| Tag | Content |
|---|
EnhancerAtlas ID | HS040-10470 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr14:73694250-73695880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr14:73695364-73695379 | GATGTCAATAGGTCA | + | 6.86 | | PPARG | MA0066.1 | chr14:73695586-73695606 | CTGGGTCATTGTCACCACAT | + | 6.08 | | RARA | MA0729.1 | chr14:73695364-73695382 | GATGTCAATAGGTCATGT | + | 6.84 | | REL | MA0101.1 | chr14:73695345-73695355 | GGGGATTTCC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 73694453 | 73695625 | | chr14 | 73695241 | 73695452 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I073226 | chr14 | 73692887 | 73696150 |
|
Enhancer Sequence | CTGAAAGTGA AGCCAGCCTG CCTGGGTTAA TGTGCTGTTG ACGGCACAGG CTGTTTGCAC 60
TGGCGATGTA GGGTGCTGCC CACTGAGCCA GGGTGCCCCA TGTGTCAGAT GGGCCCATGG 120
CGATGGAGCC AGTGCAGCCC ACTTGAGGGA GGAGACAGGG ACCGGCTCCT CTGCCTGTCC 180
ACACACATGG CAGGTCATCT TTGAGGACTC TGTTTTCTCA ATTGTCAAGG ACCAGAATTC 240
CCTCTTTCCC CTCTTGCACT ATGGATAAAG GCATAGACAT GTTATAAGTG ATTATGCAGC 300
TTTTGTCATT AAAGATATGT AATAACACGG TTCGCCAAGG TGCTCCAAGC ATTTGGTAAT 360
TATTGCATGA ATTGATTTTT GTTTTTAAAT CAAAACATAC TTTGGTAAAC ATTCCTGTGA 420
AGGGAGGCCC ATTCCAAGTC TCAGAGTTGG AGTGCCACCA AGACCCCGCC TGGAGCCCCG 480
CTGCTCTGCC AGTCAACTGA TGGGCTCCTT TACCCTCTCT CTTCCTGGCA GTGCTCCATA 540
GCGGTGGGAA AGAGGGTGAG GCCTTGCCAC TCCGCGGAGG GCCCCCTGGC CCACCCCAAT 600
GCTGAAGACA AATCTGACCC CATCTTCCCA CTGGGAACTT GGCCAACCCA GATGTTCCCG 660
CAGCCCCTCC CTCCGCTCCT CGCTCCCTGG ATGGGGCCCA CCTCCAGCGC ATTTTTCTCA 720
CTCCAAGCTC CTTCCTTGCC AGATGGCTCT GCTGGAGGAT TCTGCCCCGG GCTGGGAGGG 780
GCTGGGGACC TGATTCTCTC ATTTCCCTGT GGTTTGGCGA GTCTTCCCTC GCCCCTGTCG 840
TTTTCAGAGC GAGCCCCGCC CTTGTCTGCA GACTCTGGCT GCCTGGACAG GCAAAGGGAA 900
ATGGATGGGT CACCCTGATG CCTCCGAGCC CGGTGACAGG AGCTAAGGAT GGCAAATACA 960
GACCGAGGGG CCACCTTGCC ACTGCCTGAC CCTCCAGGGA GCTTGGGCGC CGTCCCATTT 1020
CTTAAACTCC TGGCAGTTGC CCAATAAATG GTGAGTCAGT GAAGGACTGT AGGGGTGGCT 1080
GCGGGGTCTG CGGGAGGGGA TTTCCATGCA GAATGATGTC AATAGGTCAT GTGCATGGGA 1140
ATTGTTGTGA GTAAGAACAA ACATTAACCA GCTTTTGCCC CTGTTTACAA GGCTGTGCTG 1200
GAGAGTGTGG AGCCGAAGTC AACCAGCCTT ATCCCTTCAG GAGACCTGAA TTTATAAATG 1260
GTGGTCAGGA TGAATACAAA CAGGATTCCT CCCCCAGTTC ACGTTTGTGA CATCTGGAGA 1320
GATGTATGGG TTTGTCCTGG GTCATTGTCA CCACATTGGA TGCAGGGGGA ATAAAGGATA 1380
GGGCGGTTGT TAATACATAC CCCACATTTA ACCAAGAAAA GCCACAGAGG AAGGTACTGC 1440
TTCATAAAAC CAATGTCCCT TGAGCATGTC CCTTAATATG CCACAGACAC TATGCCAAGC 1500
CCATCACAGG CATTGTCTCC TGTCCTCACC CCACCCTATG GGTAGGGCCT GTTAGCCCCA 1560
TTTTACAGAG GAGGAGGAGC GCTCCCAGAG TCACTGCCCG CAGGTAAGTG GGAGAGGCTG 1620
TGCCTCCAGC 1630
|
