| Tag | Content |
|---|
EnhancerAtlas ID | HS034-14992 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:18860690-18861840 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr19:18860936-18860951 | ATTGAGGGCGTGGCC | - | 6.83 | | ZNF263 | MA0528.1 | chr19:18861517-18861538 | GGAGGAGGAAGAGGAGGAGGA | + | 11.79 | | ZNF263 | MA0528.1 | chr19:18861526-18861547 | AGAGGAGGAGGAGGAGGACTG | + | 6.03 | | ZNF263 | MA0528.1 | chr19:18861523-18861544 | GGAAGAGGAGGAGGAGGAGGA | + | 8.67 | | ZNF263 | MA0528.1 | chr19:18861520-18861541 | GGAGGAAGAGGAGGAGGAGGA | + | 9.83 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GACAGGGGAC TCGGGTGTCT CTGCTGGGGT GAGGCAAGTC CAGCAGGTAA CCCCTGTTCT 60
CCAGGAGGTC ACAAGCTTGT GGGCAGATGG CTCTTCAAAG GAAGACTCAG ACCATGCTGA 120
GGGATCGGGG GAGGGGATCG GAAACTTTCA GAGGTGGTGC TACTTAAGTT GGATTTTGAA 180
GAGTGCATAG GAGTTTTCTA GGCAGAGAAA ACAACCCTGC AGGCGCACGT TGGCTCCCAT 240
TCCTGGATTG AGGGCGTGGC CATGAAGTCT GGGTGCTGCA CAGATGCTGG TTTCAAATGT 300
AGCGGCAGCA AGCCCACGCA AAGGAGCATT TGTCAGCTCA TGACAGAGCA GGCCAGGGGT 360
CGACTTCTAG CCACAGGTTC AGCTCCTTCC ACTGCTTCCC ACTGGACTGT TTCCTGGCTC 420
TGCTGCTGAG AACTCTCCTC GCCTGCAGCC CCTGGGCCCG TCCTAGCTAT AGCGAGTGAG 480
AAAGAGGCCA TCTCTTCCCA ACTCTTGGCC AGAGTGTCGC CTCCAGCTGA GCCATGCACA 540
CCCCTGTGGC GGGGACAGAT CTGTACCCAG GTCCTTGGCT CCAATTTGAA GCCGGGCGTG 600
GAGGCGGCAC CCTGGGAACC TTCAAGGAGG GCATATGCTG TCTTAAAAAC TGGGGCGGTG 660
CCATCAGAGA AGGGAGCTTG GAGGCTTGAG GCCAGCCCCA GGGAACCTGG TGTGGCCCAA 720
GGCACTGAAG CCAGGGAGTT GCACGTGCTT AGGGCTCACA TACCTATGCT TGTATTGCTG 780
CCGTTCACCG AGTGGGTGGT TAACACGCAA GGGAGATTCT GCTGATAGGA GGAGGAAGAG 840
GAGGAGGAGG AGGACTGTTG GCCAGAACCT CACTCCGGGG TTCCGGCTCA GCGTGCAGCA 900
GAGACGGGAG GGAGAAGAGA ATGTCTCCAT AATGAAAATG AGGCTTCTGG AACACCCAGG 960
GGTGCTGAGG ATAGCACAGT GCCTGGGGCT TCCCTGCTAT TCCTAATGAG CAGGCTGTTC 1020
TGAGGCTGCT GCCTGTCCTA CTAGGTCCCC ACAGACAGCA CGTCCGAGGG GTGGGCAACA 1080
GGATGTCACC ATCCCCTGGA ACACTGTAAC CTGGGAAAGG AGCTGTGACA TGGGACCCCT 1140
GGTGGCCTTG 1150
|
