Tag | Content |
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EnhancerAtlas ID | HS007-00305 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr1:29161180-29162720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr1:29161996-29162009 | AGCTAATTAATTT | - | 6.15 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGCCCATT CAGGTACTTC TTAAATATCC AGATGGCACT TTGTTAACGA GATTTGGTCT 60 GTAGAGTTGT TGGGATCTAT AATAAAAATC ACCCAACTAC GAGACAAGAG GGCAGTAAGA 120 TGTGCAGGAA CCTCAGGCTG CTGTCTCCTT CAGAGAAACC CCTGACTTTT CAGCTTAGAA 180 AGTCTTTCCT CCAGGGAGCC TTCTCTGATT GCTCCTCACC GCCCTTCCAG CCAACAGGTA 240 ACCCTCCTCT ATGTTCCCAC AGTGTCCTGT GTGTCCCCCG CCATTGGAAT AGGGTCTATG 300 CACTATTTCA GACACCTGTT TGCTCCCCTG TTCTGCTCTC CCCACCATGA GTGGGTGTGG 360 GGTAGAGGGA GTATATCCTT TGTTCATAGC TGGAGCCCCA GCAGAGGGTC CAACACTCAG 420 ACAGCATGTC ACTAGGTGTT TGTACAAAGG ACCTGTCCTA TTTCCAGAGG TCCAGGGTCT 480 GATATGCCAC ATCCTTGTGG GAGTCTGCGT TCTTGGGCCC CCATTGTGCC TGCTGCCCCA 540 TCCCTGGTCC AGCCACCCCT AAGCCAGAAG CAGAGCCAGG GTGGTGGGGA GGAGCTGCTC 600 TTCCCTGGCT GCCATGAGTG TGTTGTTCTT GAACTGAGGT GAACGAGGCA TCTGTCCTGC 660 TTCTTGTTGA GTGTGACCTG GCTGGCCTCC CTGCTCATGT TCAACTCTGG GGCCTGGATT 720 TCTCTGTTCC AGCCTTTAAT CTTCTCCTAT GACATGCTCT CTGGGCTTCA TTATAATTAA 780 CCACTTTCCT TCCTCAGGCT GTGCCAAAAC TGAGACAGCT AATTAATTTC TGGCCACTTG 840 CCACTCTCGT TAAGTGGTGG GCAGGGATGC AGCCTGCAGC TCTTGCTGCC CAGCTGGGCT 900 TGTTTTGCCA GTCGTGGAGG GCAACCACCC TTTGTCTGCA AATAGAGGGA GCCCCAGCTG 960 GACCCCGGCT GACTGGCAGT AGCTTCATTG AAGCTATTTG TTCCCCCACA GTGGGCAGAG 1020 CCTTTGTGAT CACTGTGGTA GATGTGCCTT GGTTTCCTCA TTTGTAAAAT CAAGGGAATG 1080 AACTTGACCT GCAGCAGGGA GAAGATTGGG TGGTGGTTAG GAGTGTGGGT TCTGGAGTCC 1140 AAGGAACCTG AGACCCAAGC TAGGCCCTGC CATCCCTAGC TGTGGGCCTC TGGGTGAGTT 1200 ACTTCATCCC TCTGAGCCTC AACATTCCCC ACCTGTAAGA TGGGGAGAGC AGTGCTCACC 1260 TCCTGTGGCG GTTGTGCGGA TTCAGTGGGT TATGGAGCAC ATGGCTGCCA CTTAGGAGGG 1320 AGACTGGCAC ATAGTGAGCG CTCGTAAACG CTCTACCCAG ACATCTCTCC TTCTAGGCTA 1380 ACATTCTATA TTCTTGATGG AAAAAAGGCC TTCTGTTGTG AGAGCTGGGG TGTGGAGCAA 1440 TTTTAACAGA CATTGCTTCT GTGTTTAGGC CATGCCTGGT GAGATGGTTA GCCCCTTCGT 1500 ATAGTTCCCT AGGGCTGCCA TAGCAAATTG CCATAAACTG 1540
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