Tag | Content |
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EnhancerAtlas ID | HS148-00856 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:101087920-101089010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr1:101088279-101088289 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr1:101088279-101088289 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr1:101088279-101088289 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr1:101088279-101088289 | AACAGCTGTT | - | 6.02 | Sox6 | MA0515.1 | chr1:101088421-101088431 | AAAACAATGG | - | 6.02 | Stat6 | MA0520.1 | chr1:101088612-101088627 | CATTTCTTGAGAAGC | + | 6.22 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_45780 | chr1:101086339-101097802 | Osteoblasts | SE_51929 | chr1:101086746-101091215 | Skeletal_Muscle_Myoblast | SE_55943 | chr1:101085569-101097753 | u87 | SE_63727 | chr1:101086919-101091372 | HSMM | SE_67718 | chr1:101085569-101097753 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 101088225 | 101088325 | chr1 | 101088583 | 101088643 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I100621 | chr1 | 101086920 | 101091298 |
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Enhancer Sequence | CTCAAAAGTC AGAGTTCTGA CCAGTATTGT TGGGGTGGGT AAAAGAACTT CACTCCCTCA 60 GATCTGAAAG TGTCCTTGCC AGAGGAGAGG GAGACCTTAT TTCAAGTGTG TTTGAATAAA 120 CATGACATAC ATAAACTTGA TTTTCCAGGT TTTGGAGAAA GCATACATTT GTCCTCTGCA 180 TCATGAAATA ATGTCCTTGG TGGCTCCTTT CAGGGCCTGT GCTGCACTCT CCTTAGTGAC 240 TATTAGCATT GGAGTTGGAC AATTTAAGGG CAGGAGTGGA GACCTGCTAC TTATAAAGGA 300 TGACTACACT TATTTAGGGA TACTGCTCAC GCTGACTCTC AGAGCAATTC TTTTGTTCCA 360 ACAGCTGTTC CCAGGGTAGG GTAATATTGG AACAGAGGCT TATGCTGCAG TATCCATTGA 420 GTGGGACTGA GGCCCCTTCA GTAGCTGAAA ATCCCCACTT CAGTGCTACT GCTTCAGCTA 480 CTGCAGCTCT TACTGTCTTC AAAAACAATG GTAAGGATTC CTTTAACCTC AGAGGAGGAA 540 TTAGCTTTTT GCAGAGACTA CAAAGAATCC ATAGGATACA AACATTTCTA TAGTCCAGGA 600 AGGAGTCCCA CATATAAAAA CAAAACTGTA ATATATTTTA TAAGTGATTT GCCTAAATAT 660 GTGAGGCTGT ATTCACTCAG TTTCTCAAGA AGCATTTCTT GAGAAGCTAC TGTGTGCCAG 720 AGCCTCCTTA GGGGGCAGGA ACTGCTTATT TATCTTCATA TCAACATCCC TAGGTAAGTG 780 CCTAGCCCAT CGTATGGGCT ACAGACTATG CAATGCTATT TCCCTTAGCC CCACCAGAGT 840 TCAGGGTCAG ACTGATGGGC AGGACTATGA ACAGATCTTC TTTCTCTCCT TGAAGGTAAC 900 TAACCTTCCA TGGGACTTGA AGCTTCAGAT TTTGGCCTTA ACCAAGTCAA CTAGCTCAAG 960 TCAGAGGGGC AGTGATTATT TGAATTGCCA AGGTATTACC TAATGAGAAT CTTTGTGACT 1020 AAGCTCTTAA AGTTGAAACT TAAGTAACAT TAGCTGAAAA ACTTGTTGGA TAAACATTGC 1080 TACTCCCTTG 1090
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