Tag | Content |
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EnhancerAtlas ID | HS188-03449 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr13:41860130-41861740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HLF | MA0043.2 | chr13:41860995-41861007 | TGTTATGTAATG | - | 6.32 | IRF1 | MA0050.2 | chr13:41860240-41860261 | AAGGGAAAACTGAAACTAGCA | - | 6.54 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 41860566 | 41860973 | chr13 | 41861230 | 41861516 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I041284 | chr13 | 41858601 | 41860927 |
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Enhancer Sequence | CGGATGTTGC AGTGAGCCGA GATCGAGCCA CTGCACTCCA GCCTGGGTGA CAGAGCAAGA 60 CTCTGTCTCA AAAAAAACAA ACAACAACAA CAACAAAAAA AAAAAAAAAA AAGGGAAAAC 120 TGAAACTAGC AGAGGTGTCA GACATACTAC CCAAAATATG TAGCAATCTT ATAGGAGAAT 180 CCTCACACAA CTTTTTGCTT AGTTGACAGG CTTTCTAAAG ACTGATCATC TCTTGCCAGT 240 GAGCATCCTG CCACTTCTTT GGAAGTGATT TGGGAATCCA AGATACATAA AAGGATCTTT 300 TCAGCCTGTT GGGTGAAATA TATAGGAAGA AAGATTCTAG CCAGAACACT TGATCCACTA 360 CATAGTTTGT CTTGCTCAAA ACCAAGATAG AAAATAGGTC TTCTAAGACT GAAGGTGCAC 420 CATCTCTGTC AACACCGGAT GATTTTATGT ATAATACTTA CGGTTCTTCT ACTTGCAAGT 480 GCTTAGATAA GTGAACCTGC TAACCCAGGA TAGTCATAAG CAGCATTGGC AAAATGGGGA 540 TTTAAAAACA ATTGTTTTAC CCATGACATT TTTATTCAGT TTGATTATTC CTTGTGAAAT 600 GAGTGTAAAT TAATCTCTAC TTCATATCTT ATCAAAATAC GATCTTCATC CTTTGATCAC 660 ATCGAGTGTT TCACACACTC CACTCCAGTA CACCCACAAC TAAGAGCAGA ATACTTCATT 720 ACAGGAAACA TGTGAATCAG AGTTCTGTTC GAAATCTTAG CCAAAGCTGG TCAATTTTTT 780 TTAACAAAAA TTCAGTATAA AATAAAACAG ACTGATCCAA AGAGCTGAGT TTGTTATACT 840 CATTTCATTA TGATATACAG TACGATGTTA TGTAATGAAC ATGGGTTGAT AAATTATTGG 900 TGCGTTAAAT GGCAATGTTT CATTAAGGAG GCTGTTCTGC TTTACCTATC GGAAAATTAC 960 TTAGAAAATG TCTGCATTTC CTATTTTAGA AACTACAGTT TTCCCAAAGA CAAAGGTCTT 1020 TAAATAGTTT AATGCTTAGT GTTCTTAACA TAACAATGCA ACTTAGTTCA GAAGGTATTT 1080 TGTCAACTCT TAATCTAAGT AAGAATAGGG GTGTGTTAGG CCATTCTTGC ATTGCTATAA 1140 AGAACAACCA CGTGGCTCAG TTATTTATAA AGAAAAGAGG TTTAATTGGC TCACGGTTTT 1200 GCAGTGTGCA AGCATGGCTC CAGCAACTGT GTGGCTTCTG GGGAGGCCTC AGGGAGCTTT 1260 CATTCATGGC GGAAGGTAAA GACAGAGCAG GCACCTCACA TGGCCAGAGC AGGAGTAAGG 1320 AGGATGGAGT AGGTGCAACA CACTTTTAAA CAACCAGATC TCGTGTGAAC TCAGAGCGAG 1380 AGCTCACTTA TCACTAAGGG GATGGTGCCA AGCCATTCAT GAGGGATCTG CCCCCATGAT 1440 CCACACTGGA GACTACATTT CAACATAAGA TTTGGAGGGG ACACATATCA AACGATATTA 1500 AGGGGATCTA AAAAAATAAG GCTTTAAGAA GTCTTGTCAT TTTAGAGCTA AATTTTAAAG 1560 AATGTGAGTC TCAACTTTTA TCTATAGAAC AAACAAAATC TTAAAGTGAC 1610
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