| Tag | Content |
|---|
EnhancerAtlas ID | HS138-41784 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr8:121873200-121874600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIL3 | MA0025.1 | chr8:121873789-121873800 | AGGTTACATAA | - | 6.14 | | NR2C2 | MA0504.1 | chr8:121873654-121873669 | GGGGGTCAGAGGGTA | + | 6.05 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 121873306 | 121873367 | | chr8 | 121873467 | 121874371 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I120860 | chr8 | 121873165 | 121874705 |
|
Enhancer Sequence | TATCTCTTTA TCTCGTTTAA TTTTTTTTTC ATTCATATCC TCCATTTGTT CCCTTCTCCA 60
AGACCCTTCA TGAGTGGGAG GGCTGCCTGA CTGTCGGGGT AGATCTGAGA CTAGACTTTC 120
CCCAGTGAGC CTAGCAGTGT GCCTATGCCT CTGCTGAAAG AAACTGCCCA CAAGTGGAAA 180
GCTCGGGGAC TCAGGGCTTG CAGCCTGATT TCTTTTGTCT CATGGGATGC TCCCTTGAGA 240
TGTCCCATGA GACATCCCAT CAGATGTCCA TGGCGCATTC CCTCTACCCT AGGAGTAGCA 300
GTCCCTGCGG GGGCAAGACT ACTGTGAATC CTGCTGCTCC TCTGGGTCTA GCCACCCAGT 360
GGGGCTGCTG TACTCCAGTC TGGTGCTGGG GAATGTCTGC AGGGGATCCA GTGATGTGAT 420
GTTCCTAGTA GTGGGTAACA GCATCATTCC TGATGGGGGT CAGAGGGTAG TGCCATAGAC 480
TCTGGGATTT CCTGGATATA AATAGGCTTG TCATAGTAAT ATACTAAATA CGTGGATAGA 540
CTCAAGGCCT CCTGGTTAGC CTGGATGATG CAAGCAATTG TGATCGCTGA GGTTACATAA 600
AAGTATTCTC CTTCCTGAGT GCTGTGTTAT TGTGCCTGCA GATGTTGCAA TGGGCTGTGC 660
CAGCTGGCCT CCAGCCAGGA GGTGGTGCTT GCCAAAGAGC ACCAGCTGCA GTGGTAGCAG 720
TGGAATTTGT GCTCGCCTTA TGTTACCCAC TGCAGGTACT CTGGTATCTC AGGTGATGGG 780
TAAGGCCATG GAGCTTCCAA ATATTCCTCT CCATTGTGTT ACACTACCAG GGTAGGTGGA 840
AGGGCAGAGC CTGGTAGGGC CTAGGTCAGG CAAGTTTGTA CTCTGGCTTC CCAAGTGTGG 900
ACACAAGCAG TGGCCCCACT GAAGATCAGA CAGCTGTTCC CTGGCTGCTG GGAGGAGCAC 960
AGCTGCCTCT GCTGCACAAA AAGATCCACG CAGGAAGCAG GGGATAGCAG GTGGCAATAA 1020
GCCCCACTCA GCTACTCAGC TCCTACTTAT CTGGCAATAC AGGTCTCACA CTTGGGTTCC 1080
AGGCAGCCTG TACTCAGAAC TCAAAACTGC CCCAGGCTCT AGGCCTACCC AACTGAGACA 1140
GAAACAGTGG CTTTCAGGTT ATACCCCTTC CAGTCCATCC ACAAAGCAGG CACCCAGCTC 1200
CTGTGCCCAT TTCTTAGCAC ACTTCCTGCT CTCCCCTTGG TTCTGGGCAT CAGGTTTCAT 1260
CCCCCTTGAG ATTATATCAC AAATATCAAT TCGGAGCTTC TGTCAACCTG TGACCACTGC 1320
CTGAGTTAGC TGGCAGACTT CTGTAAGGTC CCCTGAGACA GGATCAGGAA TGGCTTCCCT 1380
CCACCCCGCT GGAGTCTGGG 1400
|
