Tag | Content |
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EnhancerAtlas ID | HS029-12278 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr5:131722840-131724050 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr5:131723448-131723462 | ATGACTCATTTCTT | - | 7.12 | RARA(var.2) | MA0730.1 | chr5:131723962-131723979 | TGACCTTTTGTTGAACT | - | 7.01 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_25154 | chr5:131722248-131724802 | Colon_Crypt_3 | SE_26597 | chr5:131722022-131723211 | Esophagus | SE_26597 | chr5:131723314-131726622 | Esophagus | SE_54554 | chr5:131720956-131726150 | Stomach_Smooth_Muscle | SE_62219 | chr5:131721125-131837948 | Tonsil |
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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 |
GH05I132384 | chr5 | 131720053 | 131726700 |
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Enhancer Sequence | GAGGTAAGCA CCATGTGGGT GTGGGTGAGA GGGACAGACT GACCGTGATT TGAGAGCAGC 60 AGCACCCAGC CCTGAAGTCC TCCCTGCTCA CAGCAGCCCA GCCCTCTCTC CGCCCAAGCC 120 CCAACTGCCC ATTCCCCCCA TCCCCCCACT CCCCACCCCC ACACGGGCCC TGTTAACACT 180 CAGAAGTTGA GGAATAGGTT ACAGCTGCCT CACTCTTTTC ACCACGGGTT TCAGATTTTC 240 ATTTTTTACT TCCTTTCTAG GCAATCATAT ATTTTAACCA TTACTTCTAA CAATAAATAC 300 TCTTTTTGAG TAATAGGCCT TTCATAAAGT CAGCATTTGG GAAAATCATT GTTTCTTATA 360 CCTAAGGTGG CTTGTCACCT TACAAAGCTA ACCCCAAACG TAAAATGTAA AGCACAAATA 420 GATTTGGAGT TAGAAGTATT TCATCTCTTG AGTATTAGCA ATTATTCATT AAAAAGAAAA 480 AAAAAGTGTT TAGTCTCTTT CTGCCCTCCA ATGGTTAATT ATTGCATATC ATCTTGGAGT 540 CAGGTCCTTT TTGATGTCCA CCTCTTCCCC CTACCCCACC CCTCCCGTCA GCCCTGTTCT 600 CACACACCAT GACTCATTTC TTGGCTCTAC CTAGTTCCTG GTTCTTGCTT TTCCTTCCCG 660 TTCCCTCTCC TACCATCTCT GTAGCAGGCA GTTTTCCTTG GTCTCGTGAC TATGAGAGGT 720 TAGAAGCTGT AAATGCTGCC TGGTGGGGTT CTGGAATGTG TCTGTGGTCT GACTGGAAGA 780 TGAGGGGTTG GGTGTGGGAA CAGCCACAAG CAGCCCTGCT GAAGTGTGAG AGGCAGGCAT 840 GGTTGGGCTT GGAAAAGAGG GAACAGTTAT TGTAGACAGC GGAGGCCAAT GGCCACTGCC 900 AGCCCTGCAG ACTTCCCAGT GAGTGGTGGC CCAGCAGCCA CTGTCAGCAT GCACCAGAAA 960 GGGGTCCTGT GCGCAAAGGT CAGGCAGGAG TGTGGCAGAG GGCTTTTAAG TTAGGTGGTT 1020 TTGGGGGCTT TTAAGTGAGG GGTCAATCTG GGTGAATGCA TAAGCCCCAC TGGCATCTTT 1080 GAGGAAATGA GGCTATTTCA GGGGATACTT TCAGTCCAAA GTTGACCTTT TGTTGAACTT 1140 CTAACTCTGG AAAAACAAGC TCCAAACCTG GGTTTGCTTA AGAAAGCAAC ATCAGTGTGT 1200 TTAGACGTGT 1210
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