| Tag | Content |
|---|
EnhancerAtlas ID | HS030-01056 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr1:58597340-58598440 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:58597441-58597456 | GGGGGTCAGGGGTCA | + | 7.06 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCTAACAGA GAGGACCCTC AGCTGCAGGT CTGTTGGAGT ACCCTGCCGT GTGAGGTGTC 60
AGTGTGCCCC TGCTGGGGGG TGCCTCCCAG TTAGGCTGCT CGGGGGTCAG GGGTCAGGGA 120
CCCACTTGAG GAGGCAGTCT GCCCGTTCTC AGATCTCCAG CTGCTTGCTG GGAGAACCAC 180
TGCTCTCTTC AAAGCTGTCA GACAGGGACA TTTAAGTCTG CAGAGGTTAC TGCTGTCTTT 240
TTGTTTGTTT GTGCCCTGCC CCCAGAGGTG GTGCCTACAG AGGCAGGCAG GCCTCCTTGA 300
GCTGTGGTGG GCTCCACCCA GTTCGAGCTT CCTGGCTGCT TTCTTTACCT AATCAAGCCT 360
GGGCAATGGC GGGCGCCCCT CCCCCAGCCT CAATGCCGCC TTGCAGTTTG ATCTCAGACT 420
GCTGGGCTAG CAATCAGCGA GACTCCGTGG GCGTAGGACC CTCCAAGCCA GGTGCAGGAG 480
ATAATCTCGT GGTGCGCCGT TTTTTAAGCC CGTCGGAAAA GCGCAGTATT CGGGTGGGAG 540
TGACCCGATT TTCCAGGTGC GGTCCGTCAG CGATTTCTTT GACTCAGAAA GGGAACTCCC 600
TGACCCCTTG CGCTTCCCAA GTGAGGCAAT GCCTCACCCT GCTTCAGCTC GCGCACGGTG 660
CACGCACCCA CTGACCTGCG CCCACTGTCT GGCACTCCCT AGTGAGATGA ACCCGGTACC 720
TCAGATGGAA ATGCAGAAAT CACCCGTCTT CTGCGTCGCT CACGCTGGGA GCTGTAGACT 780
GGAGCTGTTC CTATTCGGCC ATCTTGGCTC CTCCCCCCGG GGCCAATCTT TTTCAAAACA 840
TCAGTCTTAA AAGTAGGTTG TCTTGCTCAT ACAGCCAGGG ATCTCTGAGG ATCCGCCTGC 900
AGTCTGCGTG AGATGAAACA TCTCGATCTA TCAACTGCCA CCCCTGAAGG AGCTGAAGGA 960
GCATCTCACT TCTTGTTTTC TCCCTAGCAG GGCCTATTTG ACAGGGTAAC ACAAACAGGA 1020
TTCTGTGCTC CTCTGAGAAT CCCCCTTCTA CATATGGGAG AGCCAGCCTC GCCAGGATGC 1080
TGTCTGGATG AGGCTCAGAC 1100
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