Tag | Content |
---|
EnhancerAtlas ID | HS104-00808 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:22458500-22459780 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:22458560-22458579 | TGGCCTGCAGGGGGCGCCA | + | 7.87 | Myod1 | MA0499.1 | chr1:22459297-22459310 | AGCAGCTGTCCCC | + | 7.04 | Myog | MA0500.1 | chr1:22459296-22459307 | CAGCAGCTGTC | - | 6.14 | SCRT1 | MA0743.1 | chr1:22458544-22458559 | TCCCACCTGTTGCTC | - | 7.46 | SCRT2 | MA0744.1 | chr1:22458546-22458559 | CCACCTGTTGCTC | - | 7.22 | Tcf12 | MA0521.1 | chr1:22459296-22459307 | CAGCAGCTGTC | - | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65544 | chr1:22451883-22461737 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 3 | ID | Chromosome | Start | End |
GH01I022133 | chr1 | 22458521 | 22458650 | GH01I022134 | chr1 | 22458693 | 22458894 | GH01I022132 | chr1 | 22459101 | 22459250 |
|
Enhancer Sequence | GCTCTCCTGC CTGTGCCCAG CCAAGGGGTC GCCTGTGGAG CCAGTCCCAC CTGTTGCTCT 60 TGGCCTGCAG GGGGCGCCAA GAGCCCGGCT ACTGGCTGTG GGCCAGGTCC ACGTTCAGGC 120 CACAGGTGTC CCTCGGTGGG GGGACAAGGA ATTGAGCCTG ACGTTGGATC CTTTCCTGCT 180 CAGACCGAGG CTTGGCCTCT TGGAGAAGGG TGGGGGCCCT GTTTGCTCTA TGATGTGGGG 240 GCACAGAGCT GGCCCATCCC CAACTCAGTC TCTGCTCCCA CAGCATGCAG CCAAGAAGGC 300 TGCATCTGGC TGTGCTGGGC CCTGGGCTCT GGTCAAGGGA GGCACCCAAG GGCAGGGGTT 360 CTCTGGGCAG GGGGGGCAGC CTCTGACCCA CCATGACCTT GGGCAAGTCC CTGCCATACT 420 TGGAGCCTGT CTCCTTATGG GTACAGTAAA CCGGTGGGTC CATATGGCCT TTCCCACTGT 480 CGGAGTTGGT GGGCCTCCTT CTACTGGCAG GGTGGGGAGT GGCCGGGCCT CAGGGGCCTG 540 CTGGCCCCAT GCCAGGCTGA TAGATGTGTC TCTGCCATTG AATAAGTAGT AAGATGGACC 600 AGGGGAGCCA CCTGCATCCC CCCACCCAGG CTCAGAACTC AGCAAGGGGA GACTGGCTGA 660 ATGACAGTCG CAGGGGCTTA GGGTGAGCTG CTGGGCTGCC GTGGCCGTGA GTCACTGGGC 720 CAGCTTCCAG GAAGGAGCTG AGCAACCTCT TCCGTTGGCA CCAGTGCCCA CCCCCAGCCC 780 CTGCCTTCAT CTGGCACAGC AGCTGTCCCC TTCCGTACAC ACGAGGCCCA GCCCCATCCC 840 CACCCCTGTT CCCCCAGACC CCAGGGTCTC GCCCGGGCAG GGCTGGGTGC CAGGGCTGGA 900 AATGGAACCG GGCACCGGCT CTAGAGAGTG AGAACCCCAG GCATTACAGG CCCTCATCCA 960 CAATGTTTCT GCTTGCCCGT TTCAGTATCC AACTAGCATT TGGCTCCATT TCACAGATGA 1020 ACAAACTGAG GCTACGGAGA TAAAGCAACT TGCTTAAAGT CCCACAGCTA GAGCGGCGAG 1080 CTGCAGTGCA AACCCAGCCC TAACTCTCAA CTCTCTTTCC TCTGTACCTG GCTGTGGATA 1140 TGCCCCATTT ACCTGCTGAG GGGGGCTAAC ACTGCCCTTG GTGCCTCACA CAGGGCACAG 1200 TGCATAGAAG GTGTTTAATA AATGCCTGCA GCAGGATGGA GGGCTCTGTC CTGACGGGGT 1260 TCCCTCTGCT TCCCTCCTGG 1280
|