| Tag | Content |
|---|
EnhancerAtlas ID | HS139-11399 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr12:328370-329780 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:329181-329200 | TACCACCCCCTCGTGGCCA | - | 6.6 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65535 | chr12:329154-329872 | Pancreatic_islets |
|
| | 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 |
| GH12I000219 | chr12 | 328927 | 329801 |
|
Enhancer Sequence | TTATAACCTT AGAACCCAAC CTGCACCATG AGGTCCTGCC CTACCCCACT TATTATTTTC 60
CACAGCTCTT TGCTCTTTTC TGTCATGGTA TCTGTCACTC ACTGTTTAAG AAATTGTATC 120
TGTTTTTACT CCTGGCATGT CACGAGCACA GCACGGCACC ACGCGGGAGG TGTTCTGTCA 180
ACAGTGTCCG GTGGATGGAG CTGCTGGCTT GCAGCATCTC GAGTTCGGGC CTGCCTCTCC 240
AGCAGATGTA TTTCTCCCCC GGTAAGACTG AGATTGAGCC CAGCACCCTC GGGGAATGCC 300
CGAGCAGCAT TCTCCAGGAA GGGGCAGCCA AGGCTGACAT ACAGCAGGAC TGCTGTCGTT 360
AATCTTCACC AACTCTTCCA ACGACAAAAA GTCAAAAACT GAAGACAAGC AAATATTTCA 420
GTGCATTTTT TTCCACTAGT GGACATGTGA AAAACTAAGA TCACCCAGGG AAGCCTGTGC 480
ACCCTTAGAC TGCAGCCCTA AGAGTCACAG GACACACCAA GGGCAGCACC AGAAGACCCA 540
TCTGAACAAA GGTGGGCACA CGGGCAGGCC CCCGAGCCTG CGCATAGGCA GGGAGAGATG 600
TAGCTGTGTG TTCAGCCACT TCCAAAACCA CACACAAAGC TACAGCCAGA AATATGTGGG 660
GCCCGGCTCC ATGCCCATAC GCAGAGGCAA GGCTGCAGAG ACACACCTGT GGCACCCTCT 720
GGGCACCCCC CCCCATGCCC ACTGACCCCG AGTGGGGGTG GACTTCCTCC CTGCAGCTCA 780
GGCCCTGACA GTAGAGCTGT GGCCATAGCA GTACCACCCC CTCGTGGCCA CATCTGGCGG 840
TGCCCCGGCA TCCGGTGTCT CCTATCCTCA GAAGAGCGAG GCGGTCCCAA GGAAGTGGCG 900
TCCCTCTGCT GGCTGAGCTG GGCAGTGCCC TCCTCTGCCA AGGCCCCCCA ACCTGCTGCA 960
CTGGGGCGTG GTCACAGCCG GCCCTCCCCC ACGTCCCCCG TGCCCAGCCT CGGTGGGCAC 1020
ACAGGCAGTT TTGGCCGCTG GGGGTAGGCG AGGACACAGC AGGGAAAGTG GGCAGGAGGA 1080
AACTGCCACC AGCCTTTCCC TCTCCTTTGG CTAGGACTCG GGTCTCCTTC ATGCGTCCCT 1140
CAATTTCCTT TCTTATTCCA CAGCACAAAG GCGGAGGAAG GAAGCTGAGG ACATGTGGAG 1200
AGAGGCTGGG CAGCCTCCTC TGGTCCACAT GCCTGATGAT GGAGGCTCTC AGCCTGGCCC 1260
CACCACCCGC CCCCATCACC GTGCTGAGTG GGCCCCAGTG AGAACTCAAT GGGGGAGGCT 1320
AGGATGGGGA GGGGCAGGGT CCTAAACCAC AACAGTAACA TGGGGAAGGG TGAAGGCAGC 1380
CAGGCAGGGG GCAGAAATCA GACAGAACCG 1410
|
