Tag | Content |
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EnhancerAtlas ID | HS095-23160 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr4:148418740-148420280 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr4:148419299-148419311 | ACAATGTAAACA | - | 6.04 | NEUROD2 | MA0668.1 | chr4:148419732-148419742 | ACCATATGGC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I147497 | chr4 | 148418821 | 148420520 |
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Enhancer Sequence | TGAGATGGAG TCTCGCTCTG TCGCCCAGGC TGGAGTGCAG TGGCGCGATC TTGGCTCACT 60 ACAAGCTCCG CCTCCCAGGT TCACACCATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA 120 CTACAGGTGC CCGCCACCAA GCCTGGCTAA TTTATTTGTA TTTTTAGTAG AGACGAGGTT 180 TCACCGTGTT AGCCAGGACG GTCTGCATCT CCTGACCTCG TGATCCGCCC ACCTCGGCCT 240 CCAAAGTGCT GGGATTACAG GCCTGAGCCA CCGCGCCCAG CCTCTCTCGG ACTTTTTGAG 300 ACCAAAGAAC ACAAAGATAC TATTTTTAAT GTGAAATACC TCTAAAAATG TTCATTGAAA 360 GTAGAAAGAT TGGCATCTTA ATACAAGATT GCCAGGGTAG GGATGGTTGT CATAGAAATT 420 TACCAAATTG GAACACATGA AGACAGAGCT AAAAGAAAAA TTTATCTTAA TATCATCAGC 480 AAAATTTGCA TTTGCAACAT CCCAAAAAGA AATTTTATTT ATGAAAACCC ACTGACCACA 540 TATGAAATGG AATCATCTTA CAATGTAAAC ACTCCCAGGA AGTCATTCAG AACTCTGTGA 600 AATGTCTGAG CACTGCATTT TTGCAATCTC ATGAATAAGA GTTTAAATGT GAGTCATTGA 660 CACTTTTCCT GCTTTTTGTT CTGGGGAAAT AGCTTCACGG TAATATTTTC ATTAATTGTA 720 TGGAGTGACT TCAGAATCAT CTCCAGCTCC TGTACCATCA TAAAGGAAGT CAACCCAGAG 780 GGAGTGGTAT GCACTAAGGT GACCGTCCAG AGCCCACTTT CAAGCACTGC TGCTTGCTCC 840 TGCTTGATTC GCTCACCCAG GGCCCAGCAA ACTACAGCTA GTGAGCCAAA TCTGGCCCAC 900 CACCTGTTTT TGTAAATGAA GTTTTATTGG AACACAGCCA TACCTATTGC TTACGTATTT 960 TCTATGGCAG CTTTTGAGTA GTTTCAACAG ACACCATATG GCCCAGAAAG CCTAAAATAT 1020 TTACTATCTG GCCATTTATG GAAAAAGTTT GTCAAGCCTG GTGGCATCTC ACCAACTGCC 1080 CTGCCCCTTC CTCTCATCCC TGGCTCTCAT CTACCTCCAT TTGGACCCAC AGGCAGTCAA 1140 AGCCCAAGAT CTGAACTTCA GAAATGTGAA TAAGGCTTCA TAACCTTTTT CTCTTTTTAA 1200 TAGAGATGGG GTTTCACTGT TTCCCAGGCT TATCTTGAAC TCTTAAACTC AAGCAATTCT 1260 CTTACCTCAA CCTTCCAAAA TACTGGGATT ACAGGCATGA GCCACTGCGA CCAGACACTT 1320 CATAACCTTT GATATTTTTA AGTGCCTAAT GCCTTAACCC CAAGAAGTAA ATGGGCATAA 1380 TCTCAAGAAA TCAAAATATG TTTTATTTTT TAAAATGGTT TGTCACTGAT CTTGAATAAA 1440 TCACTTGACC TCCCAAGTCA TTCTTTTTCT TTTTCTTCTT TTTTCGAGAA AGGGCCTCAC 1500 TCTACCACCC AGTCTGGAGT TCAGCGGCAT AACCACAGCT 1540
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