| Tag | Content |
|---|
EnhancerAtlas ID | HS073-02177 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr11:8364450-8365520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr11:8365073-8365083 | GGAAATCCCC | - | 6.02 | | TFAP2C | MA0524.2 | chr11:8364781-8364793 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr11:8364781-8364793 | TGCCCTGGGGCA | - | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I008343 | chr11 | 8364721 | 8364870 | | GH11I008344 | chr11 | 8364981 | 8365130 |
|
Enhancer Sequence | TGTGTCAGGG AAAGTGCGAT GAGCCAGGGA GGCAGGGGCA TAAGCTGGCT CTGATGCTTT 60
TGGTGGGGGC ACTGAGGCTC ATCCCCAGGC AGGCATTTGC ATCCACTGAT TTACATAAGA 120
CTTAAGAAGT CCGCTGGGAG AAGGACTTGA ACTTAAACCA CATACGATCG TTTCCTATAG 180
GGCTCCAGGG CCCTGACACA GATGGAAGTA CTCTCCTCAT GGCCCAGAGG GCAAATCCAG 240
CCGGGACAGA GCCCCAGTGG GAGCGTGGGT CATGGCCAAT GAGCATGAGG GGGCAGCGCC 300
TGTCTGGCCA CTCTGGCAGC AGTGTGTGCT GTGCCCTGGG GCAGGAAGCC ATCACAGACT 360
GAGTCACAAC ACATACACCT TGAAACCTGT CACCCAACTG TGGGTGCTCT AACTGGAAAG 420
GAGCACCGCT CGCTTTGTGA GGGAGGGCCA AAGATGGTGG GGAAGGGTCT CCCTTGCCAT 480
ATGACTGGCA GTGGGGACAG CAGCAAATTC CTGGCACGAT GAGTTCTGAG GTGACTGTGG 540
CGGTGGCCGT GGCAGTGAAA GCCTGGCAGG GCTGTGGCTC AGTCAGCTGT CCCTGTGAGC 600
ACCAGACCAC ATAAAGTACT GCTGGAAATC CCCCGCACAC TCGGGCAGAA AGAACAGGGA 660
AAGGGTGGGG ACTGGGTGCC CGCAAGGCAC TCTCACCATG GCAGCTGCAG AGATGCATTC 720
GCGCCTCACT CCTGGGCTCC TGCCCTCATC AAGGCTGGGG CGAGTCTCAT AGCTGGCCTC 780
TCCCTCTCCC CTTCCCCAGC ACCCCCTCTC CAATCTCCAC TCCTCTCCAC TGCCCCAGAC 840
TGATTGTTCC AGAACACAGT TCTCACCATG CCTTGACCCT CTGGTGGCTC CTTAGCCCTC 900
GAGGGCAGTG CCCCAGCCCC TCATCCTGGC CTCAGCTCTC ACCCCTCACC CGCTGCCAGC 960
CTCCCTAGTC TCCTTCACCT CACATAGCTC CCATTCCCCC CAAGGGAATC TAATCACCAG 1020
CTTAGCTTTG ACTGCCCTTC CACTCCTCCA CAGGAACTCA TGTGAGTCCT 1070
|
