| Tag | Content |
|---|
EnhancerAtlas ID | HS088-34961 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr22:26812220-26813660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr22:26813074-26813085 | GGTGACTCATG | + | 6.62 | | FOSL2 | MA0478.1 | chr22:26813073-26813084 | GGGTGACTCAT | + | 6.14 | | JUNB | MA0490.1 | chr22:26813073-26813084 | GGGTGACTCAT | + | 6.32 | | JUND | MA0491.1 | chr22:26813074-26813085 | GGTGACTCATG | + | 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 |
| GH22I026416 | chr22 | 26812481 | 26813547 |
|
Enhancer Sequence | AACCTACATT TGAGCCTAAA GCTCCTTGTT TTCTTCCACC AGGTGAAGTA AGAGTTTGTA 60
AAGGCAAAAA TTCTGAACAG TGCCTCCTAG GTTAACAGAA ATCATGATGA CTTTGCCAGC 120
AAAAGACTCG GAGGAACATT GAGTACACAG CCTCTCAGTT CTAGGTAGGT CATATGTGTC 180
AGCCAGTAGG TTGAGTTTAT AACAGTCACG TCGTGACCTG AACACCCTCC CACTCCACTG 240
CTGAATCAAC TAGATAGAAT CTGGCAGGGA TGATATATAA CTACCTTAGA CAGGTGTAAG 300
GGAGGGGAAA ATACAGACAA AAAGACAACA AAAAGGAAGC TTGCAAGAAA AACGAAAAAA 360
ACTGAACTAA CCCCTAATGC ATCTGATTGA GGCTTCTGCA AAACTACCAG ATGCATTCAG 420
ATCAAACTAA CTATTAAGAA ATGCAAAGAA TTGGATGCTG TCTTAGGTTG AAACAAATCA 480
AAACAAAAAA GAAATGCAAA GAAAACTTAG CTCCTTGGAG CTGTCCTAAA TTCATATACC 540
ATGCTTGAGC TTGTAACATT GATCCAGGTG ACTCCCAGTT ACGGTGTTCA CTTTGTTCCC 600
TCTAGGTATG TGCCAGGTGA TGAGGAGACA TACTGTCTGG GCTCTTCAGA CAGGCTTCTT 660
TCTCCCTGGA ACTCAGAAAA TTCCAACTAC CTAGAGTTTG CAAAGGCAGC CGGCCAGGGA 720
AGGATGCTGG CTCCAGGTCC TGGGGCCCCT CCCTGGAGGG AACAAATGCC TCTCGGATTG 780
CAGCTGCAGA AAGAGAGAGG AGAATCGGGG AATGGAATGG TGTGCTGCAG AGGCAGTGGT 840
TTGGACAGCG ACTGGGTGAC TCATGCCCCA GGCAGCTTTT TACAGGAGTT GCAAATTCCA 900
GTAATAGCAG ATCAGGAACA TCTCTCGAGG GACACCCTAC CAATCGAAGG TGTCTCTTGC 960
ACCATCTTGG CAGCGCTGAA TGGGCATCTG AATAGCTTAT CTATTCAGAT CCTTTGCCGG 1020
ATCCCAAAGG TTCTCCTTGC TTTGGCCCCT GGGCTTCCTG AAACCGGGCG GTTATTCTCC 1080
CCGGAAGTTG GAGGAATTGG ATAATATTGT CTACAGACAC CACACCTGAA TCTTATCCCT 1140
ACTACTACAA ATAGGGATGC TATTTTCTTG TCCTGTGTCC TGGATGGTGA ATTGAGTATC 1200
TTGTGCCCTG CCAAAAGCCA CTCTATGGCC ACCTCCTCTC TGTCCTAGGT TCCTGGAGGC 1260
TAACTGTGTA GCTCCCATCA ATGAGCGTCC TCTCTCTGGC TTTTAGTTAG GTATACTCTA 1320
CAGGCAGCCC CGGCAGGAAA TAAAAAGGTG GGAGGAGAGT GAGGTCATTT CTTCTGGCTT 1380
TCTCTTTGTG GAGTTACCAC AAGCTGACTG TGTCCCTTAT GAGAATAATC CAGCCCTCTC 1440
|
