| Tag | Content |
|---|
EnhancerAtlas ID | HS146-06320 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr17:25959850-25961300 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAX | MA0058.3 | chr17:25960068-25960078 | ACCACGTGCT | + | 6.02 | | NFE2L1 | MA0089.2 | chr17:25960698-25960713 | TCATGACTCAGCAGA | + | 6.91 | | Nfe2l2 | MA0150.2 | chr17:25960696-25960711 | AGTCATGACTCAGCA | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCTCCCCTG GGTTGGGACA ATTAAGCCTC ACTTGGTGAC CCATCTGGCA GTCGGAGCCA 60
CGCTTCCTCC ACATGCCGAC AGTGGGGGAA GGTCACGCGG TTCGCTGTCC TGCTGAGGAG 120
GGCTGAGTGC CATGAGGGCC TGGCTTGGAA ACCTCACTCC CACTTCTTGT CTGGCCTCAT 180
CTAGCCCAGC CTCTTTGGAG GGCCTGGGGG AAGCTGGAAC CACGTGCTGT GTGGTCCAGG 240
AAGCACTGGG AGAGCCAGGA ATAAGGATGT TCTCAGCTTA CTCATGAGAG GAAGCCTGTG 300
TGGTGGTTAG AAGCGTGGGT GCTGGGGTTC AAATCCCAGC TCTGTTGCTG ACCAGTTGTG 360
TAACTTTGAG CAAGTGACTG AACTTTTCTG TGCCTCAGTT TCCTCATCTG TAAAAGTGGC 420
CGGGGTTGCT GTGAGGATAA ATGTTCCTAG TCATGCCCAG AGCCCTCATG GACACACATG 480
GATCCAAATG CCACAGCAGC CTTAGCTGGT CAACCTCAAA ACAACACATT TGTTCTTACA 540
GTGTTGGAGG TCAGAAGTCT AAAATCAAAG TGTCATGGAA GGTGGCCAGC AGGACCATGG 600
AGCCTCTGAG GCAGCGGGGC ACCTTGGCTA AGAGCCACGT ACTGGCCTCC TGCTGGCACG 660
CAGTCTTGGC CAGCCAGGCT GAGCTCCCCA CTTCGGGGTC GGGCCTGGGT GTCCTCTGGT 720
GATGCTGAGT CCAAAACAAG GCTGCCCACA TTTTGGTTCA CAGGGCTCAG CTCTGCTTTC 780
TAGACTTCCA GATAAGAAGA GGAGGAAAAG TCCCCGGTCT CTGGGCACTA TCAGGAACAG 840
AGAGCAAGTC ATGACTCAGC AGAGGGATCG ATTTGTTCAA TGCAAAGAGC TGCACTGTCA 900
TGTCTGACAT GAGCCAGGGG CTCAGCACAC GGAATCGCAC CCAGTCCTCT CAGAACGCTG 960
CCAGCCAGGG GCTCAGCACA CAGCGTTGCA CCCAGTCCTC TCCAGAACAC TGTCGGGTGG 1020
TGTTACTGTC CTGCCATTCA GAGGAGGGAA CTGGGGCACA GGCAGGTCAA GTGACTTGGC 1080
CAGTGTCAGA ATTGCTAGTG TACAGAGCTG GGAGGCAAGC CCAGTCCCGT GGGACCATAA 1140
ATCCAGTGTG AAAATCCATC CTCCTGCACC ACATGGAACA AAAGCAGGTC CGGTTGTTTT 1200
CCTGGGTTTT CTGGACACAC TTATCCAAAT TCCACAGCAG CCTTGGCTGG CCAATCTTAA 1260
AACAACAAAT TTGCTCTCTT AATGATTTTG AAGGTCAGAT GTTAAAATCA ATGTGTCAGC 1320
AAAGTTGTTT CCTTCTGGAG GCCCCAGGGG AAAATCTGTT TCTTTTCCTT TTCCATCTTC 1380
TAGAGGCTGC CTGCAGGCCT TGGCTTATGA CCCCTCCTGC CATCTTTAAA ACCAGCAGCT 1440
TTGGCTGGGC 1450
|
| |
|
|
|
