Tag | Content |
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EnhancerAtlas ID | HS117-00375 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr1:101087960-101089010 |
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 | AAAAGAACTT CACTCCCTCA GATCTGAAAG TGTCCTTGCC AGAGGAGAGG GAGACCTTAT 60 TTCAAGTGTG TTTGAATAAA CATGACATAC ATAAACTTGA TTTTCCAGGT TTTGGAGAAA 120 GCATACATTT GTCCTCTGCA TCATGAAATA ATGTCCTTGG TGGCTCCTTT CAGGGCCTGT 180 GCTGCACTCT CCTTAGTGAC TATTAGCATT GGAGTTGGAC AATTTAAGGG CAGGAGTGGA 240 GACCTGCTAC TTATAAAGGA TGACTACACT TATTTAGGGA TACTGCTCAC GCTGACTCTC 300 AGAGCAATTC TTTTGTTCCA ACAGCTGTTC CCAGGGTAGG GTAATATTGG AACAGAGGCT 360 TATGCTGCAG TATCCATTGA GTGGGACTGA GGCCCCTTCA GTAGCTGAAA ATCCCCACTT 420 CAGTGCTACT GCTTCAGCTA CTGCAGCTCT TACTGTCTTC AAAAACAATG GTAAGGATTC 480 CTTTAACCTC AGAGGAGGAA TTAGCTTTTT GCAGAGACTA CAAAGAATCC ATAGGATACA 540 AACATTTCTA TAGTCCAGGA AGGAGTCCCA CATATAAAAA CAAAACTGTA ATATATTTTA 600 TAAGTGATTT GCCTAAATAT GTGAGGCTGT ATTCACTCAG TTTCTCAAGA AGCATTTCTT 660 GAGAAGCTAC TGTGTGCCAG AGCCTCCTTA GGGGGCAGGA ACTGCTTATT TATCTTCATA 720 TCAACATCCC TAGGTAAGTG CCTAGCCCAT CGTATGGGCT ACAGACTATG CAATGCTATT 780 TCCCTTAGCC CCACCAGAGT TCAGGGTCAG ACTGATGGGC AGGACTATGA ACAGATCTTC 840 TTTCTCTCCT TGAAGGTAAC TAACCTTCCA TGGGACTTGA AGCTTCAGAT TTTGGCCTTA 900 ACCAAGTCAA CTAGCTCAAG TCAGAGGGGC AGTGATTATT TGAATTGCCA AGGTATTACC 960 TAATGAGAAT CTTTGTGACT AAGCTCTTAA AGTTGAAACT TAAGTAACAT TAGCTGAAAA 1020 ACTTGTTGGA TAAACATTGC TACTCCCTTG 1050
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