Tag | Content |
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EnhancerAtlas ID | HS139-50382 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr7:44601060-44602430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr7:44601985-44601995 | GCCCCGCCCC | + | 6.02 | NFE2L1 | MA0089.2 | chr7:44602026-44602041 | AAAGCTGAGTCATTC | - | 6.44 | Nr2f6(var.2) | MA0728.1 | chr7:44602244-44602259 | GAGGTCAGGAGTTCA | + | 6.22 | Zfx | MA0146.2 | chr7:44602220-44602234 | GAGGCCGAGGCGGG | - | 6.01 |
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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 |
GH07I044561 | chr7 | 44601294 | 44602610 |
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Enhancer Sequence | GCTGGCTAGT TAATCTAAGC TTTTGCCAAT CTGCAAAATA AATGTGTGTG GTGGATATTA 60 AAGCCTTGCC TCTCAAATGT GGACTAGAGA CCAGCACCTT TGGGCTCACC TGGGACGGAG 120 GTGAGAACTC AAATGCAGAA CCCCAGGCTG TGCCCTAGAC GTATTCTCGT GGAAGTATGG 180 AGACACGTCC CAGAAGGCAA TGGTGGATTC AACAGGCATT GGGAGGTGCT AGCACAGAGC 240 TGGGCTGCAA CAGGCGTGCC AGGTGCCTGA GCCACTTCGG CCCCTACAGG AACCCTTGGA 300 GGGGACATTT TACCCCCACT TACAGGTGAG AACCTAGAGA AGGCCAAGAA AAGTGACATG 360 CCTTCCCTGT ATGAGACCAT ACAGTCAGAA AGTGGCCATC ATGGTCTGAC CTGGCCACTG 420 TGCCCACAGA GCACCTGGGA CATTGAGGCG AGCCACAGCA GGATGCTGCG TGGTGGAGGC 480 AACCCTTGGG GTGTTCGTCG GAAGACCCCC TTGATGTGCC TTGTTCTTTA GCCCACTGTT 540 GCCACAGATA CCCTCAGTGC ATTCTACGCC AAACCTACTG CATCTCAGCA GGTTTGCGGA 600 TAGGCTGGAG GGATAACAAG ACACTGGATG CATTGAGTTC TGAAAGCATT TCAGGATAAA 660 TAAACTAAAT ACTGTGCATT TGCCCAGTGT CATGCCTGGC ACAGAGCAGG TCTGCTTGGC 720 CAAGGCACCT TCCTCTCTGC AATGATGAAC CACTCCTTCC CTTCCTTACC CTTGTAAACA 780 TGGCTGTGAG GAATGGAAGA GCAGCAACTC ACAGCCTGTT CCACAAGGCA GGAGTCTTAC 840 ATAATGATGT TCCTGGGGAA AAGGATGACA GCTGACGGGG CACCTTCCCT GCTCAAATTC 900 AACTTTATCA CCATTGCCTC TTGGGGCCCC GCCCCTGAAG TCCAAAGTCT CACAACTAAT 960 TCCCCCAAAG CTGAGTCATT CATCCTTAGC AGATGCAGGC AGAGAATCCG CTGGGCTGGG 1020 AATGCACCCT GAGCCTTTTG TGCTCCAGGT CCAGAGGTTT CTGGGCACAC CACTGTCCTC 1080 CCATCTGCTA TCACCAGCTA TATCATCAGA ATGCTGTTGG CCGGGTGTGG TGGCTCACGC 1140 CTGTAATCCC AGAACTTTGG GAGGCCGAGG CGGGTGGATT ACCCGAGGTC AGGAGTTCAT 1200 CCTGGCCAAC ATGGTGAAAT CCCATCTCCA CAAAGATACA AAAATTAGCC AGGCATGATG 1260 GTGGGTGCCT GTAATCCCAG CTACTCAGGA GGCTGAGGCG GGAGAATCGC TTGAACCCAG 1320 GAGGCGGAGG TTGTACTGGG CCGAGATGGC GCCACTGCAC TCTAGCCTGG 1370
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