| Tag | Content |
|---|
EnhancerAtlas ID | HS127-05857 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr11:69390260-69391900 | 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 | TTCCCCTCTC TGTCTCTCTC TGCCCTTCTG TCTCCCTCTC TCTGTGTGTC TCTCTCTGTG 60
TCTCCCTCCT GTGTCTCTTT GCCCTTGTCT CTGTCTCCTT CTGTCTCTCT CTGTCTCCCT 120
CTTTCTGTCT GTCTCCATCT CCCTCTTTCT GTCTCTCTCT ACTGTCTCCC TCTCCCTATG 180
TCTCTCTCCC TTTCTCTCTC CCCACACTGA CTGAGCTTTG AGACCTTCCT CCAGCCTGTC 240
CCTCTTCCAG GACGGCTGCC CAAAGGTCTC TGAGATATGT GGGATGGACC CACACCCCCC 300
GGAGGGTTCC CAGGCCCAGG AGAAGTGGTG GTGGTGGAGG TGGAAGGAAT TTAGAACGCC 360
CAAGGCGTTA AGCGGCGGGA GATACTGACT CTTGTGGGCT TTAGTGTCTT TGTCCGCCTG 420
GTTTTCAGGT ATTCCAGAGG TAGAAAGGTC ACTTGTATGA GCACACAGAA TCGCTTCGGC 480
TGAGCGGGCA GTGTCTGGCC AGCTGTGGGG CTGTCCTGGG AAGGCAGTGG GCTCGTGGTC 540
TGCCCAGGCC AAGCTCTCCT GGATGCGTGA CCCTGGGTCA GTCACCGCAC ACTTCCAGCC 600
TGTTTCCTCC AGGGACCCTT CCAGCTCCTC TGTGCTTCTT ATCAGTGCCA GGCTGGTTGC 660
GGGGGGTGGG GAGGCCCAAG CACATTCCTT CCCCTTTTCA GACTGGAGCA GGGCAGGTTG 720
CACATCTGTG AGCTCCAGAG CAGAGGACCC AGCCCTACCT GTGAACCTTT CAAGATGCAC 780
ACCTGACCCG GTGACTTTGG GCAGAGCCTG GCTGGCCAAG GTACCCTGAC TCTGACCTTA 840
GCCAGGACAG GGCTGCCCTC CCAGCCCGGC CATCTCCGGG TATTTGCAGT TGGCCCCAAG 900
AGGAACTGGA GAGAGACTGA TTGCAGAACA GCCTAAATCC ATTCACTGCT TGCAAAGCAA 960
ACCCAAGCTC TTTCCTTCCT GCTGGTGGGA CAGTGGCAGA ATCTTAGAAG AATGGGGCCA 1020
CCGAGTGTGG GGTTCAGGGC ACAGTAATGA GACTGGCCTG GGTCCAACAC ATGAGAGCTC 1080
ACTCTGCAAA GAAGTCCGAT TAGAGATCCC GATGCCAAGC CTGGCTCAGA GCAATTTGGG 1140
CACTGCTCAT GGGATACTTA GCCATGCTAG GAAATTCTTC CCGTGACTTT ATTATCACAC 1200
ATCAAAAGTG GCTCCCCCAC CCAGCCGCAT AACCTTCTCT GCACAGAGCT GCATACCTCC 1260
TGCTGATCAG TCCTAAAAGC AGTGACCACC TCTGAAGAGT GTGCTCAGGA CGTACACCCT 1320
GTATAAGGCT GCCTCGTTGT CCCAGAATCT ACCCTCGGAA AAGAGAGACC CCCCTTATAA 1380
AGGAGTCCTT ACCAGATCGC TCATGTTATA GGTCTCCCTC TCGATATTTT GTTTTATATT 1440
TAATAGACAA TTTTTTAGCC GTTTTAGGTT TACAGAAAAA TTGAGCAGAA AGTACAGAGA 1500
ATTCCCGTCT ACTCCCTCAT CCCTCCTCCA GCTTTCCCTA TCACTAACAT CTTGCATTGA 1560
TTTGGTACAT TTGCTGCAAG TGATGAACCA ACCGCAGTAC ATTATTATTT GCTAGAGTCC 1620
ACAGTTTACA GTAGGGTTCA 1640
|
| |
|
|
|
