| Tag | Content |
|---|
EnhancerAtlas ID | HS053-11863 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr14:23605300-23607120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr14:23606283-23606299 | GTGCTTTCTAAGAACC | + | 6.26 | | HSF1 | MA0486.2 | chr14:23606662-23606675 | TTCCAGAACATTC | + | 6.62 | | ZNF263 | MA0528.1 | chr14:23605776-23605797 | GAAGGAGGGAAGGAGAAGGAA | + | 6.28 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27342 | chr14:23606678-23608362 | Esophagus |
|
| | 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 |
| GH14I023137 | chr14 | 23606522 | 23608521 |
|
Enhancer Sequence | AGAATAGTCA TTTACTTTGT AATTTGTGTA TGGAGTAGAC TGAAGCGAAC AGCAGCAGCT 60
AATCAGAAGT GTGGGAGCTG ACTGTATCCC CAAGTACCCA TAAGCAGTAA CCATCATGAA 120
CTCCCTAGGC CGGTGTCACT AGTTTCATGC AGCCATACAC ATCCCTGTCC CCTCTCCCAT 180
GCTACTGCCC CTCTACAGGG CAGTCTCATG CACCAGGTGC TCTGTGGGGC TCATCGTGCA 240
CATAGCCAGG GTCCTGCACT CACGTCCCCC CTCCACATGC AGACAAGACC AAGTGTAATT 300
GTCCAGATCC AACAGCATTT GCAAGTGTCA GGTTCACAAG AGACAGTCCT TGCCCAGCTA 360
GCCGATAACG GAGGAGACGA TGACATTAAG CATAACACAC ATCCACACAC TCTGACTCTT 420
CAGGAAGGAT CATCCTCTCC CTACCCGAGA ACACAAAGGA GTGACAGAGA GATAAAGAAG 480
GAGGGAAGGA GAAGGAAGGA AGAAGGAACT GGAAAGATGA GCAGGGGAGG CCTGGGTGGG 540
TGAGGTCTGG CCTCTGAATC GGAGGTGGAG CACACCATGC GCCACCGTTT CCTGCATGCA 600
CACACGACTA GACCACATGC ACGCAGACCG CTGCTAGGCC TGCCTGAGGG ACAAACCCCA 660
CTCTAAAGTG ACTGTAGCCA GTCACTCTCC TCCAATAGAT CTCAGGGAGC CTCACGGGTC 720
ACTGTTCCTC CACCGCTTGG CCTCGGCGGG GCCTCCGTGT GGCCACTGCT CCTGTGTAAC 780
ATGCACACGA GGTTGCTGTG GGTGAGCGTC ACAGGGTCCC GGGGTACAGG GGACACCCAC 840
ACCACCTCTT TCCAGCCCTG GGTCCTAAAA ACATTGCACT CCCTTGTTAT TTCACAGGAA 900
CTCTTCCTGA TGTGACGGCT TTGGAAGCAG CTGAACTCAC GGACTCATCT TTGGAGCAGG 960
ACTGTACTTT CTGAGGGCAG GGGGTGCTTT CTAAGAACCT GGGAGGATCC CTTGAACCAC 1020
ACAAATGGAA GTCATTCAAC ATCTGCTAGC CTCAACAGCC CCTTCTGAAG ACAGCAAAAG 1080
AAAGGGCCGG GTCCCTGGAT GCATGGAGGC AGGACCTGGG ACTCGTGGAC CCGCTCGCAC 1140
TTCTGGCTTC TGAGAGTGCT CTGGGGTGGG GGTCACGGAT AAAAGGCTCT TTCTTTGGAC 1200
AAATGTTTGC TTTCCACTTT TCCCCACCCT CTCACTTCAC ATTCTCCACC TGAGTCTCAT 1260
GGGTGGCCTC AAAAAGGCCT CTACAGCCAC CTCTCTGTTG AGCAGGGAGG AGCTCTGCAT 1320
TCTTGGGGCA ATCAGGGTGA AGCCATCCCA CCTGCAGGCT AGTTCCAGAA CATTCATGGG 1380
AGGCCAGACC CAGAGGCCCC AGGCACAAGT CTCCCTCTTG GTCCCTTTCC AAATGGGGTT 1440
CTTTTCTAGC CAGCAGCAGC CTGTTTACAG GTACAGGACT GCAGCCAAGA TACTGCCTTG 1500
CTGCCAACCA CAGCCACTGA CTGGGGGCGG CGTCAGGCAG GCTGGCGGCC TCCTCTGTCT 1560
TCTGCTCCTT TTGAAATGAG ACAGGCCACT ACATGTGAAG CACCTAGGAC CCGTATGCCA 1620
CACACATCGC AGGTGACCAC GTGAGCAGCA CACACTCCTC AGCATCCACA CTGACACACA 1680
CGCCCTCATG TGAGCAGTCA CCCCTCTGCA AGCCCAACAT CCAGATGCCC ACACAGACCC 1740
CTGCTGACAG AGACAAGCCC ACCATATACA AATAGCAAAG TGCACAGCAG AGTGGCCCCT 1800
GGCCGGGGAA GGGCCCAGGC 1820
|
