| Tag | Content |
|---|
EnhancerAtlas ID | HS138-03365 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr1:210361190-210362740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:210362272-210362287 | TGACCTCTCCCCTCC | - | 6.13 | | TEAD1 | MA0090.2 | chr1:210361718-210361728 | CACATTCCAT | + | 6.02 | | ZEB1 | MA0103.3 | chr1:210362425-210362436 | CCCACCTGCCC | + | 6.14 | | ZNF263 | MA0528.1 | chr1:210361913-210361934 | TCCACCCTCCATTCCTCCTTC | - | 6.85 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTTCCCCGC CCTTAAGAAT GTACTTATCC CAAACCTATA AGAACTAATG ATAATCCCAC 60
CACCCTTTGC TGACTCTCTT TTCGGACTCA GCCTGCCTGC ACCCAGGTGA AATAAATAGC 120
CTTATTGCTC ACACAAAGCC TGTTTGGTGG TCTCTTCACA CGGACGCGCG TGACATTTGG 180
TGCCGAAGAC CTGGGTCAGA GGGACTCCTT CGGGAGTCAT GTCCCCGGTC CTCACCCTCA 240
CTCCGTGAAG ACATCCACCT ATGACCTTGG GTCCTCAGAC CAACCAGCCC AAGGAACATC 300
TCACCAATTT CTAATCGGGT AAGCGGTCTT TTCACTCTCT TCTCCAGCCT CTCTCACTAC 360
CCTTCAATCT CCCTGTCCTT CCAATTCCAG TTATTTTTCC TCTGTAGTAG AGACAAAGGA 420
GACACATTTT ATCCGTGGAC CTAAAACTCT GGCACTGGTC ACAGACTCGG GAAGGCAGTC 480
TTCCCTTGGT GTTTAATCAC TGCGGGGATG CCTGCCTGAT TATTCACACA CATTCCATTG 540
GTGTCTGATC ACCGCAGGGA TGCCTGCCTT GGTCATTCAC CCACATTCCC CTGGTGGCAA 600
GTCAATTGTT GGGACACCTT CTTTGGCTAC TCACCCACAT TGCAGCCCAG GGCTGCTCCC 660
CACCCCGCTT CTCCGTGTCT CTACCCTTCT CTTTAAGCTT GCCTCCTTCA CTATGGGCAA 720
CCTTCCACCC TCCATTCCTC CTTCAAAACC TCTTCAACTC ACACCTGACC TAAAACCTAA 780
ATGCGTTATT TTCTTCTGCA ATACTGCTTG GCCCCAGTAC AAACTCGACA GTAGTTCCGA 840
GTGGCCACAG AATGGCACTT TCAATTTGTC TATTCTACAA GACCTAGATA ATTTTTGTCA 900
AAAAAATGGG CAAACGGTCT GAGGTGCCTG ATGTCCAGGC ATTGTTTTAC ACATCGGTCC 960
CTTCCTAATC TTTGCTCCCA ATGCAACTCA TCCCAAATCT TTCTTCTTTC TTTCCTGTCT 1020
GTTCCTTCAG TCTCCACCCC AAGCTCTGAG TCCTTTGAAT CCTCCTTTTC TATGAACCCA 1080
TCTGACCTCT CCCCTCCTCC CTAGGCTGCT CCTCGCCAGG CCGAGCCAGG TCCCAATTTT 1140
TCCTCAGCCT CTGCTCCCCC ACCCTATAAT CCTTCTATCA CCTCCCCTCC TCACACCCGG 1200
TCTGGCATAC TGTTTTGTTC CATGACTAGC CCTCCCCCAC CTGCCCAACA ATTTCCTCTT 1260
AAAGAGGTGG CTGGAGCTAA AGGCATAGTC AAGGTTAATG CTCCTTTTTC TTTAGCTGAC 1320
CTCTTCCAAA TCAGTTAGCA TTTAGGCTCT TTTTCATTAA ATATAAAAAC CCAGCCCATT 1380
TCATGGCCCG TTTGGCAACA ACCCTTAGAT GCTTTACCAC CCTAGACCCA GAGGGGCCAG 1440
AAGGTTGTCT TATTCTCCAT ATGCATTTTA TTACCCAATC CACTCCCGAC ATTAAAAAAA 1500
AAGCTCCAAA AATTAGATTC CACCCTCAAA CCCCACAACA GGACTTAATT 1550
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