| Tag | Content |
|---|
EnhancerAtlas ID | HS007-08235 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr19:33904590-33906290 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr19:33906118-33906136 | GAGGTCACATGGTCATTC | + | 6.27 | | RREB1 | MA0073.1 | chr19:33905488-33905508 | CCCCCACCCGCCCACCCCCG | + | 6.61 | | TBX20 | MA0689.1 | chr19:33905998-33906009 | CTTCACACCTC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 33904799 | 33904899 | | chr19 | 33906111 | 33906219 |
|
Enhancer Sequence | GGCACACCCC ACTCCACGAG CCCCATGAAC CCCAAGGGAA GGCCCTCGGC CCATGGTCTC 60
CCCTGCCGTG GCCCCACAAT GGTCCAAACT CTCAGTGTGA GTCTGTGAGG CTTACAGCCT 120
GGGGGTCAGT CATAGGCTGC AGAATCTCAG AGGCCAGTGT GGAGTGACAG AGAAGCTGGG 180
GGCCCAGCAG GGCGCAGCCA CCTGCCAGAG GAGCTCGCCA GCCTCCACTG ACTGCCATGG 240
CGAGTGGCTT CCCAGGCACA TCAGGACAGA TGGGACTCCT GGAGCCTGCG CCCTGTGGGA 300
AGCCGGGCTG GGGCAGAGGC CACACATTTC TGCAGAGCTG GAGGAAGTGA TTCCCTGTGA 360
CTCCGTGCCC AGAGGCCACC ACCCACCCTG CCAGGAGGGG CTGGATCTAC GGCCTGCGCT 420
CACCCGGGGA GAGGGCACAG GAGCTATGGG CAGAAGGGGC AAGGGACAGG CCTCCTGCAG 480
GTGGGGCAGG GCAGGGTGGT CTCCAGGGAT GTGGGAGAGG CAAGGCCTGG GGCACACATC 540
CTGCTTCTCC CTCCTTGGAA CGAGCTGCCT GCTGGCTGGG CCCACTCTAC AAGCTCCCAC 600
CCTGAGCGGG TAGGGCCACA GCCAAGTCTG GAGAGAAAGA CAAGCCCTGG CCCCAGGCTA 660
AGCCCAGAAC CTGCACCGGG GAGGCCTCTA GGATGGCGGA TGGTAGCACA GTCACTGCAT 720
GGATCTTTGA GCTCCAAGGG ACTGAGCCAT TCTGCCTTGG TCTTCCTCTA CTGAACCCAG 780
CTGGTGAGGG GTGTGGTCGT GGGGAGCTGC CCTCACCCCC TCCCTGAGGC CTCGGCAACA 840
GCTTTCCTGC CGGACCACAG CTGGTCCACC TGCCACCACG TGAGACAGGC CCAGGTGGCC 900
CCCACCCGCC CACCCCCGAC CAGGGCAGTC GTTGCGGCCG CCCAAGGGCA CGCCACATGG 960
CGGTCCTGCC CTGCACGTTC CAGGCCTGCC TTAGAGAACG TCCATACGAG GGAGTTTCAT 1020
CTTCTAGGCA CTGTCAACAC AAATTATGTA TAATTGTCAT GATTGGATAT TAAGCAGTTG 1080
TTATGCAGGA ACGGCTGTGG TAGATTCAAT GGGCTTTCAG ACTTGCCTTC CAAACCTCAC 1140
AGGATAATTG GGTATCTGCG AGTGAAATAT TTCCTGAAAA GAAAGGATTT CAGGAGCTGC 1200
CAGGGAAGCA AGAAAGCCAC ATGCTCCTCT CCTCAGCCGC CCCCGTATTC GTGGTGCAAG 1260
CGCTCAGGAG GCCGCTTCCA CCTCGCTCCT GGGAGTCTCA GCGCTGAGTT TCGCCACAGT 1320
CCAGGCACGT TCCTACCAAG GCAGGCAAGG GCAGTGCCCC ACATGGCAAG CCCTGTGCGC 1380
CAGGCCAGAC AGGCAGCCTC AGAAGCCACT TCACACCTCT GTGGCGCCCT CCCAGAAAGC 1440
CCGAGAAGAG GCCTGACCCA CGCCGTGGAA CAGGGGTGCT CCCTTGGCTT TGTGAGATGT 1500
GGTCCTGCAC CAACAGAAGC GAACCTCAGA GGTCACATGG TCATTCTCGA CGTGATGGCG 1560
ACAGCGGACC TCTGTGGGAC AAGTGACCTG CAGACAACCA CGGGCTGCGC TGGGACTGGC 1620
CGGCTTCAGA AAAGACAGGC AGAGGGACAG AGATGCCATC CGCATGTGCA GAGGAACTCA 1680
CATATTCTAC AAGAAAGGAG 1700
|
