Tag | Content |
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EnhancerAtlas ID | HS043-04526 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:245673000-245674510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:245673962-245673980 | CCCTCCCTCCCTCCCTCC | - | 6.03 | ZNF263 | MA0528.1 | chr1:245673966-245673987 | CCCTCCCTCCCTCCCTCTCTC | - | 6.11 | ZNF263 | MA0528.1 | chr1:245674260-245674281 | TTTTCCAGCCTTTCCTCCTTC | - | 6.48 | ZNF263 | MA0528.1 | chr1:245673962-245673983 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 |
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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 |
GH01I245510 | chr1 | 245674103 | 245674502 |
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Enhancer Sequence | ATCTTTAGTG CAGATGACTG GGACTCCACA TGGAGAAACA CAGGTGAACA GGGAGGGTTG 60 GAGAGACCAC TCAGGAATCA GTCACAGGTG ACCTTGTGCT TCCTGCTACC ATGGCTGCCC 120 CTCCCAGCCT GCCTCACCTG TGCCTTTCTC CCTTCTCCCT TCCTGCCTTC AGCTCCTCTG 180 TTGCTTCTTC TTCCTTAAAC ATCTTCACCG GTTCCTGTGC TATTACAGAG CCCCGTCTGT 240 GGGTCTCATG TCTCTGCTCC ATGCCACGCC CTCCCTTGGG CATCATCTGG GCTTTGGCTG 300 GGTCTGTGGA GGGTCCTGGG CTGCAGTGCC ATGAACAGTG GAGTGGGGCA TGCGAAGTTG 360 ACAGTCACAC TGAAAGCTCC TGCCTCGCCT CTCTACCTTC TTCTCTTTTG GGGGTTTCTT 420 TCCTGAGGCA GGGAAAAAGA AACAGGAACC CAGACCAAAC TGAGGAAAAC ACGATCAGAG 480 ATGAGATGGG GTCAGAGGCA AAGGGCTGTT TGTTGGGTTT GCACTTTCAT TACTGAGAGC 540 ATTGGAATAG TTTTAAGGCG TGCAAACTGT GAGACTAGAC AATTTCACTT AGAAAATGAA 600 ACGTGCATGC AGATGTTATT CTCATGGGGA TATATATCTG CATCTGTTTG TCTACAAGTG 660 TTCCCTTGCA GAGTCACAGA CATATACAAA ACCTGGGTTC CATCAGCTTT GTCTGCACAT 720 ACGTGGCTAA ATGTGTACAG GGATGTACAA TTAAAGATTT TAAACACTTG ATTTTGACAG 780 TATATTTTGC AGCTGCTGTG CCAAGAACCC TAAGCTACTG TGGGTTAATT GGAGTTGTAG 840 CAAGTATTTC TTTCTCGGCT GTCTCTTTTA GCAGAGCTTC TCTCTCTCTC TCTCTCTCTC 900 TCTCTCTCTC TCTCTCTTCC CCTCTCTCCC TGTTTCACCC CTCCCTGCCT GCCTGCCTCT 960 GCCCCTCCCT CCCTCCCTCC CTCTCTCTCT CTGAGATAGC AGACACCAGA GTGAAACTGG 1020 TGCAGCTTCC TTTGAGAAGC GTGCTTGCAT GTGCGGATTG GCAGGATTGT GTGAGCTCCT 1080 CTCCCATCCA TGCACTGTTC TTGGAGGGAA ATGCAATGTT GGAGCAGGGG CTGAGCTGCA 1140 CTGGGAAGGT GGCTGGGAGC TCAGTGAGGC CAGGATCATG GTTTAGCCAA AGGCTGGAAT 1200 CACAAGAATG TTTCACCAGG GTCTGCTCTG AGAGTTCTCA GACCCCCATG GATTTTAGAA 1260 TTTTCCAGCC TTTCCTCCTT CACCTTCGCA CAATTTTACT TTCTCCTGAG ATGGCCCCAG 1320 ATCTGCAAGA GACATTTGAG AGAAGCTATT TATTAGCAGA CGTGAAGAAA TGGATTCTGC 1380 ACTTGATTAT TTAGCCATGA CTTATCAATG ATGATGGATT GGAAAGCAGT GTAAGTAACG 1440 CAGTTATATA TGTTGCTGGA GTTAGGTGGT CTGTTTTCTT GCTATTTTTT TTTTACTTTA 1500 ACTTTTTCAG 1510
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