Tag | Content |
---|
EnhancerAtlas ID | HS052-21843 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr2:183969730-183970900 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr2:183970553-183970564 | TCCTGTTTACT | + | 6.32 | Nfe2l2 | MA0150.2 | chr2:183970267-183970282 | TGCTGTGTCATTCCT | - | 6.03 | ZNF263 | MA0528.1 | chr2:183970562-183970583 | CTCTCCCCTCTCCTCTCCTCA | - | 6.1 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AACTCACTCA CTATTATGAG AACAGTATGG GGGAAAACCG CCCCTGTGAT TCAATTACCT 60 CCCACTGGGT CCCTCATGCG ACACATGGGG ATTATGGGAT TACAATTCAA GATGAGATTT 120 GGTTGGGGAC ACAAAGTCAA ACCATATCAT CACCTTCCTA CTATTACCTC TCCTTTGCTC 180 ATGCAGAAGT AGTCGCTCCT CATGACCACC ACTGCTCCAG GCCCACAGTG AGTACTGCCT 240 GGCTACTACC AGGCAGTTCA CTCAAAGCCC AGGGGCTCTT CAGTCAGCTT GTGGTGAATG 300 CTGCCAGGCC TGACTCTCTC CCTTTAGGGC AGTGGGCTCT CCTATTGCCC AGGGTGGGCC 360 CAGAAATGCT ATCCAGGAGC CAAGGCCTGG AATCAGGAAT GTTAGGAGTT CACTTTGCGC 420 TCTACCCAAC TGTGGCCATG CTGGTACCCA AGCTGCAAGA CACAGTCCCC TTTATGCTTT 480 CCTCTTCTTT CCTTAAGCAG AAGGAGTCTC TCTCCATGGC CACCACAGCT GGGAATGTGC 540 TGTGTCATTC CTGAAGCCAG CATGGCCCTG GGTTTCCACC CAAGTCCCAT GGTGATTACT 600 GCCTTGGTAC CACTGATGTT TATTCAAGGC CCAAGGGCTT GTTAGTCAGC AGGTGATAAA 660 TCCTTCCACG ACTGGGTTCT TCCTTTCAAG GAAGTTGGTT TCCTTCTGAC CCAGAGTGTG 720 TCTGGAAATG TCTAGGAGCT AGGTCCTGAA ATGGGAGCAT CAGGACTCTG CTTGGTGCCC 780 TATTTTACTG TGGCTGAGCT GGCATCTAAG TTGCAAGACA ATGTCCTGTT TACTCTCCCC 840 TCTCCTCTCC TCAAGTAGAA GGAAGGAATC TCTTGAAGCT ATGAGCTGCA CTGCTTAGGG 900 TTAAAGGATA GGTGATGCAA GTATTCTCTT GACAGCCCCA GCTGGTGTCT CACTATGTAG 960 CACCACCCTA ATTCTACTGG TTTCGAGCCC AGGACAGCAC CAGGACTTGC CCTGGAATCA 1020 TAGTCCTTAC GCCCTGGATG GTCTTCCAAG TTTATTTAGG ACCCCATAGC ACTTTAGCCC 1080 ATGGTGGTGG GGCTAGCTGA AACTCAGGTT CTGACCAGTG GGTTGGACAC TTCCCATCTG 1140 GCTAGACCAG CCCTAGCCAG ATGGGAAGTG 1170
|
| |
|
|
|