Tag | Content |
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EnhancerAtlas ID | HS023-09592 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr16:57466470-57467950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr16:57466480-57466491 | AAGCAATAAAA | + | 6.32 | TFAP4 | MA0691.1 | chr16:57467545-57467555 | AACAGCTGAT | + | 6.02 |
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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 |
GH16I057431 | chr16 | 57465820 | 57467328 |
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Enhancer Sequence | CACTGAGTCC AAGCAATAAA AGAAAAAACT CCATAAACAC AGTCAGAAAC TATTAATTAC 60 AAACATACAT AAATGCTTCC TGCTGTGTAG AAGAGAACAC ACTGGCCTGG GAGGCAGAAG 120 ATGTGGGTTC ACAGTCCAGC TCTACCCCTC TGAGAGGTCT GACCTTGGGC CAACCACTTG 180 CTGATAGTTA CAGAAGTCAC CATTTGCTAA GCTCTTGCTT TGCACCAGGC ACCATATTAA 240 GCACTTATAT ACATTATCTA ACTTAATTCT GCTGACAACC TTATGAGGTA ACTATCTGTC 300 ATCCTACTTT TACCGCTGAG GAAACAGGTT TAGACACTTA GGCTGGTTCC ACAGGCTGCA 360 AAGCCTGTCT GATGCTTTTA ACCTCCATTC CATATTGCTT CCTCCTCGAT ACCTTAGTTT 420 CCATTCTATA ACATGAAGTT AAATTGTACT TCCTATGTTA CTGCAGGTGT TTTGAGGATT 480 AAATGAGAAA TGTGTCAAAA CCTTCAAAAA TAGCAGAGCT TTAGCCTCAT GTAAACCTGC 540 TACATACAAG AAAATAGGCT CTAGAGCTGC TGGTGGCAAG GTAACACCAT CAGTGGCAGA 600 CAAACCTCAC ACTTCCTGGT TCTCTGTCTA GTCAGGAGAA TGCAAGGAAG AGGCAGAGAG 660 CTGAGGCTCG GATGCAGTGT GGGCAAATCC TCGCAGGCCC TTGGGGTAAG AGTACCCTCT 720 AGTGATCATT GTCACAGCTG GATGCTCATA CCTTCCACAA GGCCAACTGT TCTAAGCTAT 780 TCCTACCCAT TCTGGAACCA TGAATCGAAA GGTTAGATTC CAAAGGATTT CTTGAAGATT 840 TAGGTTAGAC AGTCAAAACC GTACAAGTGG GAATGTACCA GTAAATATCT GTTAATGTCT 900 GCATACCTCA CAGCTGGGTC AATTCAGGCA TTTAAAAATA GGGATAGGAA GGATGAGGAT 960 GGAGCTGTGT GTGTGTGTGT GTGTGCGTGC GCGTGCGTGC ACGCGTGTGC TTGTACACAA 1020 TTTTCTAGTC AGAAGAAATA TAGTTTTATA AGTGTCTTAG CATCCTCAAA GTAAGAACAG 1080 CTGATTTTCC TGGCATGGGG AAAAAAGCAC ATGAGAACAG GAACAGGGCA CTCTCATACA 1140 CCATTACCAC TACACTGTGA GGTCTTCTGA GGAGAAACGT TAATTCTGGG ACCTGGAAGG 1200 ACCTCATTAA TTAAACTGTG TGACTCAGTC CTGTAAAATT AGGAGGCCTC GGTATCTTCT 1260 GGTGCAGAAG AAGGAGCTGA ACTAGATAAT ACCTATGTAT TATTTCAGTT TTGGATCCTA 1320 ATATGCCCAT GATAATAGTA CATTAAGTAT TCTTCTTTGT GGAAATGGCA GAAATCAAAG 1380 GACTAATCCT CTAAAAATAT CACCATCTCA TTTATTGCTG GCTCAATTTC TAACATGTCC 1440 CTCTAAGCCC ATTCAAACAG AAGAATGTCC CTAGGCCAGC 1480
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