| Tag | Content |
|---|
EnhancerAtlas ID | HS069-04546 | Organism | Homo sapiens | Tissue/cell | GM18951 | Coordinate | chr2:3306960-3308120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:3307548-3307567 | CTTCGCCCTCTGCTGGCAG | - | 6.27 |
| | | 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 |
| GH02I003302 | chr2 | 3306745 | 3308010 |
| Enhancer Sequence | CTCCGGCTGA TTAAGCAGAA AAGGAGATCA ACGTGAGGGG CTGGGTGGAA GGGGAGGGGT 60
GCCAGGCAGC TCACTCTCAC CAGCCATGCC GAGGGCCAGG CTAAGGGGAG CCTCTGGGGG 120
CCAAGCTCGG AGCCTCACCA GGGCCATGGC CCAGCAGGGG AGTCTCTGCG GCCCCCATCC 180
AGCACAAAGG AAGCCACCCC ACAGCTCTGC TGCTGCCTTA GGCTGCTGCG TGCCAGGGAC 240
CGACCACCAC CTGGAAGTCA CCGGCACTGC TGCCACCTCG ACCGCCACTC ACAGCAGCAG 300
TGGCAGCCCC CACTGTCCCC TCACGCTGCC ACGTCTGAAT CAGTCTCACC CAAATGCTCA 360
GGCCAGCAGA GTCGGGTCAC AGCGAAACTG GAAAATAGAT TTCTTATTTT CATATTGGGA 420
AATGCGACTA ATAACCTAGG AAATTTCCCC AAGCACAGGA AGACTACTCC AAAGATAAGG 480
AGCAGCCACA AACCCGCCAG ACGCCGGCAA CCTGACTTCT GAGTGTTTCC CGGCACCGTG 540
AACACAATAG ACGACACGTG ATACGGTGCG GCCTCTGCGC CCGGGAAGCT TCGCCCTCTG 600
CTGGCAGACG GCGGGATCCA TCGGGTGCTG GGAGGACCGG GAATCACAGC AGGCTGACCA 660
GCCATAACAG ACAGAGTATA ACCCCAAAGA GTCAATCGCT GTCAAAGGAA GACTGTTAAA 720
AATCTTATAC AGTCATATAA TTTGGGTTGA ATAATGAAGA TTCTCATAAA ACCCTATCAC 780
TCAAATCTCC GATTTACAGT ACTTGTTGCA TGGTTTGAAA AGATTTCCTG TTACAAAATC 840
CCCACTGTGT GATTTGCTGA CTCTGATGTA GGAAGACAGA CACGGTCACC AAGTTCACAC 900
AGAAAGGATC CATCTGAAGG GCTGGAAACG CCCAGGCACG CGGACAGGCA GCGGTGAAGC 960
CACAGAGATG ATCTTCCCAA GACCCCACGG AGCGCCACGC AAGGCTGCAG AGATCCAGGG 1020
AACAGCGTGC TGTGCGCGGG GAGGTGGTCT GGCGAGATCG GAGTTGAGAT GGCCAGGGCT 1080
GAGGAACAAA GTGTCCAGGG TTCCCAGCGT TTCTCAGAAT CACCCAGGCA ACCTCATCAG 1140
AAGACATGGT TCTGCTCCAC 1160
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