| Tag | Content |
|---|
EnhancerAtlas ID | HS188-01446 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr10:11379320-11381030 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr10:11380927-11380948 | CCCCCATCCTCACCCTGCTCC | - | 6.96 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH10I011336 | chr10 | 11378691 | 11379570 | | GH10I011337 | chr10 | 11379661 | 11379810 |
| Enhancer Sequence | AGCAAATCTT ATTCATTCCT GGTAATGAGG GACAGAAAGA GCAGCTAATG AAAACCCACA 60
GATAATCCAG AATTATTCTT CCATTCTCTG CTTTCTCCCA CCACAAACCT CCTACTCATA 120
AACTTCTCAC AAAAAAAGAA GCTTCTAATG AAAGTGAGGG AGCAGAGAAA GAGCCAAGAA 180
GCAGGAAAAG GCAGCCAAAG CCAAGGGCCT GGAGAGGGCA TACCTGCTGG TGCCGTGCAG 240
CCGCGTGGGG AGCGCTTAAC ACTGGGAGAC CCATGGTCCA GGAGACCTGG GCGCAGGCGC 300
TGAAGAGCTG CCTGCGTGTG GGGCGCCCTT CACAGTCCTC CCTTGCCAGT CAGGCACACA 360
GCTAGAACAC ACCCCTTCCG TAAAGAGCAC ACAGCCGAGG GCGTCATGGG TAGGAGGGCG 420
CTGAGTTAGT CGGGGAAGGA GGAATAAGAC CAACGTCTTC CCCTGTTGGT GTGCAGCCCT 480
GATTCCAGAG TCCCCCATGT CTCCCTAACC AGGGGCTGCA TGCTGGGAGA CCAGCACAGA 540
GTAACAGGTC AAGGCAGCTG GAAGTCACCT GCCGGGCAGG AGCTGCTTTC TGAGGAATAC 600
TCCATGTCTT GTAACCTGTC TCTACTGGTC AGCAAAGCAC CCTGGCACCA GCTTCCACGT 660
GCCTGCATCA GGAGGGTGTT TTAATACAAA CTACACACAC ACACTGTTCT CCAACTGGTC 720
ACTTATAGCT GAAGCCGCAC ATAAAAATCC CCAGTTGTGA GACACTGGAG GATCCTTCTC 780
TCATGAAGCT GCTGGGCCAT GTATAGAAAG TTCTCAGGTG CATTCTCTGG GAAGCCAGAC 840
TGCCTCGATG TGAATGCCAA CCCTACCACT GATTACCCAG GGAACCTCTG TGCCTGAATT 900
TCCTCATTAG CACAAGGAGG GTAAAAATAA TACCTAATAT GTGGGGTTGT CATGAGGATC 960
AATTAAGCCA ATACACATAA AATGATGTGC TCAGGGTCCA CGGCGCTGTG AGCACTAGGC 1020
CGGGCCGCAG GTGAATCGCA GCAGCCACAC CTAAAGACAG GGCAGCTGAA CTGGCCTCTG 1080
CTGGCCTGGC CTCTCACCTT CTCCCAGCAG GTGTCCACTT AGCTCCCTGG GTTCCCTGGG 1140
GAACTGTAGG CAAGGTCTGA CCAGAAAGTA CAGCTCTTCC AGCAGAGCTC TCTGCACTGA 1200
CAAGTCCCAG AACAGGCCTT TCCCCTTCAG AGACACTGTC CACTCTAGCG GCATCTCCCC 1260
TCACAGGCTC ACACACCACA CAGCTCCAGG AAGCCACCAA CTCATCCCAC GCTAGGAAAA 1320
GGCAACGATT CCTCACTCAG ATCCACCCCT TCCTACCTGT ATTGTATTTA GGCATCTCTT 1380
CCCCAAAAGA AAAGCCTAGC TGTCCAGTTT GGACCCAAGG CAGGAATGAC AAGGTCACCT 1440
GTAGATCTGT CTGTAACAAG CCTGTAGGTT CCAGGCCCTT CCAAGGCAAA GCGGTGCTCA 1500
ACAGCAACCT GAATGGGTAT ATGACCACCT CAGGGAGAGC AGAGGCCGGA CTTCTGAAAC 1560
AAGGGCAGGC ACACGGATGC AGCCAGGCAG AGAGCACCCG ACCCCCACCC CCATCCTCAC 1620
CCTGCTCCCA ATTCACCACA GGCACTCTGC TTTTGTTGTC TTTATTGGTG ATCCATGCAG 1680
AAGTTTGGAA AAATGATTTT GCTACTAAAA 1710
|
| |
|
|
|
