Tag | Content |
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EnhancerAtlas ID | HS108-26007 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr21:37431390-37432570 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr21:37431769-37431784 | GAGGTCAGGAGTTCA | + | 6.22 |
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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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Enhancer Sequence | ATGAAACGTT TATACTGTGA GCTAAATCAT GATCCCTACA GTAACAGAAT TCCCATTATA 60 TCAGTCCCTC TAAAACAGTT TTATCTTGCA GACCTAGTGA CTACAGCTTA ATCTACTAAA 120 AATACAAAAA ATAGCTAGGC GTGGTGGCAC ACGCCTGTAA TCCCAGCTAC TTGGGAGGCT 180 GAGGCAGGAG AATCGCTTGA ACCTGGGAGG CGGAGGTTGC AGTGAGCCGA GATCGCGCTA 240 CTGCACTCCA GCCTGGGCGA CAGAGCGAGG CTCCGTCTCA AAAAAATAAA AAAATAAATA 300 CATAAATAAA AATAAAATAA TGGCTGGGTA CAGTGGCTCA CGCCTGTAAA ACCAGCACTT 360 TGGGAGCCCG AGGCGGGCTG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA CATGGTGAAA 420 CCCCGTCTCT ACTAAAAATA CAAAAATCAG CCGGGCGTGG TGGCAGGCAC CTGTAATACC 480 AGCTACTGGG GAGGCTGAGG CAGGAGAATC GCTTGATCTC AGGAGGCGGA AGCTGCAGCT 540 AGACGAGATC ACGCCACTGC ACTCCAACCT GGGCGACAGA GCGAGACTCT GTCACAAAAA 600 ATAAATTAAA AAAATAAAAA TAAAAAATAA ATCTACTTCT AAAACATACG AGGGCAGAAA 660 TGAGCAAGAG ACAAGAACTC CAGGCAATAT TAATACCGCA CTTCCGCAGT ATAAGGTTCA 720 TTATTTGACC TAACGAAAGT CGGCATGTCC AGCTCCAGAG GCGAACGGCG GCTGGTTCGG 780 TGCGGGTCCC AGCGCTCAGT CCACAGACCG CGCCGGGAAG TGTCCCCAAG ACTCCCGGGC 840 CCTCGCGCGA GCTGTCCACC ATCACCCTGC TGAGGACCAC GTGAAGCCCG GTGACCGCCA 900 CAGACACAGG CACCGTCCCC GCCCCCATAG TCCTCAAACT CTAGCCGTGA GGCCGTCCTA 960 CGGTCCGACA CACACCGCTC CCGCAGCCAT AGGCCAGCCA GGCGAGCATC GGACCTCGGG 1020 CCTCAGGCTC CTCAGCTTTA CGCAGCGCGC CGGAGCAACA TGCGCTAAGT GTAGGACTCC 1080 ACAAGATGAG AGGTTACTGC AGCGCACACG ATAATGCCTG CCCTGGAGGG GACCTGCGAC 1140 CTAAACTCAG TTCTTTTTAC GCTGATGAAT GAAAGACTAA 1180
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