| Tag | Content |
|---|
EnhancerAtlas ID | HS023-07897 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr14:103893510-103894720 |
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 | TTTCTTTTAA GTGAAAACAA GTTTATAAAA GAAGTAAAGA AACAGGCCAG GCGCTGTGGC 60
TCACACGTGT AATCCTAGCA CATTGGGAGG CCGAGGCAGG TGGATCACCT GGGGTCAGGA 120
GTTCGAGACC AGCCTGGCCA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAATTAG 180
CCAGTCGTGG TGGTGCGCAC CTGTAATCCC AGCTACTCCA GAGGCTGAGG GAGTAGAAAC 240
TATGAAAACT TGGGAGATGG AGGTTGCAAT GAGCCGAGAT CATGTCACTG CTCTCCAGCC 300
TAGGCAACAG AGGGAGACTG TTTCAAAAAA AAAAAAAAAA GAAACAAAAG AATGGCTGCT 360
CCATAGACAG AGCAGCAGTA TCAGCTGCTT GACTGAGTCT ACTTATAGTT ATTTCTTGAT 420
TATATGCTAA ACAAGGGGTG AATTATTCAT GAGCTTTCTG GGAAAAGGGC AGAGATTTCC 480
TGGAACTGAA GGTCCCTCCC CTTTTAGGGG ACTATTTAGG GTAACTTCCC AAGGTTGCCG 540
TGGCATTTGT AAACTGTCAT GGTGGTGGTG GGAGTGTCTT TTAGCATGCT GATGCATTAT 600
AATTAGCTTA TAATGAGCAG TGAGGACAAC CAGAGGTCAC TTTCATCGCC ATCTTGGTTT 660
TGGTGGGTTT TGGCCTGCTT CTTTACCACA TCCTGTTCTA TCAGCAGGGT CTTTGTGACC 720
TGTATCTTCT GCCAAGCTCC TCCTATCTCA CCCTGTGACT AAGAATGCCT GACTTCCTGG 780
GAATGCAGCC CAGTAGGTCT CAGGCTTATT TTACCCAGCC CCTTTTCAAG ATGGAGTTGC 840
TCTGGTTCAA ACACTTCTGA CATATTTCCC CCCTCCCTTT TACAGGGGGA CCCTTAATCC 900
TTAAGAATTG TAGCGGGACA AAGATCATCT GTAACTTCTT CAAGCCAAAT AGGGGTGATG 960
ATATTCCTGC CTATTAGGGT CTCTTGTATT TAGGGTAGGG AGAAGTTTAG TTAGAAAGCA 1020
TTGTTATAGA AGCCCTTATT TTCAGTTACA CAATTTTATA AAGTTACAAT TGCTTATTGT 1080
AACCAGCTGA GTTTTAGGTT TTGTGGTTTG TTGCTTGCTT GCTTGCTTGC TTCTTAATGC 1140
CATATATCTT GGCATTTATC AGTCCATAAT TACTAAATTC TTAAAATCCA TAAATATTTA 1200
TTATTCTTTC 1210
|
