| Tag | Content |
|---|
EnhancerAtlas ID | HS150-04444 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr16:15634400-15635110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr16:15634422-15634438 | TGTTGCCATGGTAACG | + | 8.35 | | RFX1 | MA0509.2 | chr16:15634422-15634438 | TGTTGCCATGGTAACG | - | 8.4 | | RFX2 | MA0600.2 | chr16:15634422-15634438 | TGTTGCCATGGTAACG | + | 8.25 | | RFX2 | MA0600.2 | chr16:15634422-15634438 | TGTTGCCATGGTAACG | - | 8.27 | | RFX5 | MA0510.2 | chr16:15634422-15634438 | TGTTGCCATGGTAACG | + | 8.18 | | RFX5 | MA0510.2 | chr16:15634422-15634438 | TGTTGCCATGGTAACG | - | 8.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 15634400 | 15634448 | | chr16 | 15634548 | 15634975 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I015540 | chr16 | 15634401 | 15634550 |
|
Enhancer Sequence | AGAGGGCTTG AGGCATAGCA ACTGTTGCCA TGGTAACGTG CAAGTGACTG ATGTTCAGGA 60
AACACTGGCT TTGCTACCCT GAGCCACACT TTTCCTTCTT GCCTGCAAGG CGATAAGGAT 120
GTTGCACCTG GTGGCTGGTG TGAGGAGGTC AGGCGCAGCA AGAGGCAGCA CACGTAGCAG 180
TTACAGTCAC AGACTTTGCC TGCGCCAGGG TCTGTGTCCC AGCGGAGATG CTTACCGGCT 240
GTGTGGTCTT GAGCAAATTG CTCGACTTCT CTGTTACTCT GTGTGGTGTT TTCTGACGCC 300
ACTTCTGACA CCAAATGTGT TTTTTCTGAT ACCAAATACG TGCCATTTTT CTACACTAAG 360
TCTCTGATTC TTGGATGCCA ACTGGGTGCC CAAGCAATTC AATTCAGCTA TCACACTATG 420
TCCTGGAGTT AGCATCAGGT CCTGCAAGTT AAAAGACCCC ATCCCACCAG ACTGCCCCTA 480
TCTCAGATGC CAGTCGCAAG TCCGGAGCCA CCCACCCTTC TGCCTGGCCA ATTACAAACT 540
TGGGGGTTCC CACGACCACC TCCTCGGGTT TGATAGTTTG CTGGAATGAC TCACAGAGCT 600
CAGGAAAGCC CTTCACTTAT GTTTACTGGT TTATTACAAA GGACAGAACT CAGGAATAGC 660
CAAATGGAAG AGAGATGCAT TGGGCAAGGT GTGGAGAGGG AGCCGTGCAG 710
|
