| Tag | Content |
|---|
EnhancerAtlas ID | HS060-20607 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr2:203037070-203038240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr2:203037976-203037987 | AGAGATAAGGA | - | 6.02 | | HES2 | MA0616.2 | chr2:203038157-203038167 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr2:203038157-203038167 | GGCACGTGCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCTTTGAGT TGTGATGCCA TCCCTGTGTT TCTGAGAGGA AATAGTAAAA AGTCAGGGAA 60
ACATCACGAA ATTATGGCAG TATGTTTTTT AAGCCAGCAT GAATCTTGGA GGTGATCTAG 120
AAGTTCTTTT ATATTATGGA TGAAGAAACC TGAGGCCTAC AAGTCAAGAG AATCGTGCAT 180
GACAACTAAT TATTAAAACC AGGGTAACTG GAGTCTGCCC AGTGTTAGTG GTTATCTAGT 240
TCAGTTCAGT TCCGTTCAGG TCAGTTTCGT TTTGAAGACT TTTCCTTGGG CAGTTTCCAG 300
CTTCAGGAAT AAACAGCTCC AGAAGGAGCA AGTGTAATGA TTGCCTGACC TGTGCAAAGA 360
AGTGAGGAGT AGCCAGTGCT GGAAAAGTTC CTCCTAACAC TGTGGAGAAA ACAGGGAGAC 420
CAGAAGTGTG TGCCCAGGAG TCCTGGTGGT GCCACTCACC AGAATCTACA GCCTGGAAGA 480
TGGCACCATG CAAAGGTCTG GGGCTCCTTG CTCCCCACAT TGCCCAGTAT GATGCCTGCA 540
CAGTCATGGC ACAGCACACT GCCAGGCCCT GCTATCTGCA GCCTGCAGTA CTAGGTGCAA 600
AATATTCTGC TAGTCCTTAG CACCTACATG ACCTAACTCT GGTACTGCTC TATTTTTCCT 660
CTGGGAAGTA TTTCAAAGTT CTCCTTCATA TTGGAAGAGG AGGAAGTAGG AAGTGGTGCA 720
CGCTTAAGAA TGTTTCTGGT TTACTCCTAC ACAGCCCAGA CTGGGGAAGT CCCCCGGGAA 780
GTCCCCCAGA GTCCCAGAGA ACAGCAGTCG TCCCTTGATT CTGAAAATTC TCTTCACCTT 840
CCAGGAAGAA AAGCTCATTT CTAACAAGAG ACCTAAATTT GTCAAAACCC AAAAGCAGCT 900
AAAACTAGAG ATAAGGACAA CATAAGAAAG GAAAATTATA GGCCGGGCCT GGTCACTCAC 960
GCCGGTAATC CCAGCACTAT GGGAGGCCAA GGCGAGCGGA TCACCTGAGG CTGGGACTTC 1020
GAGACCAGCC TGACCAACAT GGAGAAACCC CGTCTCTACT AAAAATACAA AATTAGCTGG 1080
GCGTGGTGGC ACGTGCCTGT AATCCCAGCT ACTCAGGAGG CTGAGGCAGG AGAATCGCTT 1140
GAACCCGGGA GGCAGAGGTT GCAGTGAGCC 1170
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