| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13112 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr2:38769340-38770570 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr2:38770081-38770096 | AAAGCTGAGTCATGG | - | 6.34 |
| | | 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 |
| GH02I038540 | chr2 | 38767879 | 38771285 |
| Enhancer Sequence | AGGCTGGAGT GCAGTGGCGC GATCTCGACT CACTGCAACC TCCGCCTCAT GGGTTCAAGC 60
AATTCTCCTG TCTCAGCCTC CCAAGTAGCT GAGATTACAG ACCCCCACCA CAATGCCTGG 120
CTAATTTTTG TATTTTTAGT TGAGACGGGG TTTCACCATG TTGGTCAGGC TGGTCTCAAA 180
CTCCTGACCT CAAGTTATCC GCCCACCTCT GCCTCTCAAA GTGCTGAGAT TACATGCATG 240
AGCCACCACG CCCAGCCAGT TCCACAGACT TCTAAGGGGC TATCAGGGAA CAAATGTGTA 300
GTAAAAACTG TTCACCAAGT GTTTATGAAT CATCCAAGAA GGTCAGGATA GGTTTTTGTT 360
TTGCTTTACG GGAGACATCC TGAATCTGAA AGGCAGAAGA CACCTATCTG GCAGGTCCAG 420
GGTTAGCACA ATGTATTCAC TGCCCGTTCA AGAATAGTAA CAATGATCAT AATAACAGTC 480
ATAACTATTG TTTGTTGAGA CTATGTGCTT TAAATGCATT ATCTCACTTA ATCCTCATAC 540
CAACTTTGTC AATATTCATA TTTCACCTAC AAGAAAATAG ACTTAGTGAT GTGAAGAGAC 600
AATGTCATAC AGCACACAGT GCTAAAGTTG ATAATCAGAC CCAACTCTAT CAAACTCTAA 660
AGGCCATTTA TTTAACCACC GTGAAAGAAA ATAAAATCTC AGGACCCCGT TTCATGATGC 720
CAAAAGGAAA ACATTAAGCT GAAAGCTGAG TCATGGCCAG AAATTGCCTT TCTCTTTGTT 780
CCTAAGCAGA CAGCTACAGA TAAAAGGCCG GATGTCTCCA CAGTCAGCTA CTCTATGTTC 840
ACCTTATCAG TGATCAGTGC TGATTTACTG AGTGGGAGAC GACTACATAA TTGTCTGTTC 900
TCCTACTTGC TCCTTTTCTC TTGCAACATG TGGATTCAGT CATGTGACCA CATCCTCCCT 960
CTTTCTCTTC CAGCCTGCTT TTCCCCTTTA AATACTGAAG GCTTCAAAGT GATCTTTGAA 1020
GAAAAGCCCC GACCACATGC TGTTTCTGTG GTATCTGTGT TCCTTTCTTC CGGCCATGTC 1080
CTTAACCTTG GCAAAATAAA CTGCTAAGTT GATTGAGATC TGTCTCTGAT ACTTTTTGAT 1140
TTATACCACT ATACTTTCCA GTCTTTTTTC TTTTTTCTTT TTTTTTTTTT TTTTTTGAGA 1200
CGGAGTTTCA CTCGTTGCCC AGGCTGGAGT 1230
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