| Tag | Content |
|---|
EnhancerAtlas ID | HS145-16043 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr22:39941050-39942430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr22:39941963-39941984 | TTCAGCACCACGGACAGCAGC | + | 10.52 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 39941126 | 39941176 | | chr22 | 39941259 | 39942347 | | chr22 | 39941800 | 39942000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I039545 | chr22 | 39941881 | 39942070 |
|
Enhancer Sequence | AACCCTAGGA TATTCAGCCA AGTATTTTTC TCATATAGAA GGACAGATAA CTAAGTGAAT 60
CGGTATGGCA GGCTCTGTGC TAGCTGCTGG GGGTGCTGCA ATGAGTTATG GTATTTCCTG 120
CCTTCCAGAA GCTCCCTCTC CAGTGGGGGA CACTGGGGAG CTGGGCCTCG AAGGAGAAAG 180
GAGGGCACTC CAGGTTGGGG GGAGCAGCAT GTGCAGAGGC CTGGAGGCAT GAGTCAGTGA 240
GGGATAGGGA AAGTGTAACT GACCTCTGAG GAGCAGGTGT GTGCCAGCCA ACGAGGCCCC 300
TTTGTCTGAC CAGGGGAAGG GAAGGTTAGT GCTCCTCTCC CTCCCCAGAG GAAAACAAAA 360
TTTTAGAGAC TGTCAGAAAT GTGATGGAGC TGTCAGGAGA ACATGAAACA GCCACGTACC 420
CTGGGAAACG GAAGTCACAG CTCTGTTTGT TCTGTGACAG TGTGAAAACT CACAACCTTT 480
TCATCGAGAT GGGTAACGAA AACATGAGAA AACTGGAAGT GCTTTGGTTT GGCTCAGCTG 540
AGGACATTAC TCCAAGCCCG CCCAGGCTCT CCCCTCCGGC CTGGATTCGT TTCTGTGTCA 600
ACACTCGCCC AGCCTTGCAC AGCCGGGCAC ACGGGCGTCT CCCTCTGCAG TGGTTCCCCG 660
ACTTGTCGGC CATCTTCGCT GGTGGTGTTT TCCTTGGTCA CTGTGGTTAT TTGAAAGCGA 720
TGTCAAAGCA AACACTGCTC TCTCTCCCTG AAAACCCCTG GCAGGAGCTG CCTTTCTCAC 780
CGTCCCTGTC CTTCGTCTCC TCCTGTCCCT TCCTTCCTGC CGCAGCCTCT TCCCTCAATC 840
CTACTGAACT CCTTCCTGGG AGAGGTTAGG GCGGGAATCG CCACCTTCCA GGGCACGGAG 900
AGGCGAAGCG GAATTCAGCA CCACGGACAG CAGCCCGGCG CGCAGTTGGC GTGCGGTTGG 960
CTCAGGAAGT TATTCTGTAG GTTTTGTAGG TTTATGACCC GCTGTTGGGT AGCAAAAGGC 1020
CTTGAACGCT GACTCAGGAG GTCGGGGTGC AGGGAGCTGG ATCGGGGGTG CTGATGATGT 1080
CGGAGGAGCT CCTTGTGGAT CTGGAGATAA TTTTCCTATA AAATTCCCTC TCTCCTTTGT 1140
TTCCAAGACC CTTGACCACA CTTGCACCTT CCCCTACCAC CTCTCCCTCC ACAGTTAATA 1200
ATAACATACA TGTGTCTGTG TGTACTCGAC AGGGAATGCG AACGTATTTG CGTGAATCTG 1260
TACCTTGGTG TAATAGTGTA TTTAATACAA GTAGTATCTG GGTGTACGTG TGAGGATGTT 1320
TGTGGGATTT GTGGGTCTGT GTGAACGTGT CAGTCTCTGT GTCTGTGTGT GTGTGCACAT 1380
|
