Tag | Content |
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EnhancerAtlas ID | HS050-38172 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:127885930-127886660 |
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) |
Myog | MA0500.1 | chr2:127886047-127886058 | GACAGCTGCTG | + | 6.14 | Tcf12 | MA0521.1 | chr2:127886047-127886058 | GACAGCTGCTG | + | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_03157 | chr2:127885901-127886524 | Brain_Angular_Gyrus | SE_03883 | chr2:127885614-127886796 | Brain_Anterior_Caudate | SE_04777 | chr2:127885192-127886798 | Brain_Cingulate_Gyrus | SE_05775 | chr2:127885566-127886721 | Brain_Hippocampus_Middle | SE_07740 | chr2:127885671-127886858 | Brain_Inferior_Temporal_Lobe | SE_31713 | chr2:127885788-127886512 | Gastric |
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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 |
GH02I127128 | chr2 | 127885875 | 127886933 |
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Enhancer Sequence | GGTAGCCTTG GGCAGATGCA ATTGTGCAGG GGTGTCATCA AGGACAGAGG TTCCTTCCGT 60 TTTCCAACTC AGTCTCTCTG AGAATAGTTT GTGAGAGATT TGTCCTCACA GCTGCAGGAC 120 AGCTGCTGTG CCTCCTGCAT TAATTAGGGA GGAGGGGAGG GGCAAAAAGT AAAGAGCTGA 180 AGCGACAGCC CCCCAAGGGT GTCCCTTGTA CAGACATCCA GAAGCCCCGC CCAATGAGTG 240 ACTTTTGCCT TCATCCTGTT GGCCAGAACT GGGTCACGCA CCATGCTTAG CAACAAGGAG 300 ATCTGGGGAA GTGAGTATTA AAGCAGACAC AGCACTCTGA CCACCCTGCT GCCAGTGTGG 360 AGGCAAAGCA GGCAACCGGT GCAGGCGCCC TGGATTACCT GCCTGACCAC GTGACAGTGA 420 GGTCCTGTTG GCCACATCTG TGTGGAATTT CAGTTTCTGT TTAAGATCAT ACTGGCACCG 480 AGTAGAATTC TGTGTCTCCA GGTAAATGTA AGAGAACAGG GCAGATTTCA TAATGTCAAA 540 GTTGGCGTCA AGTCAAGAGA AGGCCAAACA ACTTCATAAT GCCCCATAAA AAAAAAGCTT 600 CACAATAGTT TGGGTAAAGT AGTTGGAGAA TTGAGTCTTC TCCTGACACC AAGTTCTATG 660 GGCATGCCAG CTAAACCTGT AAATTAAAAC AGAGCAACAG CCTGTACCCC TGCAAAGAGG 720 ATAATAAAGC 730
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