Tag | Content |
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EnhancerAtlas ID | HS092-10386 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:110243530-110244650 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr11:110244133-110244147 | ATGAGTCATTTTCT | - | 7.64 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 110243695 | 110244609 | chr11 | 110244062 | 110244430 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I110372 | chr11 | 110243104 | 110246347 |
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Enhancer Sequence | AATTTTGGAG AAATTGCCTT TGCTCACTGT GGATTCTGGA GGGTGTGAGT GATGGACAGG 60 TCCATCTGTG CATGGAGAAT GGAAAGCCCC TTCTCCAGGA TCACCCTTTA CCTTAGGAGA 120 ACACCTCAGC TCCAGGCACC AAGCAGGAGT ATCATAGGCA CTTAGCTTTA CTCCTATAGA 180 CAAATAAGAG TGGGGAGACT ATGTGGTAAG GAATGATACC CTTACACTCT TTCCAGCCCT 240 TCCCAGTCTT ACAAGGAGTG ACACACTTGG TGGCCTTCAA GCCTGTCACT GCAATTCATG 300 CAGTGGGTGG TAAGAGGACA AAGCACGCTA GGTCCCTGAT CCGACCTCCC AGGGATGACA 360 GGTCTGGCTA CTCCTCAAAC TGAACCTGAA AGAATGCAAA TGGTTCAAGT TTTCACCCTG 420 ATTCTGGCAC ACCCCGAGGC AAAAATAGCC ATTTGCCTTC ATACGAGCTT CTGTGTAGGC 480 TGTGAATAAG GAGGTTTCTA TCTCAGCTTT CTTTTTGCTC ATTTAAAGAC AACTGAGAGT 540 ACGACAGGGT AATTGTTTTG TTTTAAAGCA CTGTAATTTA GTTCCTTTCT GGACCTTCTA 600 TGTATGAGTC ATTTTCTGTA GCAGTACTAA GAGATGCAAA TAGAAAAACA TTATTTCTGA 660 AAGCTTGAGA TTTCAAGCTG GGCCTTTTAT TCACATTCTC TTGCTAGTTT TAGTTTTACT 720 TGTGACATTC ATGTTATTAG AAGAATGACA CAATTTCAAT CACATTTTTG TCCCATGTAC 780 TAATGTAGCA AACAATTTCA CAACCTTCCC TTTCTTTTAC ATGTGAGTCA TTATCATTTG 840 GTTTTGTTCT CCTTTACTCC TGAACTCACT ATCTCCTGAT CACATGTATA CACATTTCTC 900 TGATATCCTA GATCTTTATG GGTGATCAAG ATTTTTGTAT ATTCTGTTTT GTTGCTTTCA 960 TACCCGCTAG TATCCTTTTT AAGTTTGACT CTTTTATACT TTGGGAGATG CCAAACAAAT 1020 ACTTCAGGAG AAAGGAGGCA GTGTGTTGAA AGGAAGTTGA CAAAGCAAGA AGAAAAGAAG 1080 AAGAAGATAT AAGGAGGAAA CGTAGTGGCT CTTAAACAAA 1120
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