| Tag | Content |
|---|
EnhancerAtlas ID | HS145-12751 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:70173280-70174620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr2:70173453-70173463 | GGTCACGTGC | + | 6.02 | | ESR1 | MA0112.3 | chr2:70173986-70174003 | AAGGTCAAAACGACCCT | + | 6.27 | | FOSL2 | MA0478.1 | chr2:70173903-70173914 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr2:70173903-70173914 | GGGTGACTCAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09668 | chr2:70170084-70175672 | CD14 | | SE_65154 | chr2:70171871-70174956 | NHEK |
|
| | 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 |
| GH02I069945 | chr2 | 70171934 | 70176194 |
|
Enhancer Sequence | ACTCGCCTTG CCACGCTGAT ACTGTCATCC CCCAGAAGGC GGAAAAAACC ATTGCTGTGA 60
AGCATTCGAG CCAGTAATGA CCAACAGAGA CCAATAGGCT GGCCAAGTGG AAATAGAAAC 120
TCAGGGGGAG TGCCCATGTC CCCTAGGTAC CCCGGAAGGT GGTCCTGGGT GATGGTCACG 180
TGCACAGACT CTGGTCAAAT GGAGCTAAGG GTCGATGCCA ACTCCACCCT TAACACCCTC 240
GGTGACCCCA GGCAAGTATC TGGGACTCTG CTGACCCGGT CTGTAGAGTG AGGATAATAA 300
CAGCATGTAC TTCCCAGGGC TGCTAGGGGG ATTAAGTAAG GTAAAGTATG CAAACAGCTT 360
TTCCCCATGC CTGACATGCA GAAAGCATTC AGTACATATG AGCAATTATA ATCATTTTCC 420
CAGCCAAGGA GAGAACGTTC GAACACTGTC TGGCATGTGA CTTGGATTTT CAGAATACAA 480
AATTCCAACA CTCAGAGAAG AAATAAGCTT GGAAGGGAAA ATTACATTAG AGGGTGGGGA 540
AGTGTTCAAA TATGTCATTC TGACTGTGCT GTTTAGACAA CAAACAGTAG GCAGGAAGTG 600
GTTAAACCGA AAGGGGGAGC AGAGGGTGAC TCAGGGACAG AATGTGGGCA TTGACAGTGG 660
AGGGGTGGCT ATTTTCCAGG TAGTATCTCA CCTATGTGCT GTTCGGAAGG TCAAAACGAC 720
CCTAAGACCC CGCCAGCCCT ACAGGGCAGT TCCTCTCATA GAGAGACCAG ATCATACAGA 780
GGTGGCTCAG AGAGAGAGAC AGAGGGAAGC CCTTGCTAAA ATGCCCATAT GTTGCAAGTA 840
TCTCATCAGA AGAGGCCAAA TGACTTCAGT TCCCGCATTC ACACGTACCT TTGCACTGCA 900
AATTCAGAAC AACCGTAGGT AGAGCTCTAC CCAGACGGGG ACAACTCCAC ACTTCAAGTA 960
TGACCTCTGA GCAACTGCAG AGGTTGTGAT GATTCTTGGC TACTTTGCAG TTAATAACTT 1020
TGGTCAAAGA AGCTACCAGT CAATGCAGAC TAGCACAGGG CATGGAACAG TGTGTGGCCC 1080
AGAAGAGGTA TCAGTGGAAG AGTAAAGAGA TAATCAGGAT GGAACCTGGC CCTGCTTTCT 1140
TGTCACCACA CTTTATAATG TTAGGGAAAA GTATTCTTTT GGAACTCATT GCAGCAATCC 1200
CATTGCTTTC CCCTGAAAAA CAGGTGTGTT TACCTCAGGG AAACAGTGAA TCATGCAACA 1260
GATCATCTTT CTCTTCTCCC TTTGGCTGTC AGGAAACTCA GAGCCAAATT CACACTTCAC 1320
CTTTAGTAAT TTTGTGAGAA 1340
|
