Tag | Content |
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EnhancerAtlas ID | HS076-08388 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr10:104299780-104301560 |
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 | chr10:104300135-104300146 | AGTGACTCATG | + | 6.14 | KLF4 | MA0039.3 | chr10:104301012-104301023 | CCACACCCTGC | + | 6.62 | Nr2f6(var.2) | MA0728.1 | chr10:104300191-104300206 | GAGGTCAGTAGTTCA | + | 6.07 | RARA | MA0729.1 | chr10:104300191-104300209 | GAGGTCAGTAGTTCAAGA | + | 6.1 |
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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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Enhancer Sequence | TGAGTTTGGC TTCTCTCTAC TTTTGGCATG TTCCCATCAT TCTCTGAACC ACTTCCTTAC 60 TTTCTGGCAC AGTAGGAAAT TTCAGAATCA TTTTGTACTT TGCCAGCCCA GGAATCAGCC 120 ATTTATCCAG GAAGCCCTGG TTTTATTTAG TGGAGAATGG TATATAGAAG CCATGATCCG 180 GAGGCTAGGT ATTATCATTG CTCTTGGAGT GTCACTGCTC CCAGTGGCCA GAACTAGGAA 240 ACACACATGC ACATATACAC ATACCACTCT ATTTCCATAT TGGTTTCTCT CTTAAATACC 300 ATGAATTCAT ACTGATACCT CCAATTCTAA AGCTATACCT ATGGGGGCCT GGTGCAGTGA 360 CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCCCAAGTGG GTGGATCACT TGAGGTCAGT 420 AGTTCAAGAC CAGCCTGGCC AACATGGTGA AACCCCGTCT CTACCAAAAA TACAAAAATT 480 AGCCAGGTGT GTTGGTGCAC ACCTGTAGTC CCAGCTGCTC AGGAGGCTGA GGCAGGAGAA 540 TCACTTGAAC CTGGGAGGCA GAAGTTGCAG TGAGCCAAGA TCACACCACT GCACTCCAGC 600 CTGGGCAACA GAGCAAGACT CTGTCTCAAA AAATAATAAC TAACTAACTA AATAAATACT 660 ATACCCGTGG CATTCATTCC TGCCTGCCTT TAAAATATAT ATATATATAT ATTTCAGACC 720 AGGCACAGTG GCTCACACCT ACAATCCTAG CGCTCTGGGA GGCCAAGGTG GGTGGATCAC 780 TTGAGGTCAG GAGCTCGAGA CCAGCCTGGC CAACATGGTG AAACCCTGTC TCTACTAAAA 840 ATACAAAAAT TAGCTGGCCG TGATGGTGTG CGCCTGTAAT CCCAGCTACT CGGGAGGCTG 900 AGGCAGGTGA ATCACTTGAA CCCGGGAGGC GGAGGTTGCA GTGATCAGAG ATCGCGCCAT 960 TGCACTCCAG ACTGGGTGAC AGAGCAAGAC TCCATCTCGA AAAAAAAAAG TTACTTGGGT 1020 TATATCTTTT CTTCCCCCTT TCAGTGTGGT TATATGGTTG ATTTGAAATA CTGTTAGGTT 1080 CATTAATTTC TGTTTGTATT ATATTTTAGC ATTTTCTCCC TCCTCATTGA TTCTGTTTCA 1140 TTTATTTTGA GTATGTGAAA GCATTATCAC GGATCCAAAA CCAAAAGTGA GAACTATACA 1200 AAAAGGTATA TTCAAATAAA TGTTACCCAC CTCCACACCC TGCAGTGCTT TCTACCGCCT 1260 TCCCACCTAC TGTATGTAAG AATCCATCTC ATTCATTTTT GGTTTATCCT TCCCACATGG 1320 CTTTCTACAG AAATGAGTAG GTAATGTATA TTTTCCTACT TTTCTTTCTT TCTTTCTTTC 1380 TTTCTTTTTT TTTGAGATGG AGTCTCGCTC TGTCACCCAG GCTGGAGTGC AGTGGTGCGA 1440 TCTCGGCTCA CTGCAACCTC TGCCTTCTGG GTTCAAGCGA TTCCCCTGCC TCAGCCTCCC 1500 TAGTAGCTGG AACTACAGGC ATGTGCCACC ACGCCTGGCA AATTTTTGTA TTTTTAGTAG 1560 AGACGAGGTT TCACCATGTT GGCCAGGCTG GTCTCCAACT CCTGACCTCA GGTGATCTGC 1620 CTGCCTCGGC CTCCCAAAGT GCTAGGATTG CAGGCGTGAG CCACCGCGCC CGGCTTTTTT 1680 TTTTTTTTTT TTTTTTTTCC TTTTGAGACA GTTTTGCTCT TGGTGCCCAA GCTGGAGTAT 1740 AATGGTGTGA TCTCGGCTCA CCGCAACCTC CACCTCCCAG 1780
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