Tag | Content |
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EnhancerAtlas ID | HS131-07785 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr6:2542540-2544020 |
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 | AACTTGCTGA ACTGGTTCTC CCCAAATTCC TATGTTAAAG TCCTAAACCC CAGTACTTAA 60 GAACGTGGCT GTATTTGGAA ATGGGTTTTT TAAGAGGTAA TTAAATTAAA ACAAGGTCAT 120 TAGGGTGGGT CCTAACCCAA TCTGACTGGT GCCCTTATCA GAAGAGGACA TGAGGACGCA 180 GACATGCAGA GAGGGAAGAC CATGTGGGGA CACAGGGAGA AGCCAACCCT CCACCAGCCC 240 AGGAGAGAGG CCTCAGGGGA AACCAACCCT GACGACCCCT TGATCTCAGA CTCACAGCCC 300 CAAAGACTGT GAGGAGACCA GTCTCTGTTG TTCAAGTCTC TCAGTCTGTG GTGCTTGTTA 360 CACTTTCCCA GCTGCCATAC TCTCTCCCAC CTGGATCCCT GCAACAGCAT ACACCTGGTG 420 TCTCAGTGCT CACTTTGCTG CTGAGAAATA AAGATAAAAT CCTAAGCCCC TCAACCAACT 480 GAGCAGACAC TCTCTTGGCC AGGGGAACCC TAGAGAAACT GTAAAAACTG AGTTCATGGC 540 CATGATGGAT AGAAGGTCAG ACACGCCTTG CTATACCCGC TCCCTTGCTA ACCGCCACTA 600 GGTTTTCTTC CTCAATGGTT AAACAGAAAC CAGCTGTTTT GAAAGACTAG CTCCATTGCT 660 GATTTTGAAG AATCTCCTGA CTTCTGCCCC TCCCTTTTGT GGTTTCAACA CAACTGCGTT 720 CCTTCCTGAT AAGAAACCAC CAACCACAGA GTGGTTCTGC TGAGTCTATG GAGATTGCAT 780 ACTAAGGGTT TTCCTGTCCT CCACTTCACC TTCTGATCTC AGAGGGCCAA ACACTCCACT 840 CTCAGGTTAT GCTAGCACTG TCATTTTTTT GTACATGCCA CCCATGAAGA GGCATGAAGC 900 TCAATTGCAC ATGTGCACGT TTCTCCATTC GTGCCTCCTT CTGTAGCTTA CTGAATATGT 960 GCATTTGGTC ACCTGGTTCA GCATAAATCC CTTTTACATT CTTCCCACCT TCTAAGTGTC 1020 TGTTTCTAGC TTCTGGCCAG AGGCTACGCT TCCCAACCTG TCAGAATGGC TACCCTGCAG 1080 GATGCAACCC TGTATGAGAA ATCTCTCCTT TCCAAAAATA TGAACCTCAT TATTCAGTTA 1140 ACACTGCCCA GCAGGCAGTG TGGATCTCAA CACATCACTT CAACCCTTCT TTGGCTCTTC 1200 AGATAAACCC TCTGGTCTTC ACCACAGCCC TCCAGGCTCC TGCTCCAAGT TCCTTTTGTG 1260 CCTTTTTTCT CTTTTTCCTT CATGCCTCTG TCTGTTCCTC TAATGCTTTT TTTTCCCTGC 1320 CCCTGAGGAC CTTGGTTTGC ACCAGCCCCT CTACCCAGAC AGCTCTCTGT CCCGTAGCCA 1380 CCTGTGCATT ACTTTCCACT GCACATCAAA CATCCCTTCC TCAGAGAGGC TTCTCTAGTT 1440 ATGTGACCGT ATAACTCCTT GGATGTCTAT TTCATGGGAG 1480
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