Tag | Content |
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EnhancerAtlas ID | HS052-01244 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:47068530-47069850 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr1:47069089-47069100 | AAATCACAGCT | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATTCAATTA CTCTGGGACC ACATTACAGG AGACCACATG CACTTTCTAA GCACGTGCTG 60 GGCTCTGACA GCTCCTGTTC ACAGAGCTTC CCTCTCCCAT GGCTTCGCTT CATGCAATCT 120 GAGTTGCCAT CCCCCACAAC TGTCAACATC TGCAAAATAC CAGAGTAACA GGACTCCTAA 180 CCAACTCTCT GGATTACAGA GAGAGAAGTG TTGAGGTGGG AGCAGATGGG CAGAGGGGGC 240 ACCAAAGCCT CTAGCTGGCT CAGTTCCATA TAAAACCCAA CCCTGGATTT CCTCTTCACA 300 TCACTTCCAG CCCAGCCCTC TAATGAAGGG CTGAAGCTAA GGAGAGTGGG CTGAAAGCAC 360 CTGGCTGATG GGTGGTGATC CAGTGAGACA TTACACCTAC TGTCCAGCAT GTGCCTGGCG 420 CATGGGCAGT GGTGCCCTTC CCATTCTGCA GGGTCAGTTC CATCTGTAAA TCCCACTGAG 480 GCTTCAAGGC CCAGGTCACA ACAACTCTTC TCTCAGAGCC TTTCTAAAGT ACCCCAATCC 540 AAAATGACCA AGCTCCTAGA AATCACAGCT ACCATGTATT CAGCACCCAT TACATGACAG 600 GCGCCATACT AGGTGACTTC CATATAATCC TATTCACCCT TCACAATGAC CCTATTATGG 660 CCATTTCCTA GGGAAGAAAG TGAAGCTCTG GGAGGGGAAG CAGACTTGCC CCAGGACACA 720 CAGCTAAGAG GTGGAAGAGA TGAGATCTAA ACCCAGGACT CCCTGACCCT GAAGTTGAGC 780 ACTTCTAACA ACACTTCATT CCTGTGAGCC TGCCTGCCTC TGATCTGCCA CTGTCAGGGA 840 GCTTGGAGCT CTCTAGAAGA CAGGGTGCAC CTGACACTCT TATTACCTTT CCCTGTGGAC 900 AGCCATCCAC ACAGGCAGGA GCCTTTAAAT ACTGAAAATA AATGAAAACA ATTAACTTAA 960 AAATAACGCA GTACACAGAT TTCACAAATT CCTCACGTGA AAAACTATTC ATGATACTGG 1020 ACTGCCTGAG CCCTGCGCCC AGCCATAGCC TCGGTCCTGA TCCCTGGGAG AGACTGAGTC 1080 TCAAACGGGC CACAGAGTAA GCGCCATCTC GGACACCGGC CACGCCCCGA CCCCAGGCAC 1140 AGAGGTCGCA GACAGCTCGG GACAGTCCTG AAAAGCGTCC CCTTAGGCTG TCCCTCCGCA 1200 GCTGAATCGC GTCGTGACCT CGGGCAGCCG TGAAGGCCCT GACTGCCCCC TTCCGGGCAC 1260 ACGAGCTCAC TCACAGACCC CGGCCCCATT TAGCTCGGAG GAATACCTCG CAGGTCTCGC 1320
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