Tag | Content |
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EnhancerAtlas ID | HS145-09578 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr17:1460210-1461380 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr17:1460804-1460815 | GGCTGTGATTT | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09501 | chr17:1457929-1461083 | CD14 | SE_25267 | chr17:1460829-1461336 | Colon_Crypt_3 | SE_27390 | chr17:1457661-1461383 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I001554 | chr17 | 1458211 | 1461911 |
|
Enhancer Sequence | GACCCTATCT CCACTATTTA AAATAAATAT TATAAAATAA AAAAAATAAA GACAGCATGG 60 CCAAAGCAGG TGGGTTAACA AGACCCTTCC AAGCCAACAC CTGTCAGCCC AGGCACCTGG 120 TTCTCAGGCC CCAGGTACAT CCCCAGTGCC TACAGGGATT AGAGCCATCT ACCCAGCCAT 180 TCCCTCATTC TCCCTGGTTC CCAGGTTCCC CAGTCTCGTT TCTCTTTTCT GCCCTTCCCA 240 GAACCCCAAG ATCACGGTCA AGGCCCACCT CTGGCCCCCT CCCCAGGTCC CCACAGCTCT 300 TATCAGATAT GTAGCCCACC CCTGGAGGCA GTCCTCTAAA GGGCCAGTGT CTGCCCACCC 360 CTCTCGGGGG CCAACAAGCC TGGATGTCTG TCTCAACTAA ATGTGCTGCA GGCTCTGCTG 420 GCCTGATTTC ATTTTTCAAA GGTGCAGTTC ATATTGGGAA CAGAGTGGAA GTTATCACAG 480 GAGCTTCATG CTGACACTGC AGGAAAGAGA GACGGAGCCC AGTGACTGGA GGCACTATAC 540 TGGCTGACGA ACCTCACCCA AACTCGAGTT TAACTGGAAG CTGGGGCGGG GTGGGGCTGT 600 GATTTCAGAA GGAAGCAAAG AACAAGGCTG CGCCAGGAGA GGAGAGTGGA AGAAGTTCAG 660 AGAAAGAGTG AGACAAGGGA GGTTCCGTGA CAGTTTTCCG TTGTCCAAGA GACTGACTCT 720 GAGTCAGCAT GGCCTATGAA CCTTCTTACA GCAAATCCTG CTGCCAGATC CCCACATACA 780 AGGATGTCAG ACCCAGGAAC CGTAAAAGGA CAGAGGACAA GCCAAGCCTA TGTGTTATTC 840 CCTGCCCTTC GTAAAAGGAG GGTTCTGTGT CTTGGTCTTT CCAGCAGTCA CCTATCGTGG 900 CTAGGGAGAG CCTCAAGAGA TTTCCTGCCC TGCTGGTTTG TTGCACAACC AGAAAGAGCC 960 ACGCACACTT GCCAGCCGAG TCACGGACGT CCCAGAAATG CACACACTTG ATCCCATCAA 1020 TAATGCGTCC CCGGCCGGGT GTGGGGGCTC ACGCCTGTCA TCCCAGCACT TTGGGAGGCT 1080 GAGGCGGGCG GATCACTTGA GGTCGGGAGT TTGAGACCAG CCTGGCCAAC ATGGTGAAAG 1140 CCCATCTCTA CTAAAGATAT AAAAATTAGC 1170
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