| Tag | Content |
|---|
EnhancerAtlas ID | HS062-08678 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr2:3307040-3308220 | 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: 2 | Chromosome | Start | End |
| chr2 | 3307800 | 3307937 | | chr2 | 3308045 | 3308198 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I003302 | chr2 | 3306745 | 3308010 |
| Enhancer Sequence | CAGCCATGCC GAGGGCCAGG CTAAGGGGAG CCTCTGGGGG CCAAGCTCGG AGCCTCACCA 60
GGGCCATGGC CCAGCAGGGG AGTCTCTGCG GCCCCCATCC AGCACAAAGG AAGCCACCCC 120
ACAGCTCTGC TGCTGCCTTA GGCTGCTGCG TGCCAGGGAC CGACCACCAC CTGGAAGTCA 180
CCGGCACTGC TGCCACCTCG ACCGCCACTC ACAGCAGCAG TGGCAGCCCC CACTGTCCCC 240
TCACGCTGCC ACGTCTGAAT CAGTCTCACC CAAATGCTCA GGCCAGCAGA GTCGGGTCAC 300
AGCGAAACTG GAAAATAGAT TTCTTATTTT CATATTGGGA AATGCGACTA ATAACCTAGG 360
AAATTTCCCC AAGCACAGGA AGACTACTCC AAAGATAAGG AGCAGCCACA AACCCGCCAG 420
ACGCCGGCAA CCTGACTTCT GAGTGTTTCC CGGCACCGTG AACACAATAG ACGACACGTG 480
ATACGGTGCG GCCTCTGCGC CCGGGAAGCT TCGCCCTCTG CTGGCAGACG GCGGGATCCA 540
TCGGGTGCTG GGAGGACCGG GAATCACAGC AGGCTGACCA GCCATAACAG ACAGAGTATA 600
ACCCCAAAGA GTCAATCGCT GTCAAAGGAA GACTGTTAAA AATCTTATAC AGTCATATAA 660
TTTGGGTTGA ATAATGAAGA TTCTCATAAA ACCCTATCAC TCAAATCTCC GATTTACAGT 720
ACTTGTTGCA TGGTTTGAAA AGATTTCCTG TTACAAAATC CCCACTGTGT GATTTGCTGA 780
CTCTGATGTA GGAAGACAGA CACGGTCACC AAGTTCACAC AGAAAGGATC CATCTGAAGG 840
GCTGGAAACG CCCAGGCACG CGGACAGGCA GCGGTGAAGC CACAGAGATG ATCTTCCCAA 900
GACCCCACGG AGCGCCACGC AAGGCTGCAG AGATCCAGGG AACAGCGTGC TGTGCGCGGG 960
GAGGTGGTCT GGCGAGATCG GAGTTGAGAT GGCCAGGGCT GAGGAACAAA GTGTCCAGGG 1020
TTCCCAGCGT TTCTCAGAAT CACCCAGGCA ACCTCATCAG AAGACATGGT TCTGCTCCAC 1080
ATCCAGCAAC CAAGACTATG TGATCCTGAC ACCTGCAGTT CAGCCCTCCA CTCCCGTCCT 1140
GTTCAACCCT CCACTCCCGT CCAATTCAGC CCTTCAGTCC 1180
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