| Tag | Content |
|---|
EnhancerAtlas ID | HS187-12739 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr2:3307140-3308230 | 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 | AGCACAAAGG AAGCCACCCC ACAGCTCTGC TGCTGCCTTA GGCTGCTGCG TGCCAGGGAC 60
CGACCACCAC CTGGAAGTCA CCGGCACTGC TGCCACCTCG ACCGCCACTC ACAGCAGCAG 120
TGGCAGCCCC CACTGTCCCC TCACGCTGCC ACGTCTGAAT CAGTCTCACC CAAATGCTCA 180
GGCCAGCAGA GTCGGGTCAC AGCGAAACTG GAAAATAGAT TTCTTATTTT CATATTGGGA 240
AATGCGACTA ATAACCTAGG AAATTTCCCC AAGCACAGGA AGACTACTCC AAAGATAAGG 300
AGCAGCCACA AACCCGCCAG ACGCCGGCAA CCTGACTTCT GAGTGTTTCC CGGCACCGTG 360
AACACAATAG ACGACACGTG ATACGGTGCG GCCTCTGCGC CCGGGAAGCT TCGCCCTCTG 420
CTGGCAGACG GCGGGATCCA TCGGGTGCTG GGAGGACCGG GAATCACAGC AGGCTGACCA 480
GCCATAACAG ACAGAGTATA ACCCCAAAGA GTCAATCGCT GTCAAAGGAA GACTGTTAAA 540
AATCTTATAC AGTCATATAA TTTGGGTTGA ATAATGAAGA TTCTCATAAA ACCCTATCAC 600
TCAAATCTCC GATTTACAGT ACTTGTTGCA TGGTTTGAAA AGATTTCCTG TTACAAAATC 660
CCCACTGTGT GATTTGCTGA CTCTGATGTA GGAAGACAGA CACGGTCACC AAGTTCACAC 720
AGAAAGGATC CATCTGAAGG GCTGGAAACG CCCAGGCACG CGGACAGGCA GCGGTGAAGC 780
CACAGAGATG ATCTTCCCAA GACCCCACGG AGCGCCACGC AAGGCTGCAG AGATCCAGGG 840
AACAGCGTGC TGTGCGCGGG GAGGTGGTCT GGCGAGATCG GAGTTGAGAT GGCCAGGGCT 900
GAGGAACAAA GTGTCCAGGG TTCCCAGCGT TTCTCAGAAT CACCCAGGCA ACCTCATCAG 960
AAGACATGGT TCTGCTCCAC ATCCAGCAAC CAAGACTATG TGATCCTGAC ACCTGCAGTT 1020
CAGCCCTCCA CTCCCGTCCT GTTCAACCCT CCACTCCCGT CCAATTCAGC CCTTCAGTCC 1080
CGTCCAATTC 1090
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