| Tag | Content |
|---|
EnhancerAtlas ID | HS087-02630 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr1:233842730-233844120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr1:233842914-233842925 | TAATCCAATCA | + | 6.02 | | FOSL2 | MA0478.1 | chr1:233843570-233843581 | ATGAGTCATCC | - | 6.62 | | JUN(var.2) | MA0489.1 | chr1:233843351-233843365 | ATGAGTCATTTCTC | - | 6.84 | | JUNB | MA0490.1 | chr1:233843570-233843581 | ATGAGTCATCC | - | 6.62 |
|
| | 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 |
| GH01I233706 | chr1 | 233842029 | 233844573 |
|
Enhancer Sequence | TTCCACATGG CTGAGGAGGC CTCAGGAAAC TTACAATCAC AGCGGAAAGG GAAGCAGGCA 60
CCTTCTTCAC ATAGCAGCAG GAGAGAGAAG AGAAAGCAAA GGAGAAAGAG CCTTTCGTGA 120
AACCATCAGA TCAAATGAGA ACTCACTCAC GATCATGAGA ACAGCATGGG GGAAACCGCC 180
CCCATAATCC AATCACCTCT CAGTAGGTCC CTCCCTACTG GACCTAGCAG CTGATGGAAG 240
CAGCTTGGAG TTGCATAGTT CCAGGAGGAG GCACTGGTTC CTGTGTATTC TTCACTTTGT 300
CCTTATCTCC ACCCTCCATG TAGTCCAAAC TGTCTCTCCA ACTGATTGTT CTGCAGTGGT 360
CACATATGGC TGTGCAAGGG GCCAGCACTG CTGCAGCTTC CAGTGAGATA TTTCAGTTAT 420
GTGGAGCATA AGCAAGGGAG ATAAAGTAAA ATCCCTATGC TCCTGACAGC ATTGCACGGG 480
GCTTCCAGAA TGTCACGAAG CCAGCTGCTG GCACTGTTCT CAGGAGAAAA AGGACTTTTC 540
TCTGGAATGG CTCTCTTGGT GTAAGGCCTG GTGGCACATT AATAAATCAT ACACTTACGG 600
TTTAGATTAA GTCATATTTG AATGAGTCAT TTCTCTACAC AAATCTCCAC TCCCTGTGTC 660
AGCAAGGCTG ATGGGCAGAG GAGGCTGAAT GTTGGCAGGT GGTGTTATGT GATCAAGTGT 720
TTTTACTTTA ATGCCTAAGG AAGACTCTGC TAGCCAGGTG CACAATAGTC TGCACTGTTG 780
GCCTTGGCTA ATCTAATCTT AGACACCCTG TGTAATTGGG AAAGAAGGAG AAACTCTGCA 840
ATGAGTCATC CAGCAACTTG ATCCCCTGGT TTGTTTTTCA TTTTGTTTTA AGATGGGCTC 900
TAAGGTCAGG AGAATTAAGA AGTTGGATGT CTGGAAGGGG AGACGTTTTG CCCCGGAAAG 960
AGCTGCAGAG ATGTTTGCTG GGCCTGACAG CCAGCTGTGG TCAGCCAGAG AGACACATGA 1020
CAAGTAGAAC TCAGGCATCC CTGCCTTGGG AGACCAGGGC CAGGGCTTCT GTGACATGCA 1080
CTCGCTTGGA GTCCCATTGA TCCCACTGCC CCTCTGGTAG TAGTCCTGTC TTCAGCCCAG 1140
ATGAGGACTC CCAGAGTTAT CCTTGGAAGT TTCCTTCAGT TAGCAATTAC TCTGCCTGCT 1200
GTCCCGAGAC TAGACAATGC CTCCTAACAG CTCACCCCTC TGAGTCCAGC CCCTCCTCAC 1260
TTCCTGCTCT TTATTAAGAA CATTTGTTTG TTCCAAAGCT CTATAAAAGG AGGCTTATAA 1320
TCTTAAGAGT ACCCCTAAAT CACTAGCTTT TAATGAAGAT AAAATTATCT GTACAGAAAG 1380
CAGTGAAACA 1390
|
