| Tag | Content |
|---|
EnhancerAtlas ID | HS082-00024 | Organism | Homo sapiens | Tissue/cell | HCASMC | Coordinate | chr1:1489850-1491020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:1490566-1490581 | GGAGGTCAGAGGTCT | + | 6.26 |
| | | 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 |
| GH01I001554 | chr1 | 1489709 | 1491347 |
| Enhancer Sequence | CAAGGTGCCA GGACATACCA GGAAACGCCC CAAACACAGC TCGGTTTTCC TTACCAAGGT 60
TTTCTCTTTT CACTCCCTAG GGGCCTTAGT GGGACCAGAA CATCCCGGGG AGTTAGAATG 120
AGCGCAGCTG CCCATCCCAC AGGAGAACCG AGAGGCCAGG ACCACACTAC CCTGCTATGA 180
GTCACCAGGG ACTTGAAAGG GAACCCACAG GCACTGCCAC GCCAGTGTGG CTGGCACCAG 240
GGACCGCACT CTCCCACCAC GGCCTGGGAA AAAGCCATGT CAGGTGCAGC ACGCTGGCCA 300
CAGGCACTGG AGCCACGAAA GCAACAGCCC TGGGCAGCCC AGCACCATCC TGGGTTCCCT 360
GCTGCCGGCG CCAGCCCCAC GTACCCCCGA CCACCTCAGC TCCTGGCCCT CAGCCTCTCC 420
TTTGCAAACC GTGGCTGGCA GCAGAGACTT CCTTGACGTC AAGTCTCCTG AAGGTGTTGA 480
TGCTCCGTGG AAGCCTTGGT CCTTCCCCGG AAGGCCACAC CATCTTCCCT GCACGTATGA 540
CTCATCCCAG AGCATGCTAA GTGCTGCTGC CCTGACAGAC ACACCCACGA GGGGGGCCAG 600
CTATCACCTT ATTGGCCAGA TTGTCCCGGT AACTGAGTGA CGGGACACAC AGGAACACTG 660
CAGAGCCTGA CAGCCATGCC CCTGCCACAC ACACAGAAGA CTCCCCACAT CAGAGGGGAG 720
GTCAGAGGTC TCAAAGGTCA GGTTAGAGCT GGGTCAATCC GTTTCCATGG CAAAACTCAA 780
AGCACCGACA CAGGAGGCTC CGGTATCTGT GCTCCTGGTG CATGGCGGGG ATGAGACAGC 840
CTCGGCGGCG CTGGTGGAGC TCCTGGGAGC CTCGCTCCAG CGAGGACAGA GCTGCAGCTC 900
AGCACAGTGA CTGCCCAGGG CTCTGACCCA GATGCCAACA GCCTGGGCAG TGGCACCTCG 960
GCCAAGAAAG GAGGAACCAG TGCTGCAGGG GCCAGGTGGC GGCTGTGGCA GGCATGTCTG 1020
GAGGGAGTGT CGTGCATGTG GGTGACAAGA ACAGCCGAGT GTGCCACAAG CGTGGACGGC 1080
AGCTCCGTAC TCAGAAGGGC ACGGTGAGAA GAGCAGGTGA CACCGACACG GCTGTGCACA 1140
GCACGATGCT CTGGGCTCCC GGGATGGACT 1170
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