| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00026 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:913270-914260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr1:913728-913743 | GTCTTCCTGAGAACT | + | 7.03 | | Zfx | MA0146.2 | chr1:913967-913981 | CAGGCCTGGGCGGG | - | 6.74 |
| | | 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 |
| GH01I000975 | chr1 | 910651 | 915364 |
| Enhancer Sequence | CTCCCACTCC CCCCGCAACC CCGGGAACCG CCTCCCACCA CCCCGCAACC CCGGGAACCG 60
CCTGCCCCCA CCGACCAACC CCGGGAACCG CCTCCCAATC CCCCCAACCC CAGGAACCGC 120
CTCCCAACCC CCCCCAACCC CAGGAACCGC CTCCCAACCC CCCCCAACCC CAGGAACTGC 180
CTGCCCCGGG AGCCGCTTCC CCCGCAACCC CGGGAACCAC CTGCCCCGCA CACGGCCGCC 240
CCGGGAACCG CCTGCCTCCC CCTCCAACCC CAGGAACCGC CTGCCCCACC CTAACCCTGC 300
ACACTCTTGG CCTGGGAACT GCCTGCCCCG CACACGCCCG CCCCGGGAAC CGCCTGCCCC 360
AGATACATCC ATCATGGGAC ATGTCTGTCC TAAGATACAT TTGTGCTGGA CACGTCTACC 420
CTGGACACGT CTTCCCGAAA CCCCTCTGTC ATGGACACGT CTTCCTGAGA ACTGGTTGCC 480
CCGGGAACCG CCTGCCCCGG GAACCGCCCG CCCTGGACGC GTCTGTCGGA GTCACATCGC 540
CCCCGTGCTT CTTCTGCCTG AGATTTGGGT GACCTGGTTG AGTTGGGCCA GTTTGGGGGA 600
ACTGCCAGTG GAGGCCCCGT GTTCTGGTCT GTAAAGCATC TCCCAGAGGA CATCAGTGTG 660
AGATGGGCCT CGTAGAGTGC CTGACCCTGA AGGTAGCCAG GCCTGGGCGG GAACCCTGCC 720
AGAGGCTGGG GGAGGGACGC CGCCGTCACA TGGGCCCGAA CACAGGGCAA CGGCGGCGCA 780
GAGCCAACCC CCTGAACAAC CCGGGTGCTT GGACTGGGCC GCCCCATCTG GACTGTGTGC 840
TGGGATGACT GGGGGCTGGT CCCCAGGCTC CCCTGCTAGG GGATGACCCA AGCCCGGCCT 900
GCCCGGCCCC TGCGGCCCCC TGCTTGGCCA AGATCCCTGG ACAGTGTGTG CCTGGGATCT 960
GGACGGGCTG TGGGATCCGA GAGCACGTAC 990
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