| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08109 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr13:20748530-20749940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr13:20749651-20749661 | CCCAATTAGC | + | 6.02 | | MAFF | MA0495.3 | chr13:20749117-20749132 | CTGCTGAGTCATCAA | + | 6.35 | | MAFF | MA0495.3 | chr13:20749117-20749132 | CTGCTGAGTCATCAA | - | 6.36 | | NFE2L1 | MA0089.2 | chr13:20749116-20749131 | CCTGCTGAGTCATCA | - | 6.54 | | SOX10 | MA0442.2 | chr13:20749511-20749522 | AAAACAAAGAA | + | 6.62 |
|
| | 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 |
| GH13I020174 | chr13 | 20748530 | 20750306 |
|
Enhancer Sequence | TTTGCCAGCA GTAAAAATTG CCATATTTGC TTTTGTGCTC CAGCATTTAA GAGGGGCTCA 60
GAAAGTTCTT GGGAGGTGTT GTTTGCTTAA GTGGAATGGG AAGGGGACAG GACATCTCTT 120
TCCAAAACTT AGGTTTGGTG ACTCCTGGAT TTCACACTCT CTGACTGCTT GGGTGAGGGT 180
GGAATGGAGG GCTGTCCCCC ACCCTCGCAC CTGCACGGTG GCATGCTTTC CTCCTACTCC 240
AGGGAATTCC TCGTGGCCTC ATGGCCTGGG CTGTTTCTGG CTTCAAGCTC CACGTGGCCT 300
GGCCCCAGCG GTCTGGTCCA CCTTGTACTC GGTGCCCCCG CTGCCCCCTG GCCTCAGCTG 360
GAGTGACGCA CCTCATCCAT GCGGGCCTGG CGTCTGGAAG GTGGCTGGGT CTCTCGGGCT 420
TGAGCACCAT CATCTTAGCT CCAACATGTC ATTATTCCTT CCTCACTGAG GACTTTTCTG 480
CTTCCTAATT GGTTGTTGAA GATGAGGCCC CCATGCTCTT TTAAGAAAAC CTGTTGTGCC 540
CCAGGCTTGG CTGTGATGGG CACTGACTCA TACAGAAGTA GAAAGGCCTG CTGAGTCATC 600
AACACTCGTG CGACGCCCTC GCATTTTCAT TAATGATGGC CTCCCTGCCA CACGTGAATC 660
ACTCCAGCCC GAGATCTGAA ACCAGGACAC ACCCCAGGGG CGAGGTGACG CTGAGTGAGC 720
CCAGCTGTGT CCCTTTCATG AGAACTCAGA GCACAGGGCT CTGTGTGCAT GGCCGTCCCC 780
TCCAGAGAGG AGGAAGTAAA TGCCGGGATT AGTGGAAGAT CATTTCCTTC TATTTGCCTT 840
GGCTTACGTC TTTCAGAATT CAAACACGTG CACTGTTGAC CCTGCAATGG TGGAGTTTTT 900
GGATTTTCCT TCAGTCCGAT TGCTAAAATA CTTCCCTCTC ATGTGAGCTG TTGTGAAAGT 960
CATCAGCCAG ATACCATTCT AAAAACAAAG AATGTGCTTC TCGTATGTTG CATGCTGGTT 1020
ACTGAAATAT TAGGGAATTA CATAAAGGTT TTCTGGGGCA CATATTCAAG CTGAATGATA 1080
AAATTGAAGG TCACACAAAG CTAAGGTCTT TCAAATCCTG ACCCAATTAG CTCTCTGTTA 1140
GCTCTCTGAC TTTGGACAAG CTGTCTGGTC CTCTGAAGCA TACTTTGTTC GCCCTGGGTA 1200
GGGGCCCTCT GTTTTAACAG CGTTTGGCAG ATGAAAACAT TTGCAAAGCC AAAGGACAAT 1260
GAAATCTACG GAAGCCTACC ATATGCCAAT GACTCCACCA AATGTTTTCT CTTCTTGGGA 1320
TCTTCTAAAA TTCATCTGAA TACTTATAAG TTATGCAAAT TTTGGTTATT AATCTAGGTT 1380
GTATTACCTT GGGGGAAGTC AGTTAATCTC 1410
|
