| Tag | Content |
|---|
EnhancerAtlas ID | HS145-04526 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr11:70005450-70006470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr11:70005831-70005842 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr11:70005831-70005842 | CTGAGTCACCC | - | 6.02 | | Stat4 | MA0518.1 | chr11:70006294-70006308 | CGATTTCCTGGAAC | - | 6.13 |
|
| | 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 |
| GH11I070154 | chr11 | 70001071 | 70007166 |
|
Enhancer Sequence | GCCACCTCCT CTGCAGGGAG GCTCAGGAAT GAGCACACAC TGCCATCTCA GCAAGGCGGG 60
ATGGTAGAGG AAAGACAGAG GATATTGGAT AGGGAAGTAG CCGGCTCTTT TCCCAGCCTT 120
GACGTACTGG TAAACCCCTG TCACAAGGGC TTCATAGGGT TGAAGAGGAC ACAGCTTTGT 180
CTTCAACTTG GGAGTTTCAT TCAGCGAACA AACGTTGGTT GAGCACCTAG GATGTGCCCC 240
ACACGCCCCT GGTCCTGGGG ATGCGGGGGA GATGGACCAG GGAGACTGGA AGGGAGCCTG 300
CTGCAGGGCG TGCCTGTTGT GGGCCCGACT GCCCCATGGC AGGGCAGGGG ACGCGCCCGC 360
TGGGGTGGAG GGCCTCCCTC GCTGAGTCAC CCACAGGCCT GGCGCTCCAG CTGCACCTCC 420
GCATGCTGGC ACGGGGACAG ACATCCTGGA GGCCTCTTGG CAGGACCGAG GGGTTTTCCA 480
AGGAAAGCCC TTGTTCCCCG GAGCTGGCCA GGGAGTGGTC CCCACGCCTC GCAGCAGGGC 540
TTCTCCTTAG TCAGGGTGTG GTGAGGGCTG CAGGCATTTT CCTGGGCAGG GTGCAGTCAC 600
CATGTGTCAC TGGCAGATGC CTGCAGAAGC CGGTGGTAAC GGCCCAGAAC ATGAAATAAG 660
AGCTTTTCTA GGTTTCTGAA AGCTGCAGAC ACCCTCTGGG GCAAACAGAC CCATCCCAGG 720
CTGCAACTGG GAGACACACA GGGCAGCCCC AGGCCTCCTG GGCCTGCCTG TCCTGGGAGC 780
CACCTGTGAC TGTGCCAGCA GGGACCGGAC CTGCCCTCTG CACCCTTGCA TGGGAGCAAA 840
TATGCGATTT CCTGGAACAC GGGGACACAG GGTGACAAGA CAGCCTGTGT CCTGCGGGTG 900
GTTTCACGCC TGGGTGAGGA GCCTGGCTTT GCTGTGTGCT TCTCCTGCCC AGCCCTCGGT 960
CCATCCATCC TCAATGAGGG CTCAGAATGG GGCATCCACA CCCCTGGGCA GGGCGGGGCA 1020
|
