Tag | Content |
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EnhancerAtlas ID | HS042-42449 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr7:30595990-30597180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr7:30597078-30597094 | ATTTGTTTACATATTG | - | 6.15 | FOXP2 | MA0593.1 | chr7:30597079-30597090 | TTTGTTTACAT | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I030556 | chr7 | 30596175 | 30597260 |
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Enhancer Sequence | AAATTTAAGG AAGTGAGAGC ACAAATAAGA GAGTGAGAAA GAGCAGCTGG ATGTACAGAG 60 GACACATCAG GAGATAGCGG ATCATGATAC CATGAAAATC AGACTGTCAA GGCAGCATTT 120 TCTAAAAGAA GGGATGAGTA AAAGTAGGCT GGAAAATGCC ACTGGCTTGG GCACTAGGTT 180 GTGGTTGACC TTGGTGACAG CAGAGGCAGC AGAGGCCCGG CATGGCCTGG CCTCGGTGCC 240 TCTCCATGGC CATCTCCGGC ACCCTGGAGA TGCCATCCTC TGGCCATACT TGCCATTTCA 300 CGGAGCTGCC ACAGCTCTCA AGCTTCTCCA TTTTCCTTGA CCCATCCCAG TTTGTCCTCT 360 TGACCAACTC TGACTGATTC TCCAAAATTC AGCTCAACCT TAGGTCTCCA GGTCAGTTTC 420 TCCCAAAGAG GAGGAGATGC TCCCCACCCA GCCCTTTGTG TGTCCCTTCC TTTGATGACG 480 TGTGATTACA CTGTTTACTG TAAATGTCTG CCTCCTCCTC CAGTCTATGA GCTCCTTAAA 540 AACAAGGACT TAGCCTTTTG CATCTTTGTA TTCCAAGCAC TCAGCCCAGG GCCTGGCTCT 600 GAAATGAGCT CAGTGCATAT TAATGGATCA ATGCCTGGAG GGACACACCC GCTGATCTGA 660 TCCTTTTTTA GAAAAACACG ATCTGGTTGC CATGGCGCTG AAAGAGCGCT TTCTATACCT 720 GCTGTTTTCA GGATGAGCAA ATCACTTTCA GCTGACCACA CTGTGGCATC TGGCCAGCAG 780 GATCTGCAGA ATCCAGCAGG ATGGATGCTG AGCCAACTCT GAGATGGAAG AGACACTTTT 840 CCTCCTTCCG AGCAGGTAAA CTATTGAGTA ACATCAAAGA ATTTCATTTT TTCTACCCCT 900 GGAAGATTTA AAGGGCTCCT CTTTTGTCAA TATCCCCCTA GCTCTCCTGC CAGTTTTCTC 960 TCACCTCCTG TACAGTTTTT CTGTCTCCTT ATCTGCTGCT ACTCTAAGAC AGGGCTTTAG 1020 CCTATAGGCC AAATCTGGCC CACCACCTGT TTTTGCAAAT AAAGTTTTAT TGGAAGACAG 1080 CCATACCCAT TTGTTTACAT ATTGTCTATG GCTGCTTATA CTCTACAATG GTAGAGCTGT 1140 GGCAGAGATT GCATGCCTGC AAAACTGAAC ATATTTACTA TCTGGCCCCT 1190
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