| Tag | Content |
|---|
EnhancerAtlas ID | HS062-08067 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr19:10546300-10547760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr19:10546701-10546715 | AGTCCCTTGGGGCT | - | 6 | | ZNF263 | MA0528.1 | chr19:10546584-10546605 | CCCTCCCCTCTGTCCTCCCTC | - | 6.87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 10546595 | 10546955 | | chr19 | 10546647 | 10546739 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I010436 | chr19 | 10547181 | 10547350 |
|
Enhancer Sequence | CTAAGAGGGA GTCTTGGGCG GGTCACTTCA CCTCCAATGG AGCGTCTGGG CATGTGGCTG 60
TGATGTAAGG CTGGCAGCTA CCCCTGTGTC TGGGTTGCAA CCTTGGGTCC CATGGGGATG 120
TTGCTGGAGT GGCCTCTGGC CTAACTTTGG GCCACCCTGA GCAGTCAGTG GCAAGCCAGG 180
GAGGGGTGAC TCTCCATGGC TCAGGGATCT GATTCTGGGG CATCACTGGC CCTGACTCTC 240
CCCTATCCCC ACCAGCTCCC AGGCAGCAGT TCTATAGCCC TGTCCCCTCC CCTCTGTCCT 300
CCCTCAGCCC AGGGGACATC GGGTCTTGAA ACAGAAACAG CAGGGCCCCA GGGAGTGTCC 360
TCTTCCCATC CAGGCCTCTG GGCTCCTGCT GACGTGAGCT GAGTCCCTTG GGGCTGGTGG 420
ATGTGCCAGG ATGTGCTAGC TGGGCACCTG CTTGGGAACA GAGTCTCACC ATCCTAAACT 480
GCAGCTTAAA TCCTAGGCCG GGGAGTTGGA GGTGTGTAGC TATGTTCCTC TCGCCTTCTC 540
TGGAGCTGAA AAAAAATCCA CCTTAGGAGA CAGGACACAG TTCTCAGACA ATGAAGCCAC 600
CAACCCCTTG TCTCCTTATG CCATGGGAAT GTTAACAGGA CTTATATGTT GCCAGGCGCA 660
GTAGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCCGAG GCAGGTGGAT CACCTGAGAT 720
CGGGAGTTCA AGACCAGCCT GACCAACATG GAGAAACCCC GTCTCTACTA AAAATACAAA 780
ATTAGCCGGG CATGGTGATA CATGCCTGTA ATCCCAGCTA CTCGGGAGGC TGAGGCAAGA 840
GAATCTCTTG AACCTGAGAG GCGGAGGTTG CAGTGAGCCG AGATGGCGCC ACTGCACTAC 900
AGCCTAGGCA ATAAGAGCGA AACTCCGTCT CAAAAAAACA ACAAAAACCA GGACCTATAT 960
GTTAACTTAT AGAGTGGGTT GGAGCCCTCT GTCGGTTAAT GTGTATAAAG CACTTTCATA 1020
ATGCCAGGCA CACAGCAAGC ATTCAATAAA TGTCTTGTTA TTATTACTGT ATGCCTGAAA 1080
GGATCTAACC TGGCACCCAG GACACAGCAG GTGCTCAACA AATGGACACT ATTGGCTGGG 1140
TGCAGTGGCT CACGCCTGTA ATCCCAGCAC ACTGGGAGGC TGAGGCGGGT GGATCACCTG 1200
AGGTCAGGAG TTCGAGACTG GCCTGGCCAA CATGGTGAAA CCCGTCTCTA CTAAAAATAC 1260
AAAAATTAGC CAGGTGTAGT GGCGCACACC TGTAGTCCCA GCTACTCGAG AGACTGAGTC 1320
AGGAGAATTG CTTGAGCCCG GCAGCAGAGG TTGCAGTGAG CTGAGATCAC ATCACTACAC 1380
TCCAGCCTGG GTGACAGAGT GAGACTCCAT CTCAAAAATA AATAAATAAA TAAATAAATG 1440
GACATTATCA TCAAAGGTCC 1460
|
