| Tag | Content |
|---|
EnhancerAtlas ID | HS136-01835 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:229300600-229302430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr1:229301236-229301253 | AAGGGCACTCTGACCTT | - | 6.02 | | ESR1 | MA0112.3 | chr1:229301236-229301253 | AAGGGCACTCTGACCTT | + | 6.08 | | ESR2 | MA0258.2 | chr1:229301237-229301252 | AGGGCACTCTGACCT | - | 6.98 | | EWSR1-FLI1 | MA0149.1 | chr1:229301002-229301020 | GGACAGAGGGAAGGAAGT | + | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr1:229302233-229302248 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH01I229164 | chr1 | 229300122 | 229301890 |
|
Enhancer Sequence | CTTGGAAAAT GTGGTTGGGA ACTAAAGATA GGACCTAGGG CAGAGACTGG ACTGGGGCCA 60
GAGAGAATAG GGCCAGGAGC CAACCAAGAA GTCGTTGCAG AGGTCTGAAC TCCAGATTGT 120
TAACAGATAG AAAGGAAAAA GCAGAGACGC AAGGGCAAGA GAGGAGCAGA GGGAAAACCA 180
AAGCGTCAAG ATCGAACTTC TGTGGACCCA TTGAGCACCC AGGGTCCAGG GCCGGGGCCA 240
CCCAAGGGCC AGATCTGCCT TGAGGTGCCT GTCTCCGACC AGAGGGAAAC TCCCATCAGA 300
GCAGGTGTGT TTTGTTTACC AACATCCCCA AGAAGCATTC CGTTCCTCTC ACACCCTTAC 360
TGCATTCCCT CTGTGTCTCT AGATCGCAGG AGGAAGAAAA AGGGACAGAG GGAAGGAAGT 420
CCCCTTAGCT GCTGTAAGAG ATTGGTACAT TTTGTCATTT CTCTGAGCCT GTTTTCACAT 480
CAGCAAATGC AAACAGTGAC CTCCTCCAGT TGTTAGGGGA ATTAAATTAG ACAATGAAGG 540
TGTCCAGAAA ACAGCACCTC AAAATACACC ATGTTGGCAT GTTGATGGTT TTAAGTCAAA 600
GACACAAAAA ATAACGACAG CAGCGGCAGG CACAGGAAGG GCACTCTGAC CTTCTCTAAA 660
GCAGAATGTG AAACTCCCAT GTGGAAGGTG TCTCTGCTTA CTCATAGCTC AAACAATGGG 720
CCATTTTTCA CAGTGCTAAG ACCTGAAATG TAACTTGTTC TACATTAAGT TTGAGGTCTC 780
TAGGCCCTTT ATCTTCTGGC AATGTTTTGT GCCACTGTGA CCTCATAATG TTAATGTTGG 840
GAGAGACTGC GTGGCCCATC AGTGCAGCCC GATGCCTGCC CATTCTCCAT TAACTCACCC 900
CATGCTCGTG GAGACTTTAT TGCATGCTGG ATGCTGTGGT CTCCACGGGA AACGCAAACG 960
TGAAAATGAC CAGATTCTGC CTGAAGTTGC TCATAGACCA ATAAATCTAT GTTTACCATT 1020
CTGTTGGGTT AAAAAGGGGA AAAAGCCCAC TCTTGTCTCC AAGCTCCTTC TTCAACTGTG 1080
AAACGAAGAG GAATAAGTCC TGCGCATGAA TCTGTGGTTT GATCCAATGA GCCCTAGAAG 1140
CTCAAGTCTG CTTTGAGGAG GGCTAGGACA TCAGATGAAA TGCAAAAAGG AAGTCCTCAG 1200
AAAAAAGTAA TTGTATGTGT GGATGGGGTG CATGGGTGTG TGAGTGTGCA AGAGAGAAAG 1260
TGCACACACT CAATCCTCCA ACACCAACCA CAGAACAAAA TGAGCACATC TCTCTCTTGT 1320
CCCCTCTGCC TAGTGCAGGG CTCCTCACTC TCTGTGACCT CGTGTAAGTA GAAAGAGCAT 1380
CAGGTGGGAG TCAGGCCACT ACCACGCTGT TTTTTTTTTT TTTTTTTTTT TTGAAACAGA 1440
GTCTCACTCT GTTGCCTGGG CTGGAGTGCA ATGGCGCAAT CTTGGCTCAC TGCAACCTCC 1500
GCCTCCTGTG TTCAAGAGAT TCTCCTGCCT CAGCCTCTCG AGTAGCTGGG ACTACAGACA 1560
TGCACCACCA TGCCAGGCTT ATCTTTGTAT TTTCAGTAGA GATGGGGTTT CACCATGTTG 1620
GCCAGGCTGG TCTTGAACTC CTGACCTCAG TTGATCTCCT TCCTTGGCCT CCCAAAGTGC 1680
TGGGATTATA GGCGTGAGCC ACCGAGCCCG GCCCAAGTTT TCATTCTTGG ACCAGCCACT 1740
TCAATTCTTT CAACCCCAGG GTCCTTGTCT AAAAGGTGAG ATGTATATAG CGTTTATGGA 1800
AATGAGCAGA AACATTTTCA CGGAAAGGAG 1830
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