Tag | Content |
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EnhancerAtlas ID | HS047-28205 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:2542630-2543880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MNX1 | MA0707.1 | chr6:2542635-2542645 | GGTAATTAAA | + | 6.02 | PHOX2A | MA0713.1 | chr6:2542637-2542648 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr6:2542637-2542648 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr6:2542637-2542648 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr6:2542637-2542648 | TAATTAAATTA | - | 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 |
GH06I002541 | chr6 | 2542133 | 2543933 |
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Enhancer Sequence | TAAGAGGTAA TTAAATTAAA ACAAGGTCAT TAGGGTGGGT CCTAACCCAA TCTGACTGGT 60 GCCCTTATCA GAAGAGGACA TGAGGACGCA GACATGCAGA GAGGGAAGAC CATGTGGGGA 120 CACAGGGAGA AGCCAACCCT CCACCAGCCC AGGAGAGAGG CCTCAGGGGA AACCAACCCT 180 GACGACCCCT TGATCTCAGA CTCACAGCCC CAAAGACTGT GAGGAGACCA GTCTCTGTTG 240 TTCAAGTCTC TCAGTCTGTG GTGCTTGTTA CACTTTCCCA GCTGCCATAC TCTCTCCCAC 300 CTGGATCCCT GCAACAGCAT ACACCTGGTG TCTCAGTGCT CACTTTGCTG CTGAGAAATA 360 AAGATAAAAT CCTAAGCCCC TCAACCAACT GAGCAGACAC TCTCTTGGCC AGGGGAACCC 420 TAGAGAAACT GTAAAAACTG AGTTCATGGC CATGATGGAT AGAAGGTCAG ACACGCCTTG 480 CTATACCCGC TCCCTTGCTA ACCGCCACTA GGTTTTCTTC CTCAATGGTT AAACAGAAAC 540 CAGCTGTTTT GAAAGACTAG CTCCATTGCT GATTTTGAAG AATCTCCTGA CTTCTGCCCC 600 TCCCTTTTGT GGTTTCAACA CAACTGCGTT CCTTCCTGAT AAGAAACCAC CAACCACAGA 660 GTGGTTCTGC TGAGTCTATG GAGATTGCAT ACTAAGGGTT TTCCTGTCCT CCACTTCACC 720 TTCTGATCTC AGAGGGCCAA ACACTCCACT CTCAGGTTAT GCTAGCACTG TCATTTTTTT 780 GTACATGCCA CCCATGAAGA GGCATGAAGC TCAATTGCAC ATGTGCACGT TTCTCCATTC 840 GTGCCTCCTT CTGTAGCTTA CTGAATATGT GCATTTGGTC ACCTGGTTCA GCATAAATCC 900 CTTTTACATT CTTCCCACCT TCTAAGTGTC TGTTTCTAGC TTCTGGCCAG AGGCTACGCT 960 TCCCAACCTG TCAGAATGGC TACCCTGCAG GATGCAACCC TGTATGAGAA ATCTCTCCTT 1020 TCCAAAAATA TGAACCTCAT TATTCAGTTA ACACTGCCCA GCAGGCAGTG TGGATCTCAA 1080 CACATCACTT CAACCCTTCT TTGGCTCTTC AGATAAACCC TCTGGTCTTC ACCACAGCCC 1140 TCCAGGCTCC TGCTCCAAGT TCCTTTTGTG CCTTTTTTCT CTTTTTCCTT CATGCCTCTG 1200 TCTGTTCCTC TAATGCTTTT TTTTCCCTGC CCCTGAGGAC CTTGGTTTGC 1250
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