Tag | Content |
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EnhancerAtlas ID | HS180-03094 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:151913550-151914320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr1:151913717-151913728 | TCAAGGTCATT | + | 6.32 | ESRRB | MA0141.3 | chr1:151913815-151913826 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr1:151913716-151913727 | GTCAAGGTCAT | + | 6.32 | Esrra | MA0592.2 | chr1:151913814-151913825 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr1:151913717-151913727 | TCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr1:151913815-151913825 | TCAAGGTCAT | + | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_10113 | chr1:151911730-151920206 | CD14 | SE_23217 | chr1:151913044-151914904 | Colon_Crypt_1 | SE_35018 | chr1:151912751-151921049 | HeLa | SE_36600 | chr1:151912821-151915067 | HMEC | SE_64760 | chr1:151912958-151915082 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 151913574 | 151913780 | chr1 | 151913815 | 151914271 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I151940 | chr1 | 151912796 | 151920351 |
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Enhancer Sequence | CCTAGGCAGT TTGGTGCCAG AGCCTGTGTA AGTAACCATT GCACCCCACT CTGTTATGGT 60 AGAAGCTGGG CAGTCCTGAA TCAGTTCCCC AAAAATACAG TGATTTAAAT AAAATTTATT 120 AGTGTATCCT AAGTGAATCT GACTAAGCCT GTTGCTGGGG AAATCGGTCA AGGTCATTTG 180 ACTCCCTTTC TAGCTGCCCT GCCTGTCTCT CTCTCTCTCT CTCTCTCTCA CACACACACA 240 CGCACACATA CACACACAGT CTTTTTCAAG GTCATTTGAC TCCCTTTCTA GCTGCCCTGC 300 CTGTTTCTCA CTTAAACACA CACACACACA CACACATACA CACACACACA CACACGCACA 360 CACAGTCTCT CTCTCTCTCT CATAGTATTT CTTCCCCTGT CTGGCTCACT GGAAGAAATG 420 ACAATATCAT AGCTGCTCCA GGTCTGTGAA TGATGACAGT AAGGACTGGT GAAAATGAGT 480 CAGGAGCCAT TCATTGGAAA GATTGTGTAA GTGTATGTAT TGTATTTTCA CCACTAATAT 540 AGTAACTTGG TTACAGTTGC TTGGTAACTA TACACTGTTC TAAGTAATCC TTAAAAACTG 600 GCTCTGGTGA ATGCCCACAG AGATTTTTCC ACCTCTTTTT GCAGCCTCTA GTTCTCACTA 660 CTGTAACAGG GCAACAAAAA TCCCATAGTC CTTATGTCAT ACCTTTGCCC ACACTCCTCC 720 TTTGTGTTTG GCATCCACTC ATAGCACTCT TTTGCCAAGT TCTGCAAGTT 770
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