Tag | Content |
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EnhancerAtlas ID | HS147-03626 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:171786280-171787780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:171787013-171787024 | GATGAGTCACT | - | 6.02 | JUND | MA0491.1 | chr1:171787013-171787024 | GATGAGTCACT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 171786658 | 171787332 | chr1 | 171786507 | 171786551 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I171817 | chr1 | 171786346 | 171787596 |
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Enhancer Sequence | TTTGTAAAAC ACACACACAC ACACACACAC ACACACACAC AGTCTCCCAT GGTTATTAAA 60 ATAATTAAAT GGGATAACCT AAGTAAAGGC CTTAGTACAT GCTGAACACT TGGTACTTGC 120 TTATTGTTAT TTCATTGAAC ATGTTATGCT CAACAAGTTA TCTAGCTAAT ATATGCAAAG 180 TTTTGCAAGG CCAGGCCAAA GGCACAGGTC TTAAAATTAT AAAAGCTGAA GGAGTTGCAA 240 CCAAGAAAGG AAATAATTAG GGAAGAGAGA CTGGATCAGA AGCCAGGCAG CTAAGGGTAC 300 TGGCTTTTCA AATTGTGTTC TTTTGTTAAG ACTAAAATTG GAAGACAGGA GAAGCAGGGC 360 TTTTGGAATT GTGGATACCA AGCACCACTA AATGATTAAA GCAAAGTGCA GTGCTGGCTG 420 GTGGCCGTGT GCTTGTTATC TTGGAAGTGC AACCCTTGTG TCCTGTATCT GATTCATTTT 480 CAACAATTTT TTTTTTTTTT TTGTGGGTGG GGAAGAAAGA GGAGGGATGA CAGAGAAAGG 540 TTGGAAGATA CACAGGAGAG ATATTTGAGG GGAGGAGCAA ATAGACTAAT ATTCTCAGTG 600 CTTTTTAACT CATTGATTGC CAGGAGCCTG GGTGAGGCAA AGCATTGGTT TATTCAGCTT 660 TTATTCAGCT CAGTGCCCTG TTGACAACAC AATGTGTCTG AGTCACAGGG GGTCAAGTGA 720 CTGTAGCTTC TCTGATGAGT CACTGTCTTG TTTCCACTAA TGTCTCCGTG GCTGGGGCCA 780 ATTTGTTTAC TGAGAGAAAG CTACAGCTGT CTGCAGGTAC AGACATTTGT ACTCCAGAAC 840 TTACCAGCAG AGCCAAGCAG TGTGGATGTG AGGAGCTTTT GCACTCCTGG AAGGTCCTCA 900 CGGGTAACAG GCAGTGGGAG CTGCTTGATG TGATATGATG ATGCTCTTTC CTTTGATTTG 960 GTATCAAGAG AAGCAACTGT TTAGAATTAG AGCTCAGAGG ATTGAGCAAG AGTTAGAAGG 1020 TGGGAACAGG ACTAACATAT ATCACCCAGG AACCCAGTAA GACATATGGC ATATTCACAG 1080 TAGGCAATTG AAGGGTGCTG GGTAGAGAGA CTATTCACAA GGGTGTGAGC AGGGTTCAGG 1140 GAAACCAGCA AGGGATGGTG CAGGGTCTCA GAGAAAGCAA GTGTGGGGAG CCATTACTTG 1200 GCTGAAGAAG CATGAGTGGG GAGAGTGGCT ATTGGAGCAC GGGGGAGTAG AAGTTGGAGA 1260 AAGTCACCTG AGAGGAGCAG TGGCCATCAT CTTAAGGCCA CAGTCAACTT ACAGTGAACC 1320 AACAGGGATG GAGTCAGGGT TATACATACC CACTTCACTC TCCTCCCACT CTCCCATTGG 1380 AGACCCTTAT ATTGGCCACA TCTTACTGAA AGCCAGAGAG AAGGGAGTTG TTGACGTTGG 1440 CCACGCAGGC CAGCTCCTGA GGAAGAGAGC AGGGTGGAGA AGCTGGAGAG TGGCTCTGGG 1500
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