| Tag | Content |
|---|
EnhancerAtlas ID | HS148-09465 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr2:54349720-54351040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr2:54350260-54350271 | GATGAGTCACT | - | 6.02 | | JUND | MA0491.1 | chr2:54350260-54350271 | GATGAGTCACT | - | 6.32 | | ZNF263 | MA0528.1 | chr2:54350760-54350781 | TTCCCCACTTCTTCCTCCATC | - | 6.54 |
|
| | 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 |
| GH02I054121 | chr2 | 54348229 | 54351243 |
|
Enhancer Sequence | CCAGCCAACA CTGATAAAGT GCAGAAAAAT GTCTCCACAT CTACCTTTTC TTTCTATATA 60
GATATCTATC TGTTGTGCAG TATGCTTCAT ACTAGGAATC AGGACTCTCA GAAAGATTCT 120
GGGAAAATTC CTGGTGGCTT ATGAAACTTT GAGCAGTTGA TTCCTGCATG GTTCAGTGCC 180
TTGCAGAGTT AATGGGCTAG AAGTCTTGAG ACTCCTTGGC TCACCTTCCT CCCAAGGCTT 240
TAAAATAAGA GTTGTAGTTT GAGGGGCCCA ACAAATAACA CCTATCTTCA TTGTGTGAGT 300
TACTGTCAAG ACAAAGAGTA AAGCGGAGTT TTAGGAATGT GATGTCTATC TGCAGGTAAG 360
TGGACTTTAT AATGACCTGT ACTACAGAAT TAAACAGTGG CCACCCCAAA CTTCAGGCAC 420
AGGGAGGCTA CTCTAGGGTA GAGCCAGAAG TATGATCCCT GTGGGTAACT TGCTCCCAGC 480
GGGAGGAAGA AGAGGACATG CCTGGGCTGT GCATGTTTCT CCTTCTAAAT TTACCCAGTA 540
GATGAGTCAC TGCATGTCCC TGTGACAAGG GCAGGGTAGA AAGTAGCCAG GAATGACACA 600
CTAATGATAC GCCTCCTCAC AGAAGGAATT TCCGCTAGAG AGAAAGATGC TTTCTCCTGC 660
AGAAATAAGT TATAAAATCT AGAGAGAGCT CAGTCATTTA GTTCTACTTG CCGTACTTCA 720
AGAGGATCTT CACTGCAGTT GTTTTGGTAT GGAGTGATAG GAAAAAGTCA GGGAGGTTGT 780
ACGGTAAGCA AAATTGGAGA ATGACTGCCC TTGTTCTACA AATAGAGGTA GGAAGGACTA 840
CATCATAGTC CTGTTTTCTG CTTTCCTTTT TTTGTGTGTG TGGCATTAAC AAAATTGAGA 900
TATAATTTAC ATAACACTAA ATATACAGTA GTTTTTAGTA TATTCACAAT GTTTTGCAGC 960
ATTACCATTA ATTCCAGAAC ATTTCCATCA CCCCTCCTTC CCTTTACCAG CTGCTTCCCA 1020
TTCCCCACCT CATTCCCCCA TTCCCCACTT CTTCCTCCAT CCCCTGGCAT GTTAAAGTGC 1080
CTCAGGGAAG TCAGGGACAA AGTCTCTGAT GTCCTTGGCC TCTCCCTCAA GATTTCAAGA 1140
TTGCTGCTTA GCTCCAATCA TAATATTCAT ACCATGATTA GGAGAAAAAA GGGTACCAGT 1200
GCAATACCCC GACATGGAGA AACCACTAAC TCCCAGCCAA GTCAGCCCCT GTTGAAGAGC 1260
TGTCTTGAAA GTCCCAACCA GTGATACGGC TTACATTTCA TTGGCCATCC CCACTATAAG 1320
|
