| Tag | Content |
|---|
EnhancerAtlas ID | HS095-24150 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr5:72839900-72841270 |
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 | GCTGCAAAAG GCTCTCCTCT GATATACCCT TATCAACCTA AGACTGGACC CACCAAAGAG 60
AGCTGAACTG CATCCCATCT CCTCCCTGGA ATCTCATTGT TTATTGCAGA AAAGAAGACT 120
GGGGAATGCA ACCACGCCCA GATGGACATT TCACATAAGA CACGGATTGA TGCATTGGAC 180
TTCTCCCCAA ATAGGATGCT GTGTCAAAGC TGACCAAGTA TACAATGCTG TCCTTGGGAG 240
GACCCTATAG CATCTCATCA TTGTAGGTAT GGCAACATTA TCTTTCAAAG AAGAATCTAG 300
AATGGCACAA GGAGAATGGC TTATTCTTTT TAGAGGGCAG CAAGGCCAAT CTCTGTCTCA 360
ATTGGGTGGG CAGGCTCTTC CTTAAATACC TACAACCTGT TCCTGAAATA GCTGAGAGAC 420
CTTCAAGGCA GGGGCTCACT GAGAGAGGGG TGCAAGCAAT TGACCTCGTT GTTGCTGACA 480
GTCTCCTTGG CAGAGGGGCA ACACCAGGAC ATGAAAGTAA GAGGAGAGAG ATTTCATAAC 540
AGACATGCAT CATGGAGGAG GGGTAACCTG GCCTTGTGGA TAGACTCTGT GAGCTGGCAT 600
GAGTTCTGGA AGGGCGGTGC TTCAGTCAAC ACTGGTGTCC AATGTTCAAG GAAATCCTAG 660
AACAAAGGAA TCACGAGACA AGCTCTTAAG CGTTTGTTGG TACAGACTGC TGTACTGGAT 720
GTTCAGGACT CTTTTTTTAT CCAGAAGATA AACAAGGGAA GCAAACAGTC ACGTGACATC 780
TGAAGTGGGC TCTCTTTCAC ACACAGATTC ATAAAGGATG CTCAACCACA ACAAGCAATT 840
CATTGAGTAA AAAAGGTGAA TTAGTAACTC ACGGTAAAAT TACTGTTTCA GAATTTCTTG 900
TTTTGTCATG TAGGCTTAAA GGGGAACATG TTCATCTTTA CAAAAGCATC ATAGCAAGCG 960
CCAACAGGCC AGAGACAAAG GATAAATGAC TAAGTTCTTT CATAGACAGG ATGGCGATGC 1020
AAGAGGCAAG TGTGAGAATG TGGCTTGTCC ACCTGCCAGG AGATGATTGC CGCTAGAGCA 1080
GGGGTTCCCA GCCTTGATGT ACATTAGAAT CAACTGAGAA GGGATTGTAA GTCCCCATGT 1140
GGCAGCCCAG GCTAATCAAA TCAGACCATC TGGAGATAAG GCCTGGCTTC AGTATTTTCA 1200
GACCTCTCCA GATGATTCCA CTGAACATCC TAGGCAGAGA ACCAATTCCC CTTGGAGTGG 1260
AACTTTCTTC CACCACTGTA AGGTCTTCAG TCCTCTCATT CTCAGGAGAG AGAGGCTTCT 1320
GTTGAATCAA TTGATGTTGA TACAGCAGAA CAATTAGCAT AGAAGAAACC 1370
|
