| Tag | Content |
|---|
EnhancerAtlas ID | HS053-20872 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr2:46635800-46637190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr2:46635888-46635899 | GAGAGATAAGA | - | 6.32 | | TEAD1 | MA0090.2 | chr2:46636880-46636890 | ATGGAATGTG | - | 6.02 |
|
| | 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 |
| GH02I046406 | chr2 | 46633865 | 46639478 |
|
Enhancer Sequence | AGAGGCTGGG CATCTGGGGC TGGGCAGAGG CTGGGCATCT GGGGCTAGGC AGAGAGGCCT 60
GGGCTGGAAG CTCTCTGTCG AGCCACAGGA GAGATAAGAC TGAGATTGGC AGGGAGTGTG 120
AGAGAGTGAG GAAGAAGGCA AGGCCGGACC ACGAAGAAAG GGGCTGTCAC AGAGGGTGAT 180
GGGTAGGCAG AAGTCCAGCC AGCCAGGAAC CCATCCCAAC CCCGGGATCC AGCAGGAGCC 240
TTCCTCAGCC CTCTCCCCAG CCCACAGGGA AGGAGTCCAG CCCTAAAACT TGGCCTTTTG 300
CCTACCTGCC CTGCCCACAG AGCACACACA GGCGGCCTGG CCCTCCTCCC GCGCCTAGAG 360
CTGGTTGCAC AACCACCTGA GCTGGTGAGG CAAGGATAGC GTTCCCTTCC TCCCCAAGAG 420
GAGTCCAGAG GCAAGGGTTA AAAGGATTAG GCTCAGCTTT GGGAAACAAA ACCAACTCTA 480
AGTGGAAAAA CACCAGCCCT CGCTGGGCTA TTGTGAGGCG CAGTCATGGT TCCCAGTCCA 540
TATGTGGACA GGGCCTAGGA TCTGTTGACA AAAGTGACTC AGGCGTTTAC CTCAGGCCCA 600
ACGCCCGCTG GCCCAGGTCC CGTCTGGGTG TGTCATTGGC TCAAGTGAGG TCCCATGAAT 660
ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACACTCTGGA GCCAACTCTC 720
TGAGTTACCC AATCCCAGCC AATTCACCTG AAGCACCTGG CATTTCTTTC ATCACCCAAC 780
AGGTCATTGT GCTGAGCTGT CAGTGCAGAG GAGGCTTAGC TGGCTCCATC ATTCACATCA 840
CAAGCTTCAT AAATTCCTGA GGAGAGTGCC AAAGGCCGAG ATTGCTGCAG CACTTTCACT 900
GGGGGAAGAG GAGAGGCTAA GCAGGCAGGT GGTCAGGGAG AGCCAACAGA GGGAGAAATT 960
CCAGCCTCCG CTTACTCCCC CTCTGTCACT TGGTTCCACC ACATGTAGCG GCAGTGTCTG 1020
GCCCCAGTGT GCTGAGAGAA AAAAGAGAAA ACACACACAG AGAAGTGGGG ATCACAGAAC 1080
ATGGAATGTG TGTCCTCAAG GGCCCTTCCA GACCTTTAAT TAGTGTGGCT CTCTCATTTA 1140
CAGATGAAGA AACCATTTGT CAGACATTCA GCGGGTGAAG GACAAACAAG AGACAGAATC 1200
CAGGGCCTTC AACGTCCTCT CAGTGCTCTT GCCCCTACAT CACACAGACT CCAGACAAGC 1260
AGGACTGGAA GAGGCTAAGA TGACCACGAG CCTGACCCCA CACCTGCTAC TGGAGAGACC 1320
CACAGCCTCC TCATCTGGGC TCTTCTGGCC ACATGGCACA GCCTGGTGGG GTAGGTTTTA 1380
CTCATTGTGG 1390
|
