| Tag | Content |
|---|
EnhancerAtlas ID | HS131-01736 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr11:69390430-69391620 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr11:69390696-69390714 | GAGGTAGAAAGGTCACTT | + | 6.14 |
|
| | 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 |
| GH11I069576 | chr11 | 69390969 | 69391368 |
|
Enhancer Sequence | TCTCCCTATG TCTCTCTCCC TTTCTCTCTC CCCACACTGA CTGAGCTTTG AGACCTTCCT 60
CCAGCCTGTC CCTCTTCCAG GACGGCTGCC CAAAGGTCTC TGAGATATGT GGGATGGACC 120
CACACCCCCC GGAGGGTTCC CAGGCCCAGG AGAAGTGGTG GTGGTGGAGG TGGAAGGAAT 180
TTAGAACGCC CAAGGCGTTA AGCGGCGGGA GATACTGACT CTTGTGGGCT TTAGTGTCTT 240
TGTCCGCCTG GTTTTCAGGT ATTCCAGAGG TAGAAAGGTC ACTTGTATGA GCACACAGAA 300
TCGCTTCGGC TGAGCGGGCA GTGTCTGGCC AGCTGTGGGG CTGTCCTGGG AAGGCAGTGG 360
GCTCGTGGTC TGCCCAGGCC AAGCTCTCCT GGATGCGTGA CCCTGGGTCA GTCACCGCAC 420
ACTTCCAGCC TGTTTCCTCC AGGGACCCTT CCAGCTCCTC TGTGCTTCTT ATCAGTGCCA 480
GGCTGGTTGC GGGGGGTGGG GAGGCCCAAG CACATTCCTT CCCCTTTTCA GACTGGAGCA 540
GGGCAGGTTG CACATCTGTG AGCTCCAGAG CAGAGGACCC AGCCCTACCT GTGAACCTTT 600
CAAGATGCAC ACCTGACCCG GTGACTTTGG GCAGAGCCTG GCTGGCCAAG GTACCCTGAC 660
TCTGACCTTA GCCAGGACAG GGCTGCCCTC CCAGCCCGGC CATCTCCGGG TATTTGCAGT 720
TGGCCCCAAG AGGAACTGGA GAGAGACTGA TTGCAGAACA GCCTAAATCC ATTCACTGCT 780
TGCAAAGCAA ACCCAAGCTC TTTCCTTCCT GCTGGTGGGA CAGTGGCAGA ATCTTAGAAG 840
AATGGGGCCA CCGAGTGTGG GGTTCAGGGC ACAGTAATGA GACTGGCCTG GGTCCAACAC 900
ATGAGAGCTC ACTCTGCAAA GAAGTCCGAT TAGAGATCCC GATGCCAAGC CTGGCTCAGA 960
GCAATTTGGG CACTGCTCAT GGGATACTTA GCCATGCTAG GAAATTCTTC CCGTGACTTT 1020
ATTATCACAC ATCAAAAGTG GCTCCCCCAC CCAGCCGCAT AACCTTCTCT GCACAGAGCT 1080
GCATACCTCC TGCTGATCAG TCCTAAAAGC AGTGACCACC TCTGAAGAGT GTGCTCAGGA 1140
CGTACACCCT GTATAAGGCT GCCTCGTTGT CCCAGAATCT ACCCTCGGAA 1190
|
