| Tag | Content |
|---|
EnhancerAtlas ID | HS098-40114 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:134316970-134318440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr3:134317705-134317726 | GTTAACTTTCAGTTTCCTTTA | + | 7.14 | | IRF9 | MA0653.1 | chr3:134317709-134317724 | ACTTTCAGTTTCCTT | - | 6.15 |
|
| | 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 |
| GH03I134598 | chr3 | 134317599 | 134317823 |
|
Enhancer Sequence | ATTATTTTGA TGAAACACAA TACATTTCTT TCAGCCCGTA AAATCAAAGG TGTGCAAAAA 60
GGCTGTTTTC AGGGTGTAAA ACACCCCTCG TTTCCCTGTG GTGGTGCATA ACTATTATGC 120
CTCTGGGGCC TTTGTGCATT TTTCGGGCAT GAGTGACACG AGGCTGACTG GGTGGCCTTG 180
GCACCTTGTC TCTTTAGAGA AAAAGGAGAC AGTGCTTCTT TCCGATTCCC TATAAAAACC 240
AGTTTTTTGT TGAAGACCTG CCTTTCCCGC TAGTGCCTAA TACCAATTAT GTCTTTCCAG 300
AGATGGTGAG ATTGTTCTGA AAGGATTTCT TGGAAACCTT GTCTTAACAA CCCTATCGTC 360
CTAGTGTGAT AAGAATATAT GAATGGGAGG CCATTGTGGA CAGTAATAGG GCCGGGAGGC 420
TTCATCTCCC CATGGAAAGT ATAAGACACA AACAGTATAG CTGAGATCAT GAGGACCTGG 480
TTTGTAGCAG GTCGTGGGAA AGGAGAGAAG GTGGAGTTGG GAGAGCAGGT GGGAGGTGAG 540
ACACATCCAG AAGGGACTGG GTTTCATCAC CAGTGACTGC CATGAGTCTA ACTTAGTTAT 600
CTGGTTGGAT AGGGATGCAT TTACTGAACT GGGGACCCAG GAGGAGTTGG GAGTAATTTG 660
AGGGAGAGAA GTAACTCCAG TTTAGCATCT TTTGACTCGG AGATGCCTGT GGGACACCCC 720
AAAGAGGACA TCCCCGTTAA CTTTCAGTTT CCTTTAGTTC TGCTTGCAAA ATCAGACAGA 780
ACCAGCATCC TGTCAGAGGC TGTTCTTCCC CTTTGGTCCC TCTGCTGGGC TTTCTCCAGC 840
CCCTTGCCCT CAGGCAAGAG AGGAGCCAGC AGTGCAGTCT GCCAGGGGCT CCAGGGGCAG 900
GCTCTTAACA CAGCAGGGCC CTTCAGATGT TCCACAGCAG GGCCCTTCAG ATGTTCTGTA 960
ACTGACAACC CCAGGCCCAC TGCCTGCCAG CATCTGTTCA CAGAGACACG GCATCACAAA 1020
CTCTCCGGAC TGGAAGGGAC ATTGGAGGTC ATCCACTCCA GCTTTGGGGA TGGCATTTTC 1080
AGACTGTTCT AATAACTCAA GAGCTACTCC TTCTTTTGTG TGGAAGACTG TTTCTTCTGA 1140
CTTCCTCTTA ATATGCTGCC GGGTCTCCTT CCTAAGGAGA AGCATGCTGG GCCTCGTTTT 1200
TGTGGATCTA GCAGCGAGAG ACATGACGAA GCCAGATTTG GGAACACAAG TTCTTTTTGT 1260
CCTTCACACT ACAGCTACGA GAATGGTCTC CATGGTTACA GCAGCTTCTC AGAAATGTCT 1320
GGATTTTTCA TTTTCTGTAT TTCTCTAAAT GTCTAGTTTA TGAATAATCT GCTTAGGTGA 1380
CCGGCTGGAA AGTTTCTGCA TGTATATGAA TATCAAGAAG TACATATTTA TATACATTCA 1440
AAAGAAAAGT AGGCTGATAG GCATTTTTGG 1470
|
