| Tag | Content |
|---|
EnhancerAtlas ID | HS141-13230 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr3:121830280-121831500 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr3:121831305-121831315 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr3:121831305-121831315 | GGCACGTGCC | - | 6.02 | | NFIA | MA0670.1 | chr3:121830713-121830723 | ACTTGGCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr3:121831382-121831397 | CGATCTCTTGACCTC | - | 6 | | SPI1 | MA0080.4 | chr3:121830991-121831005 | TACTTCCTCATTTG | - | 6.39 | | SPIC | MA0687.1 | chr3:121830991-121831005 | TACTTCCTCATTTG | - | 7.12 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09531 | chr3:121829889-121831121 | CD14 | | SE_58952 | chr3:121771377-121831860 | Ly3 |
|
| | 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 |
| GH03I122111 | chr3 | 121829890 | 121831121 |
|
Enhancer Sequence | AGGCACCAAG CTTGAGATGG TGAGATTAAC CTGGATTATC CAGGTGGGCC CAATGTAATC 60
ACATGAGTCA GAGAACCTTT CCTAGCTGGG ATGGAGAAAT GAACTGGAAG AAGGAGAGAT 120
CTGAAACTTG AGAAGCTCAA CCCAGCATTT CTAGCTTTGA AGATGGAAGG AGGAAGCCAT 180
GAGCCAAGGA ATGTAAGTAG CTTCTAGAAG CTGGAAGTGG CTCTCAGTTG ACAGCCAGCC 240
ATTAAGGAAA TTAGGATCTC AGTTCTGCAA CTATAAGGAG CTGAATTCTG CCAAGAGACC 300
AATGTGGAAA CAGCAGATCC CTCCACAGAG ACACAAGCTT ACTGATAACT GGTAGGAATT 360
TCTCCAAAAG TGGAGCTTCC TCCTACTCCA GTGTTAATCC CTTTCTCAGA GGAGACGGTC 420
CTCAAACTAA CTAACTTGGC ACCAAAAGTC CTATCCAGTG TTTTCTCATT ATAGTTTTTC 480
TATGCCTCAA CTGTATATAT TTACCCAGTT TAGGCTGTTT AAATGAATAA AAAGGAAATG 540
CCATAGTTAT TCTAGCCAGT TTCCAATCTC TCTTCTCTTT TTTTGTTTTG TCAAATAGGG 600
CAGATAAGGC ATGAGAATTT ATAACTATGA ATTACTGTCT TTTCCCAAAC AGAAATCACC 660
CTATCAGCTT ACCCATTGGG AGAAAAACTA AAATAGCTCC CCCTGAAATT TTACTTCCTC 720
ATTTGGGTCT TGTGTGACTG AAATCTGTAT ACAATGCCCT AGCAACAACG GTTTTTACAG 780
CTTGCCTCCC TAGAACAAAC CTAGGAGTCT CAGCTGTTTC AGGAATGATT TCTTAAAGGT 840
AAAGTGCCTT TTTCAAAAGA AATTATTATT ATTTTTTTTT AATTTTTTTT TTGTGTGTGT 900
GTGAGACAGA GCCTCACTCT GTCACCAGGC TGGAGTGCAG TGGCACGATC TCAGCACACT 960
GCAACCTCTG CCTCCCAGGT TCAAGCGATT CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA 1020
CTACAGGCAC GTGCCACCAA GCCCAGGTAA TTTTTGTATT TTCAGTAGAG ATGGGTTTTC 1080
ACCATGTTGG CCAGGATGGT CTCGATCTCT TGACCTCGTG ATCCGTTTTT AACCAACATT 1140
TAAACAGAAA TATTCACAGG CTTAAAGACT GAAAGTTAGT GATATCATCA CATTTCCCCT 1200
TCAAAATGCT GAATTTGTAA 1220
|
