| Tag | Content |
|---|
EnhancerAtlas ID | HS182-06813 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr14:95036270-95037700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr14:95036427-95036438 | TGCCTCAGGCA | + | 6.02 |
| | | 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 |
| GH14I094571 | chr14 | 95037400 | 95039633 |
| Enhancer Sequence | TAGACACTCA GTAAATGCGT CCTCTGCCTG GCCCTCCTGG GTTTGCCCCA GACTCCCCTG 60
GCAGACCTGG TCCCAGACAC AAGGTATGAG AGCTCCAAGT CCCGTTCCAG TAGGTTATCC 120
AGGTTTATGG AAAGGGGACT GGGTGTGGGC AGTCAGCTGC CTCAGGCAGG GCTGGTACCT 180
TGCTCCAGAG CAGGGGCTGA GAAAGCCACG GAAAGGCAGA CACCACCAGG GCGGCTTCCA 240
CGGGGACCTG GTCAGAAGAG CCCAGTGAGG CACTGTCCCC TCCTGTGGCT ACAGAGATGT 300
GACCCGTGTC TCTCCCAGGA CAATGGCTGC GGCCAAAGAG CACACTGCAG ACCCAGAGAC 360
TCTTGCTTTT ACATCCAGGC TCTGTGCTCT GGATCTTCAG GCAAATCCTC ACCCTCTTGG 420
GCCTCAGTTT CCCCACCTTT CTGGCCTAGG TGGTCCAGCT CAGACTGGTT GAGTATGTGG 480
GGTGGATCCT CCCAGAGTCT GTGAGAATAA ACCACCCCCT CCACAGGGCA AGGCAGGTGG 540
ATGAGATGTG GTTCTGTTTG CCCTGAGCCT CGGTGATTTC TGGCAAATGC AATTCTCTGG 600
GTAGGACCTT GTGGTTTTCT TGGTGGCCAG GACATCAGTG GCAGCTGGGC TCCAGCATTG 660
TCTCCAGCCC TTGACCATGG ACACGGAGTT CCCGGGACAG TTAGAGCTGG GAACGGTCCA 720
GCCAGGAAGG ACATCTCCTT TCCTTTTCCT CGACCTAGCT CACCCTGTGC TTTCAGGGCC 780
GGGGCAACAG TTCCCACACG CTTTCCTATC AGCTGCTCAT CCTCCTCCCA GGCAGGCCAT 840
TTCACTCCCA CTCGGTGGCG TCCAGGTTGC CAGCATGTTC AAAACCAGAA TTCCTGGGTT 900
CAAGTCCCAG CTGTGCTCCT TAGAAGTAGT GTGATCCTGG GGAAGTCATT TCACGTCTCT 960
GAGCCTCAGT ATATTCATCT ATAAAGTGGG ATGATGATAA CGCTACTGAC CTCATAGGGC 1020
TGTTGGGAGG ATTAAACAGT GACTGTATAT GTCAAGTCTC ACAACAGTGC TGTGCAAACA 1080
TTAGCTATAT TATTATTGCC CTCATTCCTG CAGCCCTGAC AGTCAGTGCT GCCACCACAG 1140
GCTCTGAGCT GGGGGTCTCT CTCCACCAAA TCCCACTGCC ATCTGGGGAC CCCAAACCTT 1200
TTTCACGTTG CCACTTTCGC TACTCAGGAA AATTGACACT GAGTCCCCGC AAGGAGAAGT 1260
TCCAAAAAGG CAGAAGATTT ATAGGCCTTT CTCACCACAC TGGCGCCTGA AGTTCCTAAC 1320
TGATCTTCCA GAAGTTTCTA AATAAGACTT CAGCTCTCAG CTCTCCTCTC TTGGTAGATC 1380
CAGTGGGGGC AGAATCTCCC CTCAGAGTCT GTCCTGGACT GAAAGATTAG 1430
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