Tag | Content |
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EnhancerAtlas ID | HS092-15397 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:114616380-114618660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr13:114618124-114618136 | ACAAAGTAAACA | - | 6.18 | HSF1 | MA0486.2 | chr13:114617698-114617711 | GAACCTTCTGGAA | - | 6.15 |
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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 |
GH13I113914 | chr13 | 114616101 | 114616654 | GH13I113913 | chr13 | 114616919 | 114617562 |
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Enhancer Sequence | GCTCTGGATT CTATTTCTCC AGAAAGTGTT GACAATTTTT GCTTTAGCAG GCAATCACCT 60 TCCTCAAGAG AGGAAGTTTC TAAACCAAGG CGAGTGGTCT GCAGAGCAAA ATCAAGGCAG 120 GCAGACCTCC TCCATCCAAG AGGGCTCTTG GCTTCACTTA GGAGAGATTC ACACACACAC 180 ACCGACAGTG GAGGAAGCGT TGATCAGGAG TGATTCACAC ATGAGCCAAC AGTGGAGGAG 240 GCATTGATCA GGAGTGATTC ACACATGAGC CAACAGTGGA GGAGGCATTG ATCAGGAGTG 300 ATTCACACGT GAGCCAACAG TGGAGGAGGC ATTGATCAGG AGTGATTCAC ACGTGAGCCG 360 ACAGTGGAGG AGGCATTGAT CGGGAGATGA TTCACACGTG AGCCGACAGT GGAGGAGGCA 420 TTGATCGGGA GATGATTCAC ACGTGAGCCG ACAGTGGAGG AGGCATTGAT CGGGAGATGA 480 TTCACACGTG AGCCGACAGT GGAGGAGGCA TTGATCGGGA GATGAATCAC ACGTGAGCCG 540 ACGGTGGAGG AGGCATTGAT CGGGAGATGA ATCACACGTG AGCCGACGGT GGAGGAGGCA 600 TTGATCGGGA GATGATTCAC ACGTGAGCCA ACGGTGGAGG AGGCATTGAT CAGGAGAGAT 660 TCACACGTGA GCCGACGGTG GAGGAGGCAT TGATCAGGAG AGATTCACGC GTGAGCCAAC 720 AGTGGAGGAT GCATTGATCA GGAGATGATT CACACATGAG CCAACAGTGG AGGAGGCATT 780 GATCAGGAGA GATTCACACA TGAGCCAACG GTGGAGGAGA CATTGATCAG GAGTGATTCA 840 CATGTGAGCC AACAGTGGAG GAAGCATTGA TCAGGAGATG ATTCACACAT GAACCAACAG 900 TGAAGGAGGC ATTGATCAGG AGATGATTCA CACATGAGCC GACAGTGGAG GAGGCATTGA 960 TCAGGAGAGA TTCACACATG AGCCGACGGT GGAGGAGGCA TTGATCAGGA GTGATTCACA 1020 CGTGAGCCAA CAGTGGAGGA GGCGTTGATC AGGAGAGATT CACGCCTGAG CTGACGGTGG 1080 AGGAAGCGTT CATCAGGAGA GATTCGCACG TGAGCTGACA GTGGAGGAGG CGTTGATCAG 1140 GAGAGATTCA CACAGAATCA GACAGTGGAA GAAGCATTGA TTAGGGCGAC AGGGCACAGC 1200 CAAAGGCTGC TGCACGGACA GAGCAGGGCT GTCCACTGGC AAAGGGGCCC CCTCAGATTG 1260 CTGGCTGGCT GTTTATACCT CCACCTAATT ACACGTAAAT GAGGGGTGGG TTATTCACGA 1320 ACCTTCTGGA AAGCGGTGTG GAGGTCATGC GGTCCTGGTA ACACAGGCTG CTTCCTTTTC 1380 AGTGACCAGC GTCATTTGGC GCAGCCCCCA GAGTCTCATG ACAACGACCT TGTTCTGCTC 1440 AAGAGCCCTG TACGGTCCCC TCTTCTGTGG ATGGAAACTG AGGCACAGCA ATGACAGCAT 1500 CAACGGAGCC ACCCTGCTCC TGGCTGTGCT CTGCAGGAGC CTCCACTCGG GGGCAGAGGA 1560 CAAACAGCCC CACACTTGGA AGCACAGCTC GGGAGCAGCA GCTGAGTTGC GCTGTGAGGA 1620 GATGCCAGGC GGCTGTTTAT CCATCGGCTG CTTGCAAGTG ATGGGGCCGG GTTTACCCTC 1680 CTTTCCTGCC CATGATTTGG GCTCTTGGCA AATCAAAGGT TTAAAGATAC CAGCTCTTGG 1740 AACCACAAAG TAAACACAGC ATATCTTCCT AATTCCTTTC ACCACGCGGT GCACAGTTTT 1800 ATGTGCTAAT TGTGTTTACT GGAAGAACTC ATGGCTGGTT CAAACAAATT CTTATCGTGG 1860 AAAAAACGTC TCCCCTGCCG TCAGCTGCTG GTACTGGTGG GATAGGAGTG CAGCACGGAG 1920 CACAGAGGCT GGAGCTGGGT CAAACCGGGA GGCAAGAGTG CAGGTGCACT GCTCCTGAGC 1980 TCAGCAGGCC CCACGGCATC TGCTGTGTGT AGAGGGGCTG ACCGTAGATC GCTGCTTATT 2040 GTGGTTCCGT TTAAGAGTCC TCCCTGGCAG GATCCCTGCT CCTTAAAAGC ACAGTGCAGA 2100 GCATCTTAGC TCCGATGCAC CAAGCATGCC CCAGCTGTGC CTCAGCGAGG AGGGTGAGCT 2160 CTGGGCCAAG ACCCCCTCTC CTGGTCCGGG ACCCCTGAGC GCTTTTGACT CGGGATGACT 2220 GACAAAGTCC CTGGCCGGGT TTGTTCTTCC CAGGCTGTCC CAGTGGCTTC TGAATTTTTG 2280
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