Tag | Content |
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EnhancerAtlas ID | HS042-12024 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr13:26062870-26064340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr13:26063238-26063256 | GTTTCCCTTTCACCTTCC | - | 6.18 | NFE2L1 | MA0089.2 | chr13:26063671-26063686 | TCTGCTGTGTCATCC | - | 6.05 | Nfe2l2 | MA0150.2 | chr13:26063673-26063688 | TGCTGTGTCATCCTT | - | 6.36 | RREB1 | MA0073.1 | chr13:26063004-26063024 | CCCCCACCCCCCACCCCCCA | + | 6.63 |
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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: 1 | ID | Chromosome | Start | End |
GH13I025489 | chr13 | 26063341 | 26063370 |
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Enhancer Sequence | TACTCTATCA CACGGTCATT TTTGGTGGTG TTTTTGTCCT TTTTCTATGC TTTATCTCAT 60 GTCTTGCTGT GTACCACAGT AAGCACCACT TTTTAAAAAA TAGGTATAAA TGATTAAAGG 120 AAATTCAGAT GACTCCCCCA CCCCCCACCC CCCATTTTTG CTGTCTGGTT GACTTTACCA 180 TTTGCATCTT TCCCTGACAA CCCTGGCTAG GTTGGGATAC ACCAGGACCA GGGTACAGAG 240 TCATAGTGCC CAGGAGGACG CTTGATGGGG TGGGTATAGA TTTTAAACCA GATCTGCTTT 300 TTTGTTGAGT GGATTGTTTT CATGGCACTG GCGCTGGTTC AGTCTCTCGT GTCTCCACCT 360 GTGACAGAGT TTCCCTTTCA CCTTCCCGAT TGCTGGTGGT TATCGTTCTA AAACAGCCAA 420 GGCACTGTGA TTCTCCCTGT TGAGGGACCA TCGCTGCTTC TCTTTTGTCT CCAGTAAGAT 480 ACACAAGGCC ACTCTCGTTC TATTCCCGGC TTACCGCACC ATCTCCCCAG GCTCCTCTTC 540 CTGTGTCTGG CTGCAGCCTT TAATCACGGC ACTTTCCCTG GAACACTGTC TCCTAATCTA 600 CTCAAGTTCG TCCTCCTGGA GGGCCCTGTT TTTCAGGCTC AGGTTGCATC TCTGTAAGCA 660 AGCATTTTCT TCCTCGTCCT GCATCTCCAC CGTTTGCAGG CGGAGGCAGC CCCTCTGTGC 720 CGCAGCGTTT CTCAGACTCT TTTGCTCTGG AACTTAGCAT GCTGCACCAC ATCTATTTTT 780 ATCCATCTCT GACTCTCCTG CTCTGCTGTG TCATCCTTGA TGACAAAGTC TGTCTGTTTC 840 CCCTCGCATC CTCCCCAGCA CGACGCACAG TTCCTGCCAA TGGGAAGTGG AAAACCTTTG 900 CTGAAGGACT GCGCTCTGCA AGCGAAGGTC AGAATTGAAC AGAAAATGAG AATTGGCTTA 960 ATGTGTTGTT CTCAGATATC CCTTCACACT TAATTGCTTA TTGAACAAAG TAGAACCCCC 1020 ATGGTGATGT GCAGTTACTT ATGCCTCGGA AATTGATGTA TTGTGTAGTG TTGATGTTGT 1080 ACTTTCATAT ATAAACTACT CCTAAAAGGG GGCTGCCGAG GTAAATGCTT TTAATGCCAA 1140 TTTCTTCAGA CTTGGCAGAT GGATATCTAC CCTCAAATGG AGGTACATTT GGGATTTAAT 1200 GTGACAGCTG GCATCCTTAG TCATTTATGT TGGTCAAGGT TTAAAACTTG TGTGTTCAAC 1260 AAATTTTTTT ATGGTAGTCG GTGTATACTG TCTTGGTGCT TGGTGTTGCA GCGCAGTGGT 1320 GGAATATCGA GGGCTCTGCC TGCAAGGTTA CTCCTTAGCT TTTCGGGTAT ATTTGAGTAA 1380 GGGAAGTGTA GTAGAGAACA CACATGTTGA ATGATCCATT TCCATGGCTA AGTTCGTGGC 1440 CCCTTTTTCC TCCTGCTCTC TGGCTCATGC 1470
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