Tag | Content |
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EnhancerAtlas ID | HS062-10959 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr22:50936260-50937490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:50936797-50936816 | CAGTGCCCCCTTCTGGAAA | - | 6.79 | EWSR1-FLI1 | MA0149.1 | chr22:50936898-50936916 | CCTGCCTTCATCCCTTCC | - | 7.36 | HLF | MA0043.2 | chr22:50937369-50937381 | TGTTATGTAATG | - | 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 |
chr22 | 50936625 | 50937431 | chr22 | 50936945 | 50937290 |
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| Number: 2 | ID | Chromosome | Start | End |
GH22I050497 | chr22 | 50936222 | 50936310 | GH22I050498 | chr22 | 50936578 | 50937500 |
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Enhancer Sequence | TTCCTGCTCG GCGAGCCACA CAGCTAGAAT CATCTCACCA GCCAGGGCCT CTGCCCGTGG 60 TTCTTGTGCA GCTCTGGAGA GCTGCTCTTC CCATCCAAAG GTCTTCGATC CCCTACAGTC 120 CACAGTTCCC AGTTCTCCCC TCCACGTGCA TGGAAGCAGG ACACCCCAAT CTCATCTCTT 180 TTTTTGTTTC TTTTAAGAAA CCAGGTCTTG CTCTGTTGCC ATGCTGGGAG TGCAGGGGTG 240 CAATTAGAGC TCACTGCAGC CTCGAACTCC TGGCTCAAGT GATCCTCCTG CCTCAGCCTC 300 CTGAGTAGCT GGGACTACAC GTTCAGGCCA CCACATCTGG CTACATTTTA AATTTTTTTT 360 TTTGTAGAGA GAAGCTCTTG CTATGTTGCC CAGGTGGTCT TGAACCCCTG GCCTCAAGTG 420 ATCCTTTTGT GGCTTCCCAA AGTGCTAGGA TTACAGGAGT GACCGCTGTG CCTGGTCGTC 480 TCACCTTCTT TTGACATGGA GCCCCAGCCT TGGGAGGCAG ATGCTGAACC GTGTCCACAG 540 TGCCCCCTTC TGGAAATTCT CCACAAGCCA AGGTTTTGGA CAGCTCCAAT GTCTGGGGCT 600 ATGGCATTTC AGGCGGGAAG TCTCTGCAGA GAGCAGTACC TGCCTTCATC CCTTCCTAGA 660 TATTAATTCA CTTTCAGACA CATACTGAGC AGCTAGTGTG AGCTGTTACG GTGCTGGCTC 720 TGCAGACAGA GCTGCAGCGA AGACAGACGC CAACCCCACC CTCACACAGC CAATCCTGTG 780 CTAGTTTTTT CTGTAGAACC ACCACTGGGT TTCCAGTTGG TCTGGGTTAT CTGGTGAACT 840 CAGAGACTTT CGCTGTCTTC TGGACACTCC ACAACAGTCC AATCACCTGC GGGGACCCTG 900 ACCTCTGCAA ACCTCCGGGG GGTGGTTCCT TGGTTGGCCG CCCTCCTCTG ACGGCTCCGC 960 CTCCCTGCCG AGCCCTGGGA TCGTCCTCCC TGGCTCCTGC CTTCTCTCTC ATAGGATCTC 1020 ATTTGTTCTG ACACACTTAT TCTCAAGCCC AGTAGTTACT CTTGAATATT GCTTATAGAG 1080 GTGTGTTTCC TTGAATATTC AAGCATATGT GTTATGTAAT GGGTAATAAT AAAGTAGGAA 1140 TGTGCATATA TGAATCAGCA CAAAATAACT AAAAAAAATC CCATCTCCAA AGTCACTGAC 1200 TATTGACAAA TTCTGGACCT ACTTCTCCGT 1230
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