| Tag | Content |
|---|
EnhancerAtlas ID | HS051-26777 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr8:134120980-134122680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ETV6 | MA0645.1 | chr8:134122436-134122446 | CACTTCCGCT | - | 6.02 | | MAFK | MA0496.2 | chr8:134121528-134121547 | ACCTGCTGAGTCAGAATCT | + | 6.02 |
|
| | 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 |
| GH08I133110 | chr8 | 134122288 | 134122488 |
|
Enhancer Sequence | TATTTACCTA TGACATGCCT GTCACCATAC TGAGCACTGG GGCTATGGAC ACAATCCCTG 60
CCCCCTTTGC CATGTAGTAC TCTGGAACAA TAGGCAAATA AACTAACATC ACAGCACCTG 120
GGTCCTGAGG GCCATGGGGG CCCCTGGTTT AGCCCGGGAC AGGTTAATAA TCATCACTCA 180
AGGTTGTTGA CCATGTGCCA ACTACTGTGC TAAACACTTT TAATGCATGT TTCGTTGGGA 240
TCTGTTAATA ATTCATGCAA TAGGCATTTT TCATTATCCA CCTTGTCTAA AGAAGGAAAC 300
TGAGCTACAG AGAGAGGCAG CAATTTACTC GGGGTCCTGG AACTACAAGG TAGTTCTGCC 360
CTTTCAACCA TTATCTCTAG AGCCTGACCT TTCAACCATT ATCTGTCCTG TTTCCTGGAG 420
GAGGTGAGCC CTGAGCAAAA CCTGGATTTT CTATTATAAT CTGATTGCTG ACTGTGAAGT 480
TCCCAGGCCA ACGGCATCAG CATCACCTGG GAGCTTGTTA AAATGCACGT TCCTGGGCTC 540
CACTCTGGAC CTGCTGAGTC AGAATCTGTA TTTTATCAAG ATTTCAGTCT ACTTTAACGC 600
TTATTGGATT AAAAAGCATG TGTCTAGTTC AATAGCTGTT ATCCAGGCAA ACTAGGGAAA 660
GGTGTTTAGG CAGGAGGAAC AGCAGGCGCA AAGGCTTAAA AGTACGAGAG AACATTTGGT 720
GTTGAGGAAA CAGCACTCCT CACGTGGCCT GGGCATTTTG GTAATATTTC AGCAGCCTAG 780
TTCTCAGGAG TCACAGAAAT TGAAGGCCAA GTGGCAGCTC GTCTGGGTGG CAAGGGCAAA 840
GCACAGCTGG GTTTGTTCCC CACCTGTGTG ACTTACTCAG CTGTGTAAGA CAGCACTTAG 900
CCTCTCTGAG CCAGTTTCCT TGTCCACCCC CTCAGGATGG TTATGGGAGC AAATGAGAAG 960
AGGGTGCACC AGGGACCCAG CACAGCATCT GACACGCAAT GGGTGCTTGG TGCGTGGCAC 1020
TTGTGCTGAC CTCGGCTACT CCCTTTGCCG ACATGACTCA GGCAGCATCA TTCTCACCCC 1080
TTGGCAGTCT CCTCTAAGTT CCAGCAAATG GCATTGCACA GGGAGGAGAC AGTTTATGAA 1140
CTTGTTTTAC TCCTCTGCAG CCCAGGAGGC ATTGGTATCT TGGCTAGGGC TCTCACTATG 1200
ACCCCCTCAT GTTATGTATG AGAAAATGGT GCCCAGAGAG AGAAAGCCAC TCTCTCAAGT 1260
TTGTACAGTG ATTGCCAGAT AGCGGGTGCT GGGACTTGGA GATCCTGGTG CCCAGACCTC 1320
AGTATAGCTC CCTCATGTTA AGATTTGAAG GCAGATTATG CCTGCCACGT AGCAAAGCAG 1380
CCTGGGGAGA ACCCACTTTA GTGCCACTGC ACCGTTGTCC TTGTACCCTC CTGGGCTCCC 1440
AGAACTGAGT TCTCCCCACT TCCGCTCCAG CCCGGGGCAT TAGACCCACC CAATATCTGA 1500
GGTGGGGGCA TCATGGATTC CTTCTTTATA AAGCATCTGT GAGCAGTACT TGGCCCTCGA 1560
ATTTGGCACC TTCTGCCTTC CCCACCTGCC TTCACTCATC GCCCAATCTC CTTGTTCACA 1620
GCTCAGAGCT GAGCAAACAG GCTGCAGCAT TGAGACAGCC ACTGGAACGA ACTATTATAT 1680
TTTCTTGCAC AGTTTTTCAA 1700
|
