| Tag | Content |
|---|
EnhancerAtlas ID | HS145-03681 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr10:116079740-116081110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr10:116080660-116080671 | AAATCACAGCC | + | 6.02 | | RARA(var.2) | MA0730.1 | chr10:116080393-116080410 | TGTCCTTGGGATGACCC | - | 6.1 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_53388 | chr10:116079540-116080938 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr10 | 116079797 | 116079800 | | chr10 | 116079800 | 116080000 | | chr10 | 116080154 | 116081078 | | chr10 | 116080506 | 116080782 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I114320 | chr10 | 116079762 | 116082889 |
|
Enhancer Sequence | GGATTTTGCG TCCCTCGAGG GTGGCCGAGA CAAACATGGA AGGAGCCCGG GCACCTAATC 60
TACATGAGGA TGAGTAATGC CCCACACTGA AATACCCGAG TGAGAAACAG GTTTGCATTG 120
TGTTACTATA AACAGGAGCT GCTGGGTTAT TTGTTACAGC TGCTAGCAGT ACCCCAGGGT 180
GAGACACCAT CAGTGAAGAA CCTGGTATCT CTGGCAAGCA GGGCAGACCC CGATATCCCT 240
AGCACAGGCC AGCAGGGCAC TTATTACACA TGTGCTCAGA GAGAGGGACA TGACCCAGGG 300
GAGCGGTGTG GGGATAGGGC TGATAGAGCA GGTCAAGAAT CCAAGCAACT GGCCTTTTGC 360
AAGAAGTCAG CAAATCGCTA TGGCCGCCAA CTATAGCAAG GGGCTGGGGC CCCACGCCTA 420
TTCCTCCAGT CACAACCTGC ATGTCACACT GTTTGACCAG GCAGGACCTG AGGTCAGGCC 480
AGCTTGTAAG GCAGGTGAAG GCCTCCCTCT GTGCTGACCA TGACTGCTTC TCCCCAAGTC 540
ATCCCCAGGC CTCTCCTTGG CAGGACAGGC AGGGCTATGT TCCCTCCCAC CTCGCAGCTG 600
GTTTTCCTCC ATCTTGGAGC TTTCCTGACC CACTCCACAC AGTGAGTTCA AGCTGTCCTT 660
GGGATGACCC CTAGTCCCGG CTACGACCAA TATGAACTCA CAGTTGAGAG ACAAAACCAA 720
GAAGCGCTGG CCTTTCTGAC CACTTGTTTG TGTCGAGATG GAGTGTCTGA CCCACAAACC 780
GGCCCCCTGG TGCGTCTGGC AGGCAGGCCC CTGCTGGCCC GGCCACACCT GGGAGCAGGG 840
AAGTGCTCAC TGCGGTGAGT CACTGTTTCC ACCTTCAACG CGCATCCAGA CAGCAGCACC 900
GCACCCTCGC CTTTGGTCTG AAATCACAGC CCGACTGGTG AGCTGGCACC ACCTCGCATG 960
CTCAGTGGGT CAATGCTAAG TGCTGGCTGC CCACAAAGCC AGCGTCTTAG AATAGACTCA 1020
GCCTAAACAG GCGCTCACTT CCCACAGAGT TCCCAGCAGG AGGTGGCAGG TAAGTGTGAA 1080
GGAAGGGCAG GGGAATCCCA TCCCGCTCCC AGTCACCGGT CCCATCTCAT CCCTGGTCCT 1140
GTTCTTTTTA TTTTTATTTC AATAGTTTTT GGGGTTCAGG TGGATGCATT CTTTAATGAT 1200
GATTTCTGAG ATAGTGCACT GTCATTCGAG TGGTGTACAC TGTACCGAAT ATGTAGTCTT 1260
TTATCCCTCA CCCCCACTCC CAATCTTCCC CCGCTAGTCC CCAAAGTCCA TTATATCACT 1320
CATGCCTTTG GGTCTTCATT GCTTAGCTCC CACTTATAAG TGAGAACATA 1370
|
