| Tag | Content |
|---|
EnhancerAtlas ID | HS167-06301 | Organism | Homo sapiens | Tissue/cell | Retina | Coordinate | chr7:2309280-2311480 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr7:2310022-2310033 | AGCCTGAGGCG | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 2310942 | 2310992 | | chr7 | 2311035 | 2311281 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I002269 | chr7 | 2308801 | 2310530 |
| Enhancer Sequence | AAGGAAAACA CACAGCTTCA CCCTCTTCTA CTAGCAGCAA GAAAGCTGCT GTGGGGTATG 60
GGTCACTGTG GAGCGGGAGG TCGTCTTTCC TCAGGAGAAA CACATTTCCA TATGTTGGCT 120
TTGACATTAG TATTCTGCAA TCTCTTGACT CTCCCTTAGA TGTTTTTCTC ACCAAACAGG 180
ACAGCCTGGC TTCACAGCAG GAGCACCACA AACCTGCAGC CTCTCTCCAG AGGCACAGCC 240
ACTCCATCCG CAGACGGGGG GCAGCTCTCC AGAGAAACAG CCACTCCATC CACAGACCAG 300
GGGCGGCTCT GCAGAGAAAC GGCCCCTCCA TCCACAGACC CGGGGCGGCG TCAGCCCCAG 360
AGATACCTGA GACCCTGGTA GCTTCCAAAA ACGCAATAGA ACAGGGCAAA AGTGTCTTCC 420
TTCCTGGGAA TGCATCCATG GCGCCAGGGA CACCAGAGCC CAGGGAGCTG CTGGGCAGAG 480
GGACAGGCCC AGCCCCTGGC ACCGGAGCCC TCTCATCTGA AAGAGGCCTC CTGGGCAAAG 540
CCGTGCCTTA AAGTCAGGAG CCACCCAGGA GATACAAGGG GAAACCCTAA TATGCAGCTG 600
TTTGCGTGTC CAGGAATTCT CAGGTTTCAG AGATGCCTTA AAGATCATCT GACTCAACTC 660
TCATTTTACA AAAAAAAAAA AAAAAAAAAA AAAAAAGACC TGAGGCCCAG CATGGTGCGT 720
GCCTGTAGTC CCAGCTACTC AGAGCCTGAG GCGGGAGGAT CGCTGGAGCC CAGGGGTTCA 780
GGGCCAGCCT GGGTAACATA GTGAGACCCC ATCTCTAAAA ACAGAAAGCA AGCAAGAAAA 840
CTGAGGCCGG GAAGTGACAG AGAATGATAC CTGTGGGAAG GCCACAGGGA ACGTCCTGCC 900
CCCAGAACAG GGATATTGCC CACCTGTGAC CCACTGCACC CCTGCCCACC GCCCCTCCCA 960
GGTCCTGCCA CATTCCTCTG CTGGCAATGC AGATCGCCTC CAAAGGAAGG TTTCCAACCC 1020
CAGGGCTCAA AAGATCCCAC TGCCTGCTCC AGACATCCCC GGGGGCATCC CAGGGACATC 1080
TCAGGCACAG GGGGAAGGCC CCTCTGCCTC CGAGAGGAAC GAAGACAAAA GGAACCAAGG 1140
CTTGTGTGAA GTCAGCCTGG GAGAGGGGGT GTCTTCCTGC AGCAGGGACA AGGACAGAGG 1200
CCGTCAGGTC CCCATTCAAG ACGGGGTTTC CCTGAAATAG AGGAGAGCCT GGAAACCTCT 1260
ATTCCAGTGG AGCCCCCGCC CCTCCCCGCA CAGGGAGAGG GTCCTGCAGG CACAGGTGGA 1320
GGAGAAGCAC AGGACCCGCC TTCCCTGGAG GGGCTGGCAG CTGCTTCCTC CTCCAGGAAA 1380
CAGGAGCTGG GCTGCAGGGT TGTTTTTTGT TTTTTTGAGA CAGGGTCTCA CTCTGTCGCC 1440
CAGGCTGGAG TGCAGTGGCA CAATCACAGC TCACTGCAAG CTCCACCTCC TGGGTTCAAG 1500
CGATTCTCAT GCCTCAGCCT CCCAAGTGAC TGGGATTACA GGTGTGCACC ACCATGCCTG 1560
GCCTCAGTTT TGTTTTGGTA GAGACGAAGT CTCGCTATGT TGTCCAGGCT GGTCTCAAAC 1620
GCCTGGGCTT AAGGGACCAT CCAGCCTCGG CCTCTCCGAG CGCTGGGATT AGAGGCGTGG 1680
GCCACTGTAC CTGCGAACTG TAGCTTCTTG ACACACAATA AGGCTGTGCC GCAGCAGCTG 1740
GGAGGAGGGA AGCCCCACTC AGACCTCTGA CGGAGTGCAT GTACAACAAG TTAATTCCCG 1800
GATGCAGGTG TGGGCTGTGG CTCTGACAAG GAGGCTCAGC CTGTGTTCCA GTGGTCCTTA 1860
GTCAGACAGG GCCTTGTTTT AAGTCAACAC TTCTTCCCAT CTGGAGTCTC TGGCACCTCC 1920
CTAAACCCTC CAAACCATCC AGCCTAAATC CTCAAAGTGA CCACAGAGAT CCATGATCTC 1980
CACGCGGATT TACAAAATCC TGCAAAGTCA ACACCAGGGA CACCTCTGAA AATCACATTC 2040
AGACTGTTAT CTGGAAAGGA AAGAAGTCTT GTCCATGTCA TTCCTGCTGG GCGTCCAAAC 2100
AAGGGACCAG GAGGATAAGA AACCACACCT GAGAGAGGAA AAGGCGGGTC CGGAGGCTCG 2160
GGGACTCCCC GGGGCCGGGA CATGGGCAGG GCAGACACAC 2200
|
| |
|
|
|
