Tag | Content |
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EnhancerAtlas ID | HS052-28722 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr4:79257370-79258820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr4:79258277-79258288 | ATTTTAATTAA | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCTGCAGTC CCCTGGTGAG TTGCTTTACT TTAAATACTC TGTCAAGCTC AGTGGGGGAA 60 TGTTCCTGGT TTCTTTGTCA TTAGGATTGC CCTTGAGAGC TGTTTCTATC CTTAGGTGCT 120 TTCATCCTAG CCCAGCTGGT TTTTGTATGT ATAAAATTGT TTAGGGGAGG AAAGTCTGGG 180 TAGATCTAGC TCTTCTCTGT CCATGCCTCT TTCCGCTGGG AGCCAGCAGA TGGATGGTAC 240 CATAAGCAGC AGGGCACCCA GGTCACTGGA AATATTCTGA TAGGGAGGAA GAACTGGGTG 300 TTGGAAATCA TCCAGAGAAT GCTATGTCTT TTGGATAGGT GCTTTCAACA TTGAGAGCCT 360 CAGGAATGTA GGAGGGGTGA GAGTGCTATC CTTCTAATCA GCAGTTTATT TTCTTGCTTG 420 CTTGCTTTTT TTTTTTCTTA AATAACTCCT TATCTTCTCT TGGCCTCTTG CCAGAATCCA 480 GAGGCTTTAC TTGAAATCTG TGCCTTTGCT TCCCACCAGC CACGTGCCAG GAGGGAATTC 540 ATCAGTTCCT GCAAAATCTA CCCAGCTCCA GCCCTTCACA TCCCCTCCTC TTGGACTCAG 600 ACCTGCTTAG ACCTCCTTGT CCTTGGCAGA GAAGTTCTTA AATCTGCTTC CATGTGCTTG 660 CTCCTGCTGC TCCCTTGGCA GCGTCAATGC AGCTGCAGCT GCAGCCGCCT CTGATTCTTT 720 GCCACCCTTA TCCTTATTGC TTACACCTTA CCGTGACTCT CTTGGTTTGT TTCAGTGTTG 780 TATCTCTTGT TAATTTGGTG GTTTTTTTGG AGAAGACATA GCTTTGGCAT AACTTTGTCT 840 CTAAGGAATT GAACTTCAGA GGCAGCTCAC GATAACCTCC AGAAAGAGGA CTTTTTCTGT 900 TCTTTGTATT TTAATTAAGT ATTGCTGATA AAATAAGCAT CCCAGTGGTA GTGGCTTGAA 960 GGGAGTGTCT GGATGGTGCC TGACTCTAGA GAGAAGTTGC AGTATAGTTT GCTGTGTGTG 1020 GATTCCCCCC TCATCTGCTA GAAATTTCTG AGAAGCAAAA TGTCCCCTTC TTCTCCCTGT 1080 CCCACTCATT CTTTGAGTCA TGGTATGTTA GGGTCAGGGA GTCCTACCAC TCGTGTTTCT 1140 GCTCTGTGAC TATGATTTGA ACTTCCTTAC TTACACAGAT GGAGATGATC ATGCTGGTCT 1200 CTCTGGAATG TGTGGCCGAT TTCTCACATA TTTATAGTTC TAGATTCCAT ATTGTGTTCA 1260 TGGACAGTAC TGCCCTTGAC ATCAGAAATG CAGTCTCTAG GTCAGGTCCA AGGGTGTGCC 1320 CGGCTTGCTC AGGAATCTTC TAAAGATGAT TAGAGTTGGA GGTCTGCTTT TAATGTAATT 1380 TGTGGAATGC ATTAAATACT TCACGCATAT ACATGCTGAG CTGCTAATTC CAATCCTGGT 1440 TTTCGTCCCC 1450
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