Tag | Content |
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EnhancerAtlas ID | HS103-21296 | Organism | Homo sapiens | Tissue/cell | HUES64 | Coordinate | chr6:57183400-57184880 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr6:57184607-57184620 | GGATAATTAATTT | - | 6.98 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTACTATTT AAATTAGAAT GTATATATTC TTGAGAAGCT CACTTACCCT TTGTGAGAAT 60 GAATGAAGGT AATTCATTTC CTTCATTCAG CAATCCATTC AACAAGTATT TATTGAGGTA 120 ATTCATATCC TTCATTCAGC AATCCATTCA ACAAATATTT GTTGAGGGTT TGGTACTCAT 180 TCATTTATTT ATTGTACAAT GCATATTATT GAGTGCCATT ATGTTCTAGG TGGCAGGGAT 240 TTTGAGATGA ATAATGTTAT TTTTTGTTGA AGTTTTATTC TAGTACATGG AGACAGACAT 300 CCAAAATAAT AGTCATAATT CAGTATTTTA ACTGCTCTAG TAGAAGTAAA TGGTAGTGCT 360 GTTGAAACAA AGAAGTGGGA GTGACTGACT TAGTCTTATT AAATGAGCTT CTTAGAGAAG 420 TTGAAATGTG ATCTGGACAT ACTGAAGAAT GAGTAGAAAT TTTCCAGCAG AGAAGAAGTG 480 AAGAGTTTTT CCAAGCTGAG ATAATGGCCT ATGCAAAGGC TTGGAGCATG AAAGAGAATT 540 TCATATTTGA GCTAACAGTA ACAAGTTCAG GAATTCAGGG TGGATGGAGA AGTATGGAGG 600 GCATTTTGTG CCATGCTAAT GATATGATAT TGGGGTGTAA GAAGGATGTG GCCACCGTCC 660 TGGGGGCCTA CTTAATCCTC AGTGTGTTGC TAGAGAAAAG AATGGGCTAG ACATGAATTG 720 AAACAGAAAC ACTAGCGTTG TCTTCAGAGT TTATGTTCCA GGATATCCCT GTGGGGAAAT 780 CAGAAGGAAA GGTGAGATAC TGTTAATCAT TCTTAGAGGA GCAGGGTAAG CACTGCTAAT 840 ACAGAGAGGA GGCACTCAGT GCCTGTGTGT TGAATGAAAG AATGAAGACA AGGGAGAAAA 900 GGGTTTTAGA AAGCTTAGCA GTGTCAATAC TTCATAGGGA TTAAGATGGT GATTGAAAAG 960 TGTCCCTTGG GTTTGGCACT TGAGGTGAAA TGATAAGGGC CTGAACTATG ATAATGACAA 1020 TGGCAGTGGT AGGAAGGGAG AGAGTTAAGG GATACTGAGG AGTTAGCATT GATAGGATTT 1080 GGTGACTGGA TATGAGGAGT GAGGGAGCAG GTGTGGAGTG GCTGCAGTTC CTGCTTGGAT 1140 GATCTGATGC ATGGAAACTC TGCTGCTGGA GATGGGCATG GCAGGACGAA GAGTAGGAAT 1200 GAGGGGAGGA TAATTAATTT GGATACCCAT ACCTGTGGGA CATGGGGTTT ATGTTCAGGA 1260 GACAATTAGA AGTTCTTCAT TCTTGACTTC AAAAATGCCT CCAGAGAATA ATTCATCTGA 1320 GGAAAGATTG ATATGGTGCT TTAGGAACCT TTGAACAGTA TGTAGCATCT GTTCAGGATG 1380 GTTCATTTGG CTGTTTGGAT GGCCTTTCTT CTTCACTGTT GTGCTCTGTC CTCGGCTTCA 1440 TCAGGAAAGG AAGGGATGCT TTTTTTCTGT TGAATCTATG 1480
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