| Tag | Content |
|---|
EnhancerAtlas ID | HS176-04456 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:13379250-13380700 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr10:13380481-13380499 | CCTTCCCTGCTTCCTCCC | - | 6.84 | | JUN | MA0488.1 | chr10:13379299-13379312 | TAAATGATGTCAT | + | 6.67 | | JUND(var.2) | MA0492.1 | chr10:13379298-13379313 | GTAAATGATGTCATT | + | 6.28 | | Sox6 | MA0515.1 | chr10:13379713-13379723 | AAAACAATGG | - | 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 |
| GH10I013337 | chr10 | 13379509 | 13383397 |
|
Enhancer Sequence | CCAGGGCTGA AGTCATATTG TTTTCAAAAG AAAAAGAAGC ATTTCCCAGT AAATGATGTC 60
ATTTTATTAG GAACTTTAAA ATACAATTCA ACAGAAATGT GGTAATGAAG ATTTTTTTAT 120
TGCCACTGGA GATTTTTAAA AGTTAAGTTG CCCTTATCTA AATTTTTATC TTTTATAGAC 180
AATAAAGAGA AAATACAAAT TTTCCTTCTG ACATAAGGAT AATCAAACTC CCAAGTGTTA 240
TCACTTCCAG TGGCTGTTTA ATTGCTTGCT TTAGGCTTTC TTATACATTC CTGGAGGTCA 300
GCAATGCAGC TCAACAACCA TCTGTGGCCA CACTTTCAGT ATCATCAAGC CAGTCCACAA 360
GGCCAACAGG TGGTCTACAA CTCGCACAAG CCAATCGCTA GTTAGGGGGG TGGTGATTTA 420
GCGCCCCTTC TGTTCTGGGT GCTCTCATTT TAGGAGATGC TGGAAAACAA TGGACTGTGG 480
TTTTAGCCAT CCCTGCCACC TGGTCATGTG GGACCTGGGC TGTGGCTTAC CTGCCCAGTC 540
TCAAGAGTAT TGCTCCAGAG GAGAAAACGG ACAGATGTGC GGAAGAAATA TAGGTTTCCA 600
ATAATCTGGT ATTTGTCACT GGTACCTGAG GGTGAACACC CCCCACGTGG CTGCCTCATG 660
ATAAAGTCCC TACAGTGCAG CCTGATCCCA CTGTCCTTGC CACACACGAA GAACACCTGG 720
CATTTTATAG CAAACCAGAT TTTCCTAGTC TCTCCACTGG CTCCTCCTGG GTGGTAGCAA 780
ATTGGGGTTA AAGGTTGGGT GGATCAAAGG GTGGCTGGCT GCAACTACGC AGTAAACAAC 840
TGGGGAACAC ACCTCAGCAG TGTATCATCA GTAGCCAGGA ACTTTAACTC AGTGGTCAGA 900
AACCTACTAT GTACAGCGGC ACATCACACG GTGGTGGGTG TGCAAGTGGC TGGGTTGAGT 960
GAATTAACCA GATATCCGAA TTAATGTTTG AGGCATCTAA TTGTGATGAG ATACTAGCTC 1020
CTTAATCTCT TGAAGGAAAC ATTTAGGATC AGTCCTATTA CAGAGGACAG TAACATCTCC 1080
AGCCTAAAAC ACAGGGGTGA TGGAGGTTAC CAATGTCAAA GAAGAGAAGG TGCAAGAAAG 1140
AAGAAAATGA CAAAAACAGG CCATTGACAT GCTACTAAAC AAGAGGTGTT CTTACTCACA 1200
GCATGTACTC AGTTGCAACA GCAGCAGAGG GCCTTCCCTG CTTCCTCCCT AATTGCTTTA 1260
TGCCCAGTGC CAAGTGTGGG CAGGGGACAG GCCTGACTTC AGCAACTGCA GGAGTCTGGG 1320
CAGGGTGGGG CAGTATAGTC GGGATATAAC AGAAATAAAA CCAAAACCCC ACAGATACAT 1380
ACAAAACCCC AGCCACAACC CAAACCAAAC AAATAAGCCC TTCCAGTCAC AAAAACACAT 1440
CGGCTCACGC 1450
|
