| Tag | Content |
|---|
EnhancerAtlas ID | HS145-14253 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr20:836140-837590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr20:837034-837055 | TAAAGTAAAGTGAAAGTAGAC | - | 6.09 | | KLF14 | MA0740.1 | chr20:836227-836241 | AAGTGGGCGTGGTT | - | 6.67 | | SP3 | MA0746.2 | chr20:836228-836241 | AGTGGGCGTGGTT | - | 6.13 | | SP8 | MA0747.1 | chr20:836228-836240 | AGTGGGCGTGGT | - | 6.74 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 836323 | 836490 | | chr20 | 836645 | 837200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I000855 | chr20 | 835971 | 837830 |
|
Enhancer Sequence | CCTACCAAGC CCCAAGCACC AACTGTATGT CCAGTACAGA GCCAGCTGCT CCAGGGGAGT 60
TCGTTCCTGG GAGGGGGCAT CATGATGAAG TGGGCGTGGT TCCCATTTCC TCCAGCGTAG 120
TCTCAGAAGC GGGAAGCCAT GTGACTGAGG TTACAGCCAG GGAGGGCAGA GGCCCCCGGC 180
ACTCACCCCT CTGGGGTCCA AGCCCCGCTG GCATGTGTTG TGTCCCTGGG TAGGTGTGTC 240
ACTCCCTGTC TGTGTCTCCA GTGTTCCTGT TGGCAAATCA GGGGTGGGAC GGAGGTAAAT 300
GGAGAGGCCC TGCCCAGTCT GCTGTAATCC AGGATCTCGG ACTTAGTGGG GCCAAAGCTT 360
CCAAGTTCTC CTGATTAGTG AGGCTGCAAA AAATGTTTGG CATGTTATTC TCTCACCGTT 420
TAAATGTGGG CAAGTAACAA CTTACATGTA AAATTACCCC CATATACCAA GCATTTAAGT 480
TATTTATTAT ATCATTGCTT ACAATAGCAA ATAATTGGAA ATTATTTGAG AAATGGCTAA 540
AGAAACTCAG GCCCAGGTAC GCAAGGGAAT CCTAGGCAGC CCTCAAAAGA TGTCCTGCAA 600
ACACCTGATG TGGAATCACA AGATACACAA CACAGGTCAG TGAACAAAAC AAGTTGTGGC 660
ATGATACCCA CAGTGTGCTG CTGCTTGTGG AAGCAGGAAC ACATGTCCAT GTACTCTTGT 720
ACTGGCACAG AACCCTGGAG AATTATCCTG GGAACCCTGC ATGCTGGCTG CCCCTGGGGA 780
GGGGAACCCG AGGGTTGGGC TCAAGGGTGG GAGGCAAGAC TCACTACTTT GCACACCTTT 840
TGAATTTTGA ATCATGTGAA TGTGTTATCT GTGCAGAAAA AATAAAAATA CATTTAAAGT 900
AAAGTGAAAG TAGACAAGAA ACCTGAAACA GAGACGGACA AGCAAGCCTG CAGGCCCAGC 960
CAGCTACCGC CCCCGGGCAA CCTCATGCCA CACTGTGGGC TCTGCCCAGC TTGGTTTTGT 1020
GGCTCCACCC TCTACGGTCA TATTTGGGTT TCCACACACA CAGCACCCAA AGGAAATCCC 1080
AGCTAACGCA CATCAGGTTC TGGGCTGGGC CACCCGCCAA GGTGGTTGGT GGGCATGACA 1140
CCGCCCCGGG AATGGCGTCG TCCAAATGCC TGAGCAATGA CACGGCCTCA GATGGAATGA 1200
TGCCACTGCC CACAGTCTCA CAGGCCCTCC CATCTCGCCT TTGTTCTGCA GCCTCCAGGT 1260
GGGTGTATGG ACACTCCAAA ACAGCCATCC CTGTCAATGA ATCAGCCTGC AGGGACTGAA 1320
TTCATTCCTT CATTCATCAA TATCCATTGA GCACCTACTG TGTGCCAAAC ACTCTTCTAG 1380
GAACTGAAGA TGCAACAGAA AACAAAACAG ATAAAAATCC CTGCCCTCGA GGAGCTGACA 1440
TTCCAGAGGG 1450
|
