| Tag | Content |
|---|
EnhancerAtlas ID | HS048-29538 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:72839810-72841020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr5:72840667-72840677 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr5:72840667-72840677 | GTCACGTGAC | - | 6.02 | | Foxq1 | MA0040.1 | chr5:72839994-72840005 | CATTGTTTATT | + | 6.02 | | MITF | MA0620.2 | chr5:72840663-72840681 | AACAGTCACGTGACATCT | + | 6.12 | | MITF | MA0620.2 | chr5:72840663-72840681 | AACAGTCACGTGACATCT | - | 6.12 |
|
| | 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 |
| GH05I073544 | chr5 | 72839836 | 72841520 |
|
Enhancer Sequence | CAGTAAACTA TAGTGAAGGA GCCCAGGGAA TTTCTGAGGC ACTCTGACAT GCTGATATTT 60
TAAATTTAAG ACTCTTGAAG GTCAGCAGAT GCTGCAAAAG GCTCTCCTCT GATATACCCT 120
TATCAACCTA AGACTGGACC CACCAAAGAG AGCTGAACTG CATCCCATCT CCTCCCTGGA 180
ATCTCATTGT TTATTGCAGA AAAGAAGACT GGGGAATGCA ACCACGCCCA GATGGACATT 240
TCACATAAGA CACGGATTGA TGCATTGGAC TTCTCCCCAA ATAGGATGCT GTGTCAAAGC 300
TGACCAAGTA TACAATGCTG TCCTTGGGAG GACCCTATAG CATCTCATCA TTGTAGGTAT 360
GGCAACATTA TCTTTCAAAG AAGAATCTAG AATGGCACAA GGAGAATGGC TTATTCTTTT 420
TAGAGGGCAG CAAGGCCAAT CTCTGTCTCA ATTGGGTGGG CAGGCTCTTC CTTAAATACC 480
TACAACCTGT TCCTGAAATA GCTGAGAGAC CTTCAAGGCA GGGGCTCACT GAGAGAGGGG 540
TGCAAGCAAT TGACCTCGTT GTTGCTGACA GTCTCCTTGG CAGAGGGGCA ACACCAGGAC 600
ATGAAAGTAA GAGGAGAGAG ATTTCATAAC AGACATGCAT CATGGAGGAG GGGTAACCTG 660
GCCTTGTGGA TAGACTCTGT GAGCTGGCAT GAGTTCTGGA AGGGCGGTGC TTCAGTCAAC 720
ACTGGTGTCC AATGTTCAAG GAAATCCTAG AACAAAGGAA TCACGAGACA AGCTCTTAAG 780
CGTTTGTTGG TACAGACTGC TGTACTGGAT GTTCAGGACT CTTTTTTTAT CCAGAAGATA 840
AACAAGGGAA GCAAACAGTC ACGTGACATC TGAAGTGGGC TCTCTTTCAC ACACAGATTC 900
ATAAAGGATG CTCAACCACA ACAAGCAATT CATTGAGTAA AAAAGGTGAA TTAGTAACTC 960
ACGGTAAAAT TACTGTTTCA GAATTTCTTG TTTTGTCATG TAGGCTTAAA GGGGAACATG 1020
TTCATCTTTA CAAAAGCATC ATAGCAAGCG CCAACAGGCC AGAGACAAAG GATAAATGAC 1080
TAAGTTCTTT CATAGACAGG ATGGCGATGC AAGAGGCAAG TGTGAGAATG TGGCTTGTCC 1140
ACCTGCCAGG AGATGATTGC CGCTAGAGCA GGGGTTCCCA GCCTTGATGT ACATTAGAAT 1200
CAACTGAGAA 1210
|
