Tag | Content |
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EnhancerAtlas ID | HS098-11425 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:116679360-116680620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:116680170-116680191 | TCTTTCTTTTATTTTTATTTT | + | 6.11 | Nr2f6(var.2) | MA0728.1 | chr11:116680417-116680432 | TGAACTACTGACCTC | - | 6.07 | RARA | MA0729.1 | chr11:116680414-116680432 | TCTTGAACTACTGACCTC | - | 6.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 116679644 | 116679851 | chr11 | 116680215 | 116680518 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I116807 | chr11 | 116678420 | 116680295 | GH11I116809 | chr11 | 116680301 | 116680450 |
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Enhancer Sequence | ACACCGTCCT AAGTAAAAAG CCAGGTGCTC TTCCCCTTAC CCCAGGGGGT TTAGGATTTG 60 GGAGAAAGAG GCCTGATGGA ATATAGGGGT ACCAGGTCCA TGTGTTAACT GATCTGGGTA 120 CAAGAACAGT AACTCAAGGC CAGCCAGGGA AAGAACAGCC AAGCCGAGGC ACAGCTGCCA 180 AGTCATCACC TCTCGTTCCT TGTCCCACCA TGCCTTGTCT CAGCACGAAC ATAACCCCCT 240 CAGTTTCCCT CTTCTCCTGT CTCCTGCATA GGCAGAACCA GTTCTGAGTG ATAGCCAGGA 300 CAGCAGGTCC TCGGGTCCTC AGGCTTGCCA CTACAACCTG TTTACCCTGC GCAGACCATG 360 ATCCATCAGG TCGAGAAATG CCCCACTGCT AGATGTTTGT GTCAAAAATG CCTGCCGGTG 420 GTGCAACAGC TGGGTGGGAC CAGTGACGTG GACTTGAGTG CCACAAAATG TACCGAACAC 480 ATTCTGAGTC AACATAGTGA TGGTGTGCCA ACTCCAGATA AAGATTTTCA TTATTATTTG 540 TTTGGGTTTT GTTTATATGT ACTCCTCTTC ATCACCAAAG ATTTGAGGCT ACAGAAAATG 600 AAAATTGAAA TGGTAATAAA AGAGAGGGGC TTGCAGAGAG GACCACAGGA TGGGGAAAAT 660 AGAAATAATC GCAGAAAATC ATGACCCGAT GAAGAGCACA ATCATAGAAG CACTAACAGA 720 TGACAAGGTT GCCAGATCTT CACCATTGGT TTTGGGTTTC GTGAAAACCC GCGAAGAGAG 780 GGATTCAGTC AATTACATAT TTTTTTTCCT TCTTTCTTTT ATTTTTATTT TTTATTTTTT 840 CTTGAAATGG AGTCTCATTC CGTCACCAAG GCTGGAGTGC AGTGGTGCAA TCTTGGCTCA 900 CTGCAGCCTT CACCTCCTGA GGTTCAAGCC ATTCTCCTGA TTCAGCTTCC TGAATAGCTG 960 GGACTACAGG CATGAACCAC CATGCCTGGC TAATTTTTGT ATTTTTAGTA GAGACTGTCA 1020 CACGCGAGAC AGGGTTTCAC CATGTTTGCC AGGCTCTTGA ACTACTGACC TCAAGTGACC 1080 CGCCCACCGC AGCCTCCCAA AGTCCTGGAA TTACAGGCAT GAGCCACCGT GCCTGGCTTG 1140 TTTTAATTTT TTATTATAAA CAACACTGTG ATGAACATCC ACATAGCTAA ATGCATGCAT 1200 TCCATGATCA TTTTCTTAAG ATAATTTTTT TCTTATTATT TGTGTATTTA TTTATTTATT 1260
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