| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18919 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr3:195478140-195479240 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIA | MA0670.1 | chr3:195479022-195479032 | ACTTGGCACC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 195478515 | 195478752 | | chr3 | 195478180 | 195478230 |
| Enhancer Sequence | ACCTAGGTTA GAGGATGGCA GATGGGGGTG GGGGTGAGGC CCCATCCGGG GGGGAGACGC 60
CCTCCCACCT TGATGGGTGT ATTCATCCCT GTTTCCTCCT GGAACGGGAG CCCCAGGACC 120
CCAGCACCTT CCTCACCTGT CTCTGCACCC TTGCACTCTA GCCTAGCTCA GTGAGTGTCA 180
TGGGTCCTTG CTTAATAATG TTTGTTGAGA GTGAAGGGTT TTCCATTCTG TCCCCCCCTC 240
AGCCTCATAT GACGAGCAGA GAATCTGACA TGAATGGCCC CTACCTTGCC TCTGACACAT 300
GACTCATGAC CTCCTCCCCA GTATATTGAA CATGGGTTGT TTAGACCTAG GAGATGGTCG 360
GGGCTGGGGG TGTCAAGGTG ACTTAGGTGG AGTCTAAACT CAAAGAGTGC ATTGTCTGGC 420
GCAGGTGACA AATGTCAACA GATTTTACCG TGTGGAGTGT GGAGTGGGGA GTGCTAGGCT 480
TGCAGTAGTG ATAATAGCAG TCATCATGTT TGAATACTTG TGTGTCAGGC ACTGGACTAA 540
ATGCTTGACA CGCGTTATCA TTTAAACGGT GATACGGCCT GTTGACTCAG GTGCTATGAT 600
TGTCCCTGTG TTTACAGATG ACCTGTTATA TGATGTGTCT AGTTAGCACA CCTGCTCTAG 660
TGAGGGGCAG AGCAGGGATT CTGATTCTGG GTGTGCAGGA TTCTACAGCC CCAACCACTC 720
AGCAGTTGTG CCACTTTGCC TGTGACTGAG GTATGGCATG GCAGCCAAGA AGAGGGAGCC 780
GCCCGTTCCC TCTGGGAAGT CAGGGAAGAC TCCCGGGAGG TGAAATGTCC TTTAGTTTCT 840
TTCAGATCAT AACCAAGATG CTTAGAGGTC TCGGCTGGGG TGACTTGGCA CCCTGGCCTC 900
TGCTTATGAT GAGTCGAGGT TTCTGTCTTG GGCCTTCCTC ACTTCCTAAT GCCCTGCACC 960
TCCCATGGGG CAAGAGGCTC CGGCCTCCTC TGGCAGTTGA ATCCAGATGG ATGACAAGAT 1020
GAAGGCCGCA CAGCGATGGT TCCGCCCTGG CCTGAACCCG CCAAGCGCCC CCTCCCACCC 1080
AGAGCGCGGC CTGCAGCACT 1100
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