| Tag | Content |
|---|
EnhancerAtlas ID | HS063-03465 |
Organism | Homo sapiens |
Tissue/cell | GM18505 |
Coordinate | chr19:55116900-55118380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr19:55117372-55117382 | ACCACTTGAG | + | 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 |
| GH19I054606 | chr19 | 55117466 | 55119858 |
|
Enhancer Sequence | CTCTGATGCT CATTTTTTGC CAGTATAATC CATATTCTTG TCTCAGAAAT TTAATTTCCT 60
CTTGTATTTT TTTCAGATAT TTAAACATGT TTAATTGAAA AAGGGTCTTA TGCGTTCCTA 120
GTATTCTATT TCTTTGCACA TAATAATCCT TATCAACAAA TGTGTAGACT GATGATCATA 180
GCACTTTTTA TCATTAGAAG GATGGCTCTT GGTTGTCTAT TTTTGTTGGA CACTCACCTC 240
CTACACTCCT GAGCTACCAT GGAGGGATCC TCTCAAGGCA GTTTTTAGTA ATCCAGGACT 300
GAAAATGGGG GACTGTTCCA GCTACTGATG ACACGTGGCA TTCATTTCCC AAACATAGTG 360
TCTGCTCAGG TTGCTCCCAG AAGGAAAAAA ATGCATGTGA AATTCACACT CATGGCCGGG 420
CACGGTGGCT TATGCTTGTA ATCTCAGCAC TTTGGGAGGT CGAAGTGGGC AGACCACTTG 480
AGGCCAGGAG TTCAAGACCA GCCTGGCCAA CATGACAAAA CCCCGTCTCT ACTAAAAATG 540
CAAAAAAATT AGCCAGGCCT GGTAGTGGGC ACCTGTAATC ACAGCTACTC AGAAGGCTGA 600
AGCAGGAGAA TCACTTGGTC ATGAGAATCA GGCAGGAGAA TCACTTGGGA GGTGGAGGTT 660
ACAGTGAGTG GAGATCATGC CACTGCACTC TAGCCTGGGC AACAAGAGCA AAACTCCATC 720
TCAAAAAAAA AAAAAAAACT CATACCCACA CATGATACAG ATACCCACAT GTAAGAACTC 780
TGCAGTGAAT GAATTTGTTT CACACACACC CAGGGGAGTT GGCTCAGTGG TGGCCATGGG 840
CCTGGGTCGG TAAATAGACA TATTCCATCA CAGCTTTCAG CCTTGCCCAG AGCCCTGGCC 900
CTTCTCTGCC TGTGAGGACC CAGGGCCCCT TTTCTGTTCT GCACAGAAAT GGAAACTTCC 960
TCCCTAATGA CCCCTAATGG CACCAGACAC AGATGCCCTC TCTGTTTCGT GTGTATCCTT 1020
CTCCTTCTGA TGAACTTTCA TTTCTCATTT TCTGGACATG ACTGTGATAA CCGGGGTGTT 1080
GATGAAATAT TATGAGAAGC ATCTCTCAAG GGCAGGAACA AAGGGGCTCT CCTTAGTGGA 1140
AACATCAATC TCAGGCCTTG ATGGTGGGCG CCAGCATCCC CTCATGCCCC CACCCCTCCT 1200
GTCTTCACCT GCTCTGGAAA TTACCCATGG CTGAGCCCCC TGCAGCCCCC AGGCTCCAAT 1260
GACCCAGCTC CCCTGTGATA AATGGGGTTC ATGACAGGCT CCAAATGAGG AAACCAAGGC 1320
TCAGAGATGG GAGGTTACTG CCCAAGTTCA CACAGGCAGG GGGTGACACA AGAATATTTA 1380
AATAAAGACA AGATTTCCCC TCAAAGCAGA GTGCTAACCC CACGTATTGT CCCAGAACCT 1440
TGAACTCAGG AGCACAGGAT GGGAACAGGA GTGTTTGAAA 1480
|
