Tag | Content |
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EnhancerAtlas ID | HS105-47727 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:219509790-219510740 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:219510481-219510502 | TTTTTCTTTCCTTTTCTTTTT | + | 6.53 | Nr5a2 | MA0505.1 | chr2:219510686-219510701 | GATGGCCTTGAACTC | - | 7.49 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I218644 | chr2 | 219509118 | 219511157 |
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Enhancer Sequence | GCAAGGAGGG AAAGGGGGAG GCAATCACAA TAATTAATCA CAACAACTAA GAATCAGTCA 60 GTAAATACTT ACTGTGGGCC AGGCTCTGCA CTCAGTATCA TACATGTGTC ACCTGATGTA 120 ACCCTCCTTT TCACTACCCT ATGAAACTGG TATCTCTATT TTCCAAGTGA GAAAAACTAA 180 ATCACAGAAG TTAATAATTT GCCTAAGGTT GGTTACAAAG TAAGCCAGGA GCAGAGACAG 240 CCTAGCTTCA GGGCCTGTGT TCTAAGCCCT ATTCTGTACT GCCTTCCTAA AAGAAAGTAA 300 TCATGAATCA GCATGACCCA CTGTAGACTT CCAAGGAACT GACGTGGCTA CAACTCCACA 360 GGGCAGGTTT CTGTGCCTCA TTTCCCTTCT CCCACAGAGG CATGACAGGT CTAGAAACCC 420 CTTAGCCAGC TGTGCCATAG GTCAGAGAAC TTGCCTGGAT TTGGAAGTGG CAAGATTGGG 480 GCATGAATAT AGTGTCTATC CACTTTCCCA GGGCCAAACT CTGAGAACTC AAGTGACACC 540 TTAGTCTCTA GGCCTATACT GTAGGTCTAT ACTCCCTTCC CAGAGCCCAG AGAGTGCTCG 600 CTATGTGACT GAGCCACAGT CACAGAGGCC AGCTGTAGGC AATGGAGTTG AGACAGTGGG 660 AACAGAGAAG GGTGTTAGGA AAAGACTCTC TTTTTTCTTT CCTTTTCTTT TTTGAAACAG 720 AGTCTTACTC TGTCACCCAG GCTGGAGTAC AGTGGTGCAA TCTTGGCTCA TTGCAACCTC 780 CACCCCCCGG CTCAAGCGAT TCTAGTGCTT CAGCCTCCCA AGAAGCTGGC ATTACAGGCG 840 TCTGCTACCA TGCCCAGCTA ATTTTTGTAG TTTTAGTAGA GATGGGGTGT TGCCCAGATG 900 GCCTTGAACT CCCAAGCTCA AGCAATTTGC CCGCCCCGGC CTCTCAAAGT 950
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