Tag | Content |
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EnhancerAtlas ID | HS053-01637 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:62698190-62699320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:62698224-62698245 | TTTTACTTTTTCTTTCTTTTT | + | 7.51 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 62698531 | 62698618 | chr1 | 62698437 | 62699131 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I062232 | chr1 | 62698531 | 62698730 | GH01I062233 | chr1 | 62698781 | 62698930 |
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Enhancer Sequence | GAGATATACA GGCGTGCGCC ACTACGCCTG GCCATTTTAC TTTTTCTTTC TTTTTTTTCT 60 TTTAGAGATG GGGTCTCAAT CTGTCACCCA GGCTGGAGTG CAGTGGTGCG AAAATAACTC 120 ACTGGACTCA AACAATCCTC CTGCTTTAGC CTCCTAAGTA ACTAGGATTA CAGACATGTG 180 TCACCATGCC TGTCTATTTT TTATTTTAAA TTTTTTTTTG TAGAGATGAG GTCTTGCTAT 240 TTTGCCCAGG CTGGTCTTAA ACTCCTGGCC TCAAGCAATC CTTTCGCCTT GGCCTCCCAA 300 ACTTTTTCTG TTGAGGCCTT TGCATTTTCA AAGGGGTCTG TTATTCCCCT CAAGTTACAG 360 GCACAAGTCC AAATTCCAAG TATCCATGTA CGAGTGTGGT ATGTTTCCTG ACCTCCCTTT 420 CACGTCTCCT GTTTAGTCAC GTCTCCTGCG TAACTGAAAC TAAAGTCATT TTGAAATTGT 480 CTCCATTGCC CAACAGGTCA CACTTTTTCT TTTTTTTTCC TTTTTTCTTT TCGTGATGGA 540 GTCTCACTCT GTCGCCCAGG CTGGAGTACA GTGGCGTGAT CTTGGCTCAC TGCAAACTCC 600 ACCTCCCGCA TTCAAGCGAT TCTTATGCCT CAGCCACCCG AATAGCTGGG ATTACAGGCG 660 TGAGCCAGCG TGCCCAGCCC AGGTCAGGTC ATGCTCTTTC ACATGCCACA TCTTCCATCC 720 ACCTGCCGTT ATATCTAAAC TCCTAGGCAT CGTTATGGCT TGGCTGAAAA GCCACCTCCT 780 CTGGGAGGCG TCCTTGACTC CCTTTGTCCC ACTCAGTCTC CACAGCTCGA CTCAGGCCTC 840 CAACACTTGT CACATTTCAT AGTGGTCGTT AGCTTACACC TGCCCCCCAC CAACAAACCA 900 TTAACTCTGG AGCCCAGGAC TCTGAATGGA CACTCCACAA ATGTTTATTG AATAAATGTC 960 ACTCATGCTA AAAAAACTGG AGTGCTGTTT CTAACATGTG AATCTGAGCA TTGCTTCCTT 1020 TTTGCGGAGG AGCGGGGAAT GGTGTCTGGC TGTAACCCAG GCTTGAGTGC AGTGGTGAGA 1080 TACCGGCTCA CTGCAGCCTC TGCCTCCCCA GTTGAAGCGA TTCTCCTGCC 1130
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