Tag | Content |
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EnhancerAtlas ID | HS196-01625 | Organism | Homo sapiens | Tissue/cell | ZR75-1 | Coordinate | chr1:117562550-117564160 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr1:117563308-117563318 | ACTTGGCACC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACATTTGTGT CTTTCCAGCA TCATCTCCTT CAACTTTCCA TCGTGAATTT GAGCTTCAGC 60 CACACTGAAT TACTGGCAGC TCCTCAATTG TCCATGTTCC CTCTCACTCT CAAAGTCTTT 120 GATCTAGTTG CATCTTTTGT GTGGCAATCC TTAACCTCTT CTCCATCGGA ATAATTCCTA 180 TAAACCCTTA AGACTCAGCT CAGAATTATC TCCTCCAGGA AGTCTCCCCT CACTCCTGTA 240 TTTGGGCTAG GAGACCCTGC TGTGTGCTCA GATAGGCACT TCTATATACC TCTGTCTTAC 300 ATGAGGGACA TGAGGAACAA AAATTTTACA CTGAGGCCAG GTGTGGTGGC TCACACCTGT 360 AATCCCACAC TTTGGGAGGC CAAGGCGGGC AGATCACCTG AAGTCAGGAG TTTGAGACCA 420 GCCTGGCCAA CATAGTGAAA CCCCGTCTCT ACTGAAAATG CACAGATTAG CCAGGCATGG 480 TGGCGTGCAC CTGTAGTCCC AGCTACTCAG GAGGCTGAGG CACAAGGATC GCTTGAGCAC 540 AGGAAGTGGA GGTTGCAGTG AGCCAAGATC ATGCCACTGC ACTCCAGCCT GGGCGACAGA 600 GCAAGACTCC ATCTCAAACA AAACAAAACA ACCAAAAATC TCACACTTGA GAAAGGTTTC 660 TCAAGAGTTA TTTCAGCTGC ACATTCTAAA TGTGGAAGAC AGTGATCAGG GCAAATATCA 720 CTGTGCTGTG GTAGAATGGC TCTTTGTCTA CAAATGGCAC TTGGCACCAT CTCTAAGCCT 780 CTGTCCCTGC ACTTGTCTCC CTCTAGAGTG TGAGCCACTG AGGGAAGATA TCCACAGGGC 840 CTGGAATTGT CTGGCACATA ATATAGTGTG TGCTTCATAA ATATTTGTTG AAGGAAGAGT 900 AAAGGGACCT ATGGGCAACA TCAATAAGCA GTTAAAAAAG TAGAGTGGGT GATGTCAGCA 960 AGATGCTAGA AGAAGATTTG GGAACAAGGA TTGTCACTCA TCTTTCTGAC AAAGCAGAAA 1020 AGCTGCTGGG GTCAAAGATT AGTTGGCTCC ATATCTATAC AATGTTCCCA CAGTTAAGTG 1080 ACTGCAAAGA CACACACAGT TTTAATCACT CATGTACAAC TTCCTTTTGT TTACCCACGT 1140 TTGAAGGCAG ATACAACTAG AGTTTGGAAA TTGTGAATCC AGAAGTACTC TGCATAGTAA 1200 ACACACAAAC ACAGCATTAA TAGGGCCACT TTCTCCCAAT CTGATACATG AAATATGACA 1260 GAAGAGATGC TTGTGCTTAA ATACCGAAGC AGTATCATGT GGAAGAGAGA TACTGGGCTT 1320 GTCTGTGTGA CACTCCCTCT GCCACACCAC CCCTACCAAG CACAGGTAGC ACTAGGACTA 1380 GTGGATGGAA GTTATGAAGA GATAAAGTTC AACTTGATAT CAGAAAGCAT TCTGGAGGGG 1440 CAGAGCTGTC CAGAGATGAA ATGGGCTGCC TTGTCAGCTA GTGATGCTGT TCAAAAGCTG 1500 TATGAGCAGT GAGTGGGGCT ACTGTAGAGG GAGTTCACCC ATATGATGGC GGGAGGATGC 1560 AGTGTCATAC TTGACCTCTA ATGTCTCTAC TACCTTAACT TTCTATTTCA 1610
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