Tag | Content |
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EnhancerAtlas ID | HS044-04347 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr14:74600020-74601510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr14:74600141-74600152 | TTCTTATCTTT | + | 6.62 | IRF1 | MA0050.2 | chr14:74601201-74601222 | TAAATGAAAATGAAACTTGAA | - | 6.93 | IRF9 | MA0653.1 | chr14:74601203-74601218 | AATGAAAATGAAACT | + | 6.03 | ZNF263 | MA0528.1 | chr14:74601321-74601342 | TCCCTCTGGCCCCCCTCCCCC | - | 6.13 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 74600417 | 74601237 | chr14 | 74601306 | 74601418 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I074133 | chr14 | 74600292 | 74602151 |
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Enhancer Sequence | CCTATACTAT TTTGTTAAAA GCCTTCTAGA ATATAGGTAC CAAAAATTAA CTCACTTTAT 60 TCTTTCTAGT TTTCAGTAGT GGGGATCTGT TAAGCCTTAT TATTTAAGAA ATAGATATTA 120 ATTCTTATCT TTGGTATTTT TCTGATTTGC TTTATTGTAA CAAGAGCTGC ACATTAATTA 180 ACACATTAAT CAGTGCATGC AGAGATGGTT ACATAACAGT CTGAGCCATG AACTCAGTCC 240 AGTATTGAAA AATAAGTATC TCCAGAAGTA ATTCTTATTC TAGTATCAAA CATAACAGTC 300 CTTTAAAATT TCCTTTGGAA TGTTGAAAAG AGATCAAATG AAACCTTCAG AATGGTTATT 360 TATCAGGGAA CAAGAAACCT CCAATTTCGT TCACCCATTG TAGCTCCACT TTCTCATTTT 420 AATGCTCAAT CCACAGTGGC GATGGTAAAA GATGTCCTGC ACCTTCAGAG ATGGCAGTGG 480 GAGAGGGGAC ATCACCTTTC CATTTATTGC TTGTTGCAAT TTGGCCTGTT TACAGACAGA 540 ATTGCTCTGT GGGTTCTTTT AGTGGAGAGT GGAGGAAATC AAGATAGGAA CAAGAAATCA 600 GCATTTACAC ATGACCCATG AGTTGGCTAA TTTTTAACAT GTAGTTAAGA AATGATTACA 660 GCCTGCAGAG TCATGACCTC AACTTTTCAT CAGCTCCATT GGATTGTGCC TCAGTTTGGA 720 AATGAAGGAG GTACACGGGA AGTTTTAATT GTACCTGTGT GATTTATCCC TAGTCAGCTC 780 TTTAATTTCT TCTGGCTGTC TGAGGTTTCC GACATGCTGT AAATTTCCCC AACTTTTTCA 840 TTATCTGCAA TTTCTTTATG ACTTGTGAAT CGGAGTGGAG AGAGAGTGTG GATTTACAGC 900 AGAGATAAAC ATGTCCATAA AGTCTGTATC TGTGTCAGTA ATTGTACTGC TGTCAGTGAC 960 TGTCCTGTTT TACAGGCCTC TCTTGGGAAA GGAACAGGCT TCACTACCAG CAGCACTGAA 1020 GTGCTTGCTT TGATTTGCAT TAACTTGCTA GGAGATTAGG TAGGAATGGT GGGATAGGAA 1080 TTGATACTGG ACCTTGGCCT CTCTTGTTTG TTTGAGATCA AATGACCTCC TAGGATAACT 1140 GTGTGTTGAA GATAGAACAT GGACAGACAA TATTCATTTC CTAAATGAAA ATGAAACTTG 1200 AATTGATATG GTAGATGTGA AAAATCCTTT CTAACTTCAT TTTATAATGT ACCTTTAAGG 1260 TGACTTCCCT TTCCTATCAC TGTTGATAAT TAAACTTAGG TTCCCTCTGG CCCCCCTCCC 1320 CCATTTTCCT TTTCTTAGAA TTAAAACACA GGGTTTCACT TTTAGAGCAC TCATATCTGC 1380 TCAAGAGTGG GCCAGCTAGA GTTAAGGTGA AGACTACATC TGCCTTATCT TAATTCTCAA 1440 CTATTATTGG CTCTTTCTCA TCTGCTTAAG GTGGTGTGCC CACAACCATT 1490
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