| Tag | Content |
|---|
EnhancerAtlas ID | HS145-07214 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr14:35838630-35839700 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr14:35839113-35839124 | GGCCACACCCA | + | 6.62 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_26613 | chr14:35837778-35840348 | Esophagus | | SE_34130 | chr14:35838890-35840456 | HCC1954 | | SE_34831 | chr14:35838475-35840071 | HeLa | | SE_50091 | chr14:35834124-35838759 | Sigmoid_Colon | | SE_53368 | chr14:35837739-35838902 | Spleen | | SE_53368 | chr14:35839113-35839894 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 35838948 | 35839592 | | chr14 | 35838636 | 35838770 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I035364 | chr14 | 35833498 | 35839881 |
|
Enhancer Sequence | GTGCACAAAA AGTATCTCAG ACCCTCTCCT CACCCCACCT GATCCCGTCA AAAAGGCCTC 60
CATGAACGCC ACCCTCCATG CTGGGGTCTC GGGGCCTGCA AGATCCCAGC TCAGTGGATT 120
TGAAGGAACT GATGGGCCTG GAGTCTGGCA GTGTGAATGA ATACATTCTG GGAGCAGGCC 180
CCGCCGCAAA CTCCCGTTTC AGACCTATGG ATGTGCCAAG CACACTCCTC CCCAGGTGGG 240
GCCTCCGGAG GCACCGGGGA TCATATGTCC ATCATGGATC CGACTGAGAC CACCGCTGTA 300
CCAAGCCGGG TGCGGGGGCA CCTGGGCATA CAGGGCCCTG CAGGTGCGGC CGGGCTGCGG 360
GGAGGCCCCT CCTTCCGCAC CAGCTCCACC CGTGGTAGGG CAGGGATGAC ACTTCTCAGC 420
TCCTGGTAGG GCAGGGATGA CACTTCTCAG CTCCTGGGCC AGACGCCAAT AAGCGGACCC 480
AGGGGCCACA CCCAGTCCTA GAAGGAAAAG GGGCGGCCGG AGGTCGGGGC TCACTAGGAG 540
ATGCTGCCTT TTCTGGCACA CACCGCCCCG GGATGCTGAC AGCCAGTCAG CTTTCGGAGA 600
AACAGGAAAC GGTCTCAGAC TGGTCCACGC TTGGCACTCA TGTTTTTTTC CAGGTCTAGA 660
GAGCAGCAAG AAACGCATCC TGTTACCGTA ATATGAGTCA GATGAATCCT GTTGTGTCCT 720
CCAGGTGTCC AGATGTACAG CCCGGGTTGG GGCGGGGACT GCAACGCAAA GGAAGCTAGA 780
CTTTGCAAGC TAGAGGAGAG GTTGGGGAGC TTCTGACCAG TTCTCTAATC ACCTGAATTT 840
CACAGACCAG GAAGGGGCCT GGGAGTTGGA GCTTGCTCAT GAGTTGCAGA GCCGGACCAG 900
AACCCAGGAA TCCCAGCTTG GTGCAGCGCC CTTCCCTCTA ACCCTGCTCT CTTGGCACTC 960
AGCGTTCTCT GAGCAGCTTT TCTAAACTCT TTGCCAAAAG CCTGGAGTCT CAGACCAAAG 1020
AGGCTTAGTT GAAAACTGGT TTTTCAGAAT CCTTGGCATA TTAAGAAAAG 1070
|
