Tag | Content |
---|
EnhancerAtlas ID | HS082-08782 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr12:92172140-92173310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr12:92172684-92172697 | AAATTAATTTTTC | + | 6.11 | PHOX2A | MA0713.1 | chr12:92172679-92172690 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr12:92172679-92172690 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr12:92172679-92172690 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr12:92172679-92172690 | TAATTAAATTA | - | 6.62 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 92172402 | 92172494 | chr12 | 92172749 | 92173207 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I091776 | chr12 | 92170023 | 92173679 |
|
Enhancer Sequence | AAACCTAAGT CTGGTCACAT TTTTACTCAA TGATATTAAG TATAGATTTC AAGTTTGCAT 60 ACAGTAGCAT TTACTATAAA ATAGGAGAAT GTTACTTTTT AGGAATAATC TAAGGACAGG 120 TGTAGATGTT ATTTTTTAAT GAGGTTCAAA TTTAGCACTG TAATGAACCT CACTGAAAAA 180 GTAAAGCAGG AAATGGCAGA TTTGTTTTGA TAGAAACCAA GAATTTTAAG TGTGTGTTGG 240 CTTTACACTG TCTTTGAAAC TGTGCTATGA AAACACAGGA TCCAGGAAAT GAGCCCAGCC 300 AAGTGATTCC ACTCTCTAAA GATGTCAAAG TCGGTTCTCT GCAATATCCA AATGTTCCTC 360 TTTTGGAAGT GAAATGAGGA AAGGCCTATA TAATTTCTAG CTGAGTAAAC GAAGAGTGCT 420 TTATTCTCTT ATAAATCAGT TACAGTCCCT TAAATAAAAG CATGCTTCCT CCTGAAAGCA 480 GCTGAAAGTT TCATCTCTTT AGAAGAGGCT TTGTTTTCTC TGAAAATGGG CAGGGGGACT 540 AATTAAATTA ATTTTTCTTT GTTCCTTTAA GAAAAATAAA CTTAAAGAAA CGGAGTATCT 600 GGGTGTGTAT GTGGAAGAAA GTGACTAGCT CTGATGACCA GGCACGTCAC AGTTTCTTGT 660 TTTGACTCAA GAATGATAAA ACAGTAATGG CTTTGACCCA TTGCCCTGCT GATGTGCTGA 720 TATGAGTTTG CCATTGGTCA CTGGAAGATC AAGGTCTGCC TTTCTGCTGA CCAAGCATTC 780 TCCTAACTAT TAGTCACTGT CTTCACTTAG AGCTCTCTTT CATGACTCAG TGCAGCTCTC 840 ACATTTGGGC TGGGCAAAAC GGAAGTTCTT ACTTAATTCA ACCTGCTGCA ATAAAAATTG 900 AAACAAACAC GTCGCATTCT CCTTTTTCTT AAAAATTTTG GTAACATCAC TGTGACTAGA 960 GCAGTTAGAG AAACTCTAAA GCAGAAAATA AGAAAATCAT TGCTTAATGT GGGATTTCGA 1020 TGTGGCAGAG TGAGAGTTTT TACGGCTATA CTGACACAGA AGCATTTGCC TTTGAAAATG 1080 GGTAAACTGA GCTTAACATT TTCATGAGGC AAATTAGATG TAATATCTCA ATATCTCATA 1140 ATTTTCCTCT CAGAGAACAT CTGTTTTCTG 1170
|