| Tag | Content |
|---|
EnhancerAtlas ID | HS145-17844 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr3:122612160-122613530 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU4F2 | MA0683.1 | chr3:122612729-122612745 | ATGCATAATTTATTGG | + | 6.16 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 122612250 | 122612390 | | chr3 | 122612781 | 122613386 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I122892 | chr3 | 122611755 | 122613417 |
| Enhancer Sequence | AGATAACCAG AAAGCACGTT ACTTTGTTCA GATATGAAGA CTTTAGCTCC CGATATGTGT 60
CCCCAGGTTA GTTCTTTAGC CAGCCCCGTA GGGTCTACTA GCAAATGAAT GCATTTCAGG 120
ATTCTGCTCA GGTGAGAAGG GTGACAGGAG AGTGAGTCAC ACTGACCTCT TCCCCTTCCT 180
GTTCTTTACT TACAAACCAC ATGCCCTCGG CATGAATGGG CCCTATTTCA CCTCTTTAGT 240
TCTTTCTTAT ATAAAACACT GGACCTGATA GCGGGGTGCA GTGGCTCACG CCTGTAATCC 300
CAACATGTTG CGAGGTCAAG ACAGGAGGAT CGCTTGAGGT CAGGACTTAA AGACCAGCCT 360
GGTCTCCACC AAAATAAAAA AACACACACA CATGACTTGA TGATCTTTAA GACCATTCAA 420
TTCTTAATTC TAGCAAAAGA CAGAAAGGAG ACGATGTAGG AAGGGCTGGA GGGAGGGAGG 480
CAAATTCTCA TTTGGATATA AATGGAGATG GGGAGGCCCT ATAAGGGATA CTTTCGTTTT 540
TCACTAGTGG TGTCTTAGAG AGTTGTTTCA TGCATAATTT ATTGGATGAG TATCATTTGT 600
TCCCTAAAGG ATGCTAGGTT ATATTTTTGA ATTTTGTCAA CAAAGCAATT TTTATGAAGC 660
TGAAGATCAT ATTTTTCACA TTTACTTTGA CATATCCGTG ACTCAGATTG CGGAAACAGG 720
CCTGAACCCC CAGTGCTTCT TAGCTCAGTA ACAGTGGTGA TAATTTTGGG TGCTTGCTCT 780
ATGCCTGATA CTGTTCCAAG CACTTTCCAT GCCTCAGCCT CACAGCAAAC CCGGAGTAGG 840
TTCTATTATT AGCTCCATTT TGCATCAGAG GAGAAAACTG CCCCAGGTCA AATAGCTGGT 900
GTGTGGGGTG GAGCTGGGTT TGAGCCCAGG CCATGTGGCT GCTGCAGAGG CCCGGGCTCT 960
AACCAGGAAA CAGTAGGTGC TGGGTAGCTC TTTATCCAAA TGTGGAGGGA AGGGGGTTTT 1020
CCGAGGGCCA TGGATTTGTA CAGGCTGCCC TTTGTGCTAC ACGAAGTCCT TTAATCAATT 1080
TACTCTTCTC AGAACCCCTG CGAGGTAGGT GTCACCACCC CCATGTCACG CAGCACACAG 1140
CTGCTCAGTA AATAGTGGGG CTGGAGTTCG GAAGTCCACG GTCATCCCTC AGCATCAGGG 1200
GCCCTTGGAT CAGGGCAAGG GGCACAAGAG GCTCACAAGC ACGAGAGACT GAAGGAAAGC 1260
AAGAACTGCC TTTCCTAAAA CTGATCTAAG ACAGCGCCTG CTGACAGGAG GTCACGGCTG 1320
TGTTCCGCTT CCCGCTTCCC CTTTCACCTG CTCCCTGTTC CCACTTCACA 1370
|
| |
|
|
|
