| Tag | Content |
|---|
EnhancerAtlas ID | HS002-03108 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr14:71248450-71249930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:71249642-71249660 | CCTTCCTTCCCTGCTACC | - | 6.77 | | EWSR1-FLI1 | MA0149.1 | chr14:71249638-71249656 | CTTTCCTTCCTTCCCTGC | - | 7.24 | | Foxa2 | MA0047.2 | chr14:71248901-71248913 | TGTTTACATAGC | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_36405 | chr14:71247656-71254025 | HMEC |
|
| | 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 |
| GH14I070781 | chr14 | 71247857 | 71250079 |
|
Enhancer Sequence | CAGAGGAGGA AATGGGCTCA GGGTCGAGGA CTTTGCCCAA AGCCAGGTCT GCCTGATTCA 60
GAGCCCACAA CTGTACCAGC CCACAACTGT ACCAGCCCAG GTTCTCTGGC CACTTAGAAA 120
GAGGAGCTGT TTCACATGGA AGACTCAACT TCTTGGGAGC ATGGCTTTCC TAGTCAACAT 180
TCCAGGTCTG GGAATTGCCT AAAGAACCCA GGTGATGGGA CATGGCATCA GTGAACACTT 240
GGCTCTGTCT GAGCTGGGGC AGGCCGCCTT CCCTGGGAGG TCATAGCTAT GGCCTACCTG 300
CCCTATTACC AACTCTTGAA TCCTACCCCT TCTTTGAGGC CTAATTGTTC CATCAAGGCC 360
TCCCAGGGAA TTCTGCCTTC TCCAGACCCC ATCTCATGTA TCTTGACACG CTGCCCCCTA 420
CTACATCACA CTGTTCTGGT TGTTTAGGAT GTGTTTACAT AGCACAACTC CTAAGGATGG 480
AAAGAATGCA GTGGAAGTGA CCTCTATGTT ATGTATATAA TAAATTGACC GTATTTCTTA 540
CAGCATGTAT GCAATAGCAG GCACGTCAAT TTCTTATGAG GACATTTGGG TAATAAAATT 600
ACCCACATCG GTTGAGAATC ATGATCTATA CAAAAAGAAA ACATTCCAGG CTCTGTGACC 660
TGCACTTCAC CCCAGGCATT GCAGAGGAGA AAGGATTTGA GGGCAGAGGA GGAAGCGGTA 720
CAAGCCACCA CAGATACCAC CTTCATCCCA TCACCTTGCA GGCAAGGAAG TCCCAACCAC 780
AAAGGCTCGA AACACTGGGA GTTGCCATTG TGAACCACAA GTCCTTAATA GCCCTGGAAA 840
GCTATGAAAC ACCAATTAAA GTTTCCTATG AATCACTTTT CAACCTCTCC ATGTAAGAGC 900
AGGGAGGAAC CAACCTCAAG TACCTCCTCA GGCCAAGACT AGCTTTGCTC TGACTCACTG 960
TCTTTCAGTC TATGATATGG ATGCTTTTCT AATTCCTTCC TCCCACCTCC ATGTCCATTG 1020
CATGGGGAAG ATGAGACTTC CTAGCATCTT CCTAGTCTAC CTCTGAATAT TACTCTACAA 1080
ATCCTGTTCC CCATGAGACA GAGTTGAGGA TCTCACCATG GTAGGGAAAA TTCAAAACTA 1140
TACAAATTCT CTAGATGTTA CACCTCAGTT TCCAGGTGAA AGCCAGTCCT TTCCTTCCTT 1200
CCCTGCTACC TGGAAGGTGG GCATAACAGG CATACCCAGA AACTGCTGGG AAAACGCTCA 1260
AATGCCGTGT TCTCTGCCTT CAGTGAATGC CCATGTAAGG AAAAGTCTTA GAATATCTTA 1320
TTTTTCCTCA GTGGGGTCAC TTTTACTCTT CCTGGAAGGT CATTATCCCA GTCTCTCCAC 1380
CAATATACTA CACATCAAAT CAAGCATCAA AATGCTTGTA AGAAACCTAA AATTGGCCAG 1440
ATTCATGGTC CATGCAACTA GAGTCAAGCA TATAAAGCCA 1480
|
