| Tag | Content |
|---|
EnhancerAtlas ID | HS007-07425 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:74880980-74882480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr17:74882236-74882247 | AGGCCATAAAA | + | 6.02 | | REL | MA0101.1 | chr17:74881249-74881259 | GGAAATCCCC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 74881303 | 74881549 | | chr17 | 74881977 | 74882049 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I076885 | chr17 | 74881264 | 74882250 |
|
Enhancer Sequence | GCCTAAGTTT TGTATTTTTA GTAGAGACTG GGTTTTGCCC TGTTGCCTAG GTTGGTCTCG 60
AACTCCTGAC CTCAGGTGAT CCGCCCATCT CGGCCTCCCA AAGTGCTGGG ATTATAGGTG 120
TGAGCCACTG TGCCTGGGCT ACTGGATTTA TTTTTTAAAA AGATCATTCT GACTGCTGTG 180
TGAAAACTGG ATAAACAGGG TGGCAGGAGG GGAAGCAGTG AGGCCGTGGT GGAGATGGGG 240
AGTGCCTGCA AAGGGATCTG AGCTTCCTTG GAAATCCCCC TGAGGCATGA GGCCGTTTTC 300
CTCTCTGTGT GCATGGATCC TTCTTCTCTG ACACTGTCTG TGTGCCCTCG GATCCAGCCC 360
CTGCCCCCCA GCTCCATCTT TCTCCCTCAG ATCCAGTCCT TTGCCCCTCT TTCATTCTTT 420
TCTGCTTTCC TGTCTGCCTC CAGCGGTGCC TCTGATGCAG CCTCTGTCCG CAGGCCTGTT 480
CCCCAGGTCA GGAGCAGGCC TTTTTGGTCT CTGTTGAGGA TATTGCTGCA GGCAGCAGAG 540
CTGAAGGTCC AGTGGACCCC TGGACTCCAG GTCTGCCTTC TTGGGCTGGG GGTGGTACTG 600
CTGGCGCATC CAGTGTTTCT CTGATTTTTT TCCGGTCCTG GCCTGTGCCT CCCTCCCCTG 660
CCCTGCCCTT TGTCTCCTCC TGGGGAAGGA GGGAACTTGT AGGGGGAGGG GGAATATGCG 720
CCACCTCCCA GCTCCCTCCT GGGAAATAGC AACCATCCAT CACGACCGGC AGAGCCCATC 780
ACACCCACAG GCAGAGCCAT CAATTTCAGG GACACTGTGG TTGCTGGTTT CAGGGAGAGA 840
AATGGTGGGT GTGTCCCGGG CCTGTGAAAG CCGCCTGCTC ACACGCTCCC GTGCACAAAC 900
ACTGCTGCCC CCTCCGCACC CTGAACCTGA CTCCAGGTTA ACCAACCTGC AGCTAGACCG 960
GCAAGAATCC TGCAGGAGTG CCTGCTGCTG CATTTCCAGA AAACTCTCAG GTGCCTGCAC 1020
TTGGATTCCC CACTTAGAAA TTTCCTGTGG CTTAAAAAAA ACACGTCCCC TGTTCTTCCT 1080
CAGCCCTTTT GGAAGCTTCT GGGCTGCCGC CTTCCACTCA TGGCTGGTGT TTCCTCAGGG 1140
AAAGTAAATT TGCAATTTTA GCCTAGGAAA ACATAATTAG AGAGGCAGAT TTGCTTCAAA 1200
TGGCATCGTA TTATGTATCC TCAAGCCAAA TAGTAATGAT CTTTGAATTT TCCATAAGGC 1260
CATAAAACCA CCGAAATTTG AGGCTGTCTG GATTGAAGAG GTCAGTCCGT ATTTGTTGAA 1320
TGCCTAGTGT GTGCAGAGTC TGGGCTGGAG GTTTGAGAGC AGGTGGAGGG GACACAAAAA 1380
AGATGGAATT CCACTGCATG CCCGGTGCCC AGCCTGGCCA GTGGCCCCTC AGAGTGGGGC 1440
AGACCTGGGC GGCCTTGGGC TCTGCGAGCC TCAGGTTCTT CACGTGTGTG TTAGAGATGA 1500
|
