Tag | Content |
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EnhancerAtlas ID | HS062-08542 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr19:47893820-47895260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr19:47894642-47894653 | AAGGGGATTAG | + | 6.32 | SRF | MA0083.3 | chr19:47894011-47894027 | TTTCCAAATAAGGTCA | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 3 | ID | Chromosome | Start | End |
GH19I047390 | chr19 | 47893658 | 47893857 | GH19I047391 | chr19 | 47893862 | 47894215 | GH19I047392 | chr19 | 47894335 | 47896548 |
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Enhancer Sequence | TCTCTCACAT TCTTGGGGGC CAGAAATTGG AAGTCAAGGT GTTGGCTGGG CTGAGCTCCC 60 TCGGGAACCT GCCAGGAGTC TTCCCTGCCT CTCTCTAGCT TCTGTCACAC TGCCGGCAGT 120 CCCCTTTTAT AGAAGGGCAT GTGTCATATT GGACCAGAGC CCACCCTATG ACCTCATCTG 180 AAAAGACCCT TTTTCCAAAT AAGGTCACAT GCACAGGCGC TGGGAAGAGG AATTAGCATA 240 CCCTCTGGCG GGACACAATT CAACCCATCC TACCCCGTCT AATCCACTGG AGGGATAAAG 300 CGCTAGCCCG ACTCTGTCCC TTCTCTGCTC AGAGTTCTTC CAGGACAATG AAATATCATT 360 CAGCAATGAA AAGGAATGAC AGGCTGGGCG TGGTGACTCA CGCCTTTAAT CCTAGCTCTT 420 TGGGAGGCTG AGGCTTAAGC CCAGGAGATC GAGACCAGCC TGGACAACAT AGTGAGACCC 480 CATCTCTACA AAAGATACAA AAAATAGCTG GGCGTGGTGG TATATGCCTG TAGTCCTAGC 540 TATTTGAGAG GCTGAGGTGG GAAGATCGCT TGAGCCTGGG TGATCCAGGT TGCAGTGAGC 600 CGAGATCACA CCACTGCACT CAGCCTGGGC AACGGAGCGA GACCCTGTCT CTAAAAAAGA 660 AACAAAACAA AAAATACACA CAAAAAAATG GAATGACTGA CAGACACTAC AGCAGTGCTG 720 CAGCTGGAAG ACATGCTACT GAAAGAAGCC AGTCACAAAG GGCAGTGTAG CGTGATTCCA 780 CTTACGTGAA ATGTCCAGAA TAGGCAAACC CATGGAGACA GAAAGGGGAT TAGTGGTTGC 840 CGAGGACTGG GGGCCGGCGA TCACTGTTAG GAGGTTCAGA GTTTCTTTTG GGGATGTTGA 900 AAATATTCTA GAATTGATTG TGGTGACAGG TGCACAACCC TATAAATACA CTAAAAGCCA 960 TTGAACTGTA CGCTTTAAAT GGGTGAATTT TATGTATGAA TCAGGTCTCA ATGAAGCTGT 1020 TAACAAAAAG AACTCTATGG CTCTCCAGCG CCCCCTGGAG GGATGCAGGA TCATTGCCTT 1080 CCCTCAAGGT TCCACCAGGC CGGCCTCCCT TCCGCGGCTC CCTCTATCCT GTCAGGGCCT 1140 GTGCACCTCC GCCTTCCCCA TCTCCTGAGC TTCTCCCCTC CACCCACATC ACGCCTCATC 1200 ATCCTTCAGG TCTTAGCTCC CACCTTCCTC CTCCCGGAAG CCGACCCTGA CGCCCAGCAT 1260 GTCCCCTCTG ATGGGGCCTT TGTTCTGCAG AGGGAGGGGA GGGGCTGGTG TTAGGGGTGG 1320 ATTCCTGGAA TTCTTTTTAA AAATGTATTA TCTTTAGAGA TAGAGTCTCA TTCTGTTGCC 1380 CAGGCTGGAG TGCAGTGGCA CAATCACAGC TCACTGCAGC CTCGACCTCC TGGGCTCAAG 1440
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