| Tag | Content |
|---|
EnhancerAtlas ID | HS044-09316 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr3:149017570-149018760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr3:149018072-149018083 | GGATGACTCAT | + | 6.62 | | JUN(var.2) | MA0489.1 | chr3:149018074-149018088 | ATGACTCATTACTT | - | 6.12 | | JUN(var.2) | MA0489.1 | chr3:149018069-149018083 | AATGGATGACTCAT | + | 6.13 | | JUNB | MA0490.1 | chr3:149018072-149018083 | GGATGACTCAT | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_47116 | chr3:149012843-149020583 | Panc1 |
|
| | 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 |
| GH03I149297 | chr3 | 149015645 | 149019920 |
|
Enhancer Sequence | ACTAATATCA TAAGTGGTCA CTTCTAAGAA ACACTCCATT CTCATGTAAT TATATTTATA 60
GTAAAAATCA TAGAAGACAA TGCAGATACA AATCTGACAA CTAAGAAAAT TGTAAAAATT 120
ATGGAATAGT TTTAAAACTT TTTCCTTGAA TGTTGGCTCT TTAAACAAAG AAGCCTTAAT 180
CAGAGAAATT TACGCATAAG CATGTGATTC TGAATGAGCC TTTTCAAGGA CTTTATGTAT 240
GAGTATTTGA CTTTTGAGGT TAATAGAATC AATTCTTTAA TATGGGTTGA GAAATAAAAA 300
TAAAGTCCTA AGCTTCTCCA ACTGACTGAA CACACCATCT CTTGGCCCAG GGGACTCCAG 360
AGAAACCTTA GAAACTGAGT TCCTGGCCAT GATGGGCTAG CAGGTCGAAC ATGCCTCAGT 420
ATGCCCCATT CCTTCTAACC TTTAACCAGA ATTCTTTCCT AAGGCGTAAG TAAGCAGAAA 480
CCAGCTCTGG AAAATGAGAA ATGGATGACT CATTACTTTG TCAACTTTAG CCAGTCCTCT 540
GAGGCTGCCA CAGGACTCCC TTTCCCACAT TGCAGTTTCA ACATGACAGC TCACCAGTTA 600
AACCATAAAT CCCTTCCTGA TAAGAGACCA ACAACCATGA AGTGGTTCTG GCCAATCTAT 660
GCAGGGTGCA CAGCCAGGGC ATTTGTGTCC TCCCCTTCAT CTTTTGACAT TAGGGGGCTG 720
AAAACTCCAC TCTCAGATCA TGCTAATGCC ACAATTTTTT GTACAGGGAA TTCATGAAGA 780
GGCATAAAGC TCAATTGTGA AGCACATGTT TCTCCTTTAA TAAATATTCA TGACTCCTCC 840
TACAGCCTAA TAAAAAGGTA TTTTCAGCCA CTCTGCTCAG CATAAATTCC CGTTTCTTTC 900
AGCACTACCT TGAAGTGCCT GTTTCTGGCT TCTGGCCAGA GGTTACACTT CCCAGCGTGT 960
CAGAATGGCC ACCCTGCAGG TTGCAGCCTT TTGTGAGAAA TAAAGCTGTC CTTTCCAAAT 1020
GTATGAACCT TGTGATTCTT CAGCTGACAG GGTAATTCAT CTGAAAAACG TAGTTTTTCT 1080
TCTTGGAAGT GGACTTCCAA TATCATGATG CTAAAAACAT GTCATACTGT AATAAGAGCT 1140
GTTTTGTACT TTTACAGAAG GAATTTTTAA AAATTTATTT TTAGTTTTTG 1190
|
