| Tag | Content |
|---|
EnhancerAtlas ID | HS052-26143 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr3:50009880-50011040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr3:50010482-50010497 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 50010531 | 50010581 | | chr3 | 50010791 | 50011022 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I049972 | chr3 | 50010050 | 50011490 |
| Enhancer Sequence | ACATCCTTTA GAGCATATTA TTTCTGGAGT ATGTACATAA GGATGCAGTT TATTTACAAT 60
AGTAAAAACT AGAAACTGCC TAACTGCCCT GTATCAAAGG ATTGGCTGAC TAAATTAAGT 120
CTGAACTTAT GGCAGTGCTC GCTCTGTGCC AGGCATTGTG TGATACTTAC AAGCATTAGT 180
TCATTTAATT ATCACATATT TAATATAATC ACTCTAAATA TTAAGCATTA CTGTATGTAA 240
TTGTTCTAGA TACTGAGTGA CACAGCAGTG TATATTATCA AGTCACTGCC TCCATGGATA 300
ATGAAAAAGC AAGCAAAAGG ATTACACAAT TTTAGTCAGC AAATAAATAC TCTGAAGAAA 360
ACTAAAGTAC AGGCGGGGCA TGGTAGCTCG GCCTGTAACT CGGAGACAGA GTCTTGCTTT 420
GTCGCCCAGG CTGGAGTGTG TGGCGCGACC TTGGTGCACT GCAACCTCCA CCTCCCCAGT 480
TCAAGCAGTT CTCCTGCCGC AGCCTCCCGA GTAGCTGGGA CTACAGGCAC ACACCACCAC 540
GCCCAGCTAA TTTTTGTACT TTTAGTAGAG ACGGAGTTTC ACCACATTGG TCAGGCTGGT 600
CTTGAACTCC TGACCTCAGG TTATCTCCCT GCTTCTGCCT CCCAAAGTAC TGCCATTACA 660
GGCATGAGCC ACCAAGCCCA GCCCATTTTT GATTTTTTTG AGGCAGCGTC TCACTTTGTT 720
GCCCAGGCTG GAGTGCAGTG GCACAATCAC GGCTCACTGC AGCTTCTACC TCTTGGGCTC 780
AATCGATCCT ACCACCTCAG CCTCCTGAGT AGCTGGGACC ACGGGCATGC ATGCTAATGG 840
GGCTGTTTTT TGTATTGTGT AGTTAGGGAG ACATCACTGA GGAAGAGGCA TTCGAGCCCA 900
GGCTTGAATG CCGTGAGAGA ACAGTTTATA TGAATATGGG GAAATGAACT GCCCAGGCAG 960
TTCATGCTGA GGAAGTGCTG TGGCCCTGGA CTGTAATGAA CCCAGTACAT CATTTTATAT 1020
TTAACACATG AGAAACTGGA CACTAAAAGG TTACACAGCA AGTGAGCAGA GAGCTTGGAA 1080
TGCACACAGT ATGATTTCAG AGCTTAAGCC TTTGAAGGTT ATGCTCTTCT GCTTTTCTTT 1140
TTTTTTTTTT TTTTTTGAGA 1160
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