| Tag | Content |
|---|
EnhancerAtlas ID | HS108-31560 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr5:10688860-10690310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr5:10689617-10689632 | TGTGCTGAGTCATGA | - | 6.8 | | Nfe2l2 | MA0150.2 | chr5:10689619-10689634 | TGCTGAGTCATGACT | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_02757 | chr5:10689388-10693596 | Astrocytes | | SE_37792 | chr5:10688957-10694341 | HSMMtube | | SE_63948 | chr5:10689154-10694021 | HSMM |
|
| | 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 |
| GH05I010689 | chr5 | 10689389 | 10693893 |
|
Enhancer Sequence | TGGTCTACCC TGTGAGTACG CCACCCTTTG CAGAGGTGGA GTGGAACTCC AGGACGCAGA 60
GGCGCCATCC AGCAGTAGGG CGCCAGCCTG GAGAGGCCTC CATGTTGGGT GTTCCTGACA 120
GGCTCCTTGG TTGAGCCCAG CCCCACTGTG TAGTAGCTGC CACGTGAGGC TCTCGGGGGA 180
CCTGGCTATC AGGAATCTGT CTCCAGCACT GGTCCCCTGT GTGCACTGAG GACGGGAGTC 240
TGGAGCCCAG GGGCCTGCCA CAGTCCCGCC CTTCCTCCCT GCCCTCGGTG CTCCTCAGAG 300
GTGCTGTCCT CTGGGCGTCT CCTGCATTGA TCACGACAAG GGTGGGGTTC TATGCCTCGA 360
GTATGTACCC GGAGAAATGT GTGTGAACAG TGATGATATG AGATCATGAC AGCTCTGCTC 420
TAGCCTGAGT GCTGGAAAAC ACACACGGAA GCTGAGGCCT AGAAACCAGC CTCTGACTCC 480
CAGGGCACGC TCTTTCCTTT CCTAAACCCA CATTTAGCAC CTCACTCCCA TGTGAGCTGC 540
TCAAGACACT GTCCCATCGC AACTGCTGAA TGGCCATGGA GACCCTGGGG GCTAAAGGAG 600
ACCCCCAGCA GTAAGAATGA CCCTCCCCCC ACAGGCCCAG CTCATTCCAG GAGTGTCCAG 660
GGCCATGGTT GCAGGTTGCA GCGTCTAAGA GTCCACAGGA GTCATTCACA GATGGCGCTG 720
TCCTTGTGAA ACCCCAAATT CACGGAGATA GCTCCTTTGT GCTGAGTCAT GACTGAATCT 780
GCTGAGCTTT AGTGGCTTGG TGGATTCTGC TCATAAAGAC AGAGGATGTC AATGAAAATC 840
ATGCTAGGCT CAGCATAAGA AATGTGCCTC TGCCAACCAC TGGGTGGCGA GGGGTGAGGT 900
GAGGCCCACC GGGTGTGGCG ATGAGCCAGG GACTGGTGTC CTTTGTGCTG CATCCTATAC 960
AAAGTGGCTA GTCATTCTGC TGGATGTGGT GCTGGCGACT TGGCTGAGTG ATGGCAAGAC 1020
TGAGGGTCTG ATGCCGCAGT CAAAGGGACT CACTCAGGAT GGAAAGGCCG TGAACTTGCC 1080
CTTGTGCACA CCCTGAGGGC TGACTCCGAG CTGAGGAGCA GGGACAGGGA ATGTCACTCA 1140
GTGGCAAGCT TAGGTCAGAG CAGTCTCTTG GGGCACAACC AAAACAGTGT GCATTCCACC 1200
TAATTAACCT GGGGAAGAAC AACATGAAGG CCTGAGACTT CATCCTGCAC TGCTGTGCTC 1260
CAGCGCCCCC ATCTGTTTGG CACTGGTAAG AAATAAGGCA CTGAAAGAAA AGAACCCCAT 1320
GTGTCCAGCA CTTCCGCAGG CGAGGTCCTT GCTTTAAGAC TGCACTTTTT ACACAATATT 1380
CAAGAATTGT GTTGCATGAG AAAGTCTTAT CGAGCCGCAA GAGGCGACTC GGCGGGAAGT 1440
GACAGGACAC 1450
|
