| Tag | Content |
|---|
EnhancerAtlas ID | HS041-18599 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr7:134938590-134939690 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr7:134939110-134939125 | TGCTGACTCACAGTG | - | 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 |
| GH07I135253 | chr7 | 134938129 | 134940151 |
| Enhancer Sequence | GGTGAGAGGG ACATATCCTT GTGATCCCAA TGAATATCTC ATTGTCCTCT CAAGGGGAGC 60
CTGGCCTATG GGTGCCTGTG AGGCCTTGGG GCCACAGCTG TCCCTAGTAA CCCAGCTGGC 120
CTTTCAGCAG AGCTTCAGGG AAACCACACA TCAACATTTT CCCTCCATTC TCCCTGTTCC 180
ACCCAGGCCT AGATGGACTT GGGGAGAAGT GGGATTGTCA GAGGAGGGCT TTGTCCTCTC 240
CAAATCGACC TTACAGAGTG ACTCAAGTGC TTCTCAGCTG TGAGTGGAGT TTCATTTTGC 300
TGCAATTGGC TGGAAGACAC ATTCCTGTTT CTGTGCTGAG CTTGGACTGC AAAGACAACC 360
ATCGAGAAGC TGCCAGCCTG TCCTTGCCAG GCAATATTCA GAACTCCCTG CCCTGCTGAT 420
GGAACAGAAA AACAACCTAT TAAAAATGTT CCACTTCCCC TAGAAAAGTC AGGGGTTGCT 480
GCCAGAGGGT TCCTCATCCC GGGAGGAAGT GAGGGCTGCC TGCTGACTCA CAGTGAGTGA 540
GTGCCAGCTG TCCTACAGAC ACACAGCCTC TGTGCTCTAA GAAGCCCTTT GAAGCAGGGT 600
CCACATTGCA GGGCCTGGCT CTTAGCGGGC ATTCCTAAAT GTTGCACGAG CCCCTGCCAC 660
CTTTCCTAAA GGCTGAGCTA ACTCATCATC TTCTGAGGCC CTGCAATAAC AGTTGCTGTC 720
AGCTTTTGAA GGATTTTCAT GTCTGCTTCC AAACTGTGCT GCTTATGGTG ACATAAGCTC 780
GAGTCACACA GGGCTTCTCC CCTTGTCCCA GGCAGGCAGG AGGAAAAGAG CCTGCACAAC 840
AGGCCTCCTT TCTGCACCAG GGCTTGAGTT CCACGTTAGA CCCACTGAGC AGTGGCAACT 900
CAGTGAACTG AACTCAAGAT GTGCGGCGTG CTCCAGAGCT GCCTCAGCAG CCACAGTGGA 960
ACCAGAACTG TGGGGGCATT CTGCAGAAGA TTGAGGGATA GAGGAACTCT CGTTCCCTTG 1020
TTCCAGTGGC CACAGCTCAG AACACTAAAT TAGGGCACAG GAGCCAGTCT CACCACAGTC 1080
TCGATTTTCC AGGGGATTCC 1100
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