| Tag | Content |
|---|
EnhancerAtlas ID | HS059-14952 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr14:103893400-103894720 |
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 | TCTTTTTTTC TTGGTTTGGA GGAGACTTTC CCCTTGTCTA TAAGTAACTT AAATATAAAA 60
TGTTATAACA ATACGTTTAT TAGTTTGAAG CCCCAATTTT CTTTTTTTTT TTTCTTTTAA 120
GTGAAAACAA GTTTATAAAA GAAGTAAAGA AACAGGCCAG GCGCTGTGGC TCACACGTGT 180
AATCCTAGCA CATTGGGAGG CCGAGGCAGG TGGATCACCT GGGGTCAGGA GTTCGAGACC 240
AGCCTGGCCA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAATTAG CCAGTCGTGG 300
TGGTGCGCAC CTGTAATCCC AGCTACTCCA GAGGCTGAGG GAGTAGAAAC TATGAAAACT 360
TGGGAGATGG AGGTTGCAAT GAGCCGAGAT CATGTCACTG CTCTCCAGCC TAGGCAACAG 420
AGGGAGACTG TTTCAAAAAA AAAAAAAAAA GAAACAAAAG AATGGCTGCT CCATAGACAG 480
AGCAGCAGTA TCAGCTGCTT GACTGAGTCT ACTTATAGTT ATTTCTTGAT TATATGCTAA 540
ACAAGGGGTG AATTATTCAT GAGCTTTCTG GGAAAAGGGC AGAGATTTCC TGGAACTGAA 600
GGTCCCTCCC CTTTTAGGGG ACTATTTAGG GTAACTTCCC AAGGTTGCCG TGGCATTTGT 660
AAACTGTCAT GGTGGTGGTG GGAGTGTCTT TTAGCATGCT GATGCATTAT AATTAGCTTA 720
TAATGAGCAG TGAGGACAAC CAGAGGTCAC TTTCATCGCC ATCTTGGTTT TGGTGGGTTT 780
TGGCCTGCTT CTTTACCACA TCCTGTTCTA TCAGCAGGGT CTTTGTGACC TGTATCTTCT 840
GCCAAGCTCC TCCTATCTCA CCCTGTGACT AAGAATGCCT GACTTCCTGG GAATGCAGCC 900
CAGTAGGTCT CAGGCTTATT TTACCCAGCC CCTTTTCAAG ATGGAGTTGC TCTGGTTCAA 960
ACACTTCTGA CATATTTCCC CCCTCCCTTT TACAGGGGGA CCCTTAATCC TTAAGAATTG 1020
TAGCGGGACA AAGATCATCT GTAACTTCTT CAAGCCAAAT AGGGGTGATG ATATTCCTGC 1080
CTATTAGGGT CTCTTGTATT TAGGGTAGGG AGAAGTTTAG TTAGAAAGCA TTGTTATAGA 1140
AGCCCTTATT TTCAGTTACA CAATTTTATA AAGTTACAAT TGCTTATTGT AACCAGCTGA 1200
GTTTTAGGTT TTGTGGTTTG TTGCTTGCTT GCTTGCTTGC TTCTTAATGC CATATATCTT 1260
GGCATTTATC AGTCCATAAT TACTAAATTC TTAAAATCCA TAAATATTTA TTATTCTTTC 1320
|
