Tag | Content |
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EnhancerAtlas ID | HS177-18244 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr5:112295510-112296420 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr5:112295660-112295670 | GACACGTGCC | + | 6.02 | Npas2 | MA0626.1 | chr5:112295660-112295670 | GACACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr5:112295729-112295744 | TGAACTCCTGACCTT | - | 6.04 | STAT1 | MA0137.3 | chr5:112296289-112296300 | TTTCCTAGAAA | - | 6.14 |
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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 |
GH05I112958 | chr5 | 112293755 | 112297952 |
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Enhancer Sequence | CTATAATTTT TTGTTGTTTG TTTGCTTGAG ACAGAGTCTC ACCCTGCCAC CAAGCTGGAG 60 TGCAGTGGCA GGATCTCGGC TTACCGCAAC CTCCAACTCC CTGGTTCAAG TGATTCTCCA 120 GCCTCAGCCT CCCGAGTAGC TGGGATTACA GACACGTGCC ACCATGCCCA GCTAATTTTT 180 GTTAGAGACG GGGTTTCGCC ATGTTGGCCA GGCTGGTCTT GAACTCCTGA CCTTCGGTGA 240 TTCACCTGCC TTGGCCTCCT AAAGTGCTAG GATTACAGGC GTGAGTCATC ATGCCTGGCC 300 TCCTGGCTTA TTTCTTAAAT AATCATGGTG ACAAGTGCTC TTGGAGGTTG GAGTGAGGGT 360 GGAGGGGTTA GAAATGAGGA ATCAAACCCA CTCAGAGTAC ATGAATGAGA ATGGGGGAGG 420 AGTTGCTCCT GAAGGAAAAA CAGCTTTATG CTTCCAGAGA GAAAATGAAT GCTGAGAAGT 480 TTTTTTGTTT GTTTGGTTTT TGTTTTTTGT TTTTTAAAGA GGCAGATGCT CACTGCACTT 540 GGACTTTAGC AAAGAAAATT ACTTTTCAGA AAAGGAAAAA GAATCCCCCT TAAAATGAAA 600 GCATGTTGAT ATTCTGGCTC CTAGATCCAT CTGTGCAGGG GCCTGCTCTT CCAGCTGTCA 660 CCCTCCTTAG GCCTCTGGTG CTAGGAGCAT CTTTGAAATC ATAGATGACA GATGGGGATT 720 CTCTGACCTG GAGCCCTACC CAGGCTGCAG GCCCTCAACT ATAGCCTTTT TTTTTTTTTT 780 TTCCTAGAAA GAGGAAATCC TTCCTGCCTG CTTCTTCTCT CTTCTTCCAA CATCATAATC 840 CTCTTTCTGC AGTGCCTCAA CTCTGCTCAG AGGAAGATAA AGCTTCGCAT CATTCTTCAG 900 AGCTGTTTAC 910
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