Tag | Content |
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EnhancerAtlas ID | HS017-02814 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:206925910-206927760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:206926002-206926020 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr1:206926160-206926178 | TCTTCCTTCCCTCTTTCT | - | 6.16 | EWSR1-FLI1 | MA0149.1 | chr1:206926132-206926150 | TCTTTCTCCCTCCCTTCC | - | 6.23 | EWSR1-FLI1 | MA0149.1 | chr1:206926140-206926158 | CCTCCCTTCCATCCGTCC | - | 6.54 | EWSR1-FLI1 | MA0149.1 | chr1:206926156-206926174 | CCTTTCTTCCTTCCCTCT | - | 6.56 | EWSR1-FLI1 | MA0149.1 | chr1:206926144-206926162 | CCTTCCATCCGTCCTTTC | - | 6.64 | EWSR1-FLI1 | MA0149.1 | chr1:206925998-206926016 | TCTCCTTTCCTTCCTTCC | - | 6.82 | EWSR1-FLI1 | MA0149.1 | chr1:206926148-206926166 | CCATCCGTCCTTTCTTCC | - | 6.86 | EWSR1-FLI1 | MA0149.1 | chr1:206926095-206926113 | TTCTCCTTCCTTCCTTCC | - | 7.67 | EWSR1-FLI1 | MA0149.1 | chr1:206926152-206926170 | CCGTCCTTTCTTCCTTCC | - | 7.8 | EWSR1-FLI1 | MA0149.1 | chr1:206926099-206926117 | CCTTCCTTCCTTCCTTTT | - | 7.95 | EWSR1-FLI1 | MA0149.1 | chr1:206926006-206926024 | CCTTCCTTCCTTCCTCTC | - | 8.32 | IRF1 | MA0050.2 | chr1:206925920-206925941 | TCTCTCTTTCTGTTTTTCTTT | + | 6.37 | MEF2A | MA0052.3 | chr1:206927004-206927016 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr1:206927004-206927016 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr1:206927002-206927017 | CTACTAAAAATAGAA | + | 6.57 | SOX10 | MA0442.2 | chr1:206926085-206926096 | TTCTTTGTTTT | - | 6.62 | ZNF263 | MA0528.1 | chr1:206926095-206926116 | TTCTCCTTCCTTCCTTCCTTT | - | 6.07 | ZNF263 | MA0528.1 | chr1:206926002-206926023 | CTTTCCTTCCTTCCTTCCTCT | - | 6.14 | ZNF263 | MA0528.1 | chr1:206925998-206926019 | TCTCCTTTCCTTCCTTCCTTC | - | 6.37 | ZNF263 | MA0528.1 | chr1:206926048-206926069 | TCTTTCTTTCTTTCCTCCTTT | - | 6.39 | ZNF263 | MA0528.1 | chr1:206925994-206926015 | TCTTTCTCCTTTCCTTCCTTC | - | 6.76 |
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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 |
GH01I206753 | chr1 | 206926556 | 206926809 |
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Enhancer Sequence | CCTCCCTCTC TCTCTCTTTC TGTTTTTCTT TCTTTCTTCT TTCTTTGTTT CTTTCTCCTT 60 CCTTCCTTTT CTTTCTTTCT TCTTTCTTTC TCCTTTCCTT CCTTCCTTCC TCTCTCTTTC 120 TTCTTTCTTT CTTTTCTTTC TTTCTTTCTT TCCTCCTTTC TTTCTTTCTT CTTCTTTCTT 180 TGTTTTTCTC CTTCCTTCCT TCCTTTTTCT TTCTTTCTTC TTTCTTTCTC CCTCCCTTCC 240 ATCCGTCCTT TCTTCCTTCC CTCTTTCTTT CTTTTCTTTC TTCTTTTTTT TTCAGCGTCT 300 TGGCTCTGTC ACCCAGGCTG GAGTGCAGTG GCATGATCAC AACTCACTGC AACCTCAAAC 360 TCCCGGGCTC AAGCGATCCT CCCACCTCAG CCGCTCAAGT AGCTGGGATT ACAGGCATGT 420 ACCACCACAC CTAGCTAATT TTTTGTATTT TTTTTGTAGA GATGGGGTTT TGCCACATTG 480 CTCAGGCTGG TCTTGAACTC CTGAACTCAA GTGATCTACC TACCTTGGCC TCCCAAAGTG 540 CTGGGTCTAC AGGCGTGAGC CACTGTGCCC GGCCTCCTAG GAAACAATTT CTTGATGGTG 600 ATTTTCCATC TTTTTGCTGT GTAGGAAAGA GATTGAGCTC CATGGTAATA TGTGAGAGAG 660 AAGAGACTCA AGGGACTAAG AACCTGTACC ACAAAAGGAA GGTCTGTTTT GGAGATTTGC 720 TGGAGCTTCC CCATTGGATG TGTCATTGAA TGATGATTCA TCCTGGCCAA AAATAAAAGC 780 TTCTTAAGCT GGGTGACTCT AAGTTTGTGT GTGGTTTACG CTTGGACATG CGTTACTTTT 840 ATGACATAAA AGTGACTTCA ATCTGGTAAG ATATATTTAT AAACATAGAG GTCCTTTCAT 900 TTATTAGGAA ATTCCAATTG TGTTACGGGG TCTTCTCAAG AGATCTAAAT CTATTCTCCT 960 CTAAGATTTA GGAAATCTAA GCCGGGCATG GTGTCACTCC TGTAGTCCAA ACACCTTGGA 1020 AGGCCGAGAC GGGTGGATCA CTCAAGGCCA GGAGTTTGAG GCCAGCCTGG CCAACGTGGT 1080 GAAAGCCTGT CTCTACTAAA AATAGAAAAA TTAGCCAGGT GTGGTGGCAT GCACCTGTAA 1140 TCCCAGCTAC TTGGGAGGCT GAGACATGGG AATCACTTGA ACCTGGGAGG CAGAGGTTGG 1200 AATGAACCAC TACACTCCAG CCTGGGTGAC AGAGTGAGAC TGTCAAAAAA AAAAAAAAAA 1260 AAGTTTGAAG AAATCTGGAA TGATCATTTG TCCAGTATAT GAAACTCTGA GAATACTACA 1320 CATGTGGAAA CTAGAATCTA TCAGAAATTC CAGGATGCTC AAATATCTTC TCCCTCTCCT 1380 TCATTCACAA ATGATTTGAA CACTTATATT TTTCCTTCTA CTGCTTTCTA CTGATTTTCC 1440 TTCTACTGCT GTGAGTCTGA TGGGCTTCAA TACCATTGTG GTTGACTTAT CCAAATGTGA 1500 CTTTTCAATT CTGTGACTTT TATATCTCCA ATGACCTTTT CTTTGCCTCT ACACAGCAAT 1560 TTGCTCTAAC GGTTACAGCC TGGATTTTGT TATTCCTCAA AATGATACCA CCTCCAAAAA 1620 TCCCTTCATT TGAGCATTCC ATTCTCTTGC CACAGCCTCC TCTCTTTAGT GATTCAGATA 1680 CTCCCACTAC AACTCTTCCT TGACCTCATG ATCAACATGC TTCCTTTTCT TTTTTCAGCT 1740 CTCTCCTGCC TTTATTTCCT GCATTATTGA ACTTAGACTG CTTGGTTCAT CTTTTCATTC 1800 AGGCTCTTAG CTATACAGAC ATACCTTAGA GATATTGTGG ATTTGGTTCC 1850
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