| Tag | Content |
|---|
EnhancerAtlas ID | HS147-04954 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:233842880-233844150 |
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 | GATCATGAGA ACAGCATGGG GGAAACCGCC CCCATAATCC AATCACCTCT CAGTAGGTCC 60
CTCCCTACTG GACCTAGCAG CTGATGGAAG CAGCTTGGAG TTGCATAGTT CCAGGAGGAG 120
GCACTGGTTC CTGTGTATTC TTCACTTTGT CCTTATCTCC ACCCTCCATG TAGTCCAAAC 180
TGTCTCTCCA ACTGATTGTT CTGCAGTGGT CACATATGGC TGTGCAAGGG GCCAGCACTG 240
CTGCAGCTTC CAGTGAGATA TTTCAGTTAT GTGGAGCATA AGCAAGGGAG ATAAAGTAAA 300
ATCCCTATGC TCCTGACAGC ATTGCACGGG GCTTCCAGAA TGTCACGAAG CCAGCTGCTG 360
GCACTGTTCT CAGGAGAAAA AGGACTTTTC TCTGGAATGG CTCTCTTGGT GTAAGGCCTG 420
GTGGCACATT AATAAATCAT ACACTTACGG TTTAGATTAA GTCATATTTG AATGAGTCAT 480
TTCTCTACAC AAATCTCCAC TCCCTGTGTC AGCAAGGCTG ATGGGCAGAG GAGGCTGAAT 540
GTTGGCAGGT GGTGTTATGT GATCAAGTGT TTTTACTTTA ATGCCTAAGG AAGACTCTGC 600
TAGCCAGGTG CACAATAGTC TGCACTGTTG GCCTTGGCTA ATCTAATCTT AGACACCCTG 660
TGTAATTGGG AAAGAAGGAG AAACTCTGCA ATGAGTCATC CAGCAACTTG ATCCCCTGGT 720
TTGTTTTTCA TTTTGTTTTA AGATGGGCTC TAAGGTCAGG AGAATTAAGA AGTTGGATGT 780
CTGGAAGGGG AGACGTTTTG CCCCGGAAAG AGCTGCAGAG ATGTTTGCTG GGCCTGACAG 840
CCAGCTGTGG TCAGCCAGAG AGACACATGA CAAGTAGAAC TCAGGCATCC CTGCCTTGGG 900
AGACCAGGGC CAGGGCTTCT GTGACATGCA CTCGCTTGGA GTCCCATTGA TCCCACTGCC 960
CCTCTGGTAG TAGTCCTGTC TTCAGCCCAG ATGAGGACTC CCAGAGTTAT CCTTGGAAGT 1020
TTCCTTCAGT TAGCAATTAC TCTGCCTGCT GTCCCGAGAC TAGACAATGC CTCCTAACAG 1080
CTCACCCCTC TGAGTCCAGC CCCTCCTCAC TTCCTGCTCT TTATTAAGAA CATTTGTTTG 1140
TTCCAAAGCT CTATAAAAGG AGGCTTATAA TCTTAAGAGT ACCCCTAAAT CACTAGCTTT 1200
TAATGAAGAT AAAATTATCT GTACAGAAAG CAGTGAAACA TCACCATTCA TTCTGCAATT 1260
CCAGATTTCT 1270
|
