Tag | Content |
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EnhancerAtlas ID | HS043-01714 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:67017600-67018940 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr1:67018471-67018482 | TTTGTTTACAT | - | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_38944 | chr1:67017597-67019248 | IMR90 | SE_44891 | chr1:67018409-67020310 | NHLF | SE_46320 | chr1:67018309-67020421 | Osteoblasts |
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| 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 |
GH01I066552 | chr1 | 67018556 | 67020310 |
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Enhancer Sequence | ATTCTGCACA ACTTATCAGT GTACCAGGCT CTGAGTGAGG GGTTGTATAA ATGGTGGATC 60 ACCTATCTCT CACCATACCT CTATGAGGAG TAGTCTTAAT CCCATTTGAT AGATGAAGAA 120 ACTGAGGCTC AAGATCCCAT GCACGGCTAG GGAGTAGCAG AGCAGGATGG GACCACCGGG 180 TCCTAGCTGG TGTGATCTCT GAACCACTGT GTTTACCACC AGGCATCATG ATGGGCTTGT 240 TAAGAAAGCT GAGTTGGAGA GGTTCTTGTC CCTTGTCATG AGCGGAGACT TTATGCGGAG 300 CTGCTTGATC ACTTCTCATC AACTCCTCTG AGTTCTTGGA CATGCCCACT TTGTTGGCTA 360 TTGGCTATGT ATCTGAAAGA GTCTTTACAG ACTTCAGAAA ATTCATTTAA CAACACAATT 420 TCTGGGGCTA TGCTACCCTT GATGCTTCCA CCTCACCTTT CTTTTCTGCA CTGTGTGCTC 480 ATTTGCGCCA TCACACTGCT CCCCCTTTTC TTCTGCTCTC TTACCTGGTT GGCATAGTGC 540 TGCTGCTGCT TCCTGTGTTA CTCCTGTTCT GTGGTCTCTG CCTTTGTTCT TCCCTCACAC 600 AGGCAAGTTT ATATAGCAGC AAAGCATTGA TAAGACAGCA GCCTTTTGAG CTAGGCTGCT 660 TGACTTTACA CCTTAACCCA ATTTCACTTA CTACTCCACT ATTTTGGCTA ATTTACTTCT 720 CTTCTCTGTG CCTCTACTTT CTGTTTTCTC AGCTTTGAAA TCAATACCTG TCTCATGAAG 780 TTATTTTGAG GAATAAATAA GTTAACATAT ATAAAGTACA TAGCTTAGTG GTTGCCACAT 840 AATAATTGCT CGCCTAATTA ATCTTCTTTT TTTTGTTTAC ATTTCCATGA TAAGAGGTAA 900 TTTACATCAG GAAATCCCAT TATTTGGGTG AGAGAGAAAA CGACTTCAAC CACTATAAGG 960 AAAACGCTTC CTTCAGGAAG AAAAAGCAGA TAAGTTTTCC CTTTAAGGTG CTTCTCATTC 1020 CCTAATTTTC AAGCTCCCCT TGGCCACAGC AGTGAGTTGG CTGACTGCCA CTGGGACCTC 1080 AGAGACCAAC ACATCAGCCA AGTTTTGTTT TTCTCTTAAC TCTTGCACTT CCCATCTCCC 1140 CAACTCCCAG CTGCCCTTAT TCACAATGCT GGGACGACAG CTCCATGTTT GGGTCACGGT 1200 TGAACTGGGT CTTGCAGTCT TCAGCGGGTA GGCAGAAAGC TGGGGGAATG GTGGCTTCCT 1260 GTTCATTTGC ACCACAACAG TCAGGCACTG GGGAATAGAT GATAACTTTA TATGCATGCG 1320 GGGAACAGAG ACAGTAAAGA 1340
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