| Tag | Content |
|---|
EnhancerAtlas ID | HS121-25306 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr22:22039200-22040770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr22:22039379-22039391 | TGCCCTGAGGCA | - | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 22040375 | 22040435 | | chr22 | 22040683 | 22040746 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I021686 | chr22 | 22040599 | 22041653 |
| Enhancer Sequence | CTGTGAGTGG CGGAGGGCAC TCGGCCAAGC CCAAGCCCCG TCTTCCTGCC CATCTCATGG 60
CCTCTTGGAG TGGTCCTGGG AAAGGGGCTC ATGGGGGCCT GGGATACACG GCAGGGAGGC 120
AGCCAGGATC CCCCAGAGCT GTGGTGCCCC TGATGGCTCT GAGTGCACAG CCCTGGGGCT 180
GCCCTGAGGC AGATAGAATC TGAGAAGGCA GAAGGGGAGG GGCTGATGTC CACACTGGTC 240
GTTGAAGAAC CAAGGGGTGT GTGGGGGCAT GTAGGGGAGA TCCCTGCCAC AGAAGGTCTG 300
CCTTGTGCTG TGGTCCCAGC CTGAGCTCAG TAGCCAGGGC AGGCACGTTG AGCGGGCACA 360
TGTGGTTCTG TGGTGGCTGG GAGGGCAGGG CCCGATGTGC ACTGGGGCCC AAAGCCATGC 420
CAGGGAGAGT TGGGGCGTTT CATGGTCTGC TGCGGTGCTG ACGTGGATGG CATGCCTGGG 480
ACTGCACGGT GCCACCTGTC TGGGGCTGTC GTGTTTGCTT CTTCCTCCTG TCAGGCAGAG 540
CATGGGGATC TGGAGCTAGG GGGAGGGCAG AGACATGGGC AGGTAGCTCT GAAGTTCTCC 600
TTCTTAAAGA ATTATTCAAA TTCTGGAAAA TTTGAAAAAG AAAGCTTGTT GTCCAGTGTG 660
TCACTCCGTC TAACACACTG CCCTTAGCAC TTTGATATAT TACTTTTTTT TTTCTTTTGG 720
AAACAGGATC TTGCTATGTT GTCTAAGCTG GTCTTGAATT CCTGGCTTCA AGTGAGAGCC 780
TCCTGCCTTG GCCTCCGAAA GTGCTGGAAT TACAGGTGTG AGCCACTGTG CCTGGCTTGT 840
ATTTTCTTCT GATGGGAGAA ACCCCTTTTT CTTCCTCTAT GATAAAAAAT AACATTTATT 900
GGGGCTTTTC CCCGACCCCT GATTAAATAT GTAATGTGTT TAGTGTAGAA AGTTTGAAAC 960
TTTTAAAAAG AAATGAGGCC AGGCGTGGTG GCTCACACCT GTAATCCCAG CATTTTGGGA 1020
GGCTGAGGCA GGAGGATTGC TTGAGGCCAG GAGATCAAGA CTAGGTTAGA CAACATAGTG 1080
AGACCTTATC TCTACAAAAA ATCAGCCAGG CGTGGTGGCA TGCGCCTGTC GTCCCAGCTA 1140
CTCAGGAGGC TGAGGTCGGA GGGTCACTTG AGCCCAGGAG TTGGAGGCTG CAGTGCACCA 1200
GGATCACACA CCACTGCACT CCAGCCTGGG TACAGAGCAA GACCTTGTCT CATAAAAAAA 1260
TTAAAATAAA AATAAATGAG AAGTCAGCCA TACACTCCTA ACCCTGAGGT GGCCAGTCCT 1320
GTGTGGTATT TTATCTCCAG GGTTTCACCT GATATCATAA GAGTCGGGAT CCAGTGGAGG 1380
CCAGGGGACC CTGGCTTGGC CTAGCCTTGG CTTCTTCCTC CTGCTGGTTG GGGAGGCCCT 1440
CCTGGAGGAG AGGCACCAAG CAGGGCCTGG GGGGCAGGGG TGGCGTGTGG TTGGCTTCTA 1500
GGCAAGCGAC ACGTCCCCAC CCAACTGCCT CCCATGGCAC TGCTGAGGTG CCACCCTGGT 1560
TTCCTTGGCA 1570
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