Tag | Content |
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EnhancerAtlas ID | HS099-01937 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:209491660-209492750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:209491848-209491859 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr1:209491848-209491859 | AGTGACTCATC | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 209492000 | 209492600 | chr1 | 209491844 | 209492000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I209318 | chr1 | 209491557 | 209493106 |
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Enhancer Sequence | AGAATTCAAC TCCAAAGCCA ACCTATGTTA TCAGACTTGT TCTTAGAAAT TCATCTTTTC 60 AGTATACCCT TATGTTATCC CAGATTTAAC TCAGAAAGAA TTTAGGAGAT GAGGCTTAGC 120 TTTATAATGT CATTTATGCT AGGATCCATG TAAACAACAG ATGTCTCTCT ACTATTCCTG 180 TCACTCAAAG TGACTCATCA TAATTTCTCC ACTTTATAAG ACATGGTTCC CTCATCCTCA 240 AAAAGAGAAC AATAAGAATA TAGCCCAGGG TATCATGGGG CTCGGTGGGT TGCAAAGATG 300 TACAACATTG CACAGCATTA TAAATGCTCA GGGAACCCAA CCTTAGTGAT TGAGAGTCCC 360 TGTGCTCAGG AGACAGTGGA GATTCCAGAT CTCAATCAAC CTTCTACTTC CTAGCCTAGA 420 AAGAAATTAA GGCACCACCC CCCTCAGCCG CCCCGGGCAA ATAAATGACC TGTGGGAAAC 480 CTGAGACTCC TAGAGGGTGG GGTTAGCTCA AGACTATCCT CCCAATTTCG GCCTCAGGGA 540 AGACCTCCTC TCGGGTCTCA TAGCCTTGTT TCCCCCACCT CTATTTGTAT CTCTTCCTGG 600 GGAAAGACGA GTGCCAAAGG CAGGATATGA ACAAGTAGTT GGAAAATCGT GACTCAAGCA 660 TAAGTCATTC TCCAAACCCT GAAAAACCCT TCCTATCACT TCTACTCTCT TCTTTTTCAT 720 GATTCCTCAG GGAAAAAAAA AAAAAATTAT TGGTTCAATG TCATGGAAAG AATCTGGTAT 780 ATTTTATTTT ATCAAAATGG TTTTGAGATT TGGGGCAAGA AGGAGTCACT CACACATTTC 840 TGAGGATCCC AAAAGTTTGG ATCATGCCTC CTCTGTGGCT GGTCCCTCCC TTCTCTCTGA 900 AGAAGCTCAG TGCCTACCTC AGTGTCAGCT TCATTCAGTC AGGTGTCATT TTCAATGCCA 960 TGTCATTTGG GCAGGGCTGT CAGTCTTATT AGGATTGTTC TCCTTGGCAC TGGCAATAGC 1020 CTATGTCGTG CTTCTCCCAG CAAACAGCCT CAAGACTGGA CAATCACACC TTGCCGAATA 1080 ACTTGAGCTG 1090
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