| Tag | Content |
|---|
EnhancerAtlas ID | HS053-20913 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr2:47566910-47568180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr2:47567914-47567929 | TTGCCAAAAATAGCA | + | 7.13 | | SPI1 | MA0080.4 | chr2:47566982-47566996 | AACTTCCTCTTTTT | - | 7.64 | | SPIC | MA0687.1 | chr2:47566982-47566996 | AACTTCCTCTTTTT | - | 6.84 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23147 | chr2:47566863-47568328 | Colon_Crypt_1 | | SE_23871 | chr2:47567097-47567709 | Colon_Crypt_2 | | SE_27702 | chr2:47566744-47568425 | Fetal_Intestine | | SE_28615 | chr2:47566741-47568663 | Fetal_Intestine_Large | | SE_50655 | chr2:47566794-47568409 | Sigmoid_Colon | | SE_52751 | chr2:47566804-47568323 | Small_Intestine | | SE_56979 | chr2:47567409-47567926 | VACO_400 |
|
| | 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 |
| GH02I047339 | chr2 | 47566417 | 47568322 |
|
Enhancer Sequence | TTCTGTTGTT TTAAGCCACC TTGTCTGTGG CATTTTGTTA CAGCAGCCCT AGGGAACTAA 60
TACAATCTCT AAAACTTCCT CTTTTTGATG CTCCCAGTCT TTAGAATGTA AAGAAGCTCC 120
GCCCCTACCC ATGCATGGGC CAAGTATAAA GTGAGTGTTG ATAGCAGGAT ATTAAGTTGA 180
CAAAATAAAC CAGATTCAGG ATCTAAGAGC CACAGGGGAA AATCATGAAG TGGGGACTGG 240
TTGGACTGGT TTTTCTCATA AATCTCAATG ACTTTGATCC CAACCAGGTG GAATTTTAAA 300
GTTAATTGAT TTAGGGAGGA ACACCTGAGC AGCTGCACCG TGTGTGAGCC CTGTGCTAGG 360
CCCAGTGGGG AAGCCAGGTG AGTCAGGTGC TGCTGCCTTA CGGGAGCTCA TAGGATTCGC 420
CTCTACAGAA GGTGTGATGG AACAGGTCAG TCACTAGCCA AGGTGTGAGT AACAGGCTGT 480
GCAAGTTCAA AATCAAGAGA GTGATTCATT TCCCCTGGGG GAGCATCAGC CAGACTGCTT 540
CACTGAGGAG AAGGCAGTGG CGACATCTCT CTAAATATCT GACTGTGGAA TCCATAGCCC 600
AGAGAAGGTC TTGTGTGTCG ATTAGAGACA AGCAAAGGAA AACAAATCTA CCAGGAATGC 660
TGGTGTTTTC CTGGAGAGTG TTTCACTGAT CACGGGGTAG TGCTCTTTGC TCAGTGGAGA 720
GGTACAAAGC TGTCTAGCCC CTGCTTGCTC TGAGGGGGAA TTCTCTGGGC TCTCGGAACC 780
TCTTATTTTC CCTTCTGGTT CTCCACTTGG GGTGAGTGCT TATCACCACC TTCTGTAGAG 840
ATTGAGGAAA GTGGAGAAGG TACACAGAGG CTTTGGAGTT GCTAGCGATC TCAATGACAT 900
CTTGTAAGAG AGCTGGTGGC TCAAGAAGGA GAGAGCAGGC CCTTGTGTTG CATTTGCAGG 960
ATCTGGGGCA ATAGTACAGC CCACATATCT AAGCTCCATT TACGTTGCCA AAAATAGCAT 1020
AGGCCACACA TCTAAGCTCC ATCTACATTG ACACTCCATG ACCCCACGTG GGCCACCCCA 1080
GTGTCATGGC CCAGTCTGGA GAAGTGACCC TGCGAAAAAG CTGTGTATGC CCTGTAGGTA 1140
GACTTGACCC TTCTGTGCAA GAAATTTTGA TGTCCTGCGA GCACCCAGAA TGGTCTAGGA 1200
GAGAGGGAAC AGGCTCCAGT GGACATATTC TCTTCGCCCT GTTGACTCCC TCCTCCATGG 1260
GAAGAGACTT 1270
|
