Tag | Content |
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EnhancerAtlas ID | HS098-43769 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr4:170258180-170259900 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr4:170258590-170258601 | AATTTAATTAA | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 170258712 | 170259094 | chr4 | 170259476 | 170259663 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I169336 | chr4 | 170258000 | 170259837 |
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Enhancer Sequence | AATTTTCACA TGAATACCCC ACTCCATCAG CCATGTTGAT TAAACTGACT GACAGAGGCT 60 GAAACCAAAT CTATTCAAAT AGTCTTCTTT CTTCTTCTTT TTTTTTTTTT GAGACGGAGT 120 CTTGCTCTGT CACCCAGGCT GGAGTGCAGT GGCGTGATCT CGGCTCACTG CAACCTCTGC 180 CTCCCAGGTT CAAGCAATTC TCCTGCCCGA GCCTCCCCAG TAGCTGGGAC TACAGGCACC 240 CACCACCATG CCCAGCTAAT TTTTGTATTT TTAGCAGAGA CAGGGTTTCA CCATGTTGGC 300 CAGGTCTTGA ACTCCTAACC TCAGGTGATC CACTCACCTT GGCCTCCTAA AGTGCTGGGA 360 TTACAGATGT GAGCCACCGT GCCCGGCCCC ATTCAAATAG TCTTATGCAG AATTTAATTA 420 ACAAGACTTG AAGCAACACA ATGTGGCCTA TTTACATTGT GGAACTCAAT CATATCCCCC 480 AGAGTCCCAG CCTCAAGTTG AAACCAATCC TATAAACCAT CATGGTCTAA CTTGGAAATC 540 CAACTAGCTT GCTCTTTGTG TTTTGACTTT TCCACTTGGC TTGAGGTATT ATTCCAGATA 600 CAGCAGGATG TATTAGCACA AGGAGGAAGT CTTGGGCAAT TCAATCATTC CTAACAATCC 660 TGGCCAGTGA ATTGAAGCTA TCTGAATGCC TCACAGGGCT GAGGTTTGTT TTCCCAAAAT 720 ACTCAAAGCT CTTTTATGAC TATACTTAAG GGGTATGTGA CTATGTTTCC AGAAGAGAGG 780 CAAGTTAATG TCTGGCTTCC ACATAAGAAT TACAGTTTCT GAGATGCACA TGGTGCCCTA 840 GGGAAGAGAT GTTTGCAATT GCCGATGCCA CTCAAGGAGG ACCTGCATTC GTTGGGGACC 900 ATGGTTCATG ATGCTGCAAA TATATTCTCC TGGTTGGCTG GTTGGCATTA GGGTTTTCCA 960 CAAAGAACAG TTGAATCTAA TCCTTCTTTG TGGAGGAACT ACCTGATAGC AGTGAGTCTA 1020 ACCTGACCTT TTTGTCCATG CCACCAGCTG GTGGCATTTG TTTGTTCTGG GCGATGATTG 1080 AGTGATACCT ACAAGAAAGG GAGGGGCAAA GACATCTAGA GGTCTTGGCA AGTGTGTTGA 1140 ATGGGGTGGC AAGAACAAGT GTGTTGAATG GGGTGGCAAG AACTGGGGCT ATCCCCTGCT 1200 GCTTCTGTTA AACTTCTTGG TAAGATTAAC ACGAATGGAA ATCAAGTCCT GGTGATAATT 1260 ATCTGGCAGA GGATGGCAGG CCCAGTAGTT AGTTAAAGGC AAGGCACTTA GTGCATTGGA 1320 GTGTTTTCTT TCCTGGGGAA GATCTCAGGG TATCTTCCCA CCCTCATACT TTCTGGGGTT 1380 GGAGGAACTC TCTCCCCAGC TCTCACCACC AGAGAATCAT TGTGTTCATT CCAGTGGTTA 1440 CTCATCTCCT ACTTCACCCA CATCTTCGTC TAGATAAATT AGGTGCAAGA GGGATAAAGG 1500 CATATTTTAA AACTTTTATT TTAAGCTCAG GGGTACATGT GTAGGATTGT CATATGGGTA 1560 AACTTGTGTC ATGGGGGCTT GTTGTACAGA TTATTTTGTC ACCTAGGTTT TTTTTTTTTT 1620 TTTTTTTTTG AAACTGAGCC TCACTCTCTT GCCCAGGCTG GAGTGCAGTG GCCCATCCTT 1680 GGCTCATTGC AACCCCCGCC TCTCAGGCTG AAGCAATTTT 1720
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