| Tag | Content |
|---|
EnhancerAtlas ID | HS182-06937 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr14:103893500-103894640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr14:103894216-103894231 | GGGTCTTTGTGACCT | - | 6.34 | | IRF1 | MA0050.2 | chr14:103893839-103893860 | AAAAAAAAAAAGAAACAAAAG | - | 6.21 | | RARA(var.2) | MA0730.1 | chr14:103894132-103894149 | AGGACAACCAGAGGTCA | + | 6.62 | | STAT1 | MA0137.3 | chr14:103893964-103893975 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr14:103893964-103893975 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr14:103893964-103893978 | TTTCTGGGAAAAGG | + | 6.15 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09869 | chr14:103893831-103896534 | CD14 |
|
| | 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 |
| GH14I103426 | chr14 | 103893282 | 103895765 |
|
Enhancer Sequence | CTTTTTTTTT TTTCTTTTAA GTGAAAACAA GTTTATAAAA GAAGTAAAGA AACAGGCCAG 60
GCGCTGTGGC TCACACGTGT AATCCTAGCA CATTGGGAGG CCGAGGCAGG TGGATCACCT 120
GGGGTCAGGA GTTCGAGACC AGCCTGGCCA ACATGGTGAA ACCCCATCTC TACTAAAAAT 180
ACAAAATTAG CCAGTCGTGG TGGTGCGCAC CTGTAATCCC AGCTACTCCA GAGGCTGAGG 240
GAGTAGAAAC TATGAAAACT TGGGAGATGG AGGTTGCAAT GAGCCGAGAT CATGTCACTG 300
CTCTCCAGCC TAGGCAACAG AGGGAGACTG TTTCAAAAAA AAAAAAAAAA GAAACAAAAG 360
AATGGCTGCT CCATAGACAG AGCAGCAGTA TCAGCTGCTT GACTGAGTCT ACTTATAGTT 420
ATTTCTTGAT TATATGCTAA ACAAGGGGTG AATTATTCAT GAGCTTTCTG GGAAAAGGGC 480
AGAGATTTCC TGGAACTGAA GGTCCCTCCC CTTTTAGGGG ACTATTTAGG GTAACTTCCC 540
AAGGTTGCCG TGGCATTTGT AAACTGTCAT GGTGGTGGTG GGAGTGTCTT TTAGCATGCT 600
GATGCATTAT AATTAGCTTA TAATGAGCAG TGAGGACAAC CAGAGGTCAC TTTCATCGCC 660
ATCTTGGTTT TGGTGGGTTT TGGCCTGCTT CTTTACCACA TCCTGTTCTA TCAGCAGGGT 720
CTTTGTGACC TGTATCTTCT GCCAAGCTCC TCCTATCTCA CCCTGTGACT AAGAATGCCT 780
GACTTCCTGG GAATGCAGCC CAGTAGGTCT CAGGCTTATT TTACCCAGCC CCTTTTCAAG 840
ATGGAGTTGC TCTGGTTCAA ACACTTCTGA CATATTTCCC CCCTCCCTTT TACAGGGGGA 900
CCCTTAATCC TTAAGAATTG TAGCGGGACA AAGATCATCT GTAACTTCTT CAAGCCAAAT 960
AGGGGTGATG ATATTCCTGC CTATTAGGGT CTCTTGTATT TAGGGTAGGG AGAAGTTTAG 1020
TTAGAAAGCA TTGTTATAGA AGCCCTTATT TTCAGTTACA CAATTTTATA AAGTTACAAT 1080
TGCTTATTGT AACCAGCTGA GTTTTAGGTT TTGTGGTTTG TTGCTTGCTT GCTTGCTTGC 1140
|
