Tag | Content |
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EnhancerAtlas ID | HS175-20832 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr3:191000100-191001590 |
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) |
CDX2 | MA0465.1 | chr3:191000770-191000781 | TTTTATGGCTC | - | 6.14 | LMX1B | MA0703.2 | chr3:191000655-191000666 | AATTTAATTAA | + | 6.32 |
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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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Enhancer Sequence | ATCTAGATGA AGGAAAAAGA AAGAAAGAAA ATAAATCTAT AAAATGCAAT GCAATCAAGT 60 AGTTAACATG ATTCACTACT TGGAGAAGTG ACAGATTTGT TATGGAGTCA ATGGCAGGAA 120 GAACCCAATC AATACATCTC ATACCCGCCC ACTTCACTAA AAGCAAGCAT TCCTATGCAT 180 GCCCACACAT TCAAATAGAT GCACAAGCAT GAAGCAACAT CTTGAAATAA AAAACTGTTG 240 GATTTTCACA ATTTATGGTT TAATTTCCAG ATTCCAGGAT TAATTAACCT CAAATCTTAT 300 TAATACTAAA GCTGAGAGCA TAGAGGGCAG GTGAAAATGG GAACAATGTC TTTCATTTGA 360 CTACTTTTGA GCTAGGTGGT AGTCTTCCTG ATAGTGATGT TATTTGCAAC TATCACTTTG 420 TTCTTAACCA ACTGAATAAA CTAGAGAAAA GCTCAAATTT GAAATGAATC ATAATGGGAT 480 CACATTACTG TCTCACTATA TTAGAAAAGG ATGGCTTCAT TTTGTTTCAA GCAGCTCTTT 540 TAAAAATTAA GGCTGAATTT AATTAATTCA AAGCTGGCAA ATGTCCCATC AGTTACTCTC 600 TTTAATACTT GCTTTAATTG TGCTGGTTTT CTTTTTAAGT CAAAGTCTTT CAGTATATCT 660 CCAATTTCAA TTTTATGGCT CCAGTGATGT TATAGTATAA TGACCTCCGA TCTTGGCATT 720 TACTTGTCCC AAAAGACTTT GGATGTATCC ACTCTAAAAT TGACTCTGTT CCAGTGCATA 780 CACTGCAGCA CATGATGGTA TTAACTAAGG AGAATGACTA ATCTTTTTAC TAACCCGTTG 840 CTTTAATAAA GTTCCTGAAT AAAATCTAAA TTACTTAGTT TGATATTTAG GCTTGTTTTT 900 CCTTTACAGT TTCATTTTTC ACTATATATT TTTGTGTACC AGCCACATTA GACTACTAAT 960 TCATGAATAT ATCCTGCACT TTCTGCACTT CAGAGAGTTG CTGACATGGT TGCCTAGAAT 1020 CCTTTATTCT ACAACCTGCC ATTTTACCTA CTGATTCCTG AAGCTACTGA TCAAATGCCA 1080 CCAGAACTGT TTAGCCTTTT GGATCTTTTT TCTACTTTGA GTCATAACCT TTTTTTTCTC 1140 CTTTGGACTG CCACAACATT TTGTTTGTAT ATCTACTACA GTTCAAAATT CATTTCTTCT 1200 TTCATTAGTT ATGTATTTGC GAGTCTGCCT CCACTATCAA ATTGTAAATA CTTTGAGAGC 1260 AGTTACAGTC ATAGTCATTT CTGTCCCTAT GTGCAAGTAC CATAGTGGTT TGCGGGAAAA 1320 ATGAGTGAAA ACATGTTTGA TGTGTGACTA AATAATAACC AAAATTTCTA GTAATTGAAA 1380 GGCAAAAATA TAACCCCCTT AAACTTTACA TCCAGTTATA AAGCTATATG AGCTGAAAGA 1440 ATAATTGCAA CTCTTTGTGT CTTACTTTCT TAAGAATTCA ACCATGAACA 1490
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