| Tag | Content |
|---|
EnhancerAtlas ID | HS101-03498 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:193323740-193325740 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:193324939-193324957 | GGAAAGAGGGAATGAAGA | + | 6.16 | | HNF4G | MA0484.1 | chr1:193324481-193324496 | TGGACTTTGGACTCT | - | 9.03 | | MEF2A | MA0052.3 | chr1:193324170-193324182 | GCTAAAAATAAA | + | 6.04 | | ZNF263 | MA0528.1 | chr1:193324936-193324957 | GGAGGAAAGAGGGAATGAAGA | + | 6.14 | | ZNF263 | MA0528.1 | chr1:193324933-193324954 | GGAGGAGGAAAGAGGGAATGA | + | 6.86 |
|
| | 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 |
| GH01I193355 | chr1 | 193324190 | 193325605 |
|
Enhancer Sequence | ATGCTAAGTA GTATTTTATA AATATTGATT AGATATGTTA CTGTTCTTTG AGAGACATTC 60
CACTTGAACA AGATATTTAA GGGTTCAATT TTAGTTATAA AATGGCATAA TTAAAATGTC 120
TTTCAGTTTA TTAGTTTAAC ATATTTAATA ATTGATAATA TTTGATAGAA CATTATCTAT 180
TTAATCCAAA ATACAGACTT AAATGCACGG TAGTGCACCT TAAATGTTGT GACTTTCCTT 240
GTTTACGAGG GGATAATTCT TATCATTTGT GTTGTTACCA ATCCCCAAGG AGAGCAACAG 300
CAGATTTTTG TGTGTGTGAA CTTACTTTCA ATACAATAAA TTCCTAGATG TAGAAAAGTA 360
ATTATAAATT GTATATACTC TGAATACAAC TAAAGTTAAC CGAAAGGATT CATTTCATAT 420
TAGAGTTTAT GCTAAAAATA AAGAAAAAAT ACTATGCAAT TACACAATCT ATGTAATTAT 480
TTTCTCACTA AATGTTAATT TATTTTTCTA CAATTAATGC TTTAAGTCCT GAGATCCAAG 540
CTCTTTACTG AATTCCTAGA CTGGTGTTAA AATTCTACCC AGAATTTACA CGTCTTAACT 600
TGAGTGTTGA GTCCCTGTGT AATCAATACA ATATTTGGTA TGAAAATATT TGAACAGTTA 660
ATACTCATCA TTTCCTGTAC CTAAGGTGAT ATTTAATGGA TTGTACAGTA TGAGTCATGA 720
TATTGTGCAA CAAGAATCCT TTGGACTTTG GACTCTTATA GAGGAAGAAA CTCTTTCCAT 780
CAACATGGCT TTAAATGACC CTGATGCTCT GGCCTCATTA TCACAGAAAG CAGAACTCAT 840
ATCTTGGCAG GAAACAGGAA AGAGAATGAG AATGTAAGAA CAGAACATTC ACGTTAGAGA 900
GAAAAAGAGA ATTTGGGAAG CTTGAAGTCA TTTCTGAGAG TATTAGTTAG GATATAAACT 960
GGGCTGCTGC AACAAACCCC TGTCCCAAAA GAGGGGGGTT TAAATGAGAT AGAATTTTAT 1020
TTCTCACATA ATAGAGAGCA AGGTAGGTGA GCAGTTCAGG GCAGGTGGCA TGTCCTGCTC 1080
AGTGAGACCA TCTAAGGATC CTGGATACTG GGACAGCTTT GCCATCATTA ACATGTGACT 1140
TCTTTCTCTA GATGTCAAGC AGCTCCATTA GATGTCTCAT TTCCCAGCCA TCAGGAGGAG 1200
GAAAGAGGGA ATGAAGAACA AGCTTCTTCC TGTGGGTGTG ACCCAGAGGT TGTTCGTGTC 1260
ACTTCTATTC ACATTTGCTT GTGTAGAACT TACACAATCA TACTTAACTT CAAGAAAGAT 1320
TGGGCAACAT AGTTTATAGC GGGGAGGATT TATGCCCTGA AATTGATGGT GTCATCTTTT 1380
CATCTTCCCT CTCTCACCAT TAGCATGTAA TCTGTAACTG AATTTGAACA ATCCAACTTC 1440
CAAATGATTT CCATTTTTCT CCATATTCCT AACAACACTT TAGTCTAAAG CGTCCTCATC 1500
CTTGCCTAGT TTACTACAAT AACCTAATTG GTCAGCGTGC TTCCATTCTT GCCCCACCAA 1560
GTCATTTCTG ACACCGTGGC CGCTAATTCT TAAGAATAGA AACCAAATCA TCACTCTTCT 1620
TTAAGGCCTT TAGTGTCTAT TTCCATAGAA TAAAATCCAT ACCCTGCACC ATGAGCCGTA 1680
AGACCTGGCA ATGACCTGGC TCTAGTGTAC CCAGTGCTAT CCTTGCACCA TGCTTTCCAC 1740
CAGTCACTAT GTTCTGGCTT CTCTGGCCTC CACCTTTTTC TAGAACACAT TGATCCTTTC 1800
CCCACCTCAG GCCCTTATCC CTGCTATTCT TCATCCTGTA AAACTTTTGC TGGGATCTCC 1860
GCGTGGCTGG CTCGCCCTCA TCTCTTGGCA CTCAGCACAA ATGTCATCTA TTTTGAGAAT 1920
CTTTCCTGAC TGCCCTTTGT AAAGCAGCAT GTCTTGTTCC CAGTGACTCT TTATTGCATT 1980
ACTTTATTTA TTTTCTTCAT 2000
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