Tag | Content |
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EnhancerAtlas ID | HS141-01450 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:182399570-182400410 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK1 | MA0028.2 | chr1:182399968-182399978 | ACCGGAAGTG | + | 6.02 | ERG | MA0474.2 | chr1:182399968-182399978 | ACCGGAAGTG | + | 6.02 | ETS1 | MA0098.3 | chr1:182399968-182399978 | ACCGGAAGTG | + | 6.02 | FEV | MA0156.2 | chr1:182399968-182399978 | ACCGGAAGTG | + | 6.02 | FLI1 | MA0475.2 | chr1:182399968-182399978 | ACCGGAAGTG | + | 6.02 | YY1 | MA0095.2 | chr1:182399980-182399992 | GCAGCCATCTTG | - | 6.74 |
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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 |
GH01I182430 | chr1 | 182399444 | 182400110 |
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Enhancer Sequence | TATCGTCTTG TCTTGGGATC CCAAAATGCA GGGATTACAC GGTGCCTGGC TTTTTTTTTT 60 TTTTTTTTTT TTTTTGGTAT CTATTCTCCT TCCTCTCCTG TGCATCAGAG GAGGTGGCCT 120 GGATGCCTGC GTGGCTGCAG AGACTGAAGC AGATGGAGCC CAGTCAATCA TGGGGACTCC 180 CCTTTCCTCT CATGGTGATA CATTGAGGTG TGGGTGGGAA ATCCAGGTCT AGTTAGGGAG 240 ATGTGAGAAG GATTCTGCTG CAGGGTCTCT GGATAAAGTC CTCCCTTGTC ATAAATGTGA 300 AGAATATAAA GAAATATACT ATCTAGTATA TAGATACAGA TATATATTTA TAGAATAAAG 360 CTCTCTTTTC TGCCCCGGAC GTCTGTGAGG ATGAGGTAAC CGGAAGTGTT GCAGCCATCT 420 TGAAACCACA ATGGTTGCTA ATCTGAAGAT AAGGTCAATG AGAATGACAG AGAGAAAGCC 480 TCGAAGTAAC CTGAATCCCT GATGACTTTG TTCAGCCACT GAATTTAGCA GCTCAGGCTC 540 TGTACTACCT CTAGAGTTGT TGCTACGTGA GAAAATAAAT GTTTTACTGC TTAGGGTCCT 600 CTATTATTTA TAGCCAAAAA CATCCTAAGT GATTTACCTC ATATATCTGT AGGGTGTAAA 660 TCAAGTAATC CCTATAAAGT GTTCAGCACT GTGAAATGTT AACAATTATC ATTAATATAA 720 TATTTTATTA TGGAATTATA TACTGCTTTC TTCTTTACTA ATGTTGGGGC TGGGAAGCTG 780 ATATCCTACA ATATGGCACT TTGACATGCT GAACTGAAGA AGCCTCAAGG TCTCCCTGTT 840
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