| Tag | Content |
|---|
EnhancerAtlas ID | HS134-36990 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr22:46874770-46876240 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr22:46875184-46875199 | AATGCTGACTCATCT | - | 6.31 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 46875113 | 46875464 | | chr22 | 46875833 | 46875894 |
|
Enhancer Sequence | CACAGCAACG AGCCCAACCC AGCCCTGCAG CAGGTCCTGC TCAGAGCTCT CAGGCTCTTC 60
AGCCACTGCT CACCGCAGGC CCAGGGAGTC AGGAACGACC AGGGCCAGTC TGGAACATTC 120
CAGGCTCCAG GTCTAAAAGT GCTATCCAGC ACCCAGCCAG GCTCCTCATC CAGCCACCTC 180
AATGGCCAGA GCAGCAGGTG ACCCTCGGCC TCCCTCTGCG TGCCCCTGTG CCACTATCTC 240
CATCTTCCTC TTCTCCTTGC CCGGAGTCTC GCATGCTCAC ACCTGCGGCT GGTGCAGCAT 300
CCGCCGACGG ACGCTCCCGG GGTTTTGCTG AATCCTGGGA GCTTCTCTCC CTCCAAAATG 360
ACCTGCTGGA CTCAGGTCTG TCCCGACCCC CATGCTTGTC AGCAGTGCCT CTGAAATGCT 420
GACTCATCTC CAGGGACCAA CCTGCGTCAA GCCGCTCCTA CCCCCGAGCC CGAAGGCCCT 480
CCTGTGCAGA AAGGCTGCGG CAGCTGCCAG GGGAAAACTG TCTGGGCCCT GCCCTGGAAG 540
CCCCTACCAC TCCAGGTGAG CCTCAAGCAG ATGCCTCGTC TTTGGGAAAA AGCTACCCAC 600
GGTGGCTGAA CCGGCACTGC AGCCATGTCC CCCACAAGCT CATCACGGAG CCAGAGACCA 660
CAGCTGCCTC TGGGCAGGAG ATGCTGGGTT CCAGGGGCCA GGGATAGTGA GCTGAGACTT 720
TTTGTGGTTA TTTGGACTTT TTGGGGGGGG GCCGGGGGTG GGTAGAAAAT TAAACCTTAT 780
TTATTTTTAA AACCAAACCA CTAGGAAAAT ATATCACAGC CGGGAAGCAG CAAATGGACA 840
GGCTGTCTTA TCATTTCAAG TAATAAGCTG GTGAGAATAC AATGAGGTTG CTATCAAAAC 900
AATAAGGTGC CATGCCGGAG CAGGAACACT GCAAGCTGCG AAAGCCCCAG GCAGAAATGG 960
TATTTGGTAA CGGGGGCTGC CTCTCCTTCA CTCTCAGGGA GTCAGCTCAT CCTAGCCCAA 1020
GTTGCTTCCT TTTCCTCCCT TGAATTTCCT GTTGCCAGGG GTTTGTCTCG ACTGGACTCT 1080
GTTAATTCAG GGGCTAAGTA GGCAATGCTC GGTTTAGGTC TTCATTCCAT CTGTTCTACA 1140
AAAACCAGGT TTTTCCAAAT CCAGTACTTC ATAACTCTGT TATAATCAAG TAGCCAAATG 1200
CTCCTCTTCT ACTGTTCACT CCTATATACT AGTATGTATC ACAATCAAAA TCCCCTTCTC 1260
TTCACGGGCA AAGTGTTACT GCAAGATTGT CCTGTCGTTT TGCTACACAC AGCCTCAAGG 1320
CCCATCAGCC AGTAATTCTG CTTCCCACAA TTAGTGTGTC GTCGCCTGTC ATGTTTTTGC 1380
ATGGTCTCCA AGCTGTGGTA GACGAAATAA TGTCTCCCCC TCACCTCCCA AGAAGAGGTC 1440
CATGTCTCAA GATGCAGCAT GTCAAAATTT 1470
|
