Tag | Content |
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EnhancerAtlas ID | HS052-03751 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:231765860-231767360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr1:231766123-231766134 | ATTGACCTTGA | - | 6.02 | TFAP2A | MA0003.3 | chr1:231767157-231767168 | CGCCTCAGGCA | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 231766380 | 231766659 | chr1 | 231767036 | 231767260 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I231630 | chr1 | 231765883 | 231767386 |
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Enhancer Sequence | CAGACAGGGT TTCACCATGT TGATCAGCAT GGTCTCGATC TCCTGACCTT GTAATCTGCC 60 CGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTGCGCCG GGCCCTTTAA 120 ACAAGATTTA AAGACCAGCA CACAAAGTTT CTGAGTACAA AAAAAGGTAA TATTTTAGGT 180 TAGGGTCATT AGACCAGAAT TAGAATCATT CTTTTTTTTT CTTTTTTTAA TTAAAAAAGA 240 TGGGGTCTCC TTATTTTGGC CAGATTGACC TTGAGCCTCA AGCAACTTCT GCCTCGACCT 300 CCCAAAGTAC CAGGATTACA GATGTGAACC ATTGCACCTG GCCAGAATCA TTCTTTTGAT 360 AATAATGATG GTAATTGAGT TTATATGCTG TGTTCTCATG AATCCAAGCA GAGCCCACTG 420 TTTCCAGAGA TTCCCTTGGC AGCCACCCTG GGTTGAGGAG GGTCCCCTCC TGGCACAGCT 480 GGAACCACCG GTGAAGAGCC ATTTTTCAGT CAGCACCGTT TAGTAATATA AGACTTTTAG 540 CCTCGAGGAG TCTTCCGTTG TTAGTTCCTA ACTTTAATGA CTTTGTGGTA AAAATTCCTT 600 AGCGAATGAC TTCTGTGCAA CAATCATGTA ATTTTTAAAA TTCCAGATGC TTTAGCCGTT 660 CAGAATCCAT TTTTTCTTTC AAAACCAGAG TTCACCAGCT GTTTCTCTTG AGCGAAGACT 720 TTGCAATGAG CTTTCAAATG TTCACACCAA GTAGAAGCAG GAAGGGAGAA CTGTGGCTGG 780 GCAATGAATG AAATACTGAC ATTTAGCTGT AGAAGGTAGG CAGGGGCTCA CATGGTGTGC 840 ACAGCCCCTT ATATGACTAC TGGTCCTGTA TCTGCTTCCT TTCCCTGCCC CATTTCCCCT 900 TTGGCTTTTT GTCATGACTC AGAAATGGAT GCTAGACATT ATGGGGCTCC CTCCAGTCAC 960 TCGGGTCACT CGTCACAGAC TTATAAACAG AATCACAGAA CTTATTGTCA GATGAAGCTT 1020 CAAAACACCA GTTGGCTAAA CTCCTTGTGT TCTGGCAGGT AAGATGTCGG CATCCTTATT 1080 TAACAAATGA TGCTACTGAG AACTATGTAT GCAGAGACAT AGTCTCAAAA TAAGTGCAGT 1140 CATGCCTCGC ATAATGACGT TTTGTCAATG TCACATATGT GAGAGTGGTC CCATAAGATT 1200 ATACTGGGCT GTCAATTTCC TAATGCCTAG TATTTACTAT ACATTTTAAT GTTATTTTGT 1260 GTACTTCTAC TTAGTAAAAA AAAGTTAACT GTAAACCCGC CTCAGGCAGG TCCTTCAGGA 1320 GGTATCAGAA GAAGGCATTG TTGTCATAGG AGATGATGGC TCCATGCGTG TTTTTGCCTT 1380 GAAGGCCTTC CAACGGGACA AGGTGTGGAG GTGGAAGGCA GGGATAGTGA TGATCCTGAC 1440 CCTGGGTAGG CCCAGGCTAG TGTGTGTGTT TGTGTCTTAG TTTTTAACAA AAAGTTTGAA 1500
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