Tag | Content |
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EnhancerAtlas ID | HS076-45908 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr5:134758120-134759490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr5:134758362-134758373 | AATTTAATTAA | + | 6.32 | MEF2A | MA0052.3 | chr5:134759106-134759118 | TCTATTTTTAGG | - | 6.14 | PHOX2A | MA0713.1 | chr5:134758361-134758372 | TAATTTAATTA | + | 6.62 | PROP1 | MA0715.1 | chr5:134758361-134758372 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr5:134758361-134758372 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr5:134758361-134758372 | TAATTTAATTA | + | 6.62 |
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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: 1 | ID | Chromosome | Start | End |
GH05I135423 | chr5 | 134758801 | 134759816 |
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Enhancer Sequence | ATAGCTTTCT TCTTTATTAG TCATTAGTTA CATTCTACTG GTGATGAACC TAGAGATTAC 60 AGTATGCATT TTTGATTTAT TAAAATCTAA TATAAATGAA TATTTTTACA ATTTTCCAGA 120 CAATGCAAGG ATTTTAGAAC ATCCTAGCTC CATTTATTCC CTTTGTGTGC TATTATTGTT 180 GCATATTTTA ATTACATGCA TAATTGTATA TGCTTATATT TATTAAGATT TAATATGTAA 240 ATAATTTAAT TAATAATTTA TAATTAAATC ATATTATAAC AAATAACACA TGTATTATGA 300 TTTAATATAT AAATCATAAT ACATGTGTTA TTTGTTATAA TATGATTTAA TTATAAATAA 360 TATCAAACAT ATTTATAATC CCCCCAAGAC GTTATTATTG ATGTTTTCAA CAGTGAAAAT 420 TTATTTGGAT TTACCTGTTT ATCTTATTTT TAAATCAAAG TTTTATTTTA AATAGTTTTG 480 AACTTACAGA AAAGTTGAAA AGATAGTACA GAGAGTTCCA TGTATATTGG ACCCAACTTC 540 CCCCATGGTT AAAAATTTAC ATTATTATGG CACATTTGTA ACAACTAAGA AAACAGCATT 600 GGTGCATAAC TCTTAACTAA CCTCCGTACT TTCTTTGGAT TTCATTAGTT TTCCCTAATG 660 CTCTTTTTCT GCCATATCAT ATTCAGCCTT TGTGTCTCCT TAGGCTTCTT TGGTCTGTGA 720 CAATCTCTGA CTTTCTTTGT TTCTCCAAAT TCTCAGACCT TGAGAGTTTT GAGGAGTACT 780 GGTGGTTTGT AGAATGTCCC TCAGTTTGGG TTTATCTGAT GTTTTTCTCA TGGTTGGGGG 840 AAGAAGACCA GAGGTGAAGT GCCAGTCTTA TCACATCATA TCAAGGTACA CGCCATCAAC 900 ATGACTCATC ACTGATTATC CCAGGGCTGA GATAGTGCTG GCGAGGTTTC TCCTCCATAA 960 AGCGAGTGTT TTCCGCCTCT TTGTACTCTA TTTTTAGGAA GCAACTCAAT GAGCATGGCT 1020 TACATTTGAA AGTGGAGAGG AGAGTGAAGT CCACCTCCTG GAGCAGGGAG TAGCTACATA 1080 AATTATTTGG AATTCCTTGA TTTATTTATT CAATAATTTG TATCAGTATG GCTTCATGGA 1140 TATGTATTTT ACACTTGGGG TTATAATCCA ATACTGTAAT TTCATGTTGC TGAAATTGTT 1200 CCAGATTTAG CTGTTGAGAG CTCTTGCGGG TTGGCTCTTG AGTCATGTCC CTATGGTTTT 1260 GCTTTTTTTG AGCACTTCCT TATTTTCTGG TACTACAGGA TGAGCTTCAG GCCCAGCCTT 1320 AGAATCAGCC ATTTCTCCAA AGATCCCTGC GTGCTTTTAC CAGAAACCAA 1370
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