Tag | Content |
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EnhancerAtlas ID | HS098-29937 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:46186590-46188570 |
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) |
FOSL1 | MA0477.1 | chr2:46187398-46187409 | GATGAGTCACT | - | 6.02 | Foxd3 | MA0041.1 | chr2:46187050-46187062 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr2:46187054-46187066 | GTTTGTTTGTTT | + | 6.32 | JUND | MA0491.1 | chr2:46187398-46187409 | GATGAGTCACT | - | 6.32 | RREB1 | MA0073.1 | chr2:46187586-46187606 | GGGCAGGGAGTGGTGTGGGG | - | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I045961 | chr2 | 46187321 | 46187490 | GH02I045960 | chr2 | 46187957 | 46193089 |
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Enhancer Sequence | GGCCTTTGCT GACTGCTGTG TTTGGAGAAA GAAGATCATG TTTATTTAAA AAACAGAAGC 60 ATTAATTTCA ATCTTTGTGG CCTCAGTATT GAGGAGGGGA CTGACCTGGA GAGAGAATAG 120 ACTTTTTCTT CATGGCTAGG TGTTCCTGCT GGGCACAGGA TGGCTCAGAT CAGATTTAGG 180 GAACACTTTG ATCTGAAACT TTCTTCCTTG CTTTTCTCAA GCAGATACAA ACTTTTTGTT 240 CCCAGAGGTT AATGCCTGTG TGATGATTAT ATTTGCTCCG GAATCATCTA ACTTACCCTC 300 TTACCTTTCA AAATTCTGCA TGAAACAGCC AGGGTCCACA CAAATGAGCT AAAGTGGGGC 360 CTCTGGTCTT CTCTCTGTCA CCTCCTTATG TTCCCTGGCA TGTGTGTTGT GGTGTGAGAG 420 GGAGTTGTCT CTATGAGTTT TAATTTTCCG GGTTTTATTT GTTTGTTTGT TTGTTTACTA 480 GCAGTCTGGT TTCAAAAAAA CTTTCAGAAC TTCTTGTCAG ACCCCATATA CATTTAAAAG 540 AAATTGGCCT CTCCTCTTCC TATCTGCTAA TCATTTTTCA CATCGTTTTT TCATTTACAG 600 CATTTGGGAA GGAAAGTTCA CTTAAAAAAT CTTTAGACCA CCTGTTAGAG AAATACAAAC 660 AGAATGCTTG TTTTCTGGGA TAAAGGGGGG AAAACCTCCA TTTCATATTT TTTAATGTGT 720 GTGGTATGGT GGAAAAGACA TGAACTTTGG AACCGGTCTG GCCTTGGGAC CAAATCGAAC 780 TCCACCACTT AATAACTATG TACACCTAGA TGAGTCACTT GGATTTTCTT AGTGCCGGTT 840 TCCTCATTGT GTGGTGGAGG TAGTGATACT AATCGTGTAG AATCCTTTCG AGAAATAGAG 900 AAAATATGTT TTAATCACCT GCTATACCAT AAATCAGTGT TCCCCAACCT TTTGGTACCA 960 GGGACTGGTT TCATGGAAGA CAGTTTTTCC ACTGATGGGC AGGGAGTGGT GTGGGGGGCA 1020 GAAGGGGAAG GGCATTAGAT TCTCATAAGA AGCCCCCAAC CTAGATCCCT CACGTGTGCA 1080 GTTTACAATA GGGTTCCCGC TCCTATGAGA ATCTAATGCT GCTGCTGGTC TGACAGGAGG 1140 TGGAGCTCAG GCAATAATGC TTGCCCACCC ACCAATCACC TCCTGCTGTG CAGCCAGGTT 1200 CCTAACAGGC CACAGACCAG TACTGTGGTC CCCTGGGGAT TGGGGGCCCC TGCTGTAAAT 1260 GGTGCCTATT ATTTCTAACA TCCCGTTTTC AGTGGATTTT ATCTTTTGCT TTAGAGATGC 1320 CAAGCACCCA TCAGCCTTTG ACTGAAAAAT TCCCCAAATT TAGCTCCTGC CTCACTCTCC 1380 TTGCAGTTCC TACAATCCTT TCTGCCCCCC AGTTTTCCTA CCTGCCCAGC ACAACCTCTC 1440 CAAAAAGGAT CTGAGATTCA CCTATGTTGA ACTTATAATG GCCCTCGCAG AGGCTTTCTG 1500 TTTCAACAGG GTTGAAAGCC TGGCACTAAG GAGTAAAGCA AACACAGAGG GGCTGGAAGC 1560 AAGAGGGATC ACTTTATTTT TTAGAATACC AGGACTTTAG CGTCTCTGAA TTCCCAGCTC 1620 TCAGGAGCTA AGTCAGCCTT ACTCACTTAT ACACAGGCCC TGGTTTCCAT GTGATAGTGA 1680 TTCTAATATA AGCTGACCTA TCATAGCATT GATCCTTCCT CTGCTTCTCT CCATAGGCAG 1740 GAGTGTGTAA CACCAAGTAC AGTAGTCACA ATACCTACCT CCTTTCCCCC CCCGATTTGG 1800 TTGAGCAGTG AACAAGTCTC AGAGTTAAAA ACATTTTTCC TTGCAATGTT TACCCTGACT 1860 TTCTCCTGCT TTACCTATTA CCTCTTGAAT GAAGTATCTA CTGCTATATA ACAAGTTATC 1920 TCAAATTCAG CAGCTGAAGA TAGTAATCAA GATTTATTGT GTCATTCATT TTCCGTGAGT 1980
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