| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00991 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr22:42379140-42380160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIA | MA0670.1 | chr22:42379934-42379944 | ACTTGGCACC | - | 6.02 | | POU4F2 | MA0683.1 | chr22:42379945-42379961 | AAGAATAATTAATGAA | + | 6.81 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 42379304 | 42379957 | | chr22 | 42379600 | 42379858 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I041983 | chr22 | 42379621 | 42379770 |
|
Enhancer Sequence | TGACTCTGTG CTGTCAAAGT GCTGACCTGC AGCAAGATAA GCTCAGCTGG GGCTTGGGCC 60
AGAGTATAAA TCATCTGGAA AATCTTGCTA TAAAAAACCT CCACTGAGCT AAACAGTGTG 120
CTCAGTGACA AGGTAGATTT CTCTCCTGAG GCAGACTTCT TATCTCAAGA ACCAGTAGCA 180
AATGGGTCAG GGACCCTGGT AGCTGGGCCC CTATGGGCCA CACTCGGAGT GGCACCAACC 240
CTCCTAGCTC TCTGTCTCCT TTCCTCTCCA ATCCCTTGTC CACCAGTGAC CAAATAATCT 300
TCCCACCTTG CAAAACTTAT CGAGTCACCC AACTTACTTA AAACTCTGTA ACAAACTCTC 360
CTTTAACCTC AGGGTAAGTT TAAACTCGTA GACTGTCCTG ATTGTACCTC TTCAGCTCAT 420
CTCTGACCAC TTCCCATCTA GCATTGTACT CCTCACTCAG AAGAGGCAGT GCTCGTCCAC 480
ATGCCATGCT CTCTCCTACC CTAGAGCTTT TGCATCTGCT GTTCCCTCTG GCTAGAACTC 540
ATGACTCTTT TGAAATCAAC CTTCCGGTTT CAGCTTAGTT GCATTTCTCC AGAAGTCTTC 600
CTTAGTCCCA GAGAGACTGG GTTGGATTCC CTTGGCAATG CTGTTTCAAT ACCCTGTGGC 660
TATTCTCTTT CACAGTGGTT ATTGCAACAT ACTATAATTG TCTGCTTATG TTTTGGTCAC 720
TCTCACACTA AGCAGCTCCT TGAGGGTAAG GATCATGTTT TGTTCACGAT AGTACCTCCA 780
AATTTTAGGA CAACACTTGG CACCTAAGAA TAATTAATGA ATGAATGCTC TTAGAAAACA 840
TCTCAGAGCA AGCATGGCAA ATCCAACACC CGTGAGCCAC TTCTCTCCCC AGTGGTGTGC 900
ATGGCAGACT GCTAGTCAGT CATGGCACGT GTTCAGTGCT GAGCCCAGAT GTAGCCTTTT 960
TAACATAATG GTCTAGGTGA CTACTACCAG ATAATCAGCA GGAATGAGAA ATGCACCTTA 1020
|
