| Tag | Content |
|---|
EnhancerAtlas ID | HS034-14288 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:2119880-2120860 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr19:2120638-2120653 | CGAGGGCAGAGGGCA | + | 6.6 | | TFAP2C | MA0524.2 | chr19:2120634-2120646 | TGCCCGAGGGCA | - | 6.27 | | TFAP2C | MA0524.2 | chr19:2120634-2120646 | TGCCCGAGGGCA | + | 6.52 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGTGAGCCG AGATCACGCC ACTGCACTCC AGCCTGGGCA AAGCTTGGGA GATAGCCAGA 60
CTCTGTCTCG GGGCGAGGGG AAAAAAAGAA AATGACAGAA GTGCTCATCT CCAGGATGCA 120
GGCTGGCTGG GGACCCTTTC GGGATCCCAG AAGTCAGGCG CCTTCCTGAG CCGGGGCAGG 180
CCCAGGGTGG GGAGTGCTCG GTGTGGCCGT GATGAGCAGC AGGTAGCGGC CAGTGGTGGT 240
GATGGGGCCG GGCCCGAGGC AGTGAGGCAT AGCAGCAAAT CTCATAAATT TCCAAGAGAG 300
CCTGGAAATC CAGACTGCTG TGAGAACCGT GAGTCTCAGC AACACATTCC CACCTCCAGG 360
CAGGCCCGGT GACCCGAGCC TGCCCAGCAG TGGCTGTGAT CTGTCCTCTT GGCCAGGGAG 420
AACCTGACAT TCCTGGAGAC GGCAGGGGCA GTGTCGATAA GACCCATCCC TGCGGCCCAC 480
CTGGAACCTG GCACTGAGAC CCCTGTGCCT CCAGAGGGGC CTGGCGCAGG CAGGCTGGGG 540
CTGAGCAGGT GCCTCCCTGG GCCACCTAAC TGCCACACGG AGCTCCCACC TCACCTACAG 600
CAAACAGGGC TCAGAAGGGC TGCCACGCGC CCAGCTGGAA CTGAGCCTTG CAGATGCCCA 660
GGGCCAGCCC CCCGTCTGCA GCCCACCCCA TGGATCCTCC CACCTCCCAG TCCTAGTGCC 720
CACGGGATCT ACAATCTCCT GGGAACGCCA CAGATGCCCG AGGGCAGAGG GCAGACAGGG 780
CAGCACAGAC TCGCCTCTGT AAAGGGGGAA TGGGCCCGAC CATTGTCAGG GGACAGGTGC 840
TGGAAACCCA CGGACCTGCA AGACGGCCGG GGTGGCAGGG CGATGGGAGA CGGTAGGAAG 900
GATCTGCCAG GCACATCCCT GGTCCCTACC CCTCAGAAGC TTGGAGAAGC TGCCAGCCCA 960
GAGGCCCAGC GCCCACTCAC 980
|
