| Tag | Content |
|---|
EnhancerAtlas ID | HS092-17058 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:103893600-103894720 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
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 | CCGAGGCAGG TGGATCACCT GGGGTCAGGA GTTCGAGACC AGCCTGGCCA ACATGGTGAA 60
ACCCCATCTC TACTAAAAAT ACAAAATTAG CCAGTCGTGG TGGTGCGCAC CTGTAATCCC 120
AGCTACTCCA GAGGCTGAGG GAGTAGAAAC TATGAAAACT TGGGAGATGG AGGTTGCAAT 180
GAGCCGAGAT CATGTCACTG CTCTCCAGCC TAGGCAACAG AGGGAGACTG TTTCAAAAAA 240
AAAAAAAAAA GAAACAAAAG AATGGCTGCT CCATAGACAG AGCAGCAGTA TCAGCTGCTT 300
GACTGAGTCT ACTTATAGTT ATTTCTTGAT TATATGCTAA ACAAGGGGTG AATTATTCAT 360
GAGCTTTCTG GGAAAAGGGC AGAGATTTCC TGGAACTGAA GGTCCCTCCC CTTTTAGGGG 420
ACTATTTAGG GTAACTTCCC AAGGTTGCCG TGGCATTTGT AAACTGTCAT GGTGGTGGTG 480
GGAGTGTCTT TTAGCATGCT GATGCATTAT AATTAGCTTA TAATGAGCAG TGAGGACAAC 540
CAGAGGTCAC TTTCATCGCC ATCTTGGTTT TGGTGGGTTT TGGCCTGCTT CTTTACCACA 600
TCCTGTTCTA TCAGCAGGGT CTTTGTGACC TGTATCTTCT GCCAAGCTCC TCCTATCTCA 660
CCCTGTGACT AAGAATGCCT GACTTCCTGG GAATGCAGCC CAGTAGGTCT CAGGCTTATT 720
TTACCCAGCC CCTTTTCAAG ATGGAGTTGC TCTGGTTCAA ACACTTCTGA CATATTTCCC 780
CCCTCCCTTT TACAGGGGGA CCCTTAATCC TTAAGAATTG TAGCGGGACA AAGATCATCT 840
GTAACTTCTT CAAGCCAAAT AGGGGTGATG ATATTCCTGC CTATTAGGGT CTCTTGTATT 900
TAGGGTAGGG AGAAGTTTAG TTAGAAAGCA TTGTTATAGA AGCCCTTATT TTCAGTTACA 960
CAATTTTATA AAGTTACAAT TGCTTATTGT AACCAGCTGA GTTTTAGGTT TTGTGGTTTG 1020
TTGCTTGCTT GCTTGCTTGC TTCTTAATGC CATATATCTT GGCATTTATC AGTCCATAAT 1080
TACTAAATTC TTAAAATCCA TAAATATTTA TTATTCTTTC 1120
|
