| Tag | Content |
|---|
EnhancerAtlas ID | HS113-10837 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr14:23604820-23607120 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
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 | GAATGGCGTG AACCCGGGAG GCAGAGTGTG CAGTGAGCCA AGATTGCGCC ACTGCACTCC 60
AGCCTGGGCG ACAGAGCGAG ACTCTGCCTT AAAAAAAAAA GAAAAATTTT AAGAGAATAA 120
TTTGAATGTT CCTAGCATAA AGAAAAGACA ATATTGAAGG AGATGGGATA TCTCAATTAC 180
TCTGATTTGA TTTTTACACA TTATATCAAT GTATTGAAAC ATCATCTGTA GCTTGAAAAT 240
ATGTACATCT ATTATATACA TATGAATATG AAACTTGAAC ATAAAAATCA GCCCTCCTTC 300
CCTTTTACTC TCCTAAGAGA AAAGTGAATA TTAGAAGCTG TCAACAGTAA TTTACATGTC 360
AGTGCAAATT GGACCACTTT TTTCTTTTTT CTGGGGAAAG GCCCACCTAA GGGATGACAG 420
GCAGGGTACA GCTTGATAGG AACAAAAAGG CACATATTCA GCACACTGGG AGTTCAGAGG 480
AGAATAGTCA TTTACTTTGT AATTTGTGTA TGGAGTAGAC TGAAGCGAAC AGCAGCAGCT 540
AATCAGAAGT GTGGGAGCTG ACTGTATCCC CAAGTACCCA TAAGCAGTAA CCATCATGAA 600
CTCCCTAGGC CGGTGTCACT AGTTTCATGC AGCCATACAC ATCCCTGTCC CCTCTCCCAT 660
GCTACTGCCC CTCTACAGGG CAGTCTCATG CACCAGGTGC TCTGTGGGGC TCATCGTGCA 720
CATAGCCAGG GTCCTGCACT CACGTCCCCC CTCCACATGC AGACAAGACC AAGTGTAATT 780
GTCCAGATCC AACAGCATTT GCAAGTGTCA GGTTCACAAG AGACAGTCCT TGCCCAGCTA 840
GCCGATAACG GAGGAGACGA TGACATTAAG CATAACACAC ATCCACACAC TCTGACTCTT 900
CAGGAAGGAT CATCCTCTCC CTACCCGAGA ACACAAAGGA GTGACAGAGA GATAAAGAAG 960
GAGGGAAGGA GAAGGAAGGA AGAAGGAACT GGAAAGATGA GCAGGGGAGG CCTGGGTGGG 1020
TGAGGTCTGG CCTCTGAATC GGAGGTGGAG CACACCATGC GCCACCGTTT CCTGCATGCA 1080
CACACGACTA GACCACATGC ACGCAGACCG CTGCTAGGCC TGCCTGAGGG ACAAACCCCA 1140
CTCTAAAGTG ACTGTAGCCA GTCACTCTCC TCCAATAGAT CTCAGGGAGC CTCACGGGTC 1200
ACTGTTCCTC CACCGCTTGG CCTCGGCGGG GCCTCCGTGT GGCCACTGCT CCTGTGTAAC 1260
ATGCACACGA GGTTGCTGTG GGTGAGCGTC ACAGGGTCCC GGGGTACAGG GGACACCCAC 1320
ACCACCTCTT TCCAGCCCTG GGTCCTAAAA ACATTGCACT CCCTTGTTAT TTCACAGGAA 1380
CTCTTCCTGA TGTGACGGCT TTGGAAGCAG CTGAACTCAC GGACTCATCT TTGGAGCAGG 1440
ACTGTACTTT CTGAGGGCAG GGGGTGCTTT CTAAGAACCT GGGAGGATCC CTTGAACCAC 1500
ACAAATGGAA GTCATTCAAC ATCTGCTAGC CTCAACAGCC CCTTCTGAAG ACAGCAAAAG 1560
AAAGGGCCGG GTCCCTGGAT GCATGGAGGC AGGACCTGGG ACTCGTGGAC CCGCTCGCAC 1620
TTCTGGCTTC TGAGAGTGCT CTGGGGTGGG GGTCACGGAT AAAAGGCTCT TTCTTTGGAC 1680
AAATGTTTGC TTTCCACTTT TCCCCACCCT CTCACTTCAC ATTCTCCACC TGAGTCTCAT 1740
GGGTGGCCTC AAAAAGGCCT CTACAGCCAC CTCTCTGTTG AGCAGGGAGG AGCTCTGCAT 1800
TCTTGGGGCA ATCAGGGTGA AGCCATCCCA CCTGCAGGCT AGTTCCAGAA CATTCATGGG 1860
AGGCCAGACC CAGAGGCCCC AGGCACAAGT CTCCCTCTTG GTCCCTTTCC AAATGGGGTT 1920
CTTTTCTAGC CAGCAGCAGC CTGTTTACAG GTACAGGACT GCAGCCAAGA TACTGCCTTG 1980
CTGCCAACCA CAGCCACTGA CTGGGGGCGG CGTCAGGCAG GCTGGCGGCC TCCTCTGTCT 2040
TCTGCTCCTT TTGAAATGAG ACAGGCCACT ACATGTGAAG CACCTAGGAC CCGTATGCCA 2100
CACACATCGC AGGTGACCAC GTGAGCAGCA CACACTCCTC AGCATCCACA CTGACACACA 2160
CGCCCTCATG TGAGCAGTCA CCCCTCTGCA AGCCCAACAT CCAGATGCCC ACACAGACCC 2220
CTGCTGACAG AGACAAGCCC ACCATATACA AATAGCAAAG TGCACAGCAG AGTGGCCCCT 2280
GGCCGGGGAA GGGCCCAGGC 2300
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