| Tag | Content |
|---|
EnhancerAtlas ID | HS138-31153 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr4:148418700-148420100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| | 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 |
| GH04I147497 | chr4 | 148418821 | 148420520 |
|
Enhancer Sequence | GGAGTTTTAT ACTCAAGTAT TTTCTTGGAC TTTTTTTTTT TGAGATGGAG TCTCGCTCTG 60
TCGCCCAGGC TGGAGTGCAG TGGCGCGATC TTGGCTCACT ACAAGCTCCG CCTCCCAGGT 120
TCACACCATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA CTACAGGTGC CCGCCACCAA 180
GCCTGGCTAA TTTATTTGTA TTTTTAGTAG AGACGAGGTT TCACCGTGTT AGCCAGGACG 240
GTCTGCATCT CCTGACCTCG TGATCCGCCC ACCTCGGCCT CCAAAGTGCT GGGATTACAG 300
GCCTGAGCCA CCGCGCCCAG CCTCTCTCGG ACTTTTTGAG ACCAAAGAAC ACAAAGATAC 360
TATTTTTAAT GTGAAATACC TCTAAAAATG TTCATTGAAA GTAGAAAGAT TGGCATCTTA 420
ATACAAGATT GCCAGGGTAG GGATGGTTGT CATAGAAATT TACCAAATTG GAACACATGA 480
AGACAGAGCT AAAAGAAAAA TTTATCTTAA TATCATCAGC AAAATTTGCA TTTGCAACAT 540
CCCAAAAAGA AATTTTATTT ATGAAAACCC ACTGACCACA TATGAAATGG AATCATCTTA 600
CAATGTAAAC ACTCCCAGGA AGTCATTCAG AACTCTGTGA AATGTCTGAG CACTGCATTT 660
TTGCAATCTC ATGAATAAGA GTTTAAATGT GAGTCATTGA CACTTTTCCT GCTTTTTGTT 720
CTGGGGAAAT AGCTTCACGG TAATATTTTC ATTAATTGTA TGGAGTGACT TCAGAATCAT 780
CTCCAGCTCC TGTACCATCA TAAAGGAAGT CAACCCAGAG GGAGTGGTAT GCACTAAGGT 840
GACCGTCCAG AGCCCACTTT CAAGCACTGC TGCTTGCTCC TGCTTGATTC GCTCACCCAG 900
GGCCCAGCAA ACTACAGCTA GTGAGCCAAA TCTGGCCCAC CACCTGTTTT TGTAAATGAA 960
GTTTTATTGG AACACAGCCA TACCTATTGC TTACGTATTT TCTATGGCAG CTTTTGAGTA 1020
GTTTCAACAG ACACCATATG GCCCAGAAAG CCTAAAATAT TTACTATCTG GCCATTTATG 1080
GAAAAAGTTT GTCAAGCCTG GTGGCATCTC ACCAACTGCC CTGCCCCTTC CTCTCATCCC 1140
TGGCTCTCAT CTACCTCCAT TTGGACCCAC AGGCAGTCAA AGCCCAAGAT CTGAACTTCA 1200
GAAATGTGAA TAAGGCTTCA TAACCTTTTT CTCTTTTTAA TAGAGATGGG GTTTCACTGT 1260
TTCCCAGGCT TATCTTGAAC TCTTAAACTC AAGCAATTCT CTTACCTCAA CCTTCCAAAA 1320
TACTGGGATT ACAGGCATGA GCCACTGCGA CCAGACACTT CATAACCTTT GATATTTTTA 1380
AGTGCCTAAT GCCTTAACCC 1400
|
