Tag | Content |
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EnhancerAtlas ID | HS002-05646 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr2:191656300-191657350 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr2:191656892-191656908 | GGCAATGTAAACAATC | + | 6.1 | Foxa2 | MA0047.2 | chr2:191656893-191656905 | GCAATGTAAACA | - | 6.07 | POU2F2 | MA0507.1 | chr2:191657289-191657302 | ACATGCAAATAAA | - | 6.17 | PRDM1 | MA0508.2 | chr2:191656806-191656816 | TCACTTTCAC | + | 6.02 |
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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 |
GH02I190791 | chr2 | 191655907 | 191658721 |
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Enhancer Sequence | TTCATTTCAG AGTGAAATTC TCAAGCCCCA AATGGGTAGG TGTTTTAATT CAGCATGGAA 60 ATAAAGAGTT GCTTTTTCTG GACATATTCC CTTCCTTTTC CTGGCAGTTA CTGGTACCGA 120 CTTGCTCTTA ATTATCTCCC ATTCAATGCT AGTCATAACC ACCCGCCCAC TTCACACTTA 180 GGCAGTCCTG CCCACAGCAC TCACCCCAGC CCCCTCAGGC TGAATCATCA GCTCCCACCC 240 CCGTCCTTCC TTTCCCACTG CCATTTCCTT TTTCGCTTCA ATGCCCTTTA TAGAGGGACA 300 TTCTTGCTTT TCCAAAGCTT TTTTCCTCAT TCCTTATTAC ATCCCCTTTA AATTTTAGAA 360 AAACCGTAAT TCTTATGGAA TTTAATTTTC TTCTCATCAC TGAGGATGAT TTGTGCTTGA 420 TGCACCATAG AATCTGTGTT CATTAGTTAC CCATTAATTC TTGTGTACTT TAGGGGGACA 480 GTAGAATTTG AGAAACTGGA AATCTATCAC TTTCACTAAA ACATACATAA GATGAAACTG 540 AGTCACTTTG GAAGTTTCCA CCATGGCAGA GACAAAGGAA GTCCCAGGCC TGGGCAATGT 600 AAACAATCAA CTTACAGTTT GACATTTCTG CTTTCAACAT TCCACTCTCC CTGATTTTTT 660 TTTTAATGCT ATAATTAAGT CCTTTCAAAT TGCTAACCCT AGAGCCTCTC TTTTTTCTTA 720 GGCATACAAA GTATGGGAAG CTGAGGGCTC TAGAATTTGA CACCTGCAGG TATCCTAGCT 780 CTGATCAACC CACAGATATG TTGTACTGAT ACCAGCCCAG GCCATGAAGA CACCATTAAA 840 CATTCCACCC CTATGTGGTT TTTACTTAAA GTACTCTAAT ATTGTCAGGA GGTATCCATG 900 TATGAAGACA TATTTCTCCG CATGTTCAGG ACAAGTCATT CCTTATTATC TCATGAAGAT 960 TCTGCATACA GGTCTCACAG CTACCCCCAA CATGCAAATA AAGAAAAGAA GACATCAAGT 1020 TCAAATGATC ACTGATGGGG TTTCCTTTTG 1050
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