| Tag | Content |
|---|
EnhancerAtlas ID | HS053-35178 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr6:132654570-132656090 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RELA | MA0107.1 | chr6:132654810-132654820 | GGAAATTCCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I132333 | chr6 | 132654728 | 132656527 |
| Enhancer Sequence | TATCACAATC ACAGGGGGAA TGCCAAGAGT TGCCTCTATT CAAAAATATT AAAATTGTAC 60
GAATTATTAA AGAAAGTCAT GACCATAGAA AGTATACGAA TATAGATATA TTGGTATTCC 120
TGACACTGGA ATGAACATTT AATTTAATCT TGCTTGTAGC CTGGCTGTAT GATGGCAGAA 180
GAAATAAATA AAAAGAAATA CAAAGCAGTG CATATGGAAG TGGAGGCAAG ACACAAACAT 240
GGAAATTCCC CTGATGACAT CAAACTATGT TATTGATCCC ACATTCTTGT ACAAAGGTGG 300
GGTGTACAGA CCCAGAATGG TGACAGGCCC GTGAGCTTAC CTTCTGATGG CAAAACAGAC 360
CAGGCAAGGA GGGCCTGGCA GCCGTGGGTT ATTTATTAAC TACTGTGTGT ATTAAAGGAA 420
CAGCCCAGAA ACCAGAACAC AGACAGAAAG GGAAAGACTT CAACCTGAAA GAGGAAAACA 480
GTCTCTTCCA TTAGATCAAG TAACGGGAGC TTTCAGATAC ACTTGAGATA TCTTAGCAAG 540
AAAAGCAGAG AACAACAATA AACAGTTGCT CAAGAGTAGC CAAAACCAAG GTGGAAATTA 600
ACACTGACCA TAAAGCTGAC CTTGACAACG ACCGTTTTTC CTAATCTCAT CATCTCTTCT 660
TACGCACTTT ATCCAGGTCA AATATGCCTC ACATAGCCCC TGCAGCACAA AGAGTGCTTA 720
ATAACTATTT ATTGAATTGA AATAAAATGA ATACTACCCT TTCCATGAAG CCAACATCAA 780
TGAGGCTGAA TCATTAAATT CATTTGCCTC TTAGTTTCTT GATTATCTCC ACTATACTGC 840
ATCCCACTTC AGCTACTGAA TCCCATTGTC ACACCCTGCC CATGAGTACA CTACCTCTGA 900
AATTCTCTTT CTGTGCCTCT TTCCTTTCCT GTTAGCTCTT TCACACTTTT CCAGTTGCTC 960
AGCCAGCCAT TTTCTCCTGG AAGGTCACTG AACTCATCAC TCACCAGCAC TCACAACTGA 1020
CCCAAATGCT CAAATGGTGA ATCACTCCTG TCATCTGCTC CTTCTCATCC TCCACTAAGG 1080
ACACTGGAGA TAAACTTTAT ACAAGTATTC GCATGAGACT TCAAAGTTCA TAACTCACAC 1140
TTTTGCCTCA GAACGTCAAT CTTTCTTTGG TTTTGCTCTG CATTCTGTTC AGCTCCCTGA 1200
AGTGGCTATC CTAAAACCTT TCCCAATTTA TGCACACCTC CTAATCAGCT CTCAGCAAAT 1260
GTCTTCATTA TTTTGATGAG AGAGGAAAGC GTTTCTATCC ACTCTGTAGC TGCCTGAGGG 1320
CAGAGCTGGG GGGATAGAAT TTGATGCAAA GGACACAATA TGATTGAAAA AATCTTAAAT 1380
ATCAGGAACC CATTTTATAT ATTCATTTTT TACAATGTAG AAAGTAATGA AACGATTCAA 1440
AGAATCTACA CTTGGTGGCA TCTTATTCTA CTTAACTTGA GCTATACAGA GTGGGATGAG 1500
ACATAGAGAA CCTAAGACCA 1520
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