Tag | Content |
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EnhancerAtlas ID | HS053-02407 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:120147110-120148610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:120148485-120148496 | AGGGTGTGGCT | - | 6.02 | TCF3 | MA0522.2 | chr1:120148088-120148098 | AACACCTGCT | + | 6.02 | TP53 | MA0106.3 | chr1:120147903-120147921 | AGCCTGCCAGGACATGTC | + | 6.1 |
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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 |
GH01I119605 | chr1 | 120147764 | 120147961 |
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Enhancer Sequence | GGGTTTGGCT GTGCCACCAA GGCTGGAGTG CAGAGGTATG ATCTCTGCTC ACTGCCACCT 60 TCACCTCCTG GGCCCCATTC ATCCTCCTGC TTCAGCCTCC CGAACAGCTG GGACTATGGG 120 CAAGCACCAC TACGCCTGGC TAATTTTTGT GTTTTTAGTA GAGACGGGGT TTCACGAGGC 180 TGTCCAGGCT GGTCTTGACC TCCTGGGTGC AAGCAATCTG CCCACCTCAG CCTCCCAAAG 240 TGCTGGAATT ACAGGTGTCA GCCACCATGC TCTGCCTGTT TCTCTACTTA TTCCAAATAT 300 AAATAAGGGA TTTTCTTTGA CATGGTGCTG GAGACCCAAA ATCATGATCC CGCATCACCA 360 GCAGAATTAA ATTCAAATTT TCCCTCTTAT ACCCAACTCT CCACAGTCAC CTTACTCTCT 420 TTAAATATTT TAGTGAGTCT CCCATGACTC TAGAAATGCT TATATTCCAA GCACACCTGA 480 CAGCTCATTG CTCAGATTAC TTTTCTTAAA TGAGATGGGG TAGAAACAGA TGTTTGCTCT 540 TTCCCAATAA ATTGCTACAT ATTCTGACTT CTGTGTCCCT GTTTACTTGT TCCTTCCATG 600 GAATGTACAC CCTCCACTCC AACACCCTGA CTCTAGCCAT CCTCGAACAT CTATGTAACA 660 ACATCTTTAT CAGTTTCAGA AATCGTTTCA GAAATCGTTC TGATAACCTG ACCGGTGTTC 720 ACACAGAGCT CCAGAACAAG ACCAAGCTGA CGGTGCTGGA AGGAGACATT CTGGATGAGT 780 CATGCCTGAA GAGAGCCTGC CAGGACATGT CGGTCATCAT CCACACCACC TCCATCATAG 840 ACATCATCGG TGTCACTCAC AGAGAGTCCA TCATGAACAT CAATGTGAAA CGTACAGTAG 900 CCTGGGGAGG AGATGAAGCA AGGTGGGGAA TTAAGGATCA CAAAGAAGGA CAGGAAGGGA 960 AAAGAAGTCT CTCCACTGAA CACCTGCTAT GCTCTGGACC AAGTGTCTTT GCTGATCACT 1020 ACCAACTGGG GGAGTTCAAA GCTGCTATCT TCAGTTTTTT ACATGAGGAA ACCAGTGCTA 1080 CAGATGGCAA GTAACTTGTC CAAGGCCCCC CCAGGTAAGT AAGTAAATAG GAGAGTTAGA 1140 CTTTAAACTC ACCCCTGTGT GACTCCAAAG GCTGTGGACA CTCTTTCTAT AGTGGCTTCA 1200 ATCAAAAGTC AACTAAATTC CAACTTCAGA CTCTTGATAT CCCTCTATGG GACAGAATCA 1260 AACCTTCCAG GTGCCACCAT AGTCATCATT GTGCTACACA CAAGTCACCT TGTGCGTAGG 1320 CTTATGATAA TGAAATGGGA AAAATTCCCT CATCCCCCTC ACCAGGCATG CAATGAGGGT 1380 GTGGCTTGCT TCTTCAATGC CTCACTGCTC AAACCTCTGT GGGAGCATAG AGACAGGCAG 1440 GCTGTGGGAC TCCGACACCA TAGCAGTGTC TGGGGTGAAT GTTTACAGCT CCTGAAGCCT 1500
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