| Tag | Content |
|---|
EnhancerAtlas ID | HS180-03979 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:193324140-193325690 |
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 | CGAAAGGATT CATTTCATAT TAGAGTTTAT GCTAAAAATA AAGAAAAAAT ACTATGCAAT 60
TACACAATCT ATGTAATTAT TTTCTCACTA AATGTTAATT TATTTTTCTA CAATTAATGC 120
TTTAAGTCCT GAGATCCAAG CTCTTTACTG AATTCCTAGA CTGGTGTTAA AATTCTACCC 180
AGAATTTACA CGTCTTAACT TGAGTGTTGA GTCCCTGTGT AATCAATACA ATATTTGGTA 240
TGAAAATATT TGAACAGTTA ATACTCATCA TTTCCTGTAC CTAAGGTGAT ATTTAATGGA 300
TTGTACAGTA TGAGTCATGA TATTGTGCAA CAAGAATCCT TTGGACTTTG GACTCTTATA 360
GAGGAAGAAA CTCTTTCCAT CAACATGGCT TTAAATGACC CTGATGCTCT GGCCTCATTA 420
TCACAGAAAG CAGAACTCAT ATCTTGGCAG GAAACAGGAA AGAGAATGAG AATGTAAGAA 480
CAGAACATTC ACGTTAGAGA GAAAAAGAGA ATTTGGGAAG CTTGAAGTCA TTTCTGAGAG 540
TATTAGTTAG GATATAAACT GGGCTGCTGC AACAAACCCC TGTCCCAAAA GAGGGGGGTT 600
TAAATGAGAT AGAATTTTAT TTCTCACATA ATAGAGAGCA AGGTAGGTGA GCAGTTCAGG 660
GCAGGTGGCA TGTCCTGCTC AGTGAGACCA TCTAAGGATC CTGGATACTG GGACAGCTTT 720
GCCATCATTA ACATGTGACT TCTTTCTCTA GATGTCAAGC AGCTCCATTA GATGTCTCAT 780
TTCCCAGCCA TCAGGAGGAG GAAAGAGGGA ATGAAGAACA AGCTTCTTCC TGTGGGTGTG 840
ACCCAGAGGT TGTTCGTGTC ACTTCTATTC ACATTTGCTT GTGTAGAACT TACACAATCA 900
TACTTAACTT CAAGAAAGAT TGGGCAACAT AGTTTATAGC GGGGAGGATT TATGCCCTGA 960
AATTGATGGT GTCATCTTTT CATCTTCCCT CTCTCACCAT TAGCATGTAA TCTGTAACTG 1020
AATTTGAACA ATCCAACTTC CAAATGATTT CCATTTTTCT CCATATTCCT AACAACACTT 1080
TAGTCTAAAG CGTCCTCATC CTTGCCTAGT TTACTACAAT AACCTAATTG GTCAGCGTGC 1140
TTCCATTCTT GCCCCACCAA GTCATTTCTG ACACCGTGGC CGCTAATTCT TAAGAATAGA 1200
AACCAAATCA TCACTCTTCT TTAAGGCCTT TAGTGTCTAT TTCCATAGAA TAAAATCCAT 1260
ACCCTGCACC ATGAGCCGTA AGACCTGGCA ATGACCTGGC TCTAGTGTAC CCAGTGCTAT 1320
CCTTGCACCA TGCTTTCCAC CAGTCACTAT GTTCTGGCTT CTCTGGCCTC CACCTTTTTC 1380
TAGAACACAT TGATCCTTTC CCCACCTCAG GCCCTTATCC CTGCTATTCT TCATCCTGTA 1440
AAACTTTTGC TGGGATCTCC GCGTGGCTGG CTCGCCCTCA TCTCTTGGCA CTCAGCACAA 1500
ATGTCATCTA TTTTGAGAAT CTTTCCTGAC TGCCCTTTGT AAAGCAGCAT 1550
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