCTCCC TGACTGCATC 300 CCTGTTGAAA CCTAATGCAG GACCACGAGG CTGTGTTCCA TTGCTCTTAG GGATGATGAA 360 ACCATAGATC CCAATAACCC CTCTCTCACT CATCAGCTCC CAGGAACCCA GAGGGCCACA 420 TGGGGGAGGG AGGGATGCAG GACCCCAAGA AGAAGGGTAA ATGGAAGCCA AGAGCCAATT 480 GCCAGTTACA GAACTGTGTC GTCACATCGC GGTGCTGTGA TTCATGGTGT CCCACACTGT 540 TTGCTGTGTA CTGAGTTGGT GCTGTATTCT CACTTTGGGT TATGTGTTGC AGGGAGTGGG 600 GAACCTTCTT TCACGGCCCA GTCCCTGGGT GGCATTGTGT GTCACATGTG TCATGTGAAG 660 GCCTAGCTTA GAGCACTTTC CCAGACAGAC CCCAGGGCTG GTCCTGGTGA CCCTGATGTA 720 TCCCATAGTT TCACTCTGGG TCTGACTTGC TCATAAACAT CTCCACTCTC AACTCCCAAT 780 TCGCAAGCAA AGGGCCCCAT TCCTGGGCAG GCCCACCTGC TGGCCGTGCT ACTAATTAAT 840 GACTGCTGAT TGGCCCAAGA GGTGCACTCA TTATGCCCAA TAGAGATCAA AGCCAGATCC 900 AATCATCTGC TAAACGAGAT GTCAGATTAG GGCATTCTTC TGGGCTATTA GAAAGATTTT 960 TCTCCCTGTG TAAAGGCCTG TCAGGGCATA TGACCCTATC ACCCGCCATG AGCTGAGCCG 1020 AGGGGGCTCT GCAGCCTTTC TGTTCCTCTT ACTTTGAATG TGTCCTTTTA ATGGGACAGC 1080 CCTGTGCCAG CAGCCTGGGC ATGATCCCTG GAGAGACCAC AAAGCGTGGA GGGGATCCCC 1140 TAGGGAAGTC GTGTTTCGGC AGTCACCTCT GCCTCTTTAT TCTTGGGGTT GCTGGGTGAT 1200 TAGAGGGAAC TGCAGACTTC CCTGGGACCC TCTGCTTTCC GTTGTATCAT GGACACTTGC 1260 CTCAGTTTAC CCCCTAGGGC TGGGGATCAA GTTTAATGTT GATACCACTT TCTCAGGAGC 1320 TAGCCCCAGA CTGACACTCA TTTCAAACCA TTGGTGCACT AGCCTGACTT TCTCAACCCA 1380 AGGGTAAGAA TAGAGCCCCA GTTTTATTTA TTTATTTATT TATTTATTTT AAATTATTTT 1440 TGGAGACAGA GTCTCACTCC GTCACCCAGG CTGGAGTGCG GTGGCACAAT CTCAACTCAC 1500 TGCGATCCTG GCTCACTGCA GCCTCCACCT 1530
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