| Tag | Content |
|---|
EnhancerAtlas ID | HS187-05270 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr12:6532460-6533560 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:6532875-6532894 | CTGCCACAAGAGGGCACCC | + | 6.84 |
| | | 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 |
| GH12I006423 | chr12 | 6532321 | 6533489 |
| Enhancer Sequence | TCTCATCCCT CACCCACCTC CCACCCTCCC ACCTTTCCAA ATCTCCAATG TCTACTATTG 60
CACTCTCTGT GTCCATGTGC ACACATTATT TAGCTCCCAC TTATAAATGA GAACATGCAG 120
TATTTGACTC TGTCTCTGAA TTATTTCACT TAAGGTAATG GCCTCTAAGG GTTCCATCCA 180
CATTGCTGCA AAAGATGTAA TTTCATTCTT TTTAATGGCT GAGTAGTATT CCATGGTATA 240
AATATGCCAC ATTTTCTTTA TACAATCATC CATTGGTGGG CCCCTAGGTT GATTCCATAT 300
CCCTGCTCTT GTAAACAGTG CTGCGATAAA CGTATCTTCA AAATAACAGC CTTGAAGCCC 360
TAATTGGGCT CCTGAGAGGG CCACGTGAGA CAGTGTGAAG AGCGAAATCA CTATTCTGCC 420
ACAAGAGGGC ACCCAAAGCC CAGACAGATG GGACGACGCG CTTCCTGCCT CCATTGGAAT 480
CAAGCGCATG ACTGGATAGC AGAGGCTCCT TGGGCAGGGA GCCACAGCTT GAAGGTCCCA 540
GTTATGCAAC TGGCCCCAAG GCCCTTCTAC CCCTTCCCCA GGGGACTTCA CCAGCTCCTT 600
TTAGGACAGA GTTTGTGTAT GGTTCTTGCT GGCTTCAGTC CCTCCCGTAG AGGTGACCCT 660
GAGTAGCTGG GATTACAGGT GCCAGCATAT GCACCTGTAA TCCCTCCTCC CTGGGGAAAA 720
TCTCTGCCCT GGATGGGTAA GATCCTGACC CTGCGTGAAC GTGGCATGCG CTTCTGTTCT 780
CCACTCCCTG GAGTTCCTCC TGAGGCCGTG CAGGATCCTG TCCAGTGCTC ACAGGCATGA 840
GCATGACTTC AGGGTTGTGA GCAGAGCCCT GCAGAGGTAT GCATATGGCT ATGGAGTGGT 900
GACCTACTCG GACAGAAAGA ATAAGGAAAG GATCCAGTAG CCAGGCCAAA AGGAAGAGGC 960
ACCAAGAAGG GCTGCAGCTT GAGGGTGGAG ATTCCAGACT TCCAGATACT CTAGTGGGGG 1020
TACGATTTGG ACCCAGGAGG CAGGTTGCAA ATCTAAACCC ATCAGAAGCA TATGGACTCT 1080
TCTTTTGATT AGTTGTCAAT 1100
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