| Tag | Content |
|---|
EnhancerAtlas ID | HS040-33468 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr8:101654810-101656620 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr8:101655428-101655449 | AAAACAAAACAGAAACAAACA | - | 6.1 | | Nr2f6(var.2) | MA0728.1 | chr8:101655202-101655217 | GAGGTCAGGAGTTCA | + | 6.22 | | SPI1 | MA0080.4 | chr8:101656104-101656118 | AAAAAGAGGAAGGA | + | 6.06 | | SPIC | MA0687.1 | chr8:101656104-101656118 | AAAAAGAGGAAGGA | + | 6.38 | | ZNF740 | MA0753.2 | chr8:101655341-101655354 | TTGGGGGGGGTGG | - | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGACCTAAGG GGGACAATGA ACATAAAGGA AACTGAGTAG TTAAATGTGC CAAAAGTCAA 60
CAATCAAATC CAAATTCAAC TCCACCAAAA GAGGACCTTT TCCATGGGTC TCAGTACACA 120
GTTGAGCTAT CAAAACCACC AGCGTACTGA GAAGTATCTG GTACTACAGT TCAGCCCTAC 180
CTGTCTTTCA AAAAACTGTT TAAAGAGATC AAAAGGAAAA CATATCTGTT CTGCTCTTTT 240
ATTATGTGGT GTTTTTGTTT GTTTGGAGTA TTGTGGGTTT TTTTTAAGAC TGTGATCTGA 300
CAAATATTTT CATAAACCCC AGAACAGGGC GGGCGTGATG GCTCATGCCT GTAATCCTAG 360
CACTTTGGGA GGCTGAGGCA GGCAGATCAC CTGAGGTCAG GAGTTCAAGA CCAGCCTGGC 420
CAACATGGCA AAACCCCCTC TCTACTAAAA ATACAAAAAT TAGCCAGGTG TGGTGGCAGG 480
CACTTGTAAT CCCAGGTACC CGGGAGGCTG AGGCAGGAGA ATCACTTGAA CTTGGGGGGG 540
GTGGAGGTTG CAGTGAGCTG AGATCGCACC ACCTCACTGC AGCTTAGGTG AAAGAGCGTG 600
ACTCCGTCTC AAAAAAACAA AACAAAACAG AAACAAACAA AAAAATCCCA GAACAATCTC 660
CTGTACCAAC TACCCCTTCG TACAGCTCTG CCTTTTAACA TGAAGAGGCC TTTACAGGCC 720
AGTTGAAAAT GTCACCTACT TCCCCCACCT TACTGCATTC ACACCCCCCT ATACCTATGC 780
CAAAATGGTG ATGGCCTGGG ACAAGTAGAA TTACAGACAC AAAAGGTGTC TGTTTCTAAT 840
GTCGACTCAT TCTTCCCACC TCTCCAAGTC CCCTTGTAGT TAAAAACCCA AATTCACCAG 900
ATAAAGGGCC ACAGCTCAGA GTCTGGGTGG TGGCATCTAG CACCTAAGAG CATGGCCTAG 960
AGCTTGCATA TTATCCCATT TGTTCCTCAA AACAGCACTA CGAGGTAGAC AGATCCTCAG 1020
CACCATGAAC CTTGAGCGGG AGCAACCCCA GACTCAGGGA GATGAAGTGA CTTAAAACTA 1080
GGACATCCAA GCTGATGACT GGCAGAAGAT GGACTCAGTC TTCTCACTGC TGTCATCATC 1140
ATCACCATCA CCTTTTCCAC CAAATCTCTG CTAAGCAACT ACCAAGGCAG AATTCCATGC 1200
TGGGTGTTCC ATACCCACAA GCCTTCATTC TGTCCCTTCA TTCAAATATT TGGATTTTGC 1260
TTATAAATAA TCAGGGGAGA CAAAATATAA ACACAAAAAG AGGAAGGAGC ATGACAAGGT 1320
TGAAACATGA AGCGGCACAG CAATCAGAGA AAGGCATCTC ATGCAATCAA GGAGGACTTC 1380
CTGGAGGAGA TGGGACTGAG GTGGGCTTTG AGAAACGATT GCTCCCTTGA CAGGTAGACT 1440
AAAACCAGGA GTCATCCCAG GCAGAGGAAG TGAGCCAGGC AGAGACAAAG AGTGGGCCAG 1500
CCTGATAGGA ACAGGAGGTA TGGGTAGGGA AAGAGGAGAT CAGGTTAGGT CAGAGGGGAA 1560
GCAGCCAAGT TGGGTCAGCA CTTGGCAGGG AGGACAACTG AACCAGCGCA CACAGGCTGC 1620
ACAGCCCTCC CCTCCTACTG ACGGGTCCTT TGCAAGCTTT CCCAACTTGT CCCCATTGCC 1680
ATGTCTGATG CTGGCAGAGT GCAAAGAAAC AGAGCCCCAT ATCACTGTTC ACAGAGCCCC 1740
ATATCACTTA CACAGGATGG CCTCATCTGT AACTTGGTCA AAATGAGCTG ATTAAATGTT 1800
TCCCTCACAG 1810
|
