| Tag | Content |
|---|
EnhancerAtlas ID | HS187-18451 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr4:38732120-38733290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr4:38732923-38732942 | GTGCGCCCCCTGCTGGAGA | - | 6.72 |
| | | 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 |
| GH04I038730 | chr4 | 38732118 | 38733221 |
| Enhancer Sequence | GGTACACGCC ACCGTGCTTG GCTAATTTTT GTATTTTTTG TAGTGACAGG GTTTTGCCAT 60
GTAGCCCAGG CTGGTGTGGA ACTCCTGGGC TCAAGCAGTC CACCCACTTT GACTTCCCAA 120
AATGCTGGGA TTACAGGCCT GAGCCCCTAA CTCAGTCTTT ATTGCACAGC ATTAAAAGGG 180
TGGAAGGAGC GCTTCACAGA GCCATTCTCC TCCTCCCACC ACCATGAGAG GTACAAATTC 240
TACCAAACCT CGTCTCCTGT CTGCCTCTGG TGCAGGTTGA GGTTTGGCCT TCAGGGATTG 300
CTCCTCTGAG CTAATTTCTT GCAAAGGATG TGACAAAGGT CACTAGAGAG AAAACACCTC 360
AGCACGTGTT CCATAGGCCA ATGCGGTGAG TTCAGCACAG CCCCATCAGC ACGCAGACCA 420
TGTGAGAGGA CTCATGCATG GGAGGCCACC CACGAACAGG GCTATTTTAA TAGAATGTCT 480
TCGGGTGTGG TGAGAAAAAC CCCGGCTTGG AGTGTTTGTG GTTCATCTGG AATCAGGCAG 540
CGCTGTTATA AGCTTGGGGC CTATACAGGC TTCCTGGGTT TCTGCTTATT GATACACATT 600
GTAGGTCCTC CAAGAACGGT CCTGAATCAT TCCCTTGGTT ATGTCCATGT ACCGGATCAT 660
TCCTTTGATT AGTACACTGT AAATACTTCA AGAATGCTAG AGAAAGTTTT GAGATCAGAG 720
CCTTTCCCAC AAAAGGTCAG GAGTTCCAGT TCTCAATAAG CCGAGGTATC TGTGGTTAGA 780
GGAGTCCAGA AAATGCGGGC TGTGTGCGCC CCCTGCTGGA GAGGGAGGCC CAGGCACGCG 840
GAGCTTCTAG TTCAGGGCCG GGGTCCTCTT GAGGGTTCTC GGAGCACCTT CTCGCGGCTC 900
AGAGGGTTCT TCTTCCTGTC CTTCCAGGGC GGCCTTGCGT GAGAGCAGGA CTGCTAAGGG 960
TAATGTGGCA ATCTAGAGCC AGATTGCCGG GGTTCGAATC CTGCTTCTGC AACTGCTCTG 1020
TAACTTTTGG CAGGTCATTA AACCTCTCTG TGCCTCACCT TCCTCATCTG TAAAGTTGGG 1080
ATGATCATAT TAGAGCCTAC CTCAGAGAGT ACTTATGAGA CATAAACGAG ATAACATCTC 1140
AAACACTGAG GCACAAACAA AGCAAATGTC 1170
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