| Tag | Content |
|---|
EnhancerAtlas ID | HS052-34908 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr7:44766780-44768080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:44767760-44767781 | AAAGAAAAAGTGAAATTATCT | - | 6.06 | | IRF1 | MA0050.2 | chr7:44767708-44767729 | AAAAAAAAACAGAAAGAAAAG | - | 6.65 | | Nr2f6(var.2) | MA0728.1 | chr7:44767887-44767902 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 |
| GH07I044726 | chr7 | 44766462 | 44768001 |
|
Enhancer Sequence | AAAAAAAAAA GAATCTGGCG TAGGCTTCCC CCAGATCCTG CTTATGCCTC CTGACCAAAC 60
TTGGTGCTTC TCCATGTGAC ATGGCATGGC ATGCCTCTTG TTTCTAGAAA AACCGTGAGT 120
TACATTAAAC TTCCCTTTCA ATGGCATTGG TCTCCTCACT TTGTCACTTA GTCACCTCCA 180
TAAATTAAAA TTACATGGGT ACAAATGAGA CAATGAGCCA TATGGAAGTC TGGGAAAGGA 240
GCAGCACAGG AAAGGGTGTG GGAAATGGAA AGATAAGGAA CTTGGAGAGG TCTGGGAGTC 300
AGAAAGTCAG CCAGTGTGGC TGGAGCATAG TGAGCAAGGA GAGGAAGTAA TAGGAGATGA 360
AGGCAGGAAG ACAGCCGGGC CAGAGTGTGT CAAACCTTAA AGGGACTGGG TCTTATTTGA 420
GCATGAGTGC AGTGGGAAAC CATTACAGGG TTCTGAGAGG AGTGTCATGT GCTGGCTTAT 480
GCTTTACAGG GCCCCCTTTG GCTGCTTTCT TTGAGGTAAG GGCAGAGGCA GGGAGACCAA 540
TCACTTTTCA TCACTTCTGT TCAACATTGC ACTGGAGGTT CTACCCAGAG CAATTAGGCA 600
AGAAAATGAA ATATGGCGAG GAACAGTGGC TCACGCCTGT AATCTCAGCA CTTTGGGAGG 660
CTGTGGTGGG TGAATCACTT GAGCTCAGGA ATTCAAGACC AGCCAGGAAT TTGAGACCAG 720
CCTGGGCAAG ATGGCGAAAC CTCATCTCTA CAAAAAATAC AAAAATTAGC CAGGCATGGT 780
GGTGTGTGCC TGTAGTCCCA GCTACTCAGG AGGATTGCTT GAGCCCAGGA GGTTGAGGCT 840
GCAGTAAGTC TTGATCTGGC CACTGCACTC CAGCCTACAG AGTGCAGTCT GTAGGATGAC 900
AGAGCAAGAT CCAGCCCCTC CCCCCTCCAA AAAAAAACAG AAAGAAAAGA AAAGATGAAA 960
TAAAAGGCAT TCAGATTGCA AAAGAAAAAG TGAAATTATC TCTATTTGCA GATTACTTTA 1020
TATTTTATAT AGAGAATACT GGTTGGGTGC AATGGCTCAC GCCTGCAATC CCCAGAACTT 1080
TGGGAAGCAG AGGCAAGTTG AGCATCTGAG GTCAGGAGTT CAAGACCAGT CTGGTCAACA 1140
TGGTGAAACC CCATCCCTAC TAAAAATACA AAAATTAGCC AGGTGTGGTG GTGGGCACCT 1200
GTAATCCCAG CTTCTCCGGA GACTGAGGCA GGAGAATCAC TTGAACCCAG GAGGCAGAGG 1260
TTGCAGTGAG CCAAGATTGC ACCACTGTTC TCCTGGGTGA 1300
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