| Tag | Content |
|---|
EnhancerAtlas ID | HS076-37322 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr21:44345100-44346550 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr21:44345776-44345787 | TGTAAACAGGA | - | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 44345451 | 44346104 | | chr21 | 44345307 | 44345403 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH21I042923 | chr21 | 44343211 | 44355064 |
| Enhancer Sequence | GCTAGAGTGC AGTGGCGCGA TCTCTGCTCA CTGCAACCTC CACCTCCCGG GTTCAAGCGA 60
TCCTCCTGCC TCAGCCTCCC GAGTAGCTGG GATTACAGGG GCCTGCCACT GTGCCCAGCT 120
AATTTTTGTA TTTTTAGTAG AGACGGAGTT TCACCATGTT GACCAGGCTG GTCTCGAACT 180
CCTGATCTCG TGAATCCAAC GGCCTTGGCC TCCCAAAGTG CTGGGATTAC GGGCGTGAAC 240
CACCACGCCC GGCCATGCCA TAGCCTTCTT GGACCCATGT TGGATTTTGG GGCTGGAGAA 300
ACCAAGAGAG GCCGTGCGGA TTTTTCCCTG TTAACCGGGC TCCCAGGAAA CTTACCAGTA 360
GGCGAGATCA GTGACCGATG TGCATGCACA GAGAGGCGAC TAGAGGCTGA GGAGCTTCCT 420
TTGTCCGGCT GCTGTGGCCT GCTTTCCCAG ATGGAGGGGT GGTAGGTCCA CTGGGGACGT 480
GGACGGAAGC CCCTCGCAGG TTTCAGGGCC AGCCCCAAGG CTCTTGCATT GGTTGGAACC 540
CGGAGAGCGC GCCAACAGAC AACACGAGGC GGTGTGGAGC AACACACTGT TTTAATAAGC 600
ACCTGGATGC AGACAGACTG AGGCCTAGAA TGGCATCAGC CCCAAGTGAG GAGGGGGCAG 660
GGCTTTTATA GTTCTCTGTA AACAGGAATT GTCCCAGCCT GACGTGACTG CTATGTAGTA 720
CGCGGACGGC CTCCCCCTTG ATCTTCAGAG AGTATGTGTC TTCCAGCCAG CTCTTTTCCT 780
GCCTCTGCTA TCTTGCTGCT GGTGCAAGTT TGAGCGTTGG GACTGGGCCT GAGGAGGAGG 840
AGTTACTCAT TCCCTCAAGC TTTCAGGCCC CTGGGAGAAT CTTTCAATCA GGACTTCCTG 900
AGGCGGTGTC ACAGGTCCCT GCCCAACCTT GGCAAAATAA ACTTTCTAAA TTAACAAGAG 960
ACCTGTCTCA GCCGGGCACG GTGGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCCCAG 1020
GCGGGCAGAT CACGAGGTCA GGAGATCGAG ACCGTCCTGG CTAACACGGT GAAACCCCGT 1080
CTCTACTAAA AATACAAAAA ATTAGCCGGG CATGGTTGCA GGCGCCTGTA GTCCCAGCTA 1140
CTTGGGAGGC TGAGCCAGGA GAATGGCCTG AACCCGGGAG GCAGAGCTTG CAGTGAGCGG 1200
AGATCGCGCC ACCGCACTCC AGCCTGGACG ACAGAGCGAG CCTCCATCTC AAAAAAAAAA 1260
ACCTGTCTCA GATTTTCCAC ATCCGCACCC AAAATGGCAT CAAACTCCTG GCCTCAAGTA 1320
ACCCATCTGC CTCGGCCTCC CAAAGCGCTG GGATTACAGG CGTGAGCCAT TGTGCCTGGC 1380
CTCAAGTGGG ATTTTTTTTT TTAATTCTGA GACAGAGTCT AACTCTATTG CCCAGGCTGG 1440
ACTGCAGTGG 1450
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