Tag | Content |
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EnhancerAtlas ID | HS052-21919 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr2:191656170-191657600 |
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 | AATATGTATT TCTTTCTAAG AAAGCACGTC CTGCACAGTT TTCCATTTTG AATCTGTTTT 60 TCCCCACACC ATTAGAAGAA AGCATGGAAA ATTTCACAAT CATCTGCATT CTGTTTACAG 120 CAAATATTTT TTCATTTCAG AGTGAAATTC TCAAGCCCCA AATGGGTAGG TGTTTTAATT 180 CAGCATGGAA ATAAAGAGTT GCTTTTTCTG GACATATTCC CTTCCTTTTC CTGGCAGTTA 240 CTGGTACCGA CTTGCTCTTA ATTATCTCCC ATTCAATGCT AGTCATAACC ACCCGCCCAC 300 TTCACACTTA GGCAGTCCTG CCCACAGCAC TCACCCCAGC CCCCTCAGGC TGAATCATCA 360 GCTCCCACCC CCGTCCTTCC TTTCCCACTG CCATTTCCTT TTTCGCTTCA ATGCCCTTTA 420 TAGAGGGACA TTCTTGCTTT TCCAAAGCTT TTTTCCTCAT TCCTTATTAC ATCCCCTTTA 480 AATTTTAGAA AAACCGTAAT TCTTATGGAA TTTAATTTTC TTCTCATCAC TGAGGATGAT 540 TTGTGCTTGA TGCACCATAG AATCTGTGTT CATTAGTTAC CCATTAATTC TTGTGTACTT 600 TAGGGGGACA GTAGAATTTG AGAAACTGGA AATCTATCAC TTTCACTAAA ACATACATAA 660 GATGAAACTG AGTCACTTTG GAAGTTTCCA CCATGGCAGA GACAAAGGAA GTCCCAGGCC 720 TGGGCAATGT AAACAATCAA CTTACAGTTT GACATTTCTG CTTTCAACAT TCCACTCTCC 780 CTGATTTTTT TTTTAATGCT ATAATTAAGT CCTTTCAAAT TGCTAACCCT AGAGCCTCTC 840 TTTTTTCTTA GGCATACAAA GTATGGGAAG CTGAGGGCTC TAGAATTTGA CACCTGCAGG 900 TATCCTAGCT CTGATCAACC CACAGATATG TTGTACTGAT ACCAGCCCAG GCCATGAAGA 960 CACCATTAAA CATTCCACCC CTATGTGGTT TTTACTTAAA GTACTCTAAT ATTGTCAGGA 1020 GGTATCCATG TATGAAGACA TATTTCTCCG CATGTTCAGG ACAAGTCATT CCTTATTATC 1080 TCATGAAGAT TCTGCATACA GGTCTCACAG CTACCCCCAA CATGCAAATA AAGAAAAGAA 1140 GACATCAAGT TCAAATGATC ACTGATGGGG TTTCCTTTTG TTATGAAGCT TAGAGTTAAA 1200 AGAGATACAC TTGGGCCAGG CGCGGTGGCT CAATGCCTGT AGTCCCAGCA CTTTGGGAGG 1260 CCGAGACAGG TGGATCGTTT GAGGCCAGGA GTTTGAGACC AACCTGGCCA ACATGGCGAA 1320 ACCCCATCTC TACTAAAAAT ACACAGACTA GCTGGGCGTG GTGGTGCCCA CCTGTAATCC 1380 CAGCTACTTG GGAGGCTGAG GCAGGAAAAT AGCTTAAACC TGGGAGGCAG 1430
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