| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00542 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:22458240-22459820 |
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 | GTAGGCGGTC TCAGGCCGAA GAAGGCCAAC CTCCCCTCCC CACCCCCTGC ATTCCTGGTC 60
TCCCAGGGGC CTCCCCGCCC CTCCTTCCTA TCTACCAGGT GGTTCCCAGG GGATGCACAG 120
ACTGGTGGTG TCCTGACAAG GCCCAGGCAG GAGCTCGGAG CCCCTTGGAG GGAAGACAAG 180
GGCAGGAAGG GGGCTGAGAA GCAGCAGAGG CTGCATTTGG AAGGGGAGGG GCCCACCCGG 240
CTTCTCAGCC CTGCCTGGGT GCTCTCCTGC CTGTGCCCAG CCAAGGGGTC GCCTGTGGAG 300
CCAGTCCCAC CTGTTGCTCT TGGCCTGCAG GGGGCGCCAA GAGCCCGGCT ACTGGCTGTG 360
GGCCAGGTCC ACGTTCAGGC CACAGGTGTC CCTCGGTGGG GGGACAAGGA ATTGAGCCTG 420
ACGTTGGATC CTTTCCTGCT CAGACCGAGG CTTGGCCTCT TGGAGAAGGG TGGGGGCCCT 480
GTTTGCTCTA TGATGTGGGG GCACAGAGCT GGCCCATCCC CAACTCAGTC TCTGCTCCCA 540
CAGCATGCAG CCAAGAAGGC TGCATCTGGC TGTGCTGGGC CCTGGGCTCT GGTCAAGGGA 600
GGCACCCAAG GGCAGGGGTT CTCTGGGCAG GGGGGGCAGC CTCTGACCCA CCATGACCTT 660
GGGCAAGTCC CTGCCATACT TGGAGCCTGT CTCCTTATGG GTACAGTAAA CCGGTGGGTC 720
CATATGGCCT TTCCCACTGT CGGAGTTGGT GGGCCTCCTT CTACTGGCAG GGTGGGGAGT 780
GGCCGGGCCT CAGGGGCCTG CTGGCCCCAT GCCAGGCTGA TAGATGTGTC TCTGCCATTG 840
AATAAGTAGT AAGATGGACC AGGGGAGCCA CCTGCATCCC CCCACCCAGG CTCAGAACTC 900
AGCAAGGGGA GACTGGCTGA ATGACAGTCG CAGGGGCTTA GGGTGAGCTG CTGGGCTGCC 960
GTGGCCGTGA GTCACTGGGC CAGCTTCCAG GAAGGAGCTG AGCAACCTCT TCCGTTGGCA 1020
CCAGTGCCCA CCCCCAGCCC CTGCCTTCAT CTGGCACAGC AGCTGTCCCC TTCCGTACAC 1080
ACGAGGCCCA GCCCCATCCC CACCCCTGTT CCCCCAGACC CCAGGGTCTC GCCCGGGCAG 1140
GGCTGGGTGC CAGGGCTGGA AATGGAACCG GGCACCGGCT CTAGAGAGTG AGAACCCCAG 1200
GCATTACAGG CCCTCATCCA CAATGTTTCT GCTTGCCCGT TTCAGTATCC AACTAGCATT 1260
TGGCTCCATT TCACAGATGA ACAAACTGAG GCTACGGAGA TAAAGCAACT TGCTTAAAGT 1320
CCCACAGCTA GAGCGGCGAG CTGCAGTGCA AACCCAGCCC TAACTCTCAA CTCTCTTTCC 1380
TCTGTACCTG GCTGTGGATA TGCCCCATTT ACCTGCTGAG GGGGGCTAAC ACTGCCCTTG 1440
GTGCCTCACA CAGGGCACAG TGCATAGAAG GTGTTTAATA AATGCCTGCA GCAGGATGGA 1500
GGGCTCTGTC CTGACGGGGT TCCCTCTGCT TCCCTCCTGG CAGAGTGCTC AGGATGGGGA 1560
AGATAAGGAT GAGGGAGGAA 1580
|
