| Tag | Content |
|---|
EnhancerAtlas ID | HS187-20432 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr5:176087290-176088290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr5:176087970-176087989 | TTACCACCAGAGGGCGCCA | + | 8.45 | | EGR2 | MA0472.2 | chr5:176087994-176088005 | CCGCCCACGCA | + | 6.32 |
|
| | 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 |
| GH05I176660 | chr5 | 176087901 | 176088202 |
|
Enhancer Sequence | TATCCACTGC CATTCACTTA GGTAGGCCCT AGCTAGAGGC TGGGGTTACT GAGGCAGCTC 60
AGACCTGCCC CTGCCTTCCC AGAGCCCAGT ATCTTGTTGG AGGCAGACAA GGAAGAGTTG 120
CTAATGTGCA ATGTATACGT GGTGACAAGG ACGTGATGAT CACTGCTAAG TGGGGTCTTG 180
GGCTGGCTAC AGACAAATTT CCTGTCCCCC AGTAGAACTT AGAGCAGTTC TTTGCACCAA 240
GGGGCTCTTA CCCACAGATG ATGCAGCTTC TTCAGATATG CAAAAACACA AGGGAGCTTG 300
TAAGACTGTC CATCCCTCTA GGAGGGTCCC TGGGCCTTGG GACCAAGGTC ACCTCCCACC 360
GTCTGTTAGG ATGAGATGCA CACTCATCTG TTAGGTAGGG ACAGGTGCAT ACTGGTAGAG 420
ACAGGTGCAC ACTGTCTGGC AGCCTGGGAG TCCCCTGTCT AACCACAGGA GAGGCTGCCA 480
GCAGCTCCCT GATCAGCTTG GTGGGAGGAC ATCCTGTGAC ACCAAGATAC CCTACAGAGA 540
GAGCTGGAGG GACAGAGAAC ACCCAGGCTG GCGAGCTCCT TTATCTCTGG GTGAGGTGGT 600
CATATGGGCT GGAGAGGACG GGCAGGAGCT CCTTCTGGGG AGGCTAAGGC CACAGATGCC 660
TTGGTGGTAG CCACTCCCAG TTACCACCAG AGGGCGCCAA AGTGCCGCCC ACGCAGCTCA 720
GCCGGCTCAG CTCGCGGAAG GAGCTCTGTG TAGAGTCATT GGGGCGACCC CTAGGGCCAA 780
GCAAGCCCAT GCCATCGTTC CAGAGACCCT GGGCCCACCC CGCTGGTGCC AAATCCAGGC 840
CTTACCACCC TCTGCCCTGT CTTCTCTGGG GAGTGGAGCA AATGATGCTG CCTGCCCACG 900
GGTGCCTCTC TCAGTGCTTA CAGGGCCCGA GCCCACTTGC TGGGCTGGGT GGGTGGTGGT 960
GTCCGCCCGA TAGAGCTGGA GAAAGGGGTG AGCGTCACTC 1000
|
